Concepts (217)
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 | 8 | 2025 | 207 | 1.660 |
Why?
|
| Stereocilia | 3 | 2026 | 6 | 1.120 |
Why?
|
| Ribosomes | 3 | 2025 | 170 | 0.950 |
Why?
|
| Protein Precursors | 3 | 2026 | 85 | 0.900 |
Why?
|
| Microscopy, Electron, Transmission | 1 | 2024 | 136 | 0.860 |
Why?
|
| Image Processing, Computer-Assisted | 2 | 2025 | 677 | 0.840 |
Why?
|
| Cadherin Related Proteins | 3 | 2026 | 4 | 0.830 |
Why?
|
| Saccharomyces cerevisiae | 2 | 2025 | 567 | 0.720 |
Why?
|
| Mammals | 1 | 2022 | 219 | 0.690 |
Why?
|
| Furin | 4 | 2015 | 11 | 0.680 |
Why?
|
| Proprotein Convertase 1 | 3 | 2015 | 7 | 0.680 |
Why?
|
| Histidine | 5 | 2015 | 34 | 0.650 |
Why?
|
| Hair Cells, Auditory | 3 | 2026 | 15 | 0.570 |
Why?
|
| Models, Molecular | 8 | 2021 | 1159 | 0.560 |
Why?
|
| Proprotein Convertases | 1 | 2015 | 5 | 0.470 |
Why?
|
| Electron Microscope Tomography | 2 | 2025 | 16 | 0.460 |
Why?
|
| Peptides | 3 | 2015 | 590 | 0.440 |
Why?
|
| Membrane Proteins | 4 | 2026 | 909 | 0.440 |
Why?
|
| Organelles | 2 | 2013 | 20 | 0.420 |
Why?
|
| Mass Spectrometry | 1 | 2015 | 303 | 0.410 |
Why?
|
| Secretory Pathway | 1 | 2013 | 6 | 0.400 |
Why?
|
| Eukaryotic Cells | 1 | 2013 | 57 | 0.380 |
Why?
|
| Peptide Hydrolases | 1 | 2013 | 80 | 0.380 |
Why?
|
| Cadherins | 2 | 2026 | 82 | 0.370 |
Why?
|
| Mechanotransduction, Cellular | 2 | 2021 | 28 | 0.330 |
Why?
|
| Protein Multimerization | 4 | 2026 | 182 | 0.320 |
Why?
|
| Microscopy, Fluorescence | 2 | 2022 | 402 | 0.310 |
Why?
|
| Protozoan Proteins | 3 | 2014 | 129 | 0.280 |
Why?
|
| Hydrogen-Ion Concentration | 6 | 2015 | 462 | 0.280 |
Why?
|
| Mice | 11 | 2026 | 11003 | 0.280 |
Why?
|
| Animals | 15 | 2026 | 20961 | 0.260 |
Why?
|
| Gold | 2 | 2025 | 233 | 0.250 |
Why?
|
| Metal Nanoparticles | 2 | 2025 | 188 | 0.240 |
Why?
|
| Candida albicans | 1 | 2025 | 74 | 0.230 |
Why?
|
| Amino Acid Sequence | 7 | 2018 | 1597 | 0.220 |
Why?
|
| Cytoplasm | 1 | 2025 | 279 | 0.210 |
Why?
|
| Glutamic Acid | 1 | 2024 | 101 | 0.210 |
Why?
|
| Molecular Sequence Data | 7 | 2015 | 1997 | 0.210 |
Why?
|
| Synapses | 1 | 2024 | 191 | 0.190 |
Why?
|
| Hippocampus | 1 | 2024 | 278 | 0.190 |
Why?
|
| Electrophysiological Phenomena | 1 | 2021 | 22 | 0.180 |
Why?
|
| Molecular Conformation | 1 | 2021 | 133 | 0.180 |
Why?
|
| Hearing | 1 | 2021 | 33 | 0.180 |
Why?
|
| Software | 1 | 2024 | 388 | 0.170 |
Why?
|
| Molecular Structure | 1 | 2021 | 385 | 0.170 |
Why?
|
| Hair Cells, Vestibular | 1 | 2019 | 2 | 0.160 |
Why?
|
| Algorithms | 1 | 2024 | 1028 | 0.150 |
Why?
