 Yingming Zhao
Concepts (102)
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 | 145 | 4.170 |
Why?
| | Protein Processing, Post-Translational | 10 | 2017 | 373 | 2.800 |
Why?
| | Histones | 7 | 2018 | 295 | 2.480 |
Why?
| | Histone Code | 3 | 2018 | 18 | 1.850 |
Why?
| | Malonates | 3 | 2017 | 15 | 1.840 |
Why?
| | Sirtuins | 4 | 2015 | 45 | 1.710 |
Why?
| | Hydroxybutyrates | 3 | 2017 | 28 | 1.420 |
Why?
| | Mitochondria | 3 | 2017 | 515 | 1.110 |
Why?
| | Gene Expression Regulation | 4 | 2018 | 1895 | 1.050 |
Why?
| | Liver | 2 | 2016 | 1209 | 0.870 |
Why?
| | Food Preservatives | 1 | 2018 | 1 | 0.790 |
Why?
| | Sodium Benzoate | 1 | 2018 | 2 | 0.790 |
Why?
| | Sirtuin 2 | 1 | 2018 | 9 | 0.790 |
Why?
| | Histone Deacetylase 2 | 1 | 2017 | 6 | 0.750 |
Why?
| | Coenzyme A Ligases | 1 | 2017 | 6 | 0.730 |
Why?
| | Histone Deacetylases | 1 | 2017 | 61 | 0.710 |
Why?
| | Diabetic Ketoacidosis | 1 | 2016 | 14 | 0.670 |
Why?
| | Starvation | 1 | 2016 | 23 | 0.660 |
Why?
| | Carboxy-Lyases | 1 | 2015 | 21 | 0.640 |
Why?
| | Metabolism, Inborn Errors | 1 | 2015 | 31 | 0.640 |
Why?
| | Carbamoyl-Phosphate Synthase (Ammonia) | 1 | 2014 | 4 | 0.580 |
Why?
| | Energy Metabolism | 1 | 2016 | 256 | 0.560 |
Why?
| | Metabolic Networks and Pathways | 1 | 2013 | 71 | 0.520 |
Why?
| | Acyl Coenzyme A | 3 | 2018 | 17 | 0.520 |
Why?
| | HeLa Cells | 4 | 2017 | 504 | 0.510 |
Why?
| | Mice | 9 | 2018 | 10798 | 0.490 |
Why?
| | Amino Acid Sequence | 5 | 2014 | 2143 | 0.460 |
Why?
| | HEK293 Cells | 3 | 2018 | 619 | 0.450 |
Why?
| | Animals | 11 | 2018 | 26297 | 0.410 |
Why?
| | Epigenesis, Genetic | 3 | 2018 | 388 | 0.370 |
Why?
| | Sequence Alignment | 1 | 2009 | 356 | 0.370 |
Why?
| | Acylation | 2 | 2017 | 36 | 0.360 |
Why?
| | Malonyl Coenzyme A | 2 | 2017 | 4 | 0.340 |
Why?
| | Models, Biological | 1 | 2014 | 1768 | 0.330 |
Why?
| | Fatty Acids | 2 | 2016 | 146 | 0.300 |
Why?
| | Software | 1 | 2009 | 627 | 0.290 |
Why?
| | Promoter Regions, Genetic | 2 | 2018 | 923 | 0.270 |
Why?
| | Molecular Sequence Data | 3 | 2014 | 3161 | 0.270 |
Why?
| | Mass Spectrometry | 2 | 2014 | 178 | 0.270 |
Why?
| | Proteins | 1 | 2009 | 765 | 0.260 |
Why?
| | Humans | 11 | 2018 | 79776 | 0.230 |
Why?
| | Mice, Knockout | 2 | 2015 | 1903 | 0.200 |
Why?
| | Hep G2 Cells | 1 | 2018 | 43 | 0.200 |
Why?
| | Gene Knockout Techniques | 1 | 2018 | 72 | 0.190 |
Why?
| | Acetyltransferases | 1 | 2017 | 28 | 0.190 |
Why?
| | Acetyl Coenzyme A | 1 | 2016 | 6 | 0.180 |
Why?
| | Fatty Acids, Volatile | 1 | 2016 | 19 | 0.170 |
Why?
| | Spermatogenesis | 1 | 2016 | 53 | 0.170 |
Why?
| | Streptozocin | 1 | 2016 | 55 | 0.170 |
Why?
| | Mitochondrial Proteins | 1 | 2017 | 115 | 0.160 |
Why?
| | Chromatin Assembly and Disassembly | 1 | 2016 | 69 | 0.160 |
Why?
