Concepts (210)
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?
|
|---|
| Cryoelectron Microscopy | 6 | 2025 | 200 | 1.420 |
Why?
|
| Stereocilia | 2 | 2021 | 5 | 0.880 |
Why?
|
| Microscopy, Electron, Transmission | 1 | 2024 | 135 | 0.870 |
Why?
|
| Image Processing, Computer-Assisted | 2 | 2025 | 659 | 0.860 |
Why?
|
| Protein Precursors | 2 | 2021 | 83 | 0.850 |
Why?
|
| Cadherin Related Proteins | 2 | 2021 | 3 | 0.780 |
Why?
|
| Ribosomes | 2 | 2022 | 163 | 0.760 |
Why?
|
| Saccharomyces cerevisiae | 2 | 2025 | 564 | 0.730 |
Why?
|
| Mammals | 1 | 2022 | 218 | 0.690 |
Why?
|
| Furin | 4 | 2015 | 11 | 0.690 |
Why?
|
| Proprotein Convertase 1 | 3 | 2015 | 7 | 0.690 |
Why?
|
| Histidine | 5 | 2015 | 34 | 0.660 |
Why?
|
| Models, Molecular | 8 | 2021 | 1150 | 0.560 |
Why?
|
| Proprotein Convertases | 1 | 2015 | 5 | 0.470 |
Why?
|
| Peptides | 3 | 2015 | 574 | 0.450 |
Why?
|
| Organelles | 2 | 2013 | 20 | 0.420 |
Why?
|
| Mass Spectrometry | 1 | 2015 | 301 | 0.420 |
Why?
|
| Secretory Pathway | 1 | 2013 | 6 | 0.400 |
Why?
|
| Eukaryotic Cells | 1 | 2013 | 57 | 0.390 |
Why?
|
| Peptide Hydrolases | 1 | 2013 | 78 | 0.380 |
Why?
|
| Hair Cells, Auditory | 2 | 2021 | 14 | 0.340 |
Why?
|
| Mechanotransduction, Cellular | 2 | 2021 | 26 | 0.330 |
Why?
|
| Microscopy, Fluorescence | 2 | 2022 | 402 | 0.310 |
Why?
|
| Protozoan Proteins | 3 | 2014 | 126 | 0.290 |
Why?
|
| Hydrogen-Ion Concentration | 6 | 2015 | 458 | 0.290 |
Why?
|
| Membrane Proteins | 3 | 2021 | 899 | 0.280 |
Why?
|
| Mice | 9 | 2024 | 10863 | 0.240 |
Why?
|
| Animals | 13 | 2024 | 20715 | 0.230 |
Why?
|
| Electron Microscope Tomography | 1 | 2024 | 15 | 0.220 |
Why?
|
| Amino Acid Sequence | 7 | 2018 | 1590 | 0.220 |
Why?
|
| Glutamic Acid | 1 | 2024 | 99 | 0.210 |
Why?
|
| Molecular Sequence Data | 7 | 2015 | 1993 | 0.210 |
Why?
|
| Synapses | 1 | 2024 | 184 | 0.200 |
Why?
|
| Hippocampus | 1 | 2024 | 270 | 0.190 |
Why?
|
| Electrophysiological Phenomena | 1 | 2021 | 21 | 0.180 |
Why?
|
| Molecular Conformation | 1 | 2021 | 133 | 0.180 |
Why?
|
| Hearing | 1 | 2021 | 33 | 0.180 |
Why?
|
| Software | 1 | 2024 | 388 | 0.180 |
Why?
|
| Molecular Structure | 1 | 2021 | 384 | 0.170 |
Why?
|
| Hair Cells, Vestibular | 1 | 2019 | 2 | 0.160 |
Why?
|
| Algorithms | 1 | 2024 | 1004 | 0.150 |
Why?
|
| Multiprotein Complexes | 1 | 2019 | 154 | 0.140 |
Why?
