| The entire DSpace / Väitöskirjat ja tutkielmat / Väitöskirjat / Bio- ja ympäristötieteellinen tiedekunta | 7 / 2023 | 8 / 2023 | 9 / 2023 | 10 / 2023 | 11 / 2023 | 12 / 2023 | 1 / 2024 | 2 / 2024 | 3 / 2024 | 4 / 2024 | 5 / 2024 | 6 / 2024 | Total |
|---|
| A gene-based approach to experimental heart transplant rejection | 2 |
3 |
4 |
4 |
6 |
2 |
2 |
1 |
3 |
3 |
1 |
1 |
32 |
| A new bacterial peptidoglycan peptidase LytU and insights into substrate recognition by lysostaphin family | 3 |
13 |
9 |
4 |
5 |
3 |
4 |
1 |
5 |
3 |
3 |
2 |
55 |
| A novel multiplexed interactome proteomics approach for studying cellular signaling | 3 |
5 |
10 |
5 |
7 |
5 |
8 |
3 |
9 |
6 |
3 |
4 |
68 |
| A Novel Phytase from Bacillus : Characterization and Production of the Enzyme | 2 |
87 |
4 |
1 |
0 |
1 |
65 |
25 |
2 |
4 |
2 |
4 |
197 |
| A Physiologically Validated Animal Model of Birth Asphyxia: from Pathophysiology to Therapeutic Intervention | 4 |
15 |
3 |
0 |
8 |
1 |
3 |
2 |
0 |
3 |
1 |
1 |
41 |
| A practice approach to experimental governance : Experiences from the intersection of everyday life and local experimentation | 18 |
15 |
1 |
3 |
2 |
3 |
3 |
3 |
4 |
2 |
7 |
1 |
62 |
| A systematic-ecological approach to Baltic Sea ice studies of algae and protists | 1 |
3 |
4 |
2 |
3 |
6 |
6 |
0 |
0 |
1 |
1 |
0 |
27 |
| Acceptor specificity studies of fucosyl- and sialyltransferases | 3 |
30 |
4 |
2 |
0 |
0 |
4 |
4 |
4 |
2 |
2 |
4 |
59 |
| Acidic pH and acidic enzymes in atherosclerosis | 7 |
6 |
12 |
13 |
3 |
1 |
14 |
6 |
15 |
9 |
10 |
2 |
98 |
| Actin Dynamics in Muscle Cells | 4 |
1 |
2 |
9 |
4 |
3 |
3 |
2 |
3 |
6 |
0 |
2 |
39 |
| Actin in transcription | 0 |
0 |
0 |
0 |
0 |
0 |
24 |
38 |
10 |
3 |
4 |
4 |
83 |
| Actin regulation in dendritic spines : from synaptic plasticity to animal behavior and human neurodevelopmental disorders | 2 |
0 |
2 |
1 |
4 |
1 |
1 |
3 |
1 |
3 |
4 |
3 |
25 |
| Activation of inflammasome and protein secretion by endogenous danger and microbe-derived signals in human macrophages | 8 |
3 |
5 |
7 |
8 |
2 |
7 |
8 |
4 |
6 |
4 |
3 |
65 |
| Activation of innate immune response in human macrophages by Herpes simplex virus-1 and crystallized monosodium urate | 3 |
3 |
4 |
2 |
1 |
3 |
3 |
3 |
3 |
2 |
3 |
2 |
32 |
| Activation of innate immune responses by non-pathogenic and pathogenic bacteria in human leukocytes | 2 |
5 |
8 |
14 |
6 |
4 |
4 |
7 |
7 |
3 |
7 |
3 |
70 |
| Activation of Innate Immune Responses by Toll-Like Receptors and Influenza Viruses | 1 |
2 |
0 |
5 |
1 |
1 |
4 |
6 |
4 |
5 |
1 |
1 |
31 |
| Actors’ roles and perceptions on the opportunities to increase nature conservation effectiveness : a study of interaction between knowledge and policy process | 5 |
0 |
3 |
5 |
7 |
5 |
2 |
4 |
4 |
2 |
1 |
3 |
41 |
| Adaptation to Environmental Light Conditions in Mysid Shrimps | 0 |
2 |
3 |
4 |
5 |
5 |
1 |
6 |
5 |
3 |
1 |
0 |
35 |
| Addressing human-induced uncertainty in fisheries management : social scientific and interdisciplinary solutions using Bayesian belief networks | 1 |
2 |
3 |
1 |
2 |
1 |
4 |
6 |
1 |
6 |
7 |
6 |
40 |
| Adjustment of optically measured leaf traits to patterns of solar spectral irradiance in plant taxa from high elevations and from forest understoreys | 3 |
3 |
1 |
0 |
6 |
2 |
1 |
1 |
4 |
4 |
5 |
1 |
31 |
| Advantages and limitations of combined in situ remediation methods and mechanisms at petroleum fuel product contaminated sites | 3 |
2 |
1 |
0 |
2 |
3 |
12 |
5 |
3 |
5 |
2 |
2 |
40 |
| Affinity and Avidity of the LFA-1 Integrin is Regulated by Phosphorylation | 1 |
1 |
3 |
1 |
1 |
0 |
0 |
0 |
0 |
1 |
0 |
5 |
13 |
| Alien Species, Warming Climates, Growing Cities, and the Birds that live with them. | 4 |
5 |
12 |
9 |
13 |
6 |
7 |
42 |
19 |
21 |
8 |
17 |
163 |
| Allelopathic effects of filamentous cyanobacteria on phytoplankton in the Baltic Sea | 11 |
1 |
4 |
2 |
2 |
5 |
1 |
5 |
4 |
4 |
2 |
3 |
44 |
| Alterations of niche to stem cell communication in the aging intestine | 13 |
14 |
14 |
5 |
9 |
7 |
4 |
10 |
9 |
8 |
2 |
2 |
97 |
| 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 | 3 |
4 |
6 |
3 |
3 |
4 |
0 |
2 |
3 |
6 |
1 |
3 |
38 |
| AMIGO and its friends in developing and adult brain | 2 |
1 |
2 |
4 |
2 |
2 |
3 |
2 |
1 |
4 |
4 |
1 |
28 |
| AMIGO-Kv2.1 potassium channel complex : Identification and association with schizophrenia-related phenotypes | 0 |
2 |
5 |
2 |
6 |
3 |
6 |
1 |
3 |
4 |
4 |
6 |
42 |
| AMPA receptor ligand-binding domain : Site-directed mutagenesis study of ligand-receptor interactions | 2 |
1 |
1 |
1 |
0 |
0 |
1 |
1 |
0 |
2 |
2 |
0 |
11 |
| Amyloid angiopathy in hereditary gelsolin amyloidosis | 2 |
6 |
3 |
1 |
5 |
4 |
5 |
6 |
6 |
4 |
1 |
2 |
45 |
| An integrative perspective on visitor spatial behaviour in urban green spaces : Linking movement, motivations, values and biodiversity for participatory planning and management | 3 |
1 |
7 |
1 |
2 |
5 |
3 |
3 |
4 |
9 |
8 |
6 |
52 |
| Anaerobic Microbial Dechlorination of Polychlorinated Dibenzo-p-dioxins and Dibenzofurans in Contaminated Kymijoki River Sediments | 6 |
2 |
7 |
3 |
4 |
4 |
2 |
5 |
15 |
5 |
1 |
3 |
57 |
| Analysing Ecological Communities with Joint Species Distribution Models | 2 |
4 |
4 |
3 |
7 |
6 |
5 |
4 |
0 |
2 |
1 |
1 |
39 |
| Analysis of nuclear actin-interacting proteins and actin-regulated transcription factors | 8 |
9 |
8 |
3 |
15 |
8 |
9 |
9 |
5 |
6 |
1 |
5 |
86 |
| 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 | 3 |
0 |
1 |
2 |
2 |
0 |
0 |
0 |
0 |
1 |
6 |
0 |
15 |
| Anoxia and Oxidative Stress : Lipid Peroxidation, Mitochondrial Functions in Plants Antioxidant Status and Mitochondrial Functions in Plants | 4 |
5 |
6 |
7 |
2 |
5 |
9 |
7 |
6 |
9 |
9 |
3 |
72 |
| Ant community structure in successional mosaics of boreal forests | 1 |
2 |
5 |
2 |
1 |
3 |
1 |
0 |
2 |
3 |
0 |
3 |
23 |
| Antidepressant-induced plasticity in the adult mouse visual cortex | 5 |
4 |
3 |
6 |
4 |
7 |
4 |
4 |
8 |
4 |
3 |
8 |
60 |
| Antimicrobial resistance in the major respiratory tract pathogens : methods and epidemiology | 1 |
3 |
5 |
6 |
4 |
3 |
8 |
7 |
6 |
2 |
2 |
4 |
51 |
| Antipredator behaviour of Baltic planktivores | 2 |
1 |
2 |
3 |
2 |
4 |
1 |
1 |
1 |
1 |
2 |
3 |
23 |
| Apoplastic ROS and transcriptional response in plant stress signaling | 1 |
4 |
1 |
1 |
4 |
2 |
4 |
1 |
1 |
2 |
1 |
1 |
23 |
| Applicability of characterized variance and ecosystem interactions in water quality monitoring | 0 |
1 |
1 |
2 |
1 |
2 |
1 |
2 |
3 |
3 |
3 |
2 |
21 |
| Application of fluorescence resonance energy transfer to study syndecan-3 signaling on the surface of neural cells | 10 |
2 |
2 |
4 |
5 |
0 |
3 |
2 |
5 |
2 |
1 |
1 |
37 |
| Application of Pool-seq for variation detection and proteogenomic database creation in β-hemolytic streptococci. | 7 |
7 |
4 |
6 |
5 |
9 |
10 |
5 |
4 |
6 |
4 |
1 |
68 |
| Applications of gene sequence polymorphisms in evolutionary genetic studies of Atlantic salmon (Salmo salar) and other teleost fish species | 1 |
0 |
1 |
2 |
2 |
0 |
3 |
2 |
2 |
1 |
3 |
2 |
19 |
| Applications of residual dipolar couplings in structural studies of protein | 1 |
3 |
3 |
0 |
5 |
1 |
5 |
6 |
6 |
10 |
4 |
6 |
50 |
| Archaea in the Mycorrhizosphere of Boreal Forest Trees | 3 |
4 |
3 |
4 |
14 |
3 |
1 |
7 |
4 |
4 |
2 |
4 |
53 |
| Archaea, Bacteria, and methane production along environmental gradients in fens and bogs | 3 |
3 |
12 |
5 |
22 |
9 |
11 |
5 |
2 |
3 |
8 |
7 |
90 |
| Aspects of the antimicrobial susceptibility of Streptococcus pyogenes, Streptococcus pneumoniae and Aerococcus urinae | 13 |
15 |
4 |
3 |
2 |
7 |
11 |
4 |
4 |
1 |
5 |
5 |
74 |
| Assembling contractile actomyosin structures : From myosin folding to stress fibers governing epithelial integrity | 1 |
8 |
0 |
3 |
2 |
2 |
1 |
0 |
1 |
2 |
2 |
0 |
22 |
| Assessing oil spill risks in the northern Baltic Sea with Bayesian network applications | 2 |
1 |
4 |
2 |
0 |
1 |
3 |
8 |
2 |
5 |
4 |
0 |
32 |
| Assessing the effectiveness of different approaches to species conservation | 6 |
2 |
3 |
1 |
2 |
8 |
9 |
2 |
7 |
5 |
7 |
7 |
59 |
| Assessing the effects of climate change on Baltic Sea macroalgae : implications for the foundation species Fucus vesiculosus L. | 7 |
3 |
3 |
4 |
3 |
7 |
3 |
2 |
4 |
8 |
3 |
6 |
53 |
| Assessment of bioavailable concentrations and toxicity of arsenite and mercury in contaminated soils and sediments by bacterial biosensors | 2 |
1 |
5 |
2 |
5 |
1 |
2 |
1 |
1 |
2 |
3 |
10 |
35 |
| Assessment of copy number variations in the nebulin gene and other nemaline myopathy-causing genes | 2 |
7 |
3 |
7 |
6 |
4 |
6 |
7 |
8 |
5 |
2 |
6 |
63 |
| Assessment of natural and outer membrane vesicle (OMV) vaccine induced immunity against Neisseria meningitidis serogroup B in an infant rat infection model | 5 |
3 |
4 |
3 |
2 |
3 |
1 |
2 |
2 |
5 |
3 |
1 |
34 |
| Assignment of genetic loci and variants predisposing to migraine with aura and episodic ataxia type 2 | 0 |
3 |
4 |
1 |
3 |
1 |
2 |
2 |
5 |
2 |
1 |
3 |
27 |
| Associations between biodiversity, pollution, the commensal microbiota of children, and immune response | 3 |
10 |
8 |
11 |
15 |
7 |
7 |
4 |
7 |
3 |
2 |
2 |
79 |
| Asymmetrical flow field-flow fractionation in virus purification | 0 |
3 |
6 |
1 |
3 |
1 |
1 |
1 |
1 |
4 |
1 |
5 |
27 |
| Atheroinflammatory Properties of LDL and HDL Particles Modified by Human Mast Cell Neutral Proteases | 4 |
5 |
1 |
1 |
3 |
4 |
1 |
0 |
2 |
3 |
1 |
2 |
27 |
| Autophagosome Biogenesis : ATG4, TRIM17 and Beclin 1 localization | 3 |
2 |
4 |
3 |
1 |
4 |
2 |
3 |
4 |
4 |
16 |
2 |
48 |
| Auxin and cytokinin interactions regulate primary vascular patterning during root development in Arabidopsis thaliana | 4 |
6 |
18 |
7 |
1 |
8 |
8 |
3 |
3 |
3 |
6 |
5 |
72 |
| Avian conservation in a changing environment : species' responses and the efficiency of conservation measures | 5 |
3 |
6 |
4 |
3 |
1 |
0 |
3 |
1 |
2 |
5 |
4 |
37 |
| Avian responses in a changing climate | 11 |
20 |
9 |
2 |
3 |
3 |
3 |
0 |
3 |
2 |
1 |
1 |
58 |
| Bacterial community dynamics and perennial crop growth in motor oil-contaminated soil in a boreal climate | 2 |
1 |
2 |
0 |
0 |
1 |
7 |
0 |
1 |
5 |
2 |
2 |
23 |
| Barks and formal taxonomy in the family Annonaceae | 8 |
4 |
4 |
1 |
8 |
6 |
5 |
4 |
5 |
4 |
3 |
6 |
58 |
| Bat responses to aridity | 0 |
5 |
4 |
5 |
2 |
7 |
1 |
2 |
10 |
10 |
14 |
16 |
76 |
| Bayesian adventures among human mitochondrial lineages | 1 |
5 |
7 |
5 |
4 |
11 |
9 |
3 |
11 |
6 |
6 |
8 |
76 |
| Bayesian latent factor approaches for modeling ecological species communities | 1 |
3 |
9 |
9 |
6 |
5 |
3 |
6 |
7 |
9 |
4 |
6 |
68 |
| Bayesian Network applications for environmental risk assessment | 4 |
7 |
8 |
6 |
0 |
4 |
9 |
5 |
22 |
4 |
2 |
2 |
73 |
| Behaviour, dynamics and ecological impact of small mustelids | 1 |
5 |
3 |
4 |
1 |
10 |
6 |
8 |
5 |
3 |
5 |
2 |
53 |
| Behavioural and morphological variation in European grayling, Thymallus thymallus, populations | 2 |
2 |
2 |
2 |
1 |
2 |
8 |
2 |
0 |
3 |
2 |
0 |
26 |
| Behavioural and physiological responses to predators of captive-bred Arctic charr : significance of genetics, learning and ontogeny | 5 |
2 |
0 |
1 |
3 |
2 |
1 |
3 |
1 |
4 |
2 |
1 |
25 |
| Behavioural responses to anthropogenic disturbances | 0 |
3 |
4 |
2 |
3 |
3 |
2 |
1 |
1 |
4 |
0 |
2 |
25 |
| Behavioural, population, and genetic processes affecting metapopulation dynamics of the Glanville fritillary butterfly | 1 |
1 |
3 |
2 |
1 |
3 |
1 |
0 |
2 |
3 |
1 |
4 |
22 |
| Below-ground processes in meadow soil under elevated ozone and carbon dioxide : Greenhouse gas fluxes, N cycling and microbial communities | 2 |
2 |
2 |
0 |
0 |
0 |
0 |
2 |
0 |
1 |
0 |
0 |
9 |
| Bending the Rules of Cell Protrusions : Molecular Mechanisms and Biological Roles of Inverse-BAR Proteins in Cell Morphogenesis | 2 |
4 |
2 |
4 |
2 |
3 |
4 |
3 |
2 |
0 |
10 |
1 |
37 |
| Beneficial microbial activity supporting sustainable agriculture | 1 |
3 |
3 |
3 |
4 |
0 |
5 |
5 |
6 |
8 |
1 |
0 |
39 |
| Benthic diatom community structure in boreal streams : Distribution patterns along environmental and spatial gradients | 34 |
3 |
3 |
3 |
2 |
10 |
2 |
1 |
4 |
6 |
6 |
3 |
77 |
| Benthic fauna as mediators of carbon and nutrient cycling in the coastal Baltic Sea | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
8 |
97 |
9 |
6 |
120 |
| Benthic resting eggs in the life cycles of calanoid copepods in the northern Baltic Sea | 0 |
1 |
3 |
2 |
0 |
0 |
5 |
1 |
3 |
2 |
1 |
0 |
18 |
| Benthic-pelagic coupling in the northern Baltic Sea : importance of bioturbation and benthic predation | 1 |
0 |
1 |
4 |
2 |
3 |
2 |
1 |
4 |
2 |
1 |
0 |
21 |
| Bidirectional signalling and phosphorylation of CD11/CD18-integrins in T cells | 5 |
1 |
3 |
1 |
0 |
2 |
1 |
1 |
0 |
4 |
2 |
0 |
20 |
| Bioavailability and toxicity of chemicals in inland waters : the importance of prevailing water chemistry and implications for risk assessment | 1 |
6 |
3 |
1 |
3 |
0 |
2 |
1 |
3 |
2 |
1 |
3 |
26 |
| Biochemical effects of inherited MMR gene mutations and diet on colon cancer risk | 8 |
2 |
2 |
2 |
2 |
3 |
3 |
1 |
0 |
3 |
4 |
1 |
31 |
| Biodiversity in golf courses and its contribution to the diversity of open green spaces in an urban setting | 8 |
6 |
12 |
14 |
14 |
14 |
15 |
23 |
24 |
14 |
35 |
18 |
197 |
| Bioinformatics analysis of HPV associated host microRNA functions and identification of viral microRNA | 4 |
2 |
3 |
3 |
5 |
4 |
1 |
1 |
9 |
9 |
8 |
2 |
51 |
| Bioinformatics analysis of intron retention events associated with the minor spliceosome | 4 |
5 |
8 |
7 |
9 |
12 |
9 |
7 |
12 |
6 |
5 |
1 |
85 |
| Biological effects of contaminants in mussels (Mytilus trossulus) transplanted in northern Baltic Sea coastal areas | 5 |
1 |
3 |
2 |
5 |
4 |
1 |
2 |
6 |
5 |
0 |
5 |
39 |
| Biological Functions of Novel Mitochondrial Proteins | 2 |
5 |
8 |
6 |
6 |
2 |
9 |
8 |
5 |
9 |
3 |
2 |
65 |
| Bioluminescence of Toxic Dinoflagellates in the Baltic Sea : From Genes to Models | 6 |
6 |
3 |
2 |
6 |
6 |
2 |
19 |
9 |
20 |
8 |
22 |
109 |
| Biomarkers for exposure and for the effects of contamination with polyhalogenated aromatic hydrocarbons in Baltic ringed and grey seals | 2 |
0 |
2 |
3 |
3 |
1 |
6 |
4 |
1 |
3 |
13 |
4 |
42 |
| Bioremediation of diesel oil contaminated soil and water | 15 |
12 |
8 |
7 |
5 |
3 |
3 |
5 |
16 |
8 |
12 |
9 |
103 |
| Bird populations in a changing world : implications for North European conservation | 2 |
7 |
5 |
10 |
7 |
1 |
4 |
7 |
2 |
3 |
2 |
0 |
50 |
| Bird's eye view of European biodiversity policy under climate change | 4 |
7 |
2 |
3 |
3 |
3 |
4 |
4 |
1 |
2 |
1 |
0 |
34 |
| Black carbon deposition in the European Arctic from the preindustrial to the present | 3 |
9 |
12 |
12 |
12 |
8 |
2 |
5 |
6 |
6 |
5 |
4 |
84 |
| Blue mussel beds as biodiversity hotspots on the rocky shores of the northern Baltic Sea | 8 |
0 |
3 |
6 |
3 |
3 |
3 |
4 |
16 |
17 |
18 |
20 |
101 |
| BMP/Dpp signaling and epithelial morphogenesis in Drosophila development | 0 |
2 |
2 |
8 |
12 |
9 |
6 |
13 |
4 |
7 |
10 |
12 |
85 |
| Boosting Beneficial Microbial Exposure of Urbanites through Nature-Based Recreation and Biodiverse Elements | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
48 |
21 |
69 |
| Bovine milk TGF-(beta)2, IGF-1 and insulin in indirect heat treatments and filtration processes | 9 |
7 |
8 |
9 |
9 |
5 |
4 |
6 |
8 |
6 |
9 |
8 |
88 |
| Brain Immune Gene Network in Inbred Mouse Models of Anxiety- and Sociability-related Neuropsychiatric Disorders | 1 |
3 |
3 |
1 |
1 |
0 |
2 |
1 |
3 |
3 |
2 |
2 |
22 |
| Brain-sparing responses in brain pH and O2 levels in a rodent model of birth asphyxia : from mechanisms to novel therapeutic approaches | 3 |
4 |
1 |
1 |
1 |
3 |
5 |
2 |
4 |
1 |
2 |
4 |
31 |
| Breast cancer-predisposing genes in Finnish breast and ovarian cancer families | 0 |
1 |
1 |
4 |
1 |
0 |
1 |
0 |
2 |
5 |
4 |
2 |
21 |
| Bustle behind the scenes of action : nemosis as a model for fibroblast inflammatory activation | 4 |
0 |
2 |
2 |
0 |
3 |
1 |
0 |
0 |
1 |
0 |
1 |
14 |
| Butterflies in changing weather conditions : implications for ecology and conservation | 9 |
4 |
3 |
2 |
1 |
0 |
18 |
20 |
8 |
6 |
1 |
2 |
74 |
| Butterfly view of environmental variability in population dynamics across fragmented landscapes | 5 |
6 |
4 |
4 |
10 |
4 |
16 |
43 |
19 |
20 |
14 |
16 |
161 |
| c-Jun and its targets in fibrosarcoma and melanoma cells | 4 |
2 |
3 |
1 |
1 |
3 |
0 |
1 |
4 |
2 |
3 |
1 |
25 |
| CADASIL : molecular studies on the most common hereditary vascular dementing disorder | 4 |
4 |
5 |
10 |
13 |
2 |
1 |
3 |
2 |
4 |
4 |
1 |
53 |
| Calm or storm? : Wind power actors perceptions of Finnish wind power and its future | 33 |
74 |
3 |
1 |
3 |
0 |
2 |
0 |
6 |
2 |
5 |
2 |
131 |
| Can you see me? : Sexual signalling in an artificially lit world | 5 |
4 |
2 |
5 |
4 |
1 |
4 |
5 |
5 |
2 |
1 |
1 |
39 |
| Candidate therapeutic targets against acute myeloid leukemia identified via screening combinatorial peptide and chemical libraries | 0 |
5 |
2 |
1 |
3 |
4 |
1 |
1 |
4 |
3 |
2 |
3 |
29 |
| Cannibalism and conflict in Formica ants | 3 |
1 |
3 |
0 |
1 |
1 |
6 |
2 |
2 |
5 |
1 |
10 |
35 |
| Canonical Wnt Signaling in Hair and Mammary Gland Patterning and Development | 5 |
8 |
4 |
3 |
2 |
3 |
5 |
8 |
3 |
5 |
4 |
1 |
51 |
| Capsids, Matrices and Vesicles : Structural Insights into the Assembly of Paramyxoviruses | 2 |
2 |
3 |
4 |
3 |
3 |
7 |
1 |
6 |
4 |
4 |
2 |
41 |
| Carabid beetles (Coleoptera, Carabidae) as indicators of environmental change in Ranomafana National Park, Madagascar | 4 |
7 |
2 |
1 |
7 |
3 |
1 |
4 |
3 |
6 |
7 |
9 |
54 |
| Carabid beetles (Coleoptera, Carabidae) in boreal managed forests : meso-scale ecological patterns in relation to modern forestry | 2 |
0 |
2 |
1 |
0 |
1 |
0 |
1 |
1 |
1 |
1 |
0 |
10 |
| Carbon dioxide and methane exchange between a boreal pristine lake and the atmosphere | 8 |
7 |
10 |
5 |
5 |
2 |
3 |
0 |
2 |
4 |
1 |
1 |
48 |
| Causes and consequences of inbreeding in the ant Formica exsecta | 2 |
1 |
4 |
3 |
0 |
2 |
3 |
2 |
0 |
2 |
2 |
0 |
21 |
| Causes and consequences of variation in nestling immune function | 3 |
1 |
0 |
1 |
1 |
1 |
0 |
3 |
1 |
3 |
1 |
1 |
16 |
| Causes and consequences of within-host parasite communities | 3 |
4 |
1 |
7 |
2 |
7 |
4 |
7 |
7 |
3 |
3 |
0 |
48 |
| CD8+ T Cell Response in Experimental Chlamydia pneumoniae Infection | 1 |
4 |
2 |
5 |
6 |
2 |
5 |
5 |
4 |
3 |
5 |
2 |
44 |
| Cell cycle regulation during plant growth and development, gene expression studies in Arabidopsis thaliana (L.) Heynh. | 2 |
3 |
6 |
7 |
10 |
4 |
5 |
7 |
5 |
4 |
7 |
14 |
74 |
| Cell Cycle Regulation via Growth Factor- and Stress-Induced Pathways | 2 |
3 |
1 |
1 |
4 |
0 |
0 |
1 |
1 |
6 |
1 |
3 |
23 |
| Cell fates in nephrogenesis and spermatogenesis | 3 |
1 |
5 |
2 |
7 |
4 |
5 |
5 |
4 |
11 |
7 |
5 |
59 |
| Cell-Surface Association between Progelatinases and beta² Integrins : Role of the Complexes in Leukocyte Migration | 1 |
4 |
3 |
3 |
0 |
2 |
71 |
1 |
2 |
1 |
0 |
0 |
88 |
| Cellular differentiation in the inner ear : The role of the network of transcription factors and the Rho GTPase Cdc42 | 1 |
4 |
1 |
3 |
2 |
0 |
1 |
3 |
0 |
1 |
1 |
0 |
17 |
| Cellular fates and secretion ofAlzheimer’s disease-related proteins APP and tau | 6 |
7 |
8 |
14 |
13 |
8 |
7 |
4 |
4 |
2 |
3 |
1 |
77 |
| Cellular Membranes as a Playground for Semliki Forest Virus Replication Complex | 3 |
2 |
7 |
3 |
1 |
2 |
1 |
0 |
2 |
2 |
2 |
3 |
28 |
| Cellular Physiology and Cell-to-Cell Propagation of Tau in Neurodegeneration : The Impact of Late-Onset Alzheimer's Disease Susceptibility Genes | 4 |
5 |
3 |
2 |
2 |
4 |
0 |
1 |
7 |
4 |
3 |
2 |
37 |
| Cellular Regulation of Glial Cell Line-Derived Neurotrophic Factor | 0 |
2 |
3 |
4 |
3 |
5 |
2 |
1 |
4 |
1 |
0 |
4 |
29 |
| Chaga Genome and Convergent Evolution of Betulinate Biosynthesis in Host (Betula pendula) and the Pathogen (Inonotus obliquus) | 3 |
3 |
7 |
2 |
5 |
1 |
2 |
10 |
4 |
1 |
0 |
2 |
40 |
| Changes in soil C dynamics and N2O emissions under minimum tillage cereal crop production in boreal agroecosystems : Implications to climate change mitigation | 1 |
1 |
3 |
3 |
1 |
2 |
3 |
0 |
2 |
1 |
0 |
2 |
19 |
| Changing climate and the Baltic region biota | 11 |
2 |
2 |
5 |
5 |
7 |
6 |
4 |
1 |
7 |
2 |
1 |
53 |
| Characterisation and source identification of pollution episodes caused by long-range transported aerosols | 3 |
5 |
2 |
6 |
1 |
3 |
1 |
2 |
2 |
3 |
2 |
3 |
33 |
| Characterisation of cellular defects in Niemann-Pick type C disease | 0 |
3 |
1 |
1 |
2 |
1 |
1 |
1 |
1 |
2 |
3 |
1 |
17 |
| Characterisation of diverse microbial communities and application of novel detection techniques | 3 |
2 |
4 |
3 |
4 |
0 |
6 |
1 |
3 |
3 |
3 |
4 |
36 |
| Characterisation of the type three secretion system in Erwinia carotovora | 1 |
1 |
1 |
3 |
5 |
7 |
7 |
4 |
6 |
