| The entire DSpace / Väitöskirjat ja tutkielmat / Väitöskirjat / Bio- ja ympäristötieteellinen tiedekunta | 1 / 2023 | 2 / 2023 | 3 / 2023 | 4 / 2023 | 5 / 2023 | 6 / 2023 | 7 / 2023 | 8 / 2023 | 9 / 2023 | 10 / 2023 | 11 / 2023 | 12 / 2023 | Total |
|---|
| A gene-based approach to experimental heart transplant rejection | 10 |
4 |
10 |
2 |
5 |
6 |
2 |
3 |
4 |
4 |
6 |
2 |
58 |
| A new bacterial peptidoglycan peptidase LytU and insights into substrate recognition by lysostaphin family | 11 |
10 |
14 |
20 |
10 |
10 |
3 |
13 |
9 |
4 |
5 |
3 |
112 |
| A novel multiplexed interactome proteomics approach for studying cellular signaling | 28 |
8 |
12 |
15 |
11 |
14 |
3 |
5 |
10 |
5 |
7 |
5 |
123 |
| A Novel Phytase from Bacillus : Characterization and Production of the Enzyme | 24 |
28 |
7 |
4 |
14 |
10 |
2 |
87 |
4 |
1 |
0 |
1 |
182 |
| A Physiologically Validated Animal Model of Birth Asphyxia: from Pathophysiology to Therapeutic Intervention | 51 |
25 |
16 |
18 |
12 |
6 |
4 |
15 |
3 |
0 |
8 |
1 |
159 |
| A practice approach to experimental governance : Experiences from the intersection of everyday life and local experimentation | 10 |
5 |
3 |
14 |
5 |
4 |
18 |
15 |
1 |
3 |
2 |
3 |
83 |
| A systematic-ecological approach to Baltic Sea ice studies of algae and protists | 2 |
4 |
4 |
5 |
4 |
5 |
1 |
3 |
4 |
2 |
3 |
6 |
43 |
| Acceptor specificity studies of fucosyl- and sialyltransferases | 9 |
4 |
6 |
3 |
7 |
8 |
3 |
30 |
4 |
2 |
0 |
0 |
76 |
| Acidic pH and acidic enzymes in atherosclerosis | 8 |
3 |
6 |
8 |
9 |
8 |
7 |
6 |
12 |
13 |
3 |
1 |
84 |
| Actin Dynamics in Muscle Cells | 12 |
7 |
7 |
3 |
8 |
8 |
4 |
1 |
2 |
9 |
4 |
3 |
68 |
| Actin in transcription | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Actin regulation in dendritic spines : from synaptic plasticity to animal behavior and human neurodevelopmental disorders | 3 |
2 |
3 |
4 |
3 |
4 |
2 |
0 |
2 |
1 |
4 |
1 |
29 |
| Activation of inflammasome and protein secretion by endogenous danger and microbe-derived signals in human macrophages | 8 |
12 |
7 |
5 |
11 |
6 |
8 |
3 |
5 |
7 |
8 |
2 |
82 |
| Activation of innate immune response in human macrophages by Herpes simplex virus-1 and crystallized monosodium urate | 14 |
7 |
5 |
7 |
8 |
7 |
3 |
3 |
4 |
2 |
1 |
3 |
64 |
| Activation of innate immune responses by non-pathogenic and pathogenic bacteria in human leukocytes | 29 |
9 |
9 |
12 |
15 |
15 |
2 |
5 |
8 |
14 |
6 |
4 |
128 |
| Activation of Innate Immune Responses by Toll-Like Receptors and Influenza Viruses | 4 |
3 |
0 |
3 |
9 |
3 |
1 |
2 |
0 |
5 |
1 |
1 |
32 |
| Actors’ roles and perceptions on the opportunities to increase nature conservation effectiveness : a study of interaction between knowledge and policy process | 8 |
5 |
3 |
2 |
8 |
2 |
5 |
0 |
3 |
5 |
7 |
5 |
53 |
| Adaptation to Environmental Light Conditions in Mysid Shrimps | 9 |
6 |
8 |
16 |
10 |
3 |
0 |
2 |
3 |
4 |
5 |
5 |
71 |
| Addressing human-induced uncertainty in fisheries management : social scientific and interdisciplinary solutions using Bayesian belief networks | 4 |
1 |
1 |
1 |
4 |
7 |
1 |
2 |
3 |
1 |
2 |
1 |
28 |
| Adjustment of optically measured leaf traits to patterns of solar spectral irradiance in plant taxa from high elevations and from forest understoreys | 6 |
2 |
7 |
13 |
14 |
9 |
3 |
3 |
1 |
0 |
6 |
2 |
66 |
| Advantages and limitations of combined in situ remediation methods and mechanisms at petroleum fuel product contaminated sites | 12 |
3 |
9 |
10 |
5 |
10 |
3 |
2 |
1 |
0 |
2 |
3 |
60 |
| Affinity and Avidity of the LFA-1 Integrin is Regulated by Phosphorylation | 11 |
4 |
7 |
6 |
7 |
13 |
1 |
1 |
3 |
1 |
1 |
0 |
55 |
| Alien Species, Warming Climates, Growing Cities, and the Birds that live with them. | 0 |
0 |
0 |
0 |
0 |
126 |
4 |
5 |
12 |
9 |
13 |
6 |
175 |
| Allelopathic effects of filamentous cyanobacteria on phytoplankton in the Baltic Sea | 19 |
2 |
7 |
6 |
10 |
11 |
11 |
1 |
4 |
2 |
2 |
5 |
80 |
| Alterations of niche to stem cell communication in the aging intestine | 23 |
14 |
16 |
15 |
27 |
52 |
13 |
14 |
14 |
5 |
9 |
7 |
209 |
| Altering the 3'UTR to increase endogenous GDNF and BDNF expression | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Alternate pathways of the early secretory route in yeast | 6 |
6 |
8 |
2 |
9 |
6 |
3 |
4 |
6 |
3 |
3 |
4 |
60 |
| AMIGO and its friends in developing and adult brain | 5 |
3 |
4 |
6 |
14 |
4 |
2 |
1 |
2 |
4 |
2 |
2 |
49 |
| AMIGO-Kv2.1 potassium channel complex : Identification and association with schizophrenia-related phenotypes | 6 |
4 |
6 |
6 |
14 |
14 |
0 |
2 |
5 |
2 |
6 |
3 |
68 |
| AMPA receptor ligand-binding domain : Site-directed mutagenesis study of ligand-receptor interactions | 5 |
1 |
0 |
1 |
4 |
1 |
2 |
1 |
1 |
1 |
0 |
0 |
17 |
| Amyloid angiopathy in hereditary gelsolin amyloidosis | 13 |
4 |
6 |
0 |
7 |
4 |
2 |
6 |
3 |
1 |
5 |
4 |
55 |
| An integrative perspective on visitor spatial behaviour in urban green spaces : Linking movement, motivations, values and biodiversity for participatory planning and management | 9 |
3 |
4 |
3 |
4 |
5 |
3 |
1 |
7 |
1 |
2 |
5 |
47 |
| Anaerobic Microbial Dechlorination of Polychlorinated Dibenzo-p-dioxins and Dibenzofurans in Contaminated Kymijoki River Sediments | 8 |
4 |
2 |
1 |
8 |
2 |
6 |
2 |
7 |
3 |
4 |
4 |
51 |
| Analysing Ecological Communities with Joint Species Distribution Models | 2 |
3 |
10 |
19 |
10 |
25 |
2 |
4 |
4 |
3 |
7 |
6 |
95 |
| Analysis of nuclear actin-interacting proteins and actin-regulated transcription factors | 13 |
9 |
14 |
8 |
10 |
22 |
8 |
9 |
8 |
3 |
15 |
8 |
127 |
| Analysis of somatic mutations in leukemias | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Analyzing changes in macro-level drivers of country-specific emissions : The role of consumption, technology and trade | 2 |
0 |
4 |
2 |
10 |
6 |
3 |
0 |
1 |
2 |
2 |
0 |
32 |
| Anoxia and Oxidative Stress : Lipid Peroxidation, Mitochondrial Functions in Plants Antioxidant Status and Mitochondrial Functions in Plants | 26 |
4 |
4 |
8 |
19 |
13 |
4 |
5 |
6 |
7 |
2 |
5 |
103 |
| Ant community structure in successional mosaics of boreal forests | 5 |
2 |
2 |
6 |
7 |
7 |
1 |
2 |
5 |
2 |
1 |
3 |
43 |
| Antidepressant-induced plasticity in the adult mouse visual cortex | 13 |
2 |
6 |
6 |
13 |
5 |
5 |
4 |
3 |
6 |
4 |
7 |
74 |
| Antimicrobial resistance in the major respiratory tract pathogens : methods and epidemiology | 3 |
5 |
2 |
5 |
6 |
4 |
1 |
3 |
5 |
6 |
4 |
3 |
47 |
| Antipredator behaviour of Baltic planktivores | 2 |
4 |
5 |
2 |
6 |
4 |
2 |
1 |
2 |
3 |
2 |
4 |
37 |
| Apoplastic ROS and transcriptional response in plant stress signaling | 7 |
0 |
1 |
3 |
8 |
3 |
1 |
4 |
1 |
1 |
4 |
2 |
35 |
| Applicability of characterized variance and ecosystem interactions in water quality monitoring | 2 |
2 |
1 |
3 |
3 |
1 |
0 |
1 |
1 |
2 |
1 |
2 |
19 |
| Application of fluorescence resonance energy transfer to study syndecan-3 signaling on the surface of neural cells | 11 |
4 |
10 |
11 |
29 |
8 |
10 |
2 |
2 |
4 |
5 |
0 |
96 |
| Application of Pool-seq for variation detection and proteogenomic database creation in β-hemolytic streptococci. | 23 |
25 |
39 |
11 |
10 |
7 |
7 |
7 |
4 |
6 |
5 |
9 |
153 |
| Applications of gene sequence polymorphisms in evolutionary genetic studies of Atlantic salmon (Salmo salar) and other teleost fish species | 9 |
2 |
3 |
1 |
6 |
3 |
1 |
0 |
1 |
2 |
2 |
0 |
30 |
| Applications of residual dipolar couplings in structural studies of protein | 3 |
4 |
4 |
5 |
7 |
3 |
1 |
3 |
3 |
0 |
5 |
1 |
39 |
| Archaea in the Mycorrhizosphere of Boreal Forest Trees | 6 |
8 |
1 |
5 |
12 |
7 |
3 |
4 |
3 |
4 |
14 |
3 |
70 |
| Archaea, Bacteria, and methane production along environmental gradients in fens and bogs | 14 |
11 |
5 |
14 |
13 |
7 |
3 |
3 |
12 |
5 |
22 |
9 |
118 |
| Aspects of the antimicrobial susceptibility of Streptococcus pyogenes, Streptococcus pneumoniae and Aerococcus urinae | 26 |
23 |
44 |
29 |
36 |
13 |
13 |
15 |
4 |
3 |
2 |
7 |
215 |
| Assembling contractile actomyosin structures : From myosin folding to stress fibers governing epithelial integrity | 5 |
5 |
8 |
8 |
7 |
5 |
1 |
8 |
0 |
3 |
2 |
2 |
54 |
| Assessing oil spill risks in the northern Baltic Sea with Bayesian network applications | 10 |
5 |
2 |
5 |
10 |
8 |
2 |
1 |
4 |
2 |
0 |
1 |
50 |
| Assessing the effectiveness of different approaches to species conservation | 7 |
2 |
3 |
5 |
11 |
10 |
6 |
2 |
3 |
1 |
2 |
8 |
60 |
| Assessing the effects of climate change on Baltic Sea macroalgae : implications for the foundation species Fucus vesiculosus L. | 18 |
3 |
8 |
9 |
20 |
5 |
7 |
3 |
3 |
4 |
3 |
7 |
90 |
| Assessment of bioavailable concentrations and toxicity of arsenite and mercury in contaminated soils and sediments by bacterial biosensors | 5 |
4 |
4 |
6 |
8 |
5 |
2 |
1 |
5 |
2 |
5 |
1 |
48 |
| Assessment of copy number variations in the nebulin gene and other nemaline myopathy-causing genes | 10 |
4 |
3 |
2 |
13 |
5 |
2 |
7 |
3 |
7 |
6 |
4 |
66 |
| Assessment of natural and outer membrane vesicle (OMV) vaccine induced immunity against Neisseria meningitidis serogroup B in an infant rat infection model | 2 |
1 |
3 |
7 |
10 |
1 |
5 |
3 |
4 |
3 |
2 |
3 |
44 |
| Assignment of genetic loci and variants predisposing to migraine with aura and episodic ataxia type 2 | 20 |
5 |
4 |
6 |
11 |
6 |
0 |
3 |
4 |
1 |
3 |
1 |
64 |
| Associations between biodiversity, pollution, the commensal microbiota of children, and immune response | 10 |
9 |
18 |
16 |
12 |
13 |
3 |
10 |
8 |
11 |
15 |
7 |
132 |
| Asymmetrical flow field-flow fractionation in virus purification | 3 |
3 |
7 |
3 |
10 |
7 |
0 |
3 |
6 |
1 |
3 |
1 |
47 |
| Atheroinflammatory Properties of LDL and HDL Particles Modified by Human Mast Cell Neutral Proteases | 8 |
10 |
7 |
4 |
9 |
10 |
4 |
5 |
1 |
1 |
3 |
4 |
66 |
| Autophagosome Biogenesis : ATG4, TRIM17 and Beclin 1 localization | 5 |
9 |
4 |
4 |
11 |
3 |
3 |
2 |
4 |
3 |
1 |
4 |
53 |
| Auxin and cytokinin interactions regulate primary vascular patterning during root development in Arabidopsis thaliana | 6 |
6 |
3 |
7 |
12 |
7 |
4 |
6 |
18 |
7 |
1 |
8 |
85 |
| Avian conservation in a changing environment : species' responses and the efficiency of conservation measures | 12 |
4 |
7 |
5 |
7 |
6 |
5 |
3 |
6 |
4 |
3 |
1 |
63 |
| Avian responses in a changing climate | 0 |
0 |
0 |
0 |
0 |
62 |
11 |
20 |
9 |
2 |
3 |
3 |
110 |
| Bacterial community dynamics and perennial crop growth in motor oil-contaminated soil in a boreal climate | 9 |
6 |
3 |
16 |
10 |
6 |
2 |
1 |
2 |
0 |
0 |
1 |
56 |
| Barks and formal taxonomy in the family Annonaceae | 3 |
3 |
12 |
8 |
15 |
8 |
8 |
4 |
4 |
1 |
8 |
6 |
80 |
| Bat responses to aridity | 9 |
10 |
7 |
15 |
17 |
5 |
0 |
5 |
4 |
5 |
2 |
7 |
86 |
| Bayesian adventures among human mitochondrial lineages | 15 |
16 |
21 |
9 |
18 |
81 |
1 |
5 |
7 |
5 |
4 |
11 |
193 |
| Bayesian latent factor approaches for modeling ecological species communities | 7 |
6 |
9 |
6 |
9 |
9 |
1 |
3 |
9 |
9 |
6 |
5 |
79 |
| Bayesian Network applications for environmental risk assessment | 11 |
6 |
1 |
4 |
19 |
6 |
4 |
7 |
8 |
6 |
0 |
4 |
76 |
| Behaviour, dynamics and ecological impact of small mustelids | 2 |
6 |
5 |
6 |
2 |
4 |
1 |
5 |
3 |
4 |
1 |
10 |
49 |
| Behavioural and morphological variation in European grayling, Thymallus thymallus, populations | 2 |
6 |
3 |
5 |
5 |
4 |
2 |
2 |
2 |
2 |
1 |
2 |
36 |
| Behavioural and physiological responses to predators of captive-bred Arctic charr : significance of genetics, learning and ontogeny | 2 |
3 |
5 |
6 |
12 |
6 |
5 |
2 |
0 |
1 |
3 |
2 |
47 |
| Behavioural responses to anthropogenic disturbances | 3 |
6 |
3 |
7 |
7 |
5 |
0 |
3 |
4 |
2 |
3 |
3 |
46 |
| Behavioural, population, and genetic processes affecting metapopulation dynamics of the Glanville fritillary butterfly | 5 |
1 |
2 |
6 |
7 |
4 |
1 |
1 |
3 |
2 |
1 |
3 |
36 |
| Below-ground processes in meadow soil under elevated ozone and carbon dioxide : Greenhouse gas fluxes, N cycling and microbial communities | 1 |
2 |
0 |
4 |
7 |
1 |
2 |
2 |
2 |
0 |
0 |
0 |
21 |
| Bending the Rules of Cell Protrusions : Molecular Mechanisms and Biological Roles of Inverse-BAR Proteins in Cell Morphogenesis | 4 |
2 |
0 |
3 |
11 |
6 |
2 |
4 |
2 |
4 |
2 |
3 |
43 |
| Beneficial microbial activity supporting sustainable agriculture | 6 |
8 |
13 |
14 |
14 |
7 |
1 |
3 |
3 |
3 |
4 |
0 |
76 |
| Benthic diatom community structure in boreal streams : Distribution patterns along environmental and spatial gradients | 3 |
6 |
4 |
7 |
11 |
7 |
34 |
3 |
3 |
3 |
2 |
10 |
93 |
| Benthic fauna as mediators of carbon and nutrient cycling in the coastal Baltic Sea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Benthic resting eggs in the life cycles of calanoid copepods in the northern Baltic Sea | 0 |
2 |
1 |
6 |
7 |
2 |
0 |
1 |
3 |
2 |
0 |
0 |
24 |
| Benthic-pelagic coupling in the northern Baltic Sea : importance of bioturbation and benthic predation | 3 |
4 |
4 |
2 |
4 |
3 |
1 |
0 |
1 |
4 |
2 |
3 |
31 |
| Bidirectional signalling and phosphorylation of CD11/CD18-integrins in T cells | 1 |
2 |
9 |
2 |
8 |
4 |
5 |
1 |
3 |
1 |
0 |
2 |
38 |
| Bioavailability and toxicity of chemicals in inland waters : the importance of prevailing water chemistry and implications for risk assessment | 10 |
3 |
8 |
5 |
7 |
3 |
1 |
6 |
3 |
1 |
3 |
0 |
50 |
| Biochemical effects of inherited MMR gene mutations and diet on colon cancer risk | 6 |
1 |
8 |
10 |
16 |
11 |
8 |
2 |
2 |
2 |
2 |
3 |
71 |
| Biodiversity in golf courses and its contribution to the diversity of open green spaces in an urban setting | 53 |
54 |
39 |
27 |
45 |
25 |
8 |
6 |
12 |
14 |
14 |
14 |
311 |
| Bioinformatics analysis of HPV associated host microRNA functions and identification of viral microRNA | 13 |
15 |
7 |
14 |
8 |
2 |
4 |
2 |
3 |
3 |
5 |
4 |
80 |
| Bioinformatics analysis of intron retention events associated with the minor spliceosome | 24 |
14 |
9 |
10 |
11 |
15 |
4 |
5 |
8 |
7 |
9 |
12 |
128 |
| Biological effects of contaminants in mussels (Mytilus trossulus) transplanted in northern Baltic Sea coastal areas | 10 |
5 |
5 |
5 |
8 |
4 |
5 |
1 |
3 |
2 |
5 |
4 |
57 |
| Biological Functions of Novel Mitochondrial Proteins | 16 |
4 |
5 |
3 |
6 |
14 |
2 |
5 |
8 |
6 |
6 |
2 |
77 |
| Bioluminescence of Toxic Dinoflagellates in the Baltic Sea : From Genes to Models | 12 |
20 |
11 |
11 |
5 |
10 |
6 |
6 |
3 |
2 |
6 |
6 |
98 |
| Biomarkers for exposure and for the effects of contamination with polyhalogenated aromatic hydrocarbons in Baltic ringed and grey seals | 6 |
2 |
2 |
4 |
4 |
4 |
2 |
0 |
2 |
3 |
3 |
1 |
33 |
| Bioremediation of diesel oil contaminated soil and water | 26 |
11 |
21 |
23 |
14 |
12 |
15 |
12 |
8 |
7 |
5 |
3 |
157 |
| Bird populations in a changing world : implications for North European conservation | 5 |
7 |
8 |
5 |
9 |
7 |
2 |
7 |
5 |
10 |
7 |
1 |
73 |
| Bird's eye view of European biodiversity policy under climate change | 2 |
1 |
8 |
2 |
8 |
3 |
4 |
7 |
2 |
3 |
3 |
3 |
46 |
| Black carbon deposition in the European Arctic from the preindustrial to the present | 4 |
5 |
6 |
8 |
17 |
8 |
3 |
9 |
12 |
12 |
12 |
8 |
104 |
| Blue mussel beds as biodiversity hotspots on the rocky shores of the northern Baltic Sea | 17 |
8 |
12 |
5 |
14 |
6 |
8 |
0 |
3 |
6 |
3 |
3 |
85 |
| BMP/Dpp signaling and epithelial morphogenesis in Drosophila development | 5 |
4 |
0 |
2 |
5 |
3 |
0 |
2 |
2 |
8 |
12 |
9 |
52 |
| Boosting Beneficial Microbial Exposure of Urbanites through Nature-Based Recreation and Biodiverse Elements | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Bovine milk TGF-(beta)2, IGF-1 and insulin in indirect heat treatments and filtration processes | 24 |
20 |
15 |
10 |
25 |
10 |
9 |
7 |
8 |
9 |
9 |
5 |
151 |
| Brain Immune Gene Network in Inbred Mouse Models of Anxiety- and Sociability-related Neuropsychiatric Disorders | 5 |
2 |
3 |
7 |
4 |
3 |
1 |
3 |
3 |
1 |
1 |
0 |
33 |
| Brain-sparing responses in brain pH and O2 levels in a rodent model of birth asphyxia : from mechanisms to novel therapeutic approaches | 4 |
4 |
7 |
3 |
11 |
2 |
3 |
4 |
1 |
1 |
1 |
3 |
44 |
| Breast cancer-predisposing genes in Finnish breast and ovarian cancer families | 1 |
2 |
1 |
1 |
6 |
2 |
0 |
1 |
1 |
4 |
1 |
0 |
20 |
| Bustle behind the scenes of action : nemosis as a model for fibroblast inflammatory activation | 6 |
0 |
3 |
5 |
11 |
1 |
4 |
0 |
2 |
2 |
0 |
3 |
37 |
| Butterflies in changing weather conditions : implications for ecology and conservation | 15 |
11 |
3 |
6 |
13 |
9 |
9 |
4 |
3 |
2 |
1 |
0 |
76 |
| Butterfly view of environmental variability in population dynamics across fragmented landscapes | 2 |
150 |
24 |
6 |
8 |
14 |
5 |
6 |
4 |
4 |
10 |
4 |
237 |
| c-Jun and its targets in fibrosarcoma and melanoma cells | 1 |
3 |
3 |
2 |
3 |
2 |
4 |
2 |
3 |
1 |
1 |
3 |
28 |
| CADASIL : molecular studies on the most common hereditary vascular dementing disorder | 16 |
7 |
9 |
6 |
8 |
12 |
4 |
4 |
5 |
10 |
13 |
2 |
96 |
| Calm or storm? : Wind power actors perceptions of Finnish wind power and its future | 10 |
2 |
3 |
5 |
11 |
2 |
33 |
74 |
3 |
1 |
3 |
0 |
147 |
| Can you see me? : Sexual signalling in an artificially lit world | 297 |
46 |
41 |
15 |
14 |
11 |
5 |
4 |
2 |
5 |
4 |
1 |
445 |
| Candidate therapeutic targets against acute myeloid leukemia identified via screening combinatorial peptide and chemical libraries | 3 |
1 |
1 |
0 |
9 |
12 |
0 |
5 |
2 |
1 |
3 |
4 |
41 |
| Cannibalism and conflict in Formica ants | 4 |
1 |
7 |
4 |
9 |
8 |
3 |
1 |
3 |
0 |
1 |
1 |
42 |
| Canonical Wnt Signaling in Hair and Mammary Gland Patterning and Development | 7 |
10 |
3 |
27 |
10 |
8 |
5 |
8 |
4 |
3 |
2 |
3 |
90 |
| Capsids, Matrices and Vesicles : Structural Insights into the Assembly of Paramyxoviruses | 7 |
3 |
3 |
5 |
10 |
9 |
2 |
2 |
3 |
4 |
3 |
3 |
54 |
| Carabid beetles (Coleoptera, Carabidae) as indicators of environmental change in Ranomafana National Park, Madagascar | 4 |
4 |
3 |
9 |
10 |
17 |
4 |
7 |
2 |
1 |
7 |
3 |
71 |
| Carabid beetles (Coleoptera, Carabidae) in boreal managed forests : meso-scale ecological patterns in relation to modern forestry | 13 |
6 |
2 |
6 |
7 |
6 |
2 |
0 |
2 |
1 |
0 |
1 |
46 |
| Carbon dioxide and methane exchange between a boreal pristine lake and the atmosphere | 8 |
4 |
4 |
3 |
7 |
3 |
8 |
7 |
10 |
5 |
5 |
2 |
66 |
| Causes and consequences of inbreeding in the ant Formica exsecta | 5 |
1 |
2 |
4 |
10 |
2 |
2 |
1 |
4 |
3 |
0 |
2 |
36 |
| Causes and consequences of variation in nestling immune function | 8 |
1 |
2 |
7 |
10 |
3 |
3 |
1 |
0 |
1 |
1 |
1 |
38 |
| Causes and consequences of within-host parasite communities | 4 |
13 |
8 |
5 |
11 |
9 |
3 |
4 |
1 |
7 |
2 |
7 |
74 |
| CD8+ T Cell Response in Experimental Chlamydia pneumoniae Infection | 7 |
2 |
0 |
4 |
7 |
4 |
1 |
4 |
2 |
5 |
6 |
2 |
44 |
| Cell cycle regulation during plant growth and development, gene expression studies in Arabidopsis thaliana (L.) Heynh. | 20 |
4 |
6 |
9 |
11 |
6 |
2 |
3 |
6 |
7 |
10 |
4 |
88 |
| Cell Cycle Regulation via Growth Factor- and Stress-Induced Pathways | 3 |
2 |
2 |
3 |
6 |
3 |
2 |
3 |
1 |
1 |
4 |
0 |
30 |
| Cell fates in nephrogenesis and spermatogenesis | 6 |
1 |
5 |
6 |
6 |
4 |
3 |
1 |
5 |
2 |
7 |
4 |
50 |
| Cell-Surface Association between Progelatinases and beta² Integrins : Role of the Complexes in Leukocyte Migration | 10 |
2 |
0 |
3 |
2 |
3 |
1 |
4 |
3 |
3 |
0 |
2 |
33 |
| Cellular differentiation in the inner ear : The role of the network of transcription factors and the Rho GTPase Cdc42 | 6 |
0 |
4 |
4 |
10 |
4 |
1 |
4 |
1 |
3 |
2 |
0 |
39 |
| Cellular fates and secretion ofAlzheimer’s disease-related proteins APP and tau | 7 |
4 |
3 |
7 |
5 |
8 |
6 |
7 |
8 |
14 |
13 |
8 |
90 |
| Cellular Membranes as a Playground for Semliki Forest Virus Replication Complex | 4 |
2 |
2 |
3 |
5 |
7 |
3 |
2 |
7 |
3 |
1 |
2 |
41 |
| Cellular Physiology and Cell-to-Cell Propagation of Tau in Neurodegeneration : The Impact of Late-Onset Alzheimer's Disease Susceptibility Genes | 2 |
3 |
3 |
5 |
6 |
6 |
4 |
5 |
3 |
2 |
2 |
4 |
45 |
| Cellular Regulation of Glial Cell Line-Derived Neurotrophic Factor | 8 |
2 |
3 |
5 |
2 |
1 |
0 |
2 |
3 |
4 |
3 |
5 |
38 |
| Chaga Genome and Convergent Evolution of Betulinate Biosynthesis in Host (Betula pendula) and the Pathogen (Inonotus obliquus) | 11 |
7 |
10 |
8 |
8 |
4 |
3 |
3 |
7 |
2 |
5 |
1 |
69 |
| Changes in soil C dynamics and N2O emissions under minimum tillage cereal crop production in boreal agroecosystems : Implications to climate change mitigation | 11 |
6 |
2 |
3 |
7 |
4 |
1 |
1 |
3 |
3 |
1 |
2 |
44 |
| Changing climate and the Baltic region biota | 11 |
7 |
8 |
5 |
6 |
5 |
11 |
2 |
2 |
5 |
5 |
7 |
74 |
| Characterisation and source identification of pollution episodes caused by long-range transported aerosols | 3 |
6 |
8 |
10 |
15 |
6 |
3 |
5 |
2 |
6 |
1 |
3 |
68 |
| Characterisation of cellular defects in Niemann-Pick type C disease | 1 |
0 |
0 |
2 |
3 |
2 |
0 |
3 |
1 |
1 |
2 |
1 |
16 |
| Characterisation of diverse microbial communities and application of novel detection techniques | 16 |
8 |
6 |
9 |
12 |
7 |
3 |
2 |
4 |
3 |
4 |
0 |
74 |
| Characterisation of the type three secretion system in Erwinia carotovora | 8 |
3 |
3 |
6 |
11 |
11 |
1 |
1 |
1 |
3 |
5 |
7 |
60 |
| Characterisation, cloning and production of industrially interesting enzymes : gluconolactone oxidase of Penicillium cyaneo-fulvum and gluconate 5-dehydrogenase of Gluconobacter suboxydans | 2 |
