Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
Proteins | 17 | 2024 | 786 | 3.900 |
Why?
|
Evolution, Molecular | 18 | 2020 | 851 | 2.030 |
Why?
|
Protein Engineering | 6 | 2021 | 145 | 1.600 |
Why?
|
Epistasis, Genetic | 2 | 2019 | 90 | 1.160 |
Why?
|
Amino Acids | 6 | 2023 | 246 | 1.130 |
Why?
|
Directed Molecular Evolution | 2 | 2018 | 20 | 1.130 |
Why?
|
PDZ Domains | 5 | 2018 | 14 | 1.110 |
Why?
|
Models, Molecular | 16 | 2025 | 1312 | 0.970 |
Why?
|
Escherichia coli | 6 | 2020 | 606 | 0.950 |
Why?
|
Amino Acid Substitution | 2 | 2016 | 338 | 0.880 |
Why?
|
Circadian Rhythm Signaling Peptides and Proteins | 2 | 2014 | 22 | 0.860 |
Why?
|
Cyanobacteria | 2 | 2014 | 113 | 0.820 |
Why?
|
Allosteric Regulation | 8 | 2018 | 67 | 0.770 |
Why?
|
Anniversaries and Special Events | 1 | 2021 | 14 | 0.740 |
Why?
|
Circadian Rhythm | 2 | 2014 | 304 | 0.710 |
Why?
|
Mutation | 11 | 2023 | 4158 | 0.660 |
Why?
|
Nobel Prize | 1 | 2018 | 10 | 0.640 |
Why?
|
Amino Acid Sequence | 10 | 2023 | 2062 | 0.630 |
Why?
|
GTP-Binding Proteins | 3 | 2016 | 145 | 0.630 |
Why?
|
Protein Interaction Mapping | 2 | 2016 | 81 | 0.610 |
Why?
|
Bacterial Proteins | 3 | 2014 | 898 | 0.600 |
Why?
|
Protein Structure, Tertiary | 9 | 2014 | 740 | 0.530 |
Why?
|
Ligands | 8 | 2018 | 446 | 0.530 |
Why?
|
Cefotaxime | 1 | 2015 | 5 | 0.500 |
Why?
|
Ampicillin Resistance | 1 | 2015 | 5 | 0.500 |
Why?
|
Vision, Ocular | 2 | 2007 | 71 | 0.500 |
Why?
|
Models, Genetic | 2 | 2020 | 947 | 0.490 |
Why?
|
Signal Transduction | 9 | 2024 | 3392 | 0.480 |
Why?
|
Protein Folding | 5 | 2013 | 290 | 0.470 |
Why?
|
Models, Biological | 5 | 2018 | 1762 | 0.470 |
Why?
|
beta-Lactamases | 1 | 2015 | 56 | 0.470 |
Why?
|
Intracellular Signaling Peptides and Proteins | 1 | 2016 | 387 | 0.460 |
Why?
|
Protein Conformation | 7 | 2024 | 895 | 0.450 |
Why?
|
Biological Clocks | 1 | 2014 | 74 | 0.430 |
Why?
|
Tetrahydrofolate Dehydrogenase | 2 | 2011 | 32 | 0.420 |
Why?
|
Circadian Clocks | 2 | 2018 | 63 | 0.420 |
Why?
|
High-Throughput Nucleotide Sequencing | 1 | 2016 | 487 | 0.410 |
Why?
|
Sequence Alignment | 5 | 2016 | 354 | 0.410 |
Why?
|
Mutant Proteins | 1 | 2012 | 96 | 0.410 |
Why?
|
Binding Sites | 8 | 2016 | 1120 | 0.390 |
Why?
|
Membrane Proteins | 2 | 2016 | 1226 | 0.380 |
Why?
|
Thermodynamics | 5 | 2018 | 313 | 0.370 |
Why?
|
Conserved Sequence | 5 | 2018 | 211 | 0.360 |
Why?
|
Allosteric Site | 6 | 2018 | 22 | 0.350 |
Why?
|
Adaptation, Physiological | 1 | 2012 | 314 | 0.350 |
Why?
|
Recombinant Fusion Proteins | 2 | 2008 | 563 | 0.340 |
Why?
