Concepts (237)
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?
|
---|
Ion Channels | 41 | 2022 | 145 | 6.310 |
Why?
|
Ion Channel Gating | 30 | 2022 | 129 | 4.340 |
Why?
|
Protons | 35 | 2022 | 49 | 4.340 |
Why?
|
Zinc | 13 | 2020 | 31 | 1.290 |
Why?
|
NADPH Oxidases | 16 | 2020 | 30 | 1.230 |
Why?
|
Hydrogen-Ion Concentration | 23 | 2021 | 107 | 0.940 |
Why?
|
Membrane Potentials | 20 | 2019 | 143 | 0.830 |
Why?
|
Proton Pumps | 5 | 2008 | 10 | 0.770 |
Why?
|
Mutation | 10 | 2019 | 324 | 0.760 |
Why?
|
Animals | 32 | 2022 | 3551 | 0.760 |
Why?
|
Eosinophils | 8 | 2006 | 38 | 0.730 |
Why?
|
Pulmonary Alveoli | 7 | 2004 | 15 | 0.680 |
Why?
|
Point Mutation | 1 | 2018 | 26 | 0.600 |
Why?
|
Neutrophils | 7 | 2009 | 89 | 0.600 |
Why?
|
Patch-Clamp Techniques | 17 | 2019 | 86 | 0.510 |
Why?
|
Phagocytes | 5 | 2008 | 12 | 0.420 |
Why?
|
HEK293 Cells | 6 | 2019 | 59 | 0.410 |
Why?
|
Humans | 39 | 2020 | 26260 | 0.360 |
Why?
|
Hydrogen | 4 | 2004 | 8 | 0.360 |
Why?
|
Rats | 9 | 2018 | 634 | 0.360 |
Why?
|
Models, Theoretical | 3 | 2003 | 75 | 0.320 |
Why?
|
Protein Conformation | 5 | 2019 | 60 | 0.310 |
Why?
|
Membrane Glycoproteins | 3 | 2002 | 68 | 0.290 |
Why?
|
Mice | 10 | 2020 | 1380 | 0.280 |
Why?
|
Membrane Transport Modulators | 1 | 2007 | 1 | 0.280 |
Why?
|
Epithelial Cells | 5 | 2004 | 76 | 0.270 |
Why?
|
Electrophysiology | 10 | 2010 | 79 | 0.260 |
Why?
|
COS Cells | 6 | 2015 | 33 | 0.260 |
Why?
|
Amino Acid Sequence | 4 | 2015 | 146 | 0.240 |
Why?
|
Respiratory Burst | 8 | 2009 | 16 | 0.240 |
Why?
|
Molecular Sequence Data | 4 | 2015 | 185 | 0.240 |
Why?
|
Cell Membrane | 3 | 2019 | 79 | 0.240 |
Why?
|
Kinetics | 10 | 2010 | 158 | 0.240 |
Why?
|
Dinoflagellida | 2 | 2017 | 2 | 0.240 |
Why?
|
Snails | 3 | 2018 | 3 | 0.220 |
Why?
|
Monocytes | 2 | 2011 | 60 | 0.220 |
Why?
|
Arachidonic Acid | 2 | 2001 | 14 | 0.220 |
Why?
|
In Vitro Techniques | 8 | 2009 | 155 | 0.200 |
Why?
|
B-Lymphocytes | 2 | 2014 | 51 | 0.200 |
Why?
|
Histidine | 3 | 2018 | 5 | 0.200 |
Why?
|
Cadmium | 4 | 2018 | 9 | 0.190 |
Why?
|
Cricetinae | 2 | 2018 | 34 | 0.190 |
Why?
|
Molecular Dynamics Simulation | 3 | 2019 | 5 | 0.180 |
Why?
|
Binding Sites | 1 | 2020 | 62 | 0.180 |
Why?
|
Triple Negative Breast Neoplasms | 1 | 2020 | 14 | 0.170 |
Why?
|
Cations, Divalent | 1 | 1999 | 7 | 0.170 |
Why?
|
Energy Metabolism | 1 | 2000 | 52 | 0.170 |
Why?
|
Oocytes | 1 | 2019 | 6 | 0.170 |
Why?
