Concepts (216)
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 Proteins | 46 | 2023 | 226 | 9.340 |
Why?
|
Escherichia coli | 45 | 2023 | 616 | 6.260 |
Why?
|
Rec A Recombinases | 21 | 2022 | 37 | 5.310 |
Why?
|
Escherichia coli K12 | 12 | 2022 | 18 | 5.240 |
Why?
|
DNA Helicases | 19 | 2023 | 177 | 4.400 |
Why?
|
DNA-Binding Proteins | 34 | 2023 | 1031 | 3.980 |
Why?
|
DNA Replication | 27 | 2023 | 208 | 3.930 |
Why?
|
DNA, Bacterial | 28 | 2023 | 223 | 3.750 |
Why?
|
Bacterial Proteins | 31 | 2022 | 660 | 3.200 |
Why?
|
Gene Expression Regulation, Bacterial | 15 | 2017 | 121 | 2.430 |
Why?
|
DNA Repair | 14 | 2020 | 209 | 1.600 |
Why?
|
DNA Restriction Enzymes | 2 | 2020 | 35 | 1.470 |
Why?
|
DNA, Single-Stranded | 12 | 2023 | 90 | 1.380 |
Why?
|
Mutation | 22 | 2022 | 2137 | 1.310 |
Why?
|
Recombination, Genetic | 18 | 2020 | 210 | 1.000 |
Why?
|
Cell Division | 5 | 2018 | 388 | 0.960 |
Why?
|
Epistasis, Genetic | 3 | 2020 | 44 | 0.880 |
Why?
|
Phenotype | 10 | 2022 | 962 | 0.840 |
Why?
|
Ultraviolet Rays | 13 | 2020 | 123 | 0.830 |
Why?
|
Fimbriae Proteins | 3 | 2017 | 12 | 0.790 |
Why?
|
Geobacter | 2 | 2017 | 12 | 0.730 |
Why?
|
Evolution, Molecular | 4 | 2015 | 278 | 0.710 |
Why?
|
Mutant Proteins | 2 | 2017 | 95 | 0.680 |
Why?
|
Biofilms | 2 | 2017 | 55 | 0.680 |
Why?
|
Genes, Bacterial | 12 | 2008 | 106 | 0.680 |
Why?
|
Peptide Hydrolases | 1 | 2018 | 73 | 0.670 |
Why?
|
Chromosomes, Bacterial | 8 | 2013 | 39 | 0.670 |
Why?
|
Bacteria | 5 | 2017 | 238 | 0.630 |
Why?
|
Bacterial Adhesion | 2 | 2017 | 56 | 0.630 |
Why?
|
Suppression, Genetic | 4 | 2006 | 29 | 0.610 |
Why?
|
Adenosine Triphosphate | 2 | 2008 | 268 | 0.590 |
Why?
|
Recombinant Fusion Proteins | 9 | 2020 | 451 | 0.510 |
Why?
|
Radiation, Ionizing | 1 | 2014 | 16 | 0.500 |
Why?
|
Exodeoxyribonucleases | 4 | 2010 | 29 | 0.500 |
Why?
|
Adaptation, Biological | 1 | 2014 | 13 | 0.490 |
Why?
|
DNA Repair Enzymes | 1 | 2014 | 26 | 0.490 |
Why?
|
Base Sequence | 15 | 2012 | 1244 | 0.420 |
Why?
|
Green Fluorescent Proteins | 3 | 2007 | 313 | 0.410 |
Why?
|
Molecular Sequence Data | 16 | 2015 | 1881 | 0.390 |
Why?
|
Genes, Lethal | 3 | 2006 | 34 | 0.390 |
Why?
|
Protein Binding | 7 | 2020 | 1474 | 0.370 |
Why?
|
Alleles | 3 | 2009 | 397 | 0.340 |
Why?
|
Genome, Bacterial | 3 | 2020 | 60 | 0.330 |
Why?