3 |
5 |
7 |
12 |
5 |
2 |
2 |
6 |
0 |
3 |
2 |
49 |
| Characterization and selective modulation of chamber-specific gene regulatory networks underlying congenital and adult heart disease | 7 |
7 |
9 |
4 |
18 |
4 |
4 |
4 |
5 |
1 |
2 |
7 |
72 |
| Characterization of Drosophila melanogaster Manf an evolutionarily conserved neurotrophic factor | 4 |
1 |
2 |
4 |
8 |
6 |
3 |
2 |
1 |
5 |
6 |
4 |
46 |
| Characterization of genomic diversity in extraintestinal pathogenic Escherichia coli (ExPEC) and development of a diagnostic DNA microarray for the differentiation of ExPEC isolates causing urinary tract infections | 13 |
2 |
6 |
7 |
5 |
4 |
0 |
1 |
2 |
4 |
3 |
2 |
49 |
| Characterization of meningeal lymphatic vessels in physiological and pathological conditions | 0 |
0 |
0 |
0 |
139 |
35 |
5 |
3 |
81 |
4 |
11 |
6 |
284 |
| Characterization of New Viruses from Hypersaline Environments | 11 |
5 |
7 |
6 |
15 |
9 |
5 |
3 |
6 |
1 |
2 |
1 |
71 |
| Characterization of potato allergens | 4 |
4 |
1 |
4 |
4 |
2 |
2 |
4 |
3 |
2 |
3 |
0 |
33 |
| Characterization of small GTPase Cdc42 from the ectomycorrhizal fungus Suillus bovinus and Agrobacterium tumefaciens-mediated transformation of fungi | 19 |
2 |
2 |
6 |
11 |
7 |
7 |
9 |
6 |
2 |
3 |
2 |
76 |
| Characterization of the molecular components and function of BARE-1, Hin-Mu and Mu transposition machineries | 1 |
1 |
1 |
1 |
4 |
4 |
2 |
4 |
1 |
1 |
3 |
2 |
25 |
| Chloroinformatics | 20 |
20 |
23 |
17 |
33 |
36 |
0 |
2 |
0 |
0 |
2 |
1 |
154 |
| Chrysophyte stomatocysts and their biogeography in Finland | 4 |
1 |
7 |
3 |
8 |
6 |
2 |
2 |
6 |
3 |
3 |
1 |
46 |
| Circadian Rhythm Disruptions and Health | 12 |
12 |
1 |
7 |
10 |
4 |
2 |
2 |
4 |
1 |
3 |
0 |
58 |
| Cladocera as sentinels of aquatic mine pollution | 17 |
5 |
5 |
5 |
4 |
9 |
5 |
8 |
3 |
6 |
2 |
4 |
73 |
| Climate change and the future distribution of palsa mires : ensemble modelling, probabilities and uncertainties | 8 |
8 |
4 |
8 |
12 |
8 |
7 |
3 |
5 |
6 |
5 |
5 |
79 |
| Climate Change as a Political Process : The Rise and Fall of the Kyoto Protocol | 145 |
108 |
156 |
146 |
182 |
125 |
71 |
36 |
103 |
48 |
61 |
58 |
1239 |
| Climate change, species range shifts and uncertainty : A new era of conservation planning | 7 |
6 |
8 |
10 |
11 |
5 |
10 |
4 |
2 |
3 |
9 |
5 |
80 |
| Climate forcing on avian life history | 5 |
3 |
6 |
5 |
8 |
5 |
1 |
2 |
2 |
5 |
3 |
1 |
46 |
| Climate Impacts on Remote Subarctic Lakes in Finnish Lapland : Limnological and Palaeolimnological Assessment with a Particular Focus on Diatoms and Lake Saanajärvi | 6 |
1 |
0 |
1 |
4 |
2 |
1 |
1 |
5 |
8 |
5 |
1 |
35 |
| Climatic effect of light-absorbing impurities on snow : experimental and field observations | 11 |
2 |
3 |
3 |
4 |
5 |
2 |
2 |
5 |
0 |
1 |
0 |
38 |
| Cloister, manor and botanic gardens in medieval and early modern Finland and Sweden : An archaeobotanical approach to garden history | 10 |
6 |
11 |
10 |
19 |
8 |
7 |
7 |
10 |
2 |
25 |
20 |
135 |
| Closed-circuit hypolimnetic withdrawal : biogeochemical considerations and potential in lake restoration | 42 |
35 |
31 |
11 |
18 |
17 |
10 |
20 |
14 |
45 |
2 |
6 |
251 |
| CMGC kinases and Cancer | 10 |
6 |
8 |
8 |
27 |
19 |
17 |
3 |
5 |
8 |
9 |
4 |
124 |
| CMV-, EBV-, and HHV-6-DNAemia after liver transplantation | 10 |
7 |
5 |
5 |
5 |
2 |
1 |
2 |
3 |
1 |
0 |
2 |
43 |
| Coagulation Factor XIII (FXIII) and Vascular Endothelial Growth Factors VEGF and VEGF-C Produced by Platelers : From Clinical Findings to Molecular Characteristics | 7 |
5 |
3 |
7 |
8 |
5 |
5 |
3 |
2 |
3 |
4 |
3 |
55 |
| Coastal environmental gradients : Key to reproduction habitat mapping of freshwater fish in the Baltic Sea | 4 |
6 |
5 |
5 |
15 |
7 |
2 |
2 |
2 |
2 |
0 |
4 |
54 |
| Colour polymorphism as a proxy for adaptations to climate change : from geographical patterns to mechanisms in Tawny Owls | 14 |
19 |
20 |
17 |
16 |
29 |
8 |
47 |
53 |
7 |
6 |
3 |
239 |
| Combining biochemistry to dentistry : from in vitro Candida glabrata observations to an in vivo clinical lingonberry application | 7 |
2 |
4 |
9 |
11 |
5 |
3 |
5 |
1 |
62 |
14 |
3 |
126 |
| Coming to terms with conservation under climate change : Using species distribution models and translocation trials for estimating the need and potential of assisted migration | 13 |
1 |
2 |
6 |
6 |
8 |
5 |
1 |
6 |
1 |
1 |
0 |
50 |
| Communities of wood-inhabiting fungi : Ecological requirements and responses to forest management and fragmentation | 8 |
4 |
1 |
5 |
14 |
13 |
91 |
54 |
2 |
4 |
1 |
25 |
222 |
| Comparative and functional genome analysis of fungi for development of the protein production host Trichoderma reesei | 4 |
1 |
1 |
3 |
4 |
5 |
1 |
0 |
1 |
3 |
0 |
2 |
25 |
| Comparative Evaluation of Methods for Sequence Alignment and Annotation | 8 |
3 |
2 |
7 |
9 |
5 |
3 |
2 |
3 |
1 |
1 |
1 |
45 |
| Composition and structure of barley (Hordeum vulgare L.) grain in relation to end uses | 28 |
61 |
43 |
37 |
50 |
31 |
14 |
4 |
13 |
3 |
9 |
8 |
301 |
| Computational Approaches to Biological Network Inference and Modeling in Systems Biology | 23 |
6 |
10 |
9 |
7 |
4 |
1 |
2 |
4 |
2 |
1 |
0 |
69 |
| Computational frameworks to aid pharmacological studies : Tools, Databases and Prediction models | 7 |
8 |
5 |
5 |
6 |
4 |
2 |
4 |
25 |
11 |
1 |
7 |
85 |
| Computational genomics of lactobacilli | 11 |
9 |
9 |
36 |
9 |
6 |
2 |
4 |
3 |
0 |
6 |
6 |
101 |
| Computational investigation of oxygen reduction and proton pumping in cbb3-type Cytochrome c Oxidases | 12 |
4 |
4 |
9 |
4 |
4 |
2 |
7 |
2 |
2 |
4 |
3 |
57 |
| Computational tools for high-throughput drug combination screening, synergy scoring and predictive modelling in cancer | 45 |
35 |
39 |
23 |
27 |
20 |
12 |
12 |
19 |
9 |
6 |
10 |
257 |
| Concentrations of mercury (Hg) and cadmium (Cd), and the condition of some coastal Baltic fishes | 6 |
2 |
6 |
6 |
7 |
2 |
1 |
3 |
4 |
2 |
1 |
2 |
42 |
| Conceptual and statistical modelling of environmental effects in population dynamics | 2 |
2 |
2 |
2 |
6 |
4 |
2 |
0 |
0 |
2 |
3 |
5 |
30 |
| Condition-dependence of fitness-related traits in the Glanville fritillary butterfly | 6 |
4 |
2 |
6 |
10 |
6 |
1 |
1 |
2 |
1 |
3 |
4 |
46 |
| Connecting silvan and lacustrine ecosystems : transport of carbon from forests to adjacent water bodies | 9 |
4 |
5 |
5 |
12 |
4 |
2 |
1 |
1 |
4 |
2 |
6 |
55 |
| Connective tissue formation in wound healing : An experimental study | 7 |
9 |
13 |
18 |
27 |
17 |
8 |
6 |
5 |
4 |
3 |
2 |
119 |
| Consequences of Balanced Translocations and Loss-of-function Mutations | 14 |
15 |
18 |
13 |
87 |
9 |
5 |
5 |
12 |
3 |
5 |
1 |
187 |
| Conservation biology of Saimaa ringed seal (Phoca hispida saimensis) with reference to other European seal populations | 17 |
19 |
12 |
11 |
18 |
11 |
7 |
6 |
7 |
40 |
11 |
6 |
165 |
| Conservation genetics of endemic Indirana frogs of the Western Ghats biodiversity hotspot | 2 |
2 |
4 |
5 |
11 |
9 |
5 |
0 |
5 |
3 |
3 |
1 |
50 |
| Conservation of Atlantic salmon by supplementary stocking of juvenile fish | 14 |
9 |
5 |
13 |
19 |
9 |
3 |
2 |
8 |
4 |
2 |
1 |
89 |
| Context-dependent mate choice in the sand goby, Pomatoschistus minutus | 2 |
0 |
1 |
2 |
5 |
3 |
2 |
1 |
1 |
4 |
2 |
2 |
25 |
| Control of plankton and nutrient limitation in small boreal brown-water lakes : Evidence from small- and large-scale manipulation experiments | 7 |
0 |
1 |
1 |
5 |
1 |
2 |
2 |
1 |
3 |
1 |
3 |
27 |
| Control of vascular integrity via endothelial growth factor and integrin cell adhesion receptor pathways | 11 |
13 |
20 |
8 |
14 |
6 |
7 |
8 |
5 |
6 |
10 |
8 |
116 |
| Conversion of GDP-mannose into various GDP-deoxyhexoses in Gram-negative bacteria | 5 |
1 |
5 |
4 |
9 |
4 |
1 |
2 |
6 |
2 |
2 |
5 |
46 |
| Cooperation and conflict in conspecific brood parasitism : an alternative reproductive tactic | 6 |
4 |
2 |
2 |
4 |
2 |
1 |
1 |
2 |
2 |
5 |
3 |
34 |
| Coping with contested risks : exploring how oil spill risks are governed through governmentalities | 5 |
7 |
1 |
4 |
6 |
4 |
3 |
4 |
3 |
2 |
1 |
3 |
43 |
| Copy number variants in genes causing neuromuscular disorders | 17 |
13 |
17 |
14 |
8 |
14 |
18 |
49 |
16 |
8 |
6 |
2 |
182 |
| Cortinarius subgenus Telamonia p.p. in North Europe | 30 |
30 |
31 |
13 |
19 |
12 |
9 |
13 |
5 |
5 |
12 |
13 |
192 |
| Cracking the code of chikungunya virus : inhibitors as tools to explore alphavirus biology | 10 |
20 |
9 |
6 |
13 |
8 |
2 |
0 |
4 |
5 |
3 |
9 |
89 |
| Critical bistability and large-scale synchrony in human brain dynamics | 9 |
72 |
16 |
32 |
56 |
22 |
11 |
11 |
3 |
4 |
16 |
8 |
260 |
| Cross-reactive immune responses between enteroviruses and islet cell autoantigens | 2 |
1 |
0 |
3 |
7 |
6 |
30 |
3 |
3 |
3 |
4 |
4 |
66 |
| Crosstalk in Plant Responses to Biotic and Abiotic Stresses | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Cryo-EM in structural virology : dissecting the icosahedral capsid | 6 |
7 |
5 |
5 |
5 |
6 |
5 |
2 |
2 |
4 |
3 |
2 |
52 |
| Cultural Ecosystem Services of urban forests : a delivery from biodiversity, through the landscape, to beneficiaries | 0 |
0 |
0 |
0 |
0 |
64 |
8 |
6 |
10 |
3 |
2 |
8 |
101 |
| Culture Systems and Quality Parameters for Clinical-grade Mesenchymal stromal cells | 13 |
8 |
12 |
4 |
12 |
15 |
3 |
13 |
5 |
7 |
6 |
8 |
106 |
| Cyanobacteria and their toxins in lichen symbiosis | 9 |
6 |
8 |
12 |
14 |
7 |
4 |
3 |
2 |
1 |
3 |
2 |
71 |
| Cyclic nucleotide inactivation in osteoblasts and osteosarcoma cell lines | 2 |
6 |
0 |
3 |
18 |
5 |
2 |
1 |
2 |
1 |
6 |
1 |
47 |
| Cycling of dissolved and particulate organic matter in the pelagic marine environment : Impact of phytoplankton community mortality and microbial degradation | 32 |
3 |
14 |
4 |
11 |
8 |
3 |
3 |
4 |
0 |
4 |
2 |
88 |
| Cytokinin signaling in hybrid aspen cambial development and growth | 9 |
10 |
20 |
25 |
15 |
9 |
14 |
15 |
4 |
7 |
1 |
2 |
131 |
| Cytokinin signalling in the regulation of cambial development | 4 |
2 |
1 |
1 |
8 |
2 |
0 |
1 |
5 |
1 |
1 |
1 |
27 |
| Cytokinins regulate vascular morphogenesis in the Arabidopsis thaliana root | 6 |
2 |
1 |
4 |
15 |
4 |
2 |
4 |
6 |
1 |
13 |
7 |
65 |
| Data limited fisheries : Incorporating expert knowledge into stock assessment | 5 |
6 |
4 |
2 |
5 |
1 |
3 |
1 |
2 |
1 |
1 |
4 |
35 |
| Deadwood and wood-inhabiting fungi in urban forests - Biodiversity conservation potential in cities | 11 |
10 |
12 |
10 |
9 |
10 |
4 |
3 |
18 |
11 |
12 |
14 |
124 |
| Death pathways activated in the neurotrophic factor-deprived neurons | 8 |
3 |
1 |
1 |
8 |
3 |
1 |
0 |
3 |
3 |
6 |
3 |
40 |
| Decisions to adapt : trade-offs, maladaptation and transformations in Nordic agri-food systems | 4 |
15 |
14 |
5 |
9 |
5 |
0 |
6 |
7 |
3 |
3 |
0 |
71 |
| Degradation of 2,6-dichlorobenzonitrile and 2,6-dichlorobenzamide in groundwater sedimentary deposits and topsoil | 10 |
13 |
7 |
8 |
12 |
5 |
3 |
4 |
4 |
1 |
4 |
3 |
74 |
| Demethyl (C-11) cezomycin : a novel calcimycin antibiotic from the symbiotic, N | 4 |
2 |
2 |
3 |
7 |
3 |
2 |
0 |
4 |
1 |
1 |
0 |
29 |
| Detecting novel cancer predisposing mutations by utilizing the Finnish Cancer Registry and archival tissue material | 1 |
7 |
6 |
7 |
6 |
9 |
5 |
3 |
7 |
2 |
2 |
2 |
57 |
| Determinants of Endoplasmic Reticulum Structure and Dynamics | 6 |
2 |
3 |
7 |
74 |
11 |
1 |
2 |
3 |
12 |
15 |
25 |
161 |
| Determining the Optimal Release Window for Lake-Stocked Brown Trout : Interactions between Release Size, Prey Availability, Predation Risks and Fishing Mortality | 2 |
7 |
1 |
1 |
4 |
2 |
2 |
3 |
3 |
2 |
1 |
1 |
29 |
| Developing glutamatergic connectivity in the hippocampus : the role of tonically active kainate receptors | 3 |
1 |
0 |
4 |
12 |
12 |
1 |
3 |
3 |
3 |
8 |
8 |
58 |
| Developing more effective conservation and research : the case of the Siberian flying squirrel | 7 |
8 |
9 |
7 |
13 |
8 |
4 |
5 |
4 |
1 |
3 |
1 |
70 |
| Developing sustainability through systems thinking : perspectives to maritime traffic | 22 |
14 |
23 |
8 |
5 |
3 |
5 |
3 |
8 |
2 |
1 |
3 |
97 |
| Development and evolution of tooth renewal and dental formula in squamate reptiles | 10 |
13 |
21 |
18 |
20 |
11 |
10 |
9 |
11 |
11 |
11 |
7 |
152 |
| Development of microfluidic applications to study the role of kainate receptors in synaptogenesis | 4 |
3 |
4 |
1 |
5 |
3 |
5 |
2 |
1 |
2 |
3 |
1 |
34 |
| Development of new automated methods for quantification of immunohistochemically stained cells | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
33 |
27 |
60 |
| Development of NMR methods to study disordered proteins | 3 |
2 |
0 |
2 |
10 |
8 |
75 |
48 |
3 |
8 |
3 |
2 |
164 |
| Development of transgenic crops protected from insect damage and transgene escape | 8 |
18 |
0 |
0 |
4 |
4 |
2 |
1 |
1 |
2 |
2 |
1 |
43 |
| Developmental Growth and Regeneration Processes in Squamate Eyes | 8 |
12 |
5 |
4 |
19 |
5 |
4 |
2 |
5 |
5 |
4 |
6 |
79 |
| Developmentally Regulated Induction and Expression Mechanisms of Long-Term Potentiation at Hippocampal CA3 CA1 Synapses | 5 |
2 |
0 |
3 |
15 |
16 |
4 |
6 |
2 |
3 |
1 |
3 |
60 |
| Developmentally regulated proteins in Pinus sylvestris roots and ectomycorrhiza | 2 |
1 |
1 |
0 |
6 |
2 |
2 |
1 |
3 |
1 |
2 |
3 |
24 |
| Diamond-like carbon binding peptides evolutionary selection, characterization, and engineering | 4 |
11 |
5 |
9 |
12 |
11 |
4 |
3 |
8 |
5 |
9 |
2 |
83 |
| Diatoms, dinoflagellates and their distinct effects on the structure and function of the bacterioplankton | 21 |
11 |
24 |
19 |
26 |
15 |
15 |
9 |
6 |
6 |
9 |
3 |
164 |
| Dietary fibre components of rye bran and their fermentation in vitro | 9 |
5 |
3 |
2 |
9 |
6 |
1 |
9 |
3 |
5 |
4 |
1 |
57 |
| Differential abundance analyses of human microbiota in Parkinson’s disease | 17 |
11 |
7 |
7 |
10 |
6 |
8 |
5 |
9 |
3 |
2 |
4 |
89 |
| Differential functions of mammalian Cdk7 and CCRK kinases in regulating transcription and ciliogenesis | 13 |
4 |
6 |
4 |
6 |
12 |
6 |
5 |
3 |
3 |
2 |
2 |
66 |
| Differentiation of neural stem cells in fragile X syndrome | 13 |
8 |
6 |
4 |
4 |
3 |
5 |
2 |
6 |
3 |
1 |
2 |
57 |
| Diffusive and ship-mediated spread of dinoflagellates in the Baltic Sea with Prorocentrum minimum as a special case | 4 |
2 |
3 |
2 |
9 |
1 |
2 |
2 |
1 |
1 |
0 |
5 |
32 |
| Directional Hearing under Water : Morphology and Function of the Middle Ear of Globicephala macrorhynchus (Short-Finned Pilot Whale) | 5 |
5 |
8 |
6 |
5 |
8 |
6 |
38 |
63 |
3 |
6 |
6 |
159 |
| Discovery and evolutionary affinities of five new species of amphibians from Bangladesh | 10 |
5 |
5 |
2 |
9 |
5 |
1 |
5 |
2 |
1 |
3 |
3 |
51 |
| Discovery of oxidative enzymes for food engineering : Tyrosinase and sulfhydryl oxidase | 19 |
5 |
15 |
8 |
17 |
13 |
4 |
5 |
1 |
1 |
3 |
3 |
94 |
| Discovery of salt-loving pleolipoviruses infecting archaea : vesicle-like virion is the key to success | 8 |
4 |
7 |
2 |
10 |
4 |
1 |
3 |
0 |
7 |
3 |
3 |
52 |
| Disease dynamics, invasion and biological control of environmentally growing pathogens | 2 |
0 |
3 |
2 |
2 |
2 |
5 |
3 |
1 |
3 |
1 |
2 |
26 |
| Dispersal and related life history traits in the Glanville fritillary butterfly | 4 |
1 |
1 |
2 |
5 |
3 |
2 |
0 |
2 |
2 |
1 |
2 |
25 |
| Dissecting genetic susceptibility to gluten sensitivity : HLA-linked risk factors in coeliac disease and dermatitis herpetiformis | 10 |
6 |
7 |
9 |
6 |
6 |
4 |
3 |
13 |
7 |
5 |
3 |
79 |
| Dissecting VEGFR-2 and VEGFR-3 function : VEGFR-3 mediates lymphangiogenic signals | 6 |
2 |
5 |
3 |
6 |
3 |
1 |
7 |
0 |
1 |
1 |
5 |
40 |
| Dissipation of herbicides in surface soils and subsurface sediment slurries and development of treatment methods | 5 |
11 |
8 |
7 |
11 |
16 |
3 |
4 |
2 |
2 |
4 |
5 |
78 |
| Distribution and function of GABA receptor ρ subunits in the rat nervous system | 4 |
4 |
2 |
6 |
7 |
4 |
2 |
2 |
2 |
1 |
0 |
0 |
34 |
| Distribution of non-biting midges (Diptera, Chironomidae) in subarctic lakes of Finnish Lapland applications in lake classification and palaeolimnology | 4 |
2 |
5 |
4 |
8 |
9 |
3 |
0 |
2 |
2 |
0 |
0 |
39 |
| Disturbance in boreal spruce forest : immediate dynamics from stand to understorey level | 10 |
3 |
0 |
2 |
8 |
5 |
3 |
2 |
0 |
3 |
5 |
1 |
42 |
| Diversity and classification of the Scopulini (Lepidoptera: Geometridae, Sterrhinae) | 1 |
3 |
1 |
1 |
9 |
4 |
2 |
3 |
7 |
2 |
2 |
5 |
40 |
| Diversity and ecology of Termitomyces symbionts in Macrotermes mounds of the Tsavo Ecosystem, Kenya | 13 |
4 |
4 |
17 |
10 |
4 |
2 |
4 |
3 |
3 |
0 |
3 |
67 |
| Diversity and zoogeography of continental mysid crustaceans | 4 |
4 |
3 |
6 |
6 |
5 |
6 |
7 |
5 |
5 |
5 |
4 |
60 |
| Diversity of microfungi preserved in European Palaeogene amber | 7 |
7 |
5 |
5 |
8 |
5 |
2 |
3 |
5 |
2 |
7 |
1 |
57 |
| DNA Packaging and Host Cell Lysis : Late Events in Bacteriophage PRD1 Infection | 29 |
3 |
3 |
5 |
5 |
5 |
4 |
6 |
2 |
2 |
0 |
1 |
65 |
| Do we listen to earthworms? : Tools for evaluating the Finnish Action Plan on the sustainable use of plant protection products | 12 |
9 |
14 |
18 |
16 |
357 |
5 |
1 |
0 |
0 |
2 |
8 |
442 |
| Double-stranded RNA Bacteriophage phi6 : Self-assembly and Maturation of the Procapsid | 13 |
7 |
18 |
9 |
10 |
7 |
3 |
6 |
3 |
7 |
3 |
1 |
87 |
| Dung beetle communities in Madagascar | 7 |
8 |
6 |
10 |
13 |
7 |
2 |
8 |
4 |
3 |
8 |
2 |
78 |
| Dung beetle radiations in Madagascar | 3 |
3 |
2 |
1 |
4 |
3 |
2 |
1 |
2 |
2 |
3 |
4 |
30 |
| Dynamics of Dissolved Organic Matter and its Bioavailability to Heterotrophic Bacteria in the Gulf of Finland, Northern Baltic Sea | 3 |
3 |
3 |
5 |
7 |
3 |
2 |
0 |
0 |
1 |
4 |
2 |
33 |
| Dynamics of Finnish starlings in 1951-2005 : from monitoring to population modelling | 5 |
3 |
6 |
2 |
7 |
1 |
2 |
1 |
2 |
1 |
3 |
0 |
33 |
| Dynamics of nuclear actin | 3 |
3 |
5 |
3 |
5 |
6 |
4 |
0 |
3 |
2 |
0 |
1 |
35 |
| Dynamics of soil carbon and nitrogen in changing boreal environments | 8 |
2 |
5 |
3 |
16 |
5 |
0 |
11 |
0 |
2 |
1 |
3 |
56 |
| Early neuropathological changes in the mouse model for progressive myoclonus epilepsy of Unverricht-Lundborg type, EPM1 | 21 |
12 |
7 |
9 |
12 |
18 |
45 |
5 |
10 |
6 |
6 |
4 |
155 |
| Eco-experiential quality of urban forests : Combining ecological, restorative and aesthetic perspectives | 6 |
8 |
4 |
2 |
9 |
5 |
3 |
4 |
5 |
3 |
0 |
6 |
55 |
| Ecological and evolutionary role of seed banks for toxic dinoflagellate Alexandrium ostenfeldii | 29 |
12 |
7 |
14 |
13 |
13 |
6 |
6 |
1 |
4 |
2 |
1 |
108 |
| Ecological consequences of genetic modifications : an invasion analysis approach | 5 |
1 |
6 |
5 |
7 |
5 |
1 |
1 |
2 |
1 |
2 |
0 |
36 |
| Ecological factors shaping immune response and related life-history traits in the Glanville fritillary butterfly | 7 |
5 |
8 |
3 |
13 |
7 |
1 |
4 |
2 |
1 |
4 |
5 |
60 |
| Ecological fitness and interspecies interactions of food-spoilage-associated lactic acid bacteria : insights from the genome analyses and transcriptome profiles | 6 |
4 |
11 |
6 |
13 |
5 |
3 |
4 |
4 |
4 |
5 |
0 |
65 |
| Ecological impacts of Phlebiopsis gigantea biocontrol treatment against Heterobasidion spp. as revealed by fungal community profiling and population analyses | 10 |
3 |
6 |
3 |
12 |
4 |
1 |
1 |
2 |
1 |
3 |
1 |
47 |
| ecological rationale and conservation relevance | 5 |
2 |
7 |
1 |
5 |
9 |
2 |
0 |
2 |
0 |
1 |
2 |
36 |
| Ecological communities in variable environments : dynamics and diversity under coloured environmental stochasticity | 0 |
2 |
1 |
1 |
9 |
3 |
1 |
0 |
3 |
1 |
1 |
1 |
23 |
| Ecology of asexual reproduction in hepatics | 3 |
8 |
8 |
7 |
5 |
5 |
0 |
3 |
6 |
1 |
0 |
3 |
49 |
| Ecology of sympatric whitefish (Coregonus lavaretus (L.)) forms in a subarctic lake | 8 |
8 |
3 |
3 |
7 |
6 |
2 |
2 |
2 |
4 |
3 |
8 |
56 |
| Ecology of zooplankton in subarctic ponds, with a focus on responses to ultraviolet radiation | 9 |
3 |
3 |
4 |
3 |
1 |
2 |
3 |
6 |
4 |
4 |
5 |
47 |
| Ecology, population genetics and conservation of the African violet | 9 |
13 |
7 |
11 |
27 |
6 |
6 |
3 |
7 |
7 |
10 |
4 |
110 |
| Ectodermal organ development : Regulation by Notch and Eda pathways | 1 |
2 |
2 |
5 |
5 |
14 |
2 |
1 |
5 |
1 |
4 |
5 |
47 |
| Ectodysplasin in epithelial morphogenesis : from Tabby to TNFs | 14 |
4 |
1 |
3 |
3 |
1 |
0 |
2 |
6 |
2 |
1 |
0 |
37 |
| Effect of Light On Water Balance Through Gas Exchange | 7 |
6 |
1 |
3 |
7 |
8 |
8 |
2 |
1 |
0 |
0 |
2 |
45 |
| Effect of long-wave UV radiation on mouse melanoma : an in vitro and in vivo study | 2 |
5 |
5 |
1 |
9 |
4 |
0 |
0 |
4 |
2 |
1 |
1 |
34 |
| Effects of 17α-ethinyl estradiol on the mating system of the sand goby (Pomatoschistus minutus) | 5 |
4 |
1 |
3 |
11 |
3 |
2 |
1 |
2 |
0 |
2 |
0 |
34 |
| Effects of black carbon and Icelandic dust on snow albedo, melt and density | 16 |
12 |
9 |
15 |
16 |
10 |
5 |
2 |
4 |
2 |
2 |
2 |
95 |
| Effects of broodstock origin, rearing environment and release method on post-stocking performance of Atlantic salmon : Enriched rearing promotes post-stocking performance of Atlantic salmon | 12 |
10 |
12 |
8 |
10 |
10 |
1 |
6 |
1 |
6 |
9 |
9 |
94 |
| Effects of cyanobacteria on plankton and planktivores | 2 |
3 |
3 |
4 |
7 |
7 |
2 |
4 |
5 |
2 |
3 |
3 |
45 |
| Effects of ecological factors on dominance and immune defence in crayfish | 8 |
3 |
5 |
7 |
23 |
8 |
3 |
3 |
2 |
3 |
2 |
3 |
70 |
| Effects of embryological parameters on the success of fresh and frozen embryo transfers | 7 |
2 |
3 |
5 |
2 |
2 |
0 |
0 |
3 |
5 |
1 |
0 |
30 |
