Concepts (151)
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?
|
---|
DNA-Directed DNA Polymerase | 6 | 2017 | 79 | 2.180 |
Why?
|
Bacterial Proteins | 5 | 2016 | 878 | 1.060 |
Why?
|
Sulfotransferases | 6 | 2016 | 27 | 1.030 |
Why?
|
DNA Repair | 5 | 2017 | 579 | 0.960 |
Why?
|
DNA | 6 | 2017 | 1588 | 0.950 |
Why?
|
Virulence Factors | 3 | 2016 | 172 | 0.920 |
Why?
|
Models, Molecular | 17 | 2017 | 1070 | 0.900 |
Why?
|
Crystallography, X-Ray | 13 | 2017 | 357 | 0.810 |
Why?
|
Ribonucleotides | 2 | 2017 | 36 | 0.660 |
Why?
|
Substrate Specificity | 9 | 2017 | 283 | 0.660 |
Why?
|
Deoxyribonucleotides | 1 | 2017 | 10 | 0.590 |
Why?
|
DNA End-Joining Repair | 1 | 2017 | 34 | 0.570 |
Why?
|
Endodeoxyribonucleases | 3 | 2012 | 47 | 0.550 |
Why?
|
DNA Breaks, Double-Stranded | 2 | 2017 | 132 | 0.550 |
Why?
|
Amino Acid Sequence | 12 | 2018 | 2695 | 0.530 |
Why?
|
Deoxyribonuclease I | 1 | 2016 | 49 | 0.530 |
Why?
|
Crystallization | 3 | 2014 | 83 | 0.480 |
Why?
|
Endonucleases | 1 | 2014 | 54 | 0.470 |
Why?
|
Streptococcus pneumoniae | 3 | 2012 | 372 | 0.460 |
Why?
|
Molecular Sequence Data | 10 | 2014 | 3867 | 0.450 |
Why?
|
Streptococcus agalactiae | 1 | 2014 | 105 | 0.440 |
Why?
|
Catalytic Domain | 6 | 2017 | 158 | 0.430 |
Why?
|
Kinetics | 6 | 2017 | 1312 | 0.430 |
Why?
|
Streptococcal Infections | 1 | 2014 | 244 | 0.390 |
Why?
|
Membrane Proteins | 4 | 2012 | 1522 | 0.380 |
Why?
|
Protein Conformation | 8 | 2016 | 833 | 0.380 |
Why?
|
Catalysis | 4 | 2015 | 125 | 0.360 |
Why?
|
Sequence Alignment | 6 | 2016 | 623 | 0.360 |
Why?
|
Protein Binding | 7 | 2017 | 1741 | 0.350 |
Why?
|
Heparin | 1 | 2012 | 227 | 0.350 |
Why?
|
Periplasmic Binding Proteins | 1 | 2010 | 36 | 0.350 |
Why?
|
DNA Polymerase beta | 3 | 2015 | 14 | 0.300 |
Why?
|
Recombinant Fusion Proteins | 2 | 2010 | 767 | 0.290 |
Why?
|
Anticoagulants | 1 | 2012 | 581 | 0.280 |
Why?
|
Nucleotides | 3 | 2017 | 92 | 0.270 |
Why?
|
Nucleic Acid Conformation | 2 | 2017 | 184 | 0.260 |
Why?
|
Herpesvirus 1, Human | 1 | 2004 | 26 | 0.230 |
Why?
|
Sequence Homology, Amino Acid | 4 | 2012 | 657 | 0.230 |
Why?
|
Cell-Free Nucleic Acids | 1 | 2022 | 44 | 0.200 |
Why?
|
Hypertension, Pregnancy-Induced | 1 | 2022 | 77 | 0.190 |
Why?
|
Base Sequence | 3 | 2017 | 3091 | 0.180 |
Why?
|
Pre-Eclampsia | 1 | 2022 | 226 | 0.170 |
Why?
|
Cloning, Molecular | 3 | 2017 | 892 | 0.170 |
Why?
|
Arabidopsis Proteins | 2 | 2010 | 38 | 0.160 |
Why?
|
Arabidopsis | 2 | 2010 | 69 | 0.160 |
Why?
|
Protein Isoforms | 3 | 2016 | 408 | 0.150 |
Why?
|
Protein Conformation, beta-Strand | 1 | 2017 | 16 | 0.150 |
Why?
|
Protein Conformation, alpha-Helical | 1 | 2017 | 16 | 0.150 |
Why?
|
Receptors, Glucocorticoid | 1 | 2018 | 122 | 0.140 |
Why?