|
Archaea | 2 | 1999 | 10 | 0.320 |
Why?
|
Amino Acid Sequence | 11 | 2018 | 1498 | 0.320 |
Why?
|
Models, Biological | 4 | 2018 | 1097 | 0.300 |
Why?
|
Mutation, Missense | 3 | 2015 | 166 | 0.270 |
Why?
|
Archaeal Proteins | 3 | 1999 | 6 | 0.260 |
Why?
|
Adenosine Triphosphatases | 3 | 2004 | 220 | 0.250 |
Why?
|
DNA | 4 | 2023 | 719 | 0.230 |
Why?
|
Serine Endopeptidases | 3 | 2008 | 70 | 0.230 |
Why?
|
DNA Mutational Analysis | 3 | 2020 | 169 | 0.230 |
Why?
|
Radiation Tolerance | 2 | 2020 | 41 | 0.220 |
Why?
|
DNA Breaks, Double-Stranded | 3 | 2013 | 79 | 0.220 |
Why?
|
Phylogeny | 3 | 1999 | 303 | 0.200 |
Why?
|
Mutagenesis, Insertional | 3 | 2017 | 92 | 0.190 |
Why?
|
Ribonuclease H | 1 | 2020 | 19 | 0.190 |
Why?
|
Plasmids | 6 | 2009 | 244 | 0.190 |
Why?
|
Models, Genetic | 4 | 2005 | 244 | 0.190 |
Why?
|
Amino Acid Motifs | 1 | 2020 | 150 | 0.190 |
Why?
|
Fluorescence | 1 | 2020 | 84 | 0.190 |
Why?
|
DNA Primers | 4 | 2004 | 276 | 0.180 |
Why?
|
Replication Protein A | 5 | 2000 | 12 | 0.180 |
Why?
|
Microscopy | 1 | 2018 | 68 | 0.170 |
Why?
|
Culture Media | 2 | 2017 | 75 | 0.160 |
Why?
|
Hydrolysis | 2 | 2008 | 129 | 0.160 |
Why?
|
Conjugation, Genetic | 3 | 2015 | 12 | 0.160 |
Why?
|
Mutagenesis | 3 | 2007 | 127 | 0.160 |
Why?
|
Bacteriophage mu | 2 | 2012 | 3 | 0.160 |
Why?
|
Bioelectric Energy Sources | 1 | 2017 | 1 | 0.160 |
Why?
|
Glycerophosphates | 1 | 2017 | 2 | 0.160 |
Why?
|
Bacteriological Techniques | 1 | 2017 | 23 | 0.150 |
Why?
|
Cell Cycle Proteins | 2 | 1997 | 356 | 0.150 |
Why?
|
Cronobacter sakazakii | 1 | 2016 | 1 | 0.150 |
Why?
|
Exodeoxyribonuclease V | 2 | 2010 | 8 | 0.150 |
Why?
|
Endodeoxyribonucleases | 2 | 2010 | 37 | 0.150 |
Why?
|
Stress, Physiological | 1 | 2018 | 172 | 0.140 |
Why?
|
Membrane Microdomains | 1 | 2016 | 46 | 0.140 |
Why?
|
Mycobacterium | 1 | 2016 | 32 | 0.140 |
Why?
|
Microscopy, Fluorescence | 2 | 2010 | 371 | 0.140 |
Why?
|
Polymerase Chain Reaction | 3 | 2004 | 464 | 0.140 |
Why?
|
Protein Processing, Post-Translational | 1 | 2017 | 234 | 0.140 |
Why?
|
Cell Membrane | 1 | 2018 | 458 | 0.140 |
Why?
|
Saccharomyces cerevisiae | 2 | 1999 | 519 | 0.130 |
Why?
|
Membrane Proteins | 2 | 2016 | 753 | 0.130 |
Why?
|
Lipid Metabolism | 1 | 2016 | 193 | 0.130 |
Why?