7 |
4 |
3 |
49 |
| Characterisation, cloning and production of industrially interesting enzymes : gluconolactone oxidase of Penicillium cyaneo-fulvum and gluconate 5-dehydrogenase of Gluconobacter suboxydans | 2 |
2 |
6 |
0 |
3 |
2 |
0 |
1 |
0 |
1 |
1 |
1 |
19 |
| Characterization and selective modulation of chamber-specific gene regulatory networks underlying congenital and adult heart disease | 4 |
4 |
5 |
1 |
2 |
7 |
2 |
6 |
4 |
7 |
6 |
4 |
52 |
| Characterization of Drosophila melanogaster Manf an evolutionarily conserved neurotrophic factor | 3 |
2 |
1 |
5 |
6 |
4 |
3 |
4 |
9 |
4 |
3 |
5 |
49 |
| 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 | 0 |
1 |
2 |
4 |
3 |
2 |
4 |
2 |
12 |
3 |
5 |
5 |
43 |
| Characterization of meningeal lymphatic vessels in physiological and pathological conditions | 5 |
3 |
81 |
4 |
11 |
6 |
2 |
1 |
6 |
4 |
8 |
6 |
137 |
| Characterization of New Viruses from Hypersaline Environments | 5 |
3 |
6 |
1 |
2 |
1 |
2 |
3 |
2 |
1 |
0 |
0 |
26 |
| Characterization of potato allergens | 2 |
4 |
3 |
2 |
3 |
0 |
1 |
0 |
0 |
1 |
1 |
1 |
18 |
| Characterization of small GTPase Cdc42 from the ectomycorrhizal fungus Suillus bovinus and Agrobacterium tumefaciens-mediated transformation of fungi | 7 |
9 |
6 |
2 |
3 |
2 |
3 |
2 |
12 |
5 |
4 |
3 |
58 |
| Characterization of the molecular components and function of BARE-1, Hin-Mu and Mu transposition machineries | 2 |
4 |
1 |
1 |
3 |
2 |
0 |
1 |
2 |
1 |
2 |
3 |
22 |
| Chloroinformatics | 0 |
2 |
0 |
0 |
2 |
1 |
2 |
2 |
2 |
0 |
0 |
3 |
14 |
| Chrysophyte stomatocysts and their biogeography in Finland | 2 |
2 |
6 |
3 |
3 |
1 |
0 |
3 |
0 |
2 |
0 |
0 |
22 |
| Circadian Rhythm Disruptions and Health | 2 |
2 |
4 |
1 |
3 |
0 |
4 |
7 |
3 |
4 |
1 |
2 |
33 |
| Cladocera as sentinels of aquatic mine pollution | 5 |
8 |
3 |
6 |
2 |
4 |
5 |
13 |
9 |
6 |
3 |
3 |
67 |
| Climate change and the future distribution of palsa mires : ensemble modelling, probabilities and uncertainties | 7 |
3 |
5 |
6 |
5 |
5 |
3 |
3 |
3 |
9 |
8 |
3 |
60 |
| Climate Change as a Political Process : The Rise and Fall of the Kyoto Protocol | 71 |
36 |
103 |
48 |
61 |
58 |
42 |
54 |
87 |
65 |
116 |
46 |
787 |
| Climate change, species range shifts and uncertainty : A new era of conservation planning | 10 |
4 |
2 |
3 |
9 |
5 |
5 |
0 |
2 |
4 |
3 |
2 |
49 |
| Climate forcing on avian life history | 1 |
2 |
2 |
5 |
3 |
1 |
2 |
3 |
1 |
4 |
2 |
2 |
28 |
| Climate Impacts on Remote Subarctic Lakes in Finnish Lapland : Limnological and Palaeolimnological Assessment with a Particular Focus on Diatoms and Lake Saanajärvi | 1 |
1 |
5 |
8 |
5 |
1 |
4 |
2 |
7 |
4 |
4 |
5 |
47 |
| Climatic effect of light-absorbing impurities on snow : experimental and field observations | 2 |
2 |
5 |
0 |
1 |
0 |
1 |
2 |
0 |
3 |
2 |
2 |
20 |
| Cloister, manor and botanic gardens in medieval and early modern Finland and Sweden : An archaeobotanical approach to garden history | 7 |
7 |
10 |
2 |
25 |
20 |
24 |
20 |
20 |
26 |
22 |
16 |
199 |
| Closed-circuit hypolimnetic withdrawal : biogeochemical considerations and potential in lake restoration | 10 |
20 |
14 |
45 |
2 |
6 |
13 |
6 |
7 |
7 |
2 |
5 |
137 |
| CMGC kinases and Cancer | 17 |
3 |
5 |
8 |
9 |
4 |
6 |
1 |
2 |
2 |
1 |
2 |
60 |
| CMV-, EBV-, and HHV-6-DNAemia after liver transplantation | 1 |
2 |
3 |
1 |
0 |
2 |
0 |
0 |
1 |
1 |
2 |
0 |
13 |
| Coagulation Factor XIII (FXIII) and Vascular Endothelial Growth Factors VEGF and VEGF-C Produced by Platelers : From Clinical Findings to Molecular Characteristics | 5 |
3 |
2 |
3 |
4 |
3 |
1 |
0 |
0 |
0 |
0 |
1 |
22 |
| Coastal environmental gradients : Key to reproduction habitat mapping of freshwater fish in the Baltic Sea | 2 |
2 |
2 |
2 |
0 |
4 |
1 |
2 |
4 |
5 |
0 |
4 |
28 |
| Colour polymorphism as a proxy for adaptations to climate change : from geographical patterns to mechanisms in Tawny Owls | 8 |
47 |
53 |
7 |
6 |
3 |
11 |
0 |
6 |
3 |
4 |
8 |
156 |
| Combining biochemistry to dentistry : from in vitro Candida glabrata observations to an in vivo clinical lingonberry application | 3 |
5 |
1 |
62 |
14 |
3 |
5 |
5 |
5 |
7 |
6 |
1 |
117 |
| Coming to terms with conservation under climate change : Using species distribution models and translocation trials for estimating the need and potential of assisted migration | 5 |
1 |
6 |
1 |
1 |
0 |
1 |
1 |
2 |
3 |
1 |
2 |
24 |
| Communities of wood-inhabiting fungi : Ecological requirements and responses to forest management and fragmentation | 91 |
54 |
2 |
4 |
1 |
25 |
8 |
8 |
6 |
5 |
4 |
10 |
218 |
| Comparative and functional genome analysis of fungi for development of the protein production host Trichoderma reesei | 1 |
0 |
1 |
3 |
0 |
2 |
1 |
2 |
1 |
1 |
1 |
3 |
16 |
| Comparative Evaluation of Methods for Sequence Alignment and Annotation | 3 |
2 |
3 |
1 |
1 |
1 |
2 |
4 |
3 |
2 |
1 |
2 |
25 |
| Composition and structure of barley (Hordeum vulgare L.) grain in relation to end uses | 14 |
4 |
13 |
3 |
9 |
8 |
14 |
7 |
12 |
13 |
12 |
15 |
124 |
| Computational Approaches to Biological Network Inference and Modeling in Systems Biology | 1 |
2 |
4 |
2 |
1 |
0 |
1 |
0 |
3 |
6 |
3 |
2 |
25 |
| Computational frameworks to aid pharmacological studies : Tools, Databases and Prediction models | 2 |
4 |
25 |
11 |
1 |
7 |
2 |
0 |
3 |
3 |
8 |
2 |
68 |
| Computational genomics of lactobacilli | 2 |
4 |
3 |
0 |
6 |
6 |
3 |
49 |
25 |
2 |
0 |
2 |
102 |
| Computational investigation of oxygen reduction and proton pumping in cbb3-type Cytochrome c Oxidases | 2 |
7 |
2 |
2 |
4 |
3 |
1 |
3 |
0 |
3 |
1 |
5 |
33 |
| Computational tools for high-throughput drug combination screening, synergy scoring and predictive modelling in cancer | 12 |
12 |
19 |
9 |
6 |
10 |
9 |
5 |
16 |
23 |
23 |
9 |
153 |
| Concentrations of mercury (Hg) and cadmium (Cd), and the condition of some coastal Baltic fishes | 1 |
3 |
4 |
2 |
1 |
2 |
3 |
4 |
0 |
3 |
1 |
2 |
26 |
| Conceptual and statistical modelling of environmental effects in population dynamics | 2 |
0 |
0 |
2 |
3 |
5 |
7 |
1 |
2 |
1 |
5 |
5 |
33 |
| Condition-dependence of fitness-related traits in the Glanville fritillary butterfly | 1 |
1 |
2 |
1 |
3 |
4 |
1 |
0 |
1 |
2 |
3 |
4 |
23 |
| Connecting silvan and lacustrine ecosystems : transport of carbon from forests to adjacent water bodies | 2 |
1 |
1 |
4 |
2 |
6 |
2 |
4 |
1 |
2 |
4 |
4 |
33 |
| Connective tissue formation in wound healing : An experimental study | 8 |
6 |
5 |
4 |
3 |
2 |
3 |
1 |
4 |
2 |
3 |
1 |
42 |
| Consequences of Balanced Translocations and Loss-of-function Mutations | 5 |
5 |
12 |
3 |
5 |
1 |
3 |
5 |
9 |
5 |
7 |
6 |
66 |
| Conservation biology of Saimaa ringed seal (Phoca hispida saimensis) with reference to other European seal populations | 7 |
6 |
7 |
40 |
11 |
6 |
18 |
15 |
17 |
5 |
2 |
6 |
140 |
| Conservation genetics of endemic Indirana frogs of the Western Ghats biodiversity hotspot | 5 |
0 |
5 |
3 |
3 |
1 |
2 |
2 |
4 |
1 |
2 |
1 |
29 |
| Conservation of Atlantic salmon by supplementary stocking of juvenile fish | 3 |
2 |
8 |
4 |
2 |
1 |
3 |
3 |
0 |
5 |
5 |
0 |
36 |
| Context-dependent mate choice in the sand goby, Pomatoschistus minutus | 2 |
1 |
1 |
4 |
2 |
2 |
0 |
3 |
3 |
1 |
0 |
0 |
19 |
| Control of plankton and nutrient limitation in small boreal brown-water lakes : Evidence from small- and large-scale manipulation experiments | 2 |
2 |
1 |
3 |
1 |
3 |
3 |
5 |
0 |
2 |
3 |
2 |
27 |
| Control of vascular integrity via endothelial growth factor and integrin cell adhesion receptor pathways | 7 |
8 |
5 |
6 |
10 |
8 |
6 |
3 |
3 |
4 |
4 |
5 |
69 |
| Conversion of GDP-mannose into various GDP-deoxyhexoses in Gram-negative bacteria | 1 |
2 |
6 |
2 |
2 |
5 |
1 |
4 |
3 |
4 |
4 |
3 |
37 |
| Cooperation and conflict in conspecific brood parasitism : an alternative reproductive tactic | 1 |
1 |
2 |
2 |
5 |
3 |
2 |
3 |
4 |
5 |
3 |
3 |
34 |
| Coping with contested risks : exploring how oil spill risks are governed through governmentalities | 3 |
4 |
3 |
2 |
1 |
3 |
6 |
2 |
4 |
2 |
4 |
3 |
37 |
| Copy number variants in genes causing neuromuscular disorders | 18 |
49 |
16 |
8 |
6 |
2 |
9 |
5 |
13 |
9 |
11 |
4 |
150 |
| Cortinarius subgenus Telamonia p.p. in North Europe | 9 |
13 |
5 |
5 |
12 |
13 |
15 |
6 |
18 |
5 |
15 |
14 |
130 |
| Cracking the code of chikungunya virus : inhibitors as tools to explore alphavirus biology | 2 |
0 |
4 |
5 |
3 |
9 |
3 |
2 |
7 |
2 |
4 |
13 |
54 |
| Critical bistability and large-scale synchrony in human brain dynamics | 11 |
11 |
3 |
4 |
16 |
8 |
9 |
7 |
9 |
6 |
6 |
1 |
91 |
| Cross-reactive immune responses between enteroviruses and islet cell autoantigens | 30 |
3 |
3 |
3 |
4 |
4 |
7 |
2 |
3 |
4 |
5 |
5 |
73 |
| 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 | 5 |
2 |
2 |
4 |
3 |
2 |
1 |
2 |
3 |
6 |
5 |
2 |
37 |
| Cultural Ecosystem Services of urban forests : a delivery from biodiversity, through the landscape, to beneficiaries | 8 |
6 |
10 |
3 |
2 |
8 |
1 |
6 |
5 |
7 |
5 |
1 |
62 |
| Culture Systems and Quality Parameters for Clinical-grade Mesenchymal stromal cells | 3 |
13 |
5 |
7 |
6 |
8 |
4 |
1 |
2 |
5 |
3 |
6 |
63 |
| Cyanobacteria and their toxins in lichen symbiosis | 4 |
3 |
2 |
1 |
3 |
2 |
3 |
2 |
5 |
1 |
3 |
3 |
32 |
| Cyclic nucleotide inactivation in osteoblasts and osteosarcoma cell lines | 2 |
1 |
2 |
1 |
6 |
1 |
2 |
4 |
1 |
0 |
2 |
2 |
24 |
| Cycling of dissolved and particulate organic matter in the pelagic marine environment : Impact of phytoplankton community mortality and microbial degradation | 3 |
3 |
4 |
0 |
4 |
2 |
4 |
4 |
4 |
1 |
2 |
3 |
34 |
| Cytokinin signaling in hybrid aspen cambial development and growth | 14 |
15 |
4 |
7 |
1 |
2 |
5 |
5 |
5 |
6 |
2 |
4 |
70 |
| Cytokinin signalling in the regulation of cambial development | 0 |
1 |
5 |
1 |
1 |
1 |
1 |
3 |
2 |
4 |
3 |
2 |
24 |
| Cytokinins regulate vascular morphogenesis in the Arabidopsis thaliana root | 2 |
4 |
6 |
1 |
13 |
7 |
5 |
4 |
3 |
5 |
2 |
2 |
54 |
| Data limited fisheries : Incorporating expert knowledge into stock assessment | 3 |
1 |
2 |
1 |
1 |
4 |
3 |
2 |
4 |
4 |
6 |
2 |
33 |
| Deadwood and wood-inhabiting fungi in urban forests - Biodiversity conservation potential in cities | 4 |
3 |
18 |
11 |
12 |
14 |
4 |
7 |
0 |
6 |
10 |
8 |
97 |
| Death pathways activated in the neurotrophic factor-deprived neurons | 1 |
0 |
3 |
3 |
6 |
3 |
0 |
2 |
0 |
4 |
5 |
3 |
30 |
| Decisions to adapt : trade-offs, maladaptation and transformations in Nordic agri-food systems | 0 |
6 |
7 |
3 |
3 |
0 |
2 |
1 |
0 |
4 |
2 |
0 |
28 |
| Degradation of 2,6-dichlorobenzonitrile and 2,6-dichlorobenzamide in groundwater sedimentary deposits and topsoil | 3 |
4 |
4 |
1 |
4 |
3 |
3 |
1 |
1 |
4 |
4 |
3 |
35 |
| Demethyl (C-11) cezomycin : a novel calcimycin antibiotic from the symbiotic, N | 2 |
0 |
4 |
1 |
1 |
0 |
0 |
2 |
1 |
3 |
0 |
0 |
14 |
| Detecting novel cancer predisposing mutations by utilizing the Finnish Cancer Registry and archival tissue material | 5 |
3 |
7 |
2 |
2 |
2 |
3 |
5 |
1 |
15 |
5 |
5 |
55 |
| Determinants of Endoplasmic Reticulum Structure and Dynamics | 1 |
2 |
3 |
12 |
15 |
25 |
19 |
23 |
24 |
21 |
17 |
19 |
181 |
| Determining the Optimal Release Window for Lake-Stocked Brown Trout : Interactions between Release Size, Prey Availability, Predation Risks and Fishing Mortality | 2 |
3 |
3 |
2 |
1 |
1 |
2 |
2 |
0 |
6 |
3 |
3 |
28 |
| Developing glutamatergic connectivity in the hippocampus : the role of tonically active kainate receptors | 1 |
3 |
3 |
3 |
8 |
8 |
7 |
3 |
3 |
3 |
1 |
2 |
45 |
| Developing more effective conservation and research : the case of the Siberian flying squirrel | 4 |
5 |
4 |
1 |
3 |
1 |
2 |
8 |
2 |
5 |
2 |
1 |
38 |
| Developing sustainability through systems thinking : perspectives to maritime traffic | 5 |
3 |
8 |
2 |
1 |
3 |
3 |
4 |
4 |
10 |
12 |
3 |
58 |
| Development and evolution of tooth renewal and dental formula in squamate reptiles | 10 |
9 |
11 |
11 |
11 |
7 |
11 |
13 |
22 |
24 |
8 |
10 |
147 |
| Development of microfluidic applications to study the role of kainate receptors in synaptogenesis | 5 |
2 |
1 |
2 |
3 |
1 |
2 |
2 |
1 |
3 |
2 |
1 |
25 |
| Development of new automated methods for quantification of immunohistochemically stained cells | 0 |
0 |
0 |
0 |
33 |
27 |
14 |
3 |
6 |
2 |
11 |
2 |
98 |
| Development of NMR methods to study disordered proteins | 75 |
48 |
3 |
8 |
3 |
2 |
6 |
5 |
1 |
4 |
2 |
4 |
161 |
| Development of transgenic crops protected from insect damage and transgene escape | 2 |
1 |
1 |
2 |
2 |
1 |
2 |
4 |
3 |
4 |
1 |
1 |
24 |
| Developmental Growth and Regeneration Processes in Squamate Eyes | 4 |
2 |
5 |
5 |
4 |
6 |
2 |
5 |
1 |
1 |
2 |
1 |
38 |
| Developmentally Regulated Induction and Expression Mechanisms of Long-Term Potentiation at Hippocampal CA3 CA1 Synapses | 4 |
6 |
2 |
3 |
1 |
3 |
4 |
5 |
1 |
3 |
3 |
1 |
36 |
| Developmentally regulated proteins in Pinus sylvestris roots and ectomycorrhiza | 2 |
1 |
3 |
1 |
2 |
3 |
3 |
2 |
3 |
5 |
3 |
6 |
34 |
| Diamond-like carbon binding peptides evolutionary selection, characterization, and engineering | 4 |
3 |
8 |
5 |
9 |
2 |
3 |
2 |
6 |
3 |
3 |
4 |
52 |
| Diatoms, dinoflagellates and their distinct effects on the structure and function of the bacterioplankton | 15 |
9 |
6 |
6 |
9 |
3 |
3 |
5 |
5 |
10 |
7 |
8 |
86 |
| Dietary fibre components of rye bran and their fermentation in vitro | 1 |
9 |
3 |
5 |
4 |
1 |
2 |
0 |
2 |
2 |
5 |
0 |
34 |
| Differential abundance analyses of human microbiota in Parkinson’s disease | 8 |
5 |
9 |
3 |
2 |
4 |
9 |
7 |
4 |
6 |
1 |
1 |
59 |
| Differential functions of mammalian Cdk7 and CCRK kinases in regulating transcription and ciliogenesis | 6 |
5 |
3 |
3 |
2 |
2 |
5 |
2 |
3 |
4 |
2 |
3 |
40 |
| Differentiation of neural stem cells in fragile X syndrome | 5 |
2 |
6 |
3 |
1 |
2 |
6 |
0 |
4 |
1 |
0 |
0 |
30 |
| Diffusive and ship-mediated spread of dinoflagellates in the Baltic Sea with Prorocentrum minimum as a special case | 2 |
2 |
1 |
1 |
0 |
5 |
4 |
1 |
0 |
1 |
5 |
3 |
25 |
| Directional Hearing under Water : Morphology and Function of the Middle Ear of Globicephala macrorhynchus (Short-Finned Pilot Whale) | 6 |
38 |
63 |
3 |
6 |
6 |
2 |
7 |
3 |
4 |
3 |
6 |
147 |
| Discovery and evolutionary affinities of five new species of amphibians from Bangladesh | 1 |
5 |
2 |
1 |
3 |
3 |
2 |
4 |
2 |
12 |
7 |
1 |
43 |
| Discovery of oxidative enzymes for food engineering : Tyrosinase and sulfhydryl oxidase | 4 |
5 |
1 |
1 |
3 |
3 |
3 |
3 |
4 |
3 |
2 |
4 |
36 |
| Discovery of salt-loving pleolipoviruses infecting archaea : vesicle-like virion is the key to success | 1 |
3 |
0 |
7 |
3 |
3 |
1 |
1 |
1 |
2 |
3 |
1 |
26 |
| Disease dynamics, invasion and biological control of environmentally growing pathogens | 5 |
3 |
1 |
3 |
1 |
2 |
5 |
2 |
1 |
4 |
2 |
2 |
31 |
| Dispersal and related life history traits in the Glanville fritillary butterfly | 2 |
0 |
2 |
2 |
1 |
2 |
1 |
2 |
1 |
1 |
2 |
2 |
18 |
| Dissecting genetic susceptibility to gluten sensitivity : HLA-linked risk factors in coeliac disease and dermatitis herpetiformis | 4 |
3 |
13 |
7 |
5 |
3 |
5 |
4 |
4 |
2 |
8 |
4 |
62 |
| Dissecting VEGFR-2 and VEGFR-3 function : VEGFR-3 mediates lymphangiogenic signals | 1 |
7 |
0 |
1 |
1 |
5 |
1 |
0 |
1 |
1 |
1 |
0 |
19 |
| Dissipation of herbicides in surface soils and subsurface sediment slurries and development of treatment methods | 3 |
4 |
2 |
2 |
4 |
5 |
13 |
5 |
2 |
5 |
8 |
5 |
58 |
| Distribution and function of GABA receptor ρ subunits in the rat nervous system | 2 |
2 |
2 |
1 |
0 |
0 |
0 |
2 |
0 |
2 |
1 |
0 |
12 |
| Distribution of non-biting midges (Diptera, Chironomidae) in subarctic lakes of Finnish Lapland applications in lake classification and palaeolimnology | 3 |
0 |
2 |
2 |
0 |
0 |
2 |
1 |
1 |
3 |
0 |
0 |
14 |
| Disturbance in boreal spruce forest : immediate dynamics from stand to understorey level | 3 |
2 |
0 |
3 |
5 |
1 |
2 |
2 |
3 |
2 |
2 |
7 |
32 |
| Diversity and classification of the Scopulini (Lepidoptera: Geometridae, Sterrhinae) | 2 |
3 |
7 |
2 |
2 |
5 |
1 |
4 |
0 |
2 |
3 |
4 |
35 |
| Diversity and ecology of Termitomyces symbionts in Macrotermes mounds of the Tsavo Ecosystem, Kenya | 2 |
4 |
3 |
3 |
0 |
3 |
1 |
1 |
1 |
2 |
9 |
3 |
32 |
| Diversity and zoogeography of continental mysid crustaceans | 6 |
7 |
5 |
5 |
5 |
4 |
9 |
6 |
6 |
5 |
2 |
3 |
63 |
| Diversity of microfungi preserved in European Palaeogene amber | 2 |
3 |
5 |
2 |
7 |
1 |
2 |
4 |
1 |
4 |
3 |
3 |
37 |
| DNA Packaging and Host Cell Lysis : Late Events in Bacteriophage PRD1 Infection | 4 |
6 |
2 |
2 |
0 |
1 |
6 |
2 |
4 |
5 |
4 |
4 |
40 |
| Do we listen to earthworms? : Tools for evaluating the Finnish Action Plan on the sustainable use of plant protection products | 5 |
1 |
0 |
0 |
2 |
8 |
6 |
8 |
7 |
2 |
3 |
3 |
45 |
| Double-stranded RNA Bacteriophage phi6 : Self-assembly and Maturation of the Procapsid | 3 |
6 |
3 |
7 |
3 |
1 |
2 |
2 |
6 |
5 |
3 |
1 |
42 |
| Dung beetle communities in Madagascar | 2 |
8 |
4 |
3 |
8 |
2 |
6 |
3 |
3 |
3 |
2 |
5 |
49 |
| Dung beetle radiations in Madagascar | 2 |
1 |
2 |
2 |
3 |
4 |
2 |
4 |
3 |
3 |
2 |
7 |
35 |
| Dynamics of Dissolved Organic Matter and its Bioavailability to Heterotrophic Bacteria in the Gulf of Finland, Northern Baltic Sea | 2 |
0 |
0 |
1 |
4 |
2 |
4 |
2 |
2 |
4 |
3 |
3 |
27 |
| Dynamics of Finnish starlings in 1951-2005 : from monitoring to population modelling | 2 |
1 |
2 |
1 |
3 |
0 |
3 |
1 |
0 |
3 |
1 |
4 |
21 |
| Dynamics of nuclear actin | 4 |
0 |
3 |
2 |
0 |
1 |
2 |
2 |
0 |
4 |
1 |
3 |
22 |
| Dynamics of soil carbon and nitrogen in changing boreal environments | 0 |
11 |
0 |
2 |
1 |
3 |
2 |
4 |
0 |
2 |
2 |
2 |
29 |
| Early neuropathological changes in the mouse model for progressive myoclonus epilepsy of Unverricht-Lundborg type, EPM1 | 45 |
5 |
10 |
6 |
6 |
4 |
10 |
4 |
9 |
8 |
13 |
8 |
128 |
| Eco-experiential quality of urban forests : Combining ecological, restorative and aesthetic perspectives | 3 |
4 |
5 |
3 |
0 |
6 |
5 |
2 |
11 |
5 |
1 |
3 |
48 |
| Ecological and evolutionary role of seed banks for toxic dinoflagellate Alexandrium ostenfeldii | 6 |
6 |
1 |
4 |
2 |
1 |
2 |
1 |
3 |
0 |
4 |
0 |
30 |
| Ecological consequences of genetic modifications : an invasion analysis approach | 1 |
1 |
2 |
1 |
2 |
0 |
4 |
0 |
1 |
2 |
3 |
2 |
19 |
| Ecological factors shaping immune response and related life-history traits in the Glanville fritillary butterfly | 1 |
4 |
2 |
1 |
4 |
5 |
5 |
2 |
1 |
1 |
3 |
1 |
30 |
| Ecological fitness and interspecies interactions of food-spoilage-associated lactic acid bacteria : insights from the genome analyses and transcriptome profiles | 3 |
4 |
4 |
4 |
5 |
0 |
2 |
5 |
4 |
3 |
0 |
0 |
34 |
| Ecological impacts of Phlebiopsis gigantea biocontrol treatment against Heterobasidion spp. as revealed by fungal community profiling and population analyses | 1 |
1 |
2 |
1 |
3 |
1 |
1 |
1 |
1 |
1 |
0 |
0 |
13 |
| ecological rationale and conservation relevance | 2 |
0 |
2 |
0 |
1 |
2 |
1 |
0 |
0 |
2 |
2 |
0 |
12 |
| Ecological communities in variable environments : dynamics and diversity under coloured environmental stochasticity | 1 |
0 |
3 |
1 |
1 |
1 |
4 |
0 |
6 |
2 |
5 |
0 |
24 |
| Ecology of asexual reproduction in hepatics | 0 |
3 |
6 |
1 |
0 |
3 |
2 |
0 |
1 |
1 |
1 |
0 |
18 |
| Ecology of sympatric whitefish (Coregonus lavaretus (L.)) forms in a subarctic lake | 2 |
2 |
2 |
4 |
3 |
8 |
5 |
5 |
7 |
3 |
1 |
2 |
44 |
| Ecology of zooplankton in subarctic ponds, with a focus on responses to ultraviolet radiation | 2 |
3 |
6 |
4 |
4 |
5 |
4 |
3 |
1 |
0 |
3 |
1 |
36 |
| Ecology, population genetics and conservation of the African violet | 6 |
3 |
7 |
7 |
10 |
4 |
10 |
13 |
11 |
31 |
17 |
15 |
134 |
| Ectodermal organ development : Regulation by Notch and Eda pathways | 2 |
1 |
5 |
1 |
4 |
5 |
8 |
7 |
6 |
4 |
6 |
5 |
54 |
| Ectodysplasin in epithelial morphogenesis : from Tabby to TNFs | 0 |
2 |
6 |
2 |
1 |
0 |
3 |
3 |
1 |
2 |
7 |
0 |
27 |
| Effect of Light On Water Balance Through Gas Exchange | 8 |
2 |
1 |
0 |
0 |
2 |
4 |
3 |
6 |
3 |
3 |
2 |
34 |
| Effect of long-wave UV radiation on mouse melanoma : an in vitro and in vivo study | 0 |
0 |
4 |
2 |
1 |
1 |
1 |
2 |
2 |
3 |
1 |
2 |
19 |
| Effects of 17α-ethinyl estradiol on the mating system of the sand goby (Pomatoschistus minutus) | 2 |
1 |
2 |
0 |
2 |
0 |
0 |
1 |
1 |
3 |
4 |
0 |
16 |
| Effects of black carbon and Icelandic dust on snow albedo, melt and density | 5 |
2 |
4 |
2 |
2 |
2 |
5 |
0 |
4 |
4 |
1 |
10 |
41 |
| 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 | 1 |
6 |
1 |
6 |
9 |
9 |
7 |
6 |
6 |
11 |
6 |
4 |
72 |
| Effects of cyanobacteria on plankton and planktivores | 2 |
4 |
5 |
2 |
3 |
3 |
1 |
2 |
1 |
3 |
1 |
1 |
28 |
| Effects of ecological factors on dominance and immune defence in crayfish | 3 |
3 |
2 |
3 |
2 |
3 |
0 |
24 |
1 |
1 |
3 |
3 |
48 |