|
Electrons | 4 | 2011 | 16 | 0.170 |
Why?
|
Cell Proliferation | 1 | 2020 | 171 | 0.160 |
Why?
|
Membrane Proteins | 1 | 2020 | 159 | 0.160 |
Why?
|
HL-60 Cells | 1 | 1998 | 13 | 0.160 |
Why?
|
Tetradecanoylphorbol Acetate | 9 | 2009 | 29 | 0.150 |
Why?
|
Sequence Homology | 1 | 2018 | 2 | 0.150 |
Why?
|
Protein Domains | 1 | 2018 | 5 | 0.150 |
Why?
|
Reactive Oxygen Species | 4 | 2014 | 111 | 0.150 |
Why?
|
Rats, Sprague-Dawley | 5 | 2004 | 328 | 0.150 |
Why?
|
Models, Molecular | 4 | 2015 | 62 | 0.140 |
Why?
|
Deuterium Oxide | 1 | 1997 | 1 | 0.140 |
Why?
|
Vacuoles | 1 | 2017 | 5 | 0.140 |
Why?
|
CHO Cells | 1 | 1997 | 10 | 0.140 |
Why?
|
Chloride Channels | 1 | 1997 | 6 | 0.140 |
Why?
|
Sodium-Hydrogen Exchangers | 2 | 2009 | 5 | 0.140 |
Why?
|
Leukemia, Monocytic, Acute | 1 | 1996 | 2 | 0.130 |
Why?
|
Neoplasm Proteins | 1 | 1996 | 50 | 0.130 |
Why?
|
Aspartic Acid | 2 | 2015 | 9 | 0.130 |
Why?
|
Tryptophan | 1 | 2015 | 8 | 0.130 |
Why?
|
Mammals | 3 | 2022 | 23 | 0.120 |
Why?
|
Phagocytosis | 2 | 2009 | 40 | 0.120 |
Why?
|
Leukemia, Lymphocytic, Chronic, B-Cell | 1 | 2014 | 12 | 0.120 |
Why?
|
Protein Binding | 3 | 2015 | 118 | 0.120 |
Why?
|
Lipid Bilayers | 3 | 1997 | 50 | 0.120 |
Why?
|
Hematologic Neoplasms | 1 | 2014 | 14 | 0.120 |
Why?
|
Ion Pumps | 1 | 1994 | 1 | 0.110 |
Why?
|
Binding, Competitive | 2 | 2007 | 19 | 0.110 |
Why?
|
Structural Homology, Protein | 1 | 2013 | 4 | 0.110 |
Why?
|
Enzyme Activation | 4 | 2010 | 105 | 0.110 |
Why?
|
Basophils | 2 | 2010 | 6 | 0.100 |
Why?
|
Protein Kinase C | 2 | 2014 | 48 | 0.100 |
Why?
|
Glucose | 1 | 2011 | 54 | 0.090 |
Why?
|
Phospholipases A | 2 | 2006 | 6 | 0.090 |
Why?
|
Epithelium | 3 | 1995 | 20 | 0.090 |
Why?
|
Proton-Motive Force | 2 | 2021 | 3 | 0.090 |
Why?
|
Superoxides | 4 | 2003 | 17 | 0.090 |
Why?
|
Hydrophobic and Hydrophilic Interactions | 2 | 2021 | 8 | 0.090 |
Why?
|
Receptors, Antigen, B-Cell | 1 | 2010 | 2 | 0.090 |
Why?
|
Threonine | 1 | 2009 | 8 | 0.080 |
Why?
|
Leukocytes | 1 | 2009 | 36 | 0.080 |
Why?
|
Electric Stimulation | 3 | 2000 | 48 | 0.080 |
Why?
|
Arginine | 2 | 2022 | 15 | 0.080 |
Why?
|
Models, Biological | 3 | 2021 | 292 | 0.080 |
Why?
|
Rimantadine | 1 | 1989 | 1 | 0.080 |
Why?
|
Phosphatidylcholines | 1 | 1989 | 6 | 0.080 |
Why?
|
Erythrocyte Membrane | 1 | 1989 | 3 | 0.080 |
Why?
|
Adamantane | 1 | 1989 | 2 | 0.080 |
Why?