|
Substrate Specificity | 2 | 2009 | 306 | 0.130 |
Why?
|
DNA Damage | 3 | 2020 | 273 | 0.120 |
Why?
|
Mycobacterium tuberculosis | 1 | 2018 | 345 | 0.120 |
Why?
|
Point Mutation | 1 | 2013 | 150 | 0.120 |
Why?
|
DNA Polymerase III | 2 | 2011 | 24 | 0.120 |
Why?
|
Hardness Tests | 1 | 2012 | 1 | 0.110 |
Why?
|
Hardness | 1 | 2012 | 7 | 0.110 |
Why?
|
DNA Breaks, Single-Stranded | 1 | 2012 | 6 | 0.110 |
Why?
|
Chromosome Segregation | 1 | 2012 | 37 | 0.110 |
Why?
|
Protein Biosynthesis | 2 | 1994 | 276 | 0.110 |
Why?
|
Cytochromes | 1 | 2012 | 1 | 0.110 |
Why?
|
Sequence Alignment | 4 | 1999 | 278 | 0.110 |
Why?
|
Homologous Recombination | 1 | 2012 | 21 | 0.110 |
Why?
|
Pseudomonas putida | 1 | 1992 | 3 | 0.110 |
Why?
|
Fimbriae, Bacterial | 1 | 2012 | 19 | 0.110 |
Why?
|
Bacillus subtilis | 1 | 1992 | 28 | 0.110 |
Why?
|
Crystallography, X-Ray | 3 | 2018 | 393 | 0.110 |
Why?
|
Structure-Activity Relationship | 3 | 2018 | 342 | 0.100 |
Why?
|
Salmonella typhimurium | 1 | 1992 | 73 | 0.100 |
Why?
|
DNA Transposable Elements | 1 | 2012 | 123 | 0.100 |
Why?
|
Nucleoproteins | 2 | 2009 | 31 | 0.100 |
Why?
|
Exonucleases | 1 | 2010 | 4 | 0.100 |
Why?
|
Deoxyribonucleases | 1 | 2010 | 31 | 0.090 |
Why?
|
Bacteriophage phi X 174 | 2 | 1999 | 3 | 0.080 |
Why?
|
Microbial Viability | 1 | 2007 | 53 | 0.080 |
Why?
|
Amino Acid Substitution | 1 | 2008 | 238 | 0.080 |
Why?
|
DNA-Directed DNA Polymerase | 1 | 2007 | 11 | 0.080 |
Why?
|
Multienzyme Complexes | 1 | 2007 | 68 | 0.080 |
Why?
|
Protein Structure, Secondary | 2 | 2018 | 234 | 0.070 |
Why?
|
Genes, Dominant | 1 | 2006 | 47 | 0.070 |
Why?
|
Genes, Recessive | 1 | 2006 | 49 | 0.070 |
Why?
|
Sequence Deletion | 2 | 2004 | 113 | 0.070 |
Why?
|
Lac Operon | 2 | 1996 | 27 | 0.070 |
Why?
|
DnaB Helicases | 2 | 2016 | 2 | 0.070 |
Why?
|
Gene Expression | 2 | 2001 | 739 | 0.070 |
Why?
|
Nucleic Acid Conformation | 2 | 2018 | 222 | 0.070 |
Why?
|
Macromolecular Substances | 1 | 2005 | 150 | 0.060 |
Why?
|
Cloning, Molecular | 2 | 1999 | 348 | 0.060 |
Why?
|
Binding Sites | 3 | 2013 | 823 | 0.060 |
Why?
|
Codon | 1 | 2004 | 41 | 0.060 |
Why?
|
Genes, Reporter | 1 | 2004 | 218 | 0.060 |
Why?
|
Mutagenesis, Site-Directed | 2 | 1994 | 238 | 0.060 |
Why?
|
Protein Conformation | 2 | 2018 | 720 | 0.060 |
Why?
