 Gerald Carlson
Concepts (164)
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 | 26 | 2018 | 27 | 8.030 |
Why?
| | Protein Subunits | 13 | 2017 | 230 | 2.580 |
Why?
| | Glycogen | 3 | 2019 | 55 | 1.350 |
Why?
| | Glycogenolysis | 5 | 2018 | 8 | 1.160 |
Why?
| | Glycogen Phosphorylase | 2 | 2018 | 4 | 1.140 |
Why?
| | Proteins | 4 | 2016 | 932 | 1.110 |
Why?
| | Cross-Linking Reagents | 7 | 2016 | 205 | 1.000 |
Why?
| | Rabbits | 15 | 2015 | 758 | 0.930 |
Why?
| | Protein Structure, Quaternary | 9 | 2017 | 122 | 0.880 |
Why?
| | Protein Interaction Mapping | 3 | 2016 | 107 | 0.860 |
Why?
| | Catalytic Domain | 7 | 2017 | 217 | 0.840 |
Why?
| | Mass Spectrometry | 5 | 2016 | 659 | 0.790 |
Why?
| | Brain | 3 | 2019 | 2620 | 0.770 |
Why?
| | Models, Molecular | 10 | 2017 | 1480 | 0.750 |
Why?
| | Calcium | 9 | 2012 | 1178 | 0.740 |
Why?
| | Peptides | 3 | 2015 | 908 | 0.710 |
Why?
| | Energy Metabolism | 3 | 2019 | 831 | 0.710 |
Why?
| | Enzyme Activation | 9 | 2016 | 799 | 0.650 |
Why?
| | Protein Conformation | 9 | 2016 | 852 | 0.630 |
Why?
| | Allosteric Regulation | 4 | 2016 | 99 | 0.550 |
Why?
| | Calmodulin | 3 | 2008 | 75 | 0.540 |
Why?
| | Protein Binding | 10 | 2017 | 2103 | 0.510 |
Why?
| | Databases, Protein | 1 | 2016 | 61 | 0.500 |
Why?
| | Mutagenesis | 1 | 2016 | 181 | 0.490 |
Why?
| | Protein Structure, Secondary | 5 | 2017 | 338 | 0.480 |
Why?
| | Body Temperature | 1 | 2015 | 212 | 0.470 |
Why?
| | Phosphorylation | 7 | 2018 | 1681 | 0.470 |
Why?
| | Biomimetic Materials | 1 | 2015 | 71 | 0.470 |
Why?
| | Data Mining | 1 | 2016 | 109 | 0.470 |
Why?
| | Muscle, Skeletal | 6 | 2012 | 1627 | 0.460 |
Why?
| | Allosteric Site | 2 | 2017 | 19 | 0.410 |
Why?
| | Magnesium | 1 | 2013 | 150 | 0.400 |
Why?
| | Phosphoenolpyruvate Carboxykinase (GTP) | 2 | 2009 | 31 | 0.400 |
Why?
| | Animals | 22 | 2018 | 34479 | 0.380 |
Why?
| | Proteome | 1 | 2016 | 430 | 0.370 |
Why?
| | Computational Biology | 1 | 2016 | 598 | 0.370 |
Why?
| | Glucan 1,4-alpha-Glucosidase | 1 | 2010 | 1 | 0.350 |
Why?
| | Acarbose | 1 | 2010 | 2 | 0.350 |
Why?
| | Biochemistry | 1 | 2010 | 38 | 0.330 |
Why?
| | Biocatalysis | 1 | 2009 | 66 | 0.320 |
Why?
| | Proteomics | 1 | 2016 | 1009 | 0.320 |
Why?
| | Glyceraldehyde-3-Phosphate Dehydrogenases | 1 | 2008 | 12 | 0.300 |
Why?
| | Software | 2 | 2016 | 608 | 0.300 |
Why?
| | Deuterium Exchange Measurement | 2 | 2017 | 29 | 0.270 |
Why?
| | Multienzyme Complexes | 2 | 2016 | 68 | 0.260 |
Why?
| | High-Throughput Screening Assays | 2 | 2018 | 134 | 0.240 |
Why?
| | Circular Dichroism | 3 | 2013 | 146 | 0.240 |
Why?
| | Static Electricity | 3 | 2013 | 117 | 0.240 |
Why?
| | Proteolysis | 2 | 2016 | 162 | 0.240 |
Why?
| | Muscle Contraction | 1 | 2008 | 420 | 0.230 |
Why?
| | Scattering, Radiation | 3 | 2013 | 97 | 0.230 |
Why?
| | Protein Multimerization | 2 | 2017 | 178 | 0.220 |
Why?
| | Binding Sites | 3 | 2016 | 1236 | 0.220 |
Why?
| | Protein Interaction Domains and Motifs | 2 | 2015 | 137 | 0.210 |
Why?
