Concepts (200)
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?
|
|---|
| Protein Disulfide-Isomerases | 29 | 2005 | 32 | 2.460 |
Why?
|
| Isomerases | 16 | 1997 | 21 | 1.570 |
Why?
|
| Protein Folding | 20 | 2005 | 215 | 1.420 |
Why?
|
| Disulfides | 20 | 2005 | 60 | 1.250 |
Why?
|
| Oxidation-Reduction | 25 | 2005 | 434 | 0.760 |
Why?
|
| Glutathione | 15 | 2005 | 199 | 0.660 |
Why?
|
| Sulfhydryl Compounds | 11 | 2005 | 54 | 0.660 |
Why?
|
| Escherichia coli | 12 | 2015 | 984 | 0.610 |
Why?
|
| Kinetics | 26 | 2015 | 1087 | 0.560 |
Why?
|
| Thioredoxins | 8 | 2005 | 28 | 0.550 |
Why?
|
| beta-Lactamases | 5 | 2015 | 216 | 0.510 |
Why?
|
| Catalysis | 16 | 2011 | 137 | 0.490 |
Why?
|
| Muramidase | 6 | 2000 | 37 | 0.460 |
Why?
|
| Molecular Chaperones | 5 | 2001 | 172 | 0.440 |
Why?
|
| Ribonuclease, Pancreatic | 5 | 2002 | 20 | 0.410 |
Why?
|
| Cysteine | 6 | 2005 | 137 | 0.340 |
Why?
|
| Endoplasmic Reticulum | 5 | 2004 | 209 | 0.330 |
Why?
|
| Protein Denaturation | 11 | 2001 | 48 | 0.320 |
Why?
|
| Rats | 17 | 2005 | 3398 | 0.300 |
Why?
|
| Proteins | 5 | 1995 | 1015 | 0.290 |
Why?
|
| Oxidoreductases | 4 | 2005 | 105 | 0.270 |
Why?
|
| Oxygen | 4 | 2005 | 551 | 0.260 |
Why?
|
| Binding Sites | 9 | 2005 | 1149 | 0.250 |
Why?
|
| Hydroxymethylglutaryl CoA Reductases | 4 | 1993 | 32 | 0.250 |
Why?
|
| Sulfhydryl Reagents | 2 | 2004 | 7 | 0.250 |
Why?
|
| Cattle | 10 | 2005 | 501 | 0.240 |
Why?
|
| Microsomes, Liver | 3 | 1993 | 96 | 0.240 |
Why?
|
| Ribonucleases | 8 | 2005 | 41 | 0.230 |
Why?
|
| Protein Conformation | 6 | 2011 | 729 | 0.220 |
Why?
|
| Yeasts | 1 | 2005 | 43 | 0.220 |
Why?
|
| Recombinant Proteins | 7 | 2015 | 1323 | 0.210 |
Why?
|
| Fungal Proteins | 1 | 2005 | 135 | 0.210 |
Why?
|
| Zinc | 1 | 2004 | 128 | 0.200 |
Why?
|
| Substrate Specificity | 7 | 2015 | 285 | 0.200 |
Why?
|
| Amino Acid Sequence | 10 | 2011 | 2408 | 0.200 |
Why?
|
| Molecular Sequence Data | 11 | 2005 | 3507 | 0.190 |
Why?
|
| Animals | 29 | 2005 | 33907 | 0.190 |
Why?
|
| Saccharomyces cerevisiae | 2 | 2004 | 399 | 0.190 |
Why?
|
| Dithiothreitol | 4 | 2001 | 13 | 0.180 |
Why?
|
| Mutagenesis, Site-Directed | 7 | 2014 | 302 | 0.170 |
Why?
|
| Ampicillin Resistance | 1 | 2001 | 18 | 0.170 |
Why?
|
| Triiodothyronine | 1 | 2001 | 53 | 0.170 |
Why?
|
| Chaperonins | 3 | 1994 | 15 | 0.160 |
Why?
|
| Acyl Coenzyme A | 2 | 1990 | 23 | 0.160 |
Why?
|
| Mutation | 5 | 2015 | 6131 | 0.160 |
Why?
|
| Glutathione Disulfide | 6 | 1997 | 19 | 0.160 |
Why?
|
| Protein Structure, Tertiary | 6 | 2015 | 714 | 0.150 |
Why?
|
| Estradiol | 1 | 2001 | 470 | 0.140 |
Why?
|
| Solubility | 4 | 2001 | 117 | 0.130 |
Why?
|
| Amino Acid Substitution | 4 | 2014 | 406 | 0.130 |
Why?
