| Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
|---|
| Ion Channel Gating | 60 | 2024 | 325 | 8.570 |
Why?
|
| Potassium Channels | 59 | 2021 | 343 | 8.460 |
Why?
|
| Bacterial Proteins | 48 | 2023 | 887 | 5.780 |
Why?
|
| Ion Channels | 26 | 2023 | 246 | 4.390 |
Why?
|
| Models, Molecular | 50 | 2024 | 1296 | 3.140 |
Why?
|
| Escherichia coli Proteins | 19 | 2023 | 183 | 3.070 |
Why?
|
| Lipid Bilayers | 20 | 2023 | 136 | 2.740 |
Why?
|
| Protein Conformation | 43 | 2023 | 887 | 2.610 |
Why?
|
| Cation Transport Proteins | 6 | 2023 | 67 | 1.760 |
Why?
|
| Escherichia coli | 12 | 2023 | 605 | 1.640 |
Why?
|
| Magnesium | 6 | 2023 | 178 | 1.620 |
Why?
|
| Thermotoga maritima | 5 | 2019 | 15 | 1.610 |
Why?
|
| Molecular Dynamics Simulation | 24 | 2023 | 255 | 1.590 |
Why?
|
| Mechanotransduction, Cellular | 7 | 2023 | 80 | 1.560 |
Why?
|
| Electron Spin Resonance Spectroscopy | 33 | 2016 | 317 | 1.480 |
Why?
|
| Ciona intestinalis | 3 | 2023 | 26 | 1.430 |
Why?
|
| Protons | 8 | 2022 | 101 | 1.320 |
Why?
|
| Cryoelectron Microscopy | 6 | 2023 | 96 | 1.250 |
Why?
|
| Lipids | 3 | 2020 | 271 | 1.180 |
Why?
|
| Potassium Channels, Voltage-Gated | 6 | 2014 | 122 | 1.110 |
Why?
|
| Hair Cells, Auditory, Outer | 2 | 2023 | 17 | 1.020 |
Why?
|
| Amino Acid Sequence | 25 | 2021 | 2062 | 1.000 |
Why?
|
| Protein Structure, Secondary | 16 | 2022 | 332 | 0.900 |
Why?
|
| Crystallography, X-Ray | 21 | 2019 | 486 | 0.890 |
Why?
|
| Large-Conductance Calcium-Activated Potassium Channels | 1 | 2022 | 11 | 0.840 |
Why?
|
| Anion Transport Proteins | 1 | 2021 | 10 | 0.800 |
Why?
|
| Streptomyces lividans | 8 | 2013 | 16 | 0.790 |
Why?
|
| Molecular Sequence Data | 21 | 2015 | 3027 | 0.720 |
Why?
|
| Potassium | 7 | 2024 | 253 | 0.710 |
Why?
|
| Streptomyces | 8 | 2002 | 21 | 0.690 |
Why?
|
| Phosphoric Monoester Hydrolases | 3 | 2023 | 51 | 0.690 |
Why?
|
| Cell Membrane | 12 | 2016 | 668 | 0.670 |
Why?
|
| Potassium Channels, Inwardly Rectifying | 1 | 2020 | 121 | 0.670 |
Why?
|
| Receptors, N-Methyl-D-Aspartate | 1 | 2019 | 87 | 0.660 |
Why?
|
| Kinetics | 23 | 2024 | 1528 | 0.650 |
Why?
|
| Arabidopsis Proteins | 1 | 2020 | 137 | 0.640 |
Why?
|
| Protein Structure, Tertiary | 13 | 2014 | 740 | 0.640 |
Why?
|
| Mutation, Missense | 2 | 2019 | 277 | 0.630 |
Why?
|
| Gene Expression Regulation, Bacterial | 3 | 2014 | 213 | 0.630 |
Why?
|
| Nervous System Diseases | 1 | 2019 | 162 | 0.620 |
Why?
|
| Cell Membrane Permeability | 2 | 2016 | 120 | 0.580 |
Why?
|
| Arabidopsis | 1 | 2020 | 320 | 0.560 |
Why?
|
| Spin Labels | 9 | 2015 | 106 | 0.560 |
Why?
|
| Archaeal Proteins | 3 | 2014 | 18 | 0.550 |
Why?
