Concepts (250)
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?
|
|---|
| Shal Potassium Channels | 23 | 2026 | 47 | 3.820 |
Why?
|
| Potassium Channels | 23 | 2014 | 152 | 2.550 |
Why?
|
| Dipeptidyl-Peptidases and Tripeptidyl-Peptidases | 9 | 2014 | 19 | 2.260 |
Why?
|
| Ion Channel Gating | 14 | 2013 | 119 | 2.130 |
Why?
|
| Shaker Superfamily of Potassium Channels | 9 | 2021 | 31 | 1.580 |
Why?
|
| Oocytes | 12 | 2021 | 278 | 1.540 |
Why?
|
| Potassium Channels, Voltage-Gated | 12 | 2005 | 59 | 1.330 |
Why?
|
| Kv Channel-Interacting Proteins | 9 | 2014 | 33 | 1.190 |
Why?
|
| Protein Subunits | 10 | 2014 | 162 | 1.000 |
Why?
|
| Membrane Potentials | 13 | 2021 | 294 | 0.900 |
Why?
|
| Cell Membrane | 8 | 2009 | 448 | 0.850 |
Why?
|
| Neurons | 10 | 2021 | 1922 | 0.820 |
Why?
|
| Protein Interaction Domains and Motifs | 2 | 2013 | 134 | 0.790 |
Why?
|
| Behavior, Animal | 1 | 2026 | 496 | 0.780 |
Why?
|
| Xenopus laevis | 10 | 2021 | 118 | 0.730 |
Why?
|
| Action Potentials | 6 | 2021 | 460 | 0.640 |
Why?
|
| Cerebellum | 3 | 2013 | 415 | 0.630 |
Why?
|
| Epilepsy | 1 | 2026 | 846 | 0.570 |
Why?
|
| Repressor Proteins | 4 | 2014 | 765 | 0.570 |
Why?
|
| Animals | 44 | 2026 | 33226 | 0.470 |
Why?
|
| Amino Acid Sequence | 16 | 2014 | 2555 | 0.450 |
Why?
|
| Protein Structure, Tertiary | 13 | 2013 | 726 | 0.430 |
Why?
|
| Molecular Sequence Data | 16 | 2014 | 3604 | 0.400 |
Why?
|
| Multiprotein Complexes | 2 | 2012 | 193 | 0.400 |
Why?
|
| Static Electricity | 1 | 2013 | 44 | 0.400 |
Why?
|
| Glutathione | 1 | 2014 | 192 | 0.390 |
Why?
|
| Cricetinae | 7 | 2013 | 365 | 0.380 |
Why?
|
| Aplysia | 6 | 2003 | 13 | 0.380 |
Why?
|
| Rats | 14 | 2012 | 3394 | 0.370 |
Why?
|
| Cytoplasmic Granules | 1 | 2012 | 50 | 0.360 |
Why?
|
| Zinc | 5 | 2007 | 121 | 0.360 |
Why?
|
| Reactive Oxygen Species | 1 | 2014 | 489 | 0.350 |
Why?
|
| Conserved Sequence | 5 | 2013 | 286 | 0.330 |
Why?
|
| Potassium | 3 | 2005 | 259 | 0.320 |
Why?
|
| Kinetics | 8 | 2013 | 1092 | 0.310 |
Why?
|
| Mice, Transgenic | 4 | 2026 | 2319 | 0.300 |
Why?
|
| Patch-Clamp Techniques | 5 | 2014 | 273 | 0.300 |
Why?
|
| Nerve Tissue Proteins | 3 | 2014 | 1097 | 0.300 |
Why?
|
| CHO Cells | 6 | 2013 | 149 | 0.290 |
Why?
|
| Protein Conformation | 8 | 2013 | 801 | 0.290 |
Why?
|
| COS Cells | 9 | 2013 | 249 | 0.270 |
Why?
|
| Calcium-Binding Proteins | 4 | 2004 | 327 | 0.270 |
Why?
|
| Models, Molecular | 9 | 2013 | 1067 | 0.250 |
Why?
|
| Mutation | 8 | 2026 | 5933 | 0.240 |
Why?
|
| Gene Knock-In Techniques | 1 | 2026 | 119 | 0.230 |
Why?
|
| Protein Binding | 6 | 2013 | 1675 | 0.230 |
Why?
|
| Fear | 1 | 2026 | 199 | 0.220 |
Why?
|
| Rats, Sprague-Dawley | 5 | 2012 | 1131 | 0.220 |
Why?
|
| Cells, Cultured | 6 | 2013 | 2906 | 0.210 |
Why?
