Aaron Johnson
Concepts (92)
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?
|
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Heterochromatin | 3 | 2013 | 35 | 0.850 |
Why?
| Gene Silencing | 2 | 2013 | 175 | 0.740 |
Why?
| Chromatin Assembly and Disassembly | 3 | 2013 | 91 | 0.500 |
Why?
| Proliferating Cell Nuclear Antigen | 4 | 2006 | 49 | 0.470 |
Why?
| Saccharomyces cerevisiae | 5 | 2013 | 482 | 0.450 |
Why?
| Transcription Elongation, Genetic | 1 | 2013 | 20 | 0.440 |
Why?
| Trans-Activators | 1 | 2013 | 370 | 0.370 |
Why?
| Replication Protein C | 2 | 2006 | 4 | 0.350 |
Why?
| Escherichia coli | 6 | 2008 | 730 | 0.340 |
Why?
| Adenosine Triphosphate | 5 | 2009 | 431 | 0.340 |
Why?
| Gene Expression Regulation, Fungal | 1 | 2009 | 62 | 0.330 |
Why?
| Silent Information Regulator Proteins, Saccharomyces cerevisiae | 4 | 2013 | 9 | 0.330 |
Why?
| Histones | 2 | 2013 | 540 | 0.320 |
Why?
| DNA-Directed DNA Polymerase | 2 | 2007 | 44 | 0.310 |
Why?
| DNA Repair | 3 | 2009 | 190 | 0.310 |
Why?
| Models, Molecular | 6 | 2006 | 1390 | 0.300 |
Why?
| DNA Replication | 4 | 2008 | 203 | 0.270 |
Why?
| DNA | 4 | 2008 | 1356 | 0.260 |
Why?
| DNA Ligases | 1 | 2005 | 15 | 0.250 |
Why?
| DNA-Binding Proteins | 3 | 2009 | 1316 | 0.240 |
Why?
| Transcription, Genetic | 1 | 2009 | 1310 | 0.220 |
Why?
| Holoenzymes | 1 | 2003 | 21 | 0.220 |
Why?
| Escherichia coli Proteins | 2 | 2004 | 164 | 0.200 |
Why?
| Nucleosomes | 2 | 2013 | 125 | 0.200 |
Why?
| DNA Polymerase III | 3 | 2007 | 12 | 0.190 |
Why?
| RNA Polymerase II | 2 | 2013 | 283 | 0.160 |
Why?
| Protein Binding | 4 | 2013 | 1917 | 0.130 |
Why?
| Hydrolysis | 3 | 2006 | 179 | 0.130 |
Why?
| Protein Conformation | 4 | 2006 | 822 | 0.130 |
Why?
| Adenosine Triphosphatases | 2 | 2009 | 155 | 0.130 |
Why?
| Arginine | 2 | 2006 | 241 | 0.110 |
Why?
| DNA, Fungal | 1 | 2013 | 69 | 0.110 |
Why?
| Sirtuin 2 | 2 | 2009 | 13 | 0.110 |
Why?
| Sirtuins | 2 | 2009 | 32 | 0.100 |
Why?
| Histone Deacetylases | 2 | 2009 | 196 | 0.090 |
Why?
| Models, Genetic | 1 | 2013 | 570 | 0.090 |
Why?
| Spectrometry, Fluorescence | 2 | 2008 | 158 | 0.090 |
Why?
| Protein Structure, Tertiary | 3 | 2013 | 804 | 0.090 |
Why?
| Mass Spectrometry | 1 | 2013 | 645 | 0.090 |
Why?
| Nucleosome Assembly Protein 1 | 1 | 2009 | 1 | 0.090 |
Why?
| DNA Restriction Enzymes | 1 | 2009 | 54 | 0.090 |
Why?
| RNA Polymerase III | 1 | 2009 | 25 | 0.080 |
Why?
| NAD | 1 | 2009 | 67 | 0.080 |
Why?
| Acetylation | 1 | 2009 | 212 | 0.080 |
Why?
| Models, Biological | 3 | 2007 | 1646 | 0.080 |
Why?