| Effects of embryological parameters on the success of fresh and frozen embryo transfers | 0 |
0 |
3 |
5 |
1 |
0 |
2 |
3 |
2 |
3 |
1 |
0 |
20 |
| Effects of environmental factors, especially temperature, on the population dynamics of pikeperch (Stizostedion lucioperca (L.)) | 5 |
6 |
3 |
2 |
3 |
1 |
2 |
1 |
0 |
2 |
0 |
0 |
25 |
| Effects of environmental variation on ecological and evolutionary dynamics | 2 |
4 |
3 |
4 |
6 |
2 |
4 |
2 |
1 |
1 |
3 |
2 |
34 |
| Effects of landscape connectivity and predator-prey interactions on diving beetle assemblages in Finnish urban ponds | 3 |
2 |
3 |
2 |
4 |
12 |
8 |
7 |
3 |
9 |
4 |
1 |
58 |
| Effects of large-scale human land use on Capercaillie (Tetrao urogallus L.) populations in Finland | 8 |
4 |
7 |
1 |
5 |
6 |
5 |
5 |
1 |
15 |
7 |
7 |
71 |
| Effects of management and landscape structure on biodiversity in boreal agricultural farmland | 1 |
2 |
2 |
3 |
1 |
2 |
1 |
2 |
1 |
2 |
5 |
4 |
26 |
| Effects of microclimatic variation of snowmelt and temperature on subarcticalpine and Arctic plants | 5 |
1 |
3 |
1 |
2 |
2 |
5 |
3 |
3 |
5 |
4 |
4 |
38 |
| Effects of oxygen provision on the physiology of baker's yeast Saccharomyces cerevisiae | 0 |
1 |
7 |
5 |
2 |
1 |
5 |
5 |
10 |
19 |
4 |
6 |
65 |
| Effects of Proatherogenic and Probiotic Bacteria on Mast Cells and Inflammation | 8 |
6 |
3 |
4 |
0 |
1 |
1 |
1 |
2 |
6 |
1 |
2 |
35 |
| Effects of recreational use and fragmentation on the understorey vegetation and soil microbial communities of urban forests in southern Finland | 1 |
2 |
1 |
1 |
2 |
2 |
0 |
5 |
0 |
4 |
1 |
2 |
21 |
| Effects of tree cover on local air pollutant levels in near-road environments | 6 |
7 |
4 |
7 |
4 |
7 |
3 |
3 |
2 |
8 |
5 |
5 |
61 |
| Effects of turbidity on feeding and distribution of fish | 5 |
8 |
7 |
6 |
5 |
9 |
5 |
8 |
4 |
10 |
14 |
6 |
87 |
| Effects of urbanization on seasonal runoff generation and pollutant transport under cold climate | 4 |
5 |
6 |
8 |
3 |
5 |
4 |
10 |
6 |
8 |
6 |
3 |
68 |
| Efficient gene set analysis of high-throughput data : From omics to pathway architecture of health and disease | 4 |
3 |
6 |
3 |
5 |
3 |
6 |
3 |
10 |
2 |
7 |
3 |
55 |
| Electrogenic reactions in the heme-copper oxidase family of enzymes | 2 |
3 |
3 |
0 |
2 |
0 |
1 |
5 |
1 |
2 |
0 |
0 |
19 |
| Electron and proton transfer in NADH:ubiquinone oxidoreductase (Complex I) from Escherichia coli | 2 |
3 |
1 |
1 |
1 |
2 |
0 |
0 |
4 |
2 |
0 |
0 |
16 |
| Electron cryo-microscopy studies of bacteriophage phi8 and archaeal virus SH1 | 7 |
2 |
7 |
1 |
6 |
4 |
2 |
2 |
11 |
5 |
1 |
2 |
50 |
| Elucidating nebulin expression and function in health and disease | 5 |
3 |
7 |
3 |
3 |
2 |
6 |
4 |
9 |
4 |
4 |
6 |
56 |
| Embracing uncertainty in fisheries stock assessment using Bayesian hierarchical models | 0 |
0 |
3 |
1 |
0 |
0 |
0 |
2 |
2 |
3 |
1 |
0 |
12 |
| Enantioselective antibody fragments | 2 |
0 |
0 |
1 |
1 |
1 |
2 |
0 |
3 |
1 |
2 |
0 |
13 |
| Engineering the pentose phosphate pathway of Saccharomyces cerevisiae for production of ethanol and xylitol | 1 |
1 |
7 |
0 |
6 |
2 |
7 |
12 |
3 |
7 |
4 |
5 |
55 |
| Enriching Carnivore Conservation. An interdisciplinary approach to better understand human-carnivore interactions | 0 |
0 |
17 |
41 |
42 |
11 |
4 |
14 |
9 |
2 |
10 |
24 |
174 |
| Entry of the membrane-containing bacteriophages into their hosts | 18 |
5 |
5 |
1 |
2 |
3 |
1 |
1 |
4 |
1 |
2 |
0 |
43 |
| Environmental and climatic dependences of stable isotope ratios in tree rings on different temporal scales | 1 |
4 |
1 |
0 |
6 |
3 |
2 |
3 |
4 |
52 |
34 |
2 |
112 |
| Environmental effects of thermal and radioactive discharges from nuclear power plants in the boreal brackish-water conditions of the northern Baltic Sea | 2 |
2 |
3 |
2 |
3 |
2 |
1 |
5 |
7 |
9 |
6 |
0 |
42 |
| Environmental factors and uncertainty in fisheries management in the northern Baltic Sea | 0 |
2 |
0 |
0 |
5 |
1 |
1 |
3 |
1 |
5 |
1 |
0 |
19 |
| Enzymatic synthesis of branched polylactosamines | 1 |
1 |
0 |
2 |
2 |
2 |
3 |
3 |
3 |
4 |
2 |
1 |
24 |
| Enzymatic Synthesis of Known and Novel Oligosaccharides | 4 |
5 |
2 |
0 |
0 |
1 |
0 |
1 |
0 |
3 |
1 |
0 |
17 |
| Enzymes with radical tendencies : the PFL family | 2 |
3 |
4 |
2 |
4 |
4 |
2 |
0 |
1 |
1 |
2 |
5 |
30 |
| Epidemiology of human rhinoviruses | 13 |
51 |
1 |
2 |
4 |
6 |
75 |
26 |
6 |
6 |
4 |
1 |
195 |
| Estimating complexity and adaptation in the embryo : a statistical developmental biology approach | 3 |
0 |
6 |
2 |
2 |
1 |
1 |
1 |
4 |
13 |
10 |
7 |
50 |
| European aspen and hybrid aspen under changing environment : Leaf traits, growth and litter decomposition | 25 |
4 |
2 |
0 |
2 |
0 |
3 |
2 |
1 |
3 |
2 |
0 |
44 |
| Eutrophication interferes with sand goby mating success, sexual selection, and parental care | 3 |
1 |
1 |
2 |
1 |
1 |
3 |
6 |
1 |
2 |
3 |
2 |
26 |
| Evaluating innate and learned determinants for improving antipredator behaviour of stocked fish | 2 |
3 |
9 |
1 |
0 |
1 |
1 |
1 |
0 |
1 |
0 |
0 |
19 |
| Evaluation and management of the Finnish herring fishery | 1 |
3 |
0 |
1 |
4 |
3 |
3 |
3 |
1 |
1 |
3 |
3 |
26 |
| Evaluation of in situ remediation methods in soils contaminated with organic pollutants | 2 |
1 |
9 |
4 |
4 |
3 |
3 |
5 |
11 |
7 |
10 |
11 |
70 |
| Evaluation of methods and applications for behavioural profiling of transgenic mice | 1 |
2 |
5 |
0 |
3 |
1 |
1 |
2 |
0 |
2 |
7 |
2 |
26 |
| Evolution of life-histories in stochastic environments : Cole's paradox revisited | 1 |
0 |
3 |
3 |
2 |
8 |
5 |
0 |
1 |
2 |
2 |
8 |
35 |
| Evolution of the DUF26-containing proteins in plants | 6 |
6 |
7 |
5 |
5 |
3 |
2 |
1 |
7 |
7 |
5 |
3 |
57 |
| Evolutionary and conservation biology of the Finnish house sparrow | 5 |
5 |
1 |
1 |
2 |
3 |
3 |
5 |
1 |
2 |
5 |
3 |
36 |
| Evolutionary and ecological dimensions of disease resistance | 2 |
2 |
3 |
1 |
5 |
1 |
3 |
3 |
3 |
7 |
11 |
4 |
45 |
| Evolutionary Genetics in the Wild : from Populations to Individuals | 1 |
3 |
1 |
7 |
4 |
2 |
7 |
3 |
1 |
1 |
2 |
1 |
33 |
| Evolutionary Genomics of Prokaryotic Viruses | 1 |
6 |
3 |
1 |
5 |
2 |
1 |
2 |
1 |
1 |
4 |
2 |
29 |
| Evolutionary relationships of liverworts with a special focus on the order Porellales and the family Lejeuneaceae | 1 |
5 |
5 |
2 |
11 |
7 |
3 |
2 |
5 |
4 |
2 |
4 |
51 |
| Exercise and Falls among Frail Older People : Special Focus on People with Dementia | 0 |
2 |
13 |
5 |
5 |
1 |
3 |
6 |
8 |
4 |
1 |
2 |
50 |
| Exploring the composition, variation and interactions of unicellular organisms in the marine benthic community with DNA metabarcoding | 1 |
4 |
7 |
4 |
7 |
4 |
2 |
7 |
5 |
6 |
4 |
1 |
52 |
| Exploring the role of CDNF and MANF removal in the brain and in the unfolded protein response | 5 |
8 |
4 |
2 |
4 |
3 |
0 |
1 |
0 |
4 |
2 |
5 |
38 |
| Exploring the unknown in a well-known system : Ecology and ecosystem effects of the invasive polychaete genus Marenzelleria spp. in the northern Baltic Sea | 2 |
2 |
7 |
0 |
5 |
3 |
4 |
2 |
2 |
3 |
7 |
2 |
39 |
| Exposure-related human cancer : Molecular changes in sinonasal cancer and lung cancer, with focus on TP53 mutations | 1 |
2 |
2 |
2 |
1 |
1 |
1 |
3 |
3 |
5 |
1 |
1 |
23 |
| Expression and activation of STAT and IRF family transcription factors in mononuclear leukocytes | 0 |
2 |
4 |
0 |
1 |
3 |
2 |
0 |
0 |
3 |
1 |
1 |
17 |
| Expression and characterization of neuronal membrane receptor proteins | 1 |
1 |
3 |
3 |
5 |
1 |
2 |
2 |
3 |
2 |
5 |
0 |
28 |
| Expression and functions of KCC2 in the perinatal rodent cortex | 3 |
2 |
3 |
0 |
4 |
2 |
3 |
2 |
2 |
7 |
4 |
2 |
34 |
| Expression and regulation of human activins and their receptors | 3 |
1 |
3 |
1 |
2 |
4 |
3 |
2 |
1 |
2 |
8 |
3 |
33 |
| Expression of bacterial adhesins in E.coli : From mapping of adhesive epitopes to structure | 1 |
3 |
2 |
0 |
0 |
2 |
2 |
1 |
6 |
2 |
2 |
2 |
23 |
| Expression, Enzymatic Activities and Subcellular Localization of Hepatitis E Virus and Semliki Forest Virus Replicase Proteins | 3 |
0 |
0 |
1 |
1 |
2 |
11 |
5 |
2 |
2 |
2 |
1 |
30 |
| Extracellular ATP as a Regulator of Intracellular Signaling in Thyroid FRTL-5 Cells | 1 |
2 |
1 |
3 |
1 |
1 |
3 |
1 |
0 |
2 |
0 |
1 |
16 |
| Extracellular lipid particles in atherosclerosis and aortic stenosis | 1 |
10 |
8 |
0 |
2 |
3 |
4 |
7 |
7 |
4 |
3 |
4 |
53 |
| Extracellular Vesicles and Nanoerythrosomes : The Hidden Pearls of Blood Products | 10 |
3 |
5 |
3 |
2 |
5 |
7 |
7 |
15 |
7 |
1 |
4 |
69 |
| Extracellular vesicles in innate immunity : Proteomic investigations | 2 |
4 |
3 |
4 |
3 |
1 |
3 |
1 |
0 |
3 |
1 |
2 |
27 |
| F-actin dynamics in dendritic spines | 0 |
2 |
2 |
1 |
4 |
1 |
2 |
1 |
1 |
1 |
2 |
2 |
19 |
| Factors affecting lipid profiles in juvenile Atlantic salmon | 12 |
29 |
18 |
6 |
1 |
5 |
2 |
7 |
8 |
24 |
20 |
8 |
140 |
| 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 | 1 |
1 |
2 |
3 |
1 |
6 |
10 |
7 |
4 |
6 |
4 |
2 |
47 |
| Factors controlling carbon gas fluxes in boreal lakes | 7 |
77 |
7 |
4 |
9 |
10 |
6 |
6 |
3 |
4 |
4 |
3 |
140 |
| Factors Regulating the Substrate Specificity of A-type Phospholipases : A Mass-Spectrometric study | 4 |
1 |
5 |
3 |
2 |
8 |
3 |
1 |
3 |
9 |
7 |
5 |
51 |
| Farmland birds and habitat heterogeneity in intensively cultivated boreal agricultural landscapes | 6 |
4 |
1 |
1 |
1 |
5 |
4 |
4 |
3 |
5 |
6 |
2 |
42 |
| Fast- and drift-ice communities in the Bothnian Bay and the impact of UVA radiation on the Baltic Sea ice ecology | 8 |
0 |
5 |
1 |
2 |
2 |
5 |
4 |
2 |
8 |
5 |
3 |
45 |
| Fate and Biological Effects of Titanium Dioxide Nanoparticles in the Aquatic Environment | 1 |
4 |
1 |
0 |
1 |
3 |
1 |
3 |
3 |
6 |
2 |
4 |
29 |
| Fate and effects of Nodularia spumigena and its toxin, nodularin, in Baltic Sea planktonic food webs | 2 |
2 |
1 |
2 |
1 |
4 |
1 |
1 |
0 |
3 |
2 |
2 |
21 |
| Fate of artificial sweeteners and perfluoroalkyl acids in aquatic environment | 6 |
8 |
5 |
8 |
12 |
9 |
5 |
3 |
7 |
9 |
5 |
12 |
89 |
| Fate of Mammalian Golgi Sialyltransferases in Yeast | 1 |
2 |
3 |
0 |
0 |
2 |
6 |
1 |
2 |
4 |
4 |
1 |
26 |
| Feeding constraints and parental care in female eiders | 1 |
2 |
3 |
1 |
2 |
1 |
2 |
2 |
3 |
0 |
2 |
1 |
20 |
| FGF signaling in neurogenesis and patterning of the developing midbrain and anterior hindbrain | 3 |
3 |
3 |
4 |
8 |
3 |
6 |
1 |
2 |
3 |
2 |
1 |
39 |
| FGFR1 regulated gene-expression, cell proliferation and differentiation in the developing midbrain and hindbrain | 6 |
7 |
4 |
3 |
3 |
7 |
2 |
1 |
0 |
11 |
9 |
4 |
57 |
| Fibroblast growth factor receptor 1 in craniofacial and midbrain-hindbrain development | 1 |
2 |
0 |
1 |
7 |
1 |
4 |
0 |
4 |
3 |
3 |
2 |
28 |
| Fibroblast growth factor receptor 1 signaling in the early development of the midbrain-hindbrain and pharyngeal region | 2 |
4 |
1 |
2 |
0 |
1 |
2 |
0 |
0 |
6 |
2 |
3 |
23 |
| Fibroblast Growth Factor Signalling in the Development of the Midbrain and Anterior Hindbrain | 7 |
4 |
7 |
5 |
1 |
0 |
6 |
6 |
3 |
5 |
1 |
4 |
49 |
| Fine morphological alterations during brain injury and recovery analyzed with intravital microscopy | 5 |
1 |
5 |
2 |
1 |
3 |
2 |
0 |
2 |
3 |
3 |
1 |
28 |
| Fine-tuning of the signalling network controlling morphogenesis and stem cell development in teeth | 3 |
5 |
2 |
3 |
0 |
3 |
3 |
6 |
2 |
6 |
2 |
6 |
41 |
| Fine-tuning stress and tension in cells | 0 |
84 |
32 |
11 |
6 |
7 |
11 |
28 |
11 |
1 |
6 |
4 |
201 |
| Fire histories and tree ages in unmanaged boreal forests in Eastern Fennoscandia and Onega peninsula | 3 |
3 |
2 |
2 |
0 |
1 |
4 |
0 |
1 |
7 |
2 |
1 |
26 |
| Fish communities in South-Finnish lakes and their responses to biomanipulation assessed by experimental gillnetting | 0 |
2 |
2 |
0 |
4 |
1 |
83 |
19 |
8 |
1 |
2 |
3 |
125 |
| Fish out of place : Evaluating the impacts of fish introductions on freshwater ecosystems | 0 |
1 |
1 |
0 |
2 |
2 |
2 |
1 |
4 |
2 |
2 |
1 |
18 |
| Fisheries sustainability in the presence of predation by marine megafauna | 2 |
2 |
4 |
3 |
0 |
1 |
0 |
3 |
1 |
1 |
1 |
1 |
19 |
| Fishes of the Darkness : Water colour-regulated competitive interactions in humic lakes | 3 |
1 |
2 |
1 |
1 |
2 |
2 |
6 |
3 |
3 |
1 |
1 |
26 |
| Flagship species as fundraising tools : their role in biodiversity conservation and in environmental philanthropic behavior | 13 |
2 |
4 |
32 |
20 |
2 |
1 |
3 |
3 |
2 |
3 |
1 |
86 |
| Flight metabolic rate and dispersal in the Glanville fritillary butterfly : from genes to populations | 0 |
0 |
5 |
0 |
4 |
2 |
0 |
1 |
0 |
2 |
0 |
2 |
16 |
| Flight metabolic rate in the Glanville fritillary butterfly | 1 |
3 |
1 |
2 |
2 |
4 |
2 |
3 |
3 |
3 |
1 |
0 |
25 |
| Flower Development in Gerbera hybrida, Asteraceae | 1 |
5 |
0 |
6 |
6 |
14 |
4 |
4 |
4 |
3 |
7 |
6 |
60 |
| Fluorescence properties of Baltic Sea phytoplankton | 2 |
3 |
2 |
1 |
3 |
1 |
11 |
2 |
4 |
2 |
5 |
42 |
78 |
| Flying jewels : Taxonomy and distribution of Northern European cuckoo wasps (Hymenoptera : Chrysididae) | 16 |
11 |
0 |
1 |
2 |
8 |
5 |
2 |
6 |
7 |
5 |
11 |
74 |
| Folding and Selective Exit of Reporter Proteins from the Yeast Endoplasmic Reticulum | 4 |
4 |
4 |
5 |
4 |
2 |
5 |
2 |
1 |
3 |
6 |
1 |
41 |
| Food intake, growth and social interactions of signal crayfish, Pacifastacus leniusculus (Dana) | 6 |
1 |
8 |
3 |
5 |
2 |
6 |
6 |
6 |
8 |
10 |
7 |
68 |
| Food selection and feeding behaviour of Baltic Sea mysid shrimps | 3 |
8 |
8 |
9 |
28 |
8 |
6 |
6 |
2 |
0 |
5 |
4 |
87 |
| Forest structure and biodiversity in northern boreal forests : Effects of regeneration cutting on flying beetles and wood-decomposing fungi | 2 |
2 |
3 |
3 |
7 |
5 |
3 |
2 |
0 |
6 |
2 |
3 |
38 |
| From actin monomers to bundles : The roles of twinfilin and α-actinin in Drosophila melanogaster development | 4 |
2 |
2 |
1 |
2 |
1 |
3 |
3 |
3 |
5 |
0 |
1 |
27 |
| from biogeochemical processes during ice formation to bio-optical modelling | 0 |
1 |
2 |
4 |
1 |
3 |
2 |
2 |
0 |
0 |
2 |
0 |
17 |
| From individuals to populations : the distribution of Eurasian lynx individuals in space and time and consequences for the local population structure and dynamics | 4 |
4 |
4 |
6 |
5 |
9 |
7 |
14 |
6 |
1 |
7 |
4 |
71 |
| From locomotor behavior to cerebellum evolution and development in squamate models | 5 |
4 |
9 |
4 |
9 |
12 |
4 |
5 |
12 |
3 |
4 |
4 |
75 |
| From neural stem cells to precursors : Molecular regulation of self-renewal and differentiation | 2 |
1 |
1 |
37 |
95 |
0 |
5 |
5 |
1 |
5 |
1 |
7 |
160 |
| From the river to the open sea : a critical life phase of young Atlantic salmon migrating from the Simojoki river | 0 |
2 |
1 |
2 |
2 |
3 |
1 |
1 |
0 |
0 |
0 |
0 |
12 |
| From topics of interest to a professional field of sustainablers : Sustainability education for change-making | 6 |
14 |
14 |
13 |
8 |
8 |
6 |
8 |
3 |
12 |
17 |
1 |
110 |
| Function of the Metazoan Mediator Kinase Module in Transcription | 0 |
3 |
1 |
3 |
2 |
1 |
2 |
3 |
2 |
4 |
3 |
4 |
28 |
| Functional analysis of Cdk7-interacting proteins Mat1 and Hint in model organisms | 2 |
1 |
4 |
0 |
1 |
1 |
2 |
1 |
2 |
1 |
1 |
1 |
17 |
| Functional and cellular analysis of autoimmune regulator (AIRE) protein | 1 |
2 |
3 |
4 |
1 |
2 |
3 |
1 |
2 |
4 |
1 |
2 |
26 |
| Functional and structural analysis of RET receptor tyrosine kinase and its complexes | 2 |
8 |
2 |
4 |
8 |
1 |
3 |
4 |
3 |
12 |
12 |
2 |
61 |
| Functional and Structural Studies on Heptahelical Membrane Proteins | 2 |
0 |
1 |
5 |
2 |
2 |
2 |
3 |
4 |
3 |
2 |
1 |
27 |
| Functional characterisation of Rab22a and Munc18b, two proteins regulating vesicle transport in mammalian cells | 0 |
1 |
2 |
1 |
1 |
0 |
0 |
0 |
2 |
3 |
3 |
2 |
15 |
| Functional characterization of MutL homologue mismatch repair proteins and their variants | 24 |
8 |
5 |
2 |
5 |
27 |
27 |
5 |
3 |
1 |
5 |
4 |
116 |
| Functional Characterization of MutS Homologue Mismatch Repair Proteins and their Variants | 11 |
2 |
6 |
5 |
6 |
4 |
8 |
3 |
9 |
7 |
3 |
5 |
69 |
| Functional dissection of alternative secretory pathways in the yeast S. cerevisiae | 1 |
1 |
3 |
0 |
4 |
0 |
2 |
1 |
2 |
1 |
0 |
0 |
15 |
| Functional expression and subcellular localization of the Cl- cotransporters KCC2 and NKCC1 in rodent hippocampal and neocortical neurons | 5 |
0 |
4 |
2 |
1 |
1 |
1 |
3 |
2 |
2 |
2 |
1 |
24 |
| Functional Fertility Genomics in Sheep | 1 |
1 |
5 |
2 |
14 |
1 |
6 |
4 |
2 |
1 |
5 |
3 |
45 |
| Functional genes and gene array analysis as tools for monitoring hydrocarbon biodegradation | 2 |
3 |
2 |
2 |
3 |
4 |
2 |
4 |
1 |
3 |
3 |
6 |
35 |
| Functional genomics of the Glanville fritillary butterfly | 3 |
0 |
3 |
1 |
1 |
3 |
3 |
3 |
4 |
4 |
7 |
2 |
34 |
| Functional Mapping of Mu Transposition Machinery : MuA Protein Modification and Engineering for Hyperactivity | 4 |
6 |
3 |
2 |
7 |
9 |
4 |
8 |
13 |
14 |
8 |
3 |
81 |
| Functional Properties of Visual Pigments using A1 and A2 Chromophore : From Molecules to Ecology | 5 |
2 |
3 |
3 |
1 |
2 |
1 |
1 |
3 |
1 |
2 |
3 |
27 |
| Functional role of the Mso1p-Sec1p complex in membrane fusion regulation | 0 |
0 |
1 |
1 |
3 |
2 |
2 |
0 |
1 |
5 |
2 |
3 |
20 |
| Functional Sequence Annotation in an Error-prone Environment | 5 |
0 |
1 |
2 |
1 |
3 |
4 |
3 |
3 |
4 |
2 |
3 |
31 |
| Functional significance of minor MLH1 germline alterations found in colon cancer patients | 20 |
10 |
5 |
3 |
3 |
4 |
4 |
7 |
1 |
3 |
3 |
3 |
66 |
| Functional studies of purified transmembrane proteases, omptins, of Yersinia pestis and Salmonella enterica | 0 |
0 |
1 |
0 |
3 |
2 |
2 |
1 |
1 |
4 |
0 |
0 |
14 |
| Functional studies of the secretory pathway of filamentous fungi : The effect of unfolded protein response on protein production | 2 |
2 |
0 |
2 |
1 |
9 |
7 |
2 |
6 |
1 |
1 |
5 |
38 |
| Functional Studies on alpha2-Adrenergic Receptor Subtypes | 2 |
0 |
3 |
0 |
3 |
1 |
4 |
2 |
2 |
3 |
3 |
0 |
23 |
| Functions of Alphavirus Macrodomain-containing protein nsP3 | 2 |
5 |
4 |
2 |
1 |
2 |
6 |
4 |
1 |
1 |
3 |
2 |
33 |
| Functions of human papillomavirus E5 oncogene in epithelial cells and in the onset of cervical cancer | 1 |
1 |
2 |
1 |
3 |
0 |
2 |
0 |
3 |
1 |
4 |
0 |
18 |
| Fusion and atherogenic properties of enzymatically modified low density lipoprotein particles | 1 |
4 |
4 |
0 |
0 |
4 |
2 |
1 |
0 |
4 |
0 |
1 |
21 |
| GABAa Receptor Mediated Signalling in the Brain : Inhibition, Shunting and Excitation | 2 |
3 |
3 |
2 |
0 |
1 |
1 |
1 |
4 |
2 |
0 |
1 |
20 |
| GABAa Receptor-mediated Excitation in the Hippocampus of Adult and Newborn rats | 0 |
2 |
2 |
3 |
2 |
3 |
2 |
10 |
3 |
8 |
3 |
3 |
41 |
| GABAergic mechanisms of excitation and hypersynchrony in adult rat hippocampus | 1 |
10 |
4 |
16 |
7 |
5 |
3 |
8 |
1 |
3 |
8 |
8 |
74 |
| GABAergic Signaling and Neuronal Chloride Regulation in the Control of Network Events in the Immature Hippocampus | 2 |
3 |
2 |
4 |
3 |
3 |
3 |
0 |
3 |
1 |
2 |
2 |
28 |
| GATA transcription factors and their co-regulators guide the development of GABAergic and serotonergic neurons in the anterior brainstem | 5 |
9 |
8 |
11 |
12 |
12 |
6 |
8 |
14 |
9 |
16 |
6 |
116 |
| GDNF family receptors in peripheral target innervation and hormone production | 3 |
7 |
2 |
1 |
0 |
6 |
4 |
0 |
1 |
3 |
2 |
4 |
33 |
| GDNF Receptors : Veterans and Novices | 1 |
2 |
1 |
3 |
2 |
2 |
6 |
3 |
0 |
0 |
2 |
2 |
24 |
| GDP-L-fucose : synthesis and role in inflammation | 4 |
4 |
4 |
5 |
4 |
2 |
5 |
4 |
2 |
3 |
0 |
2 |
39 |
| Gelatinase-mediated Migration and Invasion of Cancer Cells | 2 |
2 |
3 |
1 |
16 |
3 |
3 |
11 |
4 |
6 |
2 |
0 |
53 |
| Gene Expression : From Microarrays to Functional Genomics | 2 |
3 |
4 |
5 |
2 |
3 |
2 |
1 |
2 |
1 |
1 |
0 |
26 |
| Generation and Characterization of the Cation-Chloride Cotransporter KCC2 Hypomorphic Mouse | 0 |
2 |
2 |
3 |
2 |
2 |
3 |
5 |
2 |
3 |
2 |
3 |
29 |
| Generation of Flat and Curved Membranes by Inverse-BAR Domain Proteins | 2 |
4 |
3 |
1 |
2 |
2 |
0 |
4 |
4 |
4 |
2 |
3 |
31 |
| Genetic and behavioural divergence of queen size morphs in the red ant Myrmica ruginodis | 4 |
3 |
4 |
2 |
8 |
2 |
1 |
2 |
1 |
3 |
5 |
4 |
39 |
| Genetic and environmental Influences on Atlantic Salmon Life History : vgll3 and the Physiology of Maturation | 10 |
17 |
13 |
5 |
5 |
1 |
7 |
33 |
10 |
20 |
10 |
1 |
132 |
| Genetic aspects of outcome in kidney transplantation : cytokine and thrombosis associated candidate genes and gene expression biomarkers | 4 |
2 |
2 |
4 |
2 |
5 |
4 |
5 |
2 |
11 |
13 |
5 |
59 |
| Genetic background of late-onset spinal motor neuronopathy | 2 |
2 |
4 |
2 |
2 |
3 |
2 |
5 |
5 |
4 |
3 |
2 |
36 |
| Genetic diversity and phylogeography of landlocked seals | 2 |
3 |
3 |
2 |
0 |
1 |
6 |
39 |
4 |
4 |
1 |
1 |
66 |
| Genetic mapping of traits important in barley breeding | 3 |
3 |
2 |
6 |
2 |
2 |
6 |
2 |
5 |
3 |
4 |
0 |
38 |
| Genetic profiling of the interactions between soft rot Pectobacterium species and plants | 3 |
5 |
4 |
7 |
2 |
3 |
5 |
2 |
6 |
5 |
