Concepts (213)
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?
|
|---|
| Escherichia coli | 40 | 2026 | 985 | 5.350 |
Why?
|
| Escherichia coli Proteins | 21 | 2026 | 314 | 4.360 |
Why?
|
| Transcription, Genetic | 20 | 2025 | 1363 | 4.180 |
Why?
|
| Gene Expression Regulation, Bacterial | 14 | 2023 | 166 | 2.180 |
Why?
|
| DNA-Directed RNA Polymerases | 12 | 2025 | 85 | 1.980 |
Why?
|
| DNA Replication | 7 | 2025 | 355 | 1.940 |
Why?
|
| Epigenesis, Genetic | 8 | 2019 | 756 | 1.540 |
Why?
|
| Sigma Factor | 9 | 2019 | 36 | 1.470 |
Why?
|
| Conjugation, Genetic | 2 | 2023 | 8 | 1.210 |
Why?
|
| Gene Transfer, Horizontal | 2 | 2024 | 44 | 1.040 |
Why?
|
| Pyrophosphatases | 2 | 2017 | 18 | 0.970 |
Why?
|
| DNA Damage | 8 | 2025 | 509 | 0.910 |
Why?
|
| Genomic Instability | 4 | 2025 | 245 | 0.810 |
Why?
|
| DNA Repair | 6 | 2019 | 570 | 0.800 |
Why?
|
| Genome, Viral | 1 | 2024 | 167 | 0.780 |
Why?
|
| Extracellular Vesicles | 1 | 2024 | 75 | 0.780 |
Why?
|
| Type IV Secretion Systems | 1 | 2023 | 6 | 0.770 |
Why?
|
| Mutation | 13 | 2024 | 6067 | 0.750 |
Why?
|
| Lac Operon | 4 | 2015 | 88 | 0.730 |
Why?
|
| Transcription Factors | 11 | 2019 | 2400 | 0.730 |
Why?
|
| RNA, Viral | 1 | 2024 | 499 | 0.710 |
Why?
|
| Virus Replication | 1 | 2024 | 607 | 0.670 |
Why?
|
| Anti-Bacterial Agents | 5 | 2026 | 2574 | 0.670 |
Why?
|
| Bacteria | 1 | 2024 | 521 | 0.640 |
Why?
|
| Genome, Bacterial | 2 | 2018 | 199 | 0.550 |
Why?
|
| RNA, Small Untranslated | 1 | 2017 | 20 | 0.540 |
Why?
|
| Evolution, Molecular | 4 | 2024 | 645 | 0.530 |
Why?
|
| Stress, Physiological | 4 | 2017 | 256 | 0.510 |
Why?
|
| Promoter Regions, Genetic | 8 | 2017 | 1208 | 0.490 |
Why?
|
| Amino Acid Substitution | 3 | 2014 | 404 | 0.450 |
Why?
|
| Gene Regulatory Networks | 4 | 2016 | 373 | 0.450 |
Why?
|
| Deoxyguanine Nucleotides | 1 | 2014 | 5 | 0.440 |
Why?
|
| Gene Expression Regulation, Viral | 2 | 2014 | 125 | 0.430 |
Why?
|
| Up-Regulation | 1 | 2014 | 823 | 0.360 |
Why?
|
| DNA, Bacterial | 4 | 2025 | 479 | 0.360 |
Why?
|
| Bacterial Proteins | 5 | 2023 | 947 | 0.360 |
Why?
|
| DNA Breaks, Double-Stranded | 6 | 2025 | 137 | 0.360 |
Why?
|
| Caenorhabditis elegans | 3 | 2025 | 245 | 0.350 |
Why?
|
| Lac Repressors | 3 | 2015 | 12 | 0.320 |
Why?
|
| Longevity | 2 | 2025 | 175 | 0.320 |
Why?
|
| Exodeoxyribonuclease V | 2 | 2025 | 28 | 0.270 |
Why?
|
| Drug Resistance, Bacterial | 2 | 2022 | 396 | 0.260 |
Why?