|
Amino Acid Substitution | 2 | 2010 | 393 | 0.140 |
Why?
|
Thermodynamics | 1 | 2017 | 144 | 0.140 |
Why?
|
Amino Acid Motifs | 1 | 2017 | 199 | 0.140 |
Why?
|
Receptors, Cell Surface | 2 | 2010 | 469 | 0.140 |
Why?
|
Protein Interaction Domains and Motifs | 1 | 2017 | 137 | 0.140 |
Why?
|
Adenosine Diphosphate | 1 | 2016 | 58 | 0.140 |
Why?
|
Binding Sites | 4 | 2010 | 1292 | 0.140 |
Why?
|
Mutagenesis, Site-Directed | 3 | 2012 | 316 | 0.130 |
Why?
|
Oligosaccharides | 1 | 2016 | 76 | 0.130 |
Why?
|
Protein Structure, Tertiary | 3 | 2008 | 752 | 0.130 |
Why?
|
Streptococcus pyogenes | 1 | 2016 | 77 | 0.130 |
Why?
|
Protein Multimerization | 1 | 2016 | 122 | 0.130 |
Why?
|
Escherichia coli | 2 | 2018 | 983 | 0.120 |
Why?
|
Protein Structure, Secondary | 1 | 2015 | 239 | 0.120 |
Why?
|
Protein Domains | 1 | 2016 | 233 | 0.120 |
Why?
|
Biocatalysis | 2 | 2012 | 33 | 0.120 |
Why?
|
Electrons | 1 | 2014 | 24 | 0.110 |
Why?
|
Recombinant Proteins | 1 | 2017 | 1386 | 0.110 |
Why?
|
Receptors for Activated C Kinase | 2 | 2010 | 5 | 0.110 |
Why?
|
Maltose-Binding Proteins | 2 | 2010 | 13 | 0.110 |
Why?
|
Point Mutation | 1 | 2014 | 348 | 0.110 |
Why?
|
Gene Expression | 1 | 2017 | 1565 | 0.100 |
Why?
|
Immunoglobulin E | 1 | 2013 | 162 | 0.100 |
Why?
|
DNA Damage | 1 | 2015 | 512 | 0.100 |
Why?
|
Humans | 15 | 2022 | 123180 | 0.100 |
Why?
|
Phenylalanine | 1 | 2012 | 120 | 0.100 |
Why?
|
High-Throughput Screening Assays | 1 | 2012 | 96 | 0.100 |
Why?
|
Thiophenes | 1 | 2012 | 60 | 0.100 |
Why?
|
ADAM Proteins | 1 | 2012 | 79 | 0.100 |
Why?
|
Protease Inhibitors | 1 | 2012 | 93 | 0.100 |
Why?
|
Allergens | 1 | 2013 | 249 | 0.090 |
Why?
|
Cations, Divalent | 1 | 2010 | 19 | 0.090 |
Why?
|
Dermatophagoides pteronyssinus | 1 | 2010 | 2 | 0.090 |
Why?
|
Antigens, Dermatophagoides | 1 | 2010 | 9 | 0.090 |
Why?
|
Arthropod Proteins | 1 | 2010 | 11 | 0.090 |
Why?
|
Entropy | 1 | 2010 | 26 | 0.090 |
Why?
|
Alanine | 1 | 2010 | 180 | 0.090 |
Why?
|
Chickens | 1 | 2010 | 636 | 0.080 |
Why?
|
Enzyme Inhibitors | 1 | 2012 | 570 | 0.080 |
Why?
|
Mutagenesis | 1 | 2010 | 347 | 0.080 |
Why?
|
Imidazoles | 1 | 2010 | 193 | 0.080 |
Why?
|
Sequence Analysis, DNA | 1 | 2015 | 1752 | 0.080 |
Why?
|
Animals | 7 | 2016 | 33798 | 0.080 |
Why?
|
Heparitin Sulfate | 1 | 2008 | 20 | 0.070 |
Why?
|
Saccharomyces cerevisiae Proteins | 1 | 2010 | 274 | 0.070 |
Why?
|
Protein Engineering | 1 | 2008 | 73 | 0.070 |
Why?
|
Carrier Proteins | 2 | 2010 | 1017 | 0.070 |
Why?
|
Thymine Nucleotides | 1 | 2006 | 3 | 0.070 |
Why?
|
Dideoxynucleotides | 1 | 2006 | 3 | 0.070 |
Why?
|
Saccharomyces cerevisiae | 1 | 2010 | 424 | 0.070 |
Why?
|
Recombination, Genetic | 1 | 2008 | 447 | 0.070 |
Why?