| | Methylmalonic Acid | 1 | 2015 | 6 | 0.160 |
Why?
| | Saccharomyces cerevisiae Proteins | 1 | 2017 | 269 | 0.150 |
Why?
| | Oxidation-Reduction | 1 | 2015 | 373 | 0.150 |
Why?
| | Stress, Physiological | 1 | 2016 | 239 | 0.140 |
Why?
| | Spermatozoa | 1 | 2014 | 68 | 0.140 |
Why?
| | Succinate Dehydrogenase | 1 | 2013 | 14 | 0.140 |
Why?
| | Cell Respiration | 1 | 2013 | 17 | 0.140 |
Why?
| | Pyruvate Dehydrogenase Complex | 1 | 2013 | 11 | 0.140 |
Why?
| | Consensus Sequence | 1 | 2013 | 63 | 0.140 |
Why?
| | Immunoblotting | 1 | 2014 | 280 | 0.140 |
Why?
| | Drosophila melanogaster | 1 | 2018 | 589 | 0.140 |
Why?
| | Protein Interaction Maps | 1 | 2013 | 48 | 0.130 |
Why?
| | Acetylation | 1 | 2013 | 118 | 0.130 |
Why?
| | Molecular Structure | 1 | 2014 | 286 | 0.130 |
Why?
| | Molecular Sequence Annotation | 1 | 2013 | 73 | 0.130 |
Why?
| | Glycosylation | 1 | 2013 | 133 | 0.130 |
Why?
| | Binding Sites | 1 | 2016 | 1107 | 0.130 |
Why?
| | Glucose | 1 | 2016 | 608 | 0.130 |
Why?
| | Proteome | 1 | 2013 | 99 | 0.130 |
Why?
| | Proteomics | 1 | 2014 | 183 | 0.130 |
Why?
| | Fibroblasts | 1 | 2015 | 709 | 0.120 |
Why?
| | Phosphoglycerate Kinase | 1 | 2011 | 17 | 0.120 |
Why?
| | Succinates | 1 | 2011 | 20 | 0.120 |
Why?
| | Phosphopyruvate Hydratase | 1 | 2011 | 42 | 0.120 |
Why?
| | Protein Transport | 1 | 2013 | 414 | 0.120 |
Why?
| | Antibody Specificity | 1 | 2011 | 157 | 0.120 |
Why?
| | Tandem Mass Spectrometry | 1 | 2011 | 90 | 0.120 |
Why?
| | Male | 4 | 2016 | 40685 | 0.120 |
Why?
| | Meiosis | 1 | 2011 | 77 | 0.120 |
Why?
| | Genome | 1 | 2014 | 341 | 0.110 |
Why?
| | Testis | 1 | 2011 | 170 | 0.110 |
Why?
| | Oligopeptides | 1 | 2011 | 184 | 0.110 |
Why?
| | Chromatography, High Pressure Liquid | 1 | 2011 | 318 | 0.110 |
Why?
| | Models, Molecular | 1 | 2015 | 1287 | 0.110 |
Why?
| | Kinetics | 1 | 2013 | 1604 | 0.110 |
Why?
| | Escherichia coli Proteins | 1 | 2011 | 166 | 0.110 |
Why?
| | Cell Line | 1 | 2015 | 2592 | 0.110 |
Why?
| | Antibodies | 1 | 2011 | 367 | 0.100 |
Why?
| | Blotting, Western | 1 | 2011 | 829 | 0.100 |
Why?
| | HMGB2 Protein | 1 | 2009 | 4 | 0.100 |
Why?
| | Peptide Fragments | 1 | 2011 | 472 | 0.100 |
Why?
| | Serum Albumin, Bovine | 1 | 2009 | 60 | 0.100 |
Why?
| | Disease Models, Animal | 1 | 2016 | 2215 | 0.100 |
Why?
| | Mice, Inbred C57BL | 1 | 2016 | 3090 | 0.100 |
Why?
| | False Positive Reactions | 1 | 2009 | 224 | 0.100 |
Why?
| | Escherichia coli | 1 | 2011 | 609 | 0.100 |
Why?
| | Immediate-Early Proteins | 1 | 2009 | 169 | 0.090 |
Why?
| | Rats | 1 | 2014 | 4312 | 0.090 |
Why?
| | Cells, Cultured | 1 | 2013 | 2924 | 0.090 |
Why?
| | Protein-Serine-Threonine Kinases | 1 | 2009 | 542 | 0.070 |
Why?
| | Algorithms | 1 | 2009 | 1807 | 0.050 |
Why?
|
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