|
Serine Endopeptidases | 2 | 2009 | 146 | 0.330 |
Why?
|
Molecular Sequence Data | 6 | 2016 | 3024 | 0.320 |
Why?
|
Flavoproteins | 1 | 2008 | 25 | 0.320 |
Why?
|
Autophagy | 1 | 2010 | 159 | 0.310 |
Why?
|
Receptors, Adrenergic, beta-2 | 1 | 2007 | 38 | 0.290 |
Why?
|
Second Messenger Systems | 1 | 2007 | 43 | 0.290 |
Why?
|
Rhodopsin | 2 | 2007 | 20 | 0.290 |
Why?
|
Photoreceptor Cells, Invertebrate | 2 | 2007 | 21 | 0.290 |
Why?
|
Protein Structure, Secondary | 3 | 2018 | 333 | 0.290 |
Why?
|
Databases, Protein | 3 | 2006 | 51 | 0.280 |
Why?
|
Computer Simulation | 4 | 2016 | 1101 | 0.280 |
Why?
|
Eye Proteins | 1 | 2007 | 128 | 0.270 |
Why?
|
Receptor Cross-Talk | 1 | 2006 | 33 | 0.270 |
Why?
|
Protein Binding | 5 | 2016 | 1490 | 0.260 |
Why?
|
Ampicillin | 2 | 2016 | 15 | 0.260 |
Why?
|
Molecular Docking Simulation | 2 | 2016 | 49 | 0.240 |
Why?
|
Mutagenesis | 4 | 2017 | 203 | 0.240 |
Why?
|
src Homology Domains | 1 | 2024 | 45 | 0.240 |
Why?
|
Cryptochromes | 2 | 2018 | 5 | 0.240 |
Why?
|
Receptors, Retinoic Acid | 1 | 2004 | 47 | 0.230 |
Why?
|
Potassium | 1 | 2025 | 258 | 0.220 |
Why?
|
Peptide Fragments | 1 | 2005 | 462 | 0.220 |
Why?
|
Receptors, Cytoplasmic and Nuclear | 1 | 2004 | 122 | 0.220 |
Why?
|
Genetic Techniques | 1 | 2023 | 73 | 0.220 |
Why?
|
Ceramides | 1 | 2003 | 35 | 0.210 |
Why?
|
Kinetics | 4 | 2025 | 1534 | 0.210 |
Why?
|
Drosophila Proteins | 1 | 2007 | 510 | 0.210 |
Why?
|
Potassium Channels | 1 | 2025 | 346 | 0.210 |
Why?
|
Mutagenesis, Site-Directed | 3 | 2016 | 283 | 0.200 |
Why?
|
Computational Biology | 1 | 2005 | 549 | 0.200 |
Why?
|
Structural Homology, Protein | 2 | 2018 | 19 | 0.200 |
Why?
|
Molecular Dynamics Simulation | 1 | 2024 | 263 | 0.190 |
Why?
|
Physiological Phenomena | 1 | 2021 | 7 | 0.190 |
Why?
|
Light | 3 | 2008 | 292 | 0.190 |
Why?
|
Sequence Analysis, Protein | 2 | 2016 | 28 | 0.190 |
Why?
|
Chorismate Mutase | 1 | 2020 | 1 | 0.180 |
Why?
|
RNA, Ribosomal, 23S | 1 | 2020 | 4 | 0.180 |
Why?
|
Macromolecular Substances | 1 | 2021 | 177 | 0.180 |
Why?
|
Crystallography, X-Ray | 2 | 2025 | 490 | 0.180 |
Why?
|
Rats | 3 | 2016 | 4040 | 0.170 |
Why?
|
RNA, Bacterial | 1 | 2020 | 111 | 0.170 |
Why?
|
Ribosomes | 1 | 2020 | 116 | 0.170 |
Why?
|
Recombinant Proteins | 4 | 2006 | 1008 | 0.170 |
Why?
|
Environment | 1 | 2021 | 223 | 0.170 |
Why?
|
Models, Statistical | 3 | 2020 | 574 | 0.170 |
Why?
|
Transcription, Genetic | 1 | 2004 | 1158 | 0.160 |
Why?
|
Artificial Intelligence | 1 | 2002 | 327 | 0.160 |
Why?