| Effects of environmental factors, especially temperature, on the population dynamics of pikeperch (Stizostedion lucioperca (L.)) | 7 |
4 |
12 |
9 |
15 |
4 |
5 |
6 |
3 |
2 |
3 |
1 |
71 |
| Effects of environmental variation on ecological and evolutionary dynamics | 20 |
10 |
4 |
4 |
13 |
10 |
2 |
4 |
3 |
4 |
6 |
2 |
82 |
| Effects of landscape connectivity and predator-prey interactions on diving beetle assemblages in Finnish urban ponds | 22 |
3 |
3 |
70 |
8 |
5 |
3 |
2 |
3 |
2 |
4 |
12 |
137 |
| Effects of large-scale human land use on Capercaillie (Tetrao urogallus L.) populations in Finland | 7 |
7 |
3 |
4 |
12 |
8 |
8 |
4 |
7 |
1 |
5 |
6 |
72 |
| Effects of management and landscape structure on biodiversity in boreal agricultural farmland | 2 |
3 |
4 |
3 |
10 |
3 |
1 |
2 |
2 |
3 |
1 |
2 |
36 |
| Effects of microclimatic variation of snowmelt and temperature on subarcticalpine and Arctic plants | 9 |
8 |
9 |
10 |
8 |
6 |
5 |
1 |
3 |
1 |
2 |
2 |
64 |
| Effects of oxygen provision on the physiology of baker's yeast Saccharomyces cerevisiae | 11 |
7 |
11 |
2 |
5 |
4 |
0 |
1 |
7 |
5 |
2 |
1 |
56 |
| Effects of Proatherogenic and Probiotic Bacteria on Mast Cells and Inflammation | 130 |
189 |
180 |
190 |
181 |
108 |
8 |
6 |
3 |
4 |
0 |
1 |
1000 |
| Effects of recreational use and fragmentation on the understorey vegetation and soil microbial communities of urban forests in southern Finland | 1 |
3 |
1 |
5 |
7 |
6 |
1 |
2 |
1 |
1 |
2 |
2 |
32 |
| Effects of tree cover on local air pollutant levels in near-road environments | 5 |
6 |
8 |
2 |
5 |
6 |
6 |
7 |
4 |
7 |
4 |
7 |
67 |
| Effects of turbidity on feeding and distribution of fish | 16 |
12 |
14 |
18 |
28 |
15 |
5 |
8 |
7 |
6 |
5 |
9 |
143 |
| Effects of urbanization on seasonal runoff generation and pollutant transport under cold climate | 8 |
10 |
5 |
3 |
15 |
6 |
4 |
5 |
6 |
8 |
3 |
5 |
78 |
| Efficient gene set analysis of high-throughput data : From omics to pathway architecture of health and disease | 7 |
6 |
7 |
4 |
8 |
3 |
4 |
3 |
6 |
3 |
5 |
3 |
59 |
| Electrogenic reactions in the heme-copper oxidase family of enzymes | 3 |
3 |
2 |
2 |
7 |
2 |
2 |
3 |
3 |
0 |
2 |
0 |
29 |
| Electron and proton transfer in NADH:ubiquinone oxidoreductase (Complex I) from Escherichia coli | 13 |
9 |
6 |
3 |
14 |
8 |
2 |
3 |
1 |
1 |
1 |
2 |
63 |
| Electron cryo-microscopy studies of bacteriophage phi8 and archaeal virus SH1 | 5 |
1 |
3 |
0 |
5 |
5 |
7 |
2 |
7 |
1 |
6 |
4 |
46 |
| Elucidating nebulin expression and function in health and disease | 9 |
3 |
2 |
1 |
10 |
2 |
5 |
3 |
7 |
3 |
3 |
2 |
50 |
| Embracing uncertainty in fisheries stock assessment using Bayesian hierarchical models | 1 |
2 |
9 |
3 |
6 |
6 |
0 |
0 |
3 |
1 |
0 |
0 |
31 |
| Enantioselective antibody fragments | 5 |
3 |
2 |
3 |
5 |
3 |
2 |
0 |
0 |
1 |
1 |
1 |
26 |
| Engineering the pentose phosphate pathway of Saccharomyces cerevisiae for production of ethanol and xylitol | 5 |
2 |
1 |
4 |
7 |
2 |
1 |
1 |
7 |
0 |
6 |
2 |
38 |
| Enriching Carnivore Conservation : an interdisciplinary approach to better understand human-carnivore interactions | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
17 |
41 |
42 |
11 |
111 |
| Entry of the membrane-containing bacteriophages into their hosts | 13 |
9 |
10 |
8 |
13 |
3 |
18 |
5 |
5 |
1 |
2 |
3 |
90 |
| Environmental and climatic dependences of stable isotope ratios in tree rings on different temporal scales | 3 |
5 |
4 |
6 |
5 |
3 |
1 |
4 |
1 |
0 |
6 |
3 |
41 |
| Environmental effects of thermal and radioactive discharges from nuclear power plants in the boreal brackish-water conditions of the northern Baltic Sea | 14 |
5 |
3 |
3 |
9 |
20 |
2 |
2 |
3 |
2 |
3 |
2 |
68 |
| Environmental factors and uncertainty in fisheries management in the northern Baltic Sea | 4 |
3 |
1 |
2 |
8 |
2 |
0 |
2 |
0 |
0 |
5 |
1 |
28 |
| Enzymatic synthesis of branched polylactosamines | 1 |
0 |
0 |
4 |
5 |
4 |
1 |
1 |
0 |
2 |
2 |
2 |
22 |
| Enzymatic Synthesis of Known and Novel Oligosaccharides | 4 |
1 |
2 |
6 |
5 |
1 |
4 |
5 |
2 |
0 |
0 |
1 |
31 |
| Enzymes with radical tendencies : the PFL family | 15 |
6 |
6 |
2 |
9 |
4 |
2 |
3 |
4 |
2 |
4 |
4 |
61 |
| Epidemiology of human rhinoviruses | 10 |
4 |
6 |
7 |
10 |
7 |
13 |
51 |
1 |
2 |
4 |
6 |
121 |
| Estimating complexity and adaptation in the embryo : a statistical developmental biology approach | 2 |
4 |
1 |
2 |
9 |
5 |
3 |
0 |
6 |
2 |
2 |
1 |
37 |
| European aspen and hybrid aspen under changing environment : Leaf traits, growth and litter decomposition | 3 |
1 |
0 |
0 |
6 |
8 |
25 |
4 |
2 |
0 |
2 |
0 |
51 |
| Eutrophication interferes with sand goby mating success, sexual selection, and parental care | 2 |
6 |
6 |
2 |
3 |
7 |
3 |
1 |
1 |
2 |
1 |
1 |
35 |
| Evaluating innate and learned determinants for improving antipredator behaviour of stocked fish | 1 |
0 |
2 |
5 |
3 |
0 |
2 |
3 |
9 |
1 |
0 |
1 |
27 |
| Evaluation and management of the Finnish herring fishery | 9 |
8 |
4 |
8 |
9 |
7 |
1 |
3 |
0 |
1 |
4 |
3 |
57 |
| Evaluation of in situ remediation methods in soils contaminated with organic pollutants | 12 |
7 |
4 |
7 |
13 |
8 |
2 |
1 |
9 |
4 |
4 |
3 |
74 |
| Evaluation of methods and applications for behavioural profiling of transgenic mice | 12 |
3 |
1 |
8 |
4 |
5 |
1 |
2 |
5 |
0 |
3 |
1 |
45 |
| Evolution of life-histories in stochastic environments : Cole's paradox revisited | 3 |
2 |
13 |
5 |
8 |
8 |
1 |
0 |
3 |
3 |
2 |
8 |
56 |
| Evolution of the DUF26-containing proteins in plants | 9 |
11 |
5 |
9 |
14 |
10 |
6 |
6 |
7 |
5 |
5 |
3 |
90 |
| Evolutionary and conservation biology of the Finnish house sparrow | 11 |
5 |
8 |
2 |
14 |
6 |
5 |
5 |
1 |
1 |
2 |
3 |
63 |
| Evolutionary and ecological dimensions of disease resistance | 10 |
3 |
6 |
11 |
6 |
6 |
2 |
2 |
3 |
1 |
5 |
1 |
56 |
| Evolutionary Genetics in the Wild : from Populations to Individuals | 4 |
3 |
7 |
6 |
3 |
6 |
1 |
3 |
1 |
7 |
4 |
2 |
47 |
| Evolutionary Genomics of Prokaryotic Viruses | 1 |
2 |
1 |
1 |
5 |
2 |
1 |
6 |
3 |
1 |
5 |
2 |
30 |
| Evolutionary relationships of liverworts with a special focus on the order Porellales and the family Lejeuneaceae | 5 |
5 |
2 |
7 |
11 |
8 |
1 |
5 |
5 |
2 |
11 |
7 |
69 |
| Exercise and Falls among Frail Older People : Special Focus on People with Dementia | 10 |
6 |
14 |
10 |
11 |
1 |
0 |
2 |
13 |
5 |
5 |
1 |
78 |
| Exploring the composition, variation and interactions of unicellular organisms in the marine benthic community with DNA metabarcoding | 7 |
4 |
3 |
5 |
8 |
6 |
1 |
4 |
7 |
4 |
7 |
4 |
60 |
| Exploring the role of CDNF and MANF removal in the brain and in the unfolded protein response | 12 |
16 |
9 |
11 |
6 |
5 |
5 |
8 |
4 |
2 |
4 |
3 |
85 |
| Exploring the unknown in a well-known system : Ecology and ecosystem effects of the invasive polychaete genus Marenzelleria spp. in the northern Baltic Sea | 7 |
1 |
3 |
7 |
5 |
6 |
2 |
2 |
7 |
0 |
5 |
3 |
48 |
| Exposure-related human cancer : Molecular changes in sinonasal cancer and lung cancer, with focus on TP53 mutations | 8 |
3 |
1 |
1 |
6 |
4 |
1 |
2 |
2 |
2 |
1 |
1 |
32 |
| Expression and activation of STAT and IRF family transcription factors in mononuclear leukocytes | 12 |
2 |
0 |
2 |
3 |
4 |
0 |
2 |
4 |
0 |
1 |
3 |
33 |
| Expression and characterization of neuronal membrane receptor proteins | 1 |
0 |
0 |
5 |
7 |
3 |
1 |
1 |
3 |
3 |
5 |
1 |
30 |
| Expression and functions of KCC2 in the perinatal rodent cortex | 10 |
5 |
5 |
6 |
5 |
7 |
3 |
2 |
3 |
0 |
4 |
2 |
52 |
| Expression and regulation of human activins and their receptors | 3 |
2 |
0 |
2 |
5 |
3 |
3 |
1 |
3 |
1 |
2 |
4 |
29 |
| Expression of bacterial adhesins in E.coli : From mapping of adhesive epitopes to structure | 8 |
2 |
0 |
6 |
6 |
3 |
1 |
3 |
2 |
0 |
0 |
2 |
33 |
| Expression, Enzymatic Activities and Subcellular Localization of Hepatitis E Virus and Semliki Forest Virus Replicase Proteins | 8 |
1 |
2 |
4 |
4 |
6 |
3 |
0 |
0 |
1 |
1 |
2 |
32 |
| Extended histocompatibility: Genomic prediction of kidney transplant outcome | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Extracellular ATP as a Regulator of Intracellular Signaling in Thyroid FRTL-5 Cells | 3 |
0 |
1 |
0 |
7 |
5 |
1 |
2 |
1 |
3 |
1 |
1 |
25 |
| Extracellular lipid particles in atherosclerosis and aortic stenosis | 10 |
9 |
10 |
12 |
17 |
7 |
1 |
10 |
8 |
0 |
2 |
3 |
89 |
| Extracellular Vesicles and Nanoerythrosomes : The Hidden Pearls of Blood Products | 20 |
20 |
184 |
11 |
17 |
7 |
10 |
3 |
5 |
3 |
2 |
5 |
287 |
| Extracellular vesicles in innate immunity : Proteomic investigations | 3 |
5 |
6 |
4 |
7 |
8 |
2 |
4 |
3 |
4 |
3 |
1 |
50 |
| F-actin dynamics in dendritic spines | 8 |
4 |
6 |
6 |
10 |
4 |
0 |
2 |
2 |
1 |
4 |
1 |
48 |
| Factors affecting lipid profiles in juvenile Atlantic salmon | 0 |
0 |
0 |
95 |
38 |
23 |
12 |
29 |
18 |
6 |
1 |
5 |
227 |
| Factors affecting the fatty acid profile of adipose tissues used to assess individual dietary history of grey seals and great cormorants in the Baltic Sea | 4 |
5 |
2 |
5 |
8 |
3 |
1 |
1 |
2 |
3 |
1 |
6 |
41 |
| Factors controlling carbon gas fluxes in boreal lakes | 6 |
5 |
6 |
3 |
7 |
7 |
7 |
77 |
7 |
4 |
9 |
10 |
148 |
| Factors Regulating the Substrate Specificity of A-type Phospholipases : A Mass-Spectrometric study | 5 |
3 |
2 |
1 |
5 |
7 |
4 |
1 |
5 |
3 |
2 |
8 |
46 |
| Farmland birds and habitat heterogeneity in intensively cultivated boreal agricultural landscapes | 7 |
17 |
5 |
11 |
8 |
10 |
6 |
4 |
1 |
1 |
1 |
5 |
76 |
| Fast- and drift-ice communities in the Bothnian Bay and the impact of UVA radiation on the Baltic Sea ice ecology | 5 |
1 |
5 |
6 |
7 |
4 |
8 |
0 |
5 |
1 |
2 |
2 |
46 |
| Fate and Biological Effects of Titanium Dioxide Nanoparticles in the Aquatic Environment | 7 |
5 |
2 |
4 |
11 |
4 |
1 |
4 |
1 |
0 |
1 |
3 |
43 |
| Fate and effects of Nodularia spumigena and its toxin, nodularin, in Baltic Sea planktonic food webs | 5 |
5 |
2 |
6 |
6 |
2 |
2 |
2 |
1 |
2 |
1 |
4 |
38 |
| Fate of artificial sweeteners and perfluoroalkyl acids in aquatic environment | 21 |
8 |
9 |
12 |
24 |
13 |
6 |
8 |
5 |
8 |
12 |
9 |
135 |
| Fate of Mammalian Golgi Sialyltransferases in Yeast | 6 |
6 |
2 |
0 |
3 |
2 |
1 |
2 |
3 |
0 |
0 |
2 |
27 |
| Fate of the excess phosphate in the northern Baltic Sea: Experimental perspectives | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Feeding constraints and parental care in female eiders | 0 |
1 |
1 |
3 |
6 |
3 |
1 |
2 |
3 |
1 |
2 |
1 |
24 |
| FGF signaling in neurogenesis and patterning of the developing midbrain and anterior hindbrain | 14 |
6 |
7 |
1 |
9 |
2 |
3 |
3 |
3 |
4 |
8 |
3 |
63 |
| FGFR1 regulated gene-expression, cell proliferation and differentiation in the developing midbrain and hindbrain | 3 |
6 |
6 |
1 |
13 |
8 |
6 |
7 |
4 |
3 |
3 |
7 |
67 |
| Fibroblast growth factor receptor 1 in craniofacial and midbrain-hindbrain development | 5 |
0 |
2 |
6 |
8 |
6 |
1 |
2 |
0 |
1 |
7 |
1 |
39 |
| Fibroblast growth factor receptor 1 signaling in the early development of the midbrain-hindbrain and pharyngeal region | 3 |
1 |
2 |
8 |
13 |
4 |
2 |
4 |
1 |
2 |
0 |
1 |
41 |
| Fibroblast Growth Factor Signalling in the Development of the Midbrain and Anterior Hindbrain | 8 |
5 |
3 |
6 |
8 |
8 |
7 |
4 |
7 |
5 |
1 |
0 |
62 |
| Fine morphological alterations during brain injury and recovery analyzed with intravital microscopy | 7 |
3 |
5 |
15 |
13 |
9 |
5 |
1 |
5 |
2 |
1 |
3 |
69 |
| Fine-tuning of the signalling network controlling morphogenesis and stem cell development in teeth | 1 |
2 |
3 |
7 |
9 |
4 |
3 |
5 |
2 |
3 |
0 |
3 |
42 |
| Fine-tuning stress and tension in cells | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
84 |
32 |
11 |
6 |
7 |
140 |
| Fire histories and tree ages in unmanaged boreal forests in Eastern Fennoscandia and Onega peninsula | 7 |
3 |
2 |
1 |
10 |
3 |
3 |
3 |
2 |
2 |
0 |
1 |
37 |
| Fish communities in South-Finnish lakes and their responses to biomanipulation assessed by experimental gillnetting | 3 |
9 |
6 |
13 |
4 |
3 |
0 |
2 |
2 |
0 |
4 |
1 |
47 |
| Fish out of place : Evaluating the impacts of fish introductions on freshwater ecosystems | 4 |
9 |
5 |
0 |
4 |
5 |
0 |
1 |
1 |
0 |
2 |
2 |
33 |
| Fisheries sustainability in the presence of predation by marine megafauna | 6 |
5 |
4 |
3 |
12 |
7 |
2 |
2 |
4 |
3 |
0 |
1 |
49 |
| Fishes of the Darkness : Water colour-regulated competitive interactions in humic lakes | 2 |
5 |
4 |
5 |
9 |
2 |
3 |
1 |
2 |
1 |
1 |
2 |
37 |
| Flagship species as fundraising tools : their role in biodiversity conservation and in environmental philanthropic behavior | 7 |
7 |
10 |
5 |
13 |
8 |
13 |
2 |
4 |
32 |
20 |
2 |
123 |
| Flight metabolic rate and dispersal in the Glanville fritillary butterfly : from genes to populations | 7 |
3 |
2 |
4 |
7 |
1 |
0 |
0 |
5 |
0 |
4 |
2 |
35 |
| Flight metabolic rate in the Glanville fritillary butterfly | 3 |
4 |
7 |
8 |
8 |
6 |
1 |
3 |
1 |
2 |
2 |
4 |
49 |
| Flower Development in Gerbera hybrida, Asteraceae | 3 |
1 |
3 |
3 |
7 |
10 |
1 |
5 |
0 |
6 |
6 |
14 |
59 |
| Fluorescence properties of Baltic Sea phytoplankton | 12 |
6 |
10 |
15 |
34 |
14 |
2 |
3 |
2 |
1 |
3 |
1 |
103 |
| Flying jewels : Taxonomy and distribution of Northern European cuckoo wasps (Hymenoptera : Chrysididae) | 15 |
11 |
18 |
8 |
11 |
15 |
16 |
11 |
0 |
1 |
2 |
8 |
116 |
| Folding and Selective Exit of Reporter Proteins from the Yeast Endoplasmic Reticulum | 12 |
7 |
10 |
5 |
9 |
8 |
4 |
4 |
4 |
5 |
4 |
2 |
74 |
| Food intake, growth and social interactions of signal crayfish, Pacifastacus leniusculus (Dana) | 10 |
13 |
12 |
9 |
16 |
8 |
6 |
1 |
8 |
3 |
5 |
2 |
93 |
| Food selection and feeding behaviour of Baltic Sea mysid shrimps | 24 |
9 |
6 |
12 |
6 |
4 |
3 |
8 |
8 |
9 |
28 |
8 |
125 |
| Forest structure and biodiversity in northern boreal forests : Effects of regeneration cutting on flying beetles and wood-decomposing fungi | 2 |
4 |
3 |
7 |
8 |
6 |
2 |
2 |
3 |
3 |
7 |
5 |
52 |
| From actin monomers to bundles : The roles of twinfilin and α-actinin in Drosophila melanogaster development | 16 |
6 |
5 |
3 |
8 |
2 |
4 |
2 |
2 |
1 |
2 |
1 |
52 |
| from biogeochemical processes during ice formation to bio-optical modelling | 7 |
1 |
1 |
4 |
4 |
4 |
0 |
1 |
2 |
4 |
1 |
3 |
32 |
| From individuals to populations : the distribution of Eurasian lynx individuals in space and time and consequences for the local population structure and dynamics | 11 |
8 |
7 |
9 |
18 |
10 |
4 |
4 |
4 |
6 |
5 |
9 |
95 |
| From locomotor behavior to cerebellum evolution and development in squamate models | 2 |
2 |
11 |
18 |
17 |
19 |
5 |
4 |
9 |
4 |
9 |
12 |
112 |
| From neural stem cells to precursors : Molecular regulation of self-renewal and differentiation | 9 |
4 |
6 |
3 |
16 |
4 |
2 |
1 |
1 |
37 |
95 |
0 |
178 |
| From the river to the open sea : a critical life phase of young Atlantic salmon migrating from the Simojoki river | 7 |
4 |
0 |
0 |
9 |
2 |
0 |
2 |
1 |
2 |
2 |
3 |
32 |
| From topics of interest to a professional field of sustainablers : Sustainability education for change-making | 0 |
0 |
0 |
0 |
0 |
44 |
6 |
14 |
14 |
13 |
8 |
8 |
107 |
| Function of the Metazoan Mediator Kinase Module in Transcription | 9 |
2 |
2 |
4 |
9 |
5 |
0 |
3 |
1 |
3 |
2 |
1 |
41 |
| Functional analysis of Cdk7-interacting proteins Mat1 and Hint in model organisms | 11 |
2 |
2 |
3 |
4 |
2 |
2 |
1 |
4 |
0 |
1 |
1 |
33 |
| Functional and cellular analysis of autoimmune regulator (AIRE) protein | 13 |
3 |
4 |
7 |
11 |
3 |
1 |
2 |
3 |
4 |
1 |
2 |
54 |
| Functional and structural analysis of RET receptor tyrosine kinase and its complexes | 4 |
6 |
3 |
6 |
10 |
7 |
2 |
8 |
2 |
4 |
8 |
1 |
61 |
| Functional and Structural Studies on Heptahelical Membrane Proteins | 5 |
1 |
1 |
3 |
6 |
4 |
2 |
0 |
1 |
5 |
2 |
2 |
32 |
| Functional characterisation of Rab22a and Munc18b, two proteins regulating vesicle transport in mammalian cells | 2 |
3 |
7 |
2 |
3 |
0 |
0 |
1 |
2 |
1 |
1 |
0 |
22 |
| Functional characterization of MutL homologue mismatch repair proteins and their variants | 24 |
6 |
15 |
13 |
16 |
23 |
24 |
8 |
5 |
2 |
5 |
27 |
168 |
| Functional Characterization of MutS Homologue Mismatch Repair Proteins and their Variants | 10 |
2 |
11 |
1 |
6 |
3 |
11 |
2 |
6 |
5 |
6 |
4 |
67 |
| Functional dissection of alternative secretory pathways in the yeast S. cerevisiae | 7 |
6 |
1 |
8 |
6 |
0 |
1 |
1 |
3 |
0 |
4 |
0 |
37 |
| Functional expression and subcellular localization of the Cl- cotransporters KCC2 and NKCC1 in rodent hippocampal and neocortical neurons | 8 |
0 |
2 |
1 |
8 |
5 |
5 |
0 |
4 |
2 |
1 |
1 |
37 |
| Functional Fertility Genomics in Sheep | 6 |
7 |
5 |
1 |
6 |
5 |
1 |
1 |
5 |
2 |
14 |
1 |
54 |
| Functional genes and gene array analysis as tools for monitoring hydrocarbon biodegradation | 11 |
0 |
0 |
1 |
5 |
3 |
2 |
3 |
2 |
2 |
3 |
4 |
36 |
| Functional genomics of the Glanville fritillary butterfly | 0 |
2 |
2 |
5 |
8 |
5 |
3 |
0 |
3 |
1 |
1 |
3 |
33 |
| Functional Mapping of Mu Transposition Machinery : MuA Protein Modification and Engineering for Hyperactivity | 11 |
5 |
9 |
3 |
11 |
5 |
4 |
6 |
3 |
2 |
7 |
9 |
75 |
| Functional perspective on the role of macrophytes in the coastal carbon cycle across different temporal and spatial scales | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Functional Properties of Visual Pigments using A1 and A2 Chromophore : From Molecules to Ecology | 5 |
3 |
4 |
5 |
12 |
6 |
5 |
2 |
3 |
3 |
1 |
2 |
51 |
| Functional role of the Mso1p-Sec1p complex in membrane fusion regulation | 12 |
2 |
4 |
0 |
4 |
1 |
0 |
0 |
1 |
1 |
3 |
2 |
30 |
| Functional Sequence Annotation in an Error-prone Environment | 4 |
2 |
4 |
1 |
3 |
3 |
5 |
0 |
1 |
2 |
1 |
3 |
29 |
| Functional significance of minor MLH1 germline alterations found in colon cancer patients | 11 |
7 |
13 |
13 |
18 |
22 |
20 |
10 |
5 |
3 |
3 |
4 |
129 |
| Functional studies of purified transmembrane proteases, omptins, of Yersinia pestis and Salmonella enterica | 10 |
2 |
0 |
1 |
3 |
1 |
0 |
0 |
1 |
0 |
3 |
2 |
23 |
| Functional studies of the secretory pathway of filamentous fungi : The effect of unfolded protein response on protein production | 2 |
0 |
6 |
7 |
14 |
4 |
2 |
2 |
0 |
2 |
1 |
9 |
49 |
| Functional Studies on alpha2-Adrenergic Receptor Subtypes | 10 |
1 |
2 |
3 |
10 |
2 |
2 |
0 |
3 |
0 |
3 |
1 |
37 |
| Functions of Alphavirus Macrodomain-containing protein nsP3 | 9 |
10 |
10 |
6 |
8 |
8 |
2 |
5 |
4 |
2 |
1 |
2 |
67 |
| Functions of human papillomavirus E5 oncogene in epithelial cells and in the onset of cervical cancer | 5 |
3 |
3 |
3 |
14 |
7 |
1 |
1 |
2 |
1 |
3 |
0 |
43 |
| Fusion and atherogenic properties of enzymatically modified low density lipoprotein particles | 8 |
3 |
3 |
3 |
8 |
3 |
1 |
4 |
4 |
0 |
0 |
4 |
41 |
| GABAa Receptor Mediated Signalling in the Brain : Inhibition, Shunting and Excitation | 17 |
1 |
1 |
3 |
11 |
22 |
2 |
3 |
3 |
2 |
0 |
1 |
66 |
| GABAa Receptor-mediated Excitation in the Hippocampus of Adult and Newborn rats | 8 |
27 |
17 |
19 |
1 |
3 |
0 |
2 |
2 |
3 |
2 |
3 |
87 |
| GABAergic mechanisms of excitation and hypersynchrony in adult rat hippocampus | 9 |
7 |
4 |
3 |
5 |
7 |
1 |
10 |
4 |
16 |
7 |
5 |
78 |
| GABAergic Signaling and Neuronal Chloride Regulation in the Control of Network Events in the Immature Hippocampus | 1 |
2 |
5 |
5 |
6 |
2 |
2 |
3 |
2 |
4 |
3 |
3 |
38 |
| GATA transcription factors and their co-regulators guide the development of GABAergic and serotonergic neurons in the anterior brainstem | 10 |
11 |
17 |
6 |
13 |
13 |
5 |
9 |
8 |
11 |
12 |
12 |
127 |
| GDNF family receptors in peripheral target innervation and hormone production | 0 |
8 |
9 |
9 |
8 |
4 |
3 |
7 |
2 |
1 |
0 |
6 |
57 |
| GDNF Receptors : Veterans and Novices | 8 |
3 |
2 |
1 |
13 |
8 |
1 |
2 |
1 |
3 |
2 |
2 |
46 |
| GDP-L-fucose : synthesis and role in inflammation | 2 |
8 |
4 |
6 |
8 |
4 |
4 |
4 |
4 |
5 |
4 |
2 |
55 |
| Gelatinase-mediated Migration and Invasion of Cancer Cells | 13 |
7 |
20 |
14 |
15 |
6 |
2 |
2 |
3 |
1 |
16 |
3 |
102 |
| Gene Expression : From Microarrays to Functional Genomics | 5 |
1 |
0 |
4 |
8 |
3 |
2 |
3 |
4 |
5 |
2 |
3 |
40 |
| Generation and Characterization of the Cation-Chloride Cotransporter KCC2 Hypomorphic Mouse | 3 |
3 |
1 |
1 |
4 |
1 |
0 |
2 |
2 |
3 |
2 |
2 |
24 |
| Generation of Flat and Curved Membranes by Inverse-BAR Domain Proteins | 9 |
4 |
4 |
3 |
11 |
2 |
2 |
4 |
3 |
1 |
2 |
2 |
47 |
| Genetic and behavioural divergence of queen size morphs in the red ant Myrmica ruginodis | 4 |
5 |
1 |
4 |
10 |
6 |
4 |
3 |
4 |
2 |
8 |
2 |
53 |
| Genetic and environmental Influences on Atlantic Salmon Life History : vgll3 and the Physiology of Maturation | 0 |
0 |
0 |
0 |
0 |
147 |
10 |
17 |
13 |
5 |
5 |
1 |
198 |
| Genetic aspects of outcome in kidney transplantation : cytokine and thrombosis associated candidate genes and gene expression biomarkers | 6 |
4 |
20 |
7 |
11 |
5 |
4 |
2 |
2 |
4 |
2 |
5 |
72 |
| Genetic background of late-onset spinal motor neuronopathy | 9 |
8 |
9 |
5 |
5 |
7 |
2 |
2 |
4 |
2 |
2 |
3 |
58 |
| Genetic diversity and phylogeography of landlocked seals | 3 |
4 |
5 |
5 |
11 |
6 |
2 |
3 |
3 |
2 |
0 |
1 |
45 |
| Genetic mapping of traits important in barley breeding | 5 |
0 |
2 |
5 |
3 |
3 |
3 |
3 |
2 |
6 |
2 |
2 |
36 |
| Genetic profiling of the interactions between soft rot Pectobacterium species and plants | 5 |
12 |
6 |
8 |
11 |
4 |
3 |
5 |
4 |
7 |
2 |
3 |
70 |
