Concepts (152)
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?
|
---|
Potassium Channels, Voltage-Gated | 16 | 2017 | 31 | 3.950 |
Why?
|
KCNQ1 Potassium Channel | 10 | 2014 | 16 | 2.830 |
Why?
|
Ion Channel Gating | 7 | 2015 | 40 | 1.680 |
Why?
|
Potassium | 4 | 2017 | 109 | 1.250 |
Why?
|
Cell Membrane | 4 | 2020 | 488 | 1.130 |
Why?
|
Potassium Channels | 3 | 2012 | 53 | 1.100 |
Why?
|
Calmodulin | 2 | 2014 | 18 | 0.890 |
Why?
|
CHO Cells | 9 | 2017 | 191 | 0.820 |
Why?
|
Chloride Channels | 1 | 2022 | 27 | 0.800 |
Why?
|
Protein Processing, Post-Translational | 3 | 2013 | 253 | 0.770 |
Why?
|
Membrane Potentials | 7 | 2015 | 135 | 0.770 |
Why?
|
Oocytes | 5 | 2011 | 189 | 0.770 |
Why?
|
Protons | 2 | 2020 | 59 | 0.750 |
Why?
|
Charybdotoxin | 2 | 2013 | 5 | 0.740 |
Why?
|
Wheat Germ Agglutinins | 1 | 2020 | 8 | 0.720 |
Why?
|
Cricetinae | 8 | 2014 | 376 | 0.660 |
Why?
|
Cricetulus | 7 | 2017 | 102 | 0.660 |
Why?
|
Animals | 26 | 2020 | 19467 | 0.650 |
Why?
|
Shab Potassium Channels | 1 | 2018 | 1 | 0.650 |
Why?
|
Protein Subunits | 3 | 2009 | 162 | 0.630 |
Why?
|
Potassium Channel Blockers | 3 | 2013 | 25 | 0.590 |
Why?
|
Palladium | 1 | 2017 | 6 | 0.590 |
Why?
|
Glycosylation | 5 | 2020 | 133 | 0.580 |
Why?
|
Oxazines | 1 | 2017 | 13 | 0.580 |
Why?
|
Fluorescent Dyes | 1 | 2017 | 193 | 0.520 |
Why?
|
Molecular Probe Techniques | 1 | 2015 | 6 | 0.490 |
Why?
|
Molecular Probes | 1 | 2015 | 29 | 0.480 |
Why?
|
Glycopeptides | 1 | 2014 | 12 | 0.480 |
Why?
|
Peptides | 3 | 2013 | 545 | 0.480 |
Why?
|
Protein Binding | 6 | 2015 | 1541 | 0.470 |
Why?
|
Peptide Chain Initiation, Translational | 1 | 2014 | 20 | 0.470 |
Why?
|
Ion Channels | 1 | 2015 | 86 | 0.470 |
Why?
|
Spectrum Analysis | 1 | 2014 | 51 | 0.460 |
Why?
|
Cluster Analysis | 1 | 2014 | 249 | 0.440 |
Why?
|
Neurons | 4 | 2016 | 852 | 0.420 |
Why?
|
Protein Biosynthesis | 1 | 2014 | 290 | 0.400 |
Why?
|
Pseudomonas fluorescens | 1 | 2011 | 1 | 0.390 |
Why?
|
Stenotrophomonas maltophilia | 1 | 2011 | 1 | 0.390 |
Why?
|
Pseudomonas putida | 1 | 2011 | 3 | 0.390 |
Why?
|
Disulfides | 2 | 2010 | 62 | 0.380 |
Why?
|
Protein Structure, Secondary | 2 | 2014 | 248 | 0.370 |
Why?
|
Xenopus laevis | 5 | 2016 | 66 | 0.360 |
Why?
|
Protein Interaction Domains and Motifs | 1 | 2010 | 82 | 0.340 |
Why?
|
Protein Interaction Mapping | 1 | 2010 | 70 | 0.340 |
Why?
|
Recombinant Fusion Proteins | 1 | 2011 | 500 | 0.330 |
Why?
|
Cysteine | 4 | 2013 | 107 | 0.330 |
Why?
|
Myocardium | 1 | 2011 | 261 | 0.330 |
Why?
|
Ion Transport | 2 | 2022 | 19 | 0.330 |
Why?
|
Protein Conformation | 4 | 2015 | 760 | 0.320 |
Why?
|
Patch-Clamp Techniques | 4 | 2011 | 125 | 0.310 |
Why?
|
Xenopus | 4 | 2009 | 53 | 0.300 |
Why?
