Concepts (139)
Concepts are derived automatically from a person's publications.
Concepts are listed by decreasing relevance which is based on many factors, including how many publications the person wrote about that topic, how long ago those publications were written, and how many publications other people have written on that same topic.
| Name |
Number of Publications
|
Most Recent Publication
|
Publications by All Authors
|
Concept Score
|
Why?
|
|---|
| Membrane Potentials | 10 | 2016 | 436 | 2.380 |
Why?
|
| Ion Channel Gating | 12 | 2018 | 329 | 1.970 |
Why?
|
| Phosphoric Monoester Hydrolases | 6 | 2013 | 51 | 1.600 |
Why?
|
| Histidine | 2 | 2024 | 56 | 0.990 |
Why?
|
| Electricity | 1 | 2024 | 24 | 0.920 |
Why?
|
| Ion Channels | 2 | 2016 | 246 | 0.920 |
Why?
|
| Ciona intestinalis | 5 | 2014 | 26 | 0.830 |
Why?
|
| Fishes | 1 | 2023 | 138 | 0.770 |
Why?
|
| Potassium Channels | 1 | 2023 | 343 | 0.740 |
Why?
|
| Phenylenediamines | 1 | 2016 | 7 | 0.540 |
Why?
|
| KCNQ3 Potassium Channel | 1 | 2016 | 3 | 0.540 |
Why?
|
| KCNQ2 Potassium Channel | 1 | 2016 | 5 | 0.540 |
Why?
|
| Carbamates | 1 | 2016 | 15 | 0.530 |
Why?
|
| Kinetics | 7 | 2024 | 1528 | 0.500 |
Why?
|
| Anticonvulsants | 1 | 2016 | 125 | 0.490 |
Why?
|
| Models, Biological | 3 | 2016 | 1765 | 0.430 |
Why?
|
| PTEN Phosphohydrolase | 2 | 2011 | 136 | 0.400 |
Why?
|
| Protein Structure, Tertiary | 5 | 2014 | 740 | 0.360 |
Why?
|
| Xenopus | 5 | 2018 | 126 | 0.360 |
Why?
|
| Animals | 21 | 2023 | 27380 | 0.330 |
Why?
|
| Shaker Superfamily of Potassium Channels | 2 | 2023 | 49 | 0.330 |
Why?
|
| Luminescent Proteins | 1 | 2009 | 144 | 0.310 |
Why?
|
| Oocytes | 7 | 2020 | 221 | 0.310 |
Why?
|
| Potassium | 3 | 2024 | 255 | 0.270 |
Why?
|
| Myocardial Contraction | 3 | 2003 | 252 | 0.260 |
Why?
|
| Xenopus laevis | 4 | 2020 | 138 | 0.230 |
Why?
|
| Heart | 3 | 2003 | 574 | 0.220 |
Why?
|
| Calcium | 5 | 2004 | 1175 | 0.220 |
Why?
|
| Thermodynamics | 2 | 2016 | 311 | 0.200 |
Why?
|
| Action Potentials | 5 | 2018 | 600 | 0.180 |
Why?
|
| Patch-Clamp Techniques | 2 | 2018 | 396 | 0.180 |
Why?
|
| Neuromuscular Agents | 1 | 2020 | 26 | 0.180 |
Why?
|
| Nicotinic Agonists | 1 | 2020 | 73 | 0.170 |
Why?
|
| Receptors, Nicotinic | 1 | 2020 | 131 | 0.160 |
Why?
|
| Muscle Contraction | 1 | 2000 | 284 | 0.160 |
Why?
|
| Phosphatidylinositol 4,5-Diphosphate | 1 | 2018 | 11 | 0.150 |
Why?
|
| Shab Potassium Channels | 1 | 2018 | 29 | 0.150 |
Why?
|
| Muscle, Skeletal | 2 | 2003 | 468 | 0.150 |
Why?
|
| Models, Animal | 1 | 2018 | 276 | 0.150 |
Why?
|
| Humans | 12 | 2024 | 89367 | 0.140 |
Why?
|
| Potassium Channels, Voltage-Gated | 2 | 2018 | 125 | 0.130 |
Why?
|
| Mutagenesis, Site-Directed | 2 | 2013 | 283 | 0.130 |
Why?
|
| Protein Domains | 1 | 2016 | 134 | 0.130 |
Why?
|
| Electrophysiology | 3 | 2014 | 403 | 0.130 |
Why?