2 |
1 |
45 |
| Genetic studies of population history and contemporary microevolution in grayling (Thymallus: Salmonidae) | 3 |
4 |
3 |
0 |
5 |
1 |
4 |
0 |
4 |
0 |
1 |
2 |
27 |
| Genetic Studies of the Human Complement C4 Region in MHC Class III | 1 |
0 |
2 |
2 |
1 |
0 |
1 |
0 |
1 |
2 |
1 |
3 |
14 |
| Genetic susceptibility to asbestos and tobacco smoke related non-malignant pleuropulmonary changes | 3 |
2 |
2 |
1 |
1 |
5 |
1 |
3 |
3 |
4 |
2 |
2 |
29 |
| Genetic susceptibility to celiac disease : HLA-unlinked candidate genes | 3 |
3 |
1 |
2 |
4 |
6 |
2 |
6 |
2 |
2 |
6 |
3 |
40 |
| Genetic Variation : Effect on the Risk of Cancers of Lung and Oropharynx | 1 |
3 |
0 |
3 |
1 |
1 |
2 |
1 |
2 |
3 |
1 |
2 |
20 |
| Genetically modified Pseudomonas associated with plants : aspects for environmental risk assessment | 0 |
0 |
2 |
0 |
0 |
0 |
0 |
2 |
0 |
2 |
0 |
1 |
7 |
| Genetics and Epigenetics of Nicotine Dependence : Polymorphisms and methylation of CYP2D6, MAOA, MAOB, and SLC6A3 genes as modifiers of smoking phenotypes | 8 |
18 |
3 |
6 |
2 |
5 |
5 |
11 |
14 |
5 |
6 |
6 |
89 |
| Genetics and genomics of musical abilities | 7 |
1 |
3 |
8 |
6 |
10 |
14 |
8 |
7 |
3 |
5 |
9 |
81 |
| Genetics of Local Adaptation in theThree-spined Stickleback | 4 |
1 |
2 |
2 |
3 |
2 |
2 |
0 |
1 |
3 |
0 |
4 |
24 |
| Genetics of Primary Immunodeficiency in Finland | 4 |
0 |
4 |
2 |
6 |
4 |
4 |
1 |
4 |
3 |
2 |
5 |
39 |
| Genetics of T cell co-stimulatory receptors -CD28, CTLA4, ICOS and PDCD1 in immunity and transplantation | 26 |
54 |
8 |
7 |
7 |
5 |
7 |
7 |
2 |
4 |
4 |
6 |
137 |
| Genome editing and its use to study secondary growth in Arabidopsis thaliana | 5 |
5 |
7 |
7 |
6 |
7 |
6 |
7 |
3 |
3 |
6 |
4 |
66 |
| Genomic Evolution and Diversity in Artiodactyla | 3 |
0 |
4 |
1 |
3 |
1 |
3 |
4 |
2 |
3 |
66 |
6 |
96 |
| Genomic Profiling of Gastric Cancer | 1 |
2 |
2 |
1 |
0 |
2 |
1 |
4 |
3 |
1 |
1 |
2 |
20 |
| Genomics of bacterial and archaeal virus isolates from extreme aquatic environments | 0 |
2 |
1 |
1 |
2 |
0 |
4 |
0 |
3 |
2 |
0 |
0 |
15 |
| Geographic variation in killer whale colour patterns | 13 |
10 |
10 |
5 |
9 |
10 |
9 |
7 |
9 |
20 |
5 |
11 |
118 |
| Glutamatergic Modulation of Cue-Induced Drug-Seeking Behavior in the Rat | 2 |
5 |
2 |
3 |
4 |
2 |
3 |
0 |
0 |
5 |
2 |
3 |
31 |
| Glycan Binding Proteins in Therapeutic Mesenchymal Stem Cell Research | 2 |
0 |
3 |
2 |
2 |
1 |
2 |
2 |
0 |
2 |
4 |
1 |
21 |
| Glycobiological insights in characterization and targeting of umbilical cord blood derived stem cells | 2 |
5 |
9 |
5 |
2 |
2 |
7 |
2 |
2 |
2 |
2 |
4 |
44 |
| Glycosylation and Sorting of Secretory Proteins in the Endoplasmic Reticulum of the Yeast Saccharomyces cerevisiae | 2 |
3 |
3 |
1 |
0 |
2 |
1 |
0 |
0 |
1 |
0 |
0 |
13 |
| Golgi proteomics : Identification of a novel cartilage-specific Golgi protein GoPro49 | 6 |
1 |
2 |
5 |
1 |
2 |
4 |
8 |
0 |
1 |
2 |
5 |
37 |
| GPRA and the asthma locus on chromosome 7p14-p15 | 1 |
0 |
2 |
1 |
3 |
0 |
2 |
2 |
0 |
3 |
4 |
1 |
19 |
| Growth and recruitment of burbot (Lota lota) | 3 |
1 |
10 |
1 |
1 |
14 |
11 |
6 |
11 |
10 |
6 |
2 |
76 |
| Growth and resilience of non-vascular epiphytes in the Taita Hills, Kenya | 3 |
5 |
2 |
4 |
2 |
2 |
2 |
3 |
3 |
8 |
1 |
2 |
37 |
| Habitat use and population dynamics of brown bears (Ursus arctos) in Scandinavia | 3 |
4 |
4 |
2 |
1 |
0 |
1 |
2 |
1 |
6 |
6 |
5 |
35 |
| Harmful algae in the planktonic food web of the Baltic Sea | 6 |
8 |
4 |
1 |
6 |
4 |
6 |
8 |
4 |
3 |
3 |
8 |
61 |
| Helper component-proteinase and coat protein are involved in the molecular processes of potato virus A translation and replication | 7 |
8 |
3 |
1 |
8 |
6 |
8 |
10 |
6 |
2 |
0 |
4 |
63 |
| Heparin-binding growth-associated molecule (HB-GAM) in activity-dependent neuronal plasticity in hippocampus | 0 |
1 |
3 |
10 |
4 |
4 |
2 |
3 |
1 |
5 |
8 |
3 |
44 |
| Hepatic lipid metabolism in cardiometabolic diseases : protective and adverse effects of genetic variants | 3 |
4 |
15 |
1 |
2 |
4 |
7 |
1 |
3 |
3 |
2 |
2 |
47 |
| Heterobasidion annosum and wood decay : Enzymology of cellulose, hemicellulose, and lignin degradation | 5 |
7 |
6 |
5 |
8 |
12 |
7 |
3 |
7 |
9 |
24 |
6 |
99 |
| High molecular weight cysteine proteinase inhibitors in Atlantic salmon and other fish species | 0 |
5 |
0 |
0 |
1 |
0 |
0 |
1 |
0 |
2 |
0 |
1 |
10 |
| Histopathology-selective spatial oncogenic phenotypes in non-small cell lung cancer | 2 |
5 |
2 |
2 |
4 |
5 |
7 |
6 |
7 |
8 |
2 |
2 |
52 |
| HMGB1 (Amphoterin) and AMIGO1 in Brain Development | 7 |
16 |
2 |
6 |
62 |
11 |
13 |
14 |
4 |
7 |
14 |
5 |
161 |
| Holocene carbon dynamics and atmospheric radiative forcing of different types of peatlands in Finland | 2 |
3 |
3 |
2 |
1 |
3 |
2 |
3 |
2 |
3 |
4 |
0 |
28 |
| 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 | 2 |
10 |
4 |
1 |
4 |
1 |
3 |
7 |
3 |
5 |
5 |
3 |
48 |
| Hormonal regulation of radical-induced programmed cell death in ozone-sensitive mutants of Arabidopsis thaliana | 2 |
2 |
2 |
1 |
3 |
3 |
2 |
1 |
4 |
2 |
6 |
16 |
44 |
| Host-pathogen coevolution through trade-offs and coinfection | 0 |
2 |
4 |
4 |
1 |
1 |
2 |
3 |
3 |
4 |
5 |
3 |
32 |
| How to assemble contractile actomyosin bundles in cells? | 1 |
1 |
2 |
0 |
2 |
4 |
1 |
2 |
3 |
10 |
5 |
1 |
32 |
| Human genetic variation in the Baltic Sea region : Features of population history and natural selection | 5 |
3 |
2 |
4 |
9 |
11 |
21 |
13 |
11 |
3 |
3 |
3 |
88 |
| Human parvovirus B19 : tissue persistence and prevalence of prototypic and new variants | 4 |
2 |
0 |
1 |
6 |
1 |
3 |
2 |
1 |
1 |
3 |
1 |
25 |
| Human Pathogenic Mutations in Protein Domains | 3 |
3 |
0 |
1 |
0 |
4 |
2 |
0 |
2 |
1 |
1 |
2 |
19 |
| Human picornaviruses : uncoating, assembly and interaction with cellular receptors | 1 |
0 |
2 |
10 |
6 |
11 |
5 |
4 |
4 |
1 |
3 |
6 |
53 |
| Human Protein Phosphatase Interactions and Dynamics : Proteomic and Functional Perspective | 1 |
1 |
0 |
0 |
2 |
0 |
3 |
2 |
0 |
23 |
2 |
1 |
35 |
| Human Transcription Factor Protein-Protein Interactions in Health and Disease | 3 |
8 |
2 |
4 |
8 |
2 |
1 |
2 |
1 |
3 |
11 |
7 |
52 |
| Hydroacoustic fish stock assessment in southern and northern boreal lakes : potential and constraints | 2 |
3 |
5 |
1 |
1 |
2 |
5 |
2 |
1 |
14 |
2 |
4 |
42 |
| Hydrogen peroxide in inducible plant stress responses | 0 |
5 |
3 |
4 |
1 |
3 |
3 |
2 |
8 |
4 |
2 |
1 |
36 |
| Identification of a secretion signal for the type II protein secretion pathway in Erwinia carotovora | 1 |
1 |
2 |
1 |
0 |
1 |
2 |
4 |
1 |
1 |
0 |
1 |
15 |
| Identification of evolutionary conserved mechanisms promoting rapid actin dynamics | 7 |
6 |
2 |
0 |
5 |
10 |
4 |
1 |
3 |
4 |
2 |
0 |
44 |
| IDENTIFICATION OF MANF AND CDNF INTERACTING PROTEINS AND A STUDY OF THEIR MECHANISM OF ACTION | 0 |
55 |
23 |
9 |
7 |
2 |
8 |
9 |
4 |
0 |
2 |
2 |
121 |
| Identification of molecules relevant for the invasiveness of fibrosarcomas and melanomas | 0 |
0 |
5 |
1 |
1 |
5 |
2 |
1 |
2 |
1 |
2 |
1 |
21 |
| Identification of sugar responsive transcription factors in silico | 1 |
0 |
0 |
1 |
0 |
7 |
8 |
20 |
23 |
19 |
20 |
18 |
117 |
| Identification of the fungal catabolic D-galacturonate pathway | 35 |
27 |
2 |
0 |
1 |
2 |
6 |
1 |
2 |
1 |
3 |
0 |
80 |
| Imaging Cellular Mechanisms of Oral Ectodermal Development and Disease | 1 |
0 |
5 |
0 |
2 |
1 |
1 |
0 |
2 |
3 |
2 |
0 |
17 |
| Immune response to insulin and changes in the gut immune system in children with or at risk for type 1 diabetes | 3 |
2 |
3 |
5 |
2 |
1 |
4 |
3 |
1 |
4 |
0 |
1 |
29 |
| Immune Responses to Pathogen Infection in Arabidopsis | 7 |
4 |
6 |
2 |
7 |
3 |
4 |
1 |
2 |
3 |
3 |
1 |
43 |
| Immunomodulatory Effects of Engineered Nanomaterials in Healthy and Diseased Lungs and Skin | 3 |
1 |
4 |
0 |
6 |
4 |
2 |
0 |
1 |
6 |
4 |
5 |
36 |
| Impact of land use on breeding bird populations a case study of Vuosaari harbour construction | 2 |
2 |
3 |
0 |
0 |
1 |
2 |
3 |
1 |
1 |
2 |
12 |
29 |
| Impacts of agriculture on amphibians at multiple scales | 6 |
6 |
7 |
1 |
2 |
2 |
9 |
13 |
3 |
22 |
93 |
10 |
174 |
| Impacts of soil temperature on high-latitude terrestrial biodiversity and ecosystem functioning, and climate change implications | 8 |
8 |
2 |
1 |
6 |
3 |
4 |
9 |
2 |
4 |
6 |
3 |
56 |
| Impacts of summer drought on plant-herbivore interactions : the Glanville fritillary metapopulation as a case study | 1 |
0 |
3 |
1 |
6 |
5 |
7 |
3 |
1 |
4 |
3 |
1 |
35 |
| Impacts of water-level regulation on the littoral biota of lakes in Finland : the role of hydromorphological modification in status assessment | 1 |
2 |
1 |
1 |
0 |
0 |
2 |
3 |
1 |
2 |
1 |
0 |
14 |
| Implications of bacterial viruses on pathogenic bacteria : from natural microbial communities to therapeutic applications | 1 |
1 |
6 |
5 |
8 |
3 |
4 |
1 |
1 |
4 |
2 |
0 |
36 |
| Implications of BRCA1 mutations in basal-like breast cancer development and treatment | 2 |
3 |
3 |
4 |
2 |
2 |
4 |
4 |
2 |
4 |
2 |
2 |
34 |
| Improving CNV detection from short-read MPS data in neuromuscular disorders | 7 |
16 |
21 |
9 |
16 |
8 |
9 |
9 |
10 |
10 |
8 |
3 |
126 |
| Improving Precision in Therapies for Hematological Malignancies | 7 |
2 |
11 |
22 |
7 |
4 |
3 |
3 |
8 |
4 |
3 |
6 |
80 |
| In between two worlds? : Science-policy interaction in Finnish environmental governance | 4 |
10 |
5 |
3 |
4 |
1 |
1 |
3 |
3 |
4 |
5 |
11 |
54 |
| In Vitro Cell Expansion and CTLA4 in Advanced T-Cell Therapies | 1 |
2 |
1 |
4 |
3 |
2 |
1 |
2 |
1 |
14 |
5 |
1 |
37 |
| Inbreeding Depression in the Glanville Fritillary Butterfly (Melitaea cinxia) | 1 |
2 |
3 |
0 |
1 |
3 |
3 |
3 |
1 |
1 |
3 |
1 |
22 |
| Indigenous intestinal microbiota and disease : different approaches to characterize the composition and products of human microbiota | 7 |
1 |
0 |
1 |
1 |
2 |
2 |
0 |
1 |
2 |
0 |
0 |
17 |
| Individual stress-resistance in the ant Formica exsecta | 6 |
25 |
8 |
0 |
1 |
1 |
0 |
0 |
0 |
1 |
4 |
0 |
46 |
| Induction of immunity against experimental Chlamydia pneumoniae infection | 1 |
2 |
1 |
0 |
1 |
2 |
1 |
2 |
2 |
4 |
4 |
4 |
24 |
| Influence of processing on the flavour formation of oat and rye | 2 |
3 |
3 |
25 |
3 |
4 |
5 |
3 |
4 |
2 |
2 |
3 |
59 |
| Influence of resource distribution and abundance on the population structure and dynamics of Parnassius apollo | 9 |
4 |
4 |
3 |
8 |
2 |
16 |
2 |
4 |
2 |
1 |
2 |
57 |
| Influenza A virus-host interactions and their control by viral non-structural protein NS1 | 4 |
3 |
1 |
3 |
3 |
4 |
1 |
2 |
0 |
3 |
6 |
1 |
31 |
| Inherited DNA repair capacity and individual responses to carcinogens | 0 |
0 |
0 |
3 |
3 |
0 |
1 |
0 |
1 |
5 |
1 |
2 |
16 |
| Innate immunity and its control in the pathogenesis of inflammatory rheumatic diseases | 2 |
3 |
3 |
3 |
4 |
2 |
2 |
1 |
2 |
2 |
2 |
1 |
27 |
| Integrated Analysis of Aggression in Salmonids | 3 |
3 |
3 |
3 |
4 |
3 |
0 |
1 |
2 |
4 |
3 |
1 |
30 |
| Integration of Eda signaling with other signaling pathways in oral ectodermal organogenesis | 4 |
3 |
3 |
4 |
2 |
8 |
7 |
5 |
2 |
2 |
0 |
8 |
48 |
| Interaction between Hormone and Apoplastic ROS Signaling in Regulation of Defense Responses and Cell Death | 32 |
25 |
2 |
3 |
4 |
1 |
0 |
0 |
0 |
1 |
2 |
3 |
73 |
| Interaction of GluA1 AMPA receptor with Synapse-Associated Protein 97 | 2 |
2 |
3 |
0 |
0 |
2 |
2 |
2 |
1 |
2 |
2 |
3 |
21 |
| Interactions among neuronal oscillations in the developing and adult brain | 0 |
1 |
2 |
3 |
2 |
2 |
1 |
0 |
1 |
1 |
0 |
2 |
15 |
| Interactions and Exclusions : Studies on Causal Explanation in Naturalistic Philosophy of Mind | 3 |
2 |
5 |
6 |
5 |
9 |
8 |
3 |
7 |
7 |
4 |
7 |
66 |
| Interactions between harmful algae and calanoid copepods in the Baltic Sea | 10 |
3 |
2 |
2 |
5 |
1 |
1 |
1 |
3 |
6 |
0 |
1 |
35 |
| Interactions between metals, microbes and plants : Bioremediation of arsenic and lead contaminated soils | 4 |
7 |
7 |
5 |
11 |
7 |
9 |
4 |
6 |
9 |
4 |
0 |
73 |
| Interactions between Puumala hantavirus and its host, the bank vole, in the boreal zone | 4 |
2 |
2 |
1 |
0 |
3 |
3 |
0 |
0 |
7 |
1 |
0 |
23 |
| Interactions of nandrolone and psychostimulant drugs on central monoaminergic systems | 14 |
20 |
14 |
21 |
18 |
7 |
10 |
12 |
11 |
8 |
2 |
1 |
138 |
| Intergenerational trade-offs in periodic environments : a reaction norm perspective | 3 |
0 |
0 |
2 |
4 |
1 |
6 |
3 |
2 |
3 |
3 |
1 |
28 |
| Intermolecular protein splicing and its use in biotechnological applications | 2 |
4 |
7 |
3 |
3 |
1 |
2 |
3 |
4 |
2 |
1 |
4 |
36 |
| Interplay Between Cyclase-Associated Protein, Cofilin, Profilin and Twinfilin in Actin Dynamics | 2 |
4 |
4 |
1 |
1 |
1 |
5 |
4 |
1 |
2 |
2 |
4 |
31 |
| Interplay of ecology and evolution under changing environmental conditions : Evolution experiments with heterotrophic bacteria | 2 |
1 |
3 |
1 |
2 |
2 |
3 |
0 |
1 |
2 |
2 |
0 |
19 |
| Intraspecific variation in brain size and architecture : population divergence and phenotypic plasticity | 0 |
4 |
3 |
2 |
1 |
0 |
6 |
2 |
0 |
1 |
3 |
3 |
25 |
| Intraspecific variation in phenotypic plasticity | 2 |
2 |
5 |
2 |
2 |
2 |
2 |
3 |
0 |
2 |
1 |
0 |
23 |
| Intravitreal liposomes as ocular drug delivery systems : vitreal interactions, retinal permeation and drug release characteristics | 30 |
11 |
15 |
25 |
17 |
21 |
23 |
15 |
15 |
20 |
14 |
14 |
220 |
| Introducing Wilson disease mutations into ZntA : Studies on the nucleotide and metal-binding sites of a bacterial zinc-translocating P-type ATPase | 2 |
1 |
3 |
4 |
2 |
1 |
2 |
2 |
3 |
2 |
4 |
0 |
26 |
| Introduction of hydrophobic fluorescent lipid analogues into living cultured cells and their imaging therein | 2 |
2 |
1 |
2 |
0 |
0 |
1 |
1 |
0 |
3 |
0 |
0 |
12 |
| Invertebrate predation and trophic cascades in a pelagic food web : The multiple roles of Chaoborus flavicans (Meigen) in a clay-turbid lake | 2 |
3 |
3 |
1 |
0 |
2 |
2 |
0 |
3 |
3 |
0 |
0 |
19 |
| Investigating plant resistance and infection patterns in a wild plant : case study of Plantago lanceolata | 3 |
4 |
5 |
4 |
6 |
3 |
12 |
1 |
5 |
14 |
8 |
7 |
72 |
| Involvement of non-muscle α-actinins and NUAK2 kinase in regulating actin stress fibers | 3 |
2 |
4 |
2 |
4 |
3 |
1 |
1 |
3 |
2 |
2 |
0 |
27 |
| Ion-regulatory proreins in neuronal development and communication | 2 |
2 |
2 |
4 |
1 |
2 |
2 |
2 |
3 |
5 |
2 |
4 |
31 |
| Kainate receptor auxiliary subunits NETO1 and NETO2 in anxiety and fear-related behaviors | 5 |
9 |
5 |
10 |
4 |
4 |
10 |
12 |
3 |
4 |
6 |
6 |
78 |
| Kainate-type glutamate receptors modulating network activity in developing hippocampus | 3 |
6 |
4 |
0 |
6 |
2 |
8 |
3 |
1 |
5 |
1 |
1 |
40 |
| KCC2 as a multifunctional protein in brain development and disease | 1 |
4 |
7 |
1 |
10 |
4 |
2 |
6 |
2 |
3 |
1 |
1 |
42 |
| Kin selection, social polymorphism, and reproductive allocation in ants | 4 |
3 |
1 |
21 |
3 |
5 |
1 |
3 |
3 |
5 |
6 |
2 |
57 |
| Kinship and conflicts over male production in Formica ants | 3 |
0 |
3 |
4 |
2 |
8 |
4 |
4 |
6 |
3 |
3 |
3 |
43 |
| Knowledge-based marine conservation in oil spill risk management | 3 |
3 |
3 |
1 |
5 |
5 |
3 |
4 |
2 |
4 |
3 |
5 |
41 |
| Kokonaisvaltainen lähestymistapa ympäristönsuojelutieteessä : Sisällön moniulotteisuus ympäristönsuojelijan haasteena | 7 |
26 |
43 |
46 |
54 |
31 |
45 |
33 |
47 |
10 |
5 |
2 |
349 |
| Laboratory Diagnosis and Surveillance of Acute Respiratory Tract Infections Caused by Certain Common Viruses and Mycoplasma pneumoniae | 0 |
2 |
6 |
6 |
4 |
4 |
2 |
7 |
2 |
4 |
0 |
1 |
38 |
| Lacrimal Gland Morphogenesis, Maturation and Function | 4 |
5 |
2 |
4 |
5 |
0 |
4 |
8 |
3 |
6 |
3 |
2 |
46 |
| Lactobacillus crispatus and Propionibacterium freudenreichii : A Genomic and Transcriptomic View | 51 |
64 |
2 |
1 |
0 |
1 |
0 |
0 |
2 |
4 |
4 |
4 |
133 |
| Lake-atmosphere greenhouse gas exchange in relation to atmospheric forcing and lake biogeochemistry | 0 |
1 |
5 |
1 |
2 |
7 |
0 |
1 |
3 |
2 |
5 |
2 |
29 |
| Lapin ympäristökiistojen kulttuuriset tekijät | 3 |
5 |
10 |
27 |
17 |
10 |
11 |
15 |
10 |
9 |
1 |
1 |
119 |
| Large-scale automated acoustic monitoring of birds and the challenges of field data | 6 |
4 |
3 |
2 |
3 |
0 |
5 |
21 |
3 |
8 |
6 |
4 |
65 |
| Latent TGF-beta binding protein LTBP-2 : assembly to the extracellular matrix and effects on cell adhesion | 1 |
0 |
2 |
1 |
5 |
8 |
5 |
2 |
0 |
3 |
3 |
3 |
33 |
| Leaf senescence in silver birch (Betula pendula Roth) | 2 |
3 |
1 |
0 |
1 |
1 |
1 |
0 |
0 |
1 |
2 |
0 |
12 |
| Let there be pike! : Effects of fishing on the dynamics of pike (Esox lucius) populations | 2 |
2 |
3 |
4 |
5 |
5 |
6 |
8 |
3 |
5 |
2 |
1 |
46 |
| LFA-1 Integrin beta2 Chain Phosphorylation Regulates Protein Interactions and Mediates Signals in T Cells | 12 |
15 |
5 |
4 |
8 |
9 |
5 |
34 |
9 |
8 |
8 |
8 |
125 |
| Life in extreme environments : Physiological changes in host cells during the infection of halophilic archaeal viruses | 0 |
3 |
2 |
1 |
2 |
2 |
3 |
2 |
2 |
4 |
3 |
1 |
25 |
| Life on the Edge : Structural Studies of the Extremophilic Viruses P23-77 and STIV2 | 1 |
6 |
4 |
1 |
4 |
4 |
5 |
1 |
6 |
5 |
0 |
5 |
42 |
| Light after death : the importance of spectral composition in litter decomposition processes | 2 |
2 |
4 |
22 |
22 |
0 |
0 |
0 |
1 |
5 |
1 |
0 |
59 |
| Light quality affects leaf pigments and leaf phenology | 0 |
1 |
1 |
2 |
4 |
2 |
3 |
6 |
2 |
2 |
8 |
2 |
33 |
| Lignin biosynthesis in Norway spruce : from a model system to the tree | 4 |
9 |
4 |
3 |
3 |
5 |
4 |
0 |
2 |
4 |
2 |
6 |
46 |
| Linking spatial and evolutionary dynamics in a plant-pathogen metapopulation | 5 |
4 |
0 |
3 |
5 |
4 |
2 |
4 |
4 |
4 |
1 |
3 |
39 |
| Linking taxonomy and environmental 18S-rRNA-gene sequencing of Baltic Sea protists | 3 |
4 |
5 |
4 |
5 |
9 |
11 |
1 |
2 |
7 |
6 |
3 |
60 |
| Living on voles : plastic life of the Ural owl | 4 |
2 |
2 |
0 |
3 |
1 |
3 |
2 |
1 |
5 |
3 |
1 |
27 |
| Local systems, global impacts : Using life cycle assessment to analyse the potential and constraints of industrial symbioses | 8 |
4 |
1 |
1 |
1 |
1 |
5 |
3 |
3 |
15 |
4 |
3 |
49 |
| Long-term exposure to solar blue and UV radiation in legumes : pre-acclimation to drought and accession-dependent responses in two successive generations | 4 |
1 |
2 |
3 |
4 |
3 |
2 |
0 |
0 |
3 |
1 |
3 |
26 |
| Longitudinal monitoring of parasites in individual wild primates | 3 |
2 |
9 |
2 |
3 |
2 |
3 |
2 |
2 |
1 |
0 |
0 |
29 |
| Lost before found? : On systematics and conservation of lichen genus Micarea Fr. (Pilocarpaceae, Ascomycota) | 2 |
3 |
3 |
4 |
4 |
0 |
4 |
0 |
2 |
4 |
3 |
1 |
30 |
| Luonnonsuojelu arjessa : Maanomistajien näkemyksiä ja kokemuksia yksityismaiden tilapäisestä luonnonsuojelusta ja sen uudistumisen prosessista | 4 |
1 |
4 |
10 |
18 |
9 |
11 |
15 |
15 |
13 |
10 |
9 |
119 |
| Lymphatic vessels in health and disease : Role of the VEGF-C/VEGFR-3 pathway and the transcription factor FOXC2 | 2 |
2 |
4 |
2 |
3 |
1 |
1 |
1 |
0 |
4 |
2 |
2 |
24 |
| Macroalgal contribution to benthic macrofaunal communities and food webs in shallow coastal habitats of the Baltic Sea | 4 |
11 |
2 |
2 |
3 |
7 |
4 |
3 |
11 |
5 |
1 |
4 |
57 |
| Maintaining plant species richness by cattle grazing : mesic semi-natural grasslands as focal habitats | 2 |
7 |
9 |
21 |
3 |
6 |
19 |
8 |
20 |
12 |
6 |
8 |
121 |
| Maltose and maltotriose transport into ale and lager brewer's yeast strains | 1 |
12 |
5 |
8 |
5 |
3 |
7 |
6 |
7 |
2 |
5 |
16 |
77 |
| Management of coregonid fisheries : multiform and multispecies problems | 0 |
0 |
1 |
1 |
2 |
0 |
2 |
0 |
5 |
3 |
4 |
7 |
25 |
| Management of pikeperch (Sander lucioperca) in the coastal waters of the Baltic Sea | 4 |
8 |
2 |
2 |
1 |
1 |
9 |
0 |
0 |
3 |
4 |
5 |
39 |
| Management of semi-natural grasslands for butterfly and moth communities | 39 |
6 |
5 |
4 |
6 |
0 |
1 |
5 |
5 |
6 |
6 |
9 |
92 |
| Managing forest and meadow habitats for the enhancement of urban biodiversity : messages from carabid beetles and vascular plants | 4 |
5 |
6 |
0 |
0 |
0 |
3 |
2 |
7 |
4 |
7 |
1 |
39 |
| MANF as a new regulator of the unfolded protein response and maintenance of pancreatic β-cells in mice | 5 |
2 |
5 |
2 |
5 |
5 |
2 |
4 |
9 |
4 |
6 |
6 |
55 |
| Marine icosahedral membrane-containing dsDNA bacteriophage PM2 : virion structure and host cell penetration | 2 |
3 |
4 |
1 |
1 |
0 |
2 |
2 |
2 |
6 |
2 |
1 |
26 |
| Marking one-summer old whitefish with fluorescent pigment spraying method and results of whitefish stockings in the Gulf of Bothnia | 5 |
7 |
3 |
7 |
5 |
6 |
4 |
2 |
1 |
2 |
1 |
1 |
44 |
| Mass-spectrometric analysis of glycerophospholipid metabolism | 4 |
10 |
5 |
6 |
6 |
1 |
9 |
10 |
8 |
2 |
3 |
1 |
65 |
| Mathematical models of environmental opportunist pathogen dynamics | 0 |
2 |
3 |
1 |
4 |
3 |
2 |
2 |
1 |
2 |
1 |
1 |
22 |
| Meadow plant growth and competition under elevated ozone and carbon dioxide | 1 |
3 |
1 |
3 |
5 |
2 |
3 |
1 |
2 |
5 |
4 |