|
| Heat-Shock Proteins | 2 | 1996 | 174 | 0.130 |
Why?
|
| Bacterial Proteins | 4 | 2005 | 938 | 0.130 |
Why?
|
| Thermodynamics | 6 | 2005 | 145 | 0.130 |
Why?
|
| Structure-Activity Relationship | 6 | 2015 | 552 | 0.120 |
Why?
|
| Protein Binding | 5 | 2005 | 1666 | 0.120 |
Why?
|
| Models, Molecular | 5 | 2015 | 1056 | 0.110 |
Why?
|
| Cefotaxime | 1 | 2014 | 37 | 0.110 |
Why?
|
| Alkaline Phosphatase | 1 | 1994 | 95 | 0.110 |
Why?
|
| Drug Resistance, Microbial | 1 | 2014 | 197 | 0.110 |
Why?
|
| Ceftazidime | 1 | 2015 | 47 | 0.110 |
Why?
|
| Enzymes, Immobilized | 1 | 1994 | 6 | 0.110 |
Why?
|
| Peptide Fragments | 1 | 1997 | 687 | 0.100 |
Why?
|
| NADP | 2 | 1991 | 53 | 0.100 |
Why?
|
| Guanidines | 1 | 1993 | 21 | 0.100 |
Why?
|
| Mathematics | 4 | 1995 | 71 | 0.090 |
Why?
|
| Plasmids | 4 | 2005 | 451 | 0.090 |
Why?
|
| Isoenzymes | 1 | 1993 | 211 | 0.090 |
Why?
|
| Binding, Competitive | 3 | 2001 | 145 | 0.090 |
Why?
|
| Calcium | 1 | 1996 | 1027 | 0.090 |
Why?
|
| Orotidine-5'-Phosphate Decarboxylase | 1 | 2011 | 3 | 0.090 |
Why?
|
| Base Sequence | 6 | 1996 | 2767 | 0.090 |
Why?
|
| Protein Disulfide Reductase (Glutathione) | 1 | 1991 | 2 | 0.090 |
Why?
|
| Dose-Response Relationship, Drug | 3 | 2002 | 1616 | 0.090 |
Why?
|
| Hydrolysis | 3 | 2014 | 139 | 0.090 |
Why?
|
| Enzyme Activation | 4 | 2000 | 582 | 0.090 |
Why?
|
| Catalytic Domain | 3 | 2011 | 159 | 0.080 |
Why?
|
| Liver | 6 | 1996 | 1797 | 0.080 |
Why?
|
| Peptides | 2 | 2005 | 708 | 0.080 |
Why?
|
| Acetyl-CoA C-Acetyltransferase | 1 | 1989 | 1 | 0.080 |
Why?
|
| Models, Chemical | 3 | 2005 | 78 | 0.080 |
Why?
|
| Acetyl Coenzyme A | 1 | 1989 | 16 | 0.080 |
Why?
|
| Lovastatin | 1 | 1989 | 26 | 0.080 |
Why?
|
| Acetyltransferases | 1 | 1989 | 75 | 0.080 |
Why?
|
| Gene Expression | 4 | 2015 | 1493 | 0.080 |
Why?
|
| Point Mutation | 2 | 2004 | 334 | 0.080 |
Why?
|
| Carrier Proteins | 1 | 1994 | 1006 | 0.070 |
Why?
|
| Molecular Weight | 2 | 2000 | 280 | 0.070 |
Why?
|
| In Vitro Techniques | 3 | 1996 | 809 | 0.070 |
Why?
|
| Hydroxymethylglutaryl-CoA Reductase Inhibitors | 2 | 1993 | 750 | 0.070 |
Why?
|
| Fructose-Bisphosphatase | 1 | 1987 | 3 | 0.070 |
Why?
|
| Chloroplasts | 1 | 1987 | 8 | 0.070 |
Why?
|
| Guanidine | 2 | 2001 | 9 | 0.070 |
Why?
|
| Dimerization | 2 | 2005 | 138 | 0.070 |
Why?
|
| Enzyme Stability | 2 | 2001 | 58 | 0.070 |
Why?
|
| Plants | 1 | 1987 | 50 | 0.070 |
Why?
|
| Models, Theoretical | 3 | 1995 | 363 | 0.060 |
Why?
|
| Protein Structure, Secondary | 3 | 2015 | 236 | 0.060 |
Why?
|
| DNA Primers | 3 | 1996 | 606 | 0.060 |
Why?
|
| Spectrometry, Fluorescence | 2 | 2001 | 78 | 0.060 |
Why?
|
| Periplasmic Proteins | 1 | 2005 | 6 | 0.060 |
Why?