|
| Nerve Tissue Proteins | 1 | 2019 | 511 | 0.550 |
Why?
|
| Binding Sites | 11 | 2023 | 1117 | 0.520 |
Why?
|
| Patch-Clamp Techniques | 9 | 2017 | 396 | 0.520 |
Why?
|
| Membrane Proteins | 8 | 2016 | 1215 | 0.500 |
Why?
|
| Protein Structure, Quaternary | 7 | 2017 | 99 | 0.500 |
Why?
|
| Hydrogen-Ion Concentration | 11 | 2014 | 499 | 0.490 |
Why?
|
| Methanocaldococcus | 1 | 2014 | 3 | 0.470 |
Why?
|
| Aeropyrum | 1 | 2014 | 2 | 0.470 |
Why?
|
| Axons | 6 | 1994 | 180 | 0.460 |
Why?
|
| Xenopus laevis | 10 | 2019 | 137 | 0.460 |
Why?
|
| Mutant Proteins | 5 | 2017 | 96 | 0.430 |
Why?
|
| Liposomes | 12 | 2016 | 93 | 0.430 |
Why?
|
| Ions | 4 | 2014 | 75 | 0.420 |
Why?
|
| Nanostructures | 3 | 2019 | 79 | 0.420 |
Why?
|
| Sperm Capacitation | 3 | 2022 | 4 | 0.410 |
Why?
|
| Models, Biological | 12 | 2010 | 1764 | 0.410 |
Why?
|
| Mutation | 13 | 2023 | 4132 | 0.410 |
Why?
|
| Membrane Potentials | 12 | 2021 | 436 | 0.410 |
Why?
|
| ERG1 Potassium Channel | 2 | 2024 | 15 | 0.390 |
Why?
|
| Animals | 31 | 2023 | 27324 | 0.390 |
Why?
|
| Static Electricity | 6 | 2021 | 90 | 0.390 |
Why?
|
| Ether-A-Go-Go Potassium Channels | 2 | 2024 | 27 | 0.340 |
Why?
|
| Cysteine | 9 | 2022 | 136 | 0.330 |
Why?
|
| Oocytes | 11 | 2019 | 221 | 0.310 |
Why?
|
| Sequence Homology, Amino Acid | 6 | 2021 | 418 | 0.310 |
Why?
|
| Edetic Acid | 3 | 2010 | 42 | 0.310 |
Why?
|
| Potassium Channels, Calcium-Activated | 1 | 2007 | 19 | 0.290 |
Why?
|
| Cloning, Molecular | 4 | 2014 | 646 | 0.280 |
Why?
|
| Staphylococcus aureus | 1 | 2009 | 275 | 0.270 |
Why?
|
| Ion Transport | 2 | 2023 | 81 | 0.270 |
Why?
|
| Electrophysiology | 7 | 2014 | 403 | 0.270 |
Why?
|
| Amino Acid Substitution | 7 | 2017 | 338 | 0.270 |
Why?
|
| Gram-Negative Bacteria | 1 | 2006 | 35 | 0.270 |
Why?
|
| Thermodynamics | 8 | 2016 | 311 | 0.260 |
Why?
|
| Anions | 2 | 2023 | 31 | 0.260 |
Why?
|
| Arginine | 2 | 2022 | 138 | 0.250 |
Why?
|
| Water | 4 | 2016 | 283 | 0.250 |
Why?
|
| Protein Binding | 8 | 2022 | 1487 | 0.250 |
Why?
|
| Solvents | 4 | 2014 | 96 | 0.250 |
Why?
|
| Protein Multimerization | 2 | 2017 | 175 | 0.230 |
Why?
|
| HEK293 Cells | 3 | 2024 | 638 | 0.230 |
Why?
|
| Mutagenesis, Site-Directed | 7 | 2016 | 283 | 0.230 |
Why?
|
| Electricity | 1 | 2023 | 24 | 0.230 |
Why?
|
| Models, Chemical | 3 | 2016 | 179 | 0.230 |
Why?
|
| Cochlea | 1 | 2023 | 50 | 0.220 |
Why?
|
| Protein Domains | 3 | 2021 | 133 | 0.220 |
Why?
|
| Mutagenesis | 3 | 2022 | 202 | 0.220 |
Why?
|
| Drug Design | 2 | 2022 | 125 | 0.220 |
Why?
