Concepts (104)
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?
|
|---|
| Lysine | 11 | 2018 | 150 | 2.840 |
Why?
|
| Protein Processing, Post-Translational | 10 | 2017 | 380 | 2.100 |
Why?
|
| Histones | 7 | 2018 | 327 | 1.770 |
Why?
|
| Histone Code | 3 | 2018 | 19 | 1.530 |
Why?
|
| Malonates | 3 | 2017 | 11 | 1.530 |
Why?
|
| Sirtuins | 4 | 2015 | 46 | 1.080 |
Why?
|
| Mitochondria | 3 | 2017 | 548 | 0.940 |
Why?
|
| Gene Expression Regulation | 4 | 2018 | 1975 | 0.900 |
Why?
|
| Hydroxybutyrates | 3 | 2017 | 28 | 0.820 |
Why?
|
| Liver | 2 | 2016 | 1241 | 0.740 |
Why?
|
| Food Preservatives | 1 | 2018 | 1 | 0.650 |
Why?
|
| Sodium Benzoate | 1 | 2018 | 2 | 0.650 |
Why?
|
| Sirtuin 2 | 1 | 2018 | 9 | 0.650 |
Why?
|
| Lysine Acetyltransferase 5 | 1 | 2017 | 2 | 0.620 |
Why?
|
| Histone Deacetylase 2 | 1 | 2017 | 8 | 0.620 |
Why?
|
| Coenzyme A Ligases | 1 | 2017 | 7 | 0.600 |
Why?
|
| Histone Deacetylases | 1 | 2017 | 70 | 0.590 |
Why?
|
| Diabetic Ketoacidosis | 1 | 2016 | 14 | 0.550 |
Why?
|
| Starvation | 1 | 2016 | 23 | 0.540 |
Why?
|
| Metabolism, Inborn Errors | 1 | 2015 | 30 | 0.530 |
Why?
|
| Carboxy-Lyases | 1 | 2015 | 22 | 0.530 |
Why?
|
| Energy Metabolism | 1 | 2016 | 278 | 0.470 |
Why?
|
| Metabolic Networks and Pathways | 1 | 2013 | 80 | 0.430 |
Why?
|
| HEK293 Cells | 3 | 2018 | 635 | 0.380 |
Why?
|
| HeLa Cells | 4 | 2017 | 505 | 0.350 |
Why?
|
| Mice | 9 | 2018 | 11696 | 0.340 |
Why?
|
| Amino Acid Sequence | 5 | 2014 | 2061 | 0.340 |
Why?
|
| Acyl Coenzyme A | 3 | 2018 | 17 | 0.340 |
Why?
|
| Sequence Alignment | 1 | 2009 | 353 | 0.310 |
Why?
|
| Animals | 11 | 2018 | 27171 | 0.300 |
Why?
|
| Acylation | 2 | 2017 | 40 | 0.300 |
Why?
|
| Malonyl Coenzyme A | 2 | 2017 | 4 | 0.280 |
Why?
|
| Fatty Acids | 2 | 2016 | 131 | 0.250 |
Why?
|
| Software | 1 | 2009 | 661 | 0.240 |
Why?
|
| Epigenesis, Genetic | 3 | 2018 | 502 | 0.240 |
Why?
|
| Promoter Regions, Genetic | 2 | 2018 | 956 | 0.230 |
Why?
|
| Proteins | 1 | 2009 | 786 | 0.220 |
Why?
|
| Molecular Sequence Data | 3 | 2014 | 3028 | 0.180 |
Why?
|
| Humans | 11 | 2018 | 88416 | 0.170 |
Why?
|
| Mice, Knockout | 2 | 2015 | 1987 | 0.170 |
Why?
|
| RAW 264.7 Cells | 1 | 2018 | 16 | 0.160 |
Why?
|
| Hep G2 Cells | 1 | 2018 | 48 | 0.160 |
Why?
|
| Gene Knockout Techniques | 1 | 2018 | 79 | 0.160 |
Why?
|
| Acetyltransferases | 1 | 2017 | 32 | 0.150 |
Why?
|
| Acetyl Coenzyme A | 1 | 2016 | 8 | 0.140 |
Why?
|
| Fatty Acids, Volatile | 1 | 2016 | 32 | 0.140 |
Why?
|
| Spermatogenesis | 1 | 2016 | 37 | 0.140 |
Why?
|
| Streptozocin | 1 | 2016 | 55 | 0.140 |
Why?
|
| Protein Domains | 1 | 2016 | 131 | 0.140 |
Why?
|
| Mitochondrial Proteins | 1 | 2017 | 126 | 0.140 |
Why?
|
| Chromatin Assembly and Disassembly | 1 | 2016 | 76 | 0.130 |
Why?
|
| Methylmalonic Acid | 1 | 2015 | 6 | 0.130 |
Why?
