 Gerald Carlson
Concepts (161)
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?
|
|---|
| Phosphorylase Kinase | 25 | 2018 | 26 | 8.040 |
Why?
| | Protein Subunits | 13 | 2017 | 201 | 2.660 |
Why?
| | Glycogen | 3 | 2019 | 51 | 1.390 |
Why?
| | Glycogenolysis | 5 | 2018 | 8 | 1.190 |
Why?
| | Glycogen Phosphorylase | 2 | 2018 | 4 | 1.170 |
Why?
| | Proteins | 4 | 2016 | 912 | 1.150 |
Why?
| | Cross-Linking Reagents | 7 | 2016 | 181 | 1.030 |
Why?
| | Rabbits | 14 | 2015 | 736 | 0.920 |
Why?
| | Protein Interaction Mapping | 3 | 2016 | 101 | 0.880 |
Why?
| | Protein Structure, Quaternary | 8 | 2017 | 115 | 0.850 |
Why?
| | Brain | 3 | 2019 | 2374 | 0.820 |
Why?
| | Mass Spectrometry | 5 | 2016 | 633 | 0.810 |
Why?
| | Models, Molecular | 10 | 2017 | 1378 | 0.780 |
Why?
| | Energy Metabolism | 3 | 2019 | 729 | 0.760 |
Why?
| | Peptides | 3 | 2015 | 848 | 0.750 |
Why?
| | Catalytic Domain | 6 | 2017 | 197 | 0.690 |
Why?
| | Enzyme Activation | 9 | 2016 | 787 | 0.670 |
Why?
| | Protein Conformation | 9 | 2016 | 811 | 0.650 |
Why?
| | Calcium | 8 | 2012 | 1103 | 0.650 |
Why?
| | Allosteric Regulation | 4 | 2016 | 82 | 0.570 |
Why?
| | Protein Binding | 9 | 2017 | 1896 | 0.520 |
Why?
| | Databases, Protein | 1 | 2016 | 59 | 0.510 |
Why?
| | Mutagenesis | 1 | 2016 | 170 | 0.510 |
Why?
| | Muscle, Skeletal | 6 | 2012 | 1472 | 0.500 |
Why?
| | Protein Structure, Secondary | 5 | 2017 | 325 | 0.490 |
Why?
| | Phosphorylation | 7 | 2018 | 1571 | 0.490 |
Why?
| | Body Temperature | 1 | 2015 | 208 | 0.490 |
Why?
| | Biomimetic Materials | 1 | 2015 | 64 | 0.480 |
Why?
| | Data Mining | 1 | 2016 | 100 | 0.480 |
Why?
| | Allosteric Site | 2 | 2017 | 16 | 0.430 |
Why?
| | Magnesium | 1 | 2013 | 145 | 0.410 |
Why?
| | Phosphoenolpyruvate Carboxykinase (GTP) | 2 | 2009 | 32 | 0.410 |
Why?
| | Proteome | 1 | 2016 | 339 | 0.400 |
Why?
| | Animals | 21 | 2018 | 31761 | 0.400 |
Why?
| | Computational Biology | 1 | 2016 | 530 | 0.390 |
Why?
| | Glucan 1,4-alpha-Glucosidase | 1 | 2010 | 1 | 0.360 |
Why?
| | Acarbose | 1 | 2010 | 2 | 0.360 |
Why?
| | Calmodulin | 2 | 2008 | 71 | 0.360 |
Why?
| | Proteomics | 1 | 2016 | 843 | 0.350 |
Why?
| | Biochemistry | 1 | 2010 | 40 | 0.340 |
Why?
| | Biocatalysis | 1 | 2009 | 60 | 0.330 |
Why?
| | Software | 2 | 2016 | 536 | 0.320 |
Why?
| | Glyceraldehyde-3-Phosphate Dehydrogenases | 1 | 2008 | 14 | 0.310 |
Why?
| | Deuterium Exchange Measurement | 2 | 2017 | 29 | 0.280 |
Why?
| | Multienzyme Complexes | 2 | 2016 | 64 | 0.260 |
Why?
| | High-Throughput Screening Assays | 2 | 2018 | 123 | 0.250 |
Why?
| | Circular Dichroism | 3 | 2013 | 135 | 0.250 |
Why?
| | Static Electricity | 3 | 2013 | 114 | 0.250 |
Why?
| | Proteolysis | 2 | 2016 | 143 | 0.250 |
Why?
| | Muscle Contraction | 1 | 2008 | 388 | 0.240 |
Why?
| | Scattering, Radiation | 3 | 2013 | 92 | 0.230 |
Why?
| | Protein Multimerization | 2 | 2017 | 159 | 0.230 |
Why?
| | Binding Sites | 3 | 2016 | 1176 | 0.230 |
Why?