|
Drosophila | 1 | 2003 | 522 | 0.160 |
Why?
|
Two-Hybrid System Techniques | 1 | 2018 | 56 | 0.160 |
Why?
|
Machine Learning | 1 | 2021 | 263 | 0.150 |
Why?
|
Catalytic Domain | 1 | 2018 | 156 | 0.150 |
Why?
|
Protein Kinases | 1 | 2018 | 212 | 0.140 |
Why?
|
Phosphorylation | 2 | 2012 | 1130 | 0.140 |
Why?
|
Electricity | 1 | 2016 | 24 | 0.140 |
Why?
|
ZAP-70 Protein-Tyrosine Kinase | 1 | 2016 | 18 | 0.140 |
Why?
|
Lymphocyte Specific Protein Tyrosine Kinase p56(lck) | 1 | 2016 | 34 | 0.140 |
Why?
|
Static Electricity | 1 | 2016 | 90 | 0.140 |
Why?
|
Disks Large Homolog 4 Protein | 1 | 2016 | 7 | 0.140 |
Why?
|
ras Proteins | 1 | 2017 | 130 | 0.140 |
Why?
|
Apoptosis | 1 | 2003 | 1716 | 0.130 |
Why?
|
Animals | 8 | 2018 | 27453 | 0.130 |
Why?
|
Substrate Specificity | 3 | 2018 | 352 | 0.130 |
Why?
|
Protein Domains | 1 | 2016 | 135 | 0.130 |
Why?
|
Transcription Factors | 1 | 2004 | 1658 | 0.130 |
Why?
|
Models, Chemical | 1 | 2016 | 179 | 0.130 |
Why?
|
beta-Lactam Resistance | 1 | 2015 | 11 | 0.120 |
Why?
|
Escherichia coli Proteins | 3 | 2020 | 183 | 0.120 |
Why?
|
Genetic Fitness | 1 | 2015 | 38 | 0.120 |
Why?
|
Genotype | 1 | 2019 | 1852 | 0.120 |
Why?
|
Movement | 1 | 2016 | 310 | 0.120 |
Why?
|
Cathepsin K | 1 | 2014 | 3 | 0.120 |
Why?
|
Base Sequence | 2 | 2016 | 2329 | 0.120 |
Why?
|
Receptors, Antigen, T-Cell | 1 | 2016 | 394 | 0.110 |
Why?
|
Biological Evolution | 1 | 2021 | 967 | 0.110 |
Why?
|
Phenotype | 1 | 2019 | 2447 | 0.110 |
Why?
|
Sequence Analysis, DNA | 1 | 2016 | 868 | 0.100 |
Why?
|
Time Factors | 1 | 2021 | 5330 | 0.100 |
Why?
|
Gene Expression Regulation, Bacterial | 1 | 2014 | 215 | 0.100 |
Why?
|
Reproducibility of Results | 1 | 2018 | 2762 | 0.100 |
Why?
|
Autophagy-Related Protein 8 Family | 1 | 2010 | 2 | 0.090 |
Why?
|
Humans | 12 | 2018 | 89500 | 0.090 |
Why?
|
Structure-Activity Relationship | 2 | 2016 | 413 | 0.090 |
Why?
|
Molecular Chaperones | 1 | 2010 | 123 | 0.090 |
Why?
|
HSP70 Heat-Shock Proteins | 1 | 2010 | 115 | 0.090 |
Why?
|
Enzyme Stability | 1 | 2009 | 39 | 0.080 |
Why?
|
NADP | 1 | 2008 | 45 | 0.080 |
Why?
|
Microfilament Proteins | 1 | 2010 | 212 | 0.080 |
Why?
|
Proteomics | 1 | 2010 | 231 | 0.080 |
Why?
|
Adaptor Proteins, Signal Transducing | 1 | 2010 | 312 | 0.080 |
Why?
|
Catalysis | 1 | 2008 | 205 | 0.080 |
Why?
|
Bacteriophage T4 | 1 | 2007 | 9 | 0.080 |
Why?
|
Propanolamines | 1 | 2007 | 18 | 0.080 |
Why?
|
Muramidase | 1 | 2007 | 35 | 0.070 |
Why?
