Concepts (215)
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?
|
---|
Bacteriophage T7 | 24 | 2014 | 174 | 1.890 |
Why?
|
DNA-Directed DNA Polymerase | 31 | 2017 | 486 | 1.670 |
Why?
|
Viral Proteins | 25 | 2017 | 1900 | 1.130 |
Why?
|
DNA-Directed RNA Polymerases | 9 | 2015 | 371 | 1.000 |
Why?
|
T-Phages | 14 | 1992 | 90 | 0.720 |
Why?
|
Escherichia coli | 27 | 2014 | 4217 | 0.560 |
Why?
|
DNA, Viral | 19 | 2017 | 2225 | 0.460 |
Why?
|
Genes, Viral | 9 | 2008 | 718 | 0.410 |
Why?
|
Deoxyribonucleotides | 6 | 2015 | 42 | 0.400 |
Why?
|
DNA | 11 | 2014 | 7301 | 0.390 |
Why?
|
Nucleoside-Phosphate Kinase | 1 | 2010 | 23 | 0.380 |
Why?
|
Bacteriophages | 4 | 2017 | 356 | 0.380 |
Why?
|
Thymidine | 2 | 2014 | 310 | 0.350 |
Why?
|
Exonucleases | 3 | 2004 | 47 | 0.340 |
Why?
|
Bacteriophage T4 | 3 | 2008 | 33 | 0.330 |
Why?
|
DNA, Single-Stranded | 10 | 2017 | 354 | 0.300 |
Why?
|
DNA Ligases | 2 | 2011 | 80 | 0.290 |
Why?
|
DNA Primase | 8 | 2005 | 109 | 0.270 |
Why?
|
RNA-Directed DNA Polymerase | 2 | 2008 | 248 | 0.260 |
Why?
|
Templates, Genetic | 6 | 2008 | 211 | 0.260 |
Why?
|
DNA Polymerase I | 3 | 1997 | 38 | 0.260 |
Why?
|
Thymine Nucleotides | 4 | 2014 | 63 | 0.250 |
Why?
|
RNA | 5 | 2015 | 2749 | 0.250 |
Why?
|
DNA Replication | 11 | 2017 | 1399 | 0.240 |
Why?
|
Thioredoxins | 7 | 2011 | 213 | 0.240 |
Why?
|
Oligonucleotide Probes | 2 | 2001 | 427 | 0.240 |
Why?
|
Escherichia coli Proteins | 7 | 2014 | 1050 | 0.230 |
Why?
|
Drug Resistance, Viral | 1 | 2008 | 820 | 0.220 |
Why?
|
RNA Probes | 1 | 2001 | 113 | 0.200 |
Why?
|
Thymidine Kinase | 3 | 2014 | 290 | 0.190 |
Why?
|
Isotope Labeling | 2 | 2008 | 406 | 0.190 |
Why?
|
DNA Helicases | 7 | 2011 | 859 | 0.190 |
Why?
|
Phosphotransferases | 1 | 2001 | 308 | 0.180 |
Why?
|
DNA Probes | 1 | 2001 | 560 | 0.180 |
Why?
|
Ligases | 1 | 2001 | 333 | 0.180 |
Why?
|
Manganese | 3 | 2015 | 408 | 0.170 |
Why?
|
Phosphoric Monoester Hydrolases | 1 | 2001 | 431 | 0.170 |
Why?
|
Endonucleases | 1 | 2001 | 380 | 0.160 |
Why?
|
Base Sequence | 17 | 2012 | 12797 | 0.160 |
Why?
|
Magnesium | 4 | 2012 | 813 | 0.160 |
Why?
|
Catalysis | 5 | 2007 | 761 | 0.160 |
Why?
|
Dideoxynucleotides | 2 | 2014 | 13 | 0.150 |
Why?
|
Protein Structure, Secondary | 4 | 2011 | 1246 | 0.140 |
Why?
|
Nucleic Acid Synthesis Inhibitors | 2 | 2014 | 112 | 0.140 |
Why?
