Concepts (138)
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, Tandem Pore Domain | 4 | 2005 | 16 | 0.810 |
Why?
|
| Small Ubiquitin-Related Modifier Proteins | 2 | 2012 | 12 | 0.690 |
Why?
|
| Insulin | 3 | 2014 | 1160 | 0.610 |
Why?
|
| Ion Channel Gating | 5 | 2013 | 324 | 0.550 |
Why?
|
| Insulin-Secreting Cells | 3 | 2014 | 397 | 0.480 |
Why?
|
| Cyclic GMP | 1 | 2012 | 58 | 0.410 |
Why?
|
| Glucagon-Like Peptide 1 | 1 | 2012 | 48 | 0.410 |
Why?
|
| Ion Channels | 4 | 2013 | 246 | 0.360 |
Why?
|
| Proinsulin | 1 | 2009 | 124 | 0.350 |
Why?
|
| Potassium Channels | 4 | 2005 | 340 | 0.340 |
Why?
|
| Insulin Resistance | 1 | 2009 | 377 | 0.300 |
Why?
|
| Mutation | 8 | 2013 | 3968 | 0.270 |
Why?
|
| Cell Membrane | 2 | 2005 | 666 | 0.250 |
Why?
|
| Protons | 3 | 2013 | 98 | 0.240 |
Why?
|
| Tyrosine 3-Monooxygenase | 1 | 2002 | 44 | 0.220 |
Why?
|
| Diabetes Mellitus | 1 | 2009 | 806 | 0.210 |
Why?
|
| Nerve Tissue Proteins | 1 | 2002 | 503 | 0.180 |
Why?
|
| COS Cells | 4 | 2013 | 166 | 0.160 |
Why?
|
| Glucose | 2 | 2012 | 638 | 0.160 |
Why?
|
| Zinc | 3 | 2013 | 91 | 0.140 |
Why?
|
| Eukaryotic Initiation Factor-4G | 1 | 2014 | 3 | 0.120 |
Why?
|
| Carboxypeptidase H | 1 | 2014 | 12 | 0.120 |
Why?
|
| Animals | 10 | 2014 | 26589 | 0.120 |
Why?
|
| Transfection | 3 | 2012 | 896 | 0.120 |
Why?
|
| Oocytes | 2 | 2005 | 221 | 0.110 |
Why?
|
| DNA, Complementary | 2 | 2012 | 393 | 0.110 |
Why?
|
| Potassium Channels, Voltage-Gated | 2 | 2003 | 122 | 0.110 |
Why?
|
| Membrane Proteins | 2 | 2012 | 1196 | 0.110 |
Why?
|
| Stimulation, Chemical | 1 | 2012 | 63 | 0.100 |
Why?
|
| Incretins | 1 | 2012 | 14 | 0.100 |
Why?
|
| Ubiquitin-Conjugating Enzymes | 1 | 2012 | 30 | 0.100 |
Why?
|
| Biotinylation | 1 | 2012 | 41 | 0.100 |
Why?
|
| Immunoprecipitation | 1 | 2012 | 134 | 0.100 |
Why?
|
| Aspartic Acid | 1 | 2011 | 64 | 0.100 |
Why?
|
| Fluorescence Resonance Energy Transfer | 1 | 2012 | 94 | 0.100 |
Why?
|
| Molecular Dynamics Simulation | 1 | 2013 | 245 | 0.100 |
Why?
|
| Fluorescent Antibody Technique | 1 | 2012 | 316 | 0.100 |
Why?
|
| Enzyme-Linked Immunosorbent Assay | 1 | 2012 | 376 | 0.100 |
Why?
|
| Real-Time Polymerase Chain Reaction | 1 | 2012 | 273 | 0.100 |
Why?
|
| Cells, Cultured | 2 | 2014 | 2819 | 0.090 |
Why?
|
| Down-Regulation | 1 | 2012 | 506 | 0.090 |
Why?
|
| Metabolism, Inborn Errors | 1 | 2009 | 30 | 0.090 |
Why?
|
| Amino Acid Sequence | 4 | 2013 | 2062 | 0.090 |
Why?
|
| Protein Structure, Tertiary | 3 | 2013 | 736 | 0.090 |
Why?
|
| Structure-Activity Relationship | 2 | 2010 | 408 | 0.090 |
Why?
