Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
---|
Ion Channel Gating | 60 | 2024 | 329 | 8.410 |
Why?
|
Potassium Channels | 59 | 2021 | 346 | 8.320 |
Why?
|
Bacterial Proteins | 48 | 2023 | 898 | 5.690 |
Why?
|
Ion Channels | 26 | 2023 | 246 | 4.320 |
Why?
|
Models, Molecular | 50 | 2024 | 1314 | 3.080 |
Why?
|
Escherichia coli Proteins | 19 | 2023 | 183 | 3.030 |
Why?
|
Lipid Bilayers | 20 | 2023 | 137 | 2.690 |
Why?
|
Protein Conformation | 43 | 2023 | 895 | 2.570 |
Why?
|
Cation Transport Proteins | 6 | 2023 | 67 | 1.730 |
Why?
|
Escherichia coli | 12 | 2023 | 607 | 1.610 |
Why?
|
Magnesium | 6 | 2023 | 178 | 1.600 |
Why?
|
Thermotoga maritima | 5 | 2019 | 15 | 1.580 |
Why?
|
Molecular Dynamics Simulation | 24 | 2023 | 264 | 1.550 |
Why?
|
Mechanotransduction, Cellular | 7 | 2023 | 81 | 1.540 |
Why?
|
Electron Spin Resonance Spectroscopy | 33 | 2016 | 318 | 1.460 |
Why?
|
Ciona intestinalis | 3 | 2023 | 26 | 1.410 |
Why?
|
Protons | 8 | 2022 | 101 | 1.300 |
Why?
|
Cryoelectron Microscopy | 6 | 2023 | 102 | 1.210 |
Why?
|
Lipids | 3 | 2020 | 275 | 1.160 |
Why?
|
Potassium Channels, Voltage-Gated | 6 | 2014 | 125 | 1.080 |
Why?
|
Hair Cells, Auditory, Outer | 2 | 2023 | 17 | 1.000 |
Why?
|
Amino Acid Sequence | 25 | 2021 | 2063 | 0.990 |
Why?
|
Protein Structure, Secondary | 16 | 2022 | 333 | 0.890 |
Why?
|
Crystallography, X-Ray | 21 | 2019 | 490 | 0.870 |
Why?
|
Large-Conductance Calcium-Activated Potassium Channels | 1 | 2022 | 11 | 0.820 |
Why?
|
Anion Transport Proteins | 1 | 2021 | 10 | 0.780 |
Why?
|
Streptomyces lividans | 8 | 2013 | 16 | 0.780 |
Why?
|
Molecular Sequence Data | 21 | 2015 | 3024 | 0.710 |
Why?
|
Potassium | 7 | 2024 | 258 | 0.700 |
Why?
|
Streptomyces | 8 | 2002 | 21 | 0.680 |
Why?
|
Phosphoric Monoester Hydrolases | 3 | 2023 | 51 | 0.680 |
Why?
|
Potassium Channels, Inwardly Rectifying | 1 | 2020 | 121 | 0.660 |
Why?
|
Cell Membrane | 12 | 2016 | 675 | 0.660 |
Why?
|
Receptors, N-Methyl-D-Aspartate | 1 | 2019 | 87 | 0.650 |
Why?
|
Kinetics | 23 | 2024 | 1534 | 0.640 |
Why?
|
Arabidopsis Proteins | 1 | 2020 | 138 | 0.630 |
Why?
|
Protein Structure, Tertiary | 13 | 2014 | 740 | 0.630 |
Why?
|
Mutation, Missense | 2 | 2019 | 280 | 0.620 |
Why?
|
Gene Expression Regulation, Bacterial | 3 | 2014 | 215 | 0.620 |
Why?
|
Nervous System Diseases | 1 | 2019 | 164 | 0.610 |
Why?
|
Cell Membrane Permeability | 2 | 2016 | 120 | 0.570 |
Why?
|
Arabidopsis | 1 | 2020 | 321 | 0.550 |
Why?
|
Spin Labels | 9 | 2015 | 106 | 0.550 |
Why?
|
Archaeal Proteins | 3 | 2014 | 18 | 0.540 |
Why?
|
Nerve Tissue Proteins | 1 | 2019 | 511 | 0.540 |
Why?
|
Binding Sites | 11 | 2023 | 1120 | 0.510 |
Why?
|
Patch-Clamp Techniques | 9 | 2017 | 396 | 0.510 |
Why?
|
Membrane Proteins | 8 | 2016 | 1227 | 0.490 |
Why?
|
Protein Structure, Quaternary | 7 | 2017 | 101 | 0.490 |
Why?
|
Hydrogen-Ion Concentration | 11 | 2014 | 503 | 0.490 |
Why?