|
| Sequence Alignment | 4 | 2013 | 588 | 0.210 |
Why?
|
| Heterozygote | 1 | 2026 | 691 | 0.210 |
Why?
|
| Binding Sites | 11 | 2006 | 1193 | 0.210 |
Why?
|
| Mutagenesis | 4 | 2013 | 333 | 0.200 |
Why?
|
| Cloning, Molecular | 3 | 2013 | 786 | 0.200 |
Why?
|
| Gene Expression | 4 | 2014 | 1489 | 0.190 |
Why?
|
| Amino Acid Motifs | 3 | 2013 | 193 | 0.190 |
Why?
|
| Mutation, Missense | 2 | 2026 | 889 | 0.190 |
Why?
|
| Xenopus | 5 | 2013 | 103 | 0.180 |
Why?
|
| Cell Line | 3 | 2013 | 2570 | 0.180 |
Why?
|
| Sequence Homology, Amino Acid | 6 | 2014 | 622 | 0.180 |
Why?
|
| Mice | 7 | 2026 | 17616 | 0.180 |
Why?
|
| RNA Interference | 3 | 2013 | 495 | 0.170 |
Why?
|
| Structure-Activity Relationship | 6 | 2005 | 567 | 0.170 |
Why?
|
| Electric Conductivity | 6 | 2004 | 81 | 0.160 |
Why?
|
| Transfection | 5 | 2014 | 949 | 0.160 |
Why?
|
| Cytoplasm | 2 | 2000 | 250 | 0.150 |
Why?
|
| Green Fluorescent Proteins | 3 | 2013 | 376 | 0.150 |
Why?
|
| Protein Isoforms | 2 | 2012 | 403 | 0.150 |
Why?
|
| Electrophysiology | 4 | 2010 | 250 | 0.150 |
Why?
|
| Gene Expression Regulation | 3 | 2006 | 2332 | 0.150 |
Why?
|
| HEK293 Cells | 1 | 2021 | 770 | 0.140 |
Why?
|
| Gonadotropin-Releasing Hormone | 2 | 1988 | 72 | 0.140 |
Why?
|
| Cyclic AMP-Dependent Protein Kinases | 3 | 2006 | 158 | 0.140 |
Why?
|
| Amino Acid Substitution | 3 | 2013 | 397 | 0.140 |
Why?
|
| Genetic Vectors | 5 | 2010 | 892 | 0.130 |
Why?
|
| Mice, Inbred C57BL | 1 | 2026 | 4516 | 0.130 |
Why?
|
| Biopolymers | 1 | 1995 | 19 | 0.120 |
Why?
|
| Hippocampus | 5 | 2010 | 775 | 0.120 |
Why?
|
| Blotting, Western | 3 | 2010 | 1019 | 0.120 |
Why?
|
| Potassium Channels, Inwardly Rectifying | 2 | 2006 | 39 | 0.110 |
Why?
|
| Diamide | 1 | 2014 | 3 | 0.110 |
Why?
|
| tert-Butylhydroperoxide | 1 | 2014 | 7 | 0.110 |
Why?
|
| Dithiothreitol | 1 | 2014 | 11 | 0.110 |
Why?
|
| Intracellular Membranes | 1 | 2013 | 55 | 0.100 |
Why?
|
| Cattle | 1 | 2014 | 535 | 0.100 |
Why?
|
| Algorithms | 2 | 2013 | 1639 | 0.090 |
Why?
|
| Ganglia, Sympathetic | 2 | 1990 | 8 | 0.090 |
Why?
|
| Protein Transport | 1 | 2013 | 352 | 0.090 |
Why?
|
| Muscarine | 2 | 1988 | 7 | 0.090 |
Why?
|
| Models, Neurological | 1 | 2013 | 185 | 0.090 |
Why?
|
| Microscopy, Confocal | 2 | 2004 | 361 | 0.090 |
Why?
|
| Colforsin | 3 | 2006 | 45 | 0.090 |
Why?
|
| Evolution, Molecular | 2 | 2012 | 686 | 0.080 |
Why?
|
| Dimerization | 4 | 2005 | 136 | 0.080 |
Why?
|
| Alternative Splicing | 1 | 2012 | 298 | 0.080 |
Why?
|
| Amino Acids | 1 | 2013 | 615 | 0.080 |
Why?
|
| Gene Deletion | 1 | 1993 | 769 | 0.080 |
Why?
|
| Lentivirus | 1 | 2010 | 79 | 0.080 |
Why?
|
| Models, Biological | 2 | 2013 | 1375 | 0.080 |
Why?
|
| Porosity | 1 | 2009 | 35 | 0.080 |
Why?