|
Phospholipids | 1 | 1989 | 10 | 0.080 |
Why?
|
Immunoglobulin E | 1 | 2008 | 10 | 0.080 |
Why?
|
NADPH Oxidase 2 | 3 | 2002 | 3 | 0.080 |
Why?
|
Microglia | 2 | 2000 | 136 | 0.080 |
Why?
|
Buffers | 2 | 1999 | 8 | 0.080 |
Why?
|
Hypersensitivity | 1 | 2008 | 40 | 0.070 |
Why?
|
Static Electricity | 2 | 2021 | 31 | 0.070 |
Why?
|
Temperature | 3 | 2010 | 56 | 0.070 |
Why?
|
Cells, Cultured | 4 | 2011 | 505 | 0.070 |
Why?
|
Species Specificity | 2 | 1998 | 34 | 0.070 |
Why?
|
Electric Conductivity | 3 | 2011 | 56 | 0.070 |
Why?
|
Cell Line | 4 | 2010 | 262 | 0.070 |
Why?
|
Granulocytes | 1 | 2006 | 15 | 0.070 |
Why?
|
Large-Conductance Calcium-Activated Potassium Channels | 1 | 2006 | 1 | 0.070 |
Why?
|
Blood Bactericidal Activity | 1 | 2006 | 2 | 0.070 |
Why?
|
Gene Expression Regulation | 1 | 2008 | 269 | 0.070 |
Why?
|
Biophysical Phenomena | 2 | 1996 | 25 | 0.060 |
Why?
|
Oxygen Consumption | 2 | 2003 | 37 | 0.060 |
Why?
|
Biophysics | 2 | 1996 | 28 | 0.060 |
Why?
|
Dose-Response Relationship, Drug | 2 | 2006 | 330 | 0.060 |
Why?
|
Microscopy, Confocal | 3 | 2010 | 84 | 0.060 |
Why?
|
Intracellular Membranes | 1 | 2004 | 19 | 0.060 |
Why?
|
Protein Structure, Tertiary | 2 | 2013 | 53 | 0.050 |
Why?
|
Cytosol | 1 | 2022 | 41 | 0.050 |
Why?
|
Carcinogens | 3 | 2009 | 8 | 0.050 |
Why?
|
Phosphorylation | 2 | 2014 | 134 | 0.050 |
Why?
|
Ion Transport | 3 | 2000 | 25 | 0.050 |
Why?
|
Stimulation, Chemical | 1 | 2001 | 8 | 0.050 |
Why?
|
Adult | 5 | 2009 | 7516 | 0.050 |
Why?
|
Mutation, Missense | 2 | 2013 | 24 | 0.050 |
Why?
|
Electromagnetic Fields | 1 | 2021 | 5 | 0.050 |
Why?
|
Algorithms | 2 | 2003 | 357 | 0.050 |
Why?
|
Potassium Channels, Inwardly Rectifying | 1 | 2000 | 5 | 0.040 |
Why?
|
Potassium Channels, Voltage-Gated | 1 | 2000 | 7 | 0.040 |
Why?
|
Potassium Channels | 1 | 2000 | 25 | 0.040 |
Why?
|
Chlorides | 3 | 2006 | 20 | 0.040 |
Why?
|
Cell Line, Tumor | 2 | 2014 | 229 | 0.040 |
Why?
|
Gene Knockout Techniques | 1 | 2020 | 7 | 0.040 |
Why?
|
Heterografts | 1 | 2020 | 13 | 0.040 |
Why?
|
Metals, Heavy | 1 | 2000 | 6 | 0.040 |
Why?
|
Electrochemistry | 1 | 2000 | 42 | 0.040 |
Why?
|
Gene Knockdown Techniques | 1 | 2020 | 37 | 0.040 |
Why?
|
CRISPR-Cas Systems | 1 | 2020 | 9 | 0.040 |
Why?
|
Hydrogen Peroxide | 1 | 2020 | 44 | 0.040 |
Why?
|
RNA, Small Interfering | 1 | 2020 | 70 | 0.040 |
Why?
|
Transforming Growth Factor beta | 1 | 2000 | 85 | 0.040 |
Why?
|
Solubility | 1 | 1999 | 26 | 0.040 |
Why?