|
Cluster Analysis | 2 | 2006 | 370 | 0.070 |
Why?
|
Adrenergic beta-Agonists | 1 | 2007 | 74 | 0.070 |
Why?
|
Biophysical Phenomena | 2 | 2006 | 124 | 0.070 |
Why?
|
Disulfides | 1 | 2007 | 65 | 0.070 |
Why?
|
Canidae | 1 | 2007 | 5 | 0.070 |
Why?
|
Biophysics | 2 | 2006 | 153 | 0.070 |
Why?
|
Adrenergic beta-Antagonists | 1 | 2007 | 105 | 0.070 |
Why?
|
Animals, Genetically Modified | 1 | 2007 | 183 | 0.070 |
Why?
|
Immunoglobulin Fab Fragments | 1 | 2007 | 85 | 0.070 |
Why?
|
Patch-Clamp Techniques | 1 | 2007 | 396 | 0.070 |
Why?
|
Phylogeny | 2 | 2023 | 1191 | 0.070 |
Why?
|
Oxidation-Reduction | 1 | 2007 | 388 | 0.070 |
Why?
|
Dogs | 1 | 2007 | 704 | 0.070 |
Why?
|
Saccharomyces cerevisiae | 2 | 2024 | 440 | 0.060 |
Why?
|
Proline | 1 | 2005 | 55 | 0.060 |
Why?
|
Protein Denaturation | 1 | 2005 | 106 | 0.060 |
Why?
|
Peptide Library | 1 | 2005 | 84 | 0.060 |
Why?
|
Calcium Signaling | 1 | 2006 | 138 | 0.060 |
Why?
|
Receptors, Cell Surface | 1 | 2006 | 288 | 0.060 |
Why?
|
Cyclic AMP | 1 | 2006 | 275 | 0.060 |
Why?
|
HEK293 Cells | 2 | 2018 | 646 | 0.060 |
Why?
|
Ion Transport | 1 | 2025 | 85 | 0.060 |
Why?
|
Behavior, Animal | 1 | 2007 | 378 | 0.060 |
Why?
|
Cell Membrane | 1 | 2007 | 675 | 0.060 |
Why?
|
Magnetic Resonance Spectroscopy | 1 | 2005 | 315 | 0.060 |
Why?
|
Retinoid X Receptors | 1 | 2004 | 39 | 0.060 |
Why?
|
Peptide Mapping | 1 | 2003 | 26 | 0.060 |
Why?
|
Genome | 1 | 2007 | 391 | 0.060 |
Why?
|
X-Ray Diffraction | 1 | 2024 | 127 | 0.060 |
Why?
|
Dimerization | 1 | 2004 | 143 | 0.060 |
Why?
|
Biometry | 1 | 2003 | 66 | 0.060 |
Why?
|
Ceramidases | 1 | 2003 | 4 | 0.050 |
Why?
|
Luminescent Proteins | 1 | 2003 | 144 | 0.050 |
Why?
|
Arrestins | 1 | 2003 | 9 | 0.050 |
Why?
|
Amidohydrolases | 1 | 2003 | 18 | 0.050 |
Why?
|
Cattle | 1 | 2003 | 378 | 0.050 |
Why?
|
Algorithms | 2 | 2016 | 1894 | 0.050 |
Why?
|
Clathrin | 1 | 2003 | 29 | 0.050 |
Why?
|
Retinal Degeneration | 1 | 2003 | 29 | 0.050 |
Why?
|
Green Fluorescent Proteins | 1 | 2003 | 309 | 0.050 |
Why?
|
Macrophages | 1 | 2006 | 574 | 0.050 |
Why?
|
Drosophila melanogaster | 1 | 2007 | 614 | 0.050 |
Why?
|
Necrosis | 1 | 2003 | 210 | 0.050 |
Why?
|
Research Personnel | 1 | 2002 | 71 | 0.050 |
Why?
|
Cytokines | 1 | 2006 | 806 | 0.050 |
Why?
|
Data Interpretation, Statistical | 1 | 2004 | 300 | 0.050 |
Why?
|
Genes, Insect | 1 | 2003 | 183 | 0.050 |
Why?
|
Endocytosis | 1 | 2003 | 180 | 0.050 |
Why?