|
| Allosteric Regulation | 2 | 2020 | 67 | 0.200 |
Why?
|
| Magnetic Resonance Spectroscopy | 4 | 2014 | 312 | 0.200 |
Why?
|
| Molecular Conformation | 3 | 2016 | 96 | 0.200 |
Why?
|
| Decapodiformes | 6 | 1994 | 37 | 0.200 |
Why?
|
| Antibodies | 1 | 2023 | 353 | 0.190 |
Why?
|
| Xenopus | 5 | 2013 | 126 | 0.190 |
Why?
|
| Sodium Channels | 2 | 2010 | 129 | 0.190 |
Why?
|
| Albumins | 1 | 2021 | 129 | 0.190 |
Why?
|
| HIV Protease | 2 | 2011 | 10 | 0.180 |
Why?
|
| Inflammation Mediators | 1 | 2021 | 153 | 0.180 |
Why?
|
| Kv1.2 Potassium Channel | 3 | 2012 | 22 | 0.180 |
Why?
|
| Dimerization | 2 | 2015 | 143 | 0.180 |
Why?
|
| Proteins | 2 | 2021 | 786 | 0.180 |
Why?
|
| Neutrophils | 1 | 2021 | 308 | 0.170 |
Why?
|
| Hydrogen Bonding | 4 | 2017 | 144 | 0.170 |
Why?
|
| Nuclear Magnetic Resonance, Biomolecular | 2 | 2016 | 61 | 0.170 |
Why?
|
| Recombinant Proteins | 6 | 2010 | 1012 | 0.170 |
Why?
|
| Mammals | 1 | 2021 | 235 | 0.170 |
Why?
|
| Lipid Metabolism | 2 | 2014 | 199 | 0.170 |
Why?
|
| Spectroscopy, Fourier Transform Infrared | 1 | 1998 | 31 | 0.150 |
Why?
|
| Computer Simulation | 4 | 2014 | 1097 | 0.150 |
Why?
|
| Cytoplasm | 2 | 2014 | 284 | 0.150 |
Why?
|
| Oxygen | 4 | 2010 | 742 | 0.150 |
Why?
|
| Bacteriorhodopsins | 3 | 1994 | 10 | 0.150 |
Why?
|
| Leukocytes | 1 | 2018 | 204 | 0.150 |
Why?
|
| Finite Element Analysis | 1 | 2017 | 78 | 0.150 |
Why?
|
| ATP-Binding Cassette Transporters | 2 | 2008 | 142 | 0.150 |
Why?
|
| Crystallography | 2 | 2011 | 45 | 0.150 |
Why?
|
| Sequence Alignment | 2 | 2014 | 353 | 0.150 |
Why?
|
| Gap Junctions | 2 | 2007 | 144 | 0.140 |
Why?
|
| Osmolar Concentration | 2 | 2010 | 181 | 0.140 |
Why?
|
| Peptides | 3 | 2022 | 647 | 0.140 |
Why?
|
| Light | 3 | 1994 | 292 | 0.140 |
Why?
|
| Cell Surface Display Techniques | 1 | 2015 | 16 | 0.130 |
Why?
|
| Immunoglobulin Fragments | 1 | 2015 | 24 | 0.130 |
Why?
|
| Molecular Chaperones | 1 | 2015 | 122 | 0.130 |
Why?
|
| Crystallization | 3 | 2013 | 210 | 0.120 |
Why?
|
| Potassium Channel Blockers | 2 | 2017 | 64 | 0.120 |
Why?
|
| Computational Biology | 2 | 2016 | 542 | 0.120 |
Why?
|
| Pressure | 3 | 2009 | 165 | 0.120 |
Why?
|
| Electric Conductivity | 4 | 2002 | 144 | 0.120 |
Why?
|
| Kv1.3 Potassium Channel | 2 | 2013 | 14 | 0.120 |
Why?
|
| Peptide Library | 4 | 2018 | 84 | 0.110 |
Why?
|
| Biological Transport | 1 | 2014 | 401 | 0.110 |
Why?
|
| DNA Primers | 1 | 2014 | 543 | 0.110 |
Why?
|
| Spindle Apparatus | 1 | 2013 | 65 | 0.110 |
Why?