|
Nucleic Acid Amplification Techniques | 2 | 2008 | 323 | 0.140 |
Why?
|
Promoter Regions, Genetic | 4 | 2012 | 5867 | 0.130 |
Why?
|
Cloning, Molecular | 5 | 2008 | 4320 | 0.130 |
Why?
|
Dideoxynucleosides | 1 | 1995 | 122 | 0.130 |
Why?
|
Sequence Deletion | 5 | 2014 | 1526 | 0.120 |
Why?
|
Flap Endonucleases | 1 | 2014 | 19 | 0.120 |
Why?
|
Deoxyguanine Nucleotides | 2 | 2010 | 21 | 0.120 |
Why?
|
Nucleic Acid Hybridization | 2 | 2008 | 1375 | 0.120 |
Why?
|
DNA Primers | 9 | 2017 | 2892 | 0.110 |
Why?
|
Synechococcus | 1 | 2012 | 28 | 0.110 |
Why?
|
Molecular Sequence Data | 12 | 2012 | 18111 | 0.110 |
Why?
|
DNA-Binding Proteins | 7 | 2017 | 9648 | 0.110 |
Why?
|
Aquatic Organisms | 1 | 2012 | 48 | 0.110 |
Why?
|
Nucleotides | 3 | 2013 | 464 | 0.110 |
Why?
|
Exodeoxyribonucleases | 3 | 2000 | 180 | 0.110 |
Why?
|
Suppression, Genetic | 2 | 2009 | 196 | 0.100 |
Why?
|
Genetic Complementation Test | 2 | 2010 | 562 | 0.100 |
Why?
|
Recombinant Proteins | 2 | 2001 | 6622 | 0.100 |
Why?
|
Bacteriophage M13 | 3 | 2001 | 39 | 0.100 |
Why?
|
Models, Molecular | 11 | 2011 | 5456 | 0.100 |
Why?
|
Binding Sites | 10 | 2011 | 6114 | 0.090 |
Why?
|
Phosphotransferases (Alcohol Group Acceptor) | 1 | 2012 | 437 | 0.090 |
Why?
|
RNA Ligase (ATP) | 1 | 2008 | 9 | 0.080 |
Why?
|
DNA Nucleotidylexotransferase | 1 | 2008 | 64 | 0.080 |
Why?
|
Amino Acid Sequence | 7 | 2010 | 13815 | 0.080 |
Why?
|
Deoxyribonuclease I | 1 | 2009 | 229 | 0.080 |
Why?
|
Uridine Kinase | 1 | 2007 | 6 | 0.080 |
Why?
|
Genetic Techniques | 1 | 2011 | 435 | 0.080 |
Why?
|
Escherichia coli K12 | 1 | 2007 | 34 | 0.080 |
Why?
|
Nucleotide Mapping | 1 | 1987 | 20 | 0.080 |
Why?
|
Phenylalanine | 1 | 2009 | 365 | 0.080 |
Why?
|
Substrate Specificity | 4 | 2012 | 1801 | 0.070 |
Why?
|
In Situ Nick-End Labeling | 1 | 2008 | 643 | 0.070 |
Why?
|
Sequence Analysis, DNA | 2 | 2008 | 4803 | 0.070 |
Why?
|
Phosphates | 1 | 1990 | 786 | 0.070 |
Why?
|
Kinetics | 8 | 2010 | 6473 | 0.070 |
Why?
|
Virus Replication | 4 | 2009 | 2534 | 0.070 |
Why?
|
Hydrolysis | 3 | 2004 | 682 | 0.070 |
Why?
|
Electrophoresis, Polyacrylamide Gel | 4 | 2012 | 1801 | 0.070 |
Why?
|
Siphoviridae | 1 | 2004 | 7 | 0.060 |
Why?
|
Plasmids | 4 | 2001 | 2307 | 0.060 |
Why?
|
Operon | 1 | 1985 | 363 | 0.060 |
Why?