| | Dinitrofluorobenzene | 2 | 2013 | 7 | 0.210 |
Why?
| | Substrate Specificity | 2 | 2016 | 365 | 0.200 |
Why?
| | Glycogen Phosphorylase, Muscle Form | 1 | 2002 | 1 | 0.200 |
Why?
| | Cryoelectron Microscopy | 2 | 2017 | 177 | 0.190 |
Why?
| | Protein Structure, Tertiary | 3 | 2008 | 835 | 0.180 |
Why?
| | Lafora Disease | 1 | 2019 | 2 | 0.160 |
Why?
| | Microscopy, Electron | 3 | 2012 | 417 | 0.150 |
Why?
| | Glycogen Debranching Enzyme System | 1 | 2018 | 3 | 0.150 |
Why?
| | Fluorescence Resonance Energy Transfer | 2 | 2012 | 177 | 0.150 |
Why?
| | Spectrophotometry, Ultraviolet | 2 | 2008 | 80 | 0.140 |
Why?
| | Succinimides | 2 | 2008 | 16 | 0.140 |
Why?
| | Review Literature as Topic | 1 | 2018 | 66 | 0.140 |
Why?
| | Light | 2 | 2013 | 354 | 0.140 |
Why?
| | Spectrometry, Fluorescence | 2 | 2008 | 170 | 0.140 |
Why?
| | Isoenzymes | 1 | 2018 | 304 | 0.140 |
Why?
| | Enzyme Inhibitors | 3 | 2010 | 809 | 0.140 |
Why?
| | Astrocytes | 1 | 2019 | 188 | 0.140 |
Why?
| | Hydrogen-Ion Concentration | 2 | 2008 | 536 | 0.140 |
Why?
| | Structure-Activity Relationship | 1 | 2018 | 530 | 0.130 |
Why?
| | Protein Domains | 1 | 2017 | 252 | 0.130 |
Why?
| | Glycolysis | 1 | 2018 | 293 | 0.130 |
Why?
| | Synaptic Transmission | 1 | 2018 | 258 | 0.130 |
Why?
| | Ligands | 1 | 2018 | 614 | 0.130 |
Why?
| | Amino Acid Sequence | 2 | 2012 | 2040 | 0.130 |
Why?
| | Peptide Mapping | 1 | 2015 | 61 | 0.120 |
Why?
| | Humans | 10 | 2019 | 128418 | 0.120 |
Why?
| | Workflow | 1 | 2016 | 155 | 0.120 |
Why?
| | Crystallography, X-Ray | 1 | 2015 | 433 | 0.110 |
Why?
| | Thermodynamics | 1 | 2016 | 405 | 0.110 |
Why?
| | Bridged Bicyclo Compounds | 1 | 2013 | 11 | 0.100 |
Why?
| | Cations | 1 | 2013 | 79 | 0.100 |
Why?
| | Biomedical Research | 1 | 2019 | 635 | 0.100 |
Why?
| | Molecular Docking Simulation | 1 | 2012 | 109 | 0.100 |
Why?
| | Immunochemistry | 1 | 2012 | 13 | 0.100 |
Why?
| | Oxidation-Reduction | 1 | 2015 | 1001 | 0.100 |
Why?
| | Transcriptome | 1 | 2018 | 881 | 0.090 |
Why?
| | Image Processing, Computer-Assisted | 3 | 2005 | 735 | 0.090 |
Why?
| | Neurons | 1 | 2019 | 1448 | 0.090 |
Why?
| | Tandem Mass Spectrometry | 1 | 2012 | 449 | 0.080 |
Why?
| | Holoenzymes | 1 | 2009 | 21 | 0.080 |
Why?
| | Baculoviridae | 1 | 2009 | 44 | 0.080 |
Why?
| | Kinetics | 2 | 2009 | 1615 | 0.080 |
Why?
| | Nucleotides | 1 | 2009 | 117 | 0.080 |
Why?
| | History, 20th Century | 1 | 2010 | 291 | 0.080 |
Why?
| | Tissue Extracts | 1 | 2008 | 19 | 0.080 |
Why?
| | Peptide Fragments | 1 | 2012 | 684 | 0.080 |
Why?
| | Cyclotrons | 1 | 2008 | 3 | 0.070 |
Why?
| | Troponin C | 1 | 2008 | 5 | 0.070 |
Why?
| | Algorithms | 1 | 2016 | 1618 | 0.070 |
Why?
| | Fourier Analysis | 1 | 2008 | 39 | 0.070 |
Why?
| | Enzymes, Immobilized | 1 | 2008 | 29 | 0.070 |
Why?
| | Reproducibility of Results | 1 | 2016 | 3020 | 0.070 |
Why?
| | Models, Animal | 1 | 2009 | 366 | 0.070 |
Why?
| | Career Choice | 1 | 2010 | 209 | 0.070 |
Why?