|
| Cell Membrane | 3 | 2024 | 449 | 0.240 |
Why?
|
| beta-Galactosidase | 3 | 2015 | 135 | 0.230 |
Why?
|
| RNA, Bacterial | 3 | 2015 | 57 | 0.230 |
Why?
|
| Plasmids | 2 | 2023 | 444 | 0.220 |
Why?
|
| Protein Transport | 1 | 2026 | 365 | 0.220 |
Why?
|
| Transcription Termination, Genetic | 1 | 2025 | 13 | 0.220 |
Why?
|
| Mutagenesis | 3 | 2023 | 324 | 0.210 |
Why?
|
| Mutation Rate | 1 | 2024 | 68 | 0.210 |
Why?
|
| Bacteriophage lambda | 2 | 2014 | 26 | 0.190 |
Why?
|
| Stochastic Processes | 2 | 2015 | 34 | 0.190 |
Why?
|
| Genes, Switch | 2 | 2014 | 8 | 0.180 |
Why?
|
| Green Fluorescent Proteins | 4 | 2013 | 358 | 0.170 |
Why?
|
| Sequence Analysis, RNA | 1 | 2024 | 408 | 0.170 |
Why?
|
| Bacteriophage mu | 2 | 2018 | 12 | 0.170 |
Why?
|
| Protein Conformation | 3 | 2013 | 732 | 0.170 |
Why?
|
| Amino Acid Sequence | 3 | 2013 | 2392 | 0.170 |
Why?
|
| Transcriptional Elongation Factors | 2 | 2018 | 28 | 0.160 |
Why?
|
| Transcriptional Activation | 2 | 2014 | 418 | 0.160 |
Why?
|
| Phenotype | 4 | 2020 | 4456 | 0.160 |
Why?
|
| Heat-Shock Proteins | 3 | 2006 | 174 | 0.150 |
Why?
|
| Eukaryota | 1 | 2019 | 14 | 0.150 |
Why?
|
| Gene Expression Profiling | 1 | 2026 | 1800 | 0.150 |
Why?
|
| DNA | 3 | 2023 | 1398 | 0.150 |
Why?
|
| Membrane Proteins | 2 | 2004 | 1589 | 0.140 |
Why?
|
| Viral Regulatory and Accessory Proteins | 1 | 2018 | 32 | 0.140 |
Why?
|
| Gene Expression Regulation | 3 | 2016 | 2322 | 0.140 |
Why?
|
| Protein Folding | 3 | 2004 | 214 | 0.140 |
Why?
|
| DNA Nucleotidyltransferases | 1 | 2018 | 19 | 0.140 |
Why?
|
| Amino Acids | 3 | 2010 | 564 | 0.140 |
Why?
|
| RNA Interference | 1 | 2020 | 491 | 0.140 |
Why?
|
| Models, Molecular | 2 | 2013 | 1060 | 0.140 |
Why?
|
| Protein Binding | 3 | 2017 | 1649 | 0.140 |
Why?
|
| Gene Deletion | 3 | 2017 | 766 | 0.130 |
Why?
|
| Host-Pathogen Interactions | 1 | 2020 | 253 | 0.130 |
Why?
|
| Gastrointestinal Microbiome | 1 | 2025 | 828 | 0.130 |
Why?
|
| Fluorescent Dyes | 1 | 2018 | 246 | 0.130 |
Why?
|
| Ciprofloxacin | 3 | 2023 | 64 | 0.130 |
Why?
|
| Metabolome | 1 | 2020 | 325 | 0.130 |
Why?
|
| DNA, Cruciform | 1 | 2016 | 18 | 0.130 |
Why?
|
| Recombinant Fusion Proteins | 2 | 2013 | 688 | 0.120 |
Why?
|
| Guanosine Tetraphosphate | 2 | 2023 | 6 | 0.120 |
Why?
|
| DNA Breaks, Single-Stranded | 1 | 2016 | 19 | 0.120 |
Why?