| Genetic Structure of Blood Donor Biobank and its Applications in Personalized Blood Donation and Transfusion | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Genetic studies of population history and contemporary microevolution in grayling (Thymallus: Salmonidae) | 10 |
3 |
5 |
7 |
7 |
9 |
3 |
4 |
3 |
0 |
5 |
1 |
57 |
| Genetic Studies of the Human Complement C4 Region in MHC Class III | 1 |
1 |
5 |
4 |
5 |
2 |
1 |
0 |
2 |
2 |
1 |
0 |
24 |
| Genetic susceptibility to asbestos and tobacco smoke related non-malignant pleuropulmonary changes | 32 |
34 |
31 |
35 |
39 |
33 |
3 |
2 |
2 |
1 |
1 |
5 |
218 |
| Genetic susceptibility to celiac disease : HLA-unlinked candidate genes | 5 |
2 |
4 |
6 |
6 |
4 |
3 |
3 |
1 |
2 |
4 |
6 |
46 |
| Genetic Variation : Effect on the Risk of Cancers of Lung and Oropharynx | 2 |
2 |
1 |
3 |
7 |
4 |
1 |
3 |
0 |
3 |
1 |
1 |
28 |
| Genetically modified Pseudomonas associated with plants : aspects for environmental risk assessment | 4 |
2 |
2 |
2 |
5 |
3 |
0 |
0 |
2 |
0 |
0 |
0 |
20 |
| Genetics and Epigenetics of Nicotine Dependence : Polymorphisms and methylation of CYP2D6, MAOA, MAOB, and SLC6A3 genes as modifiers of smoking phenotypes | 12 |
7 |
9 |
9 |
13 |
11 |
8 |
18 |
3 |
6 |
2 |
5 |
103 |
| Genetics and genomics of musical abilities | 3 |
1 |
8 |
6 |
19 |
2 |
7 |
1 |
3 |
8 |
6 |
10 |
74 |
| Genetics of Local Adaptation in theThree-spined Stickleback | 3 |
6 |
5 |
4 |
12 |
4 |
4 |
1 |
2 |
2 |
3 |
2 |
48 |
| Genetics of Primary Immunodeficiency in Finland | 7 |
5 |
15 |
10 |
6 |
4 |
4 |
0 |
4 |
2 |
6 |
4 |
67 |
| Genetics of T cell co-stimulatory receptors -CD28, CTLA4, ICOS and PDCD1 in immunity and transplantation | 2 |
2 |
5 |
3 |
10 |
5 |
26 |
54 |
8 |
7 |
7 |
5 |
134 |
| Genome editing and its use to study secondary growth in Arabidopsis thaliana | 13 |
14 |
28 |
26 |
20 |
18 |
5 |
5 |
7 |
7 |
6 |
7 |
156 |
| Genomic Evolution and Diversity in Artiodactyla | 15 |
1 |
5 |
9 |
15 |
4 |
3 |
0 |
4 |
1 |
3 |
1 |
61 |
| Genomic Profiling of Gastric Cancer | 12 |
9 |
9 |
9 |
6 |
6 |
1 |
2 |
2 |
1 |
0 |
2 |
59 |
| Genomics of bacterial and archaeal virus isolates from extreme aquatic environments | 7 |
0 |
6 |
6 |
4 |
2 |
0 |
2 |
1 |
1 |
2 |
0 |
31 |
| Geographic variation in killer whale colour patterns | 13 |
24 |
12 |
34 |
47 |
14 |
13 |
10 |
10 |
5 |
9 |
10 |
201 |
| Glutamatergic Modulation of Cue-Induced Drug-Seeking Behavior in the Rat | 3 |
9 |
6 |
7 |
16 |
9 |
2 |
5 |
2 |
3 |
4 |
2 |
68 |
| Glycan Binding Proteins in Therapeutic Mesenchymal Stem Cell Research | 7 |
10 |
8 |
4 |
11 |
3 |
2 |
0 |
3 |
2 |
2 |
1 |
53 |
| Glycobiological insights in characterization and targeting of umbilical cord blood derived stem cells | 30 |
12 |
21 |
10 |
38 |
22 |
2 |
5 |
9 |
5 |
2 |
2 |
158 |
| Glycosylation and Sorting of Secretory Proteins in the Endoplasmic Reticulum of the Yeast Saccharomyces cerevisiae | 9 |
3 |
3 |
2 |
4 |
0 |
2 |
3 |
3 |
1 |
0 |
2 |
32 |
| Golgi proteomics : Identification of a novel cartilage-specific Golgi protein GoPro49 | 3 |
4 |
8 |
1 |
3 |
6 |
6 |
1 |
2 |
5 |
1 |
2 |
42 |
| GPRA and the asthma locus on chromosome 7p14-p15 | 0 |
1 |
2 |
3 |
5 |
1 |
1 |
0 |
2 |
1 |
3 |
0 |
19 |
| Growth and recruitment of burbot (Lota lota) | 7 |
5 |
11 |
7 |
14 |
8 |
3 |
1 |
10 |
1 |
1 |
14 |
82 |
| Growth and resilience of non-vascular epiphytes in the Taita Hills, Kenya | 5 |
4 |
4 |
5 |
8 |
5 |
3 |
5 |
2 |
4 |
2 |
2 |
49 |
| Habitat use and population dynamics of brown bears (Ursus arctos) in Scandinavia | 5 |
4 |
2 |
6 |
8 |
5 |
3 |
4 |
4 |
2 |
1 |
0 |
44 |
| Harmful algae in the planktonic food web of the Baltic Sea | 9 |
7 |
3 |
4 |
16 |
11 |
6 |
8 |
4 |
1 |
6 |
4 |
79 |
| Helper component-proteinase and coat protein are involved in the molecular processes of potato virus A translation and replication | 4 |
9 |
5 |
10 |
8 |
4 |
7 |
8 |
3 |
1 |
8 |
6 |
73 |
| Heparin-binding growth-associated molecule (HB-GAM) in activity-dependent neuronal plasticity in hippocampus | 8 |
4 |
3 |
0 |
6 |
1 |
0 |
1 |
3 |
10 |
4 |
4 |
44 |
| Hepatic lipid metabolism in cardiometabolic diseases : protective and adverse effects of genetic variants | 4 |
7 |
2 |
4 |
10 |
14 |
3 |
4 |
15 |
1 |
2 |
4 |
70 |
| Heterobasidion annosum and wood decay : Enzymology of cellulose, hemicellulose, and lignin degradation | 6 |
10 |
9 |
6 |
13 |
8 |
5 |
7 |
6 |
5 |
8 |
12 |
95 |
| High molecular weight cysteine proteinase inhibitors in Atlantic salmon and other fish species | 6 |
4 |
5 |
0 |
4 |
1 |
0 |
5 |
0 |
0 |
1 |
0 |
26 |
| Histopathology-selective spatial oncogenic phenotypes in non-small cell lung cancer | 5 |
4 |
20 |
7 |
13 |
8 |
2 |
5 |
2 |
2 |
4 |
5 |
77 |
| HMGB1 (Amphoterin) and AMIGO1 in Brain Development | 9 |
7 |
4 |
2 |
12 |
14 |
7 |
16 |
2 |
6 |
62 |
11 |
152 |
| Holocene carbon dynamics and atmospheric radiative forcing of different types of peatlands in Finland | 6 |
6 |
4 |
1 |
5 |
3 |
2 |
3 |
3 |
2 |
1 |
3 |
39 |
| Homeostatic maintenance of the murine corneal epithelium in pathophysiological contexts | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Homeostatic maintenance of the murine corneal epithelium in pathophysiological contexts | 6 |
5 |
18 |
14 |
12 |
10 |
2 |
10 |
4 |
1 |
4 |
1 |
87 |
| Hormonal regulation of radical-induced programmed cell death in ozone-sensitive mutants of Arabidopsis thaliana | 5 |
5 |
8 |
9 |
9 |
0 |
2 |
2 |
2 |
1 |
3 |
3 |
49 |
| Host-pathogen coevolution through trade-offs and coinfection | 10 |
7 |
2 |
2 |
7 |
7 |
0 |
2 |
4 |
4 |
1 |
1 |
47 |
| How to assemble contractile actomyosin bundles in cells? | 32 |
5 |
4 |
4 |
12 |
19 |
1 |
1 |
2 |
0 |
2 |
4 |
86 |
| Human genetic variation in the Baltic Sea region : Features of population history and natural selection | 10 |
10 |
14 |
3 |
16 |
13 |
5 |
3 |
2 |
4 |
9 |
11 |
100 |
| Human parvovirus B19 : tissue persistence and prevalence of prototypic and new variants | 9 |
12 |
9 |
11 |
20 |
11 |
4 |
2 |
0 |
1 |
6 |
1 |
86 |
| Human Pathogenic Mutations in Protein Domains | 1 |
4 |
3 |
4 |
4 |
5 |
3 |
3 |
0 |
1 |
0 |
4 |
32 |
| Human picornaviruses : uncoating, assembly and interaction with cellular receptors | 4 |
3 |
3 |
7 |
10 |
8 |
1 |
0 |
2 |
10 |
6 |
11 |
65 |
| Human Protein Phosphatase Interactions and Dynamics : Proteomic and Functional Perspective | 6 |
0 |
5 |
1 |
6 |
3 |
1 |
1 |
0 |
0 |
2 |
0 |
25 |
| Human Transcription Factor Protein-Protein Interactions in Health and Disease | 6 |
7 |
10 |
7 |
6 |
12 |
3 |
8 |
2 |
4 |
8 |
2 |
75 |
| Hydroacoustic fish stock assessment in southern and northern boreal lakes : potential and constraints | 37 |
5 |
24 |
26 |
41 |
12 |
2 |
3 |
5 |
1 |
1 |
2 |
159 |
| Hydrogen peroxide in inducible plant stress responses | 9 |
2 |
3 |
1 |
7 |
9 |
0 |
5 |
3 |
4 |
1 |
3 |
47 |
| Identification of a secretion signal for the type II protein secretion pathway in Erwinia carotovora | 1 |
3 |
2 |
1 |
5 |
3 |
1 |
1 |
2 |
1 |
0 |
1 |
21 |
| Identification of evolutionary conserved mechanisms promoting rapid actin dynamics | 14 |
18 |
10 |
14 |
6 |
8 |
7 |
6 |
2 |
0 |
5 |
10 |
100 |
| Identification of MANF and CDNF interacting proteins and a study of their mechanism of action | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
55 |
23 |
9 |
7 |
2 |
96 |
| Identification of molecules relevant for the invasiveness of fibrosarcomas and melanomas | 8 |
2 |
1 |
2 |
4 |
1 |
0 |
0 |
5 |
1 |
1 |
5 |
30 |
| Identification of sugar responsive transcription factors in silico | 0 |
0 |
0 |
0 |
0 |
0 |
1 |
0 |
0 |
1 |
0 |
7 |
9 |
| Identification of the fungal catabolic D-galacturonate pathway | 9 |
9 |
1 |
6 |
9 |
5 |
35 |
27 |
2 |
0 |
1 |
2 |
106 |
| Imaging Cellular Mechanisms of Oral Ectodermal Development and Disease | 26 |
17 |
16 |
8 |
12 |
8 |
1 |
0 |
5 |
0 |
2 |
1 |
96 |
| Immune response to insulin and changes in the gut immune system in children with or at risk for type 1 diabetes | 1 |
0 |
1 |
3 |
9 |
6 |
3 |
2 |
3 |
5 |
2 |
1 |
36 |
| Immune Responses to Pathogen Infection in Arabidopsis | 19 |
20 |
16 |
16 |
31 |
32 |
7 |
4 |
6 |
2 |
7 |
3 |
163 |
| Immunomodulatory Effects of Engineered Nanomaterials in Healthy and Diseased Lungs and Skin | 1 |
3 |
3 |
4 |
7 |
4 |
3 |
1 |
4 |
0 |
6 |
4 |
40 |
| Impact of land use on breeding bird populations a case study of Vuosaari harbour construction | 6 |
6 |
4 |
1 |
10 |
3 |
2 |
2 |
3 |
0 |
0 |
1 |
38 |
| Impacts of agriculture on amphibians at multiple scales | 13 |
15 |
16 |
11 |
28 |
11 |
6 |
6 |
7 |
1 |
2 |
2 |
118 |
| Impacts of soil temperature on high-latitude terrestrial biodiversity and ecosystem functioning, and climate change implications | 31 |
1 |
7 |
10 |
25 |
12 |
8 |
8 |
2 |
1 |
6 |
3 |
114 |
| Impacts of summer drought on plant-herbivore interactions : the Glanville fritillary metapopulation as a case study | 1 |
1 |
4 |
5 |
6 |
3 |
1 |
0 |
3 |
1 |
6 |
5 |
36 |
| Impacts of water-level regulation on the littoral biota of lakes in Finland : the role of hydromorphological modification in status assessment | 6 |
5 |
4 |
2 |
11 |
0 |
1 |
2 |
1 |
1 |
0 |
0 |
33 |
| Implications of bacterial viruses on pathogenic bacteria : from natural microbial communities to therapeutic applications | 2 |
4 |
5 |
11 |
9 |
5 |
1 |
1 |
6 |
5 |
8 |
3 |
60 |
| Implications of BRCA1 mutations in basal-like breast cancer development and treatment | 9 |
6 |
7 |
6 |
15 |
9 |
2 |
3 |
3 |
4 |
2 |
2 |
68 |
| Improving CNV detection from short-read MPS data in neuromuscular disorders | 18 |
19 |
21 |
27 |
11 |
17 |
7 |
16 |
21 |
9 |
16 |
8 |
190 |
| Improving Precision in Therapies for Hematological Malignancies | 4 |
6 |
18 |
10 |
14 |
5 |
7 |
2 |
11 |
22 |
7 |
4 |
110 |
| In between two worlds? : Science-policy interaction in Finnish environmental governance | 5 |
16 |
12 |
6 |
9 |
5 |
4 |
10 |
5 |
3 |
4 |
1 |
80 |
| In Vitro Cell Expansion and CTLA4 in Advanced T-Cell Therapies | 1 |
2 |
6 |
11 |
9 |
3 |
1 |
2 |
1 |
4 |
3 |
2 |
45 |
| Inbreeding Depression in the Glanville Fritillary Butterfly (Melitaea cinxia) | 1 |
1 |
1 |
3 |
8 |
5 |
1 |
2 |
3 |
0 |
1 |
3 |
29 |
| Indigenous intestinal microbiota and disease : different approaches to characterize the composition and products of human microbiota | 6 |
3 |
2 |
3 |
3 |
6 |
7 |
1 |
0 |
1 |
1 |
2 |
35 |
| Individual stress-resistance in the ant Formica exsecta | 1 |
2 |
1 |
3 |
3 |
3 |
6 |
25 |
8 |
0 |
1 |
1 |
54 |
| Induction of immunity against experimental Chlamydia pneumoniae infection | 2 |
2 |
0 |
1 |
5 |
3 |
1 |
2 |
1 |
0 |
1 |
2 |
20 |
| Influence of processing on the flavour formation of oat and rye | 10 |
9 |
4 |
5 |
10 |
7 |
2 |
3 |
3 |
25 |
3 |
4 |
85 |
| Influence of resource distribution and abundance on the population structure and dynamics of Parnassius apollo | 15 |
9 |
6 |
9 |
16 |
3 |
9 |
4 |
4 |
3 |
8 |
2 |
88 |
| Influenza A virus-host interactions and their control by viral non-structural protein NS1 | 3 |
5 |
9 |
3 |
10 |
8 |
4 |
3 |
1 |
3 |
3 |
4 |
56 |
| Inherited DNA repair capacity and individual responses to carcinogens | 8 |
2 |
1 |
1 |
2 |
1 |
0 |
0 |
0 |
3 |
3 |
0 |
21 |
| Innate immunity and its control in the pathogenesis of inflammatory rheumatic diseases | 13 |
6 |
11 |
3 |
7 |
10 |
2 |
3 |
3 |
3 |
4 |
2 |
67 |
| Integrated Analysis of Aggression in Salmonids | 2 |
3 |
1 |
2 |
5 |
5 |
3 |
3 |
3 |
3 |
4 |
3 |
37 |
| Integration of Eda signaling with other signaling pathways in oral ectodermal organogenesis | 14 |
15 |
17 |
6 |
12 |
7 |
4 |
3 |
3 |
4 |
2 |
8 |
95 |
| Interaction between Hormone and Apoplastic ROS Signaling in Regulation of Defense Responses and Cell Death | 9 |
4 |
2 |
6 |
9 |
7 |
32 |
25 |
2 |
3 |
4 |
1 |
104 |
| Interaction of GluA1 AMPA receptor with Synapse-Associated Protein 97 | 3 |
2 |
2 |
2 |
7 |
4 |
2 |
2 |
3 |
0 |
0 |
2 |
29 |
| Interactions among neuronal oscillations in the developing and adult brain | 2 |
10 |
0 |
2 |
6 |
4 |
0 |
1 |
2 |
3 |
2 |
2 |
34 |
| Interactions and Exclusions : Studies on Causal Explanation in Naturalistic Philosophy of Mind | 12 |
1 |
3 |
9 |
4 |
5 |
3 |
2 |
5 |
6 |
5 |
9 |
64 |
| Interactions between harmful algae and calanoid copepods in the Baltic Sea | 5 |
2 |
4 |
5 |
18 |
7 |
10 |
3 |
2 |
2 |
5 |
1 |
64 |
| Interactions between metals, microbes and plants : Bioremediation of arsenic and lead contaminated soils | 22 |
19 |
6 |
2 |
9 |
12 |
4 |
7 |
7 |
5 |
11 |
7 |
111 |
| Interactions between Puumala hantavirus and its host, the bank vole, in the boreal zone | 1 |
4 |
11 |
9 |
5 |
5 |
4 |
2 |
2 |
1 |
0 |
3 |
47 |
| Interactions of nandrolone and psychostimulant drugs on central monoaminergic systems | 22 |
8 |
16 |
9 |
19 |
23 |
14 |
20 |
14 |
21 |
18 |
7 |
191 |
| Intergenerational trade-offs in periodic environments : a reaction norm perspective | 2 |
0 |
2 |
1 |
4 |
2 |
3 |
0 |
0 |
2 |
4 |
1 |
21 |
| Intermolecular protein splicing and its use in biotechnological applications | 8 |
6 |
5 |
6 |
10 |
17 |
2 |
4 |
7 |
3 |
3 |
1 |
72 |
| Interplay Between Cyclase-Associated Protein, Cofilin, Profilin and Twinfilin in Actin Dynamics | 6 |
6 |
3 |
1 |
10 |
5 |
2 |
4 |
4 |
1 |
1 |
1 |
44 |
| Interplay of ecology and evolution under changing environmental conditions : Evolution experiments with heterotrophic bacteria | 7 |
4 |
2 |
6 |
8 |
2 |
2 |
1 |
3 |
1 |
2 |
2 |
40 |
| Intraspecific variation in brain size and architecture : population divergence and phenotypic plasticity | 4 |
5 |
6 |
2 |
14 |
10 |
0 |
4 |
3 |
2 |
1 |
0 |
51 |
| Intraspecific variation in phenotypic plasticity | 10 |
6 |
5 |
3 |
9 |
6 |
2 |
2 |
5 |
2 |
2 |
2 |
54 |
| Intravitreal liposomes as ocular drug delivery systems : vitreal interactions, retinal permeation and drug release characteristics | 20 |
23 |
24 |
15 |
27 |
40 |
30 |
11 |
15 |
25 |
17 |
21 |
268 |
| Introducing Wilson disease mutations into ZntA : Studies on the nucleotide and metal-binding sites of a bacterial zinc-translocating P-type ATPase | 4 |
2 |
0 |
10 |
7 |
1 |
2 |
1 |
3 |
4 |
2 |
1 |
37 |
| Introduction of hydrophobic fluorescent lipid analogues into living cultured cells and their imaging therein | 7 |
0 |
0 |
3 |
8 |
1 |
2 |
2 |
1 |
2 |
0 |
0 |
26 |
| Invertebrate predation and trophic cascades in a pelagic food web : The multiple roles of Chaoborus flavicans (Meigen) in a clay-turbid lake | 14 |
1 |
6 |
6 |
10 |
6 |
2 |
3 |
3 |
1 |
0 |
2 |
54 |
| Investigating plant resistance and infection patterns in a wild plant : case study of Plantago lanceolata | 0 |
0 |
0 |
0 |
41 |
35 |
3 |
4 |
5 |
4 |
6 |
3 |
101 |
| Involvement of non-muscle α-actinins and NUAK2 kinase in regulating actin stress fibers | 8 |
9 |
9 |
2 |
13 |
1 |
3 |
2 |
4 |
2 |
4 |
3 |
60 |
| Ion-regulatory proreins in neuronal development and communication | 8 |
4 |
4 |
5 |
5 |
2 |
2 |
2 |
2 |
4 |
1 |
2 |
41 |
| Kainate receptor auxiliary subunits NETO1 and NETO2 in anxiety and fear-related behaviors | 6 |
11 |
16 |
9 |
13 |
14 |
5 |
9 |
5 |
10 |
4 |
4 |
106 |
| Kainate-type glutamate receptors modulating network activity in developing hippocampus | 4 |
5 |
7 |
1 |
10 |
12 |
3 |
6 |
4 |
0 |
6 |
2 |
60 |
| KCC2 as a multifunctional protein in brain development and disease | 2 |
4 |
4 |
3 |
6 |
4 |
1 |
4 |
7 |
1 |
10 |
4 |
50 |
| Kin selection, social polymorphism, and reproductive allocation in ants | 5 |
4 |
3 |
3 |
11 |
4 |
4 |
3 |
1 |
21 |
3 |
5 |
67 |
| Kinship and conflicts over male production in Formica ants | 12 |
10 |
10 |
4 |
13 |
5 |
3 |
0 |
3 |
4 |
2 |
8 |
74 |
| Knowledge-based marine conservation in oil spill risk management | 10 |
5 |
2 |
5 |
11 |
7 |
3 |
3 |
3 |
1 |
5 |
5 |
60 |
| Kokonaisvaltainen lähestymistapa ympäristönsuojelutieteessä : Sisällön moniulotteisuus ympäristönsuojelijan haasteena | 63 |
34 |
37 |
44 |
46 |
34 |
7 |
26 |
43 |
46 |
54 |
31 |
465 |
| Laboratory Diagnosis and Surveillance of Acute Respiratory Tract Infections Caused by Certain Common Viruses and Mycoplasma pneumoniae | 7 |
11 |
4 |
4 |
4 |
6 |
0 |
2 |
6 |
6 |
4 |
4 |
58 |
| Lacrimal Gland Morphogenesis, Maturation and Function | 9 |
5 |
13 |
5 |
20 |
5 |
4 |
5 |
2 |
4 |
5 |
0 |
77 |
| Lactobacillus crispatus and Propionibacterium freudenreichii : A Genomic and Transcriptomic View | 7 |
4 |
14 |
11 |
13 |
9 |
51 |
64 |
2 |
1 |
0 |
1 |
177 |
| Lake-atmosphere greenhouse gas exchange in relation to atmospheric forcing and lake biogeochemistry | 3 |
7 |
3 |
7 |
10 |
6 |
0 |
1 |
5 |
1 |
2 |
7 |
52 |
| Lapin ympäristökiistojen kulttuuriset tekijät | 29 |
29 |
13 |
16 |
19 |
4 |
3 |
5 |
10 |
27 |
17 |
10 |
182 |
| Large-scale automated acoustic monitoring of birds and the challenges of field data | 7 |
11 |
10 |
5 |
8 |
11 |
6 |
4 |
3 |
2 |
3 |
0 |
70 |
| Latent TGF-beta binding protein LTBP-2 : assembly to the extracellular matrix and effects on cell adhesion | 7 |
2 |
1 |
6 |
5 |
7 |
1 |
0 |
2 |
1 |
5 |
8 |
45 |
| Leaf senescence in silver birch (Betula pendula Roth) | 6 |
4 |
3 |
4 |
5 |
6 |
2 |
3 |
1 |
0 |
1 |
1 |
36 |
| Let there be pike! : Effects of fishing on the dynamics of pike (Esox lucius) populations | 9 |
7 |
5 |
8 |
17 |
4 |
2 |
2 |
3 |
4 |
5 |
5 |
71 |
| LFA-1 Integrin beta2 Chain Phosphorylation Regulates Protein Interactions and Mediates Signals in T Cells | 4 |
3 |
13 |
23 |
39 |
11 |
12 |
15 |
5 |
4 |
8 |
9 |
146 |
| Life in extreme environments : Physiological changes in host cells during the infection of halophilic archaeal viruses | 4 |
4 |
4 |
6 |
9 |
5 |
0 |
3 |
2 |
1 |
2 |
2 |
42 |
| Life on the Edge : Structural Studies of the Extremophilic Viruses P23-77 and STIV2 | 5 |
6 |
3 |
3 |
8 |
5 |
1 |
6 |
4 |
1 |
4 |
4 |
50 |
| Light after death : the importance of spectral composition in litter decomposition processes | 3 |
5 |
3 |
2 |
5 |
2 |
2 |
2 |
4 |
22 |
22 |
0 |
72 |
| Light quality affects leaf pigments and leaf phenology | 5 |
6 |
12 |
3 |
11 |
4 |
0 |
1 |
1 |
2 |
4 |
2 |
51 |
| Lignin biosynthesis in Norway spruce : from a model system to the tree | 5 |
7 |
2 |
8 |
7 |
9 |
4 |
9 |
4 |
3 |
3 |
5 |
66 |
| Linking spatial and evolutionary dynamics in a plant-pathogen metapopulation | 13 |
2 |
2 |
14 |
7 |
7 |
5 |
4 |
0 |
3 |
5 |
4 |
66 |
| Linking taxonomy and environmental 18S-rRNA-gene sequencing of Baltic Sea protists | 23 |
10 |
11 |
9 |
15 |
7 |
3 |
4 |
5 |
4 |
5 |
9 |
105 |
| Living on voles : plastic life of the Ural owl | 0 |
3 |
2 |
3 |
8 |
1 |
4 |
2 |
2 |
0 |
3 |
1 |
29 |
| Local systems, global impacts : Using life cycle assessment to analyse the potential and constraints of industrial symbioses | 18 |
16 |
16 |
19 |
30 |
13 |
8 |
4 |
1 |
1 |
1 |
1 |
128 |
| Long-term exposure to solar blue and UV radiation in legumes : pre-acclimation to drought and accession-dependent responses in two successive generations | 4 |
0 |
0 |
5 |
6 |
0 |
4 |
1 |
2 |
3 |
4 |
3 |
32 |
| Longitudinal monitoring of parasites in individual wild primates | 1 |
3 |
5 |
1 |
5 |
8 |
3 |
2 |
9 |
2 |
3 |
2 |
44 |
| Lost before found? : On systematics and conservation of lichen genus Micarea Fr. (Pilocarpaceae, Ascomycota) | 4 |
1 |
3 |
0 |
7 |
6 |
2 |
3 |
3 |
4 |
4 |
0 |
37 |
| Luonnonsuojelu arjessa : Maanomistajien näkemyksiä ja kokemuksia yksityismaiden tilapäisestä luonnonsuojelusta ja sen uudistumisen prosessista | 15 |
17 |
16 |
24 |
22 |
7 |
4 |
1 |
4 |
10 |
18 |
9 |
147 |
| Lymphatic vessels in health and disease : Role of the VEGF-C/VEGFR-3 pathway and the transcription factor FOXC2 | 7 |
5 |
10 |
3 |
8 |
4 |
2 |
2 |
4 |
2 |
3 |
1 |
51 |
| Macroalgal contribution to benthic macrofaunal communities and food webs in shallow coastal habitats of the Baltic Sea | 17 |
12 |
16 |
11 |
12 |
4 |
4 |
11 |
2 |
2 |
3 |
7 |
101 |
| Maintaining plant species richness by cattle grazing : mesic semi-natural grasslands as focal habitats | 5 |
7 |
3 |
5 |
8 |
2 |
2 |
7 |
9 |
21 |
3 |
6 |
78 |
| Maltose and maltotriose transport into ale and lager brewer's yeast strains | 14 |
7 |
5 |
6 |
11 |
17 |
1 |
12 |
5 |
8 |
5 |
3 |
94 |
| Management of coregonid fisheries : multiform and multispecies problems | 6 |
5 |
1 |
1 |
5 |
1 |
0 |
0 |
1 |
1 |
2 |
0 |
23 |
| Management of pikeperch (Sander lucioperca) in the coastal waters of the Baltic Sea | 6 |
0 |
9 |
9 |
6 |
6 |
4 |
8 |
2 |
2 |
1 |
1 |
54 |
| Management of semi-natural grasslands for butterfly and moth communities | 4 |
7 |
1 |
3 |
10 |
6 |
39 |
6 |
5 |
4 |
6 |
0 |
91 |
| Managing forest and meadow habitats for the enhancement of urban biodiversity : messages from carabid beetles and vascular plants | 8 |
16 |
19 |
11 |
16 |
9 |
4 |
5 |
6 |
0 |
0 |
0 |
94 |
| MANF as a new regulator of the unfolded protein response and maintenance of pancreatic β-cells in mice | 5 |
12 |
6 |
6 |
9 |
11 |
5 |
2 |
5 |
2 |
5 |
5 |
73 |
| Marine icosahedral membrane-containing dsDNA bacteriophage PM2 : virion structure and host cell penetration | 2 |
6 |
4 |
4 |
6 |
1 |
2 |
3 |
4 |
1 |
1 |
0 |
34 |
| Marking one-summer old whitefish with fluorescent pigment spraying method and results of whitefish stockings in the Gulf of Bothnia | 3 |
7 |
1 |
2 |
9 |
8 |
5 |
7 |
3 |
7 |
5 |
6 |
63 |
| Mass-spectrometric analysis of glycerophospholipid metabolism | 6 |
4 |
6 |
11 |
15 |
21 |
4 |
10 |
5 |
6 |
6 |
1 |
95 |
| Mathematical models of environmental opportunist pathogen dynamics | 5 |
1 |
2 |
1 |
7 |
1 |
0 |
2 |
3 |
1 |
4 |
3 |
30 |
| Meadow plant growth and competition under elevated ozone and carbon dioxide | 4 |
19 |
4 |
1 |
3 |
2 |
1 |
3 |
1 |
3 |
5 |
2 |
48 |
| Measuring and modelling airborne dispersal in wood decay fungi | 8 |
11 |
6 |