|
Protein Structure, Tertiary | 5 | 2011 | 3846 | 0.060 |
Why?
|
Biopolymers | 2 | 2001 | 189 | 0.060 |
Why?
|
RNA Nucleotidyltransferases | 2 | 1994 | 64 | 0.060 |
Why?
|
Phosphorylation | 2 | 2014 | 8436 | 0.050 |
Why?
|
Genetic Vectors | 1 | 1992 | 3420 | 0.050 |
Why?
|
Polynucleotide 5'-Hydroxyl-Kinase | 1 | 2001 | 8 | 0.050 |
Why?
|
Genome, Bacterial | 1 | 2006 | 760 | 0.050 |
Why?
|
Phosphorus Radioisotopes | 1 | 2001 | 104 | 0.050 |
Why?
|
Chemical Precipitation | 1 | 2001 | 179 | 0.050 |
Why?
|
Molecular Probe Techniques | 1 | 2001 | 119 | 0.050 |
Why?
|
Indicators and Reagents | 1 | 2001 | 462 | 0.050 |
Why?
|
Gene Deletion | 1 | 2008 | 2751 | 0.050 |
Why?
|
Genetics, Medical | 1 | 2001 | 338 | 0.040 |
Why?
|
Mutation | 7 | 2015 | 29786 | 0.040 |
Why?
|
Osmolar Concentration | 3 | 2010 | 683 | 0.040 |
Why?
|
Protein Binding | 5 | 2011 | 9386 | 0.040 |
Why?
|
Protein Multimerization | 2 | 1995 | 970 | 0.040 |
Why?
|
Protein Conformation | 4 | 2010 | 4011 | 0.030 |
Why?
|
Transcription, Genetic | 4 | 2015 | 7722 | 0.030 |
Why?
|
Thermus | 1 | 1995 | 11 | 0.030 |
Why?
|
Deoxycytosine Nucleotides | 2 | 1998 | 14 | 0.030 |
Why?
|
RNA, Messenger | 2 | 2001 | 13033 | 0.030 |
Why?
|
Podoviridae | 1 | 2015 | 5 | 0.030 |
Why?
|
Surface Plasmon Resonance | 2 | 2011 | 274 | 0.030 |
Why?
|
Hot Temperature | 1 | 2001 | 1354 | 0.030 |
Why?
|
Pyrophosphatases | 2 | 1999 | 137 | 0.030 |
Why?
|
Fluorine | 1 | 2015 | 83 | 0.030 |
Why?
|
Cattle | 1 | 2001 | 3922 | 0.030 |
Why?
|
Pyrimidine Phosphorylases | 1 | 2014 | 2 | 0.030 |
Why?
|
Transcription Initiation Site | 1 | 2015 | 196 | 0.030 |
Why?
|
Mutagenesis | 3 | 2005 | 1266 | 0.030 |
Why?
|
Oligodeoxyribonucleotides | 1 | 1995 | 708 | 0.030 |
Why?
|
Cyanobacteria | 1 | 2013 | 49 | 0.030 |
Why?
|
Enzyme Stability | 1 | 2013 | 210 | 0.030 |
Why?
|
RNA, Viral | 2 | 1981 | 2902 | 0.030 |
Why?
|
RNA Stability | 1 | 2015 | 321 | 0.030 |
Why?
|
Salts | 1 | 2012 | 65 | 0.030 |
Why?
|
Metals | 2 | 2012 | 719 | 0.030 |
Why?
|
Coenzymes | 1 | 2012 | 91 | 0.030 |
Why?
|
Ribonucleotides | 1 | 2012 | 117 | 0.030 |
Why?
|
Nucleic Acid Conformation | 2 | 2011 | 913 | 0.030 |
Why?
|
Gene Expression Regulation | 2 | 1992 | 12072 | 0.020 |
Why?
|
Gene Knockout Techniques | 1 | 2014 | 809 | 0.020 |
Why?
|
RNA, Transfer | 1 | 2013 | 316 | 0.020 |
Why?