|
| Rats, Inbred Strains | 3 | 1990 | 185 | 0.060 |
Why?
|
| Gene Deletion | 2 | 2005 | 769 | 0.050 |
Why?
|
| Glutaredoxins | 3 | 2005 | 31 | 0.050 |
Why?
|
| Cathepsin A | 1 | 2004 | 3 | 0.050 |
Why?
|
| Structural Homology, Protein | 1 | 2004 | 27 | 0.050 |
Why?
|
| Precipitin Tests | 1 | 2004 | 111 | 0.050 |
Why?
|
| Genetic Complementation Test | 1 | 2004 | 89 | 0.050 |
Why?
|
| Myocardium | 1 | 1989 | 859 | 0.050 |
Why?
|
| Insulin | 4 | 2005 | 1146 | 0.050 |
Why?
|
| Cloning, Molecular | 3 | 1996 | 781 | 0.050 |
Why?
|
| Time Factors | 3 | 2005 | 6190 | 0.050 |
Why?
|
| Chromosomes | 1 | 2004 | 121 | 0.050 |
Why?
|
| Chickens | 2 | 1994 | 269 | 0.050 |
Why?
|
| Crystallography, X-Ray | 2 | 2015 | 363 | 0.050 |
Why?
|
| Biocatalysis | 2 | 2015 | 37 | 0.050 |
Why?
|
| Serine | 1 | 2004 | 161 | 0.050 |
Why?
|
| Escherichia coli Proteins | 1 | 2005 | 311 | 0.050 |
Why?
|
| Anti-Bacterial Agents | 1 | 2014 | 2546 | 0.050 |
Why?
|
| Cell Division | 1 | 2004 | 721 | 0.050 |
Why?
|
| Saccharomyces cerevisiae Proteins | 1 | 2004 | 261 | 0.050 |
Why?
|
| Glycoproteins | 1 | 2004 | 346 | 0.050 |
Why?
|
| Cell Survival | 1 | 2004 | 837 | 0.040 |
Why?
|
| Models, Biological | 2 | 2005 | 1390 | 0.040 |
Why?
|
| Aprotinin | 1 | 2001 | 9 | 0.040 |
Why?
|
| Anilino Naphthalenesulfonates | 1 | 2001 | 1 | 0.040 |
Why?
|
| Bacitracin | 1 | 2001 | 1 | 0.040 |
Why?
|
| Periplasm | 1 | 2001 | 8 | 0.040 |
Why?
|
| Inclusion Bodies | 1 | 2001 | 39 | 0.040 |
Why?
|
| Ampicillin | 1 | 2001 | 59 | 0.040 |
Why?
|
| Promoter Regions, Genetic | 1 | 2004 | 1227 | 0.040 |
Why?
|
| Ultracentrifugation | 1 | 2000 | 20 | 0.040 |
Why?
|
| Citrate (si)-Synthase | 2 | 1996 | 17 | 0.040 |
Why?
|
| Glucose | 1 | 2004 | 854 | 0.040 |
Why?
|
| Electrophoresis, Polyacrylamide Gel | 2 | 2005 | 256 | 0.040 |
Why?
|
| Ligands | 1 | 2001 | 486 | 0.040 |
Why?
|
| Hot Temperature | 2 | 1996 | 141 | 0.040 |
Why?
|
| Peptide Mapping | 1 | 1997 | 33 | 0.030 |
Why?
|
| Spectrophotometry, Ultraviolet | 1 | 1997 | 39 | 0.030 |
Why?
|
| Eukaryotic Cells | 1 | 1998 | 29 | 0.030 |
Why?
|
| Membrane Proteins | 1 | 2005 | 1604 | 0.030 |
Why?
|
| Phenotype | 2 | 2005 | 4474 | 0.030 |
Why?
|
| Species Specificity | 2 | 2005 | 486 | 0.030 |
Why?
|
| Microbial Sensitivity Tests | 1 | 2001 | 840 | 0.030 |
Why?
|
| Evolution, Molecular | 1 | 2001 | 656 | 0.030 |
Why?
|
| Buffers | 1 | 1997 | 27 | 0.030 |
Why?
|
| Isomerism | 1 | 1997 | 23 | 0.030 |
Why?
|
| Oligodeoxyribonucleotides | 2 | 1994 | 123 | 0.030 |
Why?
|
| Alcohol Dehydrogenase | 1 | 1996 | 18 | 0.030 |
Why?
|
| Chromatography, High Pressure Liquid | 1 | 1997 | 325 | 0.030 |
Why?
|
| Alkylation | 1 | 1995 | 10 | 0.030 |
Why?