| | Protein Interaction Domains and Motifs | 2 | 2015 | 132 | 0.220 |
Why?
| | Dinitrofluorobenzene | 2 | 2013 | 7 | 0.210 |
Why?
| | Substrate Specificity | 2 | 2016 | 354 | 0.210 |
Why?
| | Glycogen Phosphorylase, Muscle Form | 1 | 2002 | 1 | 0.200 |
Why?
| | Cryoelectron Microscopy | 2 | 2017 | 144 | 0.200 |
Why?
| | Protein Structure, Tertiary | 3 | 2008 | 797 | 0.180 |
Why?
| | Lafora Disease | 1 | 2019 | 2 | 0.160 |
Why?
| | Microscopy, Electron | 3 | 2012 | 410 | 0.150 |
Why?
| | Glycogen Debranching Enzyme System | 1 | 2018 | 3 | 0.150 |
Why?
| | Fluorescence Resonance Energy Transfer | 2 | 2012 | 169 | 0.150 |
Why?
| | Spectrophotometry, Ultraviolet | 2 | 2008 | 73 | 0.150 |
Why?
| | Succinimides | 2 | 2008 | 15 | 0.150 |
Why?
| | Review Literature as Topic | 1 | 2018 | 61 | 0.150 |
Why?
| | Light | 2 | 2013 | 336 | 0.150 |
Why?
| | Spectrometry, Fluorescence | 2 | 2008 | 157 | 0.140 |
Why?
| | Enzyme Inhibitors | 3 | 2010 | 751 | 0.140 |
Why?
| | Astrocytes | 1 | 2019 | 162 | 0.140 |
Why?
| | Isoenzymes | 1 | 2018 | 285 | 0.140 |
Why?
| | Hydrogen-Ion Concentration | 2 | 2008 | 511 | 0.140 |
Why?
| | Structure-Activity Relationship | 1 | 2018 | 503 | 0.140 |
Why?
| | Glycolysis | 1 | 2018 | 227 | 0.140 |
Why?
| | Protein Domains | 1 | 2017 | 207 | 0.140 |
Why?
| | Synaptic Transmission | 1 | 2018 | 227 | 0.130 |
Why?
| | Ligands | 1 | 2018 | 564 | 0.130 |
Why?
| | Amino Acid Sequence | 2 | 2012 | 1988 | 0.130 |
Why?
| | Peptide Mapping | 1 | 2015 | 60 | 0.130 |
Why?
| | Humans | 10 | 2019 | 114756 | 0.130 |
Why?
| | Workflow | 1 | 2016 | 135 | 0.120 |
Why?
| | Crystallography, X-Ray | 1 | 2015 | 405 | 0.120 |
Why?
| | Thermodynamics | 1 | 2016 | 383 | 0.110 |
Why?
| | Bridged Bicyclo Compounds | 1 | 2013 | 11 | 0.110 |
Why?
| | Biomedical Research | 1 | 2019 | 585 | 0.110 |
Why?
| | Cations | 1 | 2013 | 79 | 0.110 |
Why?
| | Transcriptome | 1 | 2018 | 727 | 0.100 |
Why?
| | Oxidation-Reduction | 1 | 2015 | 927 | 0.100 |
Why?
| | Molecular Docking Simulation | 1 | 2012 | 101 | 0.100 |
Why?
| | Immunochemistry | 1 | 2012 | 11 | 0.100 |
Why?
| | Neurons | 1 | 2019 | 1281 | 0.090 |
Why?
| | Image Processing, Computer-Assisted | 3 | 2005 | 684 | 0.090 |
Why?
| | Tandem Mass Spectrometry | 1 | 2012 | 413 | 0.090 |
Why?
| | Holoenzymes | 1 | 2009 | 21 | 0.090 |
Why?
| | Baculoviridae | 1 | 2009 | 45 | 0.080 |
Why?
| | Kinetics | 2 | 2009 | 1550 | 0.080 |
Why?
| | History, 20th Century | 1 | 2010 | 265 | 0.080 |
Why?
| | Nucleotides | 1 | 2009 | 112 | 0.080 |
Why?
| | Algorithms | 1 | 2016 | 1468 | 0.080 |
Why?
| | Tissue Extracts | 1 | 2008 | 20 | 0.080 |
Why?
| | Reproducibility of Results | 1 | 2016 | 2763 | 0.080 |
Why?
| | Peptide Fragments | 1 | 2012 | 668 | 0.080 |
Why?
| | Cyclotrons | 1 | 2008 | 2 | 0.080 |
Why?
| | Enzymes, Immobilized | 1 | 2008 | 25 | 0.080 |
Why?
| | Troponin C | 1 | 2008 | 5 | 0.080 |
Why?
| | Fourier Analysis | 1 | 2008 | 39 | 0.080 |
Why?