|
Deoxyadenine Nucleotides | 1 | 1990 | 12 | 0.020 |
Why?
|
Autoanalysis | 1 | 1990 | 72 | 0.020 |
Why?
|
Scattering, Small Angle | 1 | 2010 | 59 | 0.020 |
Why?
|
Allosteric Site | 1 | 2010 | 103 | 0.020 |
Why?
|
X-Ray Diffraction | 1 | 2010 | 420 | 0.020 |
Why?
|
Avian myeloblastosis virus | 1 | 2008 | 22 | 0.020 |
Why?
|
Crystallography, X-Ray | 2 | 2007 | 2011 | 0.020 |
Why?
|
Allosteric Regulation | 1 | 2010 | 408 | 0.020 |
Why?
|
Moloney murine leukemia virus | 1 | 2008 | 139 | 0.020 |
Why?
|
Proteins | 1 | 2004 | 6103 | 0.020 |
Why?
|
Structure-Activity Relationship | 2 | 1997 | 3129 | 0.020 |
Why?
|
Histidine | 1 | 1989 | 313 | 0.020 |
Why?
|
Genes, Suppressor | 1 | 2007 | 48 | 0.020 |
Why?
|
Dithiothreitol | 1 | 1987 | 101 | 0.020 |
Why?
|
Gene Expression | 1 | 2001 | 7799 | 0.020 |
Why?
|
Hydrogen-Ion Concentration | 1 | 2012 | 2557 | 0.020 |
Why?
|
Calcium | 1 | 2001 | 5756 | 0.020 |
Why?
|
Free Radicals | 1 | 1987 | 237 | 0.020 |
Why?
|
DNA, Recombinant | 1 | 1987 | 476 | 0.020 |
Why?
|
Models, Biological | 3 | 2009 | 9583 | 0.020 |
Why?
|
Cell Physiological Phenomena | 1 | 2007 | 154 | 0.020 |
Why?
|
Solvents | 1 | 2007 | 302 | 0.020 |
Why?
|
Temperature | 1 | 2012 | 2206 | 0.020 |
Why?
|
Rifampin | 1 | 2007 | 315 | 0.020 |
Why?
|
Spinal Cord Injuries | 1 | 1994 | 931 | 0.020 |
Why?
|
Sulfinic Acids | 1 | 2005 | 13 | 0.020 |
Why?
|
Bacteriophage lambda | 1 | 1985 | 147 | 0.020 |
Why?
|
DNA, Complementary | 1 | 2008 | 2050 | 0.020 |
Why?
|
Bacterial Proteins | 2 | 1987 | 3848 | 0.010 |
Why?
|
Protein Subunits | 1 | 2007 | 959 | 0.010 |
Why?
|
History, 20th Century | 1 | 1992 | 2740 | 0.010 |
Why?
|
Image Enhancement | 1 | 1994 | 2921 | 0.010 |
Why?
|
Virulence | 1 | 2006 | 1333 | 0.010 |
Why?
|
Drosophila | 1 | 1990 | 1491 | 0.010 |
Why?
|
Surface Properties | 2 | 1997 | 1184 | 0.010 |
Why?
|
Genes | 2 | 1983 | 1893 | 0.010 |
Why?
|
Sequence Alignment | 2 | 1999 | 2256 | 0.010 |
Why?
|
Oxidation-Reduction | 1 | 1987 | 2187 | 0.010 |
Why?
|
Bacteriophage phi X 174 | 1 | 1981 | 20 | 0.010 |
Why?
|
Exodeoxyribonuclease V | 1 | 2000 | 9 | 0.010 |
Why?
|
Base Pair Mismatch | 1 | 2001 | 97 | 0.010 |
Why?
|
Polymerase Chain Reaction | 1 | 1990 | 6171 | 0.010 |
Why?
|
Crystallization | 1 | 2001 | 524 | 0.010 |
Why?