|
Scorpion Venoms | 1 | 2007 | 2 | 0.290 |
Why?
|
Binding Sites | 3 | 2015 | 869 | 0.280 |
Why?
|
Amino Acid Sequence | 4 | 2014 | 1576 | 0.280 |
Why?
|
Models, Molecular | 3 | 2015 | 1111 | 0.230 |
Why?
|
Electrophysiology | 3 | 2009 | 89 | 0.230 |
Why?
|
Long QT Syndrome | 2 | 2014 | 28 | 0.210 |
Why?
|
Humans | 17 | 2018 | 58749 | 0.210 |
Why?
|
Hydrophobic and Hydrophilic Interactions | 2 | 2014 | 246 | 0.200 |
Why?
|
Gene Expression Regulation | 1 | 2009 | 1537 | 0.200 |
Why?
|
Mutation | 4 | 2016 | 2416 | 0.200 |
Why?
|
Mutagenesis, Site-Directed | 3 | 2007 | 252 | 0.190 |
Why?
|
Cells, Cultured | 3 | 2013 | 2090 | 0.190 |
Why?
|
Molecular Conformation | 2 | 2012 | 132 | 0.180 |
Why?
|
Models, Chemical | 2 | 2012 | 133 | 0.170 |
Why?
|
Protein Transport | 3 | 2012 | 393 | 0.170 |
Why?
|
Structure-Activity Relationship | 2 | 2015 | 371 | 0.170 |
Why?
|
Molecular Sequence Data | 2 | 2014 | 1972 | 0.160 |
Why?
|
Hydrogen-Ion Concentration | 1 | 2020 | 424 | 0.160 |
Why?
|
Cytoplasm | 2 | 2012 | 270 | 0.160 |
Why?
|
Infrared Rays | 1 | 2017 | 16 | 0.150 |
Why?
|
HEK293 Cells | 3 | 2018 | 564 | 0.140 |
Why?
|
NAV1.3 Voltage-Gated Sodium Channel | 1 | 2016 | 1 | 0.140 |
Why?
|
Electrophysiological Phenomena | 1 | 2016 | 21 | 0.130 |
Why?
|
Molecular Structure | 1 | 2017 | 374 | 0.130 |
Why?
|
Autophagy | 1 | 2018 | 205 | 0.130 |
Why?
|
Superoxide Dismutase-1 | 1 | 2016 | 134 | 0.130 |
Why?
|
RNA-Binding Proteins | 1 | 2018 | 379 | 0.130 |
Why?
|
Myocytes, Cardiac | 2 | 2014 | 85 | 0.120 |
Why?
|
Consensus Sequence | 1 | 2014 | 28 | 0.120 |
Why?
|
Forecasting | 1 | 2014 | 217 | 0.110 |
Why?
|
Models, Biological | 2 | 2009 | 1134 | 0.110 |
Why?
|
Drosophila Proteins | 1 | 2018 | 677 | 0.110 |
Why?
|
Maleimides | 1 | 2013 | 7 | 0.110 |
Why?
|
Chromatography, Reverse-Phase | 1 | 2013 | 5 | 0.110 |
Why?
|
Hexosyltransferases | 1 | 2013 | 40 | 0.110 |
Why?
|
Chromatography, Gel | 1 | 2013 | 65 | 0.110 |
Why?
|
KCNQ2 Potassium Channel | 1 | 2012 | 2 | 0.100 |
Why?
|
KCNQ3 Potassium Channel | 1 | 2012 | 2 | 0.100 |
Why?
|
Tetraethylammonium | 1 | 2012 | 8 | 0.100 |
Why?
|
Potassium Channels, Tandem Pore Domain | 1 | 2012 | 3 | 0.100 |
Why?
|
Protein Folding | 1 | 2014 | 256 | 0.100 |
Why?
|
14-3-3 Proteins | 1 | 2012 | 19 | 0.100 |
Why?
|
Ions | 1 | 2012 | 52 | 0.100 |
Why?
|
Chromatography, High Pressure Liquid | 1 | 2013 | 197 | 0.100 |
Why?
|
Protein Structure, Quaternary | 1 | 2012 | 99 | 0.100 |
Why?
|
Staining and Labeling | 1 | 2013 | 123 | 0.100 |
Why?
|
Protein Kinase C | 1 | 2012 | 98 | 0.100 |
Why?
|
Cerebellum | 1 | 2012 | 92 | 0.100 |
Why?
|
Amikacin | 1 | 2011 | 1 | 0.100 |
Why?
|
Ciprofloxacin | 1 | 2011 | 20 | 0.100 |
Why?