|
Methanocaldococcus | 1 | 2014 | 3 | 0.470 |
Why?
|
Aeropyrum | 1 | 2014 | 2 | 0.460 |
Why?
|
Axons | 6 | 1994 | 181 | 0.460 |
Why?
|
Xenopus laevis | 10 | 2019 | 138 | 0.450 |
Why?
|
Mutant Proteins | 5 | 2017 | 96 | 0.420 |
Why?
|
Liposomes | 12 | 2016 | 93 | 0.420 |
Why?
|
Ions | 4 | 2014 | 75 | 0.410 |
Why?
|
Nanostructures | 3 | 2019 | 79 | 0.410 |
Why?
|
Sperm Capacitation | 3 | 2022 | 4 | 0.410 |
Why?
|
Models, Biological | 12 | 2010 | 1762 | 0.410 |
Why?
|
Mutation | 13 | 2023 | 4160 | 0.400 |
Why?
|
Membrane Potentials | 12 | 2021 | 436 | 0.400 |
Why?
|
ERG1 Potassium Channel | 2 | 2024 | 15 | 0.390 |
Why?
|
Animals | 31 | 2023 | 27481 | 0.380 |
Why?
|
Static Electricity | 6 | 2021 | 90 | 0.380 |
Why?
|
Ether-A-Go-Go Potassium Channels | 2 | 2024 | 27 | 0.330 |
Why?
|
Cysteine | 9 | 2022 | 137 | 0.320 |
Why?
|
Oocytes | 11 | 2019 | 219 | 0.310 |
Why?
|
Sequence Homology, Amino Acid | 6 | 2021 | 418 | 0.300 |
Why?
|
Edetic Acid | 3 | 2010 | 42 | 0.300 |
Why?
|
Potassium Channels, Calcium-Activated | 1 | 2007 | 19 | 0.280 |
Why?
|
Cloning, Molecular | 4 | 2014 | 645 | 0.280 |
Why?
|
Staphylococcus aureus | 1 | 2009 | 276 | 0.270 |
Why?
|
Electrophysiology | 7 | 2014 | 403 | 0.270 |
Why?
|
Ion Transport | 2 | 2023 | 85 | 0.260 |
Why?
|
Amino Acid Substitution | 7 | 2017 | 338 | 0.260 |
Why?
|
Gram-Negative Bacteria | 1 | 2006 | 35 | 0.260 |
Why?
|
Thermodynamics | 8 | 2016 | 314 | 0.260 |
Why?
|
Anions | 2 | 2023 | 31 | 0.250 |
Why?
|
Arginine | 2 | 2022 | 138 | 0.250 |
Why?
|
Water | 4 | 2016 | 284 | 0.250 |
Why?
|
Protein Binding | 8 | 2022 | 1491 | 0.240 |
Why?
|
Solvents | 4 | 2014 | 96 | 0.240 |
Why?
|
Protein Multimerization | 2 | 2017 | 178 | 0.230 |
Why?
|
HEK293 Cells | 3 | 2024 | 646 | 0.230 |
Why?
|
Mutagenesis, Site-Directed | 7 | 2016 | 283 | 0.230 |
Why?
|
Electricity | 1 | 2023 | 24 | 0.230 |
Why?
|
Models, Chemical | 3 | 2016 | 179 | 0.220 |
Why?
|
Cochlea | 1 | 2023 | 50 | 0.220 |
Why?
|
Protein Domains | 3 | 2021 | 135 | 0.220 |
Why?
|
Mutagenesis | 3 | 2022 | 203 | 0.220 |
Why?
|
Drug Design | 2 | 2022 | 123 | 0.220 |
Why?
|
Allosteric Regulation | 2 | 2020 | 67 | 0.200 |
Why?
|
Magnetic Resonance Spectroscopy | 4 | 2014 | 315 | 0.200 |
Why?
|
Molecular Conformation | 3 | 2016 | 96 | 0.190 |
Why?
|
Decapodiformes | 6 | 1994 | 38 | 0.190 |
Why?
|
Antibodies | 1 | 2023 | 353 | 0.190 |
Why?
|
Xenopus | 5 | 2013 | 126 | 0.190 |
Why?
|
Sodium Channels | 2 | 2010 | 130 | 0.190 |
Why?
|
Albumins | 1 | 2021 | 129 | 0.180 |
Why?
|
HIV Protease | 2 | 2011 | 10 | 0.180 |
Why?
|
Inflammation Mediators | 1 | 2021 | 153 | 0.180 |
Why?
|
Kv1.2 Potassium Channel | 3 | 2012 | 24 | 0.170 |
Why?
|
Dimerization | 2 | 2015 | 143 | 0.170 |
Why?
|
Proteins | 2 | 2021 | 786 | 0.170 |
Why?