2 |
32 |
| Measuring and modelling airborne dispersal in wood decay fungi | 5 |
3 |
2 |
3 |
6 |
5 |
8 |
2 |
4 |
4 |
5 |
2 |
49 |
| Mechanism of fluctuations in year class survival of vendace (Coregonus albula (L.)) larvae : an individual size based approach | 2 |
1 |
3 |
2 |
3 |
2 |
9 |
3 |
1 |
0 |
2 |
2 |
30 |
| Mechanism of RNA Translocation by a Viral Packaging Motor | 0 |
0 |
2 |
3 |
1 |
5 |
1 |
2 |
1 |
6 |
4 |
3 |
28 |
| Mechanisms and molecular regulation of mammalian tooth replacement | 2 |
4 |
2 |
1 |
0 |
2 |
3 |
6 |
9 |
7 |
5 |
4 |
45 |
| Mechanisms of Birth Asphyxia and a Novel Resuscitation Strategy | 14 |
23 |
21 |
3 |
6 |
9 |
5 |
2 |
5 |
6 |
5 |
4 |
103 |
| Mechanisms of KCC2 upregulation during development | 1 |
2 |
2 |
0 |
1 |
3 |
2 |
2 |
1 |
3 |
2 |
0 |
19 |
| Mechanisms of Sexual Selection in the Sand Goby, Pomatoschistus minutus | 1 |
2 |
2 |
3 |
0 |
0 |
0 |
2 |
2 |
1 |
0 |
1 |
14 |
| Membrane Insertion of C-tail Anchored Proteins | 1 |
2 |
1 |
0 |
1 |
1 |
0 |
2 |
0 |
2 |
0 |
0 |
10 |
| Meta-omics approach to explore microbial community of the wood ant Formica exsecta | 1 |
1 |
4 |
1 |
1 |
1 |
4 |
1 |
0 |
5 |
2 |
5 |
26 |
| Metabolism of polyunsaturated fatty acids in human bone marrow derived mesenchymal stromal cells | 2 |
1 |
1 |
1 |
1 |
1 |
0 |
1 |
2 |
8 |
1 |
0 |
19 |
| Methane processes in the coastal sediments and water column of the Baltic Sea | 10 |
7 |
7 |
15 |
14 |
6 |
10 |
8 |
6 |
9 |
6 |
3 |
101 |
| Methanogenic Archaea in boreal peatlands | 4 |
3 |
1 |
3 |
0 |
4 |
3 |
29 |
12 |
2 |
4 |
5 |
70 |
| Methicillin-resistant Staphylococcus aureus in Finland : recent changes in the epidemiology, long-term facility aspects, and phenotypic and molecular detection of isolates | 2 |
0 |
2 |
3 |
1 |
0 |
3 |
5 |
1 |
9 |
5 |
1 |
32 |
| Methods and tools for mass spectrometric lipidome analysis | 2 |
7 |
1 |
0 |
1 |
0 |
2 |
2 |
2 |
1 |
1 |
0 |
19 |
| Micro- and mesoplastics in the northern Baltic Sea : their fate in the seafloor and effects on benthic fauna | 2 |
7 |
3 |
1 |
0 |
3 |
7 |
4 |
9 |
4 |
1 |
3 |
44 |
| Microalgae : Platform for conversion of waste to high value products | 3 |
17 |
11 |
8 |
10 |
6 |
6 |
3 |
0 |
8 |
1 |
5 |
78 |
| Microarrays in Lung Cancer Research : From Comparative Analyses to Verified Findings | 1 |
3 |
2 |
0 |
1 |
0 |
1 |
1 |
2 |
4 |
2 |
1 |
18 |
| Microarrays in the Diagnosis of Human Herpesvirus infections | 3 |
3 |
2 |
3 |
0 |
2 |
9 |
0 |
1 |
3 |
0 |
2 |
28 |
| Microbe-induced activation of inflammatory cytokine response in human cells | 0 |
5 |
1 |
1 |
1 |
3 |
5 |
1 |
2 |
5 |
3 |
8 |
35 |
| Microbe-induced Innate Immune Responses in Human Dendritic Cells | 3 |
4 |
2 |
0 |
1 |
5 |
2 |
10 |
2 |
4 |
4 |
3 |
40 |
| Microbes regulate metal and nutrient cycling in Fe Mn concretions of the Gulf of Finland | 5 |
4 |
5 |
7 |
5 |
2 |
4 |
14 |
7 |
9 |
12 |
9 |
83 |
| Microbial activities in boreal soils : Biodegradation of organic contaminants at low temperature and ammonia oxidation | 2 |
2 |
0 |
1 |
2 |
3 |
1 |
7 |
2 |
4 |
0 |
3 |
27 |
| Microbial communities in Pb contaminated boreal forest soil | 5 |
5 |
12 |
59 |
8 |
4 |
1 |
3 |
0 |
4 |
0 |
1 |
102 |
| Microbial community composition in various soils and groundwater deposits and effects of long-term pesticide contamination | 1 |
2 |
1 |
1 |
5 |
1 |
1 |
1 |
2 |
1 |
0 |
2 |
18 |
| Microbial Community Profiling of Biodegradable Municipal Solid Waste Treatments : Aerobic Composting and Anaerobic Digestion | 2 |
1 |
5 |
7 |
15 |
11 |
3 |
6 |
3 |
9 |
5 |
4 |
71 |
| Microbial diversity in the municipal composting process and development of detection methods | 1 |
2 |
2 |
1 |
1 |
2 |
2 |
1 |
2 |
3 |
1 |
1 |
19 |
| Microbial ecology in atrazine and terbutryn dissipation in surface soils and subsurface sediments | 3 |
3 |
3 |
4 |
3 |
5 |
10 |
4 |
8 |
7 |
9 |
5 |
64 |
| Microbial identification by detection of ligation probes on DNA microarray | 1 |
3 |
2 |
1 |
5 |
1 |
3 |
4 |
2 |
6 |
3 |
16 |
47 |
| Micronuclei in Human peripheral Lymphocytes : Mechanistic Origin and Use as a Biomarker of Genotoxic Effects in Occupational Exosure | 0 |
7 |
4 |
1 |
2 |
3 |
8 |
3 |
7 |
5 |
5 |
3 |
48 |
| Missing-In-Metastasis (MIM) regulates cell morphology by promoting plasma membrane and actin cytoskeleton dynamics | 4 |
3 |
8 |
5 |
2 |
5 |
4 |
3 |
2 |
5 |
3 |
2 |
46 |
| Mitigating anthropogenic nitrogen loading with constructed wetlands in a boreal climate | 7 |
7 |
5 |
1 |
1 |
3 |
4 |
1 |
2 |
3 |
5 |
5 |
44 |
| Modeling ecological and evolutionary processes in spatially structured populations | 1 |
5 |
2 |
1 |
1 |
2 |
3 |
3 |
0 |
1 |
3 |
1 |
23 |
| Modelling the evolutionarily conserved MANF/CDNF protein family in Drosophila melanogaster | 4 |
2 |
7 |
17 |
7 |
6 |
7 |
4 |
5 |
4 |
4 |
1 |
68 |
| Models of Dispersal and Diversification | 1 |
0 |
1 |
3 |
3 |
3 |
1 |
1 |
1 |
4 |
2 |
1 |
21 |
| Molecular Alterations in Asbestos-Related Lung Cancer | 0 |
2 |
4 |
3 |
4 |
6 |
1 |
6 |
4 |
3 |
2 |
3 |
38 |
| Molecular and biophysical analysis of the non-catalytic PH, TH, SH3 and SH2 domains of Bruton tyrosine kinase (Btk) protein | 0 |
3 |
7 |
0 |
5 |
1 |
1 |
3 |
1 |
3 |
4 |
1 |
29 |
| Molecular and cellular basis of early development of the mammary gland | 5 |
12 |
4 |
11 |
6 |
5 |
8 |
8 |
15 |
7 |
12 |
9 |
102 |
| Molecular and cellular biology of infantile neuronal ceroid lipofuscinosis (INCL) | 6 |
1 |
2 |
4 |
1 |
2 |
4 |
2 |
0 |
3 |
2 |
0 |
27 |
| Molecular and mechanical control of plant secondary development | 2 |
5 |
6 |
2 |
30 |
5 |
8 |
8 |
1 |
2 |
1 |
4 |
74 |
| Molecular and psysiological characterization of rhizosphere bacteria and Frankia in forest soils devoid of actinorhizal plants | 2 |
2 |
5 |
5 |
2 |
3 |
1 |
2 |
0 |
8 |
3 |
3 |
36 |
| Molecular background of three lethal fetal syndromes | 5 |
3 |
5 |
1 |
1 |
3 |
1 |
1 |
4 |
3 |
6 |
0 |
33 |
| Molecular characterization of new archaeal viruses from high salinity environments | 4 |
0 |
4 |
1 |
3 |
3 |
3 |
1 |
0 |
4 |
2 |
3 |
28 |
| Molecular characterization of plant defense responses to erwinia carotovora | 2 |
5 |
0 |
6 |
0 |
1 |
1 |
1 |
4 |
6 |
1 |
4 |
31 |
| Molecular details of the double-stranded RNA virus replication and assembly | 6 |
6 |
7 |
12 |
6 |
10 |
8 |
5 |
3 |
10 |
8 |
4 |
85 |
| Molecular epidemiology of human rhinoviruses | 4 |
9 |
1 |
3 |
2 |
2 |
2 |
2 |
0 |
2 |
0 |
0 |
27 |
| Molecular epidemiology of human rotaviruses | 0 |
4 |
2 |
1 |
0 |
0 |
1 |
0 |
1 |
1 |
1 |
0 |
11 |
| Molecular epidemiology of sporadic breast cancer : The role of polymorphic genes involved in oestrogen biosynthesis and metabolism | 4 |
3 |
1 |
3 |
4 |
6 |
5 |
2 |
4 |
8 |
1 |
3 |
44 |
| Molecular Factors Affecting the Activity and Substrate Selectivity of the Pla Protease of Yersinia pestis | 1 |
3 |
0 |
3 |
0 |
2 |
4 |
2 |
1 |
1 |
3 |
1 |
21 |
| Molecular Genetics of Bipolar Disorder and Related Traits | 1 |
3 |
2 |
0 |
2 |
4 |
0 |
3 |
4 |
3 |
2 |
4 |
28 |
| Molecular Genetics of Inclusion Body Myositis and Late-Onset Rimmed-Vacuolar Distal Myopathy | 10 |
21 |
6 |
5 |
6 |
4 |
6 |
3 |
4 |
11 |
14 |
4 |
94 |
| Molecular genetics of Meckel syndrome : Ciliary genes are defective in MKS | 3 |
3 |
1 |
0 |
4 |
3 |
2 |
2 |
1 |
4 |
0 |
3 |
26 |
| Molecular genetics of RECQL4 syndromes | 1 |
4 |
4 |
4 |
3 |
4 |
3 |
6 |
2 |
2 |
1 |
4 |
38 |
| Molecular genetics of tooth agenesis | 6 |
7 |
11 |
9 |
4 |
3 |
6 |
2 |
0 |
3 |
2 |
4 |
57 |
| Molecular mechanisms controlling neuronal Bak expression | 4 |
2 |
4 |
2 |
4 |
5 |
2 |
3 |
2 |
4 |
3 |
3 |
38 |
| Molecular mechanisms of lymphangiogenesis : role of VEGFR-3 mediated signaling | 1 |
2 |
2 |
0 |
2 |
0 |
4 |
2 |
0 |
2 |
4 |
4 |
23 |
| Molecular Mechanisms of Sleep and Mood | 1 |
3 |
2 |
1 |
3 |
2 |
0 |
95 |
6 |
4 |
4 |
2 |
123 |
| Molecular Mechanisms Underlying Tooth Morphogenesis and Cell Differentiation | 0 |
1 |
4 |
1 |
2 |
4 |
2 |
1 |
4 |
4 |
4 |
5 |
32 |
| Molecular Organisation and Host-Cell Interactions of Tick-Borne Encephalitis Virus. What Makes the Virus Tick? | 10 |
12 |
11 |
11 |
5 |
2 |
5 |
4 |
18 |
13 |
4 |
3 |
98 |
| Molecular pathogenesis in hereditary non-polyposis colorectal cancer (HNPCC) syndrome | 3 |
5 |
4 |
6 |
3 |
3 |
2 |
3 |
2 |
5 |
1 |
2 |
39 |
| Molecular pathogenesis of Salla disease | 4 |
5 |
3 |
4 |
4 |
2 |
3 |
4 |
4 |
2 |
2 |
1 |
38 |
| Molecular pathomechanisms of muscular dystrophies | 3 |
3 |
4 |
5 |
3 |
3 |
1 |
9 |
7 |
11 |
3 |
3 |
55 |
| Molecular profiling of indoor microbial communities in moisture damaged and non-damaged buildings | 2 |
2 |
2 |
0 |
2 |
0 |
0 |
0 |
1 |
1 |
2 |
1 |
13 |
| Molecular Regulation of Craniofacial Bone and Palate Development | 2 |
2 |
2 |
4 |
0 |
4 |
1 |
3 |
1 |
3 |
2 |
2 |
26 |
| Molecular regulation of embryonic mammary gland development | 10 |
10 |
7 |
5 |
5 |
5 |
12 |
4 |
15 |
10 |
9 |
7 |
99 |
| Molecular Regulation of the Dendritic Spine Initiation | 0 |
54 |
9 |
3 |
5 |
2 |
5 |
5 |
4 |
2 |
0 |
1 |
90 |
| Molecular responses of plants to solar UV-B and UV-A radiation | 5 |
4 |
3 |
3 |
3 |
4 |
8 |
2 |
4 |
4 |
4 |
2 |
46 |
| Molecular Tuning of Rhodopsins for High Visual Sensitivity in Different Light Environments : Variation in Absorbance Spectrum and Opsin Sequence within and between Species | 3 |
2 |
2 |
2 |
2 |
1 |
2 |
2 |
5 |
2 |
2 |
3 |
28 |
| Monographic studies on Cryphaea (Bryopsida) | 5 |
9 |
9 |
7 |
6 |
13 |
10 |
8 |
8 |
9 |
11 |
9 |
104 |
| Monolignols and their transport during lignification in Norway spruce | 8 |
0 |
2 |
3 |
3 |
5 |
2 |
5 |
3 |
2 |
3 |
0 |
36 |
| Moonlighting Proteins of Lactobacillus crispatus : Extracellular Localization, Cell Wall Anchoring and Interactions with the Host | 7 |
5 |
4 |
3 |
1 |
4 |
0 |
0 |
2 |
9 |
2 |
0 |
37 |
| Moose hunting in Finland : management of a heavily harvested population | 3 |
4 |
6 |
5 |
6 |
14 |
4 |
10 |
9 |
4 |
6 |
4 |
75 |
| Morphogenesis of Mammalian Endoplasmic Reticulum and Golgi Apparatus throughout the Cell Cycle | 2 |
2 |
3 |
1 |
7 |
1 |
2 |
3 |
3 |
8 |
5 |
5 |
42 |
| 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 | 2 |
4 |
2 |
42 |
37 |
3 |
3 |
4 |
7 |
2 |
3 |
2 |
111 |
| mRNA Localization and Cell Motility : Roles of Heparin-Binding Proteins Amphoterin and HG-GAM in Cell Migration | 0 |
2 |
3 |
1 |
0 |
0 |
0 |
3 |
0 |
2 |
0 |
0 |
11 |
| Mu in vitro transposition applications in protein engineering | 3 |
5 |
4 |
2 |
4 |
4 |
6 |
2 |
7 |
5 |
3 |
1 |
46 |
| Mu in vitro Transposition Technology in Functional Genetics and Genomics : Applications on Mouse and Bacteriophages | 1 |
4 |
2 |
1 |
4 |
1 |
3 |
1 |
2 |
6 |
2 |
0 |
27 |
| Mucosa-Adherent Lactobacilli : Commensal and Pathogenic Characteristics | 1 |
0 |
3 |
3 |
1 |
7 |
3 |
5 |
1 |
3 |
2 |
0 |
29 |
| Mucosal antibodies to protein and capsular polysaccharide antigens of streptococcus pneumoniae in children : relation to pneumococcal carriage and acute otitis media | 1 |
4 |
0 |
1 |
2 |
1 |
4 |
3 |
0 |
2 |
1 |
2 |
21 |
| Multifunctional RNA silencing pathway polymerase QDE-1 of Neurospora crassa | 2 |
1 |
1 |
4 |
6 |
1 |
10 |
1 |
4 |
7 |
2 |
2 |
41 |
| Multiplex RT-PCR in the diagnosis of human picornaviruses and human respiratory viruses | 7 |
2 |
3 |
2 |
2 |
2 |
0 |
1 |
0 |
2 |
2 |
0 |
23 |
| Mutations as molecular tools : The metabolic-rate dependent molecular clock and DNA barcoding of allied species | 2 |
8 |
0 |
2 |
7 |
10 |
8 |
2 |
7 |
6 |
4 |
2 |
58 |
| Mycorrhizal fungi and nitrogen dynamics in drained peatland | 0 |
1 |
4 |
1 |
1 |
3 |
0 |
0 |
2 |
0 |
0 |
0 |
12 |
| Myelin plasticity in mouse resilience and susceptibility to psychosocial stress : implications for anxiety disorders | 5 |
10 |
4 |
2 |
4 |
2 |
4 |
11 |
2 |
2 |
6 |
5 |
57 |
| N-Bak : a Neuron-Specific Splice Variant of Bak with anti-Apoptotic Properties | 4 |
2 |
3 |
2 |
3 |
1 |
3 |
7 |
6 |
7 |
5 |
9 |
52 |
| N-syndecan and HB-GAM in neural migration and differentiation : Modulation of growth factor activity in brain | 0 |
1 |
1 |
1 |
3 |
2 |
2 |
1 |
2 |
1 |
5 |
1 |
20 |
| Natural stimuli and experimental setups in the study of the neural basis of social interaction | 3 |
1 |
4 |
2 |
0 |
1 |
3 |
4 |
3 |
6 |
14 |
6 |
47 |
| Natural succession and human-induced changes in the soft-bottom macrovegetation of shallow brackish bays on the southern coast of Finland | 3 |
3 |
7 |
3 |
4 |
1 |
5 |
4 |
6 |
1 |
2 |
2 |
41 |
| Natural succession of microalgal communities during the cold-water season and the impact of increased solar irradiance on sea ice algae | 1 |
1 |
1 |
1 |
2 |
0 |
5 |
3 |
3 |
2 |
0 |
2 |
21 |
| Nephrin-associated molecules in human glomerular diseases | 6 |
3 |
1 |
6 |
7 |
2 |
2 |
5 |
3 |
5 |
4 |
4 |
48 |
| Network Pharmacology Approaches for Understanding Traditional Chinese Medicine | 174 |
44 |
22 |
23 |
19 |
13 |
22 |
9 |
16 |
10 |
32 |
28 |
412 |
| Networks in urban climate policy and governance | 3 |
8 |
8 |
5 |
9 |
6 |
3 |
17 |
10 |
11 |
14 |
5 |
99 |
| Neural processing at the sensitivity limit of vision : from retinal circuits to behavior | 5 |
9 |
4 |
9 |
10 |
13 |
5 |
7 |
4 |
5 |
3 |
0 |
74 |
| Neuronal ICAM-5 regulates synaptic maturation and microglia functions | 7 |
2 |
7 |
3 |
8 |
4 |
12 |
3 |
6 |
9 |
3 |
5 |
69 |
| Neuronal K-Cl Cotransporter : Transcriptional Mechanisms of KCC2 Gene Regulation | 0 |
3 |
5 |
3 |
2 |
1 |
0 |
0 |
2 |
2 |
0 |
0 |
18 |
| Neuronal synapse formation regulated by intercellular adhesion molecules-5 (ICAM-5) | 7 |
2 |
3 |
3 |
4 |
0 |
3 |
4 |
1 |
2 |
0 |
2 |
31 |
| Neurotrophic factors and their receptors | 1 |
1 |
3 |
2 |
4 |
3 |
0 |
1 |
2 |
2 |
1 |
1 |
21 |
| Neurotrophic factors GDNF and NRTN : from basic properties to clinical trials | 3 |
5 |
3 |
2 |
0 |
2 |
0 |
7 |
1 |
3 |
2 |
5 |
33 |
| Neurotrophic Factors in Rodent Heart : From Development to Pathophysiology | 2 |
1 |
3 |
0 |
1 |
3 |
0 |
4 |
3 |
1 |
3 |
0 |
21 |
| Neurotrophic receptor TrkB activation as an orchestrator of neuronal plasticity | 52 |
3 |
8 |
5 |
2 |
5 |
2 |
1 |
1 |
2 |
8 |
4 |
93 |
| Neurotrophins and neuronal plasticity in the action of antidepressants and morphine | 1 |
4 |
1 |
0 |
0 |
0 |
0 |
1 |
1 |
1 |
0 |
0 |
9 |
| New insight into mechanisms of transcellular propagation of tau and α-synuclein in neurodegenerative diseases | 5 |
2 |
4 |
0 |
4 |
4 |
2 |
7 |
4 |
14 |
6 |
4 |
56 |
| Nitrogen cycling in aphotic coastal sandy sediments of the Baltic Sea | 1 |
0 |
2 |
2 |
2 |
0 |
3 |
2 |
1 |
2 |
1 |
46 |
62 |
| Nitrous oxide emissions from selected natural and managed northern ecosystems | 1 |
2 |
5 |
7 |
9 |
3 |
0 |
2 |
1 |
10 |
3 |
4 |
47 |
| Non-neuronal roles for GDNF and novel GDNF family receptors | 0 |
0 |
2 |
1 |
3 |
2 |
1 |
0 |
2 |
1 |
2 |
1 |
15 |
| Notch signaling in blood and lymphatic vessel development | 5 |
5 |
4 |
2 |
3 |
2 |
3 |
3 |
3 |
6 |
2 |
5 |
43 |
| Novel analytical methods for the identification of emerging contaminants in aquatic environments | 9 |
4 |
3 |
4 |
1 |
2 |
4 |
5 |
3 |
4 |
7 |
0 |
46 |
| Novel CDNF/MANF protein family : Molecular structure, expression and neurotrophic activity | 2 |
6 |
3 |
1 |
2 |
8 |
4 |
4 |
9 |
8 |
44 |
41 |
132 |
| Novel Molecular Mechanisms of Arabidopsis Disease Resistance | 1 |
1 |
3 |
2 |
1 |
4 |
3 |
4 |
1 |
2 |
0 |
2 |
24 |
| Novel molecular mechanisms of dendritic spine development | 1 |
5 |
6 |
4 |
3 |
1 |
3 |
4 |
3 |
5 |
11 |
8 |
54 |
| Novel Regulators of Vascular Development in Arabidopsis thaliana | 7 |
3 |
1 |
2 |
3 |
2 |
2 |
0 |
1 |
1 |
1 |
1 |
24 |
| Novel roles of p75 neurotrophin receptor in Low-density lipoprotein receptor regulation and lipid signaling | 3 |
6 |
2 |
0 |
4 |
1 |
2 |
2 |
5 |
5 |
3 |
1 |
34 |
| Nuclear Import Mechanisms of STAT and NF-kB Transcription Factors | 10 |
7 |
7 |
2 |
5 |
3 |
3 |
4 |
5 |
2 |
1 |
4 |
53 |
| Nutrient dynamics in eutrophic lakes : Effects of resuspension, macrophytes and oxygen | 6 |
4 |
2 |
3 |
3 |
11 |
2 |
0 |
3 |
3 |
2 |
3 |
42 |
| Occurence of the introduced black rat (Rattus rattus) and its potential effects on endemic rodents in southeastern Madagascar | 0 |
1 |
8 |
57 |
175 |
4 |
0 |
0 |
3 |
14 |
5 |
3 |
270 |
| Occurrence, habitat use and movements of the flying squirrel in human-modified forest landscapes | 4 |
4 |
4 |
1 |
3 |
3 |
3 |
3 |
2 |
5 |
10 |
0 |
42 |
| Of the interactions between eye fluke parasites and salmonid fishes | 2 |
2 |
0 |
3 |
2 |
0 |
1 |
0 |
1 |
2 |
4 |
2 |
19 |
| Oligogalacturonide signalling in plant innate immunity | 3 |
5 |
6 |
3 |
2 |
4 |
1 |
4 |
1 |
4 |
7 |
5 |
45 |
| On the deterioration and restoration of mire invertebrate communities | 5 |
1 |
5 |
1 |
1 |
1 |
1 |
1 |
0 |
1 |
0 |
2 |
19 |
| On the Development of the Turtle Scute Pattern and the Origins of its Variation | 8 |
11 |
12 |
10 |
7 |
12 |
10 |
4 |
15 |
16 |
14 |
7 |
126 |
| On the ecology of cold-water phytoplankton in the Baltic Sea | 4 |
3 |
5 |
3 |
2 |
2 |
6 |
0 |
3 |
9 |
2 |
7 |
46 |
| On the histone acetyltransferase hMOF | 1 |
1 |
7 |
4 |
6 |
5 |
1 |
2 |
4 |
2 |
0 |
1 |
34 |
| On the mechanisms of neural development in the ventral telencephalon | 4 |
2 |
4 |
5 |
3 |
2 |
2 |
4 |
3 |
4 |
5 |
2 |
40 |
| On the origin of snakes based on geometric morphometrics : morphology, paleontology, phylogeny, ecology, and development | 16 |
13 |
23 |
15 |
33 |
16 |
9 |
24 |
24 |
23 |
16 |
7 |
219 |
| On the origins and evolution of morphological complexity : a developmental perspective | 5 |
8 |
9 |
3 |
5 |
3 |
5 |
6 |
3 |
7 |
5 |
4 |
63 |
| On the phylogeny and diversity of the microsoroid ferns (Polypodiaceae) | 11 |
9 |
14 |
20 |
10 |
6 |
16 |
6 |
11 |
4 |
6 |
9 |
122 |
| On the role of bacterial production and denitrification in some less-studied Baltic Sea habitats | 0 |
1 |
1 |
1 |
15 |
1 |
6 |
4 |
4 |
1 |
2 |
1 |
37 |
| Orchestrating Plant Defences in Response to Botrytis cinerea and Apoplastic ROS : Hormone Interactions, Transcriptional and Posttranscriptional Regulation | 0 |
55 |
20 |
15 |
15 |
7 |
6 |
10 |
5 |
11 |
10 |
6 |
160 |
| Organelle specific mechanisms of neuronal cell death | 3 |
3 |
4 |
4 |
3 |
4 |
6 |
6 |
1 |
1 |
2 |
1 |
38 |
| Origin and regeneration of free-living Fucus vesiculosus in the Baltic Sea | 3 |
4 |
5 |
9 |
10 |
16 |
11 |
6 |
5 |
2 |
7 |
3 |
81 |
| ORP1L, a new Rab7 effector and regulator of late endosome functions | 2 |
2 |
3 |
2 |
0 |
0 |
0 |
3 |
1 |
5 |
3 |
3 |
24 |
| ORP2 is a sterol receptor that regulates cellular lipid metabolism | 1 |
1 |
5 |
0 |
4 |
1 |
3 |
2 |
0 |
1 |
6 |
1 |
25 |
| Outer Membrane Protease/Adhesin PgtE of Salmonella enterica : Role in Salmonella-Host Interaction | 2 |
3 |
3 |
8 |
5 |
12 |
6 |
3 |
5 |
6 |
5 |
2 |
60 |
| Overwintering ecology of northern field layer plants : snow and photosynthesis in Vaccinium vitis-idaea L. | 3 |
2 |
3 |
5 |
0 |
2 |
1 |
0 |
6 |
6 |
6 |
0 |
34 |
| Overwintering in wood plants : involvement of ABA and dehydrins | 3 |
0 |
1 |
2 |
1 |
2 |
5 |
1 |
1 |
4 |
1 |
2 |
23 |
| Oxygen reduction and proton translocation by cytochrome c oxidase | 2 |
2 |
2 |
3 |
2 |
2 |
4 |
1 |
2 |
2 |
1 |
0 |
23 |
| Ozone-induced signaling in Arabidopsis thaliana | 0 |
2 |
5 |
4 |
3 |
3 |
1 |
1 |
1 |
4 |
4 |
1 |
29 |
| Packaging Motors of Cystoviruses | 11 |
29 |
9 |
5 |
2 |
1 |
5 |
8 |
3 |
7 |
2 |
2 |
84 |
| Paracrine orchestration of intestinal regeneration and aging | 9 |
9 |
43 |
26 |
15 |
10 |
12 |
9 |
11 |
6 |
11 |
9 |
170 |
| Parasitoid foraging behaviour in a competitive environment | 1 |
3 |
2 |
5 |
6 |
2 |
8 |
5 |
2 |
5 |
1 |
2 |
42 |
| Pathogen-Induced Defense Signaling and Signal Crosstalk in Arabidopsis | 1 |
3 |
1 |
3 |
4 |
2 |
0 |
3 |
6 |
10 |
1 |
4 |
38 |
| Pathogenetic features of proteinuria studies on congenital nephrotic syndrome of the Finnish type | 5 |
0 |
1 |
0 |
2 |
1 |
0 |
1 |
2 |
5 |
1 |
2 |
20 |
| Pathogenetic mechanisms and genotype phenotype correlations in nemaline myopathies and related disorders caused by mutations in tropomyosin genes and nebulin | 8 |
1 |
4 |
2 |
7 |
3 |
9 |
8 |
5 |
4 |
15 |
6 |
72 |
| Pathogenic and Molecular Characteristics of Two Isolates of HEV-B Species | 2 |
0 |
2 |
6 |
5 |
4 |
3 |
4 |
4 |
10 |
3 |
3 |
46 |
| Pathogenic Mechanisms of Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy (PLOSL) | 2 |
3 |
3 |
6 |
1 |
0 |
1 |
2 |
1 |
2 |
1 |
0 |
22 |
| Pathogenicity, functional significance and clinical phenotype of mismatch repair gene MSH2 variants found in cancer patients | 6 |
0 |
1 |
6 |
6 |
3 |
6 |
4 |
6 |
10 |
8 |
3 |
59 |
| Pathway for the Formation of Semliki Forest Virus RNA Replication Complex | 2 |
5 |
3 |
2 |
3 |
3 |
4 |
1 |
2 |
3 |
3 |
1 |
32 |
| PCSK9 and berberine as modulators of lipoprotein receptors and neuronal cell death | 9 |
3 |
5 |
6 |
2 |
2 |
2 |
3 |
4 |
4 |
3 |
6 |
49 |
| Pentitol phosphate dehydrogenases : Discovery, characterization and use in D-arabitol and xylitol production by metabolically engineered Bacillus subtilis | 4 |
8 |
9 |
2 |
8 |
8 |
3 |
3 |
4 |
10 |
4 |
3 |
66 |