|
| Cadherins | 1 | 2018 | 80 | 0.140 |
Why?
|
| Interleukin-1 Receptor-Associated Kinases | 1 | 2018 | 34 | 0.140 |
Why?
|
| HEK293 Cells | 5 | 2021 | 622 | 0.140 |
Why?
|
| Leishmania donovani | 2 | 2014 | 4 | 0.130 |
Why?
|
| Pyrimidines | 2 | 2018 | 136 | 0.130 |
Why?
|
| Calreticulin | 1 | 2016 | 4 | 0.120 |
Why?
|
| Paracrine Communication | 1 | 2016 | 15 | 0.120 |
Why?
|
| Frameshift Mutation | 1 | 2016 | 29 | 0.120 |
Why?
|
| Deuterium | 1 | 2015 | 24 | 0.120 |
Why?
|
| Leukemia, Myeloid, Acute | 1 | 2018 | 188 | 0.120 |
Why?
|
| Molecular Chaperones | 2 | 2013 | 99 | 0.120 |
Why?
|
| Hydrogen | 1 | 2015 | 50 | 0.110 |
Why?
|
| Protein Binding | 6 | 2016 | 1603 | 0.110 |
Why?
|
| Nucleoside Transport Proteins | 1 | 2014 | 1 | 0.110 |
Why?
|
| Ubiquitin-Conjugating Enzymes | 1 | 2014 | 24 | 0.110 |
Why?
|
| Intracellular Space | 1 | 2014 | 35 | 0.110 |
Why?
|
| Anilides | 1 | 2013 | 18 | 0.100 |
Why?
|
| Monocytes | 1 | 2016 | 353 | 0.100 |
Why?
|
| Pentosyltransferases | 1 | 2013 | 2 | 0.100 |
Why?
|
| Quinolines | 1 | 2013 | 45 | 0.100 |
Why?
|
| Receptor Protein-Tyrosine Kinases | 1 | 2013 | 52 | 0.100 |
Why?
|
| Leishmania mexicana | 1 | 2013 | 7 | 0.100 |
Why?
|
| Iron-Regulatory Proteins | 1 | 2013 | 2 | 0.100 |
Why?
|
| Ubiquitination | 1 | 2014 | 113 | 0.100 |
Why?
|
| Subtilisins | 1 | 2013 | 3 | 0.100 |
Why?
|
| Enzyme Precursors | 1 | 2013 | 11 | 0.100 |
Why?
|
| Uracil | 1 | 2013 | 31 | 0.100 |
Why?
|
| Oncogenes | 1 | 2013 | 69 | 0.100 |
Why?
|
| Cathepsin B | 1 | 2013 | 14 | 0.100 |
Why?
|
| Monosaccharide Transport Proteins | 1 | 2013 | 43 | 0.100 |
Why?
|
| Membrane Transport Proteins | 1 | 2014 | 135 | 0.100 |
Why?
|
| Protein Multimerization | 3 | 2021 | 176 | 0.100 |
Why?
|
| Cathepsins | 1 | 2013 | 34 | 0.100 |
Why?
|
| Ovarian Neoplasms | 1 | 2014 | 150 | 0.100 |
Why?
|
| Flagella | 1 | 2013 | 140 | 0.090 |
Why?
|
| Plasma Membrane Neurotransmitter Transport Proteins | 1 | 2012 | 1 | 0.090 |
Why?
|
| HSP70 Heat-Shock Proteins | 1 | 2012 | 78 | 0.090 |
Why?
|
| nef Gene Products, Human Immunodeficiency Virus | 1 | 2012 | 26 | 0.090 |
Why?
|
| Caspases | 1 | 2013 | 174 | 0.090 |
Why?
|
| Proto-Oncogene Proteins | 1 | 2013 | 324 | 0.090 |
Why?
|
| Leucine | 1 | 2012 | 61 | 0.090 |
Why?