|
| RecQ Helicases | 1 | 2016 | 61 | 0.120 |
Why?
|
| Rec A Recombinases | 2 | 2017 | 27 | 0.120 |
Why?
|
| Heat-Shock Response | 2 | 2006 | 33 | 0.110 |
Why?
|
| Gene Editing | 1 | 2018 | 236 | 0.110 |
Why?
|
| Recombination, Genetic | 1 | 2016 | 422 | 0.110 |
Why?
|
| CRISPR-Cas Systems | 1 | 2018 | 316 | 0.110 |
Why?
|
| Single-Cell Analysis | 1 | 2018 | 349 | 0.110 |
Why?
|
| Operon | 1 | 2014 | 50 | 0.110 |
Why?
|
| RNA Precursors | 1 | 2015 | 42 | 0.110 |
Why?
|
| Codon, Nonsense | 1 | 2015 | 138 | 0.110 |
Why?
|
| Lysogeny | 1 | 2014 | 11 | 0.110 |
Why?
|
| Bacteriolysis | 1 | 2014 | 8 | 0.110 |
Why?
|
| Genes, Regulator | 1 | 2014 | 44 | 0.110 |
Why?
|
| Serine Endopeptidases | 2 | 2014 | 197 | 0.110 |
Why?
|
| Adenocarcinoma | 1 | 2001 | 968 | 0.100 |
Why?
|
| Protein Engineering | 1 | 2013 | 61 | 0.100 |
Why?
|
| Chromosomes, Bacterial | 1 | 2013 | 64 | 0.100 |
Why?
|
| Ribosomes | 1 | 2014 | 123 | 0.100 |
Why?
|
| Molecular Sequence Data | 3 | 2009 | 3464 | 0.100 |
Why?
|
| Biological Evolution | 1 | 2014 | 220 | 0.100 |
Why?
|
| Prostatic Neoplasms | 1 | 2001 | 1406 | 0.100 |
Why?
|
| Gene Expression Regulation, Enzymologic | 1 | 2014 | 242 | 0.100 |
Why?
|
| Homeostasis | 1 | 2016 | 712 | 0.090 |
Why?
|
| Viral Proteins | 1 | 2013 | 336 | 0.090 |
Why?
|
| Prions | 1 | 2011 | 19 | 0.080 |
Why?
|
| Polysaccharides | 2 | 2025 | 143 | 0.080 |
Why?
|
| Animals | 6 | 2025 | 33660 | 0.080 |
Why?
|
| DNA-Binding Proteins | 2 | 2019 | 1931 | 0.080 |
Why?
|
| Humans | 9 | 2025 | 130075 | 0.080 |
Why?
|
| rRNA Operon | 1 | 2009 | 3 | 0.080 |
Why?
|
| Holoenzymes | 1 | 2009 | 14 | 0.070 |
Why?
|
| Sequence Analysis, DNA | 1 | 2015 | 1690 | 0.070 |
Why?
|
| Half-Life | 1 | 2009 | 148 | 0.070 |
Why?
|
| Feedback, Physiological | 1 | 2009 | 66 | 0.070 |
Why?
|
| Mutant Proteins | 1 | 2009 | 112 | 0.070 |
Why?
|
| Protein Structure, Secondary | 1 | 2009 | 235 | 0.070 |
Why?
|
| Protein Multimerization | 1 | 2009 | 148 | 0.070 |
Why?
|
| RNA, Messenger | 1 | 2013 | 2548 | 0.060 |
Why?
|
| Kinetics | 2 | 2014 | 1087 | 0.060 |
Why?
|
| Chaperonin 10 | 2 | 2004 | 5 | 0.060 |
Why?
|
| Regulon | 1 | 2006 | 10 | 0.060 |
Why?
|
| Chaperonin 60 | 2 | 2004 | 31 | 0.060 |
Why?
|
| Genetic Variation | 1 | 2013 | 1544 | 0.060 |
Why?
|
| Luminescent Proteins | 2 | 2003 | 142 | 0.060 |
Why?