|
| Drosophila | 1 | 2013 | 782 | 0.080 |
Why?
|
| DNA, Complementary | 1 | 2009 | 435 | 0.070 |
Why?
|
| Virulence Factors, Bordetella | 1 | 1988 | 17 | 0.070 |
Why?
|
| Inositol Phosphates | 1 | 1988 | 12 | 0.070 |
Why?
|
| Pertussis Toxin | 1 | 1988 | 21 | 0.070 |
Why?
|
| Recombinant Proteins | 3 | 2004 | 1298 | 0.070 |
Why?
|
| Plasmids | 1 | 2009 | 447 | 0.070 |
Why?
|
| Substance P | 1 | 1988 | 32 | 0.070 |
Why?
|
| Phosphatidylinositols | 1 | 1988 | 31 | 0.070 |
Why?
|
| Analysis of Variance | 1 | 2010 | 950 | 0.070 |
Why?
|
| Protein Folding | 3 | 2004 | 216 | 0.070 |
Why?
|
| Acetylcholine | 1 | 1988 | 82 | 0.070 |
Why?
|
| In Situ Hybridization | 2 | 2007 | 455 | 0.070 |
Why?
|
| Crystallography, X-Ray | 4 | 2004 | 365 | 0.070 |
Why?
|
| GTP-Binding Proteins | 1 | 1988 | 159 | 0.070 |
Why?
|
| RNA, Messenger | 2 | 2012 | 2552 | 0.070 |
Why?
|
| Humans | 11 | 2021 | 126129 | 0.070 |
Why?
|
| Recombinant Fusion Proteins | 3 | 2006 | 729 | 0.070 |
Why?
|
| Protein Structure, Secondary | 3 | 2004 | 240 | 0.070 |
Why?
|
| Dendrites | 2 | 2006 | 174 | 0.060 |
Why?
|
| Mutagenesis, Site-Directed | 4 | 2004 | 299 | 0.060 |
Why?
|
| Shaw Potassium Channels | 2 | 2003 | 8 | 0.060 |
Why?
|
| Isoenzymes | 1 | 2007 | 209 | 0.060 |
Why?
|
| Andersen Syndrome | 1 | 2006 | 6 | 0.060 |
Why?
|
| Cysteine | 1 | 2007 | 138 | 0.060 |
Why?
|
| Small-Conductance Calcium-Activated Potassium Channels | 1 | 2006 | 12 | 0.060 |
Why?
|
| Eukaryotic Cells | 1 | 2006 | 29 | 0.060 |
Why?
|
| Calcium | 2 | 2004 | 1027 | 0.060 |
Why?
|
| Butadienes | 1 | 2005 | 22 | 0.060 |
Why?
|
| Pyramidal Cells | 1 | 2006 | 138 | 0.060 |
Why?
|
| Cricetulus | 1 | 2005 | 88 | 0.060 |
Why?
|
| Mitogen-Activated Protein Kinase Kinases | 1 | 2005 | 87 | 0.060 |
Why?
|
| Sulfhydryl Compounds | 1 | 2005 | 55 | 0.060 |
Why?
|
| Enzyme Inhibitors | 2 | 2005 | 566 | 0.060 |
Why?
|
| Female | 3 | 2026 | 68037 | 0.060 |
Why?
|
| Chemistry, Physical | 1 | 2004 | 30 | 0.060 |
Why?
|
| Nitriles | 1 | 2005 | 149 | 0.060 |
Why?
|
| Chemical Phenomena | 1 | 2004 | 81 | 0.060 |
Why?
|
| Protein Structure, Quaternary | 2 | 2003 | 96 | 0.050 |
Why?
|
| Nitric Oxide | 1 | 2007 | 462 | 0.050 |
Why?
|
| Sindbis Virus | 1 | 2003 | 10 | 0.050 |
Why?
|
| Endoplasmic Reticulum | 1 | 2004 | 200 | 0.050 |
Why?
|
| Phenanthrolines | 1 | 2003 | 3 | 0.050 |
Why?
|
| Crystallography | 1 | 2003 | 38 | 0.050 |
Why?
|
| Gene Expression Regulation, Viral | 1 | 2003 | 122 | 0.050 |
Why?
|
| Macromolecular Substances | 3 | 2002 | 141 | 0.050 |
Why?
|
| Phosphorylation | 5 | 2006 | 1540 | 0.050 |
Why?
|
| Surface Properties | 1 | 2002 | 80 | 0.050 |
Why?
|
| Brain | 2 | 2007 | 3031 | 0.050 |
Why?
|
| Protein Biosynthesis | 2 | 1995 | 565 | 0.040 |
Why?