|
| Tumor Suppressor Protein p53 | 1 | 2014 | 308 | 0.090 |
Why?
|
| Protein Biosynthesis | 1 | 2014 | 320 | 0.090 |
Why?
|
| Proteomics | 1 | 2013 | 283 | 0.090 |
Why?
|
| Vesicular Transport Proteins | 1 | 2012 | 113 | 0.090 |
Why?
|
| Histocompatibility Antigens Class I | 1 | 2012 | 145 | 0.090 |
Why?
|
| Down-Regulation | 1 | 2012 | 317 | 0.090 |
Why?
|
| Endosomes | 1 | 2012 | 177 | 0.080 |
Why?
|
| Glucose | 1 | 2013 | 468 | 0.080 |
Why?
|
| Escherichia coli Proteins | 1 | 2012 | 271 | 0.080 |
Why?
|
| Saccharomyces cerevisiae Proteins | 1 | 2014 | 445 | 0.080 |
Why?
|
| Binding Sites | 3 | 2021 | 906 | 0.080 |
Why?
|
| Bacteria | 1 | 2012 | 306 | 0.070 |
Why?
|
| Enzyme Activation | 3 | 2015 | 381 | 0.070 |
Why?
|
| Escherichia coli | 1 | 2012 | 707 | 0.070 |
Why?
|
| Protein Stability | 2 | 2021 | 92 | 0.070 |
Why?
|
| Models, Biological | 1 | 2013 | 1182 | 0.070 |
Why?
|
| Protein Transport | 3 | 2014 | 403 | 0.070 |
Why?
|
| Kinetics | 3 | 2014 | 763 | 0.070 |
Why?
|
| Protein Folding | 3 | 2014 | 268 | 0.070 |
Why?
|
| Janus Kinase 2 | 2 | 2018 | 16 | 0.070 |
Why?
|
| Molecular Dynamics Simulation | 2 | 2021 | 120 | 0.070 |
Why?
|
| Cell Line, Tumor | 3 | 2018 | 1470 | 0.060 |
Why?
|
| Humans | 12 | 2021 | 63527 | 0.060 |
Why?
|
| Protein Conformation | 3 | 2014 | 780 | 0.060 |
Why?
|
| Bacterial Proteins | 1 | 2012 | 767 | 0.060 |
Why?
|
| Mutation | 4 | 2018 | 2615 | 0.060 |
Why?
|
| Receptors, AMPA | 1 | 2024 | 42 | 0.050 |
Why?
|
| DNA Primers | 2 | 2013 | 292 | 0.050 |
Why?
|
| HeLa Cells | 2 | 2016 | 536 | 0.050 |
Why?
|
| Gold | 1 | 2024 | 226 | 0.050 |
Why?
|
| Substrate Specificity | 2 | 2013 | 339 | 0.050 |
Why?
|
| Metal Nanoparticles | 1 | 2024 | 186 | 0.050 |
Why?
|
| Salicylic Acid | 1 | 2021 | 2 | 0.050 |
Why?
|
| Structural Homology, Protein | 1 | 2021 | 21 | 0.040 |
Why?
|
| Anions | 1 | 2021 | 33 | 0.040 |
Why?
|
| Lipid Bilayers | 1 | 2021 | 53 | 0.040 |
Why?
|
| Chlorides | 1 | 2021 | 31 | 0.040 |
Why?
|
| Protein Structure, Tertiary | 2 | 2014 | 674 | 0.040 |
Why?
|
| Base Sequence | 2 | 2013 | 1331 | 0.040 |
Why?
|
| Protein Domains | 1 | 2021 | 149 | 0.040 |
Why?
|
| Sf9 Cells | 1 | 2018 | 8 | 0.040 |
Why?
|
| Bridged-Ring Compounds | 1 | 2018 | 9 | 0.040 |
Why?
|
| fms-Like Tyrosine Kinase 3 | 1 | 2018 | 25 | 0.040 |
Why?