|
In Vitro Techniques | 1 | 2003 | 996 | 0.050 |
Why?
|
Information Storage and Retrieval | 1 | 2002 | 121 | 0.050 |
Why?
|
Phosphoproteins | 1 | 2003 | 260 | 0.050 |
Why?
|
Saccharomyces cerevisiae Proteins | 1 | 2024 | 286 | 0.050 |
Why?
|
Research | 1 | 2002 | 251 | 0.050 |
Why?
|
Mice | 3 | 2018 | 11812 | 0.050 |
Why?
|
Cell Survival | 1 | 2003 | 982 | 0.040 |
Why?
|
Myocytes, Cardiac | 1 | 2002 | 314 | 0.040 |
Why?
|
Research Design | 1 | 2002 | 586 | 0.040 |
Why?
|
Nucleic Acid Conformation | 1 | 2020 | 345 | 0.040 |
Why?
|
ARNTL Transcription Factors | 1 | 2018 | 11 | 0.040 |
Why?
|
Period Circadian Proteins | 1 | 2018 | 10 | 0.040 |
Why?
|
CLOCK Proteins | 1 | 2018 | 15 | 0.040 |
Why?
|
B-Lymphocytes | 1 | 2002 | 740 | 0.040 |
Why?
|
Protein Interaction Domains and Motifs | 1 | 2018 | 86 | 0.040 |
Why?
|
Insect Proteins | 1 | 2018 | 89 | 0.040 |
Why?
|
Protein Interaction Maps | 1 | 2017 | 50 | 0.040 |
Why?
|
DNA Mutational Analysis | 1 | 2017 | 529 | 0.030 |
Why?
|
Biomechanical Phenomena | 1 | 2016 | 478 | 0.030 |
Why?
|
Benzoates | 1 | 2014 | 33 | 0.030 |
Why?
|
Drug Design | 1 | 2014 | 123 | 0.030 |
Why?
|
Cell Line | 1 | 2018 | 2494 | 0.030 |
Why?
|
Mice, Knockout | 1 | 2018 | 2003 | 0.030 |
Why?
|
Osteoporosis | 1 | 2014 | 121 | 0.030 |
Why?
|
Molecular Targeted Therapy | 1 | 2014 | 279 | 0.020 |
Why?
|
Circular Dichroism | 1 | 2010 | 117 | 0.020 |
Why?
|
Molecular Conformation | 1 | 2010 | 96 | 0.020 |
Why?
|
Bacterial Physiological Phenomena | 1 | 2010 | 42 | 0.020 |
Why?
|
Adenosine Triphosphatases | 1 | 2010 | 154 | 0.020 |
Why?
|
Heat-Shock Proteins | 1 | 2010 | 183 | 0.020 |
Why?
|
Carnivora | 1 | 2007 | 10 | 0.020 |
Why?
|
Pseudomonas putida | 1 | 2006 | 6 | 0.020 |
Why?
|
Biological Transport, Active | 1 | 2006 | 102 | 0.020 |
Why?
|
Nuclear Magnetic Resonance, Biomolecular | 1 | 2006 | 61 | 0.020 |
Why?
|
Repetitive Sequences, Nucleic Acid | 1 | 2007 | 135 | 0.020 |
Why?
|
Species Specificity | 1 | 2007 | 685 | 0.020 |
Why?
|
Pan troglodytes | 1 | 2007 | 202 | 0.020 |
Why?
|
Neoplasms | 1 | 2018 | 3052 | 0.010 |
Why?
|
Chymotrypsin | 1 | 2003 | 28 | 0.010 |
Why?
|
International Cooperation | 1 | 2002 | 125 | 0.010 |
Why?
|
Hemoglobins | 1 | 2003 | 193 | 0.010 |
Why?
|
Receptors, G-Protein-Coupled | 1 | 2003 | 130 | 0.010 |
Why?
|
Cooperative Behavior | 1 | 2002 | 179 | 0.010 |
Why?
|
Internet | 1 | 2002 | 321 | 0.010 |
Why?
|
Databases, Factual | 1 | 2002 | 859 | 0.010 |
Why?
|
United States | 1 | 2002 | 7033 | 0.010 |
Why?
|