7 |
15 |
11 |
5 |
3 |
2 |
3 |
6 |
5 |
82 |
| Mechanism of fluctuations in year class survival of vendace (Coregonus albula (L.)) larvae : an individual size based approach | 2 |
3 |
2 |
4 |
3 |
4 |
2 |
1 |
3 |
2 |
3 |
2 |
31 |
| Mechanism of RNA Translocation by a Viral Packaging Motor | 3 |
1 |
1 |
0 |
10 |
4 |
0 |
0 |
2 |
3 |
1 |
5 |
30 |
| Mechanisms and molecular regulation of mammalian tooth replacement | 1 |
3 |
5 |
7 |
6 |
6 |
2 |
4 |
2 |
1 |
0 |
2 |
39 |
| Mechanisms of Birth Asphyxia and a Novel Resuscitation Strategy | 48 |
56 |
69 |
57 |
76 |
74 |
14 |
23 |
21 |
3 |
6 |
9 |
456 |
| Mechanisms of KCC2 upregulation during development | 5 |
0 |
2 |
1 |
4 |
3 |
1 |
2 |
2 |
0 |
1 |
3 |
24 |
| Mechanisms of Sexual Selection in the Sand Goby, Pomatoschistus minutus | 6 |
4 |
4 |
3 |
9 |
6 |
1 |
2 |
2 |
3 |
0 |
0 |
40 |
| Membrane Insertion of C-tail Anchored Proteins | 2 |
2 |
0 |
2 |
4 |
2 |
1 |
2 |
1 |
0 |
1 |
1 |
18 |
| Meta-omics approach to explore microbial community of the wood ant Formica exsecta | 1 |
2 |
3 |
6 |
7 |
2 |
1 |
1 |
4 |
1 |
1 |
1 |
30 |
| Metabolism of polyunsaturated fatty acids in human bone marrow derived mesenchymal stromal cells | 3 |
4 |
2 |
5 |
8 |
9 |
2 |
1 |
1 |
1 |
1 |
1 |
38 |
| Methane processes in the coastal sediments and water column of the Baltic Sea | 7 |
8 |
7 |
6 |
7 |
27 |
10 |
7 |
7 |
15 |
14 |
6 |
121 |
| Methanogenic Archaea in boreal peatlands | 4 |
5 |
0 |
2 |
8 |
3 |
4 |
3 |
1 |
3 |
0 |
4 |
37 |
| Methicillin-resistant Staphylococcus aureus in Finland : recent changes in the epidemiology, long-term facility aspects, and phenotypic and molecular detection of isolates | 3 |
2 |
4 |
5 |
8 |
3 |
2 |
0 |
2 |
3 |
1 |
0 |
33 |
| Methods and tools for mass spectrometric lipidome analysis | 6 |
5 |
4 |
4 |
4 |
6 |
2 |
7 |
1 |
0 |
1 |
0 |
40 |
| Micro- and mesoplastics in the northern Baltic Sea : their fate in the seafloor and effects on benthic fauna | 23 |
16 |
31 |
25 |
30 |
12 |
2 |
7 |
3 |
1 |
0 |
3 |
153 |
| Microalgae : Platform for conversion of waste to high value products | 11 |
9 |
3 |
10 |
10 |
13 |
3 |
17 |
11 |
8 |
10 |
6 |
111 |
| Microarrays in Lung Cancer Research : From Comparative Analyses to Verified Findings | 2 |
0 |
1 |
1 |
8 |
3 |
1 |
3 |
2 |
0 |
1 |
0 |
22 |
| Microarrays in the Diagnosis of Human Herpesvirus infections | 10 |
5 |
11 |
3 |
12 |
3 |
3 |
3 |
2 |
3 |
0 |
2 |
57 |
| Microbe-induced activation of inflammatory cytokine response in human cells | 3 |
3 |
1 |
3 |
4 |
1 |
0 |
5 |
1 |
1 |
1 |
3 |
26 |
| Microbe-induced Innate Immune Responses in Human Dendritic Cells | 8 |
4 |
2 |
2 |
6 |
5 |
3 |
4 |
2 |
0 |
1 |
5 |
42 |
| Microbes regulate metal and nutrient cycling in Fe Mn concretions of the Gulf of Finland | 5 |
8 |
8 |
11 |
14 |
4 |
5 |
4 |
5 |
7 |
5 |
2 |
78 |
| Microbial activities in boreal soils : Biodegradation of organic contaminants at low temperature and ammonia oxidation | 7 |
0 |
2 |
5 |
4 |
0 |
2 |
2 |
0 |
1 |
2 |
3 |
28 |
| Microbial communities in Pb contaminated boreal forest soil | 3 |
7 |
2 |
1 |
6 |
5 |
5 |
5 |
12 |
59 |
8 |
4 |
117 |
| Microbial community composition in various soils and groundwater deposits and effects of long-term pesticide contamination | 1 |
2 |
4 |
3 |
9 |
4 |
1 |
2 |
1 |
1 |
5 |
1 |
34 |
| Microbial Community Profiling of Biodegradable Municipal Solid Waste Treatments : Aerobic Composting and Anaerobic Digestion | 5 |
6 |
4 |
17 |
11 |
9 |
2 |
1 |
5 |
7 |
15 |
11 |
93 |
| Microbial diversity in the municipal composting process and development of detection methods | 10 |
6 |
9 |
8 |
9 |
2 |
1 |
2 |
2 |
1 |
1 |
2 |
53 |
| Microbial ecology in atrazine and terbutryn dissipation in surface soils and subsurface sediments | 4 |
6 |
9 |
6 |
8 |
6 |
3 |
3 |
3 |
4 |
3 |
5 |
60 |
| Microbial identification by detection of ligation probes on DNA microarray | 11 |
0 |
2 |
2 |
7 |
2 |
1 |
3 |
2 |
1 |
5 |
1 |
37 |
| Micronuclei in Human peripheral Lymphocytes : Mechanistic Origin and Use as a Biomarker of Genotoxic Effects in Occupational Exosure | 0 |
1 |
1 |
2 |
6 |
5 |
0 |
7 |
4 |
1 |
2 |
3 |
32 |
| Missing-In-Metastasis (MIM) regulates cell morphology by promoting plasma membrane and actin cytoskeleton dynamics | 1 |
2 |
5 |
3 |
9 |
9 |
4 |
3 |
8 |
5 |
2 |
5 |
56 |
| Mitigating anthropogenic nitrogen loading with constructed wetlands in a boreal climate | 6 |
7 |
5 |
3 |
4 |
7 |
7 |
7 |
5 |
1 |
1 |
3 |
56 |
| Modeling ecological and evolutionary processes in spatially structured populations | 8 |
6 |
1 |
5 |
6 |
3 |
1 |
5 |
2 |
1 |
1 |
2 |
41 |
| Modelling the evolutionarily conserved MANF/CDNF protein family in Drosophila melanogaster | 6 |
7 |
8 |
3 |
14 |
4 |
4 |
2 |
7 |
17 |
7 |
6 |
85 |
| Models of Dispersal and Diversification | 1 |
1 |
2 |
1 |
6 |
3 |
1 |
0 |
1 |
3 |
3 |
3 |
25 |
| Molecular Alterations in Asbestos-Related Lung Cancer | 1 |
8 |
6 |
5 |
7 |
3 |
0 |
2 |
4 |
3 |
4 |
6 |
49 |
| Molecular and biophysical analysis of the non-catalytic PH, TH, SH3 and SH2 domains of Bruton tyrosine kinase (Btk) protein | 10 |
3 |
6 |
6 |
11 |
6 |
0 |
3 |
7 |
0 |
5 |
1 |
58 |
| Molecular and cellular basis of early development of the mammary gland | 7 |
4 |
17 |
49 |
62 |
33 |
5 |
12 |
4 |
11 |
6 |
5 |
215 |
| Molecular and cellular biology of infantile neuronal ceroid lipofuscinosis (INCL) | 9 |
0 |
3 |
5 |
8 |
11 |
6 |
1 |
2 |
4 |
1 |
2 |
52 |
| Molecular and mechanical control of plant secondary development | 7 |
65 |
6 |
13 |
13 |
7 |
2 |
5 |
6 |
2 |
30 |
5 |
161 |
| Molecular and psysiological characterization of rhizosphere bacteria and Frankia in forest soils devoid of actinorhizal plants | 17 |
8 |
4 |
5 |
9 |
9 |
2 |
2 |
5 |
5 |
2 |
3 |
71 |
| Molecular background of three lethal fetal syndromes | 9 |
3 |
9 |
2 |
11 |
6 |
5 |
3 |
5 |
1 |
1 |
3 |
58 |
| Molecular characterization of new archaeal viruses from high salinity environments | 4 |
4 |
11 |
6 |
10 |
4 |
4 |
0 |
4 |
1 |
3 |
3 |
54 |
| Molecular characterization of plant defense responses to erwinia carotovora | 13 |
5 |
5 |
7 |
15 |
12 |
2 |
5 |
0 |
6 |
0 |
1 |
71 |
| Molecular details of the double-stranded RNA virus replication and assembly | 7 |
8 |
11 |
12 |
16 |
14 |
6 |
6 |
7 |
12 |
6 |
10 |
115 |
| Molecular epidemiology of human rhinoviruses | 5 |
12 |
9 |
13 |
18 |
7 |
4 |
9 |
1 |
3 |
2 |
2 |
85 |
| Molecular epidemiology of human rotaviruses | 2 |
2 |
2 |
3 |
3 |
7 |
0 |
4 |
2 |
1 |
0 |
0 |
26 |
| Molecular epidemiology of sporadic breast cancer : The role of polymorphic genes involved in oestrogen biosynthesis and metabolism | 9 |
8 |
8 |
8 |
8 |
6 |
4 |
3 |
1 |
3 |
4 |
6 |
68 |
| Molecular Factors Affecting the Activity and Substrate Selectivity of the Pla Protease of Yersinia pestis | 5 |
5 |
1 |
2 |
6 |
2 |
1 |
3 |
0 |
3 |
0 |
2 |
30 |
| Molecular Genetics of Bipolar Disorder and Related Traits | 1 |
2 |
0 |
1 |
5 |
2 |
1 |
3 |
2 |
0 |
2 |
4 |
23 |
| Molecular Genetics of Inclusion Body Myositis and Late-Onset Rimmed-Vacuolar Distal Myopathy | 8 |
22 |
10 |
11 |
16 |
11 |
10 |
21 |
6 |
5 |
6 |
4 |
130 |
| Molecular genetics of Meckel syndrome : Ciliary genes are defective in MKS | 7 |
3 |
2 |
7 |
5 |
8 |
3 |
3 |
1 |
0 |
4 |
3 |
46 |
| Molecular genetics of RECQL4 syndromes | 2 |
1 |
3 |
4 |
7 |
6 |
1 |
4 |
4 |
4 |
3 |
4 |
43 |
| Molecular genetics of tooth agenesis | 16 |
8 |
8 |
16 |
17 |
9 |
6 |
7 |
11 |
9 |
4 |
3 |
114 |
| Molecular mechanisms controlling neuronal Bak expression | 6 |
8 |
3 |
6 |
8 |
4 |
4 |
2 |
4 |
2 |
4 |
5 |
56 |
| Molecular mechanisms of lymphangiogenesis : role of VEGFR-3 mediated signaling | 11 |
3 |
0 |
2 |
7 |
2 |
1 |
2 |
2 |
0 |
2 |
0 |
32 |
| Molecular Mechanisms of Sleep and Mood | 3 |
6 |
6 |
1 |
13 |
3 |
1 |
3 |
2 |
1 |
3 |
2 |
44 |
| Molecular Mechanisms Underlying Tooth Morphogenesis and Cell Differentiation | 1 |
1 |
7 |
2 |
5 |
2 |
0 |
1 |
4 |
1 |
2 |
4 |
30 |
| Molecular Organisation and Host-Cell Interactions of Tick-Borne Encephalitis Virus. What Makes the Virus Tick? | 29 |
19 |
17 |
19 |
12 |
19 |
10 |
12 |
11 |
11 |
5 |
2 |
166 |
| Molecular pathogenesis in hereditary non-polyposis colorectal cancer (HNPCC) syndrome | 5 |
6 |
9 |
7 |
12 |
6 |
3 |
5 |
4 |
6 |
3 |
3 |
69 |
| Molecular pathogenesis of Salla disease | 7 |
2 |
2 |
2 |
7 |
3 |
4 |
5 |
3 |
4 |
4 |
2 |
45 |
| Molecular pathomechanisms of muscular dystrophies | 31 |
1 |
13 |
12 |
8 |
5 |
3 |
3 |
4 |
5 |
3 |
3 |
91 |
| Molecular profiling of indoor microbial communities in moisture damaged and non-damaged buildings | 10 |
10 |
4 |
12 |
10 |
4 |
2 |
2 |
2 |
0 |
2 |
0 |
58 |
| Molecular Regulation of Craniofacial Bone and Palate Development | 6 |
0 |
1 |
0 |
6 |
0 |
2 |
2 |
2 |
4 |
0 |
4 |
27 |
| Molecular regulation of embryonic mammary gland development | 9 |
4 |
13 |
21 |
21 |
23 |
10 |
10 |
7 |
5 |
5 |
5 |
133 |
| Molecular Regulation of the Dendritic Spine Initiation | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
54 |
9 |
3 |
5 |
2 |
73 |
| Molecular responses of plants to solar UV-B and UV-A radiation | 10 |
10 |
28 |
9 |
22 |
18 |
5 |
4 |
3 |
3 |
3 |
4 |
119 |
| Molecular Tuning of Rhodopsins for High Visual Sensitivity in Different Light Environments : Variation in Absorbance Spectrum and Opsin Sequence within and between Species | 7 |
3 |
0 |
0 |
6 |
3 |
3 |
2 |
2 |
2 |
2 |
1 |
31 |
| Monographic studies on Cryphaea (Bryopsida) | 13 |
10 |
6 |
8 |
11 |
6 |
5 |
9 |
9 |
7 |
6 |
13 |
103 |
| Monolignols and their transport during lignification in Norway spruce | 0 |
0 |
0 |
41 |
24 |
7 |
8 |
0 |
2 |
3 |
3 |
5 |
93 |
| Moonlighting Proteins of Lactobacillus crispatus : Extracellular Localization, Cell Wall Anchoring and Interactions with the Host | 9 |
11 |
6 |
13 |
17 |
9 |
7 |
5 |
4 |
3 |
1 |
4 |
89 |
| Moose hunting in Finland : management of a heavily harvested population | 8 |
9 |
8 |
16 |
21 |
10 |
3 |
4 |
6 |
5 |
6 |
14 |
110 |
| Morphogenesis of Mammalian Endoplasmic Reticulum and Golgi Apparatus throughout the Cell Cycle | 3 |
5 |
6 |
4 |
9 |
5 |
2 |
2 |
3 |
1 |
7 |
1 |
48 |
| Mother-Infant Antibodies to Pneumococcal Polysaccharides and Proteins : Transfer and Persistence of Maternal Antibodies and Development of Vaccine-Induced and Naturally Acquired Antibodies in Infants | 16 |
3 |
5 |
3 |
12 |
9 |
2 |
4 |
2 |
42 |
37 |
3 |
138 |
| mRNA Localization and Cell Motility : Roles of Heparin-Binding Proteins Amphoterin and HG-GAM in Cell Migration | 6 |
2 |
2 |
2 |
5 |
2 |
0 |
2 |
3 |
1 |
0 |
0 |
25 |
| Mu in vitro transposition applications in protein engineering | 9 |
5 |
2 |
4 |
4 |
13 |
3 |
5 |
4 |
2 |
4 |
4 |
59 |
| Mu in vitro Transposition Technology in Functional Genetics and Genomics : Applications on Mouse and Bacteriophages | 1 |
0 |
1 |
1 |
6 |
2 |
1 |
4 |
2 |
1 |
4 |
1 |
24 |
| Mucosa-Adherent Lactobacilli : Commensal and Pathogenic Characteristics | 8 |
1 |
1 |
6 |
6 |
3 |
1 |
0 |
3 |
3 |
1 |
7 |
40 |
| Mucosal antibodies to protein and capsular polysaccharide antigens of streptococcus pneumoniae in children : relation to pneumococcal carriage and acute otitis media | 8 |
0 |
0 |
0 |
8 |
2 |
1 |
4 |
0 |
1 |
2 |
1 |
27 |
| Multifunctional RNA silencing pathway polymerase QDE-1 of Neurospora crassa | 4 |
3 |
2 |
11 |
10 |
11 |
2 |
1 |
1 |
4 |
6 |
1 |
56 |
| Multiplex RT-PCR in the diagnosis of human picornaviruses and human respiratory viruses | 8 |
9 |
7 |
3 |
9 |
6 |
7 |
2 |
3 |
2 |
2 |
2 |
60 |
| Mutations as molecular tools : The metabolic-rate dependent molecular clock and DNA barcoding of allied species | 5 |
1 |
2 |
1 |
7 |
10 |
2 |
8 |
0 |
2 |
7 |
10 |
55 |
| Mycorrhizal fungi and nitrogen dynamics in drained peatland | 11 |
11 |
4 |
1 |
7 |
1 |
0 |
1 |
4 |
1 |
1 |
3 |
45 |
| Myelin plasticity in mouse resilience and susceptibility to psychosocial stress : implications for anxiety disorders | 16 |
10 |
12 |
17 |
31 |
14 |
5 |
10 |
4 |
2 |
4 |
2 |
127 |
| N-Bak : a Neuron-Specific Splice Variant of Bak with anti-Apoptotic Properties | 10 |
5 |
2 |
2 |
7 |
4 |
4 |
2 |
3 |
2 |
3 |
1 |
45 |
| N-syndecan and HB-GAM in neural migration and differentiation : Modulation of growth factor activity in brain | 5 |
7 |
10 |
5 |
3 |
4 |
0 |
1 |
1 |
1 |
3 |
2 |
42 |
| Natural stimuli and experimental setups in the study of the neural basis of social interaction | 3 |
3 |
0 |
1 |
6 |
7 |
3 |
1 |
4 |
2 |
0 |
1 |
31 |
| Natural succession and human-induced changes in the soft-bottom macrovegetation of shallow brackish bays on the southern coast of Finland | 5 |
4 |
6 |
8 |
14 |
5 |
3 |
3 |
7 |
3 |
4 |
1 |
63 |
| Natural succession of microalgal communities during the cold-water season and the impact of increased solar irradiance on sea ice algae | 4 |
1 |
7 |
1 |
7 |
1 |
1 |
1 |
1 |
1 |
2 |
0 |
27 |
| Nephrin-associated molecules in human glomerular diseases | 6 |
2 |
1 |
2 |
9 |
3 |
6 |
3 |
1 |
6 |
7 |
2 |
48 |
| Network Pharmacology Approaches for Understanding Traditional Chinese Medicine | 19 |
15 |
19 |
30 |
23 |
12 |
174 |
44 |
22 |
23 |
19 |
13 |
413 |
| Networks in urban climate policy and governance | 0 |
0 |
0 |
94 |
94 |
15 |
3 |
8 |
8 |
5 |
9 |
6 |
242 |
| Neural processing at the sensitivity limit of vision : from retinal circuits to behavior | 13 |
17 |
17 |
26 |
20 |
24 |
5 |
9 |
4 |
9 |
10 |
13 |
167 |
| Neuronal ICAM-5 regulates synaptic maturation and microglia functions | 10 |
8 |
9 |
9 |
10 |
14 |
7 |
2 |
7 |
3 |
8 |
4 |
91 |
| Neuronal K-Cl Cotransporter : Transcriptional Mechanisms of KCC2 Gene Regulation | 12 |
4 |
2 |
4 |
11 |
7 |
0 |
3 |
5 |
3 |
2 |
1 |
54 |
| Neuronal synapse formation regulated by intercellular adhesion molecules-5 (ICAM-5) | 15 |
16 |
6 |
3 |
9 |
16 |
7 |
2 |
3 |
3 |
4 |
0 |
84 |
| Neurotrophic factors and their receptors | 12 |
2 |
5 |
14 |
13 |
6 |
1 |
1 |
3 |
2 |
4 |
3 |
66 |
| Neurotrophic factors GDNF and NRTN : from basic properties to clinical trials | 9 |
6 |
8 |
3 |
12 |
5 |
3 |
5 |
3 |
2 |
0 |
2 |
58 |
| Neurotrophic Factors in Rodent Heart : From Development to Pathophysiology | 9 |
1 |
2 |
3 |
4 |
2 |
2 |
1 |
3 |
0 |
1 |
3 |
31 |
| Neurotrophic receptor TrkB activation as an orchestrator of neuronal plasticity | 8 |
7 |
6 |
0 |
5 |
7 |
52 |
3 |
8 |
5 |
2 |
5 |
108 |
| Neurotrophins and neuronal plasticity in the action of antidepressants and morphine | 10 |
0 |
5 |
7 |
5 |
2 |
1 |
4 |
1 |
0 |
0 |
0 |
35 |
| New insight into mechanisms of transcellular propagation of tau and α-synuclein in neurodegenerative diseases | 6 |
4 |
4 |
12 |
18 |
5 |
5 |
2 |
4 |
0 |
4 |
4 |
68 |
| Nitrogen cycling in aphotic coastal sandy sediments of the Baltic Sea | 4 |
1 |
4 |
2 |
4 |
2 |
1 |
0 |
2 |
2 |
2 |
0 |
24 |
| Nitrous oxide emissions from selected natural and managed northern ecosystems | 18 |
11 |
2 |
7 |
13 |
11 |
1 |
2 |
5 |
7 |
9 |
3 |
89 |
| Non-neuronal roles for GDNF and novel GDNF family receptors | 4 |
2 |
1 |
2 |
3 |
1 |
0 |
0 |
2 |
1 |
3 |
2 |
21 |
| Notch signaling in blood and lymphatic vessel development | 6 |
5 |
5 |
3 |
7 |
4 |
5 |
5 |
4 |
2 |
3 |
2 |
51 |
| Novel analytical methods for the identification of emerging contaminants in aquatic environments | 9 |
5 |
7 |
4 |
17 |
10 |
9 |
4 |
3 |
4 |
1 |
2 |
75 |
| Novel CDNF/MANF protein family : Molecular structure, expression and neurotrophic activity | 14 |
4 |
9 |
3 |
8 |
4 |
2 |
6 |
3 |
1 |
2 |
8 |
64 |
| Novel Molecular Mechanisms of Arabidopsis Disease Resistance | 9 |
10 |
2 |
3 |
5 |
1 |
1 |
1 |
3 |
2 |
1 |
4 |
42 |
| Novel molecular mechanisms of dendritic spine development | 4 |
7 |
4 |
9 |
4 |
5 |
1 |
5 |
6 |
4 |
3 |
1 |
53 |
| Novel Regulators of Vascular Development in Arabidopsis thaliana | 3 |
3 |
3 |
9 |
8 |
10 |
7 |
3 |
1 |
2 |
3 |
2 |
54 |
| Novel roles of p75 neurotrophin receptor in Low-density lipoprotein receptor regulation and lipid signaling | 8 |
7 |
9 |
7 |
6 |
4 |
3 |
6 |
2 |
0 |
4 |
1 |
57 |
| Nuclear Import Mechanisms of STAT and NF-kB Transcription Factors | 11 |
5 |
1 |
7 |
16 |
9 |
10 |
7 |
7 |
2 |
5 |
3 |
83 |
| Nutrient dynamics in eutrophic lakes : Effects of resuspension, macrophytes and oxygen | 4 |
6 |
10 |
11 |
8 |
7 |
6 |
4 |
2 |
3 |
3 |
11 |
75 |
| Occurence of the introduced black rat (Rattus rattus) and its potential effects on endemic rodents in southeastern Madagascar | 2 |
4 |
4 |
4 |
10 |
7 |
0 |
1 |
8 |
57 |
175 |
4 |
276 |
| Occurrence, habitat use and movements of the flying squirrel in human-modified forest landscapes | 9 |
4 |
9 |
7 |
11 |
7 |
4 |
4 |
4 |
1 |
3 |
3 |
66 |
| Of the interactions between eye fluke parasites and salmonid fishes | 7 |
3 |
4 |
2 |
3 |
4 |
2 |
2 |
0 |
3 |
2 |
0 |
32 |
| Oligogalacturonide signalling in plant innate immunity | 7 |
6 |
5 |
17 |
11 |
9 |
3 |
5 |
6 |
3 |
2 |
4 |
78 |
| On the deterioration and restoration of mire invertebrate communities | 4 |
3 |
3 |
7 |
8 |
4 |
5 |
1 |
5 |
1 |
1 |
1 |
43 |
| On the Development of the Turtle Scute Pattern and the Origins of its Variation | 42 |
38 |
43 |
25 |
39 |
31 |
8 |
11 |
12 |
10 |
7 |
12 |
278 |
| On the ecology of cold-water phytoplankton in the Baltic Sea | 7 |
4 |
9 |
10 |
10 |
4 |
4 |
3 |
5 |
3 |
2 |
2 |
63 |
| On the histone acetyltransferase hMOF | 13 |
2 |
1 |
4 |
9 |
7 |
1 |
1 |
7 |
4 |
6 |
5 |
60 |
| On the mechanisms of neural development in the ventral telencephalon | 1 |
2 |
3 |
3 |
9 |
5 |
4 |
2 |
4 |
5 |
3 |
2 |
43 |
| On the origin of snakes based on geometric morphometrics : morphology, paleontology, phylogeny, ecology, and development | 28 |
12 |
19 |
21 |
65 |
25 |
16 |
13 |
23 |
15 |
33 |
16 |
286 |
| On the origins and evolution of morphological complexity : a developmental perspective | 11 |
24 |
10 |
12 |
7 |
5 |
5 |
8 |
9 |
3 |
5 |
3 |
102 |
| On the phylogeny and diversity of the microsoroid ferns (Polypodiaceae) | 11 |
20 |
11 |
7 |
10 |
22 |
11 |
9 |
14 |
20 |
10 |
6 |
151 |
| On the role of bacterial production and denitrification in some less-studied Baltic Sea habitats | 7 |
2 |
0 |
2 |
5 |
2 |
0 |
1 |
1 |
1 |
15 |
1 |
37 |
| Orchestrating Plant Defences in Response to Botrytis cinerea and Apoplastic ROS : Hormone Interactions, Transcriptional and Posttranscriptional Regulation | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
55 |
20 |
15 |
15 |
7 |
112 |
| Organelle specific mechanisms of neuronal cell death | 15 |
6 |
8 |
12 |
7 |
10 |
3 |
3 |
4 |
4 |
3 |
4 |
79 |
| Origin and regeneration of free-living Fucus vesiculosus in the Baltic Sea | 0 |
4 |
134 |
14 |
17 |
14 |
3 |
4 |
5 |
9 |
10 |
16 |
230 |
| ORP1L, a new Rab7 effector and regulator of late endosome functions | 8 |
2 |
1 |
3 |
5 |
7 |
2 |
2 |
3 |
2 |
0 |
0 |
35 |
| ORP2 is a sterol receptor that regulates cellular lipid metabolism | 9 |
3 |
1 |
4 |
12 |
7 |
1 |
1 |
5 |
0 |
4 |
1 |
48 |
| Outer Membrane Protease/Adhesin PgtE of Salmonella enterica : Role in Salmonella-Host Interaction | 5 |
8 |
7 |
4 |
12 |
3 |
2 |
3 |
3 |
8 |
5 |
12 |
72 |
| Overwintering ecology of northern field layer plants : snow and photosynthesis in Vaccinium vitis-idaea L. | 5 |
1 |
7 |
4 |
8 |
2 |
3 |
2 |
3 |
5 |
0 |
2 |
42 |
| Overwintering in wood plants : involvement of ABA and dehydrins | 7 |
6 |
3 |
2 |
5 |
2 |
3 |
0 |
1 |
2 |
1 |
2 |
34 |
| Oxygen reduction and proton translocation by cytochrome c oxidase | 8 |
6 |
2 |
3 |
6 |
10 |
2 |
2 |
2 |
3 |
2 |
2 |
48 |
| Ozone-induced signaling in Arabidopsis thaliana | 0 |
0 |
3 |
2 |
7 |
5 |
0 |
2 |
5 |
4 |
3 |
3 |
34 |
| Packaging Motors of Cystoviruses | 10 |
8 |
6 |
8 |
8 |
8 |
11 |
29 |
9 |
5 |
2 |
1 |
105 |
| Paracrine orchestration of intestinal regeneration and aging | 24 |
9 |
12 |
9 |
27 |
11 |
9 |
9 |
43 |
26 |
15 |
10 |
204 |
| Parasitoid foraging behaviour in a competitive environment | 5 |
4 |
4 |
0 |
11 |
8 |
1 |
3 |
2 |
5 |
6 |
2 |
51 |
| Pathogen-Induced Defense Signaling and Signal Crosstalk in Arabidopsis | 4 |
1 |
2 |
4 |
11 |
1 |
1 |
3 |
1 |
3 |
4 |
2 |
37 |
| Pathogenetic features of proteinuria studies on congenital nephrotic syndrome of the Finnish type | 13 |
10 |
6 |
3 |
8 |
7 |
5 |
0 |
1 |
0 |
2 |
1 |
56 |
| Pathogenetic mechanisms and genotype phenotype correlations in nemaline myopathies and related disorders caused by mutations in tropomyosin genes and nebulin | 10 |
16 |
8 |
6 |
18 |
15 |
8 |
1 |
4 |
2 |
7 |
3 |
98 |
| Pathogenic and Molecular Characteristics of Two Isolates of HEV-B Species | 7 |
3 |
7 |
7 |
9 |
8 |
2 |
0 |
2 |
6 |
5 |
4 |
60 |
| Pathogenic Mechanisms of Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy (PLOSL) | 1 |
3 |
6 |
3 |
6 |
3 |
2 |
3 |
3 |
6 |
1 |
0 |
37 |
| Pathogenicity, functional significance and clinical phenotype of mismatch repair gene MSH2 variants found in cancer patients | 9 |
6 |
14 |
7 |
14 |
5 |
6 |
0 |
1 |
6 |
6 |
3 |
77 |
| Pathway for the Formation of Semliki Forest Virus RNA Replication Complex | 25 |
8 |
9 |
7 |
6 |
8 |
2 |
5 |
3 |
2 |
3 |
3 |
81 |
| PCSK9 and berberine as modulators of lipoprotein receptors and neuronal cell death | 19 |
9 |
12 |
15 |
13 |
8 |
9 |
3 |
5 |
6 |
2 |
2 |
103 |
| Pentitol phosphate dehydrogenases : Discovery, characterization and use in D-arabitol and xylitol production by metabolically engineered Bacillus subtilis | 6 |
6 |
6 |
2 |
10 |
3 |
4 |
8 |
9 |
2 |
8 |
8 |
72 |
| Perception of solar UV radiation and blue light by plants : photoreceptors, transcriptome and environmental acclimation | 7 |
6 |
11 |
6 |
13 |
3 |
5 |
3 |
0 |
4 |
5 |
6 |
69 |
| Peroxidases in lignifying xylem of Norway spruce, Scots pine and silver birch | 20 |
3 |
2 |
2 |
12 |
4 |
2 |
2 |
1 |
0 |
0 |
2 |
50 |