|
| Multiprotein Complexes | 1 | 2019 | 155 | 0.140 |
Why?
|
| Interleukin-1 Receptor-Associated Kinases | 1 | 2018 | 34 | 0.140 |
Why?
|
| Proteomics | 2 | 2025 | 294 | 0.140 |
Why?
|
| HEK293 Cells | 5 | 2021 | 627 | 0.140 |
Why?
|
| Protein Biosynthesis | 2 | 2025 | 329 | 0.140 |
Why?
|
| Leishmania donovani | 2 | 2014 | 4 | 0.130 |
Why?
|
| Pyrimidines | 2 | 2018 | 146 | 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 | 192 | 0.120 |
Why?
|
| Molecular Chaperones | 2 | 2013 | 100 | 0.120 |
Why?
|
| Hydrogen | 1 | 2015 | 51 | 0.110 |
Why?
|
| Protein Binding | 6 | 2016 | 1618 | 0.110 |
Why?
|
| Nucleoside Transport Proteins | 1 | 2014 | 2 | 0.110 |
Why?
|
| Ubiquitin-Conjugating Enzymes | 1 | 2014 | 24 | 0.100 |
Why?
|
| Intracellular Space | 1 | 2014 | 35 | 0.100 |
Why?
|
| Anilides | 1 | 2013 | 18 | 0.100 |
Why?
|
| Monocytes | 1 | 2016 | 356 | 0.100 |
Why?
|
| Pentosyltransferases | 1 | 2013 | 2 | 0.100 |
Why?
|
| Quinolines | 1 | 2013 | 48 | 0.100 |
Why?
|
| Leishmania mexicana | 1 | 2013 | 7 | 0.100 |
Why?
|
| Iron-Regulatory Proteins | 1 | 2013 | 2 | 0.100 |
Why?
|
| Receptor Protein-Tyrosine Kinases | 1 | 2013 | 55 | 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 | 33 | 0.100 |
Why?
|
| Oncogenes | 1 | 2013 | 70 | 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 | 136 | 0.100 |
Why?
|
| Cathepsins | 1 | 2013 | 34 | 0.100 |
Why?
|
| Ovarian Neoplasms | 1 | 2014 | 155 | 0.090 |
Why?
|
| Flagella | 1 | 2013 | 143 | 0.090 |
Why?
|
| Plasma Membrane Neurotransmitter Transport Proteins | 1 | 2012 | 1 | 0.090 |
Why?
|
| nef Gene Products, Human Immunodeficiency Virus | 1 | 2012 | 26 | 0.090 |
Why?
|
| HSP70 Heat-Shock Proteins | 1 | 2012 | 80 | 0.090 |
Why?
|
| Caspases | 1 | 2013 | 176 | 0.090 |
Why?
|
| Proto-Oncogene Proteins | 1 | 2013 | 329 | 0.090 |
Why?
|
| Leucine | 1 | 2012 | 67 | 0.090 |
Why?
|
| Tumor Suppressor Protein p53 | 1 | 2014 | 309 | 0.090 |
Why?
|
| Vesicular Transport Proteins | 1 | 2012 | 115 | 0.090 |
Why?
|
| Histocompatibility Antigens Class I | 1 | 2012 | 145 | 0.080 |
Why?
|
| Down-Regulation | 1 | 2012 | 319 | 0.080 |
Why?
|
| Endosomes | 1 | 2012 | 178 | 0.080 |
Why?
|
| Glucose | 1 | 2013 | 470 | 0.080 |
Why?
|
| Escherichia coli Proteins | 1 | 2012 | 275 | 0.080 |
Why?
|
| Saccharomyces cerevisiae Proteins | 1 | 2014 | 446 | 0.080 |
Why?
|
| Binding Sites | 3 | 2021 | 914 | 0.070 |
Why?
|
| Humans | 13 | 2025 | 64238 | 0.070 |
Why?
|
| Enzyme Activation | 3 | 2015 | 386 | 0.070 |
Why?
|
| Bacteria | 1 | 2012 | 317 | 0.070 |
Why?
|
| Protein Stability | 2 | 2021 | 93 | 0.070 |
Why?
|
| Models, Biological | 1 | 2013 | 1187 | 0.070 |
Why?
|
| Escherichia coli | 1 | 2012 | 718 | 0.070 |
Why?