|
| Sodium | 1 | 1996 | 280 | 0.030 |
Why?
|
| Drug Stability | 1 | 1995 | 56 | 0.030 |
Why?
|
| Chaperonin 10 | 1 | 1994 | 5 | 0.030 |
Why?
|
| Tyrosine | 1 | 2015 | 144 | 0.030 |
Why?
|
| Chaperonin 60 | 1 | 1994 | 31 | 0.030 |
Why?
|
| beta-Lactam Resistance | 1 | 2015 | 48 | 0.030 |
Why?
|
| Oligopeptides | 1 | 1995 | 105 | 0.030 |
Why?
|
| Sepharose | 1 | 1994 | 11 | 0.030 |
Why?
|
| Particle Size | 1 | 1994 | 136 | 0.030 |
Why?
|
| Penicillins | 1 | 2015 | 153 | 0.030 |
Why?
|
| Hydrogen-Ion Concentration | 1 | 2015 | 409 | 0.030 |
Why?
|
| Osmolar Concentration | 1 | 1994 | 147 | 0.030 |
Why?
|
| Glutamic Acid | 1 | 2015 | 209 | 0.030 |
Why?
|
| Adenosine Triphosphate | 1 | 1994 | 263 | 0.030 |
Why?
|
| Sequence Alignment | 2 | 2011 | 585 | 0.020 |
Why?
|
| Calorimetry | 1 | 1993 | 63 | 0.020 |
Why?
|
| Chromatography, Liquid | 1 | 1994 | 237 | 0.020 |
Why?
|
| Cross-Linking Reagents | 1 | 1993 | 49 | 0.020 |
Why?
|
| Macromolecular Substances | 1 | 1993 | 129 | 0.020 |
Why?
|
| Escherichia coli Infections | 1 | 2014 | 194 | 0.020 |
Why?
|
| Urea | 1 | 1993 | 218 | 0.020 |
Why?
|
| Mycobacterium tuberculosis | 1 | 1996 | 424 | 0.020 |
Why?
|
| Chromatography, Ion Exchange | 1 | 1991 | 38 | 0.020 |
Why?
|
| Mutant Proteins | 1 | 2011 | 111 | 0.020 |
Why?
|
| Sequence Homology, Nucleic Acid | 1 | 1991 | 256 | 0.020 |
Why?
|
| Blotting, Western | 1 | 1993 | 1019 | 0.020 |
Why?
|
| Hormones | 1 | 1991 | 163 | 0.020 |
Why?
|
| Rats, Sprague-Dawley | 1 | 1993 | 1112 | 0.020 |
Why?
|
| Cholestyramine Resin | 1 | 1989 | 13 | 0.020 |
Why?
|
| Cytoplasm | 1 | 1990 | 252 | 0.020 |
Why?
|
| Enzyme Reactivators | 1 | 1988 | 2 | 0.020 |
Why?
|
| Lysine | 1 | 1989 | 166 | 0.020 |
Why?
|
| Cell Membrane | 1 | 1990 | 451 | 0.020 |
Why?
|
| Cell Nucleus | 1 | 1990 | 569 | 0.020 |
Why?
|
| Yersinia pseudotuberculosis | 1 | 2005 | 6 | 0.010 |
Why?
|
| Swine | 1 | 1989 | 1184 | 0.010 |
Why?
|
| Humans | 4 | 2014 | 130430 | 0.010 |
Why?
|
| Vibrio cholerae | 1 | 2005 | 33 | 0.010 |
Why?
|
| DNA | 1 | 1991 | 1419 | 0.010 |
Why?
|
| Haemophilus influenzae | 1 | 2005 | 134 | 0.010 |
Why?
|
| Conserved Sequence | 1 | 2005 | 281 | 0.010 |
Why?
|
| Sequence Homology, Amino Acid | 1 | 2005 | 623 | 0.010 |
Why?
|
| Male | 4 | 1993 | 64533 | 0.010 |
Why?
|
| Pseudomonas aeruginosa | 1 | 2005 | 175 | 0.010 |
Why?
|
| Phylogeny | 1 | 2005 | 706 | 0.010 |
Why?
|
| Sequence Deletion | 1 | 2004 | 521 | 0.010 |
Why?
|
| Biopolymers | 1 | 1996 | 17 | 0.010 |
Why?
|
| Microscopy, Electron | 1 | 1996 | 310 | 0.010 |
Why?
|
| Polymerase Chain Reaction | 1 | 1996 | 1458 | 0.010 |
Why?
|
| Proline | 1 | 1992 | 78 | 0.010 |
Why?
|