| Personality traits in the blue tit | 14 |
4 |
5 |
5 |
10 |
7 |
1 |
1 |
2 |
4 |
1 |
3 |
57 |
| Phagophore membrane connections and RAB24 in autophagy | 5 |
4 |
2 |
11 |
8 |
4 |
9 |
3 |
5 |
5 |
3 |
2 |
61 |
| Phosphatidylserine translocation in mammalian cells | 27 |
5 |
7 |
11 |
19 |
23 |
5 |
11 |
14 |
9 |
6 |
6 |
143 |
| Phospholipids of lipid-containing bacteriophages and their transbilayer distribution | 7 |
2 |
1 |
4 |
3 |
4 |
0 |
3 |
1 |
1 |
4 |
4 |
34 |
| Phosphoproteomic characterization of viral infection | 8 |
6 |
1 |
3 |
1 |
10 |
3 |
4 |
3 |
9 |
1 |
1 |
50 |
| Phosphorylation of the α- and β-chains of LFA-1 regulates its interaction with cytoplasmic proteins and crosstalk to VLA-4 integrin | 7 |
3 |
2 |
5 |
8 |
3 |
3 |
0 |
3 |
3 |
6 |
6 |
49 |
| Photochemical transformation of dissolved organic matter in aquatic environment : From a boreal lake and Baltic Sea to global coastal ocean | 10 |
5 |
1 |
3 |
9 |
5 |
1 |
7 |
4 |
1 |
2 |
1 |
49 |
| Phylogenetic studies of cyanobacterial lichens | 8 |
3 |
2 |
0 |
6 |
9 |
0 |
3 |
0 |
1 |
3 |
2 |
37 |
| Phylogenetics of Myrmica ants and their social parasites | 1 |
1 |
2 |
5 |
7 |
6 |
0 |
3 |
2 |
4 |
1 |
1 |
33 |
| Phylogenetics, taxon delimitation and phylogenetic diversity | 5 |
3 |
5 |
6 |
15 |
7 |
2 |
2 |
5 |
2 |
4 |
4 |
60 |
| Phylogenomics and adaptive evolution in stickleback fishes | 17 |
3 |
10 |
3 |
12 |
22 |
2 |
3 |
3 |
3 |
1 |
2 |
81 |
| Phylogeny and biogeography of liverworts (Marchantiophyta), evidence from the Southern Hemisphere family Schistochilaceae and the cosmopolitan genus Herbertus (Herbertaceae) | 25 |
11 |
24 |
20 |
19 |
20 |
14 |
8 |
9 |
12 |
7 |
14 |
183 |
| Phylogeny and evolutionary relationships of the moss families Brachytheciaceae and Meteoriaceae | 17 |
12 |
21 |
30 |
35 |
28 |
12 |
16 |
13 |
10 |
5 |
11 |
210 |
| Phylogeny and host associations of cotesia parasitoids attacking checkerspot butterflies | 3 |
6 |
7 |
3 |
6 |
5 |
5 |
4 |
7 |
4 |
3 |
1 |
54 |
| Phylogeny of a taxonomically difficult group and evolution of host location mechanism | 4 |
7 |
3 |
6 |
11 |
6 |
2 |
1 |
1 |
0 |
8 |
4 |
53 |
| Phylogeny, phyletic coevolution and phylogeography of anoplocephaline cestodes in mammals | 5 |
3 |
3 |
6 |
10 |
5 |
2 |
1 |
1 |
1 |
2 |
2 |
41 |
| Phylogeny, symbiotic interactions and chemical variation in the genus Bryoria section Implexae (Parmeliaceae, Lecanoromycetes) | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Phylogeography and Adaptive Divergence of Three-spined Stickleback Populations | 10 |
1 |
0 |
0 |
10 |
3 |
5 |
1 |
0 |
1 |
3 |
2 |
36 |
| Phylogeography and evolution of freshwater cottid fishes | 6 |
5 |
1 |
6 |
15 |
6 |
2 |
2 |
4 |
4 |
2 |
6 |
59 |
| Phylogeography and historical introgression in Stickleback fishes | 11 |
2 |
1 |
3 |
7 |
4 |
2 |
3 |
1 |
1 |
1 |
2 |
38 |
| Phylogeography and hybrid swarms : history of brackish water bivalve diversity in North European marginal seas | 3 |
1 |
3 |
4 |
5 |
3 |
3 |
0 |
2 |
1 |
2 |
0 |
27 |
| Phylogeography and population genetics of social parasitism in Myrmica ants | 4 |
2 |
2 |
2 |
7 |
4 |
2 |
2 |
3 |
3 |
0 |
1 |
32 |
| Phylogeography and Population Genetics of the Moor frog (Rana arvalis Nilsson) in Northern Europe | 5 |
7 |
3 |
4 |
10 |
4 |
4 |
6 |
4 |
2 |
2 |
4 |
55 |
| Phylogeography of amphi-boreal marine fauna | 2 |
4 |
2 |
6 |
9 |
3 |
0 |
2 |
3 |
4 |
1 |
4 |
40 |
| Physiological and Molecular Analyses of Cold Acclimation of Plants | 1 |
1 |
0 |
3 |
5 |
3 |
4 |
0 |
4 |
2 |
1 |
3 |
27 |
| Physiological Modulation of the Reverse Cholesterol Transport Pathway in vivo | 10 |
7 |
2 |
14 |
10 |
4 |
3 |
4 |
2 |
2 |
2 |
2 |
62 |
| Physiological stress and life-history strategies in the eider (Somateria mollissima) | 7 |
0 |
9 |
4 |
6 |
1 |
4 |
5 |
3 |
5 |
3 |
5 |
52 |
| Phytohormone-related crosstalk in pathogen and stomatal responses in Arabidopsis thaliana | 15 |
4 |
3 |
3 |
10 |
9 |
9 |
3 |
3 |
2 |
2 |
4 |
67 |
| Phytoplankton ecology of subarctic lakes in Finnish Lapland | 5 |
2 |
1 |
1 |
6 |
2 |
2 |
2 |
1 |
2 |
1 |
2 |
27 |
| Phytoplankton functions and community properties in the pelagic food web | 7 |
11 |
10 |
7 |
5 |
5 |
1 |
2 |
5 |
0 |
0 |
0 |
53 |
| Phytoplankton quantity as an indicator of eutrophication in Finnish coastal waters : Applications within the Water Framework Directive | 10 |
7 |
4 |
9 |
16 |
13 |
12 |
4 |
3 |
3 |
6 |
2 |
89 |
| Phytoplanktonic life in boreal humic lakes : special emphasis on autotrophic picoplankton and microbial food webs | 1 |
2 |
1 |
3 |
5 |
3 |
2 |
5 |
1 |
4 |
6 |
4 |
37 |
| Plant biomarkers as a proxy to study highly decomposed fen peat | 7 |
5 |
3 |
3 |
7 |
11 |
5 |
6 |
3 |
5 |
5 |
3 |
63 |
| Plant guard cell anion channel SLAC1 regulates stomatal closure | 8 |
5 |
5 |
4 |
11 |
8 |
4 |
4 |
1 |
1 |
5 |
5 |
61 |
| Plant oxygen deprivation stress and function of plant mitochondria under anoxia | 2 |
2 |
3 |
4 |
9 |
10 |
7 |
4 |
3 |
3 |
3 |
3 |
53 |
| Plant Tissue Cultures as Models for Tree Physiology : Somatic Embryogenesis of Tilia cordata and Lignin Biosynthesis in Picea abies Suspension Cultures as Case Studies | 18 |
5 |
1 |
2 |
5 |
9 |
4 |
7 |
10 |
6 |
5 |
5 |
77 |
| Plant-soil feedbacks as affecting ecosystem services in urban greenspaces | 8 |
3 |
4 |
2 |
8 |
4 |
4 |
5 |
1 |
1 |
2 |
3 |
45 |
| Plasma Phospholipid Transfer Protein (PLTP) : Quantitation, Biosynthesis, and Involvement in Hepatic Lipid Homeostasis | 7 |
0 |
1 |
1 |
4 |
0 |
1 |
1 |
3 |
2 |
0 |
0 |
20 |
| Plasmids and aromatic degradation in Sphingomonas for bioremediation : Aromatic ring cleavage genes in soil and rhizosphere | 7 |
3 |
8 |
7 |
5 |
9 |
1 |
4 |
3 |
1 |
1 |
1 |
50 |
| Platelet-Collagen Interaction and Microvesiculation | 4 |
1 |
0 |
5 |
3 |
3 |
3 |
1 |
1 |
0 |
0 |
1 |
22 |
| Pollination networks of the High Arctic : adding a functional perspective | 10 |
1 |
12 |
7 |
9 |
7 |
3 |
1 |
5 |
4 |
1 |
3 |
63 |
| Pollutant remediation strategies in the soil : electrokinetic remediation, biostimulation, and experimental design | 6 |
6 |
14 |
18 |
17 |
10 |
11 |
14 |
1 |
3 |
18 |
7 |
125 |
| Polyamine Metabolism During Development of Somatic and Zygotic Embryos of Picea Abies (Norway Spruce) | 21 |
6 |
1 |
3 |
12 |
5 |
2 |
5 |
3 |
2 |
3 |
3 |
66 |
| Polymorphic low penetrance genes and breast cancer : The role of genes involved in metabolism of xenobiotics, estrogens and reactive oxygen species | 20 |
8 |
10 |
9 |
9 |
13 |
3 |
5 |
1 |
5 |
4 |
5 |
92 |
| Polypore assemblages in boreal old-growth forests, and associated Coleoptera | 16 |
7 |
2 |
13 |
13 |
6 |
4 |
2 |
2 |
1 |
1 |
0 |
67 |
| Population biology of periodic Xestia moths | 1 |
1 |
0 |
1 |
5 |
6 |
3 |
3 |
0 |
0 |
0 |
0 |
20 |
| Population differentiation in sticklebacks : disentangling maternal, environmental and genetic effects | 1 |
6 |
3 |
2 |
3 |
2 |
0 |
2 |
2 |
3 |
0 |
2 |
26 |
| Population dynamics of blue mussels in a variable environment at the edge of their range | 4 |
8 |
4 |
2 |
8 |
6 |
3 |
2 |
2 |
7 |
4 |
3 |
53 |
| Population dynamics of flounders in the northern Baltic Sea : declines, cryptic species and environmental drivers | 7 |
1 |
9 |
2 |
3 |
2 |
0 |
1 |
0 |
3 |
8 |
0 |
36 |
| Population dynamics of seals : the influences of spatial and temporal structures | 2 |
12 |
0 |
5 |
6 |
8 |
0 |
3 |
4 |
0 |
4 |
4 |
48 |
| Population structure and evolution in the ant Plagiolepis pygmaea and its two social parasites Plagiolepis xene and Plagiolepis grassei | 0 |
1 |
2 |
1 |
2 |
1 |
0 |
3 |
0 |
1 |
1 |
5 |
17 |
| Positional cloning and pathway analysis of the asthma susceptibility gene, NPSR1 | 7 |
12 |
16 |
6 |
6 |
9 |
3 |
3 |
3 |
1 |
0 |
3 |
69 |
| Post-translational regulation of KCC2 in the rat hippocampus | 3 |
2 |
2 |
1 |
9 |
5 |
2 |
2 |
3 |
1 |
1 |
1 |
32 |
| Post-translational Regulation of TGF-beta Signaling in Drosophila Development | 9 |
0 |
4 |
2 |
4 |
3 |
1 |
0 |
5 |
3 |
2 |
1 |
34 |
| Postmitotic state of a cell as a challenge for regeneration : inner ear as a model | 14 |
4 |
2 |
2 |
7 |
3 |
0 |
1 |
3 |
3 |
4 |
3 |
46 |
| Posttranslational modifications of potato virus A movement related proteins CP and VPg | 5 |
0 |
0 |
1 |
2 |
5 |
0 |
1 |
0 |
1 |
1 |
1 |
17 |
| Potential of filamentous macroalgae and sessile invertebrates for bioremediation and valorization in the northern Baltic Sea | 14 |
7 |
8 |
6 |
8 |
5 |
4 |
1 |
5 |
2 |
4 |
0 |
64 |
| Potential of the slow pyrolysis products birch tar oil, wood vinegar and biochar in sustainable plant protection : pesticidal effects, soil improvement and environmental risks | 21 |
18 |
20 |
17 |
15 |
16 |
16 |
29 |
28 |
29 |
19 |
22 |
250 |
| Power dynamics and participation in post-disaster recovery | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Practices and Policies for Carbon Neutrality : Energy Transition in the Helsinki Metropolitan Area | 9 |
9 |
7 |
16 |
26 |
7 |
3 |
16 |
10 |
11 |
9 |
13 |
136 |
| Pre- and post-copulatory sexual selection in the least killifish, Heterandria formosa | 1 |
4 |
1 |
4 |
7 |
4 |
0 |
0 |
4 |
1 |
0 |
0 |
26 |
| Precautionary management of Baltic Sea cod (Gadus morhua callaris) under different harvesting and environmental scenarios | 3 |
5 |
5 |
6 |
8 |
8 |
1 |
6 |
3 |
4 |
1 |
0 |
50 |
| Precision medicine for lung cancer : models, functional assays and mechanisms | 4 |
5 |
0 |
4 |
8 |
5 |
1 |
3 |
6 |
8 |
9 |
6 |
59 |
| Preparing for the unprecedented : Moving towards quantitative understanding of oil spill impacts on Arctic marine biota | 6 |
0 |
2 |
1 |
8 |
2 |
2 |
21 |
3 |
2 |
0 |
0 |
47 |
| Present and future fluxes of nitrogen, phosphorus and carbon from catchments to lakes in a boreal landscape | 2 |
0 |
1 |
0 |
5 |
3 |
3 |
2 |
3 |
6 |
0 |
0 |
25 |
| Prevention of inflammatory cellular responses by ethanol and hemin interplay between inflammasomes and processes inhibiting inflammation | 10 |
11 |
10 |
10 |
20 |
12 |
4 |
0 |
4 |
7 |
8 |
6 |
102 |
| Probing lipid domains in model membranes and in mammalian cells | 7 |
6 |
1 |
1 |
7 |
5 |
1 |
2 |
3 |
0 |
0 |
0 |
33 |
| Production and Use of Mammalian Glycosyltransferases | 11 |
2 |
1 |
1 |
4 |
4 |
4 |
1 |
3 |
2 |
3 |
2 |
38 |
| Production of F4 Fimbrial Adhesin in Plants : a Model for Oral Porcine Vaccine against Enterotoxigenic Escherichia coli | 4 |
4 |
6 |
2 |
4 |
4 |
2 |
0 |
2 |
2 |
1 |
2 |
33 |
| Prokaryotic microorganisms, viruses, and antimicrobial agents from hypersaline environments | 6 |
8 |
12 |
7 |
7 |
5 |
6 |
8 |
5 |
1 |
0 |
4 |
69 |
| Prostatic acid phosphatase as a regulator of endo/exocytosis and lysosomal degradation | 6 |
2 |
9 |
5 |
10 |
10 |
3 |
3 |
1 |
1 |
4 |
2 |
56 |
| Protein Folding before and after Translocation into the Yeast Endoplasmic Reticulum | 3 |
0 |
6 |
1 |
10 |
0 |
1 |
0 |
1 |
4 |
2 |
3 |
31 |
| Proteolytic Modification of High Density Lipoproteins Decreases Their Ability to Induce Cholesterol Efflux from Macrophage Foam Cells | 2 |
5 |
7 |
3 |
4 |
4 |
2 |
3 |
1 |
2 |
5 |
2 |
40 |
| Proteolytic Processing as a Regulator of BMP-type Signaling in Drosophila Development | 4 |
5 |
3 |
5 |
5 |
1 |
0 |
1 |
1 |
0 |
5 |
0 |
30 |
| Proteomic Characterization of Biological Effects Induced by Engineered Nanomaterials | 4 |
3 |
1 |
1 |
10 |
4 |
3 |
3 |
6 |
0 |
1 |
1 |
37 |
| Proteomic characterization of host response to viral infection | 10 |
0 |
2 |
0 |
5 |
4 |
1 |
2 |
2 |
1 |
0 |
0 |
27 |
| Protomyces Comparative Genomics and Modulation of Arabidopsis Immunity | 6 |
1 |
1 |
5 |
9 |
4 |
5 |
2 |
5 |
6 |
3 |
4 |
51 |
| Proton translocation coupled to electron transfer reactions in terminal oxidases | 7 |
1 |
0 |
1 |
6 |
5 |
23 |
171 |
0 |
6 |
3 |
3 |
226 |
| Proximate and ultimate determinants of reproductive skew in the polygyne ant Formica fusca | 15 |
3 |
6 |
6 |
6 |
5 |
0 |
4 |
6 |
3 |
3 |
2 |
59 |
| PrsA lipoprotein and posttranslocational folding of secretory proteins in Bacillus subtilis | 7 |
26 |
2 |
9 |
7 |
4 |
0 |
4 |
3 |
1 |
3 |
2 |
68 |
| Pulmonary Infection and Atherosclerosis in an Experimental Chlamydia pneumoniae Model | 10 |
3 |
0 |
4 |
4 |
4 |
3 |
1 |
2 |
2 |
1 |
0 |
34 |
| Quality control of mitochondrial gene expression | 14 |
16 |
13 |
5 |
25 |
7 |
3 |
9 |
13 |
16 |
11 |
6 |
138 |
| Quantifying biomass and carbon processing of benthic fauna in a coastal sea : past, present and future | 3 |
5 |
1 |
10 |
7 |
5 |
2 |
4 |
1 |
2 |
2 |
2 |
44 |
| Quantitative and population genetics of the Glanville fritillary butterfly | 5 |
3 |
4 |
3 |
12 |
7 |
1 |
2 |
1 |
1 |
4 |
2 |
45 |
| Quantitative genetics in nonlinear genotype-phenotype maps | 27 |
6 |
25 |
11 |
11 |
8 |
6 |
7 |
4 |
5 |
5 |
7 |
122 |
| Quantitative PCR in the diagnosis and monitoring of human cytomegalovirus infection in organ transplant patients | 11 |
7 |
8 |
6 |
9 |
8 |
3 |
2 |
2 |
1 |
2 |
1 |
60 |
| Quorum sensing in the plant pathogen Erwinia carotovora subsp. carotovora | 20 |
3 |
6 |
4 |
5 |
2 |
1 |
3 |
5 |
5 |
3 |
4 |
61 |
| Rab8 and R-Ras as modulators of cell shape | 4 |
2 |
0 |
1 |
1 |
1 |
6 |
29 |
1 |
0 |
3 |
1 |
49 |
| Rad51c is a Tumor Suppressor in Mammary and Sebaceous Glands | 8 |
6 |
4 |
4 |
6 |
3 |
2 |
4 |
2 |
2 |
1 |
2 |
44 |
| Reactive oxygen species and SRO proteins as regulators of gene expression in Arabidopsis thaliana | 10 |
6 |
6 |
5 |
8 |
10 |
4 |
3 |
2 |
4 |
2 |
1 |
61 |
| Recent eutrophication of coastal waters in southern Finland : A palaeolimnological assessment | 9 |
2 |
0 |
4 |
6 |
0 |
2 |
0 |
2 |
0 |
3 |
2 |
30 |
| Recognition and social behaviour in Formica ants | 11 |
6 |
7 |
0 |
12 |
6 |
3 |
3 |
2 |
3 |
5 |
0 |
58 |
| Recognizing Lynch Syndrome by DNA Mismatch Repair Deficiency | 9 |
11 |
32 |
10 |
28 |
24 |
22 |
11 |
7 |
3 |
11 |
6 |
174 |
| Recombinant hantavirus proteins : antigenic properties and diagnostic applications | 7 |
0 |
1 |
1 |
9 |
1 |
1 |
2 |
1 |
3 |
2 |
4 |
32 |
| Recombinant structural proteins of rubella virus | 8 |
2 |
10 |
3 |
10 |
6 |
5 |
2 |
3 |
4 |
2 |
4 |
59 |
| Recovery of Yeast Saccharomyces cerevisiae after Thermal Insult | 2 |
5 |
6 |
2 |
11 |
7 |
1 |
3 |
1 |
5 |
1 |
5 |
49 |
| Recovery responses of acidified Finnish lakes under declining acid deposition | 12 |
2 |
2 |
1 |
8 |
5 |
0 |
2 |
0 |
2 |
1 |
0 |
35 |
| Redox-linked proton transfer by cytochrome c oxidase | 4 |
5 |
2 |
2 |
5 |
5 |
2 |
2 |
0 |
1 |
4 |
2 |
34 |
| Reduced mismatch repair gene expression and functional deficiency as indicators of Lynch syndrome | 6 |
6 |
18 |
12 |
10 |
17 |
10 |
1 |
4 |
5 |
4 |
6 |
99 |
| Refining the genetic architecture of Atlantic salmon (Salmo salar) maturation using genomics-enabled approaches | 6 |
4 |
4 |
6 |
10 |
4 |
3 |
0 |
8 |
3 |
2 |
1 |
51 |
| Regulation of Actin Dynamics in Animal Cells : The Role of ADF/cofilin and Twinfilin | 5 |
2 |
0 |
4 |
5 |
5 |
1 |
2 |
1 |
0 |
5 |
2 |
32 |
| Regulation of Cell Polarity Determinant Scribble in Drosophila and Mammals | 46 |
21 |
14 |
4 |
15 |
4 |
3 |
3 |
3 |
2 |
3 |
4 |
122 |
| Regulation of contractile actin structures in non-muscle cells | 11 |
1 |
8 |
4 |
6 |
3 |
2 |
7 |
1 |
1 |
4 |
5 |
53 |
| Regulation of GABAergic neuron identity and diversity in the developing midbrain | 3 |
6 |
4 |
1 |
10 |
3 |
2 |
0 |
2 |
4 |
1 |
5 |
41 |
| Regulation of Growth by Drosophila FoxO Transcription Factor | 7 |
2 |
2 |
1 |
8 |
8 |
1 |
0 |
0 |
2 |
1 |
5 |
37 |
| Regulation of heat shock response in yeast and mammalian cells | 7 |
4 |
3 |
3 |
8 |
6 |
0 |
4 |
0 |
0 |
1 |
2 |
38 |
| Regulation of Human Sex Hormone-Binding Globulin Gene (shbg) Expression | 19 |
16 |
15 |
12 |
7 |
26 |
1 |
1 |
4 |
0 |
3 |
4 |
108 |
| Regulation of leukocyte integrin binding to Ig-family ligands | 5 |
4 |
11 |
10 |
7 |
3 |
6 |
34 |
2 |
1 |
5 |
1 |
89 |
| Regulation of neural progenitor cell proliferation and fate by proteolytic pathways and inflammatory signals in the brain | 3 |
3 |
1 |
10 |
10 |
8 |
18 |
15 |
8 |
1 |
2 |
3 |
82 |
| Regulation of Osteoblast Differentiation and Gene Expression by Phosphodiesterases and Bioactive Peptides | 16 |
18 |
5 |
8 |
11 |
5 |
2 |
5 |
4 |
6 |
3 |
4 |
87 |
| Regulation of Stat5 activation | 9 |
1 |
0 |
3 |
6 |
2 |
0 |
0 |
2 |
1 |
5 |
3 |
32 |
| Regulation of the Actin Cytoskeleton by Twinfilin | 5 |
2 |
0 |
1 |
4 |
0 |
2 |
3 |
1 |
1 |
0 |
1 |
20 |
| Regulation of the minor spliceosome through alternative splicing and nuclear retention of the U11/U12-65K mRNA | 5 |
4 |
8 |
3 |
10 |
6 |
42 |
27 |
9 |
10 |
4 |
4 |
132 |
| Regulation of the neuronal chloride cotransporter KCC2 by neurotrophins | 4 |
2 |
4 |
1 |
4 |
1 |
0 |
0 |
0 |
4 |
3 |
2 |
25 |
| Regulatory networks controlling virulence in the plant pathogen Erwinia carotovora ssp. carotovora | 12 |
6 |
4 |
5 |
9 |
9 |
2 |
4 |
4 |
4 |
4 |
5 |
68 |
| Reindeer Parapoxvirus : Molecular Biology and Detection | 7 |
8 |
9 |
7 |
7 |
2 |
1 |
0 |
3 |
5 |
6 |
2 |
57 |
| Relationships between species traits and ecosystem processes in brackish aquatic plant communities | 2 |
3 |
3 |
8 |
6 |
6 |
3 |
2 |
4 |
4 |
3 |
2 |
46 |
| Remediation through mulching with organic matter of soil polluted by a copper-nickel smelter | 6 |
2 |
4 |
8 |
7 |
6 |
2 |
2 |
3 |
3 |
4 |
4 |
51 |
| Replication of Tula Hantavirus | 6 |
1 |
1 |
0 |
5 |
1 |
1 |
2 |
3 |
4 |
3 |
3 |
30 |
| Reproduction and dispersal of goshawks in a variable environment | 4 |
2 |
2 |
3 |
5 |
4 |
0 |
3 |
4 |
2 |
2 |
1 |
32 |
| Reproduction and population structure in European aspen | 2 |
1 |
0 |
1 |
7 |
1 |
0 |
2 |
4 |
3 |
3 |
2 |
26 |
| Reproduction, oxidative stress biomarkers and fatty acid profiles reveal salinity- and warming-induced forcing on marine zooplankton | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Reproductive partitioning in the polygynous black ant Formica fusca | 4 |
2 |
2 |
2 |
7 |
4 |
1 |
3 |
2 |
0 |
2 |
0 |
29 |
| Reserve network design in fragmented forest landscapes | 6 |
3 |
0 |
4 |
5 |
9 |
1 |
1 |
3 |
3 |
1 |
1 |
37 |
| Response of Scots pine (Pinus sylvestris L.) to a long-term Cu and Ni exposure | 4 |
2 |
3 |
4 |
10 |
1 |
0 |
4 |
1 |
4 |
1 |
4 |
38 |
| Response of the understorey vegetation of boreal forests to heavy metal loading | 21 |
2 |
7 |
2 |
6 |
1 |
0 |
4 |
3 |
5 |
2 |
2 |
55 |
| Responses of Arctic permafrost peatlands to climate changes over the past millennia | 8 |
4 |
8 |
15 |
2 |
6 |
2 |
5 |
1 |
2 |
8 |
2 |
63 |
| Responses of Auditory Supporting Cells to Hair Cell Damage and Death : Cellular Stress Signalling and Epithelial Repair | 2 |
2 |
3 |
1 |
3 |
1 |
1 |
1 |
1 |
3 |
3 |
3 |
24 |
| Responses of invertebrates to human-caused disturbances in East African tropical rainforests : conservation implications | 1 |
0 |
0 |
2 |
4 |
2 |
1 |
2 |
2 |
3 |
1 |
1 |
19 |
| Responses of Pisum Sativum to Soil Arsenate, Lead and Zinc : A Greenhouse Study of Mineral Elements, Phytase Activity, ATP And Chlorophylls | 11 |
9 |
3 |
1 |
4 |
3 |
1 |
1 |
2 |
2 |
0 |
0 |
37 |
| Responses of Scots pine to nickel and copper exposure and herbivory | 1 |
2 |
1 |
3 |
7 |
1 |
0 |
1 |
1 |
0 |
0 |
3 |
20 |
| Restoring vegetation and carbon dynamics in a cut-away peatland | 7 |
10 |
9 |
11 |
15 |
9 |
2 |
1 |
4 |
0 |
2 |
4 |
74 |
| Restrictions in the proliferative potential of inner ear hair cells and supporting cells | 4 |
2 |
6 |
8 |
7 |
2 |
0 |
3 |
2 |
2 |
3 |
0 |
39 |
| Reticulon Homology Domain Containing Protein Families of the Endoplasmic Reticulum | 6 |
6 |
5 |
1 |
7 |
10 |
5 |
3 |
5 |
16 |
15 |
19 |
98 |
| Retrotransposon BARE1 translation, localization, and VLP formation in barley | 3 |
4 |
3 |
4 |
3 |
2 |
1 |
1 |
0 |
3 |
3 |
1 |
28 |
| Revising the actin disassembly machinery : The role of GMF and twinfilin in turnover of dendritic actin arrays | 33 |
11 |
14 |
15 |
19 |
15 |
8 |
8 |
5 |
4 |
3 |
7 |
142 |
| Revision of the family Alycidae (Acariformes, Acari), with special reference to European species | 10 |
9 |
5 |
5 |
4 |
3 |
0 |
7 |
3 |
4 |
2 |
4 |
56 |
| Rhizoctonia -Scots pine interactions : detection, impact on seedling performance and host defence gene response | 5 |
0 |
2 |
6 |
6 |
5 |
1 |
1 |
2 |
1 |
3 |
5 |
37 |
| Risk factors associated to endoscopic retrograde cholangiopancreatography related complications | 4 |
5 |
9 |
3 |
11 |
7 |
8 |
1 |
11 |
12 |
4 |
5 |
80 |
| Risks out of depth? : a study on the environmental impacts of seabed mining | 10 |
24 |
19 |
9 |
17 |
14 |
5 |
6 |
13 |
2 |
9 |
6 |
134 |
| RNA-based next generation sequencing approaches in HLA genotyping and HLA expression quantification | 12 |
16 |
14 |
10 |
17 |
10 |
6 |
9 |
11 |
6 |
10 |
12 |
133 |
| Road Dust from Pavement Wear and Traction Sanding | 8 |
8 |
10 |
8 |
16 |
17 |
4 |
8 |
8 |
2 |
5 |
20 |
114 |
| Role of 3'UTR in the regulation of neurotrophic factors BDNF and GDNF | 11 |
7 |
6 |
8 |
18 |
9 |
1 |
4 |
4 |
5 |
7 |
4 |
84 |
| Role of Actin-mediated Motility of Peripheral Astrocytic Processes in Synaptic Function | 8 |
5 |
8 |
7 |
13 |
8 |
0 |
3 |
5 |
2 |
0 |
1 |
60 |
| Role of allochthonous and autochthonous dissolved organic matter (DOM) as a carbon source for bacterioplankton in boreal humic lakes | 10 |
6 |
11 |
5 |
10 |
6 |
4 |
4 |
5 |
55 |
8 |
6 |
130 |
| Role of cell cycle regulators in development of the inner ear | 8 |
1 |
1 |
3 |
8 |
6 |
0 |
2 |
1 |
2 |
3 |
2 |
37 |
| Role of cystatin B in the regulation of histone H3 tail proteolysis in the mouse brain : study on the molecular mechanisms of progressive myoclonus epilepsy type 1 | 0 |
0 |
0 |
0 |
0 |
45 |
5 |
4 |
14 |
6 |
7 |
10 |
91 |
| Role of Eda and Troy pathways in ectodermal organ development | 2 |
0 |