| Perception of solar UV radiation and blue light by plants : photoreceptors, transcriptome and environmental acclimation | 5 |
3 |
0 |
4 |
5 |
6 |
1 |
4 |
7 |
6 |
17 |
2 |
60 |
| Peroxidases in lignifying xylem of Norway spruce, Scots pine and silver birch | 2 |
2 |
1 |
0 |
0 |
2 |
1 |
3 |
0 |
2 |
0 |
2 |
15 |
| Personality traits in the blue tit | 1 |
1 |
2 |
4 |
1 |
3 |
3 |
5 |
8 |
8 |
3 |
3 |
42 |
| Phagophore membrane connections and RAB24 in autophagy | 9 |
3 |
5 |
5 |
3 |
2 |
1 |
0 |
2 |
1 |
2 |
2 |
35 |
| Phosphatidylserine translocation in mammalian cells | 5 |
11 |
14 |
9 |
6 |
6 |
3 |
8 |
4 |
5 |
3 |
3 |
77 |
| Phospholipids of lipid-containing bacteriophages and their transbilayer distribution | 0 |
3 |
1 |
1 |
4 |
4 |
2 |
1 |
8 |
6 |
18 |
7 |
55 |
| Phosphoproteomic characterization of viral infection | 3 |
4 |
3 |
9 |
1 |
1 |
1 |
2 |
3 |
4 |
3 |
1 |
35 |
| Phosphorylation of the α- and β-chains of LFA-1 regulates its interaction with cytoplasmic proteins and crosstalk to VLA-4 integrin | 3 |
0 |
3 |
3 |
6 |
6 |
3 |
0 |
2 |
6 |
4 |
3 |
39 |
| Photochemical transformation of dissolved organic matter in aquatic environment : From a boreal lake and Baltic Sea to global coastal ocean | 1 |
7 |
4 |
1 |
2 |
1 |
2 |
4 |
1 |
4 |
2 |
2 |
31 |
| Phylogenetic studies of cyanobacterial lichens | 0 |
3 |
0 |
1 |
3 |
2 |
3 |
0 |
2 |
3 |
3 |
3 |
23 |
| Phylogenetics of Myrmica ants and their social parasites | 0 |
3 |
2 |
4 |
1 |
1 |
5 |
3 |
1 |
3 |
0 |
1 |
24 |
| Phylogenetics, taxon delimitation and phylogenetic diversity | 2 |
2 |
5 |
2 |
4 |
4 |
4 |
6 |
3 |
3 |
3 |
0 |
38 |
| Phylogenomics and adaptive evolution in stickleback fishes | 2 |
3 |
3 |
3 |
1 |
2 |
0 |
0 |
1 |
6 |
5 |
1 |
27 |
| Phylogeny and biogeography of liverworts (Marchantiophyta), evidence from the Southern Hemisphere family Schistochilaceae and the cosmopolitan genus Herbertus (Herbertaceae) | 14 |
8 |
9 |
12 |
7 |
14 |
8 |
17 |
17 |
12 |
2 |
1 |
121 |
| Phylogeny and evolutionary relationships of the moss families Brachytheciaceae and Meteoriaceae | 12 |
16 |
13 |
10 |
5 |
11 |
6 |
5 |
5 |
14 |
14 |
5 |
116 |
| Phylogeny and host associations of cotesia parasitoids attacking checkerspot butterflies | 5 |
4 |
7 |
4 |
3 |
1 |
4 |
1 |
6 |
2 |
2 |
4 |
43 |
| Phylogeny of a taxonomically difficult group and evolution of host location mechanism | 2 |
1 |
1 |
0 |
8 |
4 |
3 |
2 |
1 |
3 |
7 |
2 |
34 |
| Phylogeny, phyletic coevolution and phylogeography of anoplocephaline cestodes in mammals | 2 |
1 |
1 |
1 |
2 |
2 |
4 |
3 |
7 |
4 |
9 |
4 |
40 |
| 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 | 5 |
1 |
0 |
1 |
3 |
2 |
4 |
1 |
1 |
4 |
1 |
1 |
24 |
| Phylogeography and evolution of freshwater cottid fishes | 2 |
2 |
4 |
4 |
2 |
6 |
1 |
3 |
2 |
2 |
3 |
0 |
31 |
| Phylogeography and historical introgression in Stickleback fishes | 2 |
3 |
1 |
1 |
1 |
2 |
3 |
0 |
2 |
4 |
1 |
4 |
24 |
| Phylogeography and hybrid swarms : history of brackish water bivalve diversity in North European marginal seas | 3 |
0 |
2 |
1 |
2 |
0 |
1 |
4 |
2 |
4 |
8 |
3 |
30 |
| Phylogeography and population genetics of social parasitism in Myrmica ants | 2 |
2 |
3 |
3 |
0 |
1 |
1 |
0 |
2 |
4 |
1 |
3 |
22 |
| Phylogeography and Population Genetics of the Moor frog (Rana arvalis Nilsson) in Northern Europe | 4 |
6 |
4 |
2 |
2 |
4 |
4 |
2 |
1 |
4 |
10 |
5 |
48 |
| Phylogeography of amphi-boreal marine fauna | 0 |
2 |
3 |
4 |
1 |
4 |
1 |
5 |
11 |
2 |
0 |
0 |
33 |
| Physiological and Molecular Analyses of Cold Acclimation of Plants | 4 |
0 |
4 |
2 |
1 |
3 |
1 |
3 |
3 |
4 |
2 |
2 |
29 |
| Physiological Modulation of the Reverse Cholesterol Transport Pathway in vivo | 3 |
4 |
2 |
2 |
2 |
2 |
1 |
2 |
2 |
3 |
1 |
2 |
26 |
| Physiological stress and life-history strategies in the eider (Somateria mollissima) | 4 |
5 |
3 |
5 |
3 |
5 |
3 |
4 |
3 |
3 |
3 |
2 |
43 |
| Phytohormone-related crosstalk in pathogen and stomatal responses in Arabidopsis thaliana | 9 |
3 |
3 |
2 |
2 |
4 |
5 |
0 |
8 |
5 |
3 |
2 |
46 |
| Phytoplankton ecology of subarctic lakes in Finnish Lapland | 2 |
2 |
1 |
2 |
1 |
2 |
1 |
1 |
1 |
1 |
0 |
1 |
15 |
| Phytoplankton functions and community properties in the pelagic food web | 1 |
2 |
5 |
0 |
0 |
0 |
1 |
1 |
1 |
6 |
2 |
0 |
19 |
| Phytoplankton quantity as an indicator of eutrophication in Finnish coastal waters : Applications within the Water Framework Directive | 12 |
4 |
3 |
3 |
6 |
2 |
1 |
3 |
1 |
1 |
1 |
0 |
37 |
| Phytoplanktonic life in boreal humic lakes : special emphasis on autotrophic picoplankton and microbial food webs | 2 |
5 |
1 |
4 |
6 |
4 |
2 |
3 |
2 |
2 |
1 |
0 |
32 |
| Plant biomarkers as a proxy to study highly decomposed fen peat | 5 |
6 |
3 |
5 |
5 |
3 |
4 |
5 |
5 |
2 |
2 |
4 |
49 |
| Plant guard cell anion channel SLAC1 regulates stomatal closure | 4 |
4 |
1 |
1 |
5 |
5 |
8 |
1 |
5 |
3 |
3 |
1 |
41 |
| Plant oxygen deprivation stress and function of plant mitochondria under anoxia | 7 |
4 |
3 |
3 |
3 |
3 |
1 |
0 |
4 |
10 |
5 |
1 |
44 |
| Plant Tissue Cultures as Models for Tree Physiology : Somatic Embryogenesis of Tilia cordata and Lignin Biosynthesis in Picea abies Suspension Cultures as Case Studies | 4 |
7 |
10 |
6 |
5 |
5 |
4 |
14 |
3 |
18 |
7 |
7 |
90 |
| Plant-soil feedbacks as affecting ecosystem services in urban greenspaces | 4 |
5 |
1 |
1 |
2 |
3 |
3 |
3 |
1 |
2 |
1 |
1 |
27 |
| Plasma Phospholipid Transfer Protein (PLTP) : Quantitation, Biosynthesis, and Involvement in Hepatic Lipid Homeostasis | 1 |
1 |
3 |
2 |
0 |
0 |
0 |
0 |
2 |
6 |
0 |
4 |
19 |
| Plasmids and aromatic degradation in Sphingomonas for bioremediation : Aromatic ring cleavage genes in soil and rhizosphere | 1 |
4 |
3 |
1 |
1 |
1 |
1 |
1 |
2 |
2 |
1 |
1 |
19 |
| Platelet-Collagen Interaction and Microvesiculation | 3 |
1 |
1 |
0 |
0 |
1 |
0 |
0 |
1 |
2 |
0 |
2 |
11 |
| Pollination networks of the High Arctic : adding a functional perspective | 3 |
1 |
5 |
4 |
1 |
3 |
6 |
32 |
13 |
25 |
5 |
4 |
102 |
| Pollutant remediation strategies in the soil : electrokinetic remediation, biostimulation, and experimental design | 11 |
14 |
1 |
3 |
18 |
7 |
7 |
6 |
13 |
7 |
13 |
14 |
114 |
| Polyamine Metabolism During Development of Somatic and Zygotic Embryos of Picea Abies (Norway Spruce) | 2 |
5 |
3 |
2 |
3 |
3 |
1 |
4 |
2 |
3 |
6 |
3 |
37 |
| Polymorphic low penetrance genes and breast cancer : The role of genes involved in metabolism of xenobiotics, estrogens and reactive oxygen species | 3 |
5 |
1 |
5 |
4 |
5 |
5 |
1 |
5 |
4 |
7 |
6 |
51 |
| Polypore assemblages in boreal old-growth forests, and associated Coleoptera | 4 |
2 |
2 |
1 |
1 |
0 |
2 |
0 |
5 |
8 |
10 |
1 |
36 |
| Population biology of periodic Xestia moths | 3 |
3 |
0 |
0 |
0 |
0 |
1 |
3 |
2 |
3 |
6 |
2 |
23 |
| Population differentiation in sticklebacks : disentangling maternal, environmental and genetic effects | 0 |
2 |
2 |
3 |
0 |
2 |
0 |
0 |
0 |
1 |
1 |
0 |
11 |
| Population dynamics of blue mussels in a variable environment at the edge of their range | 3 |
2 |
2 |
7 |
4 |
3 |
0 |
4 |
2 |
1 |
0 |
4 |
32 |
| Population dynamics of flounders in the northern Baltic Sea : declines, cryptic species and environmental drivers | 0 |
1 |
0 |
3 |
8 |
0 |
6 |
8 |
2 |
3 |
6 |
7 |
44 |
| Population dynamics of seals : the influences of spatial and temporal structures | 0 |
3 |
4 |
0 |
4 |
4 |
8 |
12 |
6 |
4 |
0 |
22 |
67 |
| Population structure and evolution in the ant Plagiolepis pygmaea and its two social parasites Plagiolepis xene and Plagiolepis grassei | 0 |
3 |
0 |
1 |
1 |
5 |
1 |
1 |
3 |
3 |
2 |
2 |
22 |
| Positional cloning and pathway analysis of the asthma susceptibility gene, NPSR1 | 3 |
3 |
3 |
1 |
0 |
3 |
3 |
2 |
2 |
5 |
4 |
2 |
31 |
| Post-translational regulation of KCC2 in the rat hippocampus | 2 |
2 |
3 |
1 |
1 |
1 |
1 |
0 |
1 |
2 |
0 |
2 |
16 |
| Post-translational Regulation of TGF-beta Signaling in Drosophila Development | 1 |
0 |
5 |
3 |
2 |
1 |
4 |
1 |
2 |
6 |
4 |
3 |
32 |
| Postmitotic state of a cell as a challenge for regeneration : inner ear as a model | 0 |
1 |
3 |
3 |
4 |
3 |
2 |
1 |
4 |
5 |
3 |
0 |
29 |
| Posttranslational modifications of potato virus A movement related proteins CP and VPg | 0 |
1 |
0 |
1 |
1 |
1 |
2 |
1 |
1 |
9 |
4 |
4 |
25 |
| Potential of filamentous macroalgae and sessile invertebrates for bioremediation and valorization in the northern Baltic Sea | 4 |
1 |
5 |
2 |
4 |
0 |
4 |
1 |
2 |
3 |
3 |
1 |
30 |
| Potential of the slow pyrolysis products birch tar oil, wood vinegar and biochar in sustainable plant protection : pesticidal effects, soil improvement and environmental risks | 16 |
29 |
28 |
29 |
19 |
22 |
29 |
35 |
34 |
29 |
23 |
19 |
312 |
| Power dynamics and participation in post-disaster recovery | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
7 |
34 |
10 |
4 |
5 |
60 |
| Practices and Policies for Carbon Neutrality : Energy Transition in the Helsinki Metropolitan Area | 3 |
16 |
10 |
11 |
9 |
13 |
12 |
6 |
9 |
4 |
7 |
6 |
106 |
| Pre- and post-copulatory sexual selection in the least killifish, Heterandria formosa | 0 |
0 |
4 |
1 |
0 |
0 |
0 |
0 |
0 |
5 |
0 |
1 |
11 |
| Precautionary management of Baltic Sea cod (Gadus morhua callaris) under different harvesting and environmental scenarios | 1 |
6 |
3 |
4 |
1 |
0 |
3 |
0 |
1 |
2 |
1 |
2 |
24 |
| Precision medicine for lung cancer : models, functional assays and mechanisms | 1 |
3 |
6 |
8 |
9 |
6 |
3 |
3 |
6 |
4 |
2 |
6 |
57 |
| Preparing for the unprecedented : Moving towards quantitative understanding of oil spill impacts on Arctic marine biota | 2 |
21 |
3 |
2 |
0 |
0 |
2 |
3 |
3 |
3 |
6 |
2 |
47 |
| Present and future fluxes of nitrogen, phosphorus and carbon from catchments to lakes in a boreal landscape | 3 |
2 |
3 |
6 |
0 |
0 |
0 |
3 |
1 |
2 |
2 |
2 |
24 |
| Prevention of inflammatory cellular responses by ethanol and hemin interplay between inflammasomes and processes inhibiting inflammation | 4 |
0 |
4 |
7 |
8 |
6 |
2 |
2 |
1 |
5 |
7 |
7 |
53 |
| Probing lipid domains in model membranes and in mammalian cells | 1 |
2 |
3 |
0 |
0 |
0 |
0 |
1 |
3 |
1 |
1 |
1 |
13 |
| Production and Use of Mammalian Glycosyltransferases | 4 |
1 |
3 |
2 |
3 |
2 |
1 |
1 |
0 |
1 |
3 |
0 |
21 |
| Production of F4 Fimbrial Adhesin in Plants : a Model for Oral Porcine Vaccine against Enterotoxigenic Escherichia coli | 2 |
0 |
2 |
2 |
1 |
2 |
1 |
1 |
1 |
1 |
6 |
2 |
21 |
| Prokaryotic microorganisms, viruses, and antimicrobial agents from hypersaline environments | 6 |
8 |
5 |
1 |
0 |
4 |
2 |
3 |
10 |
3 |
3 |
3 |
48 |
| Prostatic acid phosphatase as a regulator of endo/exocytosis and lysosomal degradation | 3 |
3 |
1 |
1 |
4 |
2 |
0 |
0 |
0 |
3 |
25 |
53 |
95 |
| Protein Folding before and after Translocation into the Yeast Endoplasmic Reticulum | 1 |
0 |
1 |
4 |
2 |
3 |
4 |
1 |
4 |
2 |
2 |
3 |
27 |
| Proteolytic Modification of High Density Lipoproteins Decreases Their Ability to Induce Cholesterol Efflux from Macrophage Foam Cells | 2 |
3 |
1 |
2 |
5 |
2 |
1 |
0 |
2 |
1 |
2 |
0 |
21 |
| Proteolytic Processing as a Regulator of BMP-type Signaling in Drosophila Development | 0 |
1 |
1 |
0 |
5 |
0 |
12 |
3 |
3 |
4 |
0 |
2 |
31 |
| Proteomic Characterization of Biological Effects Induced by Engineered Nanomaterials | 3 |
3 |
6 |
0 |
1 |
1 |
3 |
4 |
3 |
4 |
4 |
3 |
35 |
| Proteomic characterization of host response to viral infection | 1 |
2 |
2 |
1 |
0 |
0 |
3 |
2 |
3 |
3 |
4 |
4 |
25 |
| Protomyces Comparative Genomics and Modulation of Arabidopsis Immunity | 5 |
2 |
5 |
6 |
3 |
4 |
8 |
3 |
3 |
8 |
2 |
6 |
55 |
| Proton translocation coupled to electron transfer reactions in terminal oxidases | 23 |
171 |
0 |
6 |
3 |
3 |
4 |
9 |
5 |
4 |
4 |
2 |
234 |
| Proximate and ultimate determinants of reproductive skew in the polygyne ant Formica fusca | 0 |
4 |
6 |
3 |
3 |
2 |
4 |
3 |
3 |
3 |
3 |
0 |
34 |
| PrsA lipoprotein and posttranslocational folding of secretory proteins in Bacillus subtilis | 0 |
4 |
3 |
1 |
3 |
2 |
3 |
0 |
2 |
5 |
3 |
3 |
29 |
| Pulmonary Infection and Atherosclerosis in an Experimental Chlamydia pneumoniae Model | 3 |
1 |
2 |
2 |
1 |
0 |
1 |
1 |
1 |
3 |
2 |
0 |
17 |
| Quality control of mitochondrial gene expression | 3 |
9 |
13 |
16 |
11 |
6 |
5 |
7 |
5 |
1 |
4 |
8 |
88 |
| Quantifying biomass and carbon processing of benthic fauna in a coastal sea : past, present and future | 2 |
4 |
1 |
2 |
2 |
2 |
2 |
2 |
5 |
5 |
7 |
4 |
38 |
| Quantitative and population genetics of the Glanville fritillary butterfly | 1 |
2 |
1 |
1 |
4 |
2 |
2 |
1 |
6 |
2 |
4 |
2 |
28 |
| Quantitative genetics in nonlinear genotype-phenotype maps | 6 |
7 |
4 |
5 |
5 |
7 |
4 |
1 |
2 |
8 |
6 |
2 |
57 |
| Quantitative PCR in the diagnosis and monitoring of human cytomegalovirus infection in organ transplant patients | 3 |
2 |
2 |
1 |
2 |
1 |
1 |
1 |
15 |
5 |
2 |
11 |
46 |
| Quorum sensing in the plant pathogen Erwinia carotovora subsp. carotovora | 1 |
3 |
5 |
5 |
3 |
4 |
5 |
3 |
7 |
39 |
5 |
6 |
86 |
| Rab8 and R-Ras as modulators of cell shape | 6 |
29 |
1 |
0 |
3 |
1 |
0 |
0 |
0 |
4 |
1 |
1 |
46 |
| Rad51c is a Tumor Suppressor in Mammary and Sebaceous Glands | 2 |
4 |
2 |
2 |
1 |
2 |
1 |
2 |
1 |
3 |
5 |
2 |
27 |
| Reactive oxygen species and SRO proteins as regulators of gene expression in Arabidopsis thaliana | 4 |
3 |
2 |
4 |
2 |
1 |
7 |
4 |
4 |
6 |
1 |
5 |
43 |
| Recent eutrophication of coastal waters in southern Finland : A palaeolimnological assessment | 2 |
0 |
2 |
0 |
3 |
2 |
0 |
1 |
1 |
2 |
2 |
1 |
16 |
| Recognition and social behaviour in Formica ants | 3 |
3 |
2 |
3 |
5 |
0 |
0 |
3 |
3 |
2 |
1 |
1 |
26 |
| Recognizing Lynch Syndrome by DNA Mismatch Repair Deficiency | 22 |
11 |
7 |
3 |
11 |
6 |
19 |
6 |
4 |
3 |
4 |
2 |
98 |
| Recombinant hantavirus proteins : antigenic properties and diagnostic applications | 1 |
2 |
1 |
3 |
2 |
4 |
1 |
6 |
2 |
3 |
2 |
3 |
30 |
| Recombinant structural proteins of rubella virus | 5 |
2 |
3 |
4 |
2 |
4 |
7 |
3 |
1 |
3 |
7 |
7 |
48 |
| Recovery of Yeast Saccharomyces cerevisiae after Thermal Insult | 1 |
3 |
1 |
5 |
1 |
5 |
0 |
42 |
5 |
3 |
4 |
3 |
73 |
| Recovery responses of acidified Finnish lakes under declining acid deposition | 0 |
2 |
0 |
2 |
1 |
0 |
0 |
0 |
0 |
3 |
1 |
1 |
10 |
| Redox-linked proton transfer by cytochrome c oxidase | 2 |
2 |
0 |
1 |
4 |
2 |
0 |
3 |
1 |
2 |
1 |
0 |
18 |
| Reduced mismatch repair gene expression and functional deficiency as indicators of Lynch syndrome | 10 |
1 |
4 |
5 |
4 |
6 |
7 |
11 |
6 |
5 |
5 |
5 |
69 |
| Refining the genetic architecture of Atlantic salmon (Salmo salar) maturation using genomics-enabled approaches | 3 |
0 |
8 |
3 |
2 |
1 |
3 |
5 |
13 |
3 |
14 |
3 |
58 |
| Regulation of Actin Dynamics in Animal Cells : The Role of ADF/cofilin and Twinfilin | 1 |
2 |
1 |
0 |
5 |
2 |
1 |
4 |
1 |
4 |
2 |
3 |
26 |
| Regulation of Cell Polarity Determinant Scribble in Drosophila and Mammals | 3 |
3 |
3 |
2 |
3 |
4 |
3 |
0 |
0 |
4 |
2 |
3 |
30 |
| Regulation of contractile actin structures in non-muscle cells | 2 |
7 |
1 |
1 |
4 |
5 |
1 |
1 |
1 |
4 |
5 |
1 |
33 |
| Regulation of GABAergic neuron identity and diversity in the developing midbrain | 2 |
0 |
2 |
4 |
1 |
5 |
4 |
0 |
1 |
3 |
0 |
6 |
28 |
| Regulation of Growth by Drosophila FoxO Transcription Factor | 1 |
0 |
0 |
2 |
1 |
5 |
1 |
0 |
2 |
2 |
1 |
2 |
17 |
| Regulation of heat shock response in yeast and mammalian cells | 0 |
4 |
0 |
0 |
1 |
2 |
0 |
0 |
0 |
3 |
2 |
2 |
14 |
| Regulation of Human Sex Hormone-Binding Globulin Gene (shbg) Expression | 1 |
1 |
4 |
0 |
3 |
4 |
4 |
4 |
5 |
5 |
13 |
5 |
49 |
| Regulation of leukocyte integrin binding to Ig-family ligands | 6 |
34 |
2 |
1 |
5 |
1 |
0 |
3 |
0 |
7 |
1 |
3 |
63 |
| Regulation of neural progenitor cell proliferation and fate by proteolytic pathways and inflammatory signals in the brain | 18 |
15 |
8 |
1 |
2 |
3 |
1 |
0 |
4 |
3 |
7 |
2 |
64 |
| Regulation of Osteoblast Differentiation and Gene Expression by Phosphodiesterases and Bioactive Peptides | 2 |
5 |
4 |
6 |
3 |
4 |
2 |
1 |
6 |
8 |
5 |
5 |
51 |
| Regulation of Stat5 activation | 0 |
0 |
2 |
1 |
5 |
3 |
2 |
0 |
1 |
4 |
1 |
0 |
19 |
| Regulation of the Actin Cytoskeleton by Twinfilin | 2 |
3 |
1 |
1 |
0 |
1 |
2 |
0 |
0 |
1 |
2 |
0 |
13 |
| Regulation of the minor spliceosome through alternative splicing and nuclear retention of the U11/U12-65K mRNA | 42 |
27 |
9 |
10 |
4 |
4 |
5 |
5 |
9 |
1 |
1 |
3 |
120 |
| Regulation of the neuronal chloride cotransporter KCC2 by neurotrophins | 0 |
0 |
0 |
4 |
3 |
2 |
1 |
2 |
2 |
2 |
2 |
2 |
20 |
| Regulatory networks controlling virulence in the plant pathogen Erwinia carotovora ssp. carotovora | 2 |
4 |
4 |
4 |
4 |
5 |
2 |
3 |
5 |
3 |
6 |
7 |
49 |
| Reindeer Parapoxvirus : Molecular Biology and Detection | 1 |
0 |
3 |
5 |
6 |
2 |
2 |
1 |
3 |
3 |
2 |
3 |
31 |
| Relationships between species traits and ecosystem processes in brackish aquatic plant communities | 3 |
2 |
4 |
4 |
3 |
2 |
2 |
1 |
1 |
5 |
3 |
1 |
31 |
| Remediation through mulching with organic matter of soil polluted by a copper-nickel smelter | 2 |
2 |
3 |
3 |
4 |
4 |
3 |
3 |
3 |
1 |
2 |
3 |
33 |
| Replication of Tula Hantavirus | 1 |
2 |
3 |
4 |
3 |
3 |
1 |
2 |
3 |
3 |
1 |
1 |
27 |
| Reproduction and dispersal of goshawks in a variable environment | 0 |
3 |
4 |
2 |
2 |
1 |
4 |
3 |
3 |
3 |
2 |
0 |
27 |
| Reproduction and population structure in European aspen | 0 |
2 |
4 |
3 |
3 |
2 |
2 |
1 |
0 |
3 |
0 |
2 |
22 |
| 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 |
158 |
33 |
191 |
| Reproductive partitioning in the polygynous black ant Formica fusca | 1 |
3 |
2 |
0 |
2 |
0 |
3 |
1 |
0 |
2 |
1 |
4 |
19 |
| Reserve network design in fragmented forest landscapes | 1 |
1 |
3 |
3 |
1 |
1 |
0 |
2 |
2 |
3 |
5 |
3 |
25 |
| Response of Scots pine (Pinus sylvestris L.) to a long-term Cu and Ni exposure | 0 |
4 |
1 |
4 |
1 |
4 |
4 |
5 |
3 |
1 |
1 |
3 |
31 |
| Response of the understorey vegetation of boreal forests to heavy metal loading | 0 |
4 |
3 |
5 |
2 |
2 |
2 |
8 |
1 |
5 |
5 |
3 |
40 |
| Responses of Arctic permafrost peatlands to climate changes over the past millennia | 2 |
5 |
1 |
2 |
8 |
2 |
2 |
4 |
3 |
14 |
0 |
1 |
44 |
| Responses of Auditory Supporting Cells to Hair Cell Damage and Death : Cellular Stress Signalling and Epithelial Repair | 1 |
1 |
1 |
3 |
3 |
3 |
0 |
3 |
3 |
1 |
2 |
2 |
23 |
| Responses of invertebrates to human-caused disturbances in East African tropical rainforests : conservation implications | 1 |
2 |
2 |
3 |
1 |
1 |
0 |
2 |
0 |
1 |
1 |
4 |
18 |
| Responses of Pisum Sativum to Soil Arsenate, Lead and Zinc : A Greenhouse Study of Mineral Elements, Phytase Activity, ATP And Chlorophylls | 1 |
1 |
2 |
2 |
0 |
0 |
2 |
3 |
0 |
6 |
0 |
4 |
21 |
| Responses of Scots pine to nickel and copper exposure and herbivory | 0 |
1 |
1 |
0 |
0 |
3 |
5 |
1 |
1 |
1 |
0 |
2 |
15 |
| Restoring vegetation and carbon dynamics in a cut-away peatland | 2 |
1 |
4 |
0 |
2 |
4 |
5 |
9 |
4 |
3 |
4 |
1 |
39 |
| Restrictions in the proliferative potential of inner ear hair cells and supporting cells | 0 |
3 |
2 |
2 |
3 |
0 |
2 |
1 |
0 |
2 |
4 |
2 |
21 |
| Reticulon Homology Domain Containing Protein Families of the Endoplasmic Reticulum | 5 |
3 |
5 |
16 |
15 |
19 |
22 |
19 |
17 |
17 |
16 |
15 |
169 |
| Retrotransposon BARE1 translation, localization, and VLP formation in barley | 1 |
1 |
0 |
3 |
3 |
1 |
0 |
1 |
0 |
1 |
2 |
1 |
14 |
| Revising the actin disassembly machinery : The role of GMF and twinfilin in turnover of dendritic actin arrays | 8 |
8 |
5 |
4 |
3 |
7 |
4 |
5 |
2 |
3 |
11 |
3 |
63 |
| Revision of the family Alycidae (Acariformes, Acari), with special reference to European species | 0 |
7 |
3 |
4 |
2 |
4 |
7 |
2 |
36 |
25 |
6 |
8 |
104 |
| Rhizoctonia -Scots pine interactions : detection, impact on seedling performance and host defence gene response | 1 |
1 |
2 |
1 |
3 |
5 |
1 |
8 |
1 |
4 |
5 |
0 |
32 |
| Risk factors associated to endoscopic retrograde cholangiopancreatography related complications | 8 |
1 |
11 |
12 |
4 |
5 |
5 |
6 |
2 |
7 |
1 |
3 |
65 |
| Risks out of depth? : a study on the environmental impacts of seabed mining | 5 |
6 |
13 |
2 |
9 |
6 |
12 |
1 |
7 |
7 |
6 |
4 |
78 |
| RNA-based next generation sequencing approaches in HLA genotyping and HLA expression quantification | 6 |
9 |
11 |
6 |
10 |
12 |
10 |
10 |
9 |
5 |
6 |
5 |
99 |
| Road Dust from Pavement Wear and Traction Sanding | 4 |
8 |
8 |
2 |
5 |
20 |
10 |
2 |
7 |
6 |
7 |
14 |
93 |
| Role of 3'UTR in the regulation of neurotrophic factors BDNF and GDNF | 1 |
4 |
4 |
5 |
7 |
4 |
5 |
2 |
3 |
9 |
10 |
6 |
60 |
| Role of Actin-mediated Motility of Peripheral Astrocytic Processes in Synaptic Function | 0 |
3 |
5 |
2 |
0 |
1 |
3 |
0 |
1 |
2 |
2 |
1 |
20 |
| Role of allochthonous and autochthonous dissolved organic matter (DOM) as a carbon source for bacterioplankton in boreal humic lakes | 4 |