|
Threonine | 1 | 2011 | 14 | 0.100 |
Why?
|
Microinjections | 1 | 2011 | 65 | 0.100 |
Why?
|
Endocytosis | 1 | 2012 | 148 | 0.100 |
Why?
|
Asparagine | 1 | 2011 | 24 | 0.100 |
Why?
|
Drug Resistance, Multiple | 1 | 2011 | 34 | 0.090 |
Why?
|
Action Potentials | 1 | 2011 | 103 | 0.090 |
Why?
|
Point Mutation | 1 | 2011 | 162 | 0.090 |
Why?
|
Protein Isoforms | 1 | 2011 | 192 | 0.090 |
Why?
|
Computational Biology | 1 | 2012 | 323 | 0.090 |
Why?
|
Arrhythmias, Cardiac | 1 | 2011 | 142 | 0.090 |
Why?
|
Polysaccharides | 1 | 2011 | 143 | 0.090 |
Why?
|
HeLa Cells | 1 | 2011 | 527 | 0.090 |
Why?
|
Nerve Tissue Proteins | 1 | 2012 | 418 | 0.080 |
Why?
|
Quaternary Ammonium Compounds | 1 | 2009 | 27 | 0.080 |
Why?
|
Boronic Acids | 1 | 2009 | 27 | 0.080 |
Why?
|
DNA, Complementary | 1 | 2009 | 166 | 0.080 |
Why?
|
Small Molecule Libraries | 1 | 2009 | 58 | 0.080 |
Why?
|
Transfection | 1 | 2010 | 669 | 0.080 |
Why?
|
Amino Acids | 1 | 2009 | 140 | 0.070 |
Why?
|
Membrane Proteins | 1 | 2013 | 835 | 0.070 |
Why?
|
Mice, Transgenic | 1 | 2011 | 1214 | 0.070 |
Why?
|
Biochemistry | 1 | 2008 | 50 | 0.070 |
Why?
|
Crystallography, X-Ray | 1 | 2008 | 418 | 0.070 |
Why?
|
Ligands | 1 | 2008 | 420 | 0.070 |
Why?
|
RecQ Helicases | 1 | 2006 | 9 | 0.070 |
Why?
|
Golgi Apparatus | 1 | 2006 | 62 | 0.070 |
Why?
|
COS Cells | 1 | 2006 | 176 | 0.070 |
Why?
|
Anti-Bacterial Agents | 1 | 2011 | 710 | 0.060 |
Why?
|
Endoplasmic Reticulum | 1 | 2006 | 168 | 0.060 |
Why?
|
KCNQ Potassium Channels | 1 | 2004 | 3 | 0.060 |
Why?
|
Protein Structure, Tertiary | 1 | 2006 | 660 | 0.060 |
Why?
|
Kidney | 1 | 2006 | 391 | 0.060 |
Why?
|
Amino Acid Substitution | 1 | 2004 | 250 | 0.060 |
Why?
|
Time Factors | 1 | 2010 | 3544 | 0.050 |
Why?
|
Recombinant Proteins | 1 | 2004 | 688 | 0.050 |
Why?
|
Cell Line | 1 | 2006 | 2010 | 0.050 |
Why?
|
Genetic Vectors | 1 | 2007 | 787 | 0.050 |
Why?
|
Proton Pumps | 1 | 2018 | 6 | 0.040 |
Why?
|
Monocarboxylic Acid Transporters | 1 | 2018 | 11 | 0.040 |
Why?
|
Salivary Glands | 1 | 2018 | 46 | 0.040 |
Why?
|
TOR Serine-Threonine Kinases | 1 | 2018 | 112 | 0.040 |
Why?
|
Mice | 1 | 2011 | 10171 | 0.040 |
Why?
|
Sodium | 1 | 2016 | 59 | 0.030 |
Why?
|
Drosophila melanogaster | 1 | 2018 | 479 | 0.030 |
Why?
|
Receptors, Metabotropic Glutamate | 1 | 2012 | 30 | 0.030 |
Why?
|
Amino Acid Motifs | 1 | 2012 | 151 | 0.020 |
Why?
|
Male | 1 | 2011 | 27214 | 0.020 |
Why?
|
Rats, Sprague-Dawley | 1 | 2012 | 569 | 0.020 |
Why?
|
Rats | 1 | 2014 | 1900 | 0.020 |
Why?
|
Signal Transduction | 1 | 2018 | 2870 | 0.020 |
Why?
|
Female | 1 | 2007 | 30508 | 0.020 |
Why?
|