|
| Trypsin | 1 | 2001 | 81 | 0.040 |
Why?
|
| Two-Hybrid System Techniques | 1 | 2001 | 62 | 0.040 |
Why?
|
| Kv1.1 Potassium Channel | 1 | 2001 | 35 | 0.040 |
Why?
|
| Models, Chemical | 1 | 2001 | 82 | 0.040 |
Why?
|
| Mitogen-Activated Protein Kinase 1 | 1 | 2000 | 101 | 0.040 |
Why?
|
| Male | 1 | 2026 | 62225 | 0.040 |
Why?
|
| Thermodynamics | 1 | 2000 | 140 | 0.040 |
Why?
|
| Point Mutation | 1 | 2001 | 337 | 0.040 |
Why?
|
| Receptors, Muscarinic | 2 | 1990 | 9 | 0.040 |
Why?
|
| In Vitro Techniques | 3 | 2003 | 821 | 0.040 |
Why?
|
| Chromatography, High Pressure Liquid | 2 | 2000 | 340 | 0.040 |
Why?
|
| Substrate Specificity | 1 | 1999 | 283 | 0.040 |
Why?
|
| Ions | 2 | 2002 | 22 | 0.040 |
Why?
|
| Caenorhabditis elegans | 1 | 1999 | 237 | 0.030 |
Why?
|
| Proteins | 1 | 2003 | 1020 | 0.030 |
Why?
|
| Chromatography, Affinity | 1 | 1995 | 56 | 0.030 |
Why?
|
| Chromatography, Gel | 1 | 1995 | 80 | 0.030 |
Why?
|
| Precipitin Tests | 1 | 1995 | 136 | 0.030 |
Why?
|
| Nickel | 1 | 1995 | 21 | 0.030 |
Why?
|
| Cross-Linking Reagents | 1 | 1995 | 50 | 0.030 |
Why?
|
| Molecular Weight | 1 | 1995 | 298 | 0.030 |
Why?
|
| Genetic Predisposition to Disease | 1 | 2006 | 3260 | 0.030 |
Why?
|
| Dose-Response Relationship, Drug | 3 | 2005 | 1598 | 0.030 |
Why?
|
| Organ Culture Techniques | 2 | 2006 | 145 | 0.030 |
Why?
|
| Enzyme Activation | 2 | 2002 | 582 | 0.030 |
Why?
|
| Tetraethylammonium Compounds | 1 | 1992 | 4 | 0.020 |
Why?
|
| Tetraethylammonium | 1 | 1992 | 11 | 0.020 |
Why?
|
| Myocardium | 2 | 2007 | 837 | 0.020 |
Why?
|
| Time Factors | 3 | 2002 | 6030 | 0.020 |
Why?
|
| Polymerase Chain Reaction | 1 | 1995 | 1490 | 0.020 |
Why?
|
| Electrochemistry | 1 | 1991 | 25 | 0.020 |
Why?
|
| Protein Processing, Post-Translational | 1 | 1993 | 348 | 0.020 |
Why?
|
| Blotting, Northern | 1 | 1991 | 236 | 0.020 |
Why?
|
| Sequence Homology, Nucleic Acid | 1 | 1991 | 252 | 0.020 |
Why?
|
| Tissue Distribution | 1 | 1991 | 364 | 0.020 |
Why?
|
| Anura | 1 | 1990 | 22 | 0.020 |
Why?
|
| Guanosine 5'-O-(3-Thiotriphosphate) | 1 | 1988 | 14 | 0.020 |
Why?
|
| Guanine Nucleotides | 1 | 1988 | 13 | 0.020 |
Why?
|
| Rana pipiens | 1 | 1988 | 29 | 0.020 |
Why?
|
| Synaptic Transmission | 2 | 2006 | 321 | 0.020 |
Why?
|
| Ranidae | 1 | 1988 | 6 | 0.020 |
Why?
|
| Dialysis | 1 | 1988 | 18 | 0.020 |
Why?
|
| Fura-2 | 1 | 1988 | 11 | 0.020 |
Why?
|
| Guanosine Triphosphate | 1 | 1988 | 38 | 0.020 |
Why?
|
| Type C Phospholipases | 1 | 1988 | 16 | 0.020 |
Why?
|
| Fishes | 1 | 1988 | 30 | 0.020 |
Why?
|
| Thionucleotides | 1 | 1988 | 21 | 0.020 |
Why?
|
| Atropine | 1 | 1988 | 26 | 0.020 |
Why?
|
| Sympathetic Nervous System | 1 | 1988 | 55 | 0.020 |
Why?
|
| Benzofurans | 1 | 1988 | 32 | 0.020 |
Why?