4 |
5 |
55 |
8 |
6 |
5 |
6 |
9 |
9 |
8 |
4 |
123 |
| Role of cell cycle regulators in development of the inner ear | 0 |
2 |
1 |
2 |
3 |
2 |
0 |
3 |
1 |
3 |
1 |
1 |
19 |
| 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 | 5 |
4 |
14 |
6 |
7 |
10 |
5 |
4 |
10 |
10 |
8 |
7 |
90 |
| Role of Eda and Troy pathways in ectodermal organ development | 1 |
1 |
1 |
4 |
2 |
0 |
1 |
3 |
3 |
6 |
4 |
4 |
30 |
| Role of HMGB1 in cells of the circulation | 2 |
1 |
2 |
2 |
7 |
5 |
3 |
2 |
0 |
2 |
0 |
2 |
28 |
| Role of IL-21 in Regulation of Leukocyte Functions | 2 |
1 |
2 |
0 |
1 |
1 |
3 |
0 |
0 |
1 |
1 |
0 |
12 |
| Role of lignan sources in tumour formation in multiple intestinal neoplasia mice | 9 |
2 |
3 |
1 |
2 |
0 |
1 |
1 |
0 |
1 |
1 |
1 |
22 |
| Role of LKB1 in stem cell fate determination and tumorigenesis | 2 |
5 |
8 |
6 |
6 |
3 |
7 |
3 |
9 |
8 |
10 |
8 |
75 |
| Role of oscillations in visual perception : attention and working memory | 5 |
4 |
5 |
27 |
9 |
3 |
2 |
4 |
9 |
1 |
4 |
5 |
78 |
| Role of RAGE as an Amphoterin Receptor : From Development to Disease | 2 |
1 |
4 |
4 |
4 |
9 |
10 |
95 |
1 |
4 |
4 |
4 |
142 |
| Role of resuspension and silicate in internal phosphorus loading | 2 |
2 |
4 |
4 |
3 |
2 |
2 |
3 |
2 |
4 |
1 |
2 |
31 |
| Role of Temperature in the Biological Activity of a Boreal Forest | 2 |
2 |
1 |
1 |
1 |
2 |
4 |
2 |
12 |
4 |
2 |
4 |
37 |
| Role of the inflammasome pathway in atherosclerosis | 3 |
4 |
2 |
3 |
5 |
5 |
0 |
1 |
2 |
5 |
3 |
2 |
35 |
| Role of WRKY Transcription Factors in Arabidopsis Development and Stress Responses | 9 |
7 |
20 |
4 |
3 |
7 |
2 |
2 |
12 |
10 |
22 |
25 |
123 |
| Roles of GDNF family receptor GFRα2 in the peripheral nervous system | 2 |
5 |
4 |
1 |
5 |
1 |
0 |
2 |
0 |
3 |
2 |
3 |
28 |
| 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 | 0 |
5 |
4 |
2 |
2 |
2 |
1 |
1 |
1 |
2 |
1 |
0 |
21 |
| Salmonella enterica, Listeria monocytogenes and Clostridium perfringens : Diversity of Human Isolates Studied by Phenotypic and Molecular Methods | 5 |
8 |
1 |
1 |
2 |
4 |
3 |
2 |
2 |
2 |
1 |
3 |
34 |
| SARS-CoV-2 entry mechanisms and antiviral strategies | 0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
0 |
100 |
11 |
2 |
113 |
| Sea-ice ecology in the Baltic Sea with special emphasis on bacteria | 0 |
1 |
1 |
0 |
2 |
5 |
2 |
4 |
5 |
4 |
3 |
1 |
28 |
| Search for genetic variants conferring susceptibility to obesity and related metabolic traits | 1 |
3 |
3 |
6 |
6 |
3 |
2 |
2 |
2 |
4 |
1 |
3 |
36 |
| Secchi depth in the Baltic Sea an indicator of eutrophication | 0 |
5 |
2 |
4 |
7 |
3 |
2 |
4 |
7 |
4 |
1 |
5 |
44 |
| Secondary metabolites in Gerbera hybrida | 12 |
9 |
1 |
1 |
2 |
4 |
2 |
3 |
4 |
1 |
1 |
1 |
41 |
| Sediment resuspension as a water quality regulator in lakes | 8 |
7 |
6 |
6 |
7 |
6 |
4 |
5 |
7 |
18 |
53 |
3 |
130 |
| Sedimentary sea-ice proxies in the Arctic: seasonal production, vertical export and taxonomic insights | 13 |
23 |
11 |
28 |
14 |
12 |
10 |
12 |
9 |
11 |
2 |
7 |
152 |
| Sedimentary zooplankton remains as indicators of lake ecological quality and trophic structure | 2 |
2 |
5 |
4 |
4 |
2 |
5 |
2 |
5 |
7 |
0 |
1 |
39 |
| Selective glycoprotein exit from yeast endoplasmic reticulum | 5 |
3 |
4 |
4 |
5 |
1 |
3 |
3 |
4 |
2 |
7 |
1 |
42 |
| Self-assembly of hydrophobin proteins from the fungus Trichoderma reesei | 3 |
4 |
4 |
0 |
1 |
2 |
4 |
5 |
1 |
2 |
2 |
2 |
30 |
| Senescence Ecology : Aging in a Population of Wild Brown Mouse Lemurs (Microcebus rufus) | 2 |
2 |
1 |
8 |
16 |
1 |
6 |
1 |
5 |
1 |
3 |
3 |
49 |
| Serum amyloid A (SAA) : Proinflammatory functions and their regulation by serum lipoproteins | 4 |
4 |
5 |
7 |
4 |
10 |
6 |
4 |
3 |
4 |
9 |
5 |
65 |
| Setting priorities for conservation : protected area effectiveness, management, and quality of governance | 6 |
5 |
5 |
3 |
7 |
1 |
6 |
7 |
4 |
5 |
5 |
2 |
56 |
| Sex chromosome evolution and speciation in stickleback fishes | 9 |
6 |
12 |
0 |
7 |
0 |
5 |
1 |
7 |
2 |
6 |
2 |
57 |
| Shaking Environmental Education Paradigms. Practitioners’ narratives, contextual elements, and biocultural approaches | 0 |
0 |
107 |
19 |
15 |
7 |
10 |
8 |
6 |
5 |
2 |
4 |
183 |
| Short- and long-term consequences of food resources on Ural owl Strix uralensis reproduction | 2 |
1 |
2 |
0 |
0 |
3 |
1 |
3 |
3 |
1 |
2 |
2 |
20 |
| Short-term effects of variable retention on epigaeic spiders and carabid beetles in Finland | 3 |
5 |
2 |
1 |
0 |
0 |
1 |
1 |
0 |
1 |
0 |
2 |
16 |
| Short-term plant-decomposer feedbacks in grassland plants | 1 |
0 |
2 |
1 |
3 |
1 |
1 |
1 |
0 |
2 |
0 |
0 |
12 |
| Should I stay or should I go? : Reproductive and dispersal strategies of site-specific liverwort species | 1 |
2 |
9 |
3 |
5 |
8 |
3 |
4 |
1 |
6 |
0 |
0 |
42 |
| Signaling through the Jak-Stat pathway : Regulation of tyrosine kinase activity | 1 |
4 |
1 |
2 |
4 |
4 |
7 |
3 |
7 |
3 |
4 |
7 |
47 |
| Silicon and its impacts on phosphorus in eutrophic freshwater lakes | 1 |
3 |
3 |
4 |
4 |
1 |
1 |
4 |
4 |
0 |
1 |
2 |
28 |
| Social polymorphism and dispersal in Formica ants | 2 |
3 |
4 |
7 |
10 |
8 |
5 |
5 |
2 |
6 |
6 |
2 |
60 |
| Socio-Ecological Resilience of a Small-Scale Hilsa Shad (Tenualosa ilisha) Fishery in the Gangetic River Systems of Bangladesh | 5 |
2 |
4 |
9 |
2 |
2 |
6 |
20 |
5 |
4 |
4 |
6 |
69 |
| Soil microbial dynamics and the condition of Norway spruce on the Bothnian land-uplift coast | 3 |
1 |
1 |
5 |
1 |
0 |
2 |
1 |
0 |
0 |
0 |
0 |
14 |
| Sostdc1 Plays an Essential Role in Mammalian Tooth Patterning : Insight into the Rodent Dental Evolution | 5 |
12 |
29 |
29 |
7 |
0 |
4 |
9 |
9 |
10 |
5 |
13 |
132 |
| Spacing behaviour of the Siberian flying squirrel : effects of landscape structure | 8 |
2 |
4 |
2 |
2 |
2 |
1 |
12 |
4 |
2 |
2 |
3 |
44 |
| Spatial and temporal determinants of Finnish farmland bird populations | 0 |
5 |
2 |
3 |
2 |
7 |
5 |
5 |
1 |
4 |
1 |
6 |
41 |
| Spatial conservation prioritization for Finnish forest conservation management | 2 |
8 |
3 |
48 |
4 |
6 |
6 |
5 |
3 |
7 |
2 |
3 |
97 |
| Spatial ecology of a specialist insect herbivore : the leaf-mining moth Tischeria ekebladella on the pedunculate oak Quercus robur | 1 |
6 |
1 |
3 |
4 |
2 |
1 |
1 |
1 |
1 |
3 |
0 |
24 |
| Spatial ecology of an oak-associated herbivore community : A metacommunity of herbivores | 1 |
3 |
4 |
3 |
2 |
4 |
2 |
5 |
9 |
4 |
3 |
5 |
45 |
| Spatial ecology of dung beetles | 2 |
2 |
4 |
6 |
5 |
6 |
10 |
7 |
4 |
8 |
8 |
4 |
66 |
| Spatial ecology of food webs : herbivore-parasitoid communities on the pedunculate oak | 4 |
1 |
1 |
2 |
3 |
1 |
6 |
1 |
0 |
0 |
2 |
4 |
25 |
| Spatial population dynamics in reserve-network design | 1 |
0 |
2 |
1 |
1 |
2 |
1 |
1 |
2 |
1 |
0 |
0 |
12 |
| Spatial processes in ecology and evolution, and implications for conservation | 1 |
1 |
4 |
4 |
1 |
1 |
8 |
2 |
1 |
6 |
4 |
3 |
36 |
| Spatial variability in benthic macrofauna communities and associated ecosystem functions across coastal habitats | 6 |
38 |
3 |
9 |
3 |
5 |
6 |
4 |
7 |
4 |
8 |
3 |
96 |
| Spatiotemporality of carbon fluxes along a boreal land-stream-lake continuum | 1 |
5 |
3 |
2 |
0 |
0 |
3 |
1 |
9 |
6 |
4 |
7 |
41 |
| Species turnover of aquatic organisms in space and time : Patterns in community composition and diversity | 1 |
0 |
3 |
9 |
2 |
2 |
3 |
3 |
1 |
2 |
4 |
1 |
31 |
| Species-based and community-level approaches to conservation prioritization | 1 |
0 |
0 |
1 |
3 |
1 |
3 |
44 |
2 |
4 |
2 |
2 |
63 |
| Spectral and thermal properties of amphibian visual pigments related to molecular structure | 1 |
0 |
2 |
0 |
1 |
0 |
0 |
3 |
2 |
3 |
2 |
4 |
18 |
| Sphagnum-associated methanotrophs : a resilient CH4 biofilter in pristine and disturbed peatlands | 0 |
2 |
2 |
2 |
1 |
1 |
4 |
2 |
4 |
2 |
3 |
1 |
24 |
| Spring bloom dynamics in the Baltic Sea : from the environment to macroelements and microbial interactions | 2 |
4 |
2 |
1 |
4 |
3 |
3 |
5 |
6 |
2 |
7 |
6 |
45 |
| Springtime Episode Acidification as a Regulatory Factor of Estuary Spawning Fish Recruitment | 2 |
6 |
1 |
4 |
7 |
1 |
1 |
8 |
3 |
3 |
1 |
1 |
38 |
| Staphylococcus aureus and Lactobacillus crispatus : Adhesive characteristics of two Gram-positive bacterial species | 0 |
4 |
3 |
3 |
3 |
1 |
0 |
3 |
1 |
2 |
4 |
4 |
28 |
| Statistical methods for detecting signals of natural selection in the wild | 1 |
3 |
6 |
2 |
2 |
5 |
3 |
0 |
2 |
3 |
3 |
1 |
31 |
| Steps towards comprehensive Bayesian decision analysis in fisheries and environmental management | 9 |
5 |
2 |
0 |
2 |
0 |
10 |
1 |
3 |
4 |
3 |
5 |
44 |
| Sticky business : diversity and evolution of Mycocaliciales (Ascomycota) on plant exudates | 4 |
3 |
6 |
1 |
1 |
1 |
5 |
10 |
1 |
3 |
4 |
2 |
41 |
| Strategies to Improve Standardization and Robustness of Toxicogenomics Data Analysis | 1 |
2 |
1 |
6 |
0 |
4 |
6 |
4 |
8 |
7 |
3 |
8 |
50 |
| Stress and developmental responses in Arabidopsis thaliana : regulation through the transcription factor-interacting protein RCD1 | 1 |
2 |
3 |
3 |
3 |
0 |
5 |
9 |
2 |
10 |
3 |
7 |
48 |
| Stress responses of Gram-positive bacteria to cationic antimicrobial peptides | 1 |
0 |
1 |
2 |
2 |
2 |
0 |
2 |
3 |
1 |
0 |
1 |
15 |
| Strong in the Real Way : Protein-Protein and Protein-Lipid Interactions in Tick-Borne Encephalitis Virus Stability and Assembly | 6 |
13 |
6 |
5 |
6 |
5 |
7 |
4 |
7 |
7 |
5 |
3 |
74 |
| Structural and biochemical studies of a posttranslational modification platform in early Eukaryota | 2 |
2 |
9 |
0 |
1 |
0 |
3 |
0 |
2 |
7 |
3 |
3 |
32 |
| Structural and functional characterization of leucine-rich repeat synaptic adhesion molecules | 3 |
0 |
1 |
3 |
4 |
2 |
0 |
1 |
2 |
9 |
3 |
0 |
28 |
| Structural and functional roles of KCC2 in developing cortex | 1 |
3 |
4 |
4 |
1 |
4 |
2 |
1 |
0 |
1 |
3 |
3 |
27 |
| Structural and Functional Studies on Trimeric Autotransporters | 1 |
0 |
0 |
2 |
3 |
4 |
1 |
2 |
1 |
4 |
1 |
3 |
22 |
| Structural basis of cytoskeletal regulation by twinfilin | 1 |
2 |
1 |
4 |
1 |
2 |
1 |
1 |
1 |
3 |
3 |
2 |
22 |
| Structural Evolution of Function and Stability in Muconate Lactonizing Enzymes | 2 |
2 |
0 |
1 |
4 |
3 |
1 |
4 |
0 |
1 |
1 |
7 |
26 |
| Structural stability and binding properties of soluble and membrane-anchored recombinant antibodies | 0 |
1 |
2 |
2 |
1 |
1 |
1 |
2 |
2 |
3 |
2 |
3 |
20 |
| Structural Studies of Membrane-Bound Pyrophosphatases | 14 |
8 |
2 |
2 |
2 |
7 |
7 |
5 |
5 |
3 |
10 |
5 |
70 |
| Structural Studies on Inteins | 2 |
4 |
2 |
2 |
2 |
3 |
5 |
4 |
3 |
2 |
0 |
3 |
32 |
| Structural studies on lysosomal proteins | 1 |
4 |
3 |
3 |
0 |
3 |
1 |
0 |
4 |
3 |
2 |
2 |
26 |
| Structural studies on members of the picornavirus superfamily | 2 |
4 |
3 |
2 |
2 |
2 |
2 |
3 |
1 |
2 |
1 |
2 |
26 |
| Structural studies on viral receptor-binding proteins | 2 |
1 |
1 |
2 |
4 |
2 |
1 |
2 |
4 |
1 |
3 |
1 |
24 |
| Structure and Assembly of Membrane-Containing dsDNA Bacteriophages | 0 |
1 |
4 |
1 |
1 |
2 |
0 |
0 |
0 |
3 |
1 |
1 |
14 |
| Structure and Dynamics of Coil-like Molecules by Residual Dipolar Couplings | 2 |
1 |
1 |
2 |
0 |
2 |
1 |
1 |
1 |
1 |
2 |
3 |
17 |
| Structure and function of GDNF receptor alpha splice variants | 0 |
0 |
0 |
4 |
1 |
1 |
5 |
0 |
2 |
1 |
2 |
3 |
19 |
| Structure and Function of PH and WW domains | 7 |
3 |
3 |
4 |
6 |
2 |
5 |
2 |
2 |
2 |
8 |
1 |
45 |
| Structure, function and intracellular dynamics of alphavirus replication complexes | 5 |
35 |
6 |
2 |
6 |
9 |
12 |
7 |
6 |
4 |
5 |
1 |
98 |
| Structure-function relations in AMPA receptors | 0 |
1 |
1 |
1 |
1 |
1 |
0 |
0 |
0 |
2 |
1 |
1 |
9 |
| Structure-function relationships in the omptin family of enterobacterial proteases/adhesins | 6 |
2 |
2 |
5 |
3 |
2 |
1 |
2 |
0 |
1 |
2 |
1 |
27 |
| Structure-Function Studies of GDNF Family Ligand-RET signalling | 2 |
5 |
2 |
1 |
8 |
0 |
2 |
3 |
1 |
1 |
1 |
3 |
29 |
| Studies on dinoflagellates in the northern Baltic Sea | 10 |
4 |
7 |
3 |
8 |
1 |
7 |
3 |
9 |
5 |
1 |
5 |
63 |
| Studies on palmitoyl-protein thioesterase 1 : Implications for synaptic functions | 1 |
1 |
4 |
3 |
1 |
0 |
0 |
0 |
0 |
1 |
1 |
1 |
13 |
| Studies on planktonic brackish water microprotozoans with special emphasis on the role of ciliates as grazers | 4 |
3 |
3 |
3 |
2 |
1 |
1 |
6 |
0 |
4 |
2 |
1 |
30 |
| Studies on the neurotrophic factor Manf and the pleiotropic factor Lin-28 during Drosophila development | 4 |
1 |
1 |
7 |
1 |
6 |
6 |
5 |
5 |
8 |
2 |
4 |
50 |
| Studying connectivity in the neonatal EEG | 2 |
2 |
7 |
7 |
2 |
1 |
6 |
3 |
1 |
7 |
4 |
2 |
44 |
| Submerged macrophytes modify food web interactions and stability of lake littoral ecosystems | 2 |
0 |
2 |
3 |
1 |
2 |
0 |
0 |
1 |
1 |
0 |
2 |
14 |
| Substance flow analysis in Finland : Four case studies on N and P flows | 1 |
2 |
5 |
0 |
2 |
4 |
3 |
2 |
2 |
5 |
1 |
2 |
29 |
| Substrate Selectivity and Molecular Adaptation in the Outer Membrane Proteases of Yersinia pestis and Salmonella enterica | 5 |
4 |
0 |
3 |
0 |
4 |
0 |
6 |
8 |
4 |
1 |
1 |
36 |
| Successional and spatial patterns of bacterial communities in hydrocarbon-contaminated soils and Populus rhizosphere | 1 |
4 |
3 |
4 |
0 |
2 |
3 |
1 |
0 |
2 |
1 |
1 |
22 |
| Surface protein Pls of methicillin-resistant Staphylococcus aureus : role in adhesion, invasion and pathogenesis, and evolutionary aspects | 1 |
0 |
1 |
3 |
1 |
3 |
3 |
3 |
4 |
3 |
1 |
2 |
25 |
| Surface Proteins of Lactobacillus crispatus : Adhesive Properties and Cell Wall Anchoring | 1 |
3 |
3 |
1 |
3 |
1 |
3 |
4 |
4 |
3 |
4 |
3 |
33 |
| Sustainability Conceptualisation, Operationalisation, and Realisation : Perspectives on Urban Transportation Policy-Making and Planning | 5 |
10 |
15 |
23 |
15 |
4 |
12 |
4 |
8 |
9 |
2 |
9 |
116 |
| Sustainable development indicators : Much wanted, less used? | 5 |
2 |
3 |
2 |
0 |
1 |
2 |
3 |
1 |
8 |
0 |
2 |
29 |
| Sustainable forest management : ecologically sound and socially accepted | 1 |
5 |
11 |
3 |
1 |
2 |
7 |
1 |
3 |
3 |
2 |
5 |
44 |
| Sustainable harvesting in variable environments | 3 |
1 |
3 |
4 |
3 |
2 |
2 |
0 |
0 |
6 |
2 |
2 |
28 |
| Sustained inhibition of hippocampal networks in perinatal development | 4 |
3 |
3 |
2 |
3 |
1 |
1 |
1 |
2 |
2 |
2 |
0 |
24 |
| Swimming through troubled waters : Eutrophication of the Baltic Sea and parasites of the threespine stickleback | 2 |
4 |
1 |
3 |
1 |
0 |
4 |
0 |
2 |
3 |
1 |
1 |
22 |
| Symplastically transmitted signals regulate pattern formation during root development in Arabidopsis thaliana | 3 |
3 |
2 |
3 |
2 |
2 |
0 |
0 |
0 |
1 |
4 |
1 |
21 |
| Synaptic mechanisms of Hebbian and homeostatic plasticity driven by intrinsic activity in the developing hippocampus | 0 |
0 |
4 |
5 |
4 |
5 |
2 |
4 |
1 |
10 |
9 |
2 |
46 |
| Syndecan-3 in neural plasticity : From cell surface interactions to cytoskeletal regulation | 5 |
4 |
6 |
3 |
3 |
2 |
1 |
2 |
3 |
1 |
0 |
2 |
32 |
| Synthesis of neoglycoconjugates and oligosaccharides with potential anti-Helicobacter pylori activity | 0 |
1 |
3 |
1 |
0 |
1 |
3 |
3 |
0 |
5 |
1 |
2 |
20 |
| Systematizing morphology : a total evidence approach to ditrysian phylogenetics (Lepidoptera) | 0 |
3 |
3 |
2 |
2 |
0 |
0 |
0 |
0 |
3 |
2 |
2 |
17 |
| Systemic signaling in plant gas exchange | 4 |
7 |
5 |
14 |
2 |
3 |
2 |
0 |
6 |
3 |
3 |
1 |
50 |
| Systems biology view of receptor tyrosine kinase functions and their oncofusions | 1 |
5 |
4 |
1 |
4 |
5 |
7 |
1 |
2 |
6 |
4 |
6 |
46 |
| Systems Toxicology Approach in Nanosafety : From In vivo Towards In vitro Testing | 1 |
5 |
1 |
1 |
0 |
1 |
0 |
4 |
2 |
1 |
1 |
0 |
17 |
| Systems-level neural mechanisms of conscious perception in health and schizophrenia | 0 |
0 |
4 |
0 |
2 |
2 |
1 |
5 |
5 |
5 |
1 |
3 |
28 |
| Taphrina as model phytopathogenic yeasts infecting the model plant Arabidopsis and woody plant Betula pendula | 6 |
7 |
6 |
11 |
7 |
10 |
6 |
10 |
3 |
9 |
15 |
2 |
92 |
| Targeting GDNF receptors with small molecules for the treatment of Parkinson’s disease | 1 |
6 |
16 |
14 |
3 |
6 |
4 |
5 |
8 |
7 |
4 |
4 |
78 |
| Targeting STAT3 and kinases in lymphoid malignancies | 5 |
13 |
10 |
7 |
4 |
4 |
5 |
6 |
7 |
6 |
11 |
5 |
83 |
| Tau pathology : secretion and internalization as the key for understanding protein propagation | 3 |
5 |
2 |
5 |
5 |
1 |
4 |
1 |
2 |
0 |
9 |
3 |
40 |
| Taxon delineation in gelechioid moths : from phylogenetics to DNA barcoding | 4 |
4 |
1 |
8 |
3 |
3 |
2 |
3 |
6 |
4 |
1 |
3 |
42 |
| Taxonomic and phylogenetic studies on Salicornioideae (Amaranthaceae) | 3 |
3 |
4 |
1 |
9 |
5 |
1 |
4 |
9 |
8 |
16 |
3 |
66 |
| Taxonomic Studies of the Bartramiaceae, Bryopsida | 4 |
1 |
2 |
5 |
3 |
8 |
4 |
10 |
4 |
5 |
7 |
2 |
55 |
| Taxonomy and phylogeny of brown-rot fungi in the Antrodia complex (Polyporales, Basidiomycota) | 6 |
5 |
4 |
3 |
8 |
1 |
8 |
3 |
3 |
6 |
1 |
3 |
51 |
| Taxonomy and phylogeny of the manna lichens and allied species (Megasporaceae) | 12 |
32 |
6 |
2 |
4 |
6 |
6 |
5 |
3 |
9 |
7 |
4 |
96 |
| Taxonomy and phylogeny of white-rot polypores : case studies in Hymenochaetales and Polyporales (Basidiomycota) | 3 |
6 |
2 |
4 |
5 |
1 |
3 |
5 |
3 |
3 |
3 |
2 |
40 |
| Telecouplings in a globalizing world : linking food consumption to outsourced resource use and displaced environmental impacts | 3 |
6 |
9 |
7 |
12 |
8 |
5 |
7 |
6 |
3 |
10 |
3 |
79 |
| Temporal and Density-dependent Variability as Source for Uncertainty in Fish Population Dynamics | 2 |
1 |
2 |
1 |
0 |
0 |
0 |
1 |
1 |
1 |
1 |
0 |
10 |
| Temporal and regional patterns of atmospheric components affecting acidification in Finland | 1 |
2 |
1 |
1 |
1 |
0 |
1 |
0 |
0 |
2 |
0 |
0 |
9 |
| Temporal and spatial turnover of freshwater diatoms : Implications for bioassessment | 2 |
2 |
1 |
0 |
1 |
6 |
5 |
6 |
3 |
2 |
2 |
1 |
31 |
| Temporal habitat dynamics and conservation planning : The case of the false heath fritillary | 0 |
3 |
1 |
0 |
2 |
1 |
2 |
6 |
1 |
1 |
6 |
2 |
25 |
| The bacterial and fungal communities in the nests of the ant Formica exsecta | 2 |
2 |
2 |
0 |
1 |
1 |
6 |
4 |
5 |
6 |
5 |
4 |
38 |
| The biodiversity hypothesis of allergy : The interrelations between the skin microbiota, allergic diseases and exposure to microbes in residential environments | 11 |
5 |
12 |
6 |
7 |
2 |
9 |
12 |
7 |
13 |
9 |
4 |
97 |
| The biological functions of mouse twinfilin isoforms | 2 |
2 |
0 |
2 |
4 |
1 |
1 |
3 |
0 |
1 |
1 |
2 |
19 |
| The BMX Tyrosine Kinase : A Signal Mediator in Hematopoietic and Endothelial/Epithelial Cells | 1 |
1 |
1 |
1 |
1 |
2 |
2 |
4 |
3 |
3 |
3 |
1 |
23 |
| The community of medium-sized carnivores : the interactions between species, habitats and rabies | 5 |
2 |
5 |
2 |
1 |
1 |
4 |
1 |
3 |
1 |
0 |
1 |
26 |
| The consequences of spatial environmental variability on dispersal and on the spatial distribution of species | 2 |
3 |
1 |
3 |
1 |
1 |
5 |
1 |
1 |
26 |
4 |
6 |
54 |
| The contributions of soil, ground vegetation and trees to the methane exchange of boreal forest | 8 |
10 |
7 |
14 |
8 |
3 |
4 |
10 |
6 |
6 |
4 |
3 |
83 |
| The cysteine-rich receptor-like kinase CRK2 during stress responses in Arabidopsis thaliana | 17 |
8 |
6 |
33 |
9 |
5 |
2 |
6 |
3 |
5 |
6 |
6 |
106 |
| The Developmental Basis for the Evolution of Muroid Dentition | 0 |
1 |
11 |
1 |
2 |
0 |
7 |
2 |
5 |
3 |
7 |
6 |
45 |
| The DISC1 gene network in major mental illnesses in Finland | 1 |
6 |
3 |
1 |
0 |
6 |
1 |
3 |
2 |
9 |
3 |
6 |
41 |
| The easy explanation - exploring the link between drought and food security in the East and Horn of Africa | 1 |
2 |
3 |
0 |
1 |
1 |
9 |
9 |
1 |
1 |
1 |
0 |
29 |
| The Ecology and Evolution of Melitaeine Butterflies | 0 |
3 |
2 |
3 |
6 |
9 |
28 |
40 |
5 |
4 |
3 |
6 |
109 |
| The ecophysiology of plasma membrane aquaporins in Arabidopsis thaliana and Fagus sylvatica | 2 |
7 |
2 |
3 |
2 |
5 |
3 |
0 |
3 |
4 |
14 |
2 |
47 |
| The effect of lignin content and lignin modification on Norway spruce wood properties and decay resistance | 2 |
5 |
2 |
0 |
1 |
1 |
12 |
0 |
1 |
2 |
0 |
2 |
28 |
| The effect of living environment and environmental exposure on the composition of microbial community in soil, on human skin and in the gut | 1 |
4 |
10 |
7 |
6 |
8 |
7 |
2 |
7 |
5 |
0 |
2 |
59 |
| The effect of turbidity on the ecology of pike larvae | 5 |
1 |
2 |
3 |
4 |
4 |
7 |
2 |
2 |
5 |
5 |
4 |
44 |
| The effects of eutrophication on alternative reproductive tactics in threespine sticklebacks | 1 |
1 |
2 |
2 |
1 |
1 |
1 |
0 |
2 |
1 |
0 |
0 |
12 |
| 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 | 3 |
7 |
3 |
5 |
7 |
3 |
5 |
4 |
9 |
8 |
17 |
4 |
75 |
| The effects of habitat changes, conservation measures and interspecific interactions on forest-dwelling hawks | 0 |
2 |
2 |
4 |
1 |
2 |
15 |
10 |
11 |
5 |
6 |
8 |
66 |
| The effects of habitat edges and trampling intensity on vegetation in urban forests | 2 |
12 |
13 |
10 |
6 |
7 |
16 |
11 |
15 |
10 |
4 |