|
Neutrophils | 1 | 2021 | 311 | 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 | 1008 | 0.170 |
Why?
|
Mammals | 1 | 2021 | 237 | 0.170 |
Why?
|
Lipid Metabolism | 2 | 2014 | 201 | 0.160 |
Why?
|
Computer Simulation | 4 | 2014 | 1101 | 0.150 |
Why?
|
Spectroscopy, Fourier Transform Infrared | 1 | 1998 | 30 | 0.150 |
Why?
|
Cytoplasm | 2 | 2014 | 285 | 0.150 |
Why?
|
Oxygen | 4 | 2010 | 744 | 0.150 |
Why?
|
Bacteriorhodopsins | 3 | 1994 | 10 | 0.150 |
Why?
|
Leukocytes | 1 | 2018 | 208 | 0.150 |
Why?
|
Finite Element Analysis | 1 | 2017 | 78 | 0.150 |
Why?
|
ATP-Binding Cassette Transporters | 2 | 2008 | 143 | 0.150 |
Why?
|
Crystallography | 2 | 2011 | 45 | 0.140 |
Why?
|
Sequence Alignment | 2 | 2014 | 354 | 0.140 |
Why?
|
Gap Junctions | 2 | 2007 | 144 | 0.140 |
Why?
|
Osmolar Concentration | 2 | 2010 | 182 | 0.140 |
Why?
|
Peptides | 3 | 2022 | 649 | 0.140 |
Why?
|
Light | 3 | 1994 | 292 | 0.130 |
Why?
|
Cell Surface Display Techniques | 1 | 2015 | 16 | 0.130 |
Why?
|
Immunoglobulin Fragments | 1 | 2015 | 24 | 0.130 |
Why?
|
Molecular Chaperones | 1 | 2015 | 123 | 0.120 |
Why?
|
Crystallization | 3 | 2013 | 215 | 0.120 |
Why?
|
Potassium Channel Blockers | 2 | 2017 | 64 | 0.120 |
Why?
|
Pressure | 3 | 2009 | 165 | 0.120 |
Why?
|
Computational Biology | 2 | 2016 | 550 | 0.110 |
Why?
|
Electric Conductivity | 4 | 2002 | 144 | 0.110 |
Why?
|
Kv1.3 Potassium Channel | 2 | 2013 | 14 | 0.110 |
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 | 2449 | 0.100 |
Why?
|
Structure-Activity Relationship | 2 | 2010 | 413 | 0.100 |
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 | 2384 | 0.100 |
Why?
|
Solubility | 1 | 2012 | 183 | 0.100 |
Why?
|
Protein Engineering | 2 | 2010 | 145 | 0.100 |
Why?
|
Shaker Superfamily of Potassium Channels | 3 | 2010 | 49 | 0.100 |
Why?
|
DNA, Complementary | 1 | 2012 | 391 | 0.100 |
Why?
|
Caenorhabditis elegans Proteins | 1 | 2013 | 113 | 0.100 |
Why?
|
Adenosine Triphosphate | 2 | 1991 | 316 | 0.100 |
Why?
|
Up-Regulation | 1 | 2014 | 725 | 0.090 |
Why?
|
Phosphorylation | 5 | 1991 | 1130 | 0.090 |
Why?
|
Aspartic Acid | 1 | 2011 | 64 | 0.090 |
Why?
|
Caenorhabditis elegans | 1 | 2013 | 231 | 0.090 |
Why?
|
In Vitro Techniques | 6 | 2009 | 996 | 0.090 |
Why?
|
Tryptophan | 1 | 2011 | 97 | 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 | 89613 | 0.090 |
Why?
|
Drosophila | 2 | 1993 | 522 | 0.090 |
Why?
|
Scorpion Venoms | 1 | 2009 | 25 | 0.090 |
Why?
|
Neurotoxins | 1 | 2009 | 49 | 0.090 |
Why?
|
Rats | 3 | 2011 | 4041 | 0.080 |
Why?
|
Protein Subunits | 2 | 2012 | 123 | 0.080 |
Why?
|
Time Factors | 3 | 2007 | 5337 | 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 | 7216 | 0.070 |
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 | 2763 | 0.070 |
Why?
|
Female | 8 | 2019 | 46401 | 0.060 |
Why?
|
Solutions | 3 | 2016 | 86 | 0.060 |
Why?
|
Male | 4 | 2022 | 42488 | 0.060 |
Why?
|
Methanococcus | 1 | 2005 | 5 | 0.060 |
Why?
|
Sodium | 2 | 2016 | 331 | 0.060 |
Why?
|
Methionine | 1 | 2005 | 67 | 0.060 |
Why?