|
| Synapses | 1 | 1992 | 433 | 0.020 |
Why?
|
| Homeostasis | 1 | 1992 | 685 | 0.020 |
Why?
|
| Drug Resistance | 1 | 1988 | 248 | 0.020 |
Why?
|
| Adenosine Triphosphate | 1 | 1988 | 267 | 0.020 |
Why?
|
| Nerve Tissue | 1 | 2007 | 6 | 0.020 |
Why?
|
| Ion Transport | 1 | 2007 | 48 | 0.020 |
Why?
|
| Fluorescent Dyes | 1 | 1988 | 249 | 0.020 |
Why?
|
| Disulfides | 1 | 2007 | 78 | 0.020 |
Why?
|
| Base Sequence | 1 | 1991 | 2773 | 0.020 |
Why?
|
| Microscopy, Electron, Transmission | 1 | 2006 | 130 | 0.020 |
Why?
|
| Oxidation-Reduction | 1 | 2007 | 420 | 0.020 |
Why?
|
| Intracellular Fluid | 1 | 2005 | 20 | 0.010 |
Why?
|
| Cyclic AMP | 1 | 2006 | 223 | 0.010 |
Why?
|
| Glutathione Transferase | 1 | 2006 | 145 | 0.010 |
Why?
|
| Magnetic Resonance Spectroscopy | 1 | 2006 | 277 | 0.010 |
Why?
|
| Mass Spectrometry | 1 | 2006 | 351 | 0.010 |
Why?
|
| Down-Regulation | 1 | 2006 | 651 | 0.010 |
Why?
|
| DNA Mutational Analysis | 1 | 2006 | 780 | 0.010 |
Why?
|
| MAP Kinase Signaling System | 1 | 2005 | 299 | 0.010 |
Why?
|
| Tryptophan | 1 | 2004 | 94 | 0.010 |
Why?
|
| Phenylalanine | 1 | 2004 | 120 | 0.010 |
Why?
|
| 8-Bromo Cyclic Adenosine Monophosphate | 1 | 2002 | 20 | 0.010 |
Why?
|
| Phosphopeptides | 1 | 2002 | 25 | 0.010 |
Why?
|
| Luminescent Proteins | 1 | 2003 | 155 | 0.010 |
Why?
|
| Protein Denaturation | 1 | 2002 | 47 | 0.010 |
Why?
|
| Spectrometry, Fluorescence | 1 | 2002 | 78 | 0.010 |
Why?
|
| Phylogeny | 1 | 2004 | 718 | 0.010 |
Why?
|
| Hydrogen-Ion Concentration | 1 | 2002 | 422 | 0.010 |
Why?
|
| Urea | 1 | 2002 | 225 | 0.010 |
Why?
|
| Myocytes, Cardiac | 1 | 2006 | 609 | 0.010 |
Why?
|
| Electrocardiography | 1 | 2006 | 918 | 0.010 |
Why?
|
| Antibody Specificity | 1 | 2000 | 197 | 0.010 |
Why?
|
| Threonine | 1 | 2000 | 60 | 0.010 |
Why?
|
| Animals, Newborn | 1 | 2003 | 1014 | 0.010 |
Why?
|
| Oligopeptides | 1 | 2000 | 115 | 0.010 |
Why?
|
| Antibodies | 1 | 2000 | 352 | 0.010 |
Why?
|
| Serine | 1 | 2000 | 161 | 0.010 |
Why?
|
| Sequence Analysis | 1 | 1999 | 51 | 0.010 |
Why?
|
| Dentate Gyrus | 1 | 1999 | 36 | 0.010 |
Why?
|
| Hydrogen Bonding | 1 | 1998 | 82 | 0.010 |
Why?
|
| Crystallization | 1 | 1998 | 82 | 0.010 |
Why?
|
| Immunohistochemistry | 1 | 2000 | 1604 | 0.010 |
Why?
|
| Escherichia coli | 1 | 2002 | 968 | 0.010 |
Why?
|
| Cerebral Cortex | 1 | 1999 | 442 | 0.010 |
Why?
|
| Electroencephalography | 1 | 1999 | 845 | 0.010 |
Why?
|
| Transcription, Genetic | 1 | 1999 | 1381 | 0.010 |
Why?
|
| Receptors, Neurotransmitter | 1 | 1990 | 20 | 0.010 |
Why?
|
| Phenotype | 1 | 1999 | 4313 | 0.000 |
Why?
|
| Signal Transduction | 1 | 2000 | 4472 | 0.000 |
Why?
|
| Adolescent | 1 | 2006 | 19986 | 0.000 |
Why?
|