|
| Protein Transport | 3 | 2014 | 405 | 0.070 |
Why?
|
| Kinetics | 3 | 2014 | 766 | 0.070 |
Why?
|
| Protein Folding | 3 | 2014 | 268 | 0.070 |
Why?
|
| Janus Kinase 2 | 2 | 2018 | 19 | 0.060 |
Why?
|
| Molecular Dynamics Simulation | 2 | 2021 | 123 | 0.060 |
Why?
|
| Cell Line, Tumor | 3 | 2018 | 1494 | 0.060 |
Why?
|
| Protein Conformation | 3 | 2014 | 784 | 0.060 |
Why?
|
| Mutation | 4 | 2018 | 2629 | 0.060 |
Why?
|
| Bacterial Proteins | 1 | 2012 | 775 | 0.060 |
Why?
|
| Hyphae | 1 | 2025 | 18 | 0.060 |
Why?
|
| Organelle Biogenesis | 1 | 2025 | 18 | 0.060 |
Why?
|
| Dimerization | 1 | 2025 | 146 | 0.060 |
Why?
|
| Receptors, N-Methyl-D-Aspartate | 1 | 2025 | 90 | 0.060 |
Why?
|
| Fungal Proteins | 1 | 2025 | 149 | 0.060 |
Why?
|
| Receptors, AMPA | 1 | 2024 | 42 | 0.050 |
Why?
|
| DNA Primers | 2 | 2013 | 295 | 0.050 |
Why?
|
| HeLa Cells | 2 | 2016 | 540 | 0.050 |
Why?
|
| Substrate Specificity | 2 | 2013 | 340 | 0.050 |
Why?
|
| Salicylic Acid | 1 | 2021 | 2 | 0.040 |
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 | 1332 | 0.040 |
Why?
|
| Protein Domains | 1 | 2021 | 154 | 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 | 0.030 |
Why?
|
| Benzothiazoles | 1 | 2018 | 20 | 0.030 |
Why?
|
| Nitriles | 1 | 2018 | 79 | 0.030 |
Why?
|
| Xenograft Model Antitumor Assays | 1 | 2018 | 195 | 0.030 |
Why?
|
| Pyrazoles | 1 | 2018 | 87 | 0.030 |
Why?
|
| Mice, SCID | 1 | 2018 | 517 | 0.030 |
Why?
|
| Protein Kinase Inhibitors | 1 | 2018 | 189 | 0.030 |
Why?
|
| Mice, Inbred NOD | 1 | 2018 | 526 | 0.030 |
Why?
|
| Imaging, Three-Dimensional | 1 | 2018 | 288 | 0.030 |
Why?
|
| Thrombocythemia, Essential | 1 | 2016 | 3 | 0.030 |
Why?
|
| Extracellular Space | 1 | 2016 | 29 | 0.030 |
Why?
|
| Primary Myelofibrosis | 1 | 2016 | 11 | 0.030 |
Why?
|
| Culture Media, Conditioned | 1 | 2016 | 52 | 0.030 |
Why?
|
| COS Cells | 1 | 2015 | 174 | 0.030 |
Why?
|
| Real-Time Polymerase Chain Reaction | 1 | 2016 | 209 | 0.030 |
Why?
|
| Bone Marrow | 1 | 2016 | 175 | 0.030 |
Why?
|
| Cell Culture Techniques | 1 | 2016 | 183 | 0.030 |
Why?
|
| Blotting, Western | 1 | 2016 | 614 | 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 | 51 | 0.030 |
Why?
|
| Phosphoribosyl Pyrophosphate | 1 | 2013 | 1 | 0.030 |
Why?
|
| Thiouracil | 1 | 2013 | 1 | 0.030 |
Why?
|
| Spectrophotometry | 1 | 2013 | 34 | 0.030 |
Why?
|
| Immunohistochemistry | 1 | 2016 | 901 | 0.030 |
Why?
|
| Cations, Divalent | 1 | 2013 | 23 | 0.030 |
Why?
|
| Lysine | 1 | 2014 | 87 | 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?
|
| Chromatography, Gel | 1 | 2013 | 65 | 0.030 |
Why?
|
| Hemochromatosis Protein | 1 | 2013 | 6 | 0.030 |
Why?