|
| Mice | 3 | 2014 | 11356 | 0.080 |
Why?
|
| Mice, Inbred C57BL | 2 | 2014 | 3095 | 0.080 |
Why?
|
| Electrophysiology | 2 | 2010 | 401 | 0.080 |
Why?
|
| Hydrogen-Ion Concentration | 2 | 2010 | 493 | 0.080 |
Why?
|
| Animals, Newborn | 1 | 2009 | 510 | 0.080 |
Why?
|
| Electric Conductivity | 2 | 2011 | 144 | 0.080 |
Why?
|
| Molecular Sequence Data | 4 | 2013 | 3030 | 0.080 |
Why?
|
| Protein Binding | 3 | 2010 | 1457 | 0.080 |
Why?
|
| Humans | 13 | 2014 | 86653 | 0.070 |
Why?
|
| Chronic Disease | 1 | 2009 | 971 | 0.070 |
Why?
|
| Xenopus | 2 | 2003 | 125 | 0.070 |
Why?
|
| Xenopus Proteins | 1 | 2005 | 34 | 0.070 |
Why?
|
| Two-Hybrid System Techniques | 1 | 2005 | 55 | 0.070 |
Why?
|
| Cell Line | 3 | 2010 | 2469 | 0.070 |
Why?
|
| Disease Progression | 1 | 2009 | 1531 | 0.060 |
Why?
|
| Cysteine Endopeptidases | 1 | 2005 | 87 | 0.060 |
Why?
|
| Xenopus laevis | 1 | 2005 | 137 | 0.060 |
Why?
|
| Endopeptidases | 1 | 2005 | 116 | 0.060 |
Why?
|
| Diabetes Mellitus, Type 2 | 1 | 2014 | 1375 | 0.060 |
Why?
|
| Terminology as Topic | 1 | 2005 | 217 | 0.060 |
Why?
|
| Charybdotoxin | 1 | 2003 | 8 | 0.060 |
Why?
|
| Infant, Newborn | 1 | 2009 | 2379 | 0.060 |
Why?
|
| Prokaryotic Cells | 1 | 2003 | 15 | 0.060 |
Why?
|
| 14-3-3 Proteins | 1 | 2002 | 10 | 0.060 |
Why?
|
| Eukaryotic Cells | 1 | 2003 | 43 | 0.060 |
Why?
|
| Amino Acid Motifs | 1 | 2002 | 116 | 0.050 |
Why?
|
| Paralyses, Familial Periodic | 1 | 2002 | 2 | 0.050 |
Why?
|
| Models, Biological | 1 | 2009 | 1749 | 0.050 |
Why?
|
| Epilepsy, Absence | 1 | 2002 | 8 | 0.050 |
Why?
|
| Long QT Syndrome | 1 | 2002 | 34 | 0.050 |
Why?
|
| Biological Transport | 1 | 2002 | 396 | 0.050 |
Why?
|
| Protein Isoforms | 1 | 2002 | 270 | 0.050 |
Why?
|
| Peptides | 1 | 2005 | 639 | 0.050 |
Why?
|
| Protein Subunits | 3 | 2010 | 122 | 0.050 |
Why?
|
| Gene Deletion | 1 | 2002 | 329 | 0.050 |
Why?
|
| Potassium Channels, Inwardly Rectifying | 1 | 2002 | 119 | 0.050 |
Why?
|
| Histidine | 2 | 2011 | 55 | 0.050 |
Why?
|
| Membrane Potentials | 3 | 2010 | 435 | 0.050 |
Why?
|
| Peptide Fragments | 1 | 2002 | 460 | 0.050 |
Why?
|
| Escherichia coli | 1 | 2003 | 597 | 0.050 |
Why?
|
| Saccharomyces cerevisiae | 1 | 2003 | 434 | 0.040 |
Why?
|
| Models, Molecular | 3 | 2010 | 1286 | 0.040 |
Why?
|
| Kinetics | 2 | 2010 | 1513 | 0.040 |
Why?
|
| Rats | 1 | 2002 | 3992 | 0.030 |
Why?
|
| Sterol Regulatory Element Binding Protein 1 | 1 | 2014 | 12 | 0.030 |
Why?
|
| Receptor, Insulin | 1 | 2014 | 54 | 0.030 |
Why?