| | Dimerization | 1 | 2008 | 188 | 0.070 |
Why?
| | Surface Properties | 1 | 2008 | 393 | 0.070 |
Why?
| | Spectrometry, Mass, Electrospray Ionization | 1 | 2008 | 167 | 0.070 |
Why?
| | Cytosol | 1 | 2008 | 214 | 0.070 |
Why?
| | Troponin I | 1 | 2008 | 75 | 0.070 |
Why?
| | Cations, Divalent | 1 | 2007 | 54 | 0.070 |
Why?
| | Models, Biological | 2 | 2006 | 1691 | 0.070 |
Why?
| | Enzyme Stability | 1 | 2007 | 67 | 0.070 |
Why?
| | Spectroscopy, Fourier Transform Infrared | 1 | 2007 | 82 | 0.070 |
Why?
| | Structural Homology, Protein | 1 | 2006 | 25 | 0.070 |
Why?
| | Phosphoserine | 1 | 2006 | 33 | 0.070 |
Why?
| | Mutant Proteins | 1 | 2006 | 98 | 0.070 |
Why?
| | Recombinant Proteins | 1 | 2009 | 1281 | 0.060 |
Why?
| | Two-Hybrid System Techniques | 2 | 2006 | 56 | 0.060 |
Why?
| | Sequence Deletion | 1 | 2006 | 178 | 0.060 |
Why?
| | Chromatography, Liquid | 1 | 2008 | 374 | 0.060 |
Why?
| | Point Mutation | 1 | 2006 | 223 | 0.060 |
Why?
| | X-Rays | 1 | 2005 | 29 | 0.060 |
Why?
| | Mutation | 1 | 2016 | 3689 | 0.060 |
Why?
| | Microtubule-Associated Proteins | 1 | 2006 | 190 | 0.060 |
Why?
| | Caspases | 1 | 2005 | 242 | 0.060 |
Why?
| | Temperature | 1 | 2007 | 625 | 0.060 |
Why?
| | Internet | 1 | 2008 | 617 | 0.050 |
Why?
| | Amino Acids | 1 | 2006 | 474 | 0.050 |
Why?
| | Molecular Sequence Data | 1 | 2006 | 2819 | 0.050 |
Why?
| | Hydrolysis | 1 | 2002 | 184 | 0.050 |
Why?
| | Hypoglycemic Agents | 1 | 2010 | 1212 | 0.050 |
Why?
| | DNA Primers | 1 | 2002 | 510 | 0.040 |
Why?
| | Base Sequence | 1 | 2002 | 2135 | 0.040 |
Why?
| | Mice | 3 | 2008 | 16602 | 0.030 |
Why?
| | Female | 2 | 2015 | 68154 | 0.030 |
Why?
| | United States | 1 | 2010 | 13830 | 0.030 |
Why?
| | Catalysis | 1 | 2012 | 305 | 0.020 |
Why?
| | Cell Line | 2 | 2006 | 2731 | 0.020 |
Why?
| | Signal Transduction | 1 | 2002 | 4826 | 0.020 |
Why?
| | Crystallization | 1 | 2008 | 137 | 0.020 |
Why?
| | Molecular Structure | 1 | 2008 | 464 | 0.020 |
Why?
| | Lac Operon | 1 | 2006 | 45 | 0.020 |
Why?
| | beta-Galactosidase | 1 | 2006 | 75 | 0.020 |
Why?
| | src Homology Domains | 1 | 2006 | 37 | 0.020 |
Why?
| | Yeasts | 1 | 2006 | 52 | 0.020 |
Why?
| | Minor Histocompatibility Antigens | 1 | 2006 | 46 | 0.020 |
Why?
| | Immunoprecipitation | 1 | 2006 | 157 | 0.020 |
Why?
| | Ethylenediamines | 1 | 2005 | 6 | 0.020 |
Why?
| | Staurosporine | 1 | 2005 | 20 | 0.020 |
Why?
| | Plasmids | 1 | 2006 | 354 | 0.010 |
Why?
| | Myoblasts | 1 | 2005 | 80 | 0.010 |
Why?
| | Caspase 3 | 1 | 2005 | 228 | 0.010 |
Why?
| | Doxorubicin | 1 | 2005 | 322 | 0.010 |
Why?
| | Blotting, Western | 1 | 2006 | 1164 | 0.010 |
Why?
| | Cell Culture Techniques | 1 | 2005 | 345 | 0.010 |
Why?
| | Adenosine Triphosphate | 1 | 2005 | 471 | 0.010 |
Why?
| | Ultraviolet Rays | 1 | 2005 | 384 | 0.010 |
Why?
| | Cell Differentiation | 1 | 2005 | 1900 | 0.010 |
Why?
| | Apoptosis | 1 | 2005 | 2435 | 0.010 |
Why?
| | Time Factors | 1 | 2005 | 6482 | 0.010 |
Why?
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