|
| Stress, Physiological | 1 | 2016 | 231 | 0.120 |
Why?
|
| Saccharomyces cerevisiae Proteins | 1 | 2017 | 282 | 0.120 |
Why?
|
| Carbamoyl-Phosphate Synthase (Ammonia) | 1 | 2014 | 4 | 0.120 |
Why?
|
| Oxidation-Reduction | 1 | 2015 | 380 | 0.120 |
Why?
|
| Drosophila melanogaster | 1 | 2018 | 604 | 0.110 |
Why?
|
| Succinate Dehydrogenase | 1 | 2013 | 17 | 0.110 |
Why?
|
| Cell Respiration | 1 | 2013 | 18 | 0.110 |
Why?
|
| Pyruvate Dehydrogenase Complex | 1 | 2013 | 13 | 0.110 |
Why?
|
| Consensus Sequence | 1 | 2013 | 65 | 0.110 |
Why?
|
| Binding Sites | 1 | 2016 | 1113 | 0.110 |
Why?
|
| Protein Interaction Maps | 1 | 2013 | 49 | 0.110 |
Why?
|
| Acetylation | 1 | 2013 | 132 | 0.110 |
Why?
|
| Molecular Sequence Annotation | 1 | 2013 | 68 | 0.110 |
Why?
|
| Glucose | 1 | 2016 | 630 | 0.110 |
Why?
|
| Glycosylation | 1 | 2013 | 129 | 0.110 |
Why?
|
| Fibroblasts | 1 | 2015 | 754 | 0.100 |
Why?
|
| Proteome | 1 | 2013 | 130 | 0.100 |
Why?
|
| Phosphoglycerate Kinase | 1 | 2011 | 17 | 0.100 |
Why?
|
| Phosphopyruvate Hydratase | 1 | 2011 | 41 | 0.100 |
Why?
|
| Succinates | 1 | 2011 | 21 | 0.100 |
Why?
|
| Protein Transport | 1 | 2013 | 419 | 0.100 |
Why?
|
| Antibody Specificity | 1 | 2011 | 130 | 0.100 |
Why?
|
| Tandem Mass Spectrometry | 1 | 2011 | 104 | 0.090 |
Why?
|
| Testis | 1 | 2011 | 152 | 0.090 |
Why?
|
| Models, Molecular | 1 | 2015 | 1295 | 0.090 |
Why?
|
| Meiosis | 1 | 2011 | 82 | 0.090 |
Why?
|
| Cell Line | 1 | 2015 | 2498 | 0.090 |
Why?
|
| Kinetics | 1 | 2013 | 1528 | 0.090 |
Why?
|
| Chromatography, High Pressure Liquid | 1 | 2011 | 315 | 0.090 |
Why?
|
| Oligopeptides | 1 | 2011 | 191 | 0.090 |
Why?
|
| Escherichia coli Proteins | 1 | 2011 | 182 | 0.090 |
Why?
|
| Blotting, Western | 1 | 2011 | 797 | 0.090 |
Why?
|
| Antibodies | 1 | 2011 | 354 | 0.090 |
Why?
|
| Peptide Fragments | 1 | 2011 | 460 | 0.090 |
Why?
|
| HMGB2 Protein | 1 | 2009 | 4 | 0.080 |
Why?
|
| Mice, Inbred C57BL | 1 | 2016 | 3196 | 0.080 |
Why?
|
| Serum Albumin, Bovine | 1 | 2009 | 45 | 0.080 |
Why?
|
| Disease Models, Animal | 1 | 2016 | 2340 | 0.080 |
Why?
|
| Male | 4 | 2016 | 41926 | 0.080 |
Why?
|
| False Positive Reactions | 1 | 2009 | 222 | 0.080 |
Why?
|
| Escherichia coli | 1 | 2011 | 604 | 0.080 |
Why?
|
| Rats | 1 | 2014 | 4032 | 0.080 |
Why?
|
| Cells, Cultured | 1 | 2013 | 2873 | 0.080 |
Why?
|
| Immediate-Early Proteins | 1 | 2009 | 166 | 0.070 |
Why?
|
| Models, Biological | 1 | 2014 | 1764 | 0.070 |
Why?
|
| Mass Spectrometry | 2 | 2014 | 193 | 0.060 |
Why?
|
| Algorithms | 1 | 2009 | 1860 | 0.050 |
Why?
|
| Spermatozoa | 1 | 2014 | 62 | 0.030 |
Why?
|
| Immunoblotting | 1 | 2014 | 273 | 0.030 |
Why?
|
| Molecular Structure | 1 | 2014 | 289 | 0.030 |
Why?
|
| Proteomics | 1 | 2014 | 227 | 0.030 |
Why?
|
| Genome | 1 | 2014 | 376 | 0.020 |
Why?
|