Concepts (142)
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 | 23 | 2025 | 986 | 1.050 |
Why?
|
| Transcription, Genetic | 13 | 2025 | 1697 | 1.010 |
Why?
|
| Escherichia coli Proteins | 11 | 2018 | 305 | 0.780 |
Why?
|
| DNA-Directed RNA Polymerases | 8 | 2025 | 121 | 0.450 |
Why?
|
| Epigenesis, Genetic | 8 | 2019 | 677 | 0.430 |
Why?
|
| Gene Expression Regulation, Bacterial | 6 | 2017 | 158 | 0.420 |
Why?
|
| DNA Replication | 5 | 2025 | 352 | 0.370 |
Why?
|
| DNA Repair | 5 | 2018 | 585 | 0.280 |
Why?
|
| Pyrophosphatases | 2 | 2017 | 20 | 0.260 |
Why?
|
| Transcription Termination, Genetic | 1 | 2025 | 13 | 0.240 |
Why?
|
| DNA Damage | 3 | 2025 | 513 | 0.240 |
Why?
|
| DNA Breaks, Double-Stranded | 4 | 2025 | 131 | 0.220 |
Why?
|
| Lac Operon | 5 | 2015 | 95 | 0.200 |
Why?
|
| Gene Expression Regulation, Viral | 2 | 2014 | 132 | 0.200 |
Why?
|
| DNA, Bacterial | 4 | 2016 | 478 | 0.150 |
Why?
|
| RNA, Small Untranslated | 1 | 2017 | 21 | 0.150 |
Why?
|
| Sigma Factor | 1 | 2017 | 35 | 0.140 |
Why?
|
| Genomic Instability | 1 | 2019 | 228 | 0.140 |
Why?
|
| Genome, Bacterial | 1 | 2018 | 187 | 0.140 |
Why?
|
| Bacteriophage lambda | 2 | 2014 | 27 | 0.140 |
Why?
|
| Genes, Switch | 2 | 2014 | 10 | 0.140 |
Why?
|
| DNA, Cruciform | 1 | 2016 | 18 | 0.140 |
Why?
|
| DNA Breaks, Single-Stranded | 1 | 2016 | 20 | 0.130 |
Why?
|
| RecQ Helicases | 1 | 2016 | 62 | 0.130 |
Why?
|
| Transcription Factors | 5 | 2018 | 2580 | 0.130 |
Why?
|
| Mutation | 9 | 2015 | 5825 | 0.120 |
Why?
|
| Recombination, Genetic | 1 | 2016 | 448 | 0.120 |
Why?
|
| Chromosome Inversion | 1 | 1995 | 74 | 0.120 |
Why?
|
| Gene Deletion | 2 | 2014 | 789 | 0.120 |
Why?
|
| Deoxyguanine Nucleotides | 1 | 2014 | 5 | 0.120 |
Why?
|
| Lysogeny | 1 | 2014 | 10 | 0.120 |
Why?
|
| Bacteriolysis | 1 | 2014 | 8 | 0.120 |
Why?
|
| Gene Regulatory Networks | 3 | 2015 | 351 | 0.110 |
Why?
|
| Genes, Regulator | 1 | 2014 | 56 | 0.110 |
Why?
|
| Multigene Family | 1 | 1995 | 298 | 0.110 |
Why?
|
| Stress, Physiological | 2 | 2017 | 254 | 0.110 |
Why?
|
| Chromosomes, Bacterial | 1 | 2013 | 64 | 0.110 |
Why?
|
| Protein Engineering | 1 | 2013 | 73 | 0.110 |
Why?
|
| Models, Genetic | 1 | 1995 | 759 | 0.100 |
Why?
|
| Amino Acid Substitution | 2 | 2013 | 393 | 0.100 |
Why?
|
| Viral Proteins | 1 | 2013 | 347 | 0.090 |
Why?
|
| Lac Repressors | 4 | 2015 | 15 | 0.090 |
Why?
|
| DNA, Single-Stranded | 2 | 2025 | 74 | 0.090 |
Why?
|
| Promoter Regions, Genetic | 4 | 2017 | 1327 | 0.090 |
Why?
|
| Recombinant Fusion Proteins | 1 | 2013 | 766 | 0.090 |
Why?
|
| Evolution, Molecular | 1 | 2013 | 669 | 0.080 |
Why?