|
| Phenylurea Compounds | 1 | 2018 | 31 | 0.040 |
Why?
|
| Benzothiazoles | 1 | 2018 | 19 | 0.030 |
Why?
|
| Nitriles | 1 | 2018 | 70 | 0.030 |
Why?
|
| Xenograft Model Antitumor Assays | 1 | 2018 | 190 | 0.030 |
Why?
|
| Pyrazoles | 1 | 2018 | 79 | 0.030 |
Why?
|
| Mice, SCID | 1 | 2018 | 516 | 0.030 |
Why?
|
| Protein Kinase Inhibitors | 1 | 2018 | 188 | 0.030 |
Why?
|
| Mice, Inbred NOD | 1 | 2018 | 523 | 0.030 |
Why?
|
| Imaging, Three-Dimensional | 1 | 2018 | 286 | 0.030 |
Why?
|
| Thrombocythemia, Essential | 1 | 2016 | 3 | 0.030 |
Why?
|
| Extracellular Space | 1 | 2016 | 28 | 0.030 |
Why?
|
| Primary Myelofibrosis | 1 | 2016 | 11 | 0.030 |
Why?
|
| Culture Media, Conditioned | 1 | 2016 | 51 | 0.030 |
Why?
|
| COS Cells | 1 | 2015 | 175 | 0.030 |
Why?
|
| Real-Time Polymerase Chain Reaction | 1 | 2016 | 206 | 0.030 |
Why?
|
| Bone Marrow | 1 | 2016 | 175 | 0.030 |
Why?
|
| Cell Culture Techniques | 1 | 2016 | 182 | 0.030 |
Why?
|
| Blotting, Western | 1 | 2016 | 612 | 0.030 |
Why?
|
| Endopeptidase K | 1 | 2014 | 4 | 0.030 |
Why?
|
| Microsomes | 1 | 2014 | 11 | 0.030 |
Why?
|
| Sequence Homology | 1 | 2014 | 20 | 0.030 |
Why?
|
| Deubiquitinating Enzymes | 1 | 2014 | 5 | 0.030 |
Why?
|
| SEC Translocation Channels | 1 | 2014 | 38 | 0.030 |
Why?
|
| Proto-Oncogene Proteins c-mdm2 | 1 | 2014 | 32 | 0.030 |
Why?
|
| Sulfhydryl Compounds | 1 | 2014 | 50 | 0.030 |
Why?
|
| Phosphoribosyl Pyrophosphate | 1 | 2013 | 1 | 0.030 |
Why?
|
| Thiouracil | 1 | 2013 | 1 | 0.030 |
Why?
|
| Spectrophotometry | 1 | 2013 | 35 | 0.030 |
Why?
|
| Immunohistochemistry | 1 | 2016 | 897 | 0.030 |
Why?
|
| Cations, Divalent | 1 | 2013 | 23 | 0.030 |
Why?
|
| Lysine | 1 | 2014 | 83 | 0.030 |
Why?
|
| Enzyme Stability | 1 | 2013 | 47 | 0.030 |
Why?
|
| Conserved Sequence | 1 | 2014 | 173 | 0.030 |
Why?
|
| Zinc Fingers | 1 | 2014 | 103 | 0.030 |
Why?
|
| Hemochromatosis Protein | 1 | 2013 | 5 | 0.030 |
Why?
|
| Chromatography, Gel | 1 | 2013 | 65 | 0.030 |
Why?
|
| Mutagenesis, Site-Directed | 1 | 2014 | 248 | 0.030 |
Why?
|
| Fluorouracil | 1 | 2013 | 66 | 0.030 |
Why?
|
| Cysteine Endopeptidases | 1 | 2014 | 95 | 0.030 |
Why?
|
| Feedback, Physiological | 1 | 2013 | 59 | 0.030 |
Why?