4 |
2 |
8 |
3 |
1 |
1 |
1 |
4 |
2 |
0 |
28 |
| Role of HMGB1 in cells of the circulation | 4 |
4 |
0 |
4 |
9 |
5 |
2 |
1 |
2 |
2 |
7 |
5 |
45 |
| Role of IL-21 in Regulation of Leukocyte Functions | 5 |
5 |
1 |
3 |
6 |
2 |
2 |
1 |
2 |
0 |
1 |
1 |
29 |
| Role of lignan sources in tumour formation in multiple intestinal neoplasia mice | 11 |
1 |
2 |
8 |
12 |
6 |
9 |
2 |
3 |
1 |
2 |
0 |
57 |
| Role of LKB1 in stem cell fate determination and tumorigenesis | 3 |
4 |
14 |
6 |
8 |
8 |
2 |
5 |
8 |
6 |
6 |
3 |
73 |
| Role of oscillations in visual perception : attention and working memory | 7 |
3 |
11 |
7 |
4 |
10 |
5 |
4 |
5 |
27 |
9 |
3 |
95 |
| Role of RAGE as an Amphoterin Receptor : From Development to Disease | 10 |
8 |
5 |
3 |
15 |
1 |
2 |
1 |
4 |
4 |
4 |
9 |
66 |
| Role of resuspension and silicate in internal phosphorus loading | 6 |
12 |
7 |
2 |
12 |
2 |
2 |
2 |
4 |
4 |
3 |
2 |
58 |
| Role of Temperature in the Biological Activity of a Boreal Forest | 2 |
3 |
1 |
1 |
7 |
8 |
2 |
2 |
1 |
1 |
1 |
2 |
31 |
| Role of the inflammasome pathway in atherosclerosis | 4 |
5 |
6 |
16 |
7 |
10 |
3 |
4 |
2 |
3 |
5 |
5 |
70 |
| Role of WRKY Transcription Factors in Arabidopsis Development and Stress Responses | 16 |
16 |
15 |
18 |
14 |
13 |
9 |
7 |
20 |
4 |
3 |
7 |
142 |
| Roles of GDNF family receptor GFRα2 in the peripheral nervous system | 9 |
5 |
1 |
6 |
4 |
3 |
2 |
5 |
4 |
1 |
5 |
1 |
46 |
| ROS signaling, phytohormone signaling and toxin tolerance : defense mechanisms in Arabidopsis thaliana against Botrytis cinerea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Salivary Antibodies to Capsular Polysaccharides Induced by Polysaccharide-Protein Conjugate Vaccines in Infants | 8 |
7 |
3 |
6 |
12 |
10 |
0 |
5 |
4 |
2 |
2 |
2 |
61 |
| Salmonella enterica, Listeria monocytogenes and Clostridium perfringens : Diversity of Human Isolates Studied by Phenotypic and Molecular Methods | 21 |
8 |
8 |
9 |
11 |
7 |
5 |
8 |
1 |
1 |
2 |
4 |
85 |
| SARS-CoV-2 entry mechanisms and antiviral strategies | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Sea-ice ecology in the Baltic Sea with special emphasis on bacteria | 5 |
0 |
4 |
1 |
4 |
8 |
0 |
1 |
1 |
0 |
2 |
5 |
31 |
| Search for genetic variants conferring susceptibility to obesity and related metabolic traits | 12 |
5 |
6 |
4 |
9 |
3 |
1 |
3 |
3 |
6 |
6 |
3 |
61 |
| Secchi depth in the Baltic Sea an indicator of eutrophication | 9 |
5 |
6 |
8 |
3 |
4 |
0 |
5 |
2 |
4 |
7 |
3 |
56 |
| Secondary metabolites in Gerbera hybrida | 1 |
1 |
6 |
5 |
27 |
15 |
12 |
9 |
1 |
1 |
2 |
4 |
84 |
| Sediment resuspension as a water quality regulator in lakes | 9 |
36 |
20 |
28 |
38 |
15 |
8 |
7 |
6 |
6 |
7 |
6 |
186 |
| Sedimentary sea-ice proxies in the Arctic: seasonal production, vertical export and taxonomic insights | 0 |
0 |
0 |
0 |
87 |
54 |
13 |
23 |
11 |
28 |
14 |
12 |
242 |
| Sedimentary zooplankton remains as indicators of lake ecological quality and trophic structure | 7 |
5 |
3 |
5 |
10 |
2 |
2 |
2 |
5 |
4 |
4 |
2 |
51 |
| Selective glycoprotein exit from yeast endoplasmic reticulum | 2 |
5 |
10 |
7 |
5 |
4 |
5 |
3 |
4 |
4 |
5 |
1 |
55 |
| Self-assembly of hydrophobin proteins from the fungus Trichoderma reesei | 1 |
3 |
3 |
4 |
9 |
7 |
3 |
4 |
4 |
0 |
1 |
2 |
41 |
| Senescence Ecology : Aging in a Population of Wild Brown Mouse Lemurs (Microcebus rufus) | 17 |
4 |
10 |
5 |
11 |
17 |
2 |
2 |
1 |
8 |
16 |
1 |
94 |
| Serum amyloid A (SAA) : Proinflammatory functions and their regulation by serum lipoproteins | 4 |
5 |
6 |
3 |
14 |
8 |
4 |
4 |
5 |
7 |
4 |
10 |
74 |
| Setting priorities for conservation : protected area effectiveness, management, and quality of governance | 5 |
4 |
6 |
1 |
5 |
5 |
6 |
5 |
5 |
3 |
7 |
1 |
53 |
| Sex chromosome evolution and speciation in stickleback fishes | 7 |
17 |
8 |
2 |
13 |
13 |
9 |
6 |
12 |
0 |
7 |
0 |
94 |
| Shaking Environmental Education Paradigms. Practitioners’ narratives, contextual elements, and biocultural approaches | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
107 |
19 |
15 |
7 |
148 |
| Short- and long-term consequences of food resources on Ural owl Strix uralensis reproduction | 8 |
5 |
4 |
11 |
11 |
5 |
2 |
1 |
2 |
0 |
0 |
3 |
52 |
| Short-term effects of variable retention on epigaeic spiders and carabid beetles in Finland | 3 |
3 |
2 |
2 |
9 |
5 |
3 |
5 |
2 |
1 |
0 |
0 |
35 |
| Short-term plant-decomposer feedbacks in grassland plants | 6 |
3 |
0 |
4 |
10 |
9 |
1 |
0 |
2 |
1 |
3 |
1 |
40 |
| Should I stay or should I go? : Reproductive and dispersal strategies of site-specific liverwort species | 9 |
3 |
6 |
3 |
16 |
7 |
1 |
2 |
9 |
3 |
5 |
8 |
72 |
| Signaling through the Jak-Stat pathway : Regulation of tyrosine kinase activity | 8 |
3 |
6 |
3 |
3 |
11 |
1 |
4 |
1 |
2 |
4 |
4 |
50 |
| Silicon and its impacts on phosphorus in eutrophic freshwater lakes | 15 |
8 |
3 |
4 |
9 |
5 |
1 |
3 |
3 |
4 |
4 |
1 |
60 |
| Social polymorphism and dispersal in Formica ants | 10 |
9 |
12 |
9 |
11 |
9 |
2 |
3 |
4 |
7 |
10 |
8 |
94 |
| Socio-Ecological Resilience of a Small-Scale Hilsa Shad (Tenualosa ilisha) Fishery in the Gangetic River Systems of Bangladesh | 8 |
11 |
22 |
8 |
17 |
7 |
5 |
2 |
4 |
9 |
2 |
2 |
97 |
| Soil microbial dynamics and the condition of Norway spruce on the Bothnian land-uplift coast | 5 |
2 |
2 |
5 |
9 |
3 |
3 |
1 |
1 |
5 |
1 |
0 |
37 |
| Sostdc1 Plays an Essential Role in Mammalian Tooth Patterning : Insight into the Rodent Dental Evolution | 6 |
5 |
3 |
6 |
13 |
3 |
5 |
12 |
29 |
29 |
7 |
0 |
118 |
| Spacing behaviour of the Siberian flying squirrel : effects of landscape structure | 4 |
3 |
5 |
7 |
9 |
6 |
8 |
2 |
4 |
2 |
2 |
2 |
54 |
| Spatial and temporal determinants of Finnish farmland bird populations | 3 |
3 |
2 |
2 |
8 |
2 |
0 |
5 |
2 |
3 |
2 |
7 |
39 |
| Spatial conservation prioritization for Finnish forest conservation management | 8 |
6 |
3 |
5 |
13 |
7 |
2 |
8 |
3 |
48 |
4 |
6 |
113 |
| Spatial ecology of a specialist insect herbivore : the leaf-mining moth Tischeria ekebladella on the pedunculate oak Quercus robur | 2 |
2 |
1 |
6 |
9 |
2 |
1 |
6 |
1 |
3 |
4 |
2 |
39 |
| Spatial ecology of an oak-associated herbivore community : A metacommunity of herbivores | 4 |
0 |
1 |
2 |
8 |
3 |
1 |
3 |
4 |
3 |
2 |
4 |
35 |
| Spatial ecology of dung beetles | 5 |
4 |
3 |
5 |
10 |
4 |
2 |
2 |
4 |
6 |
5 |
6 |
56 |
| Spatial ecology of food webs : herbivore-parasitoid communities on the pedunculate oak | 5 |
3 |
0 |
3 |
10 |
5 |
4 |
1 |
1 |
2 |
3 |
1 |
38 |
| Spatial population dynamics in reserve-network design | 3 |
1 |
1 |
1 |
6 |
0 |
1 |
0 |
2 |
1 |
1 |
2 |
19 |
| Spatial processes in ecology and evolution, and implications for conservation | 4 |
3 |
2 |
5 |
9 |
3 |
1 |
1 |
4 |
4 |
1 |
1 |
38 |
| Spatial variability in benthic macrofauna communities and associated ecosystem functions across coastal habitats | 1 |
4 |
13 |
16 |
17 |
10 |
6 |
38 |
3 |
9 |
3 |
5 |
125 |
| Spatiotemporality of carbon fluxes along a boreal land-stream-lake continuum | 7 |
2 |
14 |
1 |
7 |
4 |
1 |
5 |
3 |
2 |
0 |
0 |
46 |
| Species turnover of aquatic organisms in space and time : Patterns in community composition and diversity | 6 |
3 |
1 |
7 |
8 |
5 |
1 |
0 |
3 |
9 |
2 |
2 |
47 |
| Species-based and community-level approaches to conservation prioritization | 7 |
3 |
1 |
6 |
8 |
6 |
1 |
0 |
0 |
1 |
3 |
1 |
37 |
| Spectral and thermal properties of amphibian visual pigments related to molecular structure | 5 |
3 |
1 |
5 |
6 |
3 |
1 |
0 |
2 |
0 |
1 |
0 |
27 |
| Sphagnum-associated methanotrophs : a resilient CH4 biofilter in pristine and disturbed peatlands | 9 |
2 |
7 |
1 |
15 |
3 |
0 |
2 |
2 |
2 |
1 |
1 |
45 |
| Spring bloom dynamics in the Baltic Sea : from the environment to macroelements and microbial interactions | 5 |
7 |
4 |
4 |
11 |
8 |
2 |
4 |
2 |
1 |
4 |
3 |
55 |
| Springtime Episode Acidification as a Regulatory Factor of Estuary Spawning Fish Recruitment | 4 |
4 |
2 |
3 |
10 |
5 |
2 |
6 |
1 |
4 |
7 |
1 |
49 |
| Staphylococcus aureus and Lactobacillus crispatus : Adhesive characteristics of two Gram-positive bacterial species | 8 |
2 |
8 |
10 |
11 |
3 |
0 |
4 |
3 |
3 |
3 |
1 |
56 |
| Statistical methods for detecting signals of natural selection in the wild | 3 |
1 |
1 |
6 |
8 |
8 |
1 |
3 |
6 |
2 |
2 |
5 |
46 |
| Steps towards comprehensive Bayesian decision analysis in fisheries and environmental management | 17 |
7 |
7 |
6 |
12 |
11 |
9 |
5 |
2 |
0 |
2 |
0 |
78 |
| Sticky business : diversity and evolution of Mycocaliciales (Ascomycota) on plant exudates | 18 |
11 |
6 |
9 |
9 |
51 |
4 |
3 |
6 |
1 |
1 |
1 |
120 |
| Strategies to Improve Standardization and Robustness of Toxicogenomics Data Analysis | 4 |
1 |
3 |
2 |
8 |
3 |
1 |
2 |
1 |
6 |
0 |
4 |
35 |
| Stress and developmental responses in Arabidopsis thaliana : regulation through the transcription factor-interacting protein RCD1 | 3 |
5 |
3 |
1 |
10 |
5 |
1 |
2 |
3 |
3 |
3 |
0 |
39 |
| Stress responses of Gram-positive bacteria to cationic antimicrobial peptides | 6 |
3 |
1 |
0 |
6 |
1 |
1 |
0 |
1 |
2 |
2 |
2 |
25 |
| Strong in the Real Way : Protein-Protein and Protein-Lipid Interactions in Tick-Borne Encephalitis Virus Stability and Assembly | 15 |
12 |
20 |
10 |
18 |
10 |
6 |
13 |
6 |
5 |
6 |
5 |
126 |
| Structural and biochemical studies of a posttranslational modification platform in early Eukaryota | 3 |
6 |
1 |
3 |
4 |
3 |
2 |
2 |
9 |
0 |
1 |
0 |
34 |
| Structural and functional characterization of leucine-rich repeat synaptic adhesion molecules | 14 |
9 |
6 |
7 |
13 |
8 |
3 |
0 |
1 |
3 |
4 |
2 |
70 |
| Structural and functional roles of KCC2 in developing cortex | 5 |
2 |
2 |
1 |
7 |
6 |
1 |
3 |
4 |
4 |
1 |
4 |
40 |
| Structural and Functional Studies on Trimeric Autotransporters | 5 |
1 |
5 |
1 |
9 |
4 |
1 |
0 |
0 |
2 |
3 |
4 |
35 |
| Structural basis of cytoskeletal regulation by twinfilin | 4 |
2 |
3 |
2 |
3 |
3 |
1 |
2 |
1 |
4 |
1 |
2 |
28 |
| Structural Evolution of Function and Stability in Muconate Lactonizing Enzymes | 3 |
2 |
2 |
3 |
1 |
5 |
2 |
2 |
0 |
1 |
4 |
3 |
28 |
| Structural stability and binding properties of soluble and membrane-anchored recombinant antibodies | 4 |
2 |
2 |
1 |
4 |
3 |
0 |
1 |
2 |
2 |
1 |
1 |
23 |
| Structural Studies of Membrane-Bound Pyrophosphatases | 3 |
2 |
0 |
4 |
6 |
8 |
14 |
8 |
2 |
2 |
2 |
7 |
58 |
| Structural Studies on Inteins | 9 |
3 |
4 |
2 |
7 |
5 |
2 |
4 |
2 |
2 |
2 |
3 |
45 |
| Structural studies on lysosomal proteins | 7 |
1 |
6 |
6 |
12 |
3 |
1 |
4 |
3 |
3 |
0 |
3 |
49 |
| Structural studies on members of the picornavirus superfamily | 17 |
1 |
1 |
2 |
6 |
8 |
2 |
4 |
3 |
2 |
2 |
2 |
50 |
| Structural studies on viral receptor-binding proteins | 11 |
3 |
5 |
1 |
6 |
3 |
2 |
1 |
1 |
2 |
4 |
2 |
41 |
| Structure and Assembly of Membrane-Containing dsDNA Bacteriophages | 6 |
4 |
5 |
3 |
4 |
1 |
0 |
1 |
4 |
1 |
1 |
2 |
32 |
| Structure and Dynamics of Coil-like Molecules by Residual Dipolar Couplings | 6 |
0 |
0 |
1 |
3 |
0 |
2 |
1 |
1 |
2 |
0 |
2 |
18 |
| Structure and function of GDNF receptor alpha splice variants | 4 |
1 |
3 |
1 |
3 |
1 |
0 |
0 |
0 |
4 |
1 |
1 |
19 |
| Structure and Function of PH and WW domains | 18 |
12 |
9 |
5 |
5 |
3 |
7 |
3 |
3 |
4 |
6 |
2 |
77 |
| Structure, function and intracellular dynamics of alphavirus replication complexes | 8 |
4 |
5 |
3 |
10 |
2 |
5 |
35 |
6 |
2 |
6 |
9 |
95 |
| Structure-function relations in AMPA receptors | 8 |
2 |
3 |
3 |
6 |
2 |
0 |
1 |
1 |
1 |
1 |
1 |
29 |
| Structure-function relationships in the omptin family of enterobacterial proteases/adhesins | 14 |
6 |
4 |
5 |
9 |
6 |
6 |
2 |
2 |
5 |
3 |
2 |
64 |
| Structure-Function Studies of GDNF Family Ligand-RET signalling | 8 |
4 |
7 |
3 |
6 |
7 |
2 |
5 |
2 |
1 |
8 |
0 |
53 |
| Studies on dinoflagellates in the northern Baltic Sea | 9 |
12 |
7 |
7 |
21 |
7 |
10 |
4 |
7 |
3 |
8 |
1 |
96 |
| Studies on palmitoyl-protein thioesterase 1 : Implications for synaptic functions | 8 |
0 |
0 |
1 |
4 |
2 |
1 |
1 |
4 |
3 |
1 |
0 |
25 |
| Studies on planktonic brackish water microprotozoans with special emphasis on the role of ciliates as grazers | 6 |
1 |
0 |
2 |
5 |
1 |
4 |
3 |
3 |
3 |
2 |
1 |
31 |
| Studies on the neurotrophic factor Manf and the pleiotropic factor Lin-28 during Drosophila development | 8 |
5 |
6 |
2 |
8 |
4 |
4 |
1 |
1 |
7 |
1 |
6 |
53 |
| Studying connectivity in the neonatal EEG | 7 |
4 |
4 |
7 |
16 |
4 |
2 |
2 |
7 |
7 |
2 |
1 |
63 |
| Submerged macrophytes modify food web interactions and stability of lake littoral ecosystems | 4 |
3 |
2 |
16 |
5 |
8 |
2 |
0 |
2 |
3 |
1 |
2 |
48 |
| Substance flow analysis in Finland : Four case studies on N and P flows | 8 |
10 |
7 |
11 |
6 |
7 |
1 |
2 |
5 |
0 |
2 |
4 |
63 |
| Substrate Selectivity and Molecular Adaptation in the Outer Membrane Proteases of Yersinia pestis and Salmonella enterica | 5 |
5 |
0 |
3 |
7 |
6 |
5 |
4 |
0 |
3 |
0 |
4 |
42 |
| Successional and spatial patterns of bacterial communities in hydrocarbon-contaminated soils and Populus rhizosphere | 6 |
1 |
7 |
4 |
6 |
9 |
1 |
4 |
3 |
4 |
0 |
2 |
47 |
| Surface protein Pls of methicillin-resistant Staphylococcus aureus : role in adhesion, invasion and pathogenesis, and evolutionary aspects | 7 |
3 |
2 |
6 |
7 |
1 |
1 |
0 |
1 |
3 |
1 |
3 |
35 |
| Surface Proteins of Lactobacillus crispatus : Adhesive Properties and Cell Wall Anchoring | 9 |
10 |
3 |
1 |
9 |
4 |
1 |
3 |
3 |
1 |
3 |
1 |
48 |
| Sustainability Conceptualisation, Operationalisation, and Realisation : Perspectives on Urban Transportation Policy-Making and Planning | 38 |
28 |
39 |
13 |
18 |
9 |
5 |
10 |
15 |
23 |
15 |
4 |
217 |
| Sustainable development indicators : Much wanted, less used? | 8 |
8 |
12 |
7 |
12 |
8 |
5 |
2 |
3 |
2 |
0 |
1 |
68 |
| Sustainable forest management : ecologically sound and socially accepted | 18 |
14 |
7 |
7 |
8 |
13 |
1 |
5 |
11 |
3 |
1 |
2 |
90 |
| Sustainable harvesting in variable environments | 2 |
3 |
5 |
5 |
5 |
3 |
3 |
1 |
3 |
4 |
3 |
2 |
39 |
| Sustained inhibition of hippocampal networks in perinatal development | 0 |
26 |
38 |
18 |
7 |
5 |
4 |
3 |
3 |
2 |
3 |
1 |
110 |
| Swimming through troubled waters : Eutrophication of the Baltic Sea and parasites of the threespine stickleback | 5 |
3 |
1 |
10 |
7 |
6 |
2 |
4 |
1 |
3 |
1 |
0 |
43 |
| Symplastically transmitted signals regulate pattern formation during root development in Arabidopsis thaliana | 12 |
6 |
4 |
5 |
6 |
4 |
3 |
3 |
2 |
3 |
2 |
2 |
52 |
| Synaptic mechanisms of Hebbian and homeostatic plasticity driven by intrinsic activity in the developing hippocampus | 11 |
7 |
5 |
2 |
6 |
6 |
0 |
0 |
4 |
5 |
4 |
5 |
55 |
| Syndecan-3 in neural plasticity : From cell surface interactions to cytoskeletal regulation | 8 |
4 |
3 |
12 |
9 |
7 |
5 |
4 |
6 |
3 |
3 |
2 |
66 |
| Synthesis of neoglycoconjugates and oligosaccharides with potential anti-Helicobacter pylori activity | 8 |
7 |
5 |
5 |
5 |
6 |
0 |
1 |
3 |
1 |
0 |
1 |
42 |
| Systematizing morphology : a total evidence approach to ditrysian phylogenetics (Lepidoptera) | 7 |
2 |
4 |
5 |
7 |
4 |
0 |
3 |
3 |
2 |
2 |
0 |
39 |
| Systemic signaling in plant gas exchange | 0 |
0 |
126 |
20 |
12 |
8 |
4 |
7 |
5 |
14 |
2 |
3 |
201 |
| Systems biology view of receptor tyrosine kinase functions and their oncofusions | 11 |
4 |
9 |
7 |
6 |
3 |
1 |
5 |
4 |
1 |
4 |
5 |
60 |
| Systems Toxicology Approach in Nanosafety : From In vivo Towards In vitro Testing | 3 |
6 |
6 |
10 |
11 |
3 |
1 |
5 |
1 |
1 |
0 |
1 |
48 |
| Systems-level neural mechanisms of conscious perception in health and schizophrenia | 4 |
3 |
2 |
2 |
3 |
6 |
0 |
0 |
4 |
0 |
2 |
2 |
28 |
| Taphrina as model phytopathogenic yeasts infecting the model plant Arabidopsis and woody plant Betula pendula | 9 |
13 |
5 |
9 |
16 |
13 |
6 |
7 |
6 |
11 |
7 |
10 |
112 |
| Targeting GDNF receptors with small molecules for the treatment of Parkinson’s disease | 17 |
26 |
32 |
25 |
23 |
13 |
1 |
6 |
16 |
14 |
3 |
6 |
182 |
| Targeting STAT3 and kinases in lymphoid malignancies | 11 |
7 |
10 |
8 |
11 |
8 |
5 |
13 |
10 |
7 |
4 |
4 |
98 |
| Tau pathology : secretion and internalization as the key for understanding protein propagation | 4 |
2 |
0 |
3 |
5 |
10 |
3 |
5 |
2 |
5 |
5 |
1 |
45 |
| Taxon delineation in gelechioid moths : from phylogenetics to DNA barcoding | 1 |
4 |
2 |
4 |
10 |
4 |
4 |
4 |
1 |
8 |
3 |
3 |
48 |
| Taxonomic and phylogenetic studies on Salicornioideae (Amaranthaceae) | 8 |
5 |
5 |
4 |
10 |
3 |
3 |
3 |
4 |
1 |
9 |
5 |
60 |
| Taxonomic Studies of the Bartramiaceae, Bryopsida | 1 |
8 |
5 |
8 |
12 |
16 |
4 |
1 |
2 |
5 |
3 |
8 |
73 |
| Taxonomy and phylogeny of brown-rot fungi in the Antrodia complex (Polyporales, Basidiomycota) | 10 |
12 |
12 |
17 |
28 |
32 |
6 |
5 |
4 |
3 |
8 |
1 |
138 |
| Taxonomy and phylogeny of the manna lichens and allied species (Megasporaceae) | 13 |
14 |
20 |
38 |
55 |
21 |
12 |
32 |
6 |
2 |
4 |
6 |
223 |
| Taxonomy and phylogeny of white-rot polypores : case studies in Hymenochaetales and Polyporales (Basidiomycota) | 14 |
2 |
1 |
0 |
11 |
10 |
3 |
6 |
2 |
4 |
5 |
1 |
59 |
| Telecouplings in a globalizing world : linking food consumption to outsourced resource use and displaced environmental impacts | 15 |
16 |
14 |
5 |
15 |
4 |
3 |
6 |
9 |
7 |
12 |
8 |
114 |
| Temporal and Density-dependent Variability as Source for Uncertainty in Fish Population Dynamics | 4 |
3 |
2 |
2 |
5 |
3 |
2 |
1 |
2 |
1 |
0 |
0 |
25 |
| Temporal and regional patterns of atmospheric components affecting acidification in Finland | 7 |
2 |
0 |
3 |
2 |
1 |
1 |
2 |
1 |
1 |
1 |
0 |
21 |
| Temporal and spatial turnover of freshwater diatoms : Implications for bioassessment | 6 |
3 |
1 |
8 |
6 |
1 |
2 |
2 |
1 |
0 |
1 |
6 |
37 |
| Temporal habitat dynamics and conservation planning : The case of the false heath fritillary | 5 |
1 |
5 |
2 |
7 |
2 |
0 |
3 |
1 |
0 |
2 |
1 |
29 |
| The bacterial and fungal communities in the nests of the ant Formica exsecta | 5 |
1 |
5 |
4 |
19 |
2 |
2 |
2 |
2 |
0 |
1 |
1 |
44 |
| The biodiversity hypothesis of allergy : The interrelations between the skin microbiota, allergic diseases and exposure to microbes in residential environments | 15 |
6 |
5 |
5 |
9 |
8 |
11 |
5 |
12 |
6 |
7 |
2 |
91 |
| The biological functions of mouse twinfilin isoforms | 3 |
4 |
6 |
1 |
7 |
3 |
2 |
2 |
0 |
2 |
4 |
1 |
35 |
| The BMX Tyrosine Kinase : A Signal Mediator in Hematopoietic and Endothelial/Epithelial Cells | 13 |
2 |
5 |
2 |
6 |
3 |
1 |
1 |
1 |
1 |
1 |
2 |
38 |
| The community of medium-sized carnivores : the interactions between species, habitats and rabies | 3 |
5 |
4 |
1 |
7 |
3 |
5 |
2 |
5 |
2 |
1 |
1 |
39 |
| The consequences of spatial environmental variability on dispersal and on the spatial distribution of species | 0 |
3 |
4 |
9 |
3 |
2 |
2 |
3 |
1 |
3 |
1 |
1 |
32 |
| The contributions of soil, ground vegetation and trees to the methane exchange of boreal forest | 6 |
6 |
6 |
14 |
16 |
4 |
8 |
10 |
7 |
14 |
8 |
3 |
102 |
| The cysteine-rich receptor-like kinase CRK2 during stress responses in Arabidopsis thaliana | 10 |
8 |
6 |
24 |
28 |
9 |
17 |
8 |
6 |
33 |
9 |
5 |
163 |
| The Developmental Basis for the Evolution of Muroid Dentition | 15 |
4 |
1 |
4 |
7 |
3 |
0 |
1 |
11 |
1 |
2 |
0 |
49 |
| The DISC1 gene network in major mental illnesses in Finland | 8 |
10 |
8 |
10 |
8 |
3 |
1 |
6 |
3 |
1 |
0 |
6 |
64 |
| The easy explanation - exploring the link between drought and food security in the East and Horn of Africa | 8 |
4 |
8 |
8 |
15 |
9 |
1 |
2 |
3 |
0 |
1 |
1 |
60 |
| The Ecology and Evolution of Melitaeine Butterflies | 5 |
2 |
7 |
6 |
10 |
2 |
0 |
3 |
2 |
3 |
6 |
9 |
55 |
| The ecophysiology of plasma membrane aquaporins in Arabidopsis thaliana and Fagus sylvatica | 36 |
36 |
36 |
14 |
11 |
4 |
2 |
7 |
2 |
3 |
2 |
5 |
158 |
| The effect of lignin content and lignin modification on Norway spruce wood properties and decay resistance | 6 |
4 |
4 |
3 |
10 |
6 |
2 |
5 |
2 |
0 |
1 |
1 |
44 |
| The effect of living environment and environmental exposure on the composition of microbial community in soil, on human skin and in the gut | 7 |
6 |
3 |
8 |
5 |
4 |
1 |
4 |
10 |
7 |
6 |
8 |
69 |
| The effect of turbidity on the ecology of pike larvae | 10 |
6 |
1 |
6 |
9 |
2 |
5 |
1 |
2 |
3 |
4 |
4 |
53 |
| The effects of eutrophication on alternative reproductive tactics in threespine sticklebacks | 3 |
1 |
2 |
2 |
6 |
3 |
1 |
1 |
2 |
2 |
1 |
1 |
25 |
| The effects of forestry practices on ectomycorrhizal fungal communities and seedling establishment : Integrated studies on biodiversity, podzol profile, clear-cut logging impacts and seedling inoculation | 7 |
8 |
11 |
12 |
8 |
5 |
3 |
7 |
3 |
5 |
7 |
3 |
79 |
| The effects of habitat changes, conservation measures and interspecific interactions on forest-dwelling hawks | 8 |
3 |
3 |
3 |
13 |
5 |
0 |
2 |
2 |
4 |
1 |
2 |
46 |
| The effects of habitat edges and trampling intensity on vegetation in urban forests | 5 |
2 |
8 |
9 |
17 |
10 |
2 |
12 |
13 |
10 |
6 |
7 |
101 |
| The effects of recent eutrophication on freshwater fish communities and fishery on the northern coast of the Gulf of Finland, Baltic Sea | 4 |
4 |
8 |
3 |
17 |
10 |
2 |
3 |
6 |
2 |
9 |
3 |
71 |
| The Emerging Phenotype : Ecological Genetics of Color, Form and Sex in the Common Frog | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| The Endoplasmic Reticulum Subdomains and its Membrane Contact Sites | 17 |
11 |
11 |
11 |
14 |
9 |
6 |
6 |
9 |