|
| Adenosine Triphosphatases | 2 | 2003 | 189 | 0.060 |
Why?
|
| DNA Polymerase III | 1 | 2025 | 26 | 0.060 |
Why?
|
| DNA, Single-Stranded | 1 | 2025 | 69 | 0.050 |
Why?
|
| Carrier Proteins | 1 | 2009 | 996 | 0.050 |
Why?
|
| Molecular Chaperones | 1 | 2004 | 172 | 0.050 |
Why?
|
| Models, Genetic | 2 | 2018 | 749 | 0.050 |
Why?
|
| Ribonucleases | 1 | 2003 | 41 | 0.050 |
Why?
|
| ATP-Dependent Proteases | 1 | 2003 | 13 | 0.050 |
Why?
|
| Prokaryotic Cells | 1 | 2002 | 7 | 0.050 |
Why?
|
| Eukaryotic Cells | 1 | 2002 | 29 | 0.050 |
Why?
|
| Drug Resistance, Microbial | 1 | 2023 | 195 | 0.050 |
Why?
|
| Thermodynamics | 1 | 2003 | 144 | 0.050 |
Why?
|
| Pharmaceutical Preparations | 1 | 2023 | 78 | 0.050 |
Why?
|
| Substrate Specificity | 1 | 2003 | 287 | 0.050 |
Why?
|
| Colistin | 1 | 2022 | 30 | 0.050 |
Why?
|
| Temperature | 1 | 2003 | 290 | 0.050 |
Why?
|
| Adenosine Triphosphate | 1 | 2003 | 265 | 0.040 |
Why?
|
| Protein Structure, Tertiary | 1 | 2003 | 716 | 0.040 |
Why?
|
| Mice | 3 | 2025 | 18160 | 0.040 |
Why?
|
| Lymphatic Metastasis | 1 | 2001 | 425 | 0.040 |
Why?
|
| RNA | 1 | 2023 | 509 | 0.040 |
Why?
|
| Dose-Response Relationship, Drug | 1 | 2003 | 1604 | 0.040 |
Why?
|
| Neoplasm Invasiveness | 1 | 2001 | 631 | 0.040 |
Why?
|
| Lymph Nodes | 1 | 2001 | 356 | 0.040 |
Why?
|
| Microbial Sensitivity Tests | 1 | 2022 | 848 | 0.040 |
Why?
|
| Phleomycins | 1 | 2018 | 6 | 0.040 |
Why?
|
| Exonucleases | 1 | 2018 | 27 | 0.040 |
Why?
|
| Chromosomal Instability | 1 | 2019 | 59 | 0.040 |
Why?
|
| DNA-Directed DNA Polymerase | 1 | 2019 | 87 | 0.040 |
Why?
|
| Gene Knockout Techniques | 1 | 2018 | 131 | 0.030 |
Why?
|
| Multivariate Analysis | 1 | 2001 | 1374 | 0.030 |
Why?
|
| Cell Division | 1 | 2019 | 718 | 0.030 |
Why?
|
| Membrane Transport Proteins | 1 | 2019 | 179 | 0.030 |
Why?
|
| Bacterial Load | 1 | 2017 | 34 | 0.030 |
Why?
|
| Unfolded Protein Response | 1 | 2017 | 66 | 0.030 |
Why?
|
| Rad51 Recombinase | 1 | 2016 | 33 | 0.030 |
Why?
|
| Mitochondrial Dynamics | 1 | 2017 | 49 | 0.030 |
Why?
|
| Caenorhabditis elegans Proteins | 1 | 2017 | 103 | 0.030 |
Why?
|
| Reactive Oxygen Species | 1 | 2019 | 521 | 0.030 |
Why?
|
| Survival Rate | 1 | 2001 | 2107 | 0.030 |
Why?
|
| DNA, Neoplasm | 1 | 2016 | 282 | 0.030 |
Why?
|
| Amyloid beta-Peptides | 1 | 2017 | 230 | 0.030 |
Why?