|
Tetraethylammonium Compounds | 3 | 1993 | 14 | 0.060 |
Why?
|
Tetraethylammonium | 3 | 1993 | 24 | 0.060 |
Why?
|
Open Reading Frames | 1 | 2005 | 121 | 0.060 |
Why?
|
Hydrophobic and Hydrophilic Interactions | 1 | 2004 | 95 | 0.060 |
Why?
|
Maleimides | 1 | 2002 | 26 | 0.050 |
Why?
|
Membrane Transport Proteins | 1 | 2023 | 170 | 0.050 |
Why?
|
Dialysis | 2 | 1991 | 24 | 0.050 |
Why?
|
Semen | 1 | 2021 | 13 | 0.050 |
Why?
|
Fertilization | 1 | 2021 | 41 | 0.050 |
Why?
|
Mechanoreceptors | 1 | 2001 | 36 | 0.050 |
Why?
|
Spermatozoa | 1 | 2021 | 62 | 0.050 |
Why?
|
Molecular Structure | 1 | 2001 | 292 | 0.050 |
Why?
|
Rubidium Radioisotopes | 2 | 1998 | 4 | 0.050 |
Why?
|
Stress, Mechanical | 1 | 2001 | 253 | 0.040 |
Why?
|
Signal Transduction | 2 | 2010 | 3397 | 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 | 563 | 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?
|
Biopolymers | 1 | 1997 | 26 | 0.040 |
Why?
|
Electric Stimulation | 1 | 1998 | 365 | 0.040 |
Why?
|
Hot Temperature | 1 | 1997 | 207 | 0.030 |
Why?
|
Oxygen Isotopes | 1 | 2016 | 15 | 0.030 |
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 | 462 | 0.030 |
Why?
|
Reactive Oxygen Species | 1 | 2018 | 490 | 0.030 |
Why?
|
Electrochemistry | 2 | 1994 | 60 | 0.030 |
Why?
|
Microscopy, Polarization | 1 | 2015 | 10 | 0.030 |
Why?
|
Arrhythmias, Cardiac | 1 | 2017 | 200 | 0.030 |
Why?
|
Gene Deletion | 1 | 2016 | 341 | 0.030 |
Why?
|
Sensory Rhodopsins | 1 | 1994 | 1 | 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 | 18 | 0.030 |
Why?
|
Microtubules | 1 | 2013 | 123 | 0.030 |
Why?
|
Amino Acid Motifs | 1 | 2012 | 116 | 0.030 |
Why?
|
Protein Stability | 1 | 2012 | 101 | 0.030 |
Why?
|
Isoleucine | 1 | 2011 | 19 | 0.020 |
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 | 49 | 0.020 |
Why?
|
Micelles | 2 | 2008 | 48 | 0.020 |
Why?
|
Sequence Analysis, Protein | 1 | 2010 | 28 | 0.020 |
Why?
|
Drosophila melanogaster | 2 | 1994 | 614 | 0.020 |
Why?
|
Phenylalanine | 1 | 2010 | 35 | 0.020 |
Why?
|
Intercellular Signaling Peptides and Proteins | 1 | 2009 | 182 | 0.020 |
Why?
|
Protein Renaturation | 1 | 2008 | 4 | 0.020 |
Why?
|
Lysophosphatidylcholines | 1 | 2008 | 17 | 0.020 |
Why?
|
Cross-Linking Reagents | 1 | 2008 | 88 | 0.020 |
Why?
|
Ligands | 1 | 2009 | 447 | 0.020 |
Why?
|
Myocardium | 1 | 2011 | 572 | 0.020 |
Why?
|
Immunoglobulin Fab Fragments | 1 | 2009 | 85 | 0.020 |
Why?
|
Asparagine | 1 | 2007 | 30 | 0.020 |
Why?
|
Histidine | 1 | 2007 | 56 | 0.020 |
Why?
|
Models, Neurological | 1 | 1990 | 411 | 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 | 806 | 0.020 |
Why?
|
Fluorescent Dyes | 1 | 2006 | 245 | 0.020 |
Why?
|
Carbon | 1 | 2005 | 90 | 0.020 |
Why?
|
Monte Carlo Method | 1 | 2005 | 185 | 0.020 |
Why?
|
T-Lymphocytes | 1 | 2009 | 1221 | 0.010 |
Why?
|
Software | 1 | 2007 | 667 | 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 | 32 | 0.010 |
Why?
|
Transfection | 1 | 1994 | 909 | 0.010 |
Why?
|
Leishmania mexicana | 1 | 1987 | 1 | 0.000 |
Why?
|
Dimethyl Sulfoxide | 1 | 1987 | 38 | 0.000 |
Why?
|
Copper | 1 | 1987 | 78 | 0.000 |
Why?
|