|
| Fluorescent Dyes | 3 | 2008 | 244 | 0.120 |
Why?
|
| Protein Multimerization | 1 | 2016 | 176 | 0.120 |
Why?
|
| Structure-Activity Relationship | 2 | 2020 | 413 | 0.120 |
Why?
|
| Mutation | 2 | 2024 | 4143 | 0.110 |
Why?
|
| Hydrogen-Ion Concentration | 1 | 2014 | 501 | 0.110 |
Why?
|
| Hydrophobic and Hydrophilic Interactions | 1 | 2013 | 94 | 0.110 |
Why?
|
| Microscopy, Fluorescence | 3 | 2012 | 428 | 0.110 |
Why?
|
| Intermediate-Conductance Calcium-Activated Potassium Channels | 1 | 2013 | 5 | 0.110 |
Why?
|
| Protons | 1 | 2013 | 101 | 0.110 |
Why?
|
| KCNQ1 Potassium Channel | 1 | 2013 | 17 | 0.110 |
Why?
|
| Ear, Inner | 1 | 2013 | 33 | 0.110 |
Why?
|
| Fluorescence | 2 | 2013 | 103 | 0.110 |
Why?
|
| Kv1.2 Potassium Channel | 1 | 2012 | 24 | 0.100 |
Why?
|
| Electrochemical Techniques | 1 | 2012 | 8 | 0.100 |
Why?
|
| Myocytes, Cardiac | 3 | 2004 | 314 | 0.100 |
Why?
|
| Biocatalysis | 1 | 2012 | 50 | 0.100 |
Why?
|
| Myocardium | 1 | 2013 | 571 | 0.090 |
Why?
|
| Recombinant Fusion Proteins | 1 | 2011 | 565 | 0.080 |
Why?
|
| Fluorometry | 1 | 2009 | 30 | 0.080 |
Why?
|
| Ion Transport | 1 | 2009 | 81 | 0.080 |
Why?
|
| Mutant Proteins | 1 | 2008 | 96 | 0.080 |
Why?
|
| Staining and Labeling | 1 | 2008 | 168 | 0.080 |
Why?
|
| Signal Transduction | 2 | 2016 | 3386 | 0.080 |
Why?
|
| Enzyme Activation | 1 | 2009 | 698 | 0.080 |
Why?
|
| Temperature | 1 | 2008 | 405 | 0.070 |
Why?
|
| Recombinant Proteins | 1 | 2009 | 1012 | 0.070 |
Why?
|
| Binding Sites | 1 | 2009 | 1117 | 0.070 |
Why?
|
| Clathrin | 1 | 2006 | 29 | 0.070 |
Why?
|
| Decapodiformes | 1 | 2006 | 37 | 0.070 |
Why?
|
| Synaptic Vesicles | 1 | 2006 | 38 | 0.070 |
Why?
|
| Protein Conformation | 1 | 2008 | 891 | 0.060 |
Why?
|
| Protein Binding | 1 | 2009 | 1488 | 0.060 |
Why?
|
| Endocytosis | 1 | 2006 | 180 | 0.060 |
Why?
|
| Ryanodine Receptor Calcium Release Channel | 2 | 2003 | 25 | 0.060 |
Why?
|
| Strontium | 1 | 2004 | 6 | 0.060 |
Why?
|
| Cations, Divalent | 1 | 2004 | 39 | 0.060 |
Why?
|
| Cells, Cultured | 1 | 2009 | 2884 | 0.060 |
Why?
|
| Heterocyclic Compounds, 3-Ring | 2 | 2003 | 31 | 0.060 |
Why?
|
| Synapses | 1 | 2006 | 280 | 0.050 |
Why?
|
| Rats | 4 | 2004 | 4041 | 0.050 |
Why?
|
| Calcium Channels | 1 | 2003 | 182 | 0.050 |
Why?
|
| Time Factors | 2 | 2008 | 5339 | 0.050 |
Why?
|
| CHO Cells | 2 | 2012 | 188 | 0.050 |
Why?
|
| Cricetinae | 2 | 2012 | 558 | 0.050 |
Why?
|
| Cell Membrane | 2 | 2014 | 672 | 0.050 |
Why?
|
| Azo Compounds | 1 | 2020 | 13 | 0.050 |
Why?
|
| Isomerism | 1 | 2020 | 29 | 0.050 |
Why?
|
| Quaternary Ammonium Compounds | 1 | 2020 | 81 | 0.040 |
Why?