|
| Muscarinic Agonists | 1 | 2007 | 6 | 0.070 |
Why?
|
| Pilocarpine | 1 | 2007 | 12 | 0.070 |
Why?
|
| Rec A Recombinases | 3 | 2017 | 26 | 0.070 |
Why?
|
| Sjogren's Syndrome | 1 | 2007 | 89 | 0.060 |
Why?
|
| DNA-Binding Proteins | 1 | 2013 | 2043 | 0.060 |
Why?
|
| DNA Polymerase III | 1 | 2025 | 27 | 0.060 |
Why?
|
| beta-Galactosidase | 2 | 2015 | 145 | 0.060 |
Why?
|
| DNA Helicases | 2 | 2013 | 231 | 0.060 |
Why?
|
| Mutagenesis | 2 | 1997 | 346 | 0.050 |
Why?
|
| Stochastic Processes | 2 | 2015 | 34 | 0.050 |
Why?
|
| Green Fluorescent Proteins | 2 | 2013 | 389 | 0.050 |
Why?
|
| Protein Binding | 2 | 2017 | 1736 | 0.050 |
Why?
|
| Exodeoxyribonuclease V | 2 | 2017 | 23 | 0.050 |
Why?
|
| Genes, Bacterial | 3 | 1991 | 209 | 0.040 |
Why?
|
| DNA | 2 | 2018 | 1597 | 0.040 |
Why?
|
| Eukaryota | 1 | 2019 | 21 | 0.040 |
Why?
|
| Amino Acids | 3 | 2010 | 664 | 0.040 |
Why?
|
| Phenotype | 3 | 2015 | 4255 | 0.040 |
Why?
|
| Transcriptional Elongation Factors | 1 | 2018 | 25 | 0.040 |
Why?
|
| Molecular Sequence Data | 5 | 1995 | 3877 | 0.040 |
Why?
|
| Models, Molecular | 2 | 2013 | 1068 | 0.040 |
Why?
|
| Base Sequence | 4 | 1995 | 3090 | 0.030 |
Why?
|
| Rad51 Recombinase | 1 | 2016 | 29 | 0.030 |
Why?
|
| Repressor Proteins | 2 | 1993 | 815 | 0.030 |
Why?
|
| DNA, Neoplasm | 1 | 2016 | 301 | 0.030 |
Why?
|
| Single-Cell Analysis | 1 | 2018 | 275 | 0.030 |
Why?
|
| Templates, Genetic | 1 | 1995 | 97 | 0.030 |
Why?
|
| RNA, Bacterial | 1 | 2015 | 54 | 0.030 |
Why?
|
| Sequence Homology, Nucleic Acid | 1 | 1995 | 286 | 0.030 |
Why?
|
| Codon, Nonsense | 1 | 2015 | 131 | 0.030 |
Why?
|
| RNA Precursors | 1 | 2015 | 67 | 0.030 |
Why?
|
| Tumor Suppressor p53-Binding Protein 1 | 1 | 2013 | 12 | 0.030 |
Why?
|
| Cytidine Deaminase | 1 | 2013 | 31 | 0.030 |
Why?
|
| Ku Autoantigen | 1 | 2013 | 21 | 0.030 |
Why?
|
| Bacteriophage mu | 1 | 2013 | 12 | 0.030 |
Why?
|
| Synthetic Biology | 1 | 2013 | 14 | 0.030 |
Why?
|
| Virus Activation | 1 | 2014 | 87 | 0.030 |
Why?
|
| Nitroimidazoles | 1 | 1993 | 44 | 0.030 |
Why?
|
| Mutagens | 1 | 1993 | 84 | 0.030 |
Why?
|
| Genes, Reporter | 1 | 2013 | 380 | 0.020 |
Why?
|
| Neoplasm Proteins | 1 | 2016 | 669 | 0.020 |
Why?
|
| Quinolines | 1 | 1993 | 98 | 0.020 |
Why?
|
| Kinetics | 1 | 2014 | 1323 | 0.020 |
Why?
|
| Models, Theoretical | 1 | 2014 | 359 | 0.020 |
Why?
|
| HeLa Cells | 1 | 2013 | 806 | 0.020 |
Why?
|
| Bacterial Proteins | 2 | 1997 | 890 | 0.020 |
Why?
|
| Aminacrine | 1 | 1991 | 1 | 0.020 |
Why?
|
| Protein Conformation | 1 | 2013 | 830 | 0.020 |
Why?