|
| Phenotype | 1 | 2019 | 2439 | 0.110 |
Why?
|
| Structure-Activity Relationship | 2 | 2010 | 412 | 0.110 |
Why?
|
| Cadmium | 1 | 2012 | 28 | 0.100 |
Why?
|
| Multiprotein Complexes | 1 | 2013 | 96 | 0.100 |
Why?
|
| Periplasmic Binding Proteins | 2 | 2014 | 25 | 0.100 |
Why?
|
| Coordination Complexes | 1 | 2012 | 20 | 0.100 |
Why?
|
| Electrophoresis, Polyacrylamide Gel | 1 | 2012 | 269 | 0.100 |
Why?
|
| Circular Dichroism | 2 | 2005 | 117 | 0.100 |
Why?
|
| Genetic Vectors | 1 | 2014 | 446 | 0.100 |
Why?
|
| Disease Models, Animal | 1 | 2019 | 2362 | 0.100 |
Why?
|
| Solubility | 1 | 2012 | 179 | 0.100 |
Why?
|
| Protein Engineering | 2 | 2010 | 141 | 0.100 |
Why?
|
| Shaker Superfamily of Potassium Channels | 3 | 2010 | 49 | 0.100 |
Why?
|
| DNA, Complementary | 1 | 2012 | 392 | 0.100 |
Why?
|
| Caenorhabditis elegans Proteins | 1 | 2013 | 113 | 0.100 |
Why?
|
| Adenosine Triphosphate | 2 | 1991 | 316 | 0.100 |
Why?
|
| Up-Regulation | 1 | 2014 | 727 | 0.100 |
Why?
|
| Aspartic Acid | 1 | 2011 | 64 | 0.100 |
Why?
|
| Phosphorylation | 5 | 1991 | 1130 | 0.100 |
Why?
|
| Caenorhabditis elegans | 1 | 2013 | 230 | 0.090 |
Why?
|
| In Vitro Techniques | 6 | 2009 | 996 | 0.090 |
Why?
|
| Tryptophan | 1 | 2011 | 92 | 0.090 |
Why?
|
| Muscle Proteins | 1 | 2011 | 133 | 0.090 |
Why?
|
| Acrosome Reaction | 2 | 2021 | 2 | 0.090 |
Why?
|
| Biophysical Phenomena | 5 | 2010 | 124 | 0.090 |
Why?
|
| Electrons | 1 | 2010 | 50 | 0.090 |
Why?
|
| Structural Homology, Protein | 1 | 2010 | 19 | 0.090 |
Why?
|
| Humans | 12 | 2024 | 89073 | 0.090 |
Why?
|
| Drosophila | 2 | 1993 | 521 | 0.090 |
Why?
|
| Scorpion Venoms | 1 | 2009 | 25 | 0.090 |
Why?
|
| Neurotoxins | 1 | 2009 | 49 | 0.090 |
Why?
|
| Rats | 3 | 2011 | 4041 | 0.090 |
Why?
|
| Protein Subunits | 2 | 2012 | 123 | 0.090 |
Why?
|
| Time Factors | 3 | 2007 | 5320 | 0.080 |
Why?
|
| Haemophilus influenzae | 1 | 2008 | 15 | 0.080 |
Why?
|
| Rubidium | 2 | 1999 | 9 | 0.080 |
Why?
|
| HIV Protease Inhibitors | 1 | 2009 | 21 | 0.080 |
Why?
|
| Diffusion | 3 | 2016 | 93 | 0.080 |
Why?
|
| Child | 1 | 2019 | 7149 | 0.080 |
Why?
|
| Methanobacterium | 1 | 2007 | 2 | 0.070 |
Why?
|
| Spectrophotometry, Infrared | 2 | 2017 | 18 | 0.070 |
Why?
|
| Mycobacterium tuberculosis | 1 | 2009 | 195 | 0.070 |
Why?
|
| Likelihood Functions | 1 | 2007 | 251 | 0.070 |
Why?
|
| Detergents | 2 | 2015 | 34 | 0.070 |
Why?
|
| Spectrometry, Fluorescence | 1 | 2006 | 85 | 0.070 |
Why?
|
| Biophysics | 4 | 1994 | 153 | 0.070 |
Why?
|
| Reproducibility of Results | 1 | 2012 | 2752 | 0.070 |
Why?