|
| Binding Sites | 1 | 2018 | 1134 | 0.030 |
Why?
|
| Models, Animal | 1 | 2017 | 449 | 0.030 |
Why?
|
| Disease Progression | 1 | 2001 | 2191 | 0.030 |
Why?
|
| Neoplasm Recurrence, Local | 1 | 2001 | 1265 | 0.030 |
Why?
|
| Mitochondria | 1 | 2020 | 768 | 0.030 |
Why?
|
| Tumor Suppressor p53-Binding Protein 1 | 1 | 2013 | 14 | 0.030 |
Why?
|
| Cytidine Deaminase | 1 | 2013 | 31 | 0.030 |
Why?
|
| Ku Autoantigen | 1 | 2013 | 21 | 0.030 |
Why?
|
| Virus Activation | 1 | 2014 | 87 | 0.030 |
Why?
|
| Synthetic Biology | 1 | 2013 | 13 | 0.030 |
Why?
|
| RNA, Transfer | 1 | 2014 | 57 | 0.030 |
Why?
|
| Chromatin Immunoprecipitation | 1 | 2014 | 223 | 0.020 |
Why?
|
| Selection, Genetic | 1 | 2014 | 150 | 0.020 |
Why?
|
| Open Reading Frames | 1 | 2014 | 199 | 0.020 |
Why?
|
| Feedback | 1 | 2014 | 143 | 0.020 |
Why?
|
| Time Factors | 1 | 2003 | 6165 | 0.020 |
Why?
|
| Genes, Reporter | 1 | 2013 | 340 | 0.020 |
Why?
|
| Neoplasm Proteins | 1 | 2016 | 679 | 0.020 |
Why?
|
| DNA Helicases | 1 | 2013 | 234 | 0.020 |
Why?
|
| Signal Transduction | 1 | 2004 | 4645 | 0.020 |
Why?
|
| HeLa Cells | 1 | 2013 | 689 | 0.020 |
Why?
|
| Models, Theoretical | 1 | 2014 | 358 | 0.020 |
Why?
|
| Base Sequence | 2 | 2006 | 2729 | 0.020 |
Why?
|
| Homologous Recombination | 1 | 2011 | 97 | 0.020 |
Why?
|
| Protein Interaction Domains and Motifs | 1 | 2011 | 136 | 0.020 |
Why?
|
| Mutagenesis, Site-Directed | 1 | 2011 | 300 | 0.020 |
Why?
|
| Intracellular Signaling Peptides and Proteins | 1 | 2013 | 583 | 0.020 |
Why?
|
| Guanosine Pentaphosphate | 1 | 2010 | 2 | 0.020 |
Why?
|
| Genome-Wide Association Study | 1 | 2017 | 1827 | 0.020 |
Why?
|
| Aging | 1 | 2017 | 1238 | 0.020 |
Why?
|
| Mutagenesis, Insertional | 1 | 2010 | 150 | 0.020 |
Why?
|
| DNA Transposable Elements | 1 | 2010 | 178 | 0.020 |
Why?
|
| Point Mutation | 1 | 2010 | 332 | 0.020 |
Why?
|
| Proteins | 1 | 2013 | 1004 | 0.020 |
Why?
|
| Algorithms | 1 | 2014 | 1662 | 0.020 |
Why?
|
| Porins | 1 | 2004 | 37 | 0.010 |
Why?
|
| HSP70 Heat-Shock Proteins | 1 | 2004 | 72 | 0.010 |
Why?
|
| Endopeptidases | 1 | 2004 | 106 | 0.010 |
Why?
|
| Bacterial Outer Membrane Proteins | 1 | 2004 | 116 | 0.010 |
Why?
|
| Directed Molecular Evolution | 1 | 2002 | 12 | 0.010 |
Why?
|
| Protein Isoforms | 1 | 2002 | 422 | 0.010 |
Why?
|
| Neoplasms | 1 | 2016 | 2977 | 0.010 |
Why?
|
| Male | 1 | 2001 | 64382 | 0.010 |
Why?
|