| Recombination, Genetic | 1 | 2009 | 177 | 0.080 |
Why?
| Multiprotein Complexes | 1 | 2009 | 145 | 0.080 |
Why?
| Mutation | 3 | 2009 | 3364 | 0.070 |
Why?
| Lysine | 1 | 2009 | 246 | 0.070 |
Why?
| Proteomics | 1 | 2013 | 859 | 0.070 |
Why?
| Multienzyme Complexes | 1 | 2007 | 64 | 0.070 |
Why?
| Chromatography, Gel | 2 | 2006 | 128 | 0.070 |
Why?
| Saccharomyces cerevisiae Proteins | 1 | 2009 | 336 | 0.070 |
Why?
| Cell Cycle Proteins | 1 | 2009 | 553 | 0.060 |
Why?
| DNA Ligase ATP | 1 | 2005 | 4 | 0.060 |
Why?
| Nuclear Proteins | 1 | 2009 | 594 | 0.060 |
Why?
| Kinetics | 2 | 2003 | 1569 | 0.050 |
Why?
| Amino Acid Motifs | 1 | 2003 | 198 | 0.050 |
Why?
| Electrophoresis, Polyacrylamide Gel | 1 | 2003 | 312 | 0.050 |
Why?
| Catalytic Domain | 1 | 2003 | 202 | 0.050 |
Why?
| Protein Subunits | 3 | 2007 | 204 | 0.040 |
Why?
| Proteins | 1 | 2005 | 920 | 0.040 |
Why?
| Dose-Response Relationship, Drug | 1 | 2003 | 1870 | 0.040 |
Why?
| Time Factors | 2 | 2008 | 6171 | 0.040 |
Why?
| DNA Damage | 2 | 2008 | 357 | 0.030 |
Why?
| Macromolecular Substances | 2 | 2004 | 200 | 0.030 |
Why?
| Xenopus Proteins | 1 | 2013 | 56 | 0.030 |
Why?
| Mutagenesis, Site-Directed | 2 | 2004 | 346 | 0.030 |
Why?
| Xenopus laevis | 1 | 2013 | 118 | 0.030 |
Why?
| Amino Acid Substitution | 1 | 2013 | 267 | 0.030 |
Why?
| Mutation, Missense | 1 | 2013 | 296 | 0.020 |
Why?
| Humans | 3 | 2013 | 115739 | 0.020 |
Why?
| Chromosomal Proteins, Non-Histone | 1 | 2009 | 99 | 0.020 |
Why?
| Bacteriophage M13 | 1 | 2008 | 10 | 0.020 |
Why?
| Photons | 1 | 2008 | 57 | 0.020 |
Why?
| Diffusion | 1 | 2008 | 120 | 0.020 |
Why?
| Biochemistry | 1 | 2008 | 40 | 0.020 |
Why?
| Molecular Conformation | 1 | 2008 | 139 | 0.020 |
Why?
| Lasers | 1 | 2008 | 121 | 0.020 |
Why?
| Fluorescence Resonance Energy Transfer | 1 | 2008 | 176 | 0.020 |
Why?
| Surface Plasmon Resonance | 1 | 2006 | 82 | 0.020 |
Why?
| Enzyme Activation | 1 | 2007 | 793 | 0.020 |
Why?
| Cloning, Molecular | 1 | 2006 | 523 | 0.020 |
Why?
| Nucleic Acid Conformation | 1 | 2008 | 672 | 0.020 |
Why?
| Protein Structure, Quaternary | 1 | 2004 | 115 | 0.010 |
Why?
| Solutions | 1 | 2004 | 150 | 0.010 |
Why?
| DNA, Bacterial | 1 | 2003 | 309 | 0.010 |
Why?
| Fluorescent Dyes | 1 | 2004 | 304 | 0.010 |
Why?
| Transcription Factors | 1 | 2009 | 1528 | 0.010 |
Why?
| Binding Sites | 1 | 2003 | 1177 | 0.010 |
Why?
| Base Sequence | 1 | 2003 | 2114 | 0.010 |
Why?
| Animals | 1 | 2013 | 32104 | 0.010 |
Why?
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