|
Promoter Regions, Genetic | 2 | 2004 | 614 | 0.060 |
Why?
|
Temperature | 1 | 2004 | 281 | 0.060 |
Why?
|
Rad51 Recombinase | 3 | 1998 | 26 | 0.060 |
Why?
|
Deltaproteobacteria | 1 | 2001 | 3 | 0.050 |
Why?
|
Transformation, Bacterial | 1 | 2001 | 12 | 0.050 |
Why?
|
RNA | 1 | 2005 | 358 | 0.050 |
Why?
|
Dimerization | 1 | 2001 | 137 | 0.050 |
Why?
|
Models, Molecular | 2 | 2013 | 1060 | 0.050 |
Why?
|
Intrinsically Disordered Proteins | 1 | 2020 | 10 | 0.050 |
Why?
|
Sulfolobus | 2 | 1998 | 2 | 0.050 |
Why?
|
Single Molecule Imaging | 1 | 2020 | 18 | 0.050 |
Why?
|
DNA Primase | 1 | 2000 | 3 | 0.050 |
Why?
|
Recombinant Proteins | 2 | 1999 | 631 | 0.050 |
Why?
|
beta-Galactosidase | 2 | 1996 | 77 | 0.040 |
Why?
|
RNA, Ribosomal, 16S | 1 | 1999 | 62 | 0.040 |
Why?
|
DNA, Archaeal | 1 | 1998 | 1 | 0.040 |
Why?
|
Centrifugation, Density Gradient | 1 | 2018 | 29 | 0.040 |
Why?
|
Cell Fractionation | 1 | 2018 | 28 | 0.040 |
Why?
|
Genetic Complementation Test | 2 | 2001 | 51 | 0.040 |
Why?
|
Protein Domains | 1 | 2018 | 124 | 0.040 |
Why?
|
Peptidoglycan | 1 | 2018 | 53 | 0.040 |
Why?
|
Repressor Proteins | 2 | 1996 | 307 | 0.040 |
Why?
|
Halobacteriaceae | 1 | 1996 | 1 | 0.040 |
Why?
|
Methanococcus | 1 | 1996 | 5 | 0.040 |
Why?
|
Dose-Response Relationship, Radiation | 1 | 1996 | 50 | 0.040 |
Why?
|
Genetic Markers | 1 | 1996 | 108 | 0.040 |
Why?
|
Genetic Vectors | 1 | 2001 | 653 | 0.040 |
Why?
|
Restriction Mapping | 1 | 1994 | 53 | 0.030 |
Why?
|
Selection, Genetic | 1 | 2015 | 69 | 0.030 |
Why?
|
Genomic Instability | 1 | 2015 | 53 | 0.030 |
Why?
|
Transduction, Genetic | 1 | 1996 | 194 | 0.030 |
Why?
|
Half-Life | 1 | 1994 | 63 | 0.030 |
Why?
|
Coliphages | 1 | 1993 | 12 | 0.030 |
Why?
|
Replication Origin | 2 | 2007 | 35 | 0.030 |
Why?
|
Genes, Viral | 1 | 1993 | 55 | 0.030 |
Why?
|
Proviruses | 1 | 1993 | 18 | 0.030 |
Why?
|
Regulatory Sequences, Nucleic Acid | 1 | 1994 | 93 | 0.030 |
Why?
|
Fluorescence Resonance Energy Transfer | 1 | 2013 | 68 | 0.030 |
Why?
|
Peptide Mapping | 1 | 2013 | 31 | 0.030 |
Why?
|
Zinc | 1 | 2013 | 82 | 0.030 |
Why?
|
Two-Hybrid System Techniques | 1 | 2013 | 60 | 0.030 |
Why?
|
Binding, Competitive | 1 | 2013 | 100 | 0.030 |
Why?
|
Protein Interaction Domains and Motifs | 1 | 2013 | 83 | 0.030 |
Why?
|
Entropy | 1 | 2012 | 17 | 0.030 |
Why?