|
Proteins | 1 | 2000 | 64 | 0.040 |
Why?
|
Cell Movement | 1 | 2020 | 76 | 0.040 |
Why?
|
Ions | 2 | 2015 | 41 | 0.040 |
Why?
|
Amino Acids | 1 | 2019 | 15 | 0.040 |
Why?
|
Cryopreservation | 1 | 2019 | 16 | 0.040 |
Why?
|
Gene Expression Regulation, Neoplastic | 1 | 2020 | 106 | 0.040 |
Why?
|
Up-Regulation | 1 | 2000 | 166 | 0.040 |
Why?
|
Benzopyrans | 2 | 2009 | 7 | 0.040 |
Why?
|
Immunohistochemistry | 1 | 2020 | 349 | 0.040 |
Why?
|
Isotonic Solutions | 2 | 2011 | 9 | 0.040 |
Why?
|
Mice, Knockout | 2 | 2010 | 298 | 0.040 |
Why?
|
Maleimides | 2 | 2009 | 6 | 0.040 |
Why?
|
Indoles | 2 | 2009 | 34 | 0.040 |
Why?
|
Enzyme Inhibitors | 2 | 2009 | 114 | 0.040 |
Why?
|
Male | 4 | 2004 | 14168 | 0.040 |
Why?
|
N-Formylmethionine Leucyl-Phenylalanine | 2 | 2008 | 11 | 0.040 |
Why?
|
Fluorescent Dyes | 2 | 2009 | 34 | 0.040 |
Why?
|
Hematoporphyrins | 1 | 1997 | 1 | 0.030 |
Why?
|
Mass Spectrometry | 1 | 2017 | 36 | 0.030 |
Why?
|
Diffusion | 1 | 1996 | 23 | 0.030 |
Why?
|
Tumor Cells, Cultured | 1 | 1996 | 115 | 0.030 |
Why?
|
Signal Transduction | 2 | 2010 | 417 | 0.030 |
Why?
|
Cell Differentiation | 1 | 1996 | 129 | 0.030 |
Why?
|
Zinc Compounds | 2 | 2006 | 3 | 0.030 |
Why?
|
Macrophages | 1 | 1996 | 101 | 0.030 |
Why?
|
Egtazic Acid | 1 | 1995 | 11 | 0.030 |
Why?
|
Tritium | 1 | 2015 | 7 | 0.030 |
Why?
|
Molecular Conformation | 1 | 2015 | 8 | 0.030 |
Why?
|
Water | 1 | 2015 | 25 | 0.030 |
Why?
|
Protein Isoforms | 1 | 2014 | 45 | 0.030 |
Why?
|
Amphibians | 1 | 1994 | 1 | 0.030 |
Why?
|
Vertebrates | 1 | 1994 | 1 | 0.030 |
Why?
|
Amiloride | 1 | 1994 | 4 | 0.030 |
Why?
|
Mathematics | 2 | 1997 | 31 | 0.030 |
Why?
|
Carrier Proteins | 1 | 1994 | 103 | 0.030 |
Why?
|
Sodium | 1 | 1994 | 50 | 0.030 |
Why?
|
Granulomatous Disease, Chronic | 2 | 2005 | 5 | 0.030 |
Why?
|
Phylogeny | 1 | 2013 | 40 | 0.030 |
Why?
|
Potassium | 2 | 2004 | 42 | 0.030 |
Why?
|
Open Reading Frames | 1 | 2011 | 9 | 0.020 |
Why?
|
Mutant Proteins | 1 | 2011 | 6 | 0.020 |
Why?
|
Sucrose | 1 | 2011 | 17 | 0.020 |
Why?
|
Osmolar Concentration | 1 | 2011 | 19 | 0.020 |
Why?
|
Substrate Specificity | 1 | 2011 | 20 | 0.020 |
Why?
|
Lysine | 1 | 2011 | 12 | 0.020 |
Why?
|
Leukocytes, Mononuclear | 1 | 2011 | 54 | 0.020 |
Why?
|
Permeability | 1 | 2011 | 110 | 0.020 |
Why?
|
Protein Interaction Domains and Motifs | 1 | 2010 | 5 | 0.020 |
Why?