|
| Protein Conformation | 2 | 2010 | 881 | 0.030 |
Why?
|
| Endoplasmic Reticulum Stress | 1 | 2014 | 83 | 0.030 |
Why?
|
| Protein Biosynthesis | 1 | 2014 | 378 | 0.030 |
Why?
|
| Isotonic Solutions | 1 | 2011 | 17 | 0.030 |
Why?
|
| Osmolar Concentration | 1 | 2011 | 181 | 0.030 |
Why?
|
| HEK293 Cells | 1 | 2013 | 615 | 0.030 |
Why?
|
| Permeability | 1 | 2011 | 137 | 0.030 |
Why?
|
| Sucrose | 1 | 2011 | 64 | 0.030 |
Why?
|
| Open Reading Frames | 1 | 2011 | 117 | 0.030 |
Why?
|
| Mutant Proteins | 1 | 2011 | 94 | 0.030 |
Why?
|
| Trans-Activators | 1 | 2014 | 429 | 0.030 |
Why?
|
| Lysine | 1 | 2011 | 147 | 0.020 |
Why?
|
| Substrate Specificity | 1 | 2011 | 347 | 0.020 |
Why?
|
| Basophils | 1 | 2010 | 25 | 0.020 |
Why?
|
| Homeodomain Proteins | 1 | 2014 | 536 | 0.020 |
Why?
|
| Protein Interaction Domains and Motifs | 1 | 2010 | 86 | 0.020 |
Why?
|
| Dimerization | 1 | 2010 | 143 | 0.020 |
Why?
|
| Mice, Knockout | 1 | 2014 | 1924 | 0.020 |
Why?
|
| Green Fluorescent Proteins | 1 | 2010 | 305 | 0.020 |
Why?
|
| Protein Multimerization | 1 | 2010 | 173 | 0.020 |
Why?
|
| Patch-Clamp Techniques | 1 | 2010 | 396 | 0.020 |
Why?
|
| Temperature | 1 | 2010 | 396 | 0.020 |
Why?
|
| Genome-Wide Association Study | 1 | 2014 | 1621 | 0.020 |
Why?
|
| Methanococcus | 1 | 2003 | 5 | 0.010 |
Why?
|
| Signal Transduction | 1 | 2014 | 3243 | 0.010 |
Why?
|
| Mesylates | 1 | 2003 | 15 | 0.010 |
Why?
|
| Archaea | 1 | 2003 | 18 | 0.010 |
Why?
|
| Sequence Homology, Amino Acid | 1 | 2003 | 416 | 0.010 |
Why?
|
| Female | 2 | 2003 | 44537 | 0.010 |
Why?
|
| Polymorphism, Single-Stranded Conformational | 1 | 2002 | 29 | 0.010 |
Why?
|
| Guinea Pigs | 1 | 2002 | 171 | 0.010 |
Why?
|
| Cysteine | 1 | 2003 | 135 | 0.010 |
Why?
|
| Cloning, Molecular | 1 | 2003 | 646 | 0.010 |
Why?
|
| Potassium | 1 | 2003 | 281 | 0.010 |
Why?
|
| Mutagenesis, Insertional | 1 | 2002 | 111 | 0.010 |
Why?
|
| Amino Acid Substitution | 1 | 2002 | 339 | 0.010 |
Why?
|
| DNA Mutational Analysis | 1 | 2002 | 526 | 0.010 |
Why?
|
| Dose-Response Relationship, Drug | 1 | 2003 | 1961 | 0.010 |
Why?
|
| Base Sequence | 1 | 2003 | 2330 | 0.010 |
Why?
|
| Evolution, Molecular | 1 | 2003 | 813 | 0.010 |
Why?
|
| Neurons | 1 | 2005 | 1546 | 0.010 |
Why?
|
| DNA | 1 | 2002 | 1294 | 0.010 |
Why?
|
| Phenotype | 1 | 2002 | 2380 | 0.010 |
Why?
|
| Polymorphism, Single Nucleotide | 1 | 2002 | 2357 | 0.010 |
Why?
|
| Male | 1 | 2014 | 40973 | 0.010 |
Why?
|
| Child | 1 | 2002 | 6928 | 0.010 |
Why?
|
| Adolescent | 1 | 2002 | 8982 | 0.010 |
Why?
|