|
Biophysics | 1 | 2012 | 40 | 0.030 |
Why?
|
Pressure | 1 | 2012 | 64 | 0.030 |
Why?
|
Transposases | 1 | 2012 | 11 | 0.030 |
Why?
|
Protein Multimerization | 1 | 2013 | 153 | 0.030 |
Why?
|
Ribosomes | 1 | 1994 | 151 | 0.030 |
Why?
|
Electron Transport | 1 | 2012 | 19 | 0.030 |
Why?
|
Saccharomyces cerevisiae Proteins | 1 | 1996 | 408 | 0.030 |
Why?
|
Holoenzymes | 1 | 2011 | 3 | 0.030 |
Why?
|
Protein Isoforms | 1 | 2012 | 182 | 0.030 |
Why?
|
Phosphates | 1 | 1992 | 83 | 0.030 |
Why?
|
Surface Properties | 1 | 2012 | 251 | 0.030 |
Why?
|
Reverse Transcriptase Polymerase Chain Reaction | 1 | 2012 | 485 | 0.020 |
Why?
|
Protein Transport | 1 | 2012 | 371 | 0.020 |
Why?
|
Peptide Chain Initiation, Translational | 1 | 1990 | 21 | 0.020 |
Why?
|
Genome | 1 | 2012 | 245 | 0.020 |
Why?
|
RNA, Messenger | 1 | 1994 | 1362 | 0.020 |
Why?
|
Luminescent Proteins | 1 | 2009 | 116 | 0.020 |
Why?
|
Hydrogen-Ion Concentration | 1 | 2009 | 389 | 0.020 |
Why?
|
Kinetics | 1 | 2009 | 697 | 0.020 |
Why?
|
Sensitivity and Specificity | 1 | 2009 | 965 | 0.020 |
Why?
|
Transcription, Genetic | 1 | 1990 | 811 | 0.020 |
Why?
|
Cell Nucleus | 1 | 2009 | 565 | 0.020 |
Why?
|
Time Factors | 1 | 2012 | 3161 | 0.020 |
Why?
|
Nitrogen Fixation | 1 | 2001 | 1 | 0.010 |
Why?
|
Blotting, Southern | 1 | 2001 | 44 | 0.010 |
Why?
|
Electroporation | 1 | 2001 | 33 | 0.010 |
Why?
|
Microbial Sensitivity Tests | 1 | 2001 | 152 | 0.010 |
Why?
|
Molecular Weight | 2 | 1993 | 177 | 0.010 |
Why?
|
Templates, Genetic | 1 | 1999 | 14 | 0.010 |
Why?
|
Open Reading Frames | 1 | 1999 | 78 | 0.010 |
Why?
|
Genes, Archaeal | 1 | 1998 | 1 | 0.010 |
Why?
|
Oligodeoxyribonucleotides | 1 | 1999 | 226 | 0.010 |
Why?
|
Consensus Sequence | 1 | 1997 | 29 | 0.010 |
Why?
|
Conserved Sequence | 1 | 1997 | 167 | 0.010 |
Why?
|
Anti-Bacterial Agents | 1 | 2001 | 588 | 0.010 |
Why?
|
Humans | 2 | 1999 | 50631 | 0.010 |
Why?
|
Deoxyribonuclease EcoRI | 1 | 1993 | 1 | 0.010 |
Why?
|
Reading Frames | 1 | 1993 | 2 | 0.010 |
Why?
|
Bacteriophage lambda | 1 | 1993 | 20 | 0.010 |
Why?
|
Deoxyribonucleases, Type II Site-Specific | 1 | 1993 | 23 | 0.010 |
Why?
|
Sequence Analysis, DNA | 1 | 1993 | 359 | 0.010 |
Why?
|
Chromosome Mapping | 1 | 1984 | 266 | 0.000 |
Why?
|
Animals | 1 | 1997 | 17863 | 0.000 |
Why?
|