6 |
3 |
8 |
111 |
| The environment in the headlines : Newspaper coverage of climate change and eutrophication in Finland | 9 |
9 |
4 |
12 |
11 |
8 |
5 |
9 |
4 |
15 |
7 |
2 |
95 |
| The establishment of efficient methods to culture immunosuppressive mesenchymal stromal cells from cord blood and bone marrow | 8 |
1 |
5 |
5 |
8 |
6 |
5 |
1 |
6 |
4 |
5 |
2 |
56 |
| The evolution of new enterovirus types EV-94, EV-96 and EV-97 | 4 |
7 |
1 |
6 |
10 |
15 |
6 |
31 |
21 |
86 |
15 |
10 |
212 |
| The Extracellular Regulation of Bone Morphogenetic Proteins in Drosophila and Sawfly Wing | 13 |
2 |
3 |
6 |
9 |
3 |
3 |
1 |
2 |
6 |
3 |
0 |
51 |
| The family Herbertaceae and its novel systematic position within liverworts | 13 |
7 |
10 |
14 |
12 |
11 |
6 |
3 |
1 |
2 |
3 |
2 |
84 |
| The fate and effects of lead (Pb) at active and abandoned shooting ranges in a boreal forest ecosystem | 9 |
6 |
7 |
1 |
8 |
5 |
2 |
5 |
5 |
4 |
4 |
1 |
57 |
| The fate of urban-derived contaminants in boreal environments | 4 |
3 |
1 |
4 |
5 |
4 |
0 |
1 |
1 |
3 |
1 |
0 |
27 |
| The function and regulation of the U11-48K protein in U12-dependent splicing | 4 |
5 |
0 |
2 |
8 |
3 |
6 |
3 |
2 |
0 |
3 |
1 |
37 |
| The genome packaging machinery of dsDNA bacteriophage PRD1 | 10 |
2 |
6 |
2 |
10 |
7 |
6 |
1 |
8 |
4 |
2 |
3 |
61 |
| The Gerbera cDNA Microarray : A Tool for Large-Scale Identification of Genes Involved in Flower Development | 1 |
3 |
0 |
4 |
6 |
3 |
1 |
4 |
2 |
0 |
0 |
4 |
28 |
| The Growth Responses of Fish to Differences in Acidity-Related Lake Charasteristics and Fish Species Composition | 3 |
6 |
2 |
2 |
9 |
8 |
0 |
5 |
1 |
1 |
3 |
2 |
42 |
| The HELCOM Ecosystem Approach : time for quantification, integration and measures | 14 |
6 |
14 |
5 |
11 |
5 |
6 |
2 |
1 |
0 |
2 |
5 |
71 |
| The hERG1 (KV11.1) potassium channel : its modulation and the functional characterisation of genetic variants | 8 |
8 |
7 |
13 |
9 |
10 |
4 |
6 |
4 |
3 |
4 |
4 |
80 |
| The high- and low-activity forms of human plasma phospholipid transfer protein (PLTP) | 12 |
2 |
1 |
3 |
11 |
5 |
5 |
2 |
2 |
3 |
4 |
4 |
54 |
| The Human Microbiome in Parkinson’s Disease and Primary Sclerosing Cholangitis | 7 |
1 |
6 |
4 |
14 |
1 |
1 |
0 |
2 |
5 |
4 |
4 |
49 |
| The Human UDP-Glucuronosyltransferases : Studies on Substrate Binding and Catalytic Mechanism | 7 |
7 |
4 |
6 |
11 |
6 |
7 |
9 |
2 |
6 |
7 |
2 |
74 |
| The impact of FSC certification on timber tree regeneration and floristic composition in Honduran community forests | 5 |
2 |
2 |
5 |
11 |
5 |
2 |
0 |
3 |
1 |
3 |
1 |
40 |
| The Impact of Membrane Phospholipid Composition and Extracellular Vesicles on the Immunoregulative Properties of Human Mesenchymal Stromal Cells | 8 |
1 |
4 |
7 |
6 |
2 |
0 |
4 |
5 |
1 |
3 |
4 |
45 |
| The impacts of forestry on polyporous fungi in boreal forests | 3 |
2 |
2 |
5 |
6 |
5 |
1 |
7 |
5 |
4 |
1 |
1 |
42 |
| The impacts of temperature on the long-term variation in migration and breeding performance of birds | 3 |
0 |
0 |
3 |
9 |
4 |
4 |
5 |
5 |
6 |
6 |
5 |
50 |
| The importance of forested mire margin plant communities for the diversity of managed boreal forests in Finland | 8 |
4 |
3 |
3 |
7 |
7 |
0 |
6 |
2 |
2 |
4 |
7 |
53 |
| The influence of eutrophication on sexual selection in sticklebacks | 2 |
3 |
5 |
4 |
10 |
3 |
2 |
1 |
1 |
2 |
1 |
4 |
38 |
| The integration of developmental signals during root procambial patterning in Arabidopsis thaliana | 12 |
2 |
4 |
8 |
10 |
3 |
1 |
2 |
3 |
1 |
1 |
3 |
50 |
| The life cycle and genetic structure of the red alga Furcellaria lumbricalis on a salinity gradient | 7 |
6 |
23 |
7 |
21 |
8 |
1 |
4 |
5 |
3 |
2 |
2 |
89 |
| The limits of visual sensitivity and its circadian control | 7 |
7 |
12 |
10 |
5 |
10 |
1 |
2 |
6 |
6 |
3 |
1 |
70 |
| The limits to traffic volume growth : The content and procedure of administrative futures studies on Finnish transport CO2 policy | 8 |
6 |
8 |
12 |
11 |
9 |
8 |
4 |
16 |
5 |
6 |
4 |
97 |
| The Mads World of Floral Regulators in Gerbera Hybrida | 8 |
7 |
3 |
3 |
10 |
4 |
5 |
3 |
1 |
4 |
1 |
1 |
50 |
| The mast cell as a regulator of atherosclerotic plaque stability | 12 |
5 |
11 |
2 |
6 |
3 |
2 |
4 |
4 |
5 |
1 |
7 |
62 |
| The Mechanisms, Applications, and Target Site Selection of Bacteriophage Mu Minimal in vitro DNA Transposition Reaction | 0 |
1 |
1 |
3 |
3 |
3 |
1 |
5 |
2 |
3 |
3 |
0 |
25 |
| The Molecular Basis of Hydrolethalus Syndrome | 1 |
2 |
3 |
3 |
10 |
2 |
0 |
3 |
1 |
2 |
0 |
1 |
28 |
| The neuronal cell adhesion molecule ICAM-5 | 7 |
5 |
6 |
9 |
12 |
10 |
1 |
6 |
6 |
5 |
4 |
3 |
74 |
| The nuclear import mechanism of SRF co-activator MKL1 | 8 |
3 |
6 |
10 |
9 |
5 |
5 |
3 |
4 |
5 |
2 |
2 |
62 |
| The NUP98-NSD1 fusion gene in acute myeloid leukemia | 31 |
23 |
16 |
18 |
15 |
10 |
11 |
6 |
5 |
7 |
2 |
6 |
150 |
| The Population Consequences of Sex and Conflict | 3 |
2 |
3 |
2 |
6 |
1 |
4 |
4 |
1 |
0 |
1 |
1 |
28 |
| The Power of Perspectives : Developing and Implementing Inter and Transdisciplinary Methods to Address Wicked Socio-Environmental Problems | 8 |
18 |
24 |
12 |
13 |
13 |
7 |
7 |
8 |
2 |
4 |
0 |
116 |
| The Pseudomonas syringae-derived HrpA pilins : molecular characterization and biotechnological application of the transcripts | 7 |
1 |
3 |
2 |
4 |
2 |
2 |
2 |
0 |
2 |
0 |
0 |
25 |
| The range expansion of the European map butterfly in Finland | 1 |
1 |
8 |
6 |
4 |
2 |
1 |
3 |
2 |
1 |
1 |
2 |
32 |
| The regulation of U12-dependent splicing and its significance to mRNA stability | 4 |
2 |
5 |
8 |
4 |
5 |
3 |
3 |
2 |
1 |
2 |
5 |
44 |
| The role of a tapeworm Diphyllobothrium ditremum Creplin in the regulation mechanisms of a subarctic whitefish (Coregonus lavaretus (L.)) population | 5 |
2 |
5 |
4 |
5 |
1 |
1 |
2 |
4 |
5 |
4 |
5 |
43 |
| The role of bioactive lipid mediators and extracellular vesicles in mesenchymal stromal cell immunomodulation | 10 |
4 |
15 |
2 |
9 |
11 |
1 |
5 |
2 |
2 |
2 |
0 |
63 |
| The Role of Calcium and Protein Phosphatases in Cold Signal Transduction in Arabidopsis thaliana | 2 |
2 |
0 |
4 |
6 |
3 |
1 |
3 |
2 |
3 |
3 |
1 |
30 |
| The role of cortical oscillations in the estimation and maintenance of sensory and duration information in working memory | 8 |
7 |
4 |
4 |
5 |
4 |
5 |
0 |
5 |
1 |
3 |
1 |
47 |
| The role of cyclase-associated protein (CAP) in actin dynamics during cell motility and morphogenesis | 5 |
1 |
5 |
4 |
16 |
5 |
7 |
5 |
1 |
0 |
3 |
8 |
60 |
| The role of cysteine-rich receptor-like protein kinases in ROS signaling in Arabidopsis thaliana | 2 |
17 |
12 |
12 |
22 |
13 |
8 |
6 |
1 |
3 |
2 |
3 |
101 |
| The role of environmental factors in regulating planktivorous predation : Interactive effects of turbulence and visibility conditions | 3 |
6 |
6 |
2 |
2 |
3 |
3 |
3 |
2 |
5 |
4 |
3 |
42 |
| The role of hybrids in the process of speciation : a study of naturally occurring Formica wood ant hybrids | 8 |
2 |
10 |
1 |
11 |
6 |
7 |
3 |
3 |
3 |
3 |
2 |
59 |
| The role of Kainate receptor auxiliary subunits NETO1 and NETO2 in development of hippocampal circuitry | 5 |
3 |
1 |
6 |
13 |
6 |
0 |
1 |
1 |
3 |
3 |
2 |
44 |
| The role of MADS and TCP transcription factors in Gerbera hybrida flower development | 4 |
4 |
3 |
2 |
4 |
5 |
4 |
5 |
1 |
1 |
0 |
0 |
33 |
| The role of marine heatwaves for biodiversity and ecosystem functioning in coastal waters | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| The Role of Mast Cells in Foam Cell Formation, Growth Inhibition, and Apoptosis of Smooth Muscle Cells | 11 |
2 |
3 |
0 |
3 |
5 |
0 |
3 |
1 |
1 |
1 |
3 |
33 |
| The role of multi-scale phase synchronization and cross-frequency interactions in cognitive integration | 7 |
8 |
4 |
6 |
8 |
4 |
4 |
3 |
6 |
17 |
7 |
7 |
81 |
| The role of phosphorus as a regulator of bloom-forming diazotrophic cyanobacteria in the Baltic Sea | 13 |
6 |
8 |
2 |
3 |
10 |
0 |
4 |
5 |
4 |
2 |
2 |
59 |
| The role of productivity in the ecological and evolutionary dynamics of predator-prey interaction | 3 |
2 |
4 |
4 |
7 |
6 |
3 |
1 |
4 |
3 |
2 |
1 |
40 |
| The role of the feeding migration and diet of Atlantic salmon (Salmo salar L.) in yolk-sac-fry mortality in the Baltic Sea | 1 |
8 |
5 |
4 |
8 |
4 |
1 |
5 |
4 |
0 |
2 |
1 |
43 |
| The Role of TRKB Receptor Complex Proteins and the Lipid Environment In the Mechanism of Antidepressant Drug Action | 14 |
9 |
11 |
8 |
5 |
11 |
4 |
37 |
12 |
15 |
11 |
14 |
151 |
| The role of zooplankton in littoral communities : Diversity and food web interactions in the Baltic Sea | 15 |
4 |
5 |
4 |
9 |
8 |
5 |
6 |
3 |
3 |
5 |
2 |
69 |
| The roles of nitrification and nitrate reduction pathways in nitrogen cycling of Baltic Sea | 9 |
3 |
8 |
4 |
10 |
7 |
6 |
4 |
5 |
2 |
1 |
1 |
60 |
| The Roles of Template RNA and Replication Proteins in the Formation of Semliki Forest Virus Replication Spherules | 5 |
6 |
4 |
5 |
7 |
3 |
0 |
7 |
4 |
3 |
2 |
0 |
46 |
| The Roles of WOL and APL in Phloem Development in Arabidopsis thaliana Roots | 9 |
10 |
7 |
3 |
6 |
5 |
3 |
4 |
2 |
31 |
12 |
6 |
98 |
| The scent of brood recognition in Formica ants | 4 |
8 |
13 |
15 |
7 |
12 |
5 |
4 |
2 |
2 |
1 |
0 |
73 |
| The serine proteinases of Fusarium grown on cereal proteins and in barley grain and their inhibition by barley proteins | 3 |
4 |
2 |
4 |
5 |
4 |
0 |
1 |
2 |
1 |
0 |
4 |
30 |
| The Size of Major Mammalian Sensory Organs as Measured from Cranial Characters, and Their Relation to the Biology and Evolution of Mammals | 12 |
13 |
9 |
13 |
7 |
9 |
11 |
27 |
26 |
20 |
2 |
0 |
149 |
| The Structure and Dynamics of the Actin Cytoskeleton in the Axon Initial Segment | 9 |
5 |
5 |
1 |
10 |
6 |
0 |
2 |
0 |
0 |
1 |
0 |
39 |
| The Togavirus RNA Replication Complex | 48 |
20 |
41 |
45 |
40 |
32 |
7 |
26 |
7 |
17 |
28 |
21 |
332 |
| The toxicity of Fusarium mycotoxins enniatin and moniliformin | 6 |
14 |
8 |
4 |
25 |
10 |
5 |
0 |
4 |
3 |
4 |
7 |
90 |
| The Transcriptional Regulation of Retrotransposon BARE | 10 |
5 |
3 |
5 |
4 |
1 |
5 |
1 |
2 |
0 |
0 |
1 |
37 |
| The viral coat protein is regulated by HSP70 and HSP40 in Potato virus A infection | 5 |
4 |
3 |
2 |
4 |
5 |
1 |
1 |
4 |
3 |
8 |
3 |
43 |
| The visual preferences for forest regeneration and field afforestation : four case studies in Finland | 7 |
15 |
5 |
8 |
11 |
8 |
1 |
0 |
4 |
4 |
8 |
6 |
77 |
| The VP1 intracapsid hook and uncoating of enteroviruses | 11 |
5 |
3 |
4 |
12 |
5 |
10 |
22 |
27 |
10 |
5 |
4 |
118 |
| Theoretical Studies on Coupled Electron and Proton Transfer in Cytochrome c Oxidase | 20 |
5 |
8 |
9 |
9 |
15 |
2 |
3 |
1 |
2 |
4 |
1 |
79 |
| Thyroid Hormone Control of Cardiac Substrate Metabolism | 1 |
4 |
0 |
3 |
7 |
2 |
0 |
4 |
3 |
1 |
2 |
2 |
29 |
| Time to rest : Signals in shoot apex developmental transitions underlying dormancy | 5 |
3 |
1 |
2 |
8 |
4 |
1 |
3 |
0 |
2 |
5 |
1 |
35 |
| Tinkering with cusp patterning : Developmental Genetic Mechanisms in Mouse Molar Development | 5 |
2 |
4 |
8 |
11 |
5 |
7 |
4 |
10 |
16 |
8 |
2 |
82 |
| Tissue culture and cryopreservation in the utilization and conservation of genetic resources of Norway spruce (Picea abies) and elms (Ulmus glabra, U. laevis) | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Tissue-Adherence in Lactic Acid Bacteria : Identification and Characterization of the Collagen-Binding S-Layer Protein of Lactobacillus crispatus | 4 |
5 |
4 |
2 |
9 |
5 |
7 |
4 |
4 |
7 |
7 |
5 |
63 |
| Tissue-specific genetic and epigenetic alterations in Mlh1 heterozygous tissues | 3 |
4 |
2 |
6 |
6 |
3 |
1 |
5 |
16 |
6 |
5 |
8 |
65 |
| To be or not to be a Queen : Caste-specific gene expression patterns in ants | 7 |
5 |
3 |
7 |
10 |
7 |
3 |
3 |
1 |
1 |
3 |
2 |
52 |
| To Move or to Convene : Regulatory Circuits of Mat Fimbriae in Escherichia coli | 3 |
3 |
3 |
8 |
5 |
1 |
2 |
3 |
2 |
3 |
2 |
5 |
40 |
| To the root of the stem cell problem : The evolutionary importance of the epithelial stem cell niche during tooth development | 7 |
3 |
1 |
2 |
3 |
0 |
0 |
2 |
2 |
5 |
0 |
3 |
28 |
| Tonically Active Kainate Receptors (tKARs) : A Novel Mechanism Regulating Neuronal Function in the Brain | 4 |
5 |
2 |
6 |
7 |
4 |
1 |
2 |
5 |
1 |
7 |
1 |
45 |
| Towards a better understanding of the systematics and diversity of Cortinarius, with an emphasis on species growing in boreal and temperate zones of Europe and North America | 19 |
5 |
5 |
5 |
12 |
4 |
2 |
6 |
12 |
10 |
7 |
3 |
90 |
| Towards ecological intensification of agriculture : from management to soil bacterial and nitrogen-cycling communities | 3 |
2 |
5 |
9 |
13 |
8 |
2 |
5 |
4 |
2 |
6 |
3 |
62 |
| Towards immunomodulatory urban greening : enhancing urban indoor and outdoor microbial communities with indoor vegetation and novel plant substrates | 24 |
20 |
15 |
9 |
13 |
12 |
8 |
2 |
1 |
7 |
4 |
4 |
119 |
| Towards inclusivity in ecosystem governance : The epistemic dimension of human-nature connections and its implications for sustainability science | 10 |
13 |
15 |
21 |
12 |
10 |
6 |
6 |
3 |
0 |
21 |
6 |
123 |
| Traditional medicinal uses and biological activities of some plant extracts of African Combretum Loefl., Terminalia L. and Pteleopsis Engl. species | 13 |
19 |
28 |
25 |
17 |
17 |
34 |
15 |
14 |
8 |
5 |
3 |
198 |
| Trait-based analysis of phytoplankton along a salinity gradient | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Trait-based prediction of extinction risk | 47 |
21 |
24 |
13 |
22 |
9 |
10 |
52 |
54 |
15 |
14 |
4 |
285 |
| Transcription factor Foxi3 in Hair Follicle Development and Homeostasis | 7 |
5 |
6 |
12 |
8 |
18 |
4 |
4 |
5 |
5 |
9 |
7 |
90 |
| Transcription factor function and interactions during human preimplantation development | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
55 |
11 |
3 |
37 |
106 |
| Transcription Factors Foxi3 and Sox2 in the Regulation of Tooth Development | 3 |
6 |
3 |
3 |
7 |
10 |
10 |
141 |
0 |
0 |
2 |
2 |
187 |
| Transcriptional analysis of persistent Chlamydia pneumoniae infection in vitro | 11 |
4 |
5 |
2 |
12 |
8 |
1 |
4 |
2 |
3 |
3 |
3 |
58 |
| Transcriptional control of dietary sugar metabolism and homeostasis by Mondo-Mlx transcription factors | 7 |
6 |
7 |
10 |
12 |
21 |
1 |
5 |
3 |
23 |
49 |
9 |
153 |
| Transcriptional Regulation of GABAergic neuron differentiation in the developing diencephalon, midbrain and anterior hindbrain | 10 |
7 |
10 |
4 |
13 |
12 |
6 |
4 |
9 |
5 |
2 |
5 |
87 |
| Transcriptional regulators involved in nutrient-dependent growth control | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
| Transcriptome and glycome profiling of human hematopoietic CD133+ and CD34+ cells | 2 |
4 |
2 |
3 |
6 |
5 |
3 |
3 |
3 |
5 |
2 |
5 |
43 |
| Transcriptome and proteome analysis of xylose-metabolising Saccharomyces cerevisiae | 8 |
5 |
4 |
4 |
6 |
5 |
0 |
1 |
0 |
3 |
2 |
2 |
40 |
| Transcriptomic analysis of food-related microorganisms : Cheese microbiota, food spoilage lactic acid bacteria, and foodborne pathogens | 4 |
7 |
7 |
12 |
10 |
13 |
7 |
9 |
6 |
6 |
6 |
4 |
91 |
| Transcriptomic data integration for precision medicine in leukemia | 6 |
5 |
8 |
1 |
12 |
5 |
5 |
3 |
2 |
6 |
2 |
11 |
66 |
| Transformation and removal of riverine dissolved organic matter in Baltic Sea estuaries | 3 |
2 |
8 |
3 |
11 |
3 |
0 |
2 |
5 |
4 |
0 |
1 |
42 |
| Trapped in the net : restriction of TRKB function by perineuronal nets inhibits plasticity in the central nervous system | 7 |
3 |
3 |
2 |
6 |
7 |
3 |
4 |
2 |
4 |
9 |
7 |
57 |
| Trauma-induced cellular stress signalling and hair cell death in the cochlea | 3 |
0 |
3 |
11 |
6 |
11 |
1 |
2 |
3 |
4 |
5 |
2 |
51 |
| Trichoderma reesei strains for production of cellulases for the textile industry | 15 |
25 |
18 |
25 |
26 |
9 |
8 |
7 |
17 |
7 |
9 |
7 |
173 |
| Trimeric autotransporters and their ligands : structural studies | 6 |
8 |
7 |
7 |
8 |
23 |
4 |
3 |
3 |
1 |
3 |
6 |
79 |
| Trophic Interactions and Impacts of Non-indigenous Species in Baltic Sea Coastal Ecosystems | 4 |
2 |
4 |
8 |
8 |
3 |
2 |
4 |
7 |
1 |
5 |
3 |
51 |
| Trypsinogens and trypsin inhibitor (PSTI/TATI) -expression in urogenital organs and tumors | 7 |
1 |
9 |
1 |
7 |
6 |
2 |
0 |
2 |
0 |
0 |
2 |
37 |
| Tula hantavirus nucleocapsid protein | 6 |
2 |
0 |
2 |
6 |
5 |
0 |
1 |
5 |
3 |
2 |
1 |
33 |
| Tumor Necrosis Factors and Chemokines in Hair Development | 6 |
6 |
2 |
5 |
8 |
5 |
6 |
4 |
7 |
14 |
10 |
6 |
79 |
| Tumorigenic transformation induced by Ornithine and S-adenosylmethionine decarboxylases : Search for common denominators in oncogenic signaling | 5 |
4 |
4 |
1 |
5 |
3 |
1 |
0 |
1 |
2 |
3 |
3 |
32 |
| Type III Secretion System of Phytopathogenic Bacterium Pseudomonas syringae : From Gene to Function | 8 |
2 |
5 |
6 |
13 |
9 |
8 |
4 |
7 |
6 |
2 |
2 |
72 |
| U12-type Spliceosome : Localization and Effects of Splicing Efficiency on Gene Expression | 3 |
10 |
7 |
5 |
12 |
4 |
2 |
1 |
5 |
5 |
2 |
2 |
58 |
| Uncovering a sugar tolerance network : SIK3 and Cabut as downstream effectors of Mondo-Mlx | 5 |
8 |
15 |
8 |
10 |
4 |
7 |
4 |
3 |
6 |
8 |
3 |
81 |
| Understanding the biodiversity and ecological importance of ctenophores Lessons from Arctic and Baltic Mertensia ovum | 19 |
5 |
18 |
8 |
16 |
13 |
6 |
3 |
6 |
6 |
8 |
3 |
111 |
| Unravelling Molecular and Cellular Disease Mechanisms in Infantile Neuronal Ceroid Lipofuscinosis (INCL) | 1 |
3 |
5 |
4 |
11 |
3 |
0 |
0 |
1 |
2 |
0 |
1 |
31 |
| Urban ecosystem services at the plant-soil interface | 8 |
7 |
3 |
8 |
7 |
2 |
3 |
2 |
5 |
2 |
6 |
5 |
58 |
| Urban ecosystems-response to disturbances, resilience and ecological memory | 4 |
5 |
10 |
3 |
11 |
7 |
3 |
3 |
141 |
5 |
7 |
4 |
203 |
| Urban futures and climate change : understanding vulnerability dynamics | 4 |
18 |
7 |
6 |
14 |
6 |
11 |
31 |
14 |
1 |
3 |
0 |
115 |
| Urban woodland ecology : Methodological perspectives and empirical studies | 3 |
4 |
8 |
6 |
9 |
5 |
2 |
3 |
2 |
3 |
4 |
0 |
49 |
| Use of ecological information in urban planning | 4 |
4 |
2 |
4 |
7 |
4 |
1 |
3 |
4 |
2 |
2 |
3 |
40 |
| Using a combination of bioassays, bioaccumulation kinetics and mixture toxicity tests to assess the ecotoxicological risk of CCA contaminated soils in Finland | 9 |
1 |
4 |
4 |
4 |
11 |
4 |
2 |
3 |
2 |
3 |
2 |
49 |
| Using modern and fossil pollen data for climate and human influence reconstructions in China | 5 |
13 |
8 |
25 |
62 |
12 |
16 |
46 |
45 |
214 |
8 |
4 |
458 |
| Utility of Type I Collagen-Derived Markers as Reflectors of Bone Turnover in Different Clinical Situations | 6 |
5 |
3 |
4 |
9 |
3 |
1 |
3 |
2 |
5 |
1 |
2 |
44 |
| Vascular Diversity and the Functional Role of Peptidases in Angiogenesis | 5 |
3 |
3 |
0 |
3 |
4 |
1 |
1 |
2 |
2 |
2 |
3 |
29 |
| Vegetated roofs as habitats for arthropods in urban areas | 2 |
5 |
3 |
4 |
9 |
22 |
0 |
2 |
2 |
1 |
5 |
0 |
55 |
| Vegetation and carbon dynamics of high-latitude peatlands in a changing climate : from early Holocene to recent past | 12 |
18 |
5 |
17 |
9 |
4 |
6 |
13 |
0 |
1 |
5 |
6 |
96 |
| VEGF-C: The evolutionary origin, activation, and potential as a drug target | 0 |
0 |
0 |
0 |
24 |
93 |
9 |
8 |
10 |
8 |
1 |
2 |
155 |
| VEGFR-2 and VEGFR-3 Specific Signaling in Lymphangiogenesis and Angiogenesis | 9 |
7 |
2 |
5 |
6 |
4 |
0 |
4 |
1 |
3 |
0 |
3 |
44 |
| VEGFR-3 Ligands and Lymphangiogenesis | 4 |
2 |
4 |
0 |
8 |
3 |
2 |
2 |
2 |
3 |
5 |
0 |
35 |
| Virus - host cell interactions in echovirus 1 infection | 7 |
1 |
7 |
4 |
7 |
3 |
0 |
0 |
4 |
20 |
66 |
6 |
125 |
| Virus-host interactions of emerging respiratory pathogens | 2 |
1 |
5 |
5 |
5 |
5 |
2 |
0 |
2 |
0 |
0 |
1 |
28 |
| Virus-host systems in sea ice | 5 |
4 |
3 |
6 |
5 |
4 |
2 |
2 |
4 |
2 |
10 |
12 |
59 |
| Vole population dynamics : experiments on predation | 0 |
5 |
8 |
9 |
4 |
6 |
3 |
3 |
1 |
4 |
7 |
2 |
52 |
| Voles and their trophic interactions in a changing landscape | 4 |
1 |
7 |
4 |
12 |
12 |
9 |
13 |
8 |
8 |
5 |
4 |
87 |
| Voluntary alcohol drinking : relation to corticosteroids and alcohol-mediated testosterone elevation | 8 |
2 |
9 |
3 |
12 |
2 |
5 |
1 |
1 |
2 |
4 |
2 |
51 |
| Water quality estimation by optical remote sensing in boreal lakes | 9 |
6 |
8 |
5 |
8 |
5 |
4 |
6 |
3 |
3 |
2 |
3 |
62 |
| Waterbirds in a changing world : effects of climate, habitat and conservation policy on European waterbirds | 3 |
8 |
4 |
8 |
12 |
8 |
3 |
8 |
4 |
2 |
15 |
13 |
88 |
| Western diet and genetic predisposition as risk factors of colon cancer | 10 |
9 |
9 |
5 |
8 |
9 |
3 |
4 |
4 |
2 |
5 |
0 |
68 |
| What Makes Us Anxious : A Cross-Species Multi-omics Approach to the Biological Basis of Anxiety Disorders | 10 |
5 |
5 |
7 |
10 |
6 |
2 |
4 |
8 |
1 |
4 |
2 |
64 |
| When do we attain our objectives? : On the role of indicators, values and uncertainty in environmental management | 7 |
4 |
3 |
4 |
7 |
2 |
4 |
4 |
4 |
2 |
3 |
4 |
48 |
| Where and how to conserve : Extending the scope of spatial reserve network design | 3 |
1 |
3 |
0 |
2 |
2 |
0 |
1 |
2 |
2 |
1 |
1 |
18 |
| Wood-inhabiting Basidiomycetes in the Caucasus Region : Systematics and Biogeography | 6 |
2 |
5 |
1 |
6 |
8 |
1 |
1 |
2 |
3 |
0 |
1 |
36 |
| Yeast Saccharomyces cerevisiae as a tool in cloning and analysis of fungal genes : Applications for biomass hydrolysis and utilisation | 10 |
3 |
2 |
64 |
13 |
7 |
1 |
0 |
1 |
2 |
3 |
1 |
107 |
| Ympäristö ylittää oppiainerajat : Arvolatautuneisuus ja monialaisuus koulun ympäristöopetuksen haasteina | 36 |
38 |
120 |
77 |
39 |
28 |
12 |
10 |
24 |
44 |
69 |
24 |
521 |