|
| Prions | 1 | 2011 | 13 | 0.020 |
Why?
|
| Amino Acid Sequence | 2 | 2013 | 2704 | 0.020 |
Why?
|
| Humans | 6 | 2025 | 124703 | 0.020 |
Why?
|
| Intracellular Signaling Peptides and Proteins | 1 | 2013 | 555 | 0.020 |
Why?
|
| Guanosine Pentaphosphate | 1 | 2010 | 2 | 0.020 |
Why?
|
| Frameshift Mutation | 1 | 1991 | 180 | 0.020 |
Why?
|
| rRNA Operon | 1 | 2009 | 3 | 0.020 |
Why?
|
| Guanosine Tetraphosphate | 1 | 2009 | 6 | 0.020 |
Why?
|
| Holoenzymes | 1 | 2009 | 10 | 0.020 |
Why?
|
| Half-Life | 1 | 2009 | 157 | 0.020 |
Why?
|
| Feedback, Physiological | 1 | 2009 | 69 | 0.020 |
Why?
|
| Mutant Proteins | 1 | 2009 | 115 | 0.020 |
Why?
|
| Sequence Analysis, DNA | 1 | 2015 | 1758 | 0.020 |
Why?
|
| Protein Multimerization | 1 | 2009 | 128 | 0.020 |
Why?
|
| Proteins | 1 | 2013 | 1036 | 0.020 |
Why?
|
| Salivation | 1 | 2007 | 6 | 0.020 |
Why?
|
| Administration, Buccal | 1 | 2007 | 5 | 0.020 |
Why?
|
| Transcriptional Activation | 1 | 2009 | 484 | 0.020 |
Why?
|
| Drug Implants | 1 | 2007 | 42 | 0.020 |
Why?
|
| RNA, Messenger | 1 | 2013 | 2814 | 0.020 |
Why?
|
| Delayed-Action Preparations | 1 | 2007 | 110 | 0.020 |
Why?
|
| Genetic Variation | 1 | 2013 | 1497 | 0.020 |
Why?
|
| Statistics, Nonparametric | 1 | 2007 | 429 | 0.020 |
Why?
|
| Animals | 2 | 2019 | 34028 | 0.020 |
Why?
|
| Tears | 1 | 2007 | 172 | 0.020 |
Why?
|
| Pain Measurement | 1 | 2007 | 361 | 0.020 |
Why?
|
| Gene Expression Regulation | 1 | 2013 | 2520 | 0.010 |
Why?
|
| Carrier Proteins | 1 | 2009 | 1022 | 0.010 |
Why?
|
| Pilot Projects | 1 | 2007 | 1391 | 0.010 |
Why?
|
| Neoplasms | 1 | 2016 | 2788 | 0.010 |
Why?
|
| DNA Polymerase I | 1 | 1997 | 10 | 0.010 |
Why?
|
| Exodeoxyribonucleases | 1 | 1997 | 51 | 0.010 |
Why?
|
| Cyclic AMP | 1 | 1997 | 246 | 0.010 |
Why?
|
| Serine Endopeptidases | 1 | 1997 | 177 | 0.010 |
Why?
|
| Mice | 1 | 2013 | 17580 | 0.010 |
Why?
|
| Base Composition | 1 | 1993 | 71 | 0.010 |
Why?
|
| Cells, Cultured | 1 | 1997 | 3038 | 0.010 |
Why?
|
| Genetic Complementation Test | 1 | 1991 | 88 | 0.010 |
Why?
|
| Codon | 1 | 1991 | 97 | 0.010 |
Why?
|
| Substrate Specificity | 1 | 1991 | 292 | 0.010 |
Why?
|
| Dose-Response Relationship, Drug | 1 | 1993 | 1688 | 0.000 |
Why?
|
| Aged | 1 | 2007 | 19763 | 0.000 |
Why?
|
| Protein Biosynthesis | 1 | 1991 | 663 | 0.000 |
Why?
|
| Time Factors | 1 | 1997 | 6308 | 0.000 |
Why?
|
| Middle Aged | 1 | 2007 | 26796 | 0.000 |
Why?
|
| Genotype | 1 | 1991 | 2556 | 0.000 |
Why?
|
| Male | 1 | 2007 | 61264 | 0.000 |
Why?
|
| Female | 1 | 2007 | 66557 | 0.000 |
Why?
|