| | Career Choice | 1 | 2010 | 177 | 0.080 |
Why?
| | Models, Animal | 1 | 2009 | 345 | 0.070 |
Why?
| | Dimerization | 1 | 2008 | 176 | 0.070 |
Why?
| | Troponin I | 1 | 2008 | 68 | 0.070 |
Why?
| | Cytosol | 1 | 2008 | 208 | 0.070 |
Why?
| | Spectrometry, Mass, Electrospray Ionization | 1 | 2008 | 162 | 0.070 |
Why?
| | Models, Biological | 2 | 2006 | 1630 | 0.070 |
Why?
| | Surface Properties | 1 | 2008 | 387 | 0.070 |
Why?
| | Cations, Divalent | 1 | 2007 | 50 | 0.070 |
Why?
| | Enzyme Stability | 1 | 2007 | 62 | 0.070 |
Why?
| | Spectroscopy, Fourier Transform Infrared | 1 | 2007 | 76 | 0.070 |
Why?
| | Structural Homology, Protein | 1 | 2006 | 23 | 0.070 |
Why?
| | Phosphoserine | 1 | 2006 | 33 | 0.070 |
Why?
| | Mutant Proteins | 1 | 2006 | 95 | 0.070 |
Why?
| | Recombinant Proteins | 1 | 2009 | 1233 | 0.070 |
Why?
| | Sequence Deletion | 1 | 2006 | 167 | 0.070 |
Why?
| | Chromatography, Liquid | 1 | 2008 | 348 | 0.070 |
Why?
| | Point Mutation | 1 | 2006 | 216 | 0.060 |
Why?
| | Mutation | 1 | 2016 | 3350 | 0.060 |
Why?
| | X-Rays | 1 | 2005 | 30 | 0.060 |
Why?
| | Microtubule-Associated Proteins | 1 | 2006 | 174 | 0.060 |
Why?
| | Temperature | 1 | 2007 | 575 | 0.060 |
Why?
| | Caspases | 1 | 2005 | 245 | 0.060 |
Why?
| | Internet | 1 | 2008 | 596 | 0.050 |
Why?
| | Amino Acids | 1 | 2006 | 448 | 0.050 |
Why?
| | Hypoglycemic Agents | 1 | 2010 | 1009 | 0.050 |
Why?
| | Molecular Sequence Data | 1 | 2006 | 2791 | 0.050 |
Why?
| | Mice | 3 | 2008 | 14916 | 0.040 |
Why?
| | Female | 2 | 2015 | 59507 | 0.030 |
Why?
| | United States | 1 | 2010 | 12176 | 0.030 |
Why?
| | Catalysis | 1 | 2012 | 292 | 0.020 |
Why?
| | Cell Line | 2 | 2006 | 2639 | 0.020 |
Why?
| | Signal Transduction | 1 | 2002 | 4521 | 0.020 |
Why?
| | Crystallization | 1 | 2008 | 136 | 0.020 |
Why?
| | Molecular Structure | 1 | 2008 | 438 | 0.020 |
Why?
| | Lac Operon | 1 | 2006 | 44 | 0.020 |
Why?
| | Two-Hybrid System Techniques | 1 | 2006 | 52 | 0.020 |
Why?
| | beta-Galactosidase | 1 | 2006 | 62 | 0.020 |
Why?
| | src Homology Domains | 1 | 2006 | 33 | 0.020 |
Why?
| | Yeasts | 1 | 2006 | 49 | 0.020 |
Why?
| | Minor Histocompatibility Antigens | 1 | 2006 | 41 | 0.020 |
Why?
| | Immunoprecipitation | 1 | 2006 | 152 | 0.020 |
Why?
| | Ethylenediamines | 1 | 2005 | 6 | 0.020 |
Why?
| | Staurosporine | 1 | 2005 | 21 | 0.020 |
Why?
| | Plasmids | 1 | 2006 | 345 | 0.020 |
Why?
| | Myoblasts | 1 | 2005 | 76 | 0.010 |
Why?
| | Caspase 3 | 1 | 2005 | 236 | 0.010 |
Why?
| | Doxorubicin | 1 | 2005 | 286 | 0.010 |
Why?
| | Blotting, Western | 1 | 2006 | 1151 | 0.010 |
Why?
| | Adenosine Triphosphate | 1 | 2005 | 431 | 0.010 |
Why?
| | Cell Culture Techniques | 1 | 2005 | 343 | 0.010 |
Why?
| | Ultraviolet Rays | 1 | 2005 | 366 | 0.010 |
Why?
| | Cell Differentiation | 1 | 2005 | 1699 | 0.010 |
Why?
| | Apoptosis | 1 | 2005 | 2369 | 0.010 |
Why?
| | Time Factors | 1 | 2005 | 6124 | 0.010 |
Why?
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