|
DNA Mutational Analysis | 1 | 1989 | 4186 | 0.010 |
Why?
|
Rec A Recombinases | 1 | 1999 | 51 | 0.010 |
Why?
|
Databases, Genetic | 1 | 2006 | 1783 | 0.010 |
Why?
|
Iron | 1 | 1987 | 1774 | 0.010 |
Why?
|
Animals | 4 | 2008 | 168757 | 0.010 |
Why?
|
Host-Pathogen Interactions | 1 | 2007 | 1477 | 0.010 |
Why?
|
DNA, Circular | 1 | 1998 | 97 | 0.010 |
Why?
|
Biotinylation | 1 | 1998 | 179 | 0.010 |
Why?
|
Peptide Fragments | 2 | 2001 | 5097 | 0.010 |
Why?
|
Chemistry, Physical | 1 | 1997 | 156 | 0.010 |
Why?
|
Macromolecular Substances | 1 | 1999 | 1454 | 0.010 |
Why?
|
Chemical Phenomena | 1 | 1997 | 518 | 0.010 |
Why?
|
Adenosine Triphosphate | 2 | 1994 | 2025 | 0.010 |
Why?
|
Repressor Proteins | 1 | 2007 | 3023 | 0.010 |
Why?
|
Oxygen | 1 | 1987 | 4189 | 0.010 |
Why?
|
Sequence Homology, Amino Acid | 1 | 1999 | 2839 | 0.010 |
Why?
|
Cytidine Triphosphate | 1 | 1994 | 17 | 0.010 |
Why?
|
Proteome | 1 | 2004 | 1799 | 0.010 |
Why?
|
Magnetic Resonance Spectroscopy | 1 | 2004 | 3760 | 0.010 |
Why?
|
Contusions | 1 | 1994 | 81 | 0.010 |
Why?
|
Chromatography, DEAE-Cellulose | 1 | 1992 | 87 | 0.010 |
Why?
|
DNA, Bacterial | 1 | 1998 | 1465 | 0.010 |
Why?
|
Isoelectric Focusing | 1 | 1992 | 181 | 0.010 |
Why?
|
Fluorescence Polarization | 1 | 1992 | 132 | 0.010 |
Why?
|
Chromatography, Gel | 1 | 1992 | 668 | 0.010 |
Why?
|
Chromatography, Affinity | 1 | 1992 | 549 | 0.010 |
Why?
|
Models, Genetic | 1 | 1981 | 3494 | 0.010 |
Why?
|
Spectrometry, Fluorescence | 1 | 1992 | 689 | 0.010 |
Why?
|
Molecular Weight | 1 | 1992 | 2255 | 0.010 |
Why?
|
Edema | 1 | 1994 | 789 | 0.010 |
Why?
|
Microscopy, Electron | 1 | 1992 | 2645 | 0.010 |
Why?
|
Recombinant Fusion Proteins | 1 | 1997 | 3772 | 0.000 |
Why?
|
Magnetic Resonance Imaging | 1 | 1994 | 35421 | 0.000 |
Why?
|
Prostheses and Implants | 1 | 1994 | 1387 | 0.000 |
Why?
|
Equipment Design | 1 | 1994 | 3582 | 0.000 |
Why?
|
Rats, Sprague-Dawley | 1 | 1994 | 8301 | 0.000 |
Why?
|
Hemorrhage | 1 | 1994 | 3461 | 0.000 |
Why?
|
Models, Theoretical | 1 | 1994 | 3589 | 0.000 |
Why?
|
Genes, Regulator | 1 | 1980 | 378 | 0.000 |
Why?
|
Cell Line | 1 | 1992 | 15997 | 0.000 |
Why?
|
Rats | 1 | 1994 | 24260 | 0.000 |
Why?
|
Humans | 1 | 2001 | 744343 | 0.000 |
Why?
|
Concepts
(215)
Derived automatically from this person's publications.
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Co-Authors
(4)
People in Profiles who have published with this person.
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Similar People
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People who share similar concepts with this person.
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