|
| Female | 8 | 2019 | 46014 | 0.060 |
Why?
|
| Solutions | 3 | 2016 | 85 | 0.060 |
Why?
|
| Male | 4 | 2022 | 42254 | 0.060 |
Why?
|
| Methanococcus | 1 | 2005 | 5 | 0.060 |
Why?
|
| Sodium | 2 | 2016 | 331 | 0.060 |
Why?
|
| Methionine | 1 | 2005 | 65 | 0.060 |
Why?
|
| Tetraethylammonium Compounds | 3 | 1993 | 14 | 0.060 |
Why?
|
| Open Reading Frames | 1 | 2005 | 119 | 0.060 |
Why?
|
| Tetraethylammonium | 3 | 1993 | 24 | 0.060 |
Why?
|
| Hydrophobic and Hydrophilic Interactions | 1 | 2004 | 94 | 0.060 |
Why?
|
| Maleimides | 1 | 2002 | 26 | 0.050 |
Why?
|
| Membrane Transport Proteins | 1 | 2023 | 169 | 0.050 |
Why?
|
| Dialysis | 2 | 1991 | 24 | 0.050 |
Why?
|
| Semen | 1 | 2021 | 13 | 0.050 |
Why?
|
| Fertilization | 1 | 2021 | 40 | 0.050 |
Why?
|
| Mechanoreceptors | 1 | 2001 | 36 | 0.050 |
Why?
|
| Spermatozoa | 1 | 2021 | 62 | 0.050 |
Why?
|
| Molecular Structure | 1 | 2001 | 289 | 0.050 |
Why?
|
| Rubidium Radioisotopes | 2 | 1998 | 4 | 0.050 |
Why?
|
| Stress, Mechanical | 1 | 2001 | 253 | 0.050 |
Why?
|
| Signal Transduction | 2 | 2010 | 3374 | 0.040 |
Why?
|
| Microscopy, Atomic Force | 1 | 2019 | 53 | 0.040 |
Why?
|
| Toxins, Biological | 1 | 2018 | 7 | 0.040 |
Why?
|
| Respiratory Burst | 1 | 2018 | 18 | 0.040 |
Why?
|
| Recombinant Fusion Proteins | 2 | 2013 | 565 | 0.040 |
Why?
|
| Sequence Deletion | 1 | 1999 | 205 | 0.040 |
Why?
|
| Hydrogen | 1 | 1998 | 47 | 0.040 |
Why?
|
| Quantitative Structure-Activity Relationship | 1 | 2017 | 8 | 0.040 |
Why?
|
| Electric Stimulation | 1 | 1998 | 354 | 0.040 |
Why?
|
| Biopolymers | 1 | 1997 | 26 | 0.040 |
Why?
|
| Oxygen Isotopes | 1 | 2016 | 15 | 0.040 |
Why?
|
| Hot Temperature | 1 | 1997 | 208 | 0.040 |
Why?
|
| Carbon Isotopes | 1 | 2016 | 74 | 0.030 |
Why?
|
| Isotope Labeling | 1 | 2016 | 52 | 0.030 |
Why?
|
| Energy Transfer | 1 | 2016 | 25 | 0.030 |
Why?
|
| Peptide Fragments | 1 | 1998 | 463 | 0.030 |
Why?
|
| Electrochemistry | 2 | 1994 | 60 | 0.030 |
Why?
|
| Microscopy, Polarization | 1 | 2015 | 10 | 0.030 |
Why?
|
| Reactive Oxygen Species | 1 | 2018 | 490 | 0.030 |
Why?
|
| Arrhythmias, Cardiac | 1 | 2017 | 197 | 0.030 |
Why?
|
| Sensory Rhodopsins | 1 | 1994 | 1 | 0.030 |
Why?
|
| Gene Deletion | 1 | 2016 | 342 | 0.030 |
Why?
|
| Halorhodopsins | 1 | 1994 | 5 | 0.030 |
Why?
|
| Halobacterium | 1 | 1994 | 2 | 0.030 |
Why?
|
| Phenylmercury Compounds | 1 | 1994 | 1 | 0.030 |
Why?
|
| Databases, Protein | 1 | 2014 | 51 | 0.030 |
Why?
|
| Sulfhydryl Compounds | 1 | 1994 | 71 | 0.030 |
Why?