|
| Glycerol | 1 | 2013 | 32 | 0.030 |
Why?
|
| Zinc | 1 | 2014 | 92 | 0.030 |
Why?
|
| Chromatography, Affinity | 1 | 2013 | 48 | 0.030 |
Why?
|
| Mutagenesis | 1 | 2013 | 133 | 0.030 |
Why?
|
| GPI-Linked Proteins | 1 | 2013 | 40 | 0.030 |
Why?
|
| Urea | 1 | 2013 | 38 | 0.030 |
Why?
|
| Sequence Alignment | 1 | 2014 | 299 | 0.030 |
Why?
|
| Plasmids | 1 | 2014 | 292 | 0.020 |
Why?
|
| Protons | 1 | 2013 | 62 | 0.020 |
Why?
|
| Circular Dichroism | 1 | 2013 | 108 | 0.020 |
Why?
|
| Disulfides | 1 | 2013 | 64 | 0.020 |
Why?
|
| Cytosol | 1 | 2014 | 180 | 0.020 |
Why?
|
| Endoplasmic Reticulum | 1 | 2014 | 174 | 0.020 |
Why?
|
| Thermodynamics | 1 | 2013 | 196 | 0.020 |
Why?
|
| Sequence Homology, Amino Acid | 1 | 2013 | 363 | 0.020 |
Why?
|
| Hydrophobic and Hydrophilic Interactions | 1 | 2014 | 265 | 0.020 |
Why?
|
| Protein Isoforms | 1 | 2013 | 197 | 0.020 |
Why?
|
| Dogs | 1 | 2014 | 330 | 0.020 |
Why?
|
| Calcium | 1 | 2016 | 576 | 0.020 |
Why?
|
| Animals, Genetically Modified | 1 | 2013 | 299 | 0.020 |
Why?
|
| Temperature | 1 | 2013 | 307 | 0.020 |
Why?
|
| Cell Nucleus | 1 | 2016 | 628 | 0.020 |
Why?
|
| Sequence Analysis, DNA | 1 | 2013 | 417 | 0.020 |
Why?
|
| Flow Cytometry | 1 | 2013 | 664 | 0.020 |
Why?
|
| Cytokines | 1 | 2016 | 934 | 0.020 |
Why?
|
| Cell Survival | 1 | 2013 | 576 | 0.020 |
Why?
|
| DNA Damage | 1 | 2014 | 287 | 0.020 |
Why?
|
| Protein Structure, Secondary | 1 | 2012 | 260 | 0.020 |
Why?
|
| Recombinant Proteins | 1 | 2013 | 705 | 0.020 |
Why?
|
| Structure-Activity Relationship | 1 | 2012 | 373 | 0.020 |
Why?
|
| Amino Acids | 1 | 2012 | 147 | 0.020 |
Why?
|
| Crystallography, X-Ray | 1 | 2012 | 432 | 0.020 |
Why?
|
| Evolution, Molecular | 1 | 2012 | 322 | 0.020 |
Why?
|
| Cell Line | 1 | 2014 | 2041 | 0.020 |
Why?
|
| Child | 1 | 2018 | 4541 | 0.020 |
Why?
|
| Aged, 80 and over | 1 | 2018 | 5468 | 0.020 |
Why?
|
| Young Adult | 1 | 2018 | 4714 | 0.020 |
Why?
|
| Adolescent | 1 | 2018 | 6259 | 0.020 |
Why?
|
| Time Factors | 1 | 2013 | 3708 | 0.010 |
Why?
|
| Female | 2 | 2018 | 32939 | 0.010 |
Why?
|
| Aged | 1 | 2018 | 14451 | 0.010 |
Why?
|
| Adult | 1 | 2018 | 16895 | 0.010 |
Why?
|
| Middle Aged | 1 | 2018 | 17656 | 0.010 |
Why?
|
| Male | 1 | 2018 | 29931 | 0.010 |
Why?
|