|
| Anura | 1 | 2000 | 20 | 0.040 |
Why?
|
| Amino Acid Sequence | 2 | 2014 | 2062 | 0.040 |
Why?
|
| Muscle Fibers, Skeletal | 1 | 2000 | 49 | 0.040 |
Why?
|
| Molecular Sequence Data | 2 | 2014 | 3027 | 0.040 |
Why?
|
| Light | 1 | 2020 | 293 | 0.040 |
Why?
|
| Ligands | 1 | 2020 | 445 | 0.040 |
Why?
|
| Electric Stimulation | 1 | 2000 | 356 | 0.040 |
Why?
|
| Adaptation, Physiological | 1 | 2000 | 314 | 0.040 |
Why?
|
| In Vitro Techniques | 1 | 2000 | 996 | 0.040 |
Why?
|
| Receptors, Muscarinic | 1 | 2018 | 48 | 0.040 |
Why?
|
| Sodium | 1 | 2018 | 331 | 0.040 |
Why?
|
| Models, Theoretical | 1 | 2000 | 491 | 0.040 |
Why?
|
| HEK293 Cells | 1 | 2018 | 640 | 0.030 |
Why?
|
| Heart Ventricles | 1 | 2000 | 779 | 0.030 |
Why?
|
| Static Electricity | 1 | 2014 | 90 | 0.030 |
Why?
|
| Protein Stability | 1 | 2013 | 100 | 0.030 |
Why?
|
| Voltage-Sensitive Dye Imaging | 1 | 2013 | 3 | 0.030 |
Why?
|
| Sequence Homology, Amino Acid | 1 | 2014 | 418 | 0.030 |
Why?
|
| Electric Conductivity | 1 | 2013 | 144 | 0.030 |
Why?
|
| Phosphatidylinositols | 1 | 2012 | 20 | 0.030 |
Why?
|
| Protein Subunits | 1 | 2013 | 123 | 0.030 |
Why?
|
| Crystallography, X-Ray | 1 | 2014 | 486 | 0.030 |
Why?
|
| Genes, Reporter | 1 | 2012 | 275 | 0.030 |
Why?
|
| Electron Spin Resonance Spectroscopy | 1 | 2014 | 317 | 0.020 |
Why?
|
| Mutation, Missense | 1 | 2012 | 277 | 0.020 |
Why?
|
| Cricetulus | 1 | 2011 | 127 | 0.020 |
Why?
|
| Escherichia coli | 1 | 2014 | 605 | 0.020 |
Why?
|
| Molecular Dynamics Simulation | 1 | 2012 | 260 | 0.020 |
Why?
|
| Models, Molecular | 1 | 2014 | 1303 | 0.020 |
Why?
|
| Auxilins | 1 | 2006 | 1 | 0.020 |
Why?
|
| Calcium-Binding Proteins | 1 | 2006 | 121 | 0.020 |
Why?
|
| Neurotransmitter Agents | 1 | 2006 | 108 | 0.020 |
Why?
|
| Sarcoplasmic Reticulum | 1 | 2004 | 25 | 0.020 |
Why?
|
| Synaptic Transmission | 1 | 2006 | 228 | 0.010 |
Why?
|
| Sarcolemma | 1 | 2003 | 31 | 0.010 |
Why?
|
| Calcium Channels, L-Type | 1 | 2003 | 38 | 0.010 |
Why?
|
| Calcium Channels, T-Type | 1 | 2003 | 25 | 0.010 |
Why?
|
| Coronary Circulation | 1 | 2003 | 131 | 0.010 |
Why?
|
| Animals, Newborn | 1 | 2003 | 524 | 0.010 |
Why?
|
| Rats, Wistar | 1 | 2003 | 302 | 0.010 |
Why?
|
| Artifacts | 1 | 2003 | 247 | 0.010 |
Why?
|
| Mice, Inbred BALB C | 1 | 2003 | 1088 | 0.010 |
Why?
|
| Reaction Time | 1 | 2000 | 310 | 0.010 |
Why?
|
| Age Factors | 1 | 2003 | 1871 | 0.010 |
Why?
|
| Male | 2 | 2003 | 42423 | 0.010 |
Why?
|
| Female | 2 | 2003 | 46222 | 0.010 |
Why?
|
| Mice | 1 | 2003 | 11764 | 0.000 |
Why?
|
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Concepts
(139)
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