|
| Mutagenesis, Site-Directed | 1 | 2014 | 248 | 0.030 |
Why?
|
| Feedback, Physiological | 1 | 2013 | 59 | 0.020 |
Why?
|
| Fluorouracil | 1 | 2013 | 69 | 0.020 |
Why?
|
| Cysteine Endopeptidases | 1 | 2014 | 97 | 0.020 |
Why?
|
| Glycerol | 1 | 2013 | 33 | 0.020 |
Why?
|
| Zinc | 1 | 2014 | 93 | 0.020 |
Why?
|
| Mutagenesis | 1 | 2013 | 133 | 0.020 |
Why?
|
| GPI-Linked Proteins | 1 | 2013 | 40 | 0.020 |
Why?
|
| Sequence Alignment | 1 | 2014 | 302 | 0.020 |
Why?
|
| Urea | 1 | 2013 | 39 | 0.020 |
Why?
|
| Chromatography, Affinity | 1 | 2013 | 49 | 0.020 |
Why?
|
| Protons | 1 | 2013 | 65 | 0.020 |
Why?
|
| Plasmids | 1 | 2014 | 293 | 0.020 |
Why?
|
| Circular Dichroism | 1 | 2013 | 108 | 0.020 |
Why?
|
| Cytosol | 1 | 2014 | 181 | 0.020 |
Why?
|
| Disulfides | 1 | 2013 | 66 | 0.020 |
Why?
|
| Endoplasmic Reticulum | 1 | 2014 | 175 | 0.020 |
Why?
|
| Sequence Homology, Amino Acid | 1 | 2013 | 365 | 0.020 |
Why?
|
| Thermodynamics | 1 | 2013 | 199 | 0.020 |
Why?
|
| Protein Isoforms | 1 | 2013 | 199 | 0.020 |
Why?
|
| Dogs | 1 | 2014 | 332 | 0.020 |
Why?
|
| Hydrophobic and Hydrophilic Interactions | 1 | 2014 | 272 | 0.020 |
Why?
|
| Calcium | 1 | 2016 | 580 | 0.020 |
Why?
|
| Animals, Genetically Modified | 1 | 2013 | 302 | 0.020 |
Why?
|
| Temperature | 1 | 2013 | 312 | 0.020 |
Why?
|
| Cell Nucleus | 1 | 2016 | 632 | 0.020 |
Why?
|
| Sequence Analysis, DNA | 1 | 2013 | 416 | 0.020 |
Why?
|
| Flow Cytometry | 1 | 2013 | 668 | 0.020 |
Why?
|
| Cytokines | 1 | 2016 | 944 | 0.020 |
Why?
|
| Cell Survival | 1 | 2013 | 582 | 0.020 |
Why?
|
| DNA Damage | 1 | 2014 | 289 | 0.020 |
Why?
|
| Protein Structure, Secondary | 1 | 2012 | 260 | 0.020 |
Why?
|
| Recombinant Proteins | 1 | 2013 | 704 | 0.020 |
Why?
|
| Structure-Activity Relationship | 1 | 2012 | 374 | 0.020 |
Why?
|
| Amino Acids | 1 | 2012 | 148 | 0.020 |
Why?
|
| Crystallography, X-Ray | 1 | 2012 | 436 | 0.020 |
Why?
|
| Evolution, Molecular | 1 | 2012 | 324 | 0.020 |
Why?
|
| Cell Line | 1 | 2014 | 2055 | 0.020 |
Why?
|
| Child | 1 | 2018 | 4583 | 0.020 |
Why?
|
| Aged, 80 and over | 1 | 2018 | 5520 | 0.020 |
Why?
|
| Young Adult | 1 | 2018 | 4776 | 0.020 |
Why?
|
| Adolescent | 1 | 2018 | 6304 | 0.020 |
Why?
|
| Time Factors | 1 | 2013 | 3724 | 0.010 |
Why?
|
| Female | 2 | 2018 | 33350 | 0.010 |
Why?
|
| Aged | 1 | 2018 | 14648 | 0.010 |
Why?
|
| Adult | 1 | 2018 | 17116 | 0.010 |
Why?
|
| Middle Aged | 1 | 2018 | 17898 | 0.010 |
Why?
|
| Male | 1 | 2018 | 30294 | 0.010 |
Why?
|