|
Protein Multimerization | 1 | 2010 | 14 | 0.020 |
Why?
|
Protein Subunits | 1 | 2010 | 18 | 0.020 |
Why?
|
Structure-Activity Relationship | 1 | 2010 | 35 | 0.020 |
Why?
|
Green Fluorescent Proteins | 1 | 2010 | 22 | 0.020 |
Why?
|
Dimerization | 1 | 2010 | 19 | 0.020 |
Why?
|
Oncogene Protein v-akt | 1 | 2010 | 8 | 0.020 |
Why?
|
Syk Kinase | 1 | 2010 | 9 | 0.020 |
Why?
|
Protein-Tyrosine Kinases | 1 | 2010 | 13 | 0.020 |
Why?
|
Immunoblotting | 1 | 2010 | 53 | 0.020 |
Why?
|
Protein Kinase C-delta | 1 | 2009 | 9 | 0.020 |
Why?
|
Amino Acid Substitution | 1 | 2009 | 23 | 0.020 |
Why?
|
Transfection | 1 | 2010 | 111 | 0.020 |
Why?
|
Naphthols | 1 | 2009 | 3 | 0.020 |
Why?
|
Rhodamines | 1 | 2009 | 4 | 0.020 |
Why?
|
Intracellular Signaling Peptides and Proteins | 1 | 2010 | 51 | 0.020 |
Why?
|
Mitochondria | 1 | 2010 | 66 | 0.020 |
Why?
|
Cell Aggregation | 1 | 1989 | 1 | 0.020 |
Why?
|
Erythrocyte Deformability | 1 | 1989 | 1 | 0.020 |
Why?
|
Membrane Fluidity | 1 | 1989 | 7 | 0.020 |
Why?
|
Erythrocytes | 1 | 1989 | 20 | 0.020 |
Why?
|
Lipids | 1 | 1989 | 47 | 0.020 |
Why?
|
Antibodies, Anti-Idiotypic | 1 | 2008 | 7 | 0.020 |
Why?
|
Histamine | 1 | 2008 | 6 | 0.020 |
Why?
|
Proton Pump Inhibitors | 1 | 2008 | 13 | 0.020 |
Why?
|
Okadaic Acid | 1 | 2006 | 5 | 0.020 |
Why?
|
Arachidonic Acids | 1 | 2006 | 7 | 0.020 |
Why?
|
Group IV Phospholipases A2 | 1 | 2006 | 5 | 0.020 |
Why?
|
Mice, SCID | 1 | 2006 | 45 | 0.020 |
Why?
|
Mice, Inbred BALB C | 1 | 2006 | 101 | 0.020 |
Why?
|
Staphylococcus aureus | 1 | 2006 | 64 | 0.020 |
Why?
|
Mice, Inbred C57BL | 1 | 2006 | 420 | 0.020 |
Why?
|
Acids | 1 | 2004 | 2 | 0.010 |
Why?
|
Fluoresceins | 1 | 2004 | 5 | 0.010 |
Why?
|
Female | 1 | 2019 | 14520 | 0.010 |
Why?
|
Transgenes | 1 | 2001 | 12 | 0.010 |
Why?
|
Kv1.3 Potassium Channel | 1 | 2000 | 1 | 0.010 |
Why?
|
Delayed Rectifier Potassium Channels | 1 | 2000 | 1 | 0.010 |
Why?
|
Mice, Inbred Strains | 1 | 2000 | 25 | 0.010 |
Why?
|
Neurotoxins | 1 | 2000 | 15 | 0.010 |
Why?
|
Animals, Newborn | 1 | 2000 | 39 | 0.010 |
Why?
|
Reverse Transcriptase Polymerase Chain Reaction | 1 | 2000 | 134 | 0.010 |
Why?
|
RNA, Messenger | 1 | 2000 | 290 | 0.010 |
Why?
|
Picrates | 1 | 1997 | 1 | 0.010 |
Why?
|
Adsorption | 1 | 1997 | 7 | 0.010 |
Why?
|
Surface Properties | 1 | 1997 | 140 | 0.010 |
Why?
|
Light | 1 | 1997 | 57 | 0.010 |
Why?
|
Electricity | 1 | 1990 | 8 | 0.010 |
Why?
|