|
Mutation | 2 | 2014 | 5767 | 0.070 |
Why?
|
Asthma | 1 | 2013 | 744 | 0.060 |
Why?
|
Chromatography, Ion Exchange | 1 | 2004 | 68 | 0.060 |
Why?
|
Ions | 1 | 2004 | 22 | 0.060 |
Why?
|
Hydrogen Bonding | 1 | 2004 | 79 | 0.060 |
Why?
|
Models, Chemical | 1 | 2004 | 85 | 0.060 |
Why?
|
Chromatography, High Pressure Liquid | 1 | 2004 | 338 | 0.050 |
Why?
|
Lysine | 1 | 2004 | 198 | 0.050 |
Why?
|
Polysaccharides | 1 | 2004 | 144 | 0.050 |
Why?
|
Glutamine | 1 | 2004 | 195 | 0.050 |
Why?
|
Plasmids | 1 | 2004 | 511 | 0.050 |
Why?
|
DNA Mutational Analysis | 1 | 2004 | 790 | 0.050 |
Why?
|
DNA-Binding Proteins | 2 | 2010 | 2055 | 0.050 |
Why?
|
Fetus | 1 | 2022 | 578 | 0.040 |
Why?
|
Zebrafish Proteins | 1 | 2016 | 105 | 0.030 |
Why?
|
DNA Replication | 1 | 2017 | 350 | 0.030 |
Why?
|
Glucocorticoids | 1 | 2018 | 377 | 0.030 |
Why?
|
Mice | 2 | 2013 | 17542 | 0.030 |
Why?
|
Zebrafish | 1 | 2016 | 386 | 0.030 |
Why?
|
Cockroaches | 1 | 2013 | 6 | 0.030 |
Why?
|
Digestion | 1 | 2013 | 37 | 0.030 |
Why?
|
Micrococcal Nuclease | 1 | 2012 | 7 | 0.030 |
Why?
|
Organic Chemicals | 1 | 2012 | 59 | 0.030 |
Why?
|
Crystallography | 1 | 2012 | 40 | 0.030 |
Why?
|
Fluorescence | 1 | 2012 | 93 | 0.030 |
Why?
|
Protein Unfolding | 1 | 2012 | 10 | 0.030 |
Why?
|
Magnetic Resonance Spectroscopy | 1 | 2013 | 288 | 0.020 |
Why?
|
Transgenes | 1 | 2013 | 334 | 0.020 |
Why?
|
Environmental Exposure | 1 | 2013 | 217 | 0.020 |
Why?
|
Scattering, Small Angle | 1 | 2010 | 8 | 0.020 |
Why?
|
Ligands | 1 | 2012 | 533 | 0.020 |
Why?
|
X-Ray Diffraction | 1 | 2010 | 95 | 0.020 |
Why?
|
Mismatch Repair Endonuclease PMS2 | 1 | 2010 | 9 | 0.020 |
Why?
|
MutL Proteins | 1 | 2010 | 19 | 0.020 |
Why?
|
Lipids | 1 | 2013 | 514 | 0.020 |
Why?
|
DNA Repair Enzymes | 1 | 2010 | 40 | 0.020 |
Why?
|
Pregnancy | 1 | 2022 | 7146 | 0.020 |
Why?
|
Infant, Newborn | 1 | 2022 | 8115 | 0.020 |
Why?
|
Adenosine Triphosphatases | 1 | 2010 | 208 | 0.020 |
Why?
|
Electrophoretic Mobility Shift Assay | 1 | 2008 | 49 | 0.020 |
Why?
|
Nuclear Magnetic Resonance, Biomolecular | 1 | 2008 | 43 | 0.020 |
Why?
|
Carbohydrate Conformation | 1 | 2008 | 16 | 0.020 |
Why?
|
Escherichia coli Proteins | 1 | 2010 | 303 | 0.020 |
Why?
|
Protein Biosynthesis | 1 | 2010 | 664 | 0.020 |
Why?
|
DNA Primers | 1 | 2008 | 660 | 0.020 |
Why?
|
Reproducibility of Results | 1 | 2012 | 2840 | 0.020 |
Why?
|
Transcription, Genetic | 1 | 2010 | 1702 | 0.020 |
Why?
|
Feasibility Studies | 1 | 2008 | 756 | 0.020 |
Why?
|
Retrospective Studies | 1 | 2022 | 16062 | 0.010 |
Why?
|
Signal Transduction | 1 | 2008 | 4494 | 0.010 |
Why?
|
Female | 1 | 2022 | 65562 | 0.010 |
Why?
|