|
| Halobacterium salinarum | 1 | 1993 | 3 | 0.030 |
Why?
|
| Thiocyanates | 1 | 1993 | 11 | 0.030 |
Why?
|
| Proton Pumps | 1 | 1993 | 4 | 0.030 |
Why?
|
| Tetrodotoxin | 1 | 1993 | 50 | 0.030 |
Why?
|
| Nitrates | 1 | 1993 | 35 | 0.030 |
Why?
|
| Sucrose | 1 | 2013 | 65 | 0.030 |
Why?
|
| Voltage-Gated Sodium Channels | 1 | 2012 | 17 | 0.030 |
Why?
|
| Microtubules | 1 | 2013 | 123 | 0.030 |
Why?
|
| Amino Acid Motifs | 1 | 2012 | 116 | 0.030 |
Why?
|
| Protein Stability | 1 | 2012 | 100 | 0.030 |
Why?
|
| Isoleucine | 1 | 2011 | 17 | 0.030 |
Why?
|
| Nickel | 2 | 2008 | 13 | 0.020 |
Why?
|
| Photolysis | 1 | 1991 | 13 | 0.020 |
Why?
|
| Spectrophotometry, Ultraviolet | 1 | 1991 | 44 | 0.020 |
Why?
|
| Biotransformation | 1 | 1991 | 50 | 0.020 |
Why?
|
| Micelles | 2 | 2008 | 48 | 0.020 |
Why?
|
| Sequence Analysis, Protein | 1 | 2010 | 28 | 0.020 |
Why?
|
| Drosophila melanogaster | 2 | 1994 | 613 | 0.020 |
Why?
|
| Phenylalanine | 1 | 2010 | 35 | 0.020 |
Why?
|
| Intercellular Signaling Peptides and Proteins | 1 | 2009 | 181 | 0.020 |
Why?
|
| Protein Renaturation | 1 | 2008 | 4 | 0.020 |
Why?
|
| Lysophosphatidylcholines | 1 | 2008 | 17 | 0.020 |
Why?
|
| Cross-Linking Reagents | 1 | 2008 | 87 | 0.020 |
Why?
|
| Ligands | 1 | 2009 | 443 | 0.020 |
Why?
|
| Immunoglobulin Fab Fragments | 1 | 2009 | 83 | 0.020 |
Why?
|
| Myocardium | 1 | 2011 | 571 | 0.020 |
Why?
|
| Asparagine | 1 | 2007 | 30 | 0.020 |
Why?
|
| Histidine | 1 | 2007 | 56 | 0.020 |
Why?
|
| Models, Neurological | 1 | 1990 | 409 | 0.020 |
Why?
|
| Cyclic N-Oxides | 1 | 1987 | 33 | 0.020 |
Why?
|
| Amphotericin B | 1 | 1987 | 34 | 0.020 |
Why?
|
| Rhodamines | 1 | 2006 | 18 | 0.020 |
Why?
|
| Cytokines | 1 | 2009 | 802 | 0.020 |
Why?
|
| Fluorescent Dyes | 1 | 2006 | 243 | 0.020 |
Why?
|
| Carbon | 1 | 2005 | 90 | 0.020 |
Why?
|
| Monte Carlo Method | 1 | 2005 | 186 | 0.020 |
Why?
|
| T-Lymphocytes | 1 | 2009 | 1223 | 0.010 |
Why?
|
| Software | 1 | 2007 | 665 | 0.010 |
Why?
|
| Chemistry | 1 | 1994 | 54 | 0.010 |
Why?
|
| Chemical Phenomena | 1 | 1994 | 72 | 0.010 |
Why?
|
| Darkness | 1 | 1994 | 49 | 0.010 |
Why?
|
| Baculoviridae | 1 | 1994 | 34 | 0.010 |
Why?
|
| Moths | 1 | 1994 | 31 | 0.010 |
Why?
|
| Transfection | 1 | 1994 | 911 | 0.010 |
Why?
|
| Leishmania mexicana | 1 | 1987 | 1 | 0.000 |
Why?
|
| Dimethyl Sulfoxide | 1 | 1987 | 38 | 0.000 |
Why?
|
| Copper | 1 | 1987 | 77 | 0.000 |
Why?
|