5 |
111 |
| The effects of recent eutrophication on freshwater fish communities and fishery on the northern coast of the Gulf of Finland, Baltic Sea | 2 |
3 |
6 |
2 |
9 |
3 |
2 |
13 |
3 |
5 |
5 |
5 |
58 |
| 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 | 6 |
6 |
9 |
6 |
3 |
8 |
6 |
7 |
6 |
10 |
9 |
4 |
80 |
| The environment in the headlines : Newspaper coverage of climate change and eutrophication in Finland | 5 |
9 |
4 |
15 |
7 |
2 |
4 |
4 |
2 |
3 |
4 |
2 |
61 |
| The establishment of efficient methods to culture immunosuppressive mesenchymal stromal cells from cord blood and bone marrow | 5 |
1 |
6 |
4 |
5 |
2 |
7 |
4 |
2 |
4 |
5 |
1 |
46 |
| The evolution of new enterovirus types EV-94, EV-96 and EV-97 | 6 |
31 |
21 |
86 |
15 |
10 |
3 |
3 |
3 |
5 |
5 |
1 |
189 |
| The Extracellular Regulation of Bone Morphogenetic Proteins in Drosophila and Sawfly Wing | 3 |
1 |
2 |
6 |
3 |
0 |
6 |
5 |
2 |
5 |
4 |
1 |
38 |
| The family Herbertaceae and its novel systematic position within liverworts | 6 |
3 |
1 |
2 |
3 |
2 |
2 |
3 |
5 |
3 |
5 |
5 |
40 |
| The fate and effects of lead (Pb) at active and abandoned shooting ranges in a boreal forest ecosystem | 2 |
5 |
5 |
4 |
4 |
1 |
5 |
2 |
7 |
4 |
1 |
2 |
42 |
| The fate of urban-derived contaminants in boreal environments | 0 |
1 |
1 |
3 |
1 |
0 |
2 |
2 |
0 |
2 |
0 |
0 |
12 |
| The function and regulation of the U11-48K protein in U12-dependent splicing | 6 |
3 |
2 |
0 |
3 |
1 |
3 |
0 |
0 |
1 |
1 |
1 |
21 |
| The genome packaging machinery of dsDNA bacteriophage PRD1 | 6 |
1 |
8 |
4 |
2 |
3 |
2 |
2 |
3 |
6 |
2 |
0 |
39 |
| The Gerbera cDNA Microarray : A Tool for Large-Scale Identification of Genes Involved in Flower Development | 1 |
4 |
2 |
0 |
0 |
4 |
1 |
1 |
0 |
1 |
0 |
0 |
14 |
| The Growth Responses of Fish to Differences in Acidity-Related Lake Charasteristics and Fish Species Composition | 0 |
5 |
1 |
1 |
3 |
2 |
3 |
1 |
1 |
3 |
0 |
1 |
21 |
| The HELCOM Ecosystem Approach : time for quantification, integration and measures | 6 |
2 |
1 |
0 |
2 |
5 |
8 |
1 |
2 |
10 |
6 |
9 |
52 |
| The hERG1 (KV11.1) potassium channel : its modulation and the functional characterisation of genetic variants | 4 |
6 |
4 |
3 |
4 |
4 |
4 |
5 |
3 |
7 |
0 |
0 |
44 |
| The high- and low-activity forms of human plasma phospholipid transfer protein (PLTP) | 5 |
2 |
2 |
3 |
4 |
4 |
2 |
1 |
3 |
2 |
4 |
1 |
33 |
| The Human Microbiome in Parkinson’s Disease and Primary Sclerosing Cholangitis | 1 |
0 |
2 |
5 |
4 |
4 |
4 |
0 |
1 |
3 |
5 |
1 |
30 |
| The Human UDP-Glucuronosyltransferases : Studies on Substrate Binding and Catalytic Mechanism | 7 |
9 |
2 |
6 |
7 |
2 |
4 |
3 |
4 |
3 |
8 |
5 |
60 |
| The impact of FSC certification on timber tree regeneration and floristic composition in Honduran community forests | 2 |
0 |
3 |
1 |
3 |
1 |
2 |
4 |
7 |
7 |
4 |
2 |
36 |
| The Impact of Membrane Phospholipid Composition and Extracellular Vesicles on the Immunoregulative Properties of Human Mesenchymal Stromal Cells | 0 |
4 |
5 |
1 |
3 |
4 |
1 |
2 |
3 |
43 |
3 |
11 |
80 |
| The impacts of forestry on polyporous fungi in boreal forests | 1 |
7 |
5 |
4 |
1 |
1 |
64 |
12 |
3 |
3 |
2 |
3 |
106 |
| The impacts of temperature on the long-term variation in migration and breeding performance of birds | 4 |
5 |
5 |
6 |
6 |
5 |
3 |
3 |
3 |
5 |
0 |
1 |
46 |
| The importance of forested mire margin plant communities for the diversity of managed boreal forests in Finland | 0 |
6 |
2 |
2 |
4 |
7 |
4 |
1 |
3 |
9 |
1 |
1 |
40 |
| The influence of eutrophication on sexual selection in sticklebacks | 2 |
1 |
1 |
2 |
1 |
4 |
6 |
1 |
4 |
10 |
3 |
4 |
39 |
| The integration of developmental signals during root procambial patterning in Arabidopsis thaliana | 1 |
2 |
3 |
1 |
1 |
3 |
3 |
5 |
5 |
3 |
6 |
6 |
39 |
| The life cycle and genetic structure of the red alga Furcellaria lumbricalis on a salinity gradient | 1 |
4 |
5 |
3 |
2 |
2 |
6 |
4 |
6 |
23 |
5 |
8 |
69 |
| The limits of visual sensitivity and its circadian control | 1 |
2 |
6 |
6 |
3 |
1 |
2 |
1 |
8 |
5 |
6 |
3 |
44 |
| The limits to traffic volume growth : The content and procedure of administrative futures studies on Finnish transport CO2 policy | 8 |
4 |
16 |
5 |
6 |
4 |
5 |
2 |
5 |
5 |
6 |
4 |
70 |
| The Mads World of Floral Regulators in Gerbera Hybrida | 5 |
3 |
1 |
4 |
1 |
1 |
0 |
6 |
1 |
17 |
4 |
1 |
44 |
| The mast cell as a regulator of atherosclerotic plaque stability | 2 |
4 |
4 |
5 |
1 |
7 |
1 |
1 |
0 |
1 |
1 |
2 |
29 |
| The Mechanisms, Applications, and Target Site Selection of Bacteriophage Mu Minimal in vitro DNA Transposition Reaction | 1 |
5 |
2 |
3 |
3 |
0 |
1 |
2 |
0 |
3 |
0 |
8 |
28 |
| The Molecular Basis of Hydrolethalus Syndrome | 0 |
3 |
1 |
2 |
0 |
1 |
1 |
5 |
9 |
1 |
7 |
7 |
37 |
| The neuronal cell adhesion molecule ICAM-5 | 1 |
6 |
6 |
5 |
4 |
3 |
3 |
0 |
2 |
2 |
1 |
2 |
35 |
| The nuclear import mechanism of SRF co-activator MKL1 | 5 |
3 |
4 |
5 |
2 |
2 |
2 |
2 |
0 |
4 |
1 |
0 |
30 |
| The NUP98-NSD1 fusion gene in acute myeloid leukemia | 11 |
6 |
5 |
7 |
2 |
6 |
5 |
3 |
2 |
9 |
11 |
16 |
83 |
| The Population Consequences of Sex and Conflict | 4 |
4 |
1 |
0 |
1 |
1 |
1 |
0 |
1 |
2 |
0 |
2 |
17 |
| The Power of Perspectives : Developing and Implementing Inter and Transdisciplinary Methods to Address Wicked Socio-Environmental Problems | 7 |
7 |
8 |
2 |
4 |
0 |
6 |
4 |
2 |
0 |
9 |
4 |
53 |
| The Pseudomonas syringae-derived HrpA pilins : molecular characterization and biotechnological application of the transcripts | 2 |
2 |
0 |
2 |
0 |
0 |
0 |
1 |
0 |
2 |
1 |
0 |
10 |
| The range expansion of the European map butterfly in Finland | 1 |
3 |
2 |
1 |
1 |
2 |
0 |
2 |
1 |
0 |
1 |
0 |
14 |
| The regulation of U12-dependent splicing and its significance to mRNA stability | 3 |
3 |
2 |
1 |
2 |
5 |
2 |
3 |
1 |
5 |
2 |
2 |
31 |
| The role of a tapeworm Diphyllobothrium ditremum Creplin in the regulation mechanisms of a subarctic whitefish (Coregonus lavaretus (L.)) population | 1 |
2 |
4 |
5 |
4 |
5 |
4 |
1 |
2 |
2 |
3 |
3 |
36 |
| The role of bioactive lipid mediators and extracellular vesicles in mesenchymal stromal cell immunomodulation | 1 |
5 |
2 |
2 |
2 |
0 |
2 |
5 |
2 |
6 |
11 |
4 |
42 |
| The Role of Calcium and Protein Phosphatases in Cold Signal Transduction in Arabidopsis thaliana | 1 |
3 |
2 |
3 |
3 |
1 |
0 |
0 |
0 |
1 |
3 |
0 |
17 |
| The role of cortical oscillations in the estimation and maintenance of sensory and duration information in working memory | 5 |
0 |
5 |
1 |
3 |
1 |
2 |
1 |
5 |
3 |
6 |
3 |
35 |
| The role of cyclase-associated protein (CAP) in actin dynamics during cell motility and morphogenesis | 7 |
5 |
1 |
0 |
3 |
8 |
2 |
0 |
3 |
4 |
1 |
2 |
36 |
| The role of cysteine-rich receptor-like protein kinases in ROS signaling in Arabidopsis thaliana | 8 |
6 |
1 |
3 |
2 |
3 |
2 |
6 |
2 |
4 |
12 |
10 |
59 |
| The role of environmental factors in regulating planktivorous predation : Interactive effects of turbulence and visibility conditions | 3 |
3 |
2 |
5 |
4 |
3 |
4 |
2 |
3 |
3 |
6 |
3 |
41 |
| The role of hybrids in the process of speciation : a study of naturally occurring Formica wood ant hybrids | 7 |
3 |
3 |
3 |
3 |
2 |
4 |
1 |
5 |
7 |
5 |
9 |
52 |
| The role of Kainate receptor auxiliary subunits NETO1 and NETO2 in development of hippocampal circuitry | 0 |
1 |
1 |
3 |
3 |
2 |
3 |
1 |
9 |
3 |
1 |
2 |
29 |
| The role of MADS and TCP transcription factors in Gerbera hybrida flower development | 4 |
5 |
1 |
1 |
0 |
0 |
5 |
1 |
0 |
2 |
3 |
1 |
23 |
| The Role of Mast Cells in Foam Cell Formation, Growth Inhibition, and Apoptosis of Smooth Muscle Cells | 0 |
3 |
1 |
1 |
1 |
3 |
3 |
0 |
0 |
2 |
1 |
3 |
18 |
| The role of multi-scale phase synchronization and cross-frequency interactions in cognitive integration | 4 |
3 |
6 |
17 |
7 |
7 |
6 |
14 |
8 |
28 |
4 |
9 |
113 |
| The role of phosphorus as a regulator of bloom-forming diazotrophic cyanobacteria in the Baltic Sea | 0 |
4 |
5 |
4 |
2 |
2 |
8 |
3 |
4 |
4 |
2 |
3 |
41 |
| The role of productivity in the ecological and evolutionary dynamics of predator-prey interaction | 3 |
1 |
4 |
3 |
2 |
1 |
2 |
6 |
1 |
4 |
4 |
7 |
38 |
| The role of the feeding migration and diet of Atlantic salmon (Salmo salar L.) in yolk-sac-fry mortality in the Baltic Sea | 1 |
5 |
4 |
0 |
2 |
1 |
1 |
1 |
3 |
4 |
2 |
1 |
25 |
| The Role of TRKB Receptor Complex Proteins and the Lipid Environment In the Mechanism of Antidepressant Drug Action | 4 |
37 |
12 |
15 |
11 |
14 |
15 |
9 |
7 |
6 |
4 |
5 |
139 |
| The role of zooplankton in littoral communities : Diversity and food web interactions in the Baltic Sea | 5 |
6 |
3 |
3 |
5 |
2 |
4 |
1 |
5 |
3 |
2 |
0 |
39 |
| The roles of nitrification and nitrate reduction pathways in nitrogen cycling of Baltic Sea | 6 |
4 |
5 |
2 |
1 |
1 |
2 |
2 |
1 |
2 |
1 |
3 |
30 |
| The Roles of Template RNA and Replication Proteins in the Formation of Semliki Forest Virus Replication Spherules | 0 |
7 |
4 |
3 |
2 |
0 |
2 |
2 |
2 |
1 |
24 |
33 |
80 |
| The Roles of WOL and APL in Phloem Development in Arabidopsis thaliana Roots | 3 |
4 |
2 |
31 |
12 |
6 |
7 |
9 |
6 |
9 |
12 |
9 |
110 |
| The scent of brood recognition in Formica ants | 5 |
4 |
2 |
2 |
1 |
0 |
0 |
1 |
2 |
6 |
0 |
1 |
24 |
| The serine proteinases of Fusarium grown on cereal proteins and in barley grain and their inhibition by barley proteins | 0 |
1 |
2 |
1 |
0 |
4 |
3 |
2 |
3 |
5 |
3 |
2 |
26 |
| The Size of Major Mammalian Sensory Organs as Measured from Cranial Characters, and Their Relation to the Biology and Evolution of Mammals | 11 |
27 |
26 |
20 |
2 |
0 |
3 |
0 |
3 |
3 |
1 |
3 |
99 |
| The Structure and Dynamics of the Actin Cytoskeleton in the Axon Initial Segment | 0 |
2 |
0 |
0 |
1 |
0 |
2 |
3 |
0 |
1 |
2 |
6 |
17 |
| The Togavirus RNA Replication Complex | 7 |
26 |
7 |
17 |
28 |
21 |
11 |
12 |
21 |
16 |
15 |
0 |
181 |
| The toxicity of Fusarium mycotoxins enniatin and moniliformin | 5 |
0 |
4 |
3 |
4 |
7 |
3 |
3 |
3 |
3 |
1 |
0 |
36 |
| The Transcriptional Regulation of Retrotransposon BARE | 5 |
1 |
2 |
0 |
0 |
1 |
0 |
0 |
2 |
2 |
1 |
3 |
17 |
| The viral coat protein is regulated by HSP70 and HSP40 in Potato virus A infection | 1 |
1 |
4 |
3 |
8 |
3 |
3 |
3 |
7 |
2 |
7 |
3 |
45 |
| The visual preferences for forest regeneration and field afforestation : four case studies in Finland | 1 |
0 |
4 |
4 |
8 |
6 |
5 |
7 |
3 |
12 |
7 |
5 |
62 |
| The VP1 intracapsid hook and uncoating of enteroviruses | 10 |
22 |
27 |
10 |
5 |
4 |
3 |
3 |
7 |
18 |
0 |
2 |
111 |
| Theoretical Studies on Coupled Electron and Proton Transfer in Cytochrome c Oxidase | 2 |
3 |
1 |
2 |
4 |
1 |
3 |
4 |
4 |
5 |
48 |
40 |
117 |
| Thyroid Hormone Control of Cardiac Substrate Metabolism | 0 |
4 |
3 |
1 |
2 |
2 |
0 |
1 |
0 |
2 |
1 |
0 |
16 |
| Time to rest : Signals in shoot apex developmental transitions underlying dormancy | 1 |
3 |
0 |
2 |
5 |
1 |
2 |
4 |
3 |
2 |
6 |
4 |
33 |
| Tinkering with cusp patterning : Developmental Genetic Mechanisms in Mouse Molar Development | 7 |
4 |
10 |
16 |
8 |
2 |
4 |
1 |
4 |
5 |
3 |
3 |
67 |
| Tissue-Adherence in Lactic Acid Bacteria : Identification and Characterization of the Collagen-Binding S-Layer Protein of Lactobacillus crispatus | 7 |
4 |
4 |
7 |
7 |
5 |
2 |
4 |
1 |
1 |
2 |
1 |
45 |
| Tissue-specific genetic and epigenetic alterations in Mlh1 heterozygous tissues | 1 |
5 |
16 |
6 |
5 |
8 |
4 |
2 |
2 |
4 |
7 |
3 |
63 |
| To be or not to be a Queen : Caste-specific gene expression patterns in ants | 3 |
3 |
1 |
1 |
3 |
2 |
7 |
3 |
2 |
3 |
2 |
2 |
32 |
| To Move or to Convene : Regulatory Circuits of Mat Fimbriae in Escherichia coli | 2 |
3 |
2 |
3 |
2 |
5 |
3 |
5 |
2 |
5 |
7 |
0 |
39 |
| To the root of the stem cell problem : The evolutionary importance of the epithelial stem cell niche during tooth development | 0 |
2 |
2 |
5 |
0 |
3 |
1 |
2 |
2 |
3 |
1 |
0 |
21 |
| Tonically Active Kainate Receptors (tKARs) : A Novel Mechanism Regulating Neuronal Function in the Brain | 1 |
2 |
5 |
1 |
7 |
1 |
8 |
4 |
2 |
3 |
4 |
3 |
41 |
| 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 | 2 |
6 |
12 |
10 |
7 |
3 |
4 |
4 |
1 |
2 |
2 |
4 |
57 |
| Towards ecological intensification of agriculture : from management to soil bacterial and nitrogen-cycling communities | 2 |
5 |
4 |
2 |
6 |
3 |
2 |
2 |
5 |
6 |
5 |
5 |
47 |
| Towards immunomodulatory urban greening : enhancing urban indoor and outdoor microbial communities with indoor vegetation and novel plant substrates | 8 |
2 |
1 |
7 |
4 |
4 |
6 |
4 |
3 |
6 |
5 |
1 |
51 |
| Towards inclusivity in ecosystem governance : The epistemic dimension of human-nature connections and its implications for sustainability science | 6 |
6 |
3 |
0 |
21 |
6 |
6 |
8 |
13 |
22 |
25 |
10 |
126 |
| Traditional medicinal uses and biological activities of some plant extracts of African Combretum Loefl., Terminalia L. and Pteleopsis Engl. species | 34 |
15 |
14 |
8 |
5 |
3 |
9 |
6 |
6 |
9 |
10 |
14 |
133 |
| 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 | 10 |
52 |
54 |
15 |
14 |
4 |
8 |
5 |
9 |
7 |
4 |
1 |
183 |
| Transcription factor Foxi3 in Hair Follicle Development and Homeostasis | 4 |
4 |
5 |
5 |
9 |
7 |
3 |
10 |
5 |
2 |
2 |
9 |
65 |
| Transcription factor function and interactions during human preimplantation development | 0 |
0 |
55 |
11 |
3 |
37 |
4 |
14 |
5 |
4 |
10 |
8 |
151 |
| Transcription Factors Foxi3 and Sox2 in the Regulation of Tooth Development | 10 |
141 |
0 |
0 |
2 |
2 |
4 |
3 |
6 |
14 |
35 |
6 |
223 |
| Transcriptional analysis of persistent Chlamydia pneumoniae infection in vitro | 1 |
4 |
2 |
3 |
3 |
3 |
3 |
1 |
5 |
4 |
4 |
1 |
34 |
| Transcriptional control of dietary sugar metabolism and homeostasis by Mondo-Mlx transcription factors | 1 |
5 |
3 |
23 |
49 |
9 |
7 |
5 |
16 |
15 |
16 |
3 |
152 |
| Transcriptional Regulation of GABAergic neuron differentiation in the developing diencephalon, midbrain and anterior hindbrain | 6 |
4 |
9 |
5 |
2 |
5 |
4 |
1 |
2 |
2 |
4 |
1 |
45 |
| 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 | 3 |
3 |
3 |
5 |
2 |
5 |
1 |
2 |
0 |
4 |
4 |
3 |
35 |
| Transcriptome and proteome analysis of xylose-metabolising Saccharomyces cerevisiae | 0 |
1 |
0 |
3 |
2 |
2 |
1 |
1 |
1 |
5 |
5 |
5 |
26 |
| Transcriptomic analysis of food-related microorganisms : Cheese microbiota, food spoilage lactic acid bacteria, and foodborne pathogens | 7 |
9 |
6 |
6 |
6 |
4 |
21 |
10 |
20 |
10 |
15 |
6 |
120 |
| Transcriptomic data integration for precision medicine in leukemia | 5 |
3 |
2 |
6 |
2 |
11 |
4 |
2 |
5 |
6 |
3 |
2 |
51 |
| Transformation and removal of riverine dissolved organic matter in Baltic Sea estuaries | 0 |
2 |
5 |
4 |
0 |
1 |
4 |
2 |
2 |
2 |
0 |
0 |
22 |
| Trapped in the net : restriction of TRKB function by perineuronal nets inhibits plasticity in the central nervous system | 3 |
4 |
2 |
4 |
9 |
7 |
4 |
3 |
5 |
1 |
1 |
3 |
46 |
| Trauma-induced cellular stress signalling and hair cell death in the cochlea | 1 |
2 |
3 |
4 |
5 |
2 |
3 |
1 |
2 |
2 |
1 |
1 |
27 |
| Trichoderma reesei strains for production of cellulases for the textile industry | 8 |
7 |
17 |
7 |
9 |
7 |
7 |
7 |
12 |
7 |
3 |
2 |
93 |
| Trimeric autotransporters and their ligands : structural studies | 4 |
3 |
3 |
1 |
3 |
6 |
5 |
4 |
2 |
2 |
6 |
1 |
40 |
| Trophic Interactions and Impacts of Non-indigenous Species in Baltic Sea Coastal Ecosystems | 2 |
4 |
7 |
1 |
5 |
3 |
2 |
1 |
1 |
5 |
2 |
5 |
38 |
| Trypsinogens and trypsin inhibitor (PSTI/TATI) -expression in urogenital organs and tumors | 2 |
0 |
2 |
0 |
0 |
2 |
3 |
5 |
1 |
2 |
0 |
2 |
19 |
| Tula hantavirus nucleocapsid protein | 0 |
1 |
5 |
3 |
2 |
1 |
3 |
3 |
2 |
5 |
0 |
2 |
27 |
| Tumor Necrosis Factors and Chemokines in Hair Development | 6 |
4 |
7 |
14 |
10 |
6 |
8 |
2 |
6 |
7 |
5 |
4 |
79 |
| Tumorigenic transformation induced by Ornithine and S-adenosylmethionine decarboxylases : Search for common denominators in oncogenic signaling | 1 |
0 |
1 |
2 |
3 |
3 |
2 |
0 |
2 |
2 |
0 |
1 |
17 |
| Type III Secretion System of Phytopathogenic Bacterium Pseudomonas syringae : From Gene to Function | 8 |
4 |
7 |
6 |
2 |
2 |
4 |
5 |
1 |
1 |
2 |
0 |
42 |
| U12-type Spliceosome : Localization and Effects of Splicing Efficiency on Gene Expression | 2 |
1 |
5 |
5 |
2 |
2 |
2 |
3 |
1 |
4 |
2 |
8 |
37 |
| Uncovering a sugar tolerance network : SIK3 and Cabut as downstream effectors of Mondo-Mlx | 7 |
4 |
3 |
6 |
8 |
3 |
9 |
10 |
1 |
3 |
4 |
2 |
60 |
| Understanding the biodiversity and ecological importance of ctenophores Lessons from Arctic and Baltic Mertensia ovum | 6 |
3 |
6 |
6 |
8 |
3 |
5 |
4 |
5 |
4 |
5 |
1 |
56 |
| Unravelling Molecular and Cellular Disease Mechanisms in Infantile Neuronal Ceroid Lipofuscinosis (INCL) | 0 |
0 |
1 |
2 |
0 |
1 |
4 |
1 |
1 |
1 |
1 |
3 |
15 |
| Urban ecosystem services at the plant-soil interface | 3 |
2 |
5 |
2 |
6 |
5 |
7 |
4 |
3 |
4 |
8 |
6 |
55 |
| Urban ecosystems-response to disturbances, resilience and ecological memory | 3 |
3 |
141 |
5 |
7 |
4 |
1 |
9 |
5 |
6 |
2 |
2 |
188 |
| Urban futures and climate change : understanding vulnerability dynamics | 11 |
31 |
14 |
1 |
3 |
0 |
4 |
11 |
6 |
2 |
2 |
3 |
88 |
| Urban woodland ecology : Methodological perspectives and empirical studies | 2 |
3 |
2 |
3 |
4 |
0 |
4 |
2 |
3 |
2 |
2 |
1 |
28 |
| Use of ecological information in urban planning | 1 |
3 |
4 |
2 |
2 |
3 |
3 |
3 |
5 |
3 |
6 |
0 |
35 |
| Using a combination of bioassays, bioaccumulation kinetics and mixture toxicity tests to assess the ecotoxicological risk of CCA contaminated soils in Finland | 4 |
2 |
3 |
2 |
3 |
2 |
4 |
3 |
2 |
8 |
9 |
5 |
47 |
| Using modern and fossil pollen data for climate and human influence reconstructions in China | 16 |
46 |
45 |
214 |
8 |
4 |
1 |
2 |
2 |
2 |
3 |
2 |
345 |
| Utility of Type I Collagen-Derived Markers as Reflectors of Bone Turnover in Different Clinical Situations | 1 |
3 |
2 |
5 |
1 |
2 |
0 |
2 |
5 |
5 |
1 |
1 |
28 |
| Vascular Diversity and the Functional Role of Peptidases in Angiogenesis | 1 |
1 |
2 |
2 |
2 |
3 |
5 |
1 |
2 |
4 |
6 |
2 |
31 |
| Vegetated roofs as habitats for arthropods in urban areas | 0 |
2 |
2 |
1 |
5 |
0 |
0 |
2 |
0 |
2 |
5 |
3 |
22 |
| Vegetation and carbon dynamics of high-latitude peatlands in a changing climate : from early Holocene to recent past | 6 |
13 |
0 |
1 |
5 |
6 |
4 |
6 |
5 |
7 |
8 |
3 |
64 |
| VEGF-C: The evolutionary origin, activation, and potential as a drug target | 9 |
8 |
10 |
8 |
1 |
2 |
9 |
5 |
5 |
5 |
2 |
5 |
69 |
| VEGFR-2 and VEGFR-3 Specific Signaling in Lymphangiogenesis and Angiogenesis | 0 |
4 |
1 |
3 |
0 |
3 |
0 |
3 |
0 |
2 |
1 |
2 |
19 |
| VEGFR-3 Ligands and Lymphangiogenesis | 2 |
2 |
2 |
3 |
5 |
0 |
3 |
0 |
1 |
2 |
1 |
1 |
22 |
| Virus - host cell interactions in echovirus 1 infection | 0 |
0 |
4 |
20 |
66 |
6 |
4 |
1 |
3 |
4 |
6 |
1 |
115 |
| Virus-host interactions of emerging respiratory pathogens | 2 |
0 |
2 |
0 |
0 |
1 |
2 |
3 |
3 |
1 |
2 |
0 |
16 |
| Virus-host systems in sea ice | 2 |
2 |
4 |
2 |
10 |
12 |
11 |
7 |
5 |
2 |
2 |
1 |
60 |
| Vole population dynamics : experiments on predation | 3 |
3 |
1 |
4 |
7 |
2 |
6 |
1 |
6 |
6 |
4 |
3 |
46 |
| Voles and their trophic interactions in a changing landscape | 9 |
13 |
8 |
8 |
5 |
4 |
0 |
9 |
5 |
3 |
5 |
2 |
71 |
| Voluntary alcohol drinking : relation to corticosteroids and alcohol-mediated testosterone elevation | 5 |
1 |
1 |
2 |
4 |
2 |
2 |
3 |
3 |
6 |
3 |
5 |
37 |
| Water quality estimation by optical remote sensing in boreal lakes | 4 |
6 |
3 |
3 |
2 |
3 |
2 |
1 |
11 |
5 |
3 |
3 |
46 |
| Waterbirds in a changing world : effects of climate, habitat and conservation policy on European waterbirds | 3 |
8 |
4 |
2 |
15 |
13 |
7 |
4 |
7 |
8 |
7 |
4 |
82 |
| Western diet and genetic predisposition as risk factors of colon cancer | 3 |
4 |
4 |
2 |
5 |
0 |
1 |
2 |
0 |
3 |
4 |
1 |
29 |
| What Makes Us Anxious : A Cross-Species Multi-omics Approach to the Biological Basis of Anxiety Disorders | 2 |
4 |
8 |
1 |
4 |
2 |
9 |
7 |
9 |
11 |
6 |
4 |
67 |
| When do we attain our objectives? : On the role of indicators, values and uncertainty in environmental management | 4 |
4 |
4 |
2 |
3 |
4 |
11 |
3 |
2 |
5 |
1 |
4 |
47 |
| Where and how to conserve : Extending the scope of spatial reserve network design | 0 |
1 |
2 |
2 |
1 |
1 |
1 |
0 |
0 |
3 |
2 |
4 |
17 |
| Wood-inhabiting Basidiomycetes in the Caucasus Region : Systematics and Biogeography | 1 |
1 |
2 |
3 |
0 |
1 |
6 |
3 |
3 |
4 |
2 |
4 |
30 |
| Yeast Saccharomyces cerevisiae as a tool in cloning and analysis of fungal genes : Applications for biomass hydrolysis and utilisation | 1 |
0 |
1 |
2 |
3 |
1 |
2 |
1 |
3 |
3 |
1 |
1 |
19 |
| Ympäristö ylittää oppiainerajat : Arvolatautuneisuus ja monialaisuus koulun ympäristöopetuksen haasteina | 12 |
10 |
24 |
44 |
69 |
24 |
44 |
35 |
27 |
39 |
28 |
11 |
367 |