Concepts (132)
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?
|
|---|
| Retina | 29 | 2020 | 289 | 3.590 |
Why?
|
| Zinc | 17 | 2014 | 131 | 3.310 |
Why?
|
| Electroretinography | 10 | 2020 | 21 | 1.160 |
Why?
|
| Presynaptic Terminals | 3 | 2013 | 54 | 0.920 |
Why?
|
| Histidine | 7 | 2013 | 43 | 0.910 |
Why?
|
| Retinal Rod Photoreceptor Cells | 4 | 2008 | 17 | 0.770 |
Why?
|
| Chelating Agents | 5 | 2013 | 52 | 0.640 |
Why?
|
| Photoreceptor Cells | 7 | 2020 | 39 | 0.430 |
Why?
|
| Connexins | 2 | 2004 | 28 | 0.420 |
Why?
|
| Light | 7 | 2020 | 185 | 0.420 |
Why?
|
| Carrier Proteins | 2 | 2007 | 321 | 0.420 |
Why?
|
| Oocytes | 2 | 2004 | 149 | 0.400 |
Why?
|
| Animals | 36 | 2014 | 16992 | 0.390 |
Why?
|
| Retinal Cone Photoreceptor Cells | 1 | 2013 | 31 | 0.380 |
Why?
|
| Membrane Proteins | 2 | 2007 | 561 | 0.370 |
Why?
|
| Dark Adaptation | 4 | 2020 | 17 | 0.330 |
Why?
|
| Calcium | 2 | 2013 | 491 | 0.330 |
Why?
|
| Cell Survival | 1 | 2013 | 945 | 0.320 |
Why?
|
| gamma-Aminobutyric Acid | 6 | 2001 | 81 | 0.280 |
Why?
|
| Excitatory Amino Acid Agonists | 3 | 2013 | 43 | 0.280 |
Why?
|
| Photoreceptor Cells, Vertebrate | 2 | 2020 | 33 | 0.270 |
Why?
|
| Xenopus | 2 | 2004 | 48 | 0.260 |
Why?
|
| Receptors, GABA | 3 | 2002 | 28 | 0.250 |
Why?
|
| Ion Channel Gating | 1 | 2004 | 82 | 0.220 |
Why?
|
| Neurons | 7 | 2004 | 1263 | 0.210 |
Why?
|
| Adaptation, Ocular | 3 | 2007 | 12 | 0.210 |
Why?
|
| Cycloleucine | 1 | 2003 | 2 | 0.200 |
Why?
|
| Gap Junctions | 1 | 2003 | 49 | 0.200 |
Why?
|
| Turtles | 4 | 1991 | 31 | 0.190 |
Why?
|
| Microscopy, Fluorescence | 3 | 2013 | 256 | 0.190 |
Why?
|
| Patch-Clamp Techniques | 5 | 2003 | 228 | 0.190 |
Why?
|
| Glutamic Acid | 2 | 2013 | 131 | 0.190 |
Why?
|
| Membrane Potentials | 6 | 2003 | 222 | 0.180 |
Why?
|
| Glycine | 1 | 2001 | 47 | 0.170 |
Why?
|
| Visual Pathways | 1 | 2001 | 40 | 0.170 |
Why?
|
| Serotonin | 2 | 1998 | 123 | 0.170 |
Why?
|
| Kainic Acid | 2 | 2013 | 48 | 0.150 |
Why?
|
| Zimeldine | 1 | 1998 | 1 | 0.140 |
Why?
|
| N-Methylaspartate | 1 | 1998 | 59 | 0.140 |
Why?
|
| Excitatory Amino Acid Antagonists | 1 | 1998 | 92 | 0.140 |
Why?
|
| Fluorescent Dyes | 2 | 2013 | 182 | 0.130 |
Why?
|
| Picrotoxin | 5 | 2003 | 14 | 0.130 |
Why?
|
| Neurons, Afferent | 1 | 1996 | 44 | 0.130 |
Why?
|
| Potassium | 2 | 1998 | 109 | 0.120 |
Why?
|
| Afferent Pathways | 1 | 1996 | 43 | 0.120 |
Why?
|
| Fishes | 4 | 1996 | 73 | 0.120 |
Why?
|
| Cation Transport Proteins | 2 | 2007 | 35 | 0.120 |
Why?
|
| Dose-Response Relationship, Drug | 2 | 2013 | 1124 | 0.120 |
Why?
|
| Vision, Ocular | 2 | 1991 | 43 | 0.120 |
Why?
|
| Membrane Transport Proteins | 2 | 2007 | 100 | 0.120 |
Why?
|
| Retinal Neurons | 1 | 2014 | 2 | 0.110 |
Why?
|
| Electrophysiological Phenomena | 1 | 2014 | 20 | 0.110 |
Why?
|
| Glutamine | 1 | 2014 | 36 | 0.110 |
Why?
|
| Trace Elements | 1 | 2014 | 35 | 0.110 |
Why?
|
| GABA Antagonists | 3 | 2003 | 29 | 0.110 |
Why?
|
| Eye | 2 | 2013 | 77 | 0.100 |
Why?
|
| Zebrafish | 2 | 2007 | 146 | 0.100 |
Why?
|
| Necrosis | 1 | 2013 | 54 | 0.100 |
Why?
|
| Ambystoma | 1 | 2013 | 4 | 0.100 |
Why?
|
| Xanthenes | 1 | 2013 | 11 | 0.100 |
Why?
|
| Data Interpretation, Statistical | 1 | 2013 | 125 | 0.100 |
Why?
|
| Calcium Channels, L-Type | 1 | 2013 | 20 | 0.100 |
Why?
|
| Ethylenediamines | 1 | 2013 | 8 | 0.100 |
Why?
|
| Aniline Compounds | 1 | 2013 | 28 | 0.100 |
Why?
|
| Calcium Channel Blockers | 1 | 2013 | 55 | 0.100 |
Why?
|
| Synaptic Vesicles | 2 | 1991 | 31 | 0.090 |
Why?
|
| Neurotransmitter Agents | 1 | 1991 | 69 | 0.090 |
Why?
|
| Synapses | 4 | 1981 | 185 | 0.080 |
Why?
|
| Rats | 2 | 2007 | 3735 | 0.070 |
Why?
|
| Feedback, Physiological | 1 | 2008 | 32 | 0.070 |
Why?
|
| Cells, Cultured | 2 | 2003 | 1621 | 0.070 |
Why?
|
| Bicuculline | 3 | 2002 | 18 | 0.060 |
Why?
|
| Homeostasis | 1 | 2007 | 192 | 0.060 |
Why?
|
| Ocular Physiological Phenomena | 2 | 1978 | 9 | 0.060 |
Why?
|
| Rats, Long-Evans | 1 | 2005 | 108 | 0.060 |
Why?
|
| Potassium Channels, Voltage-Gated | 1 | 2004 | 13 | 0.060 |
Why?
|
| Immunoenzyme Techniques | 1 | 2004 | 114 | 0.050 |
Why?
|
| Mice | 2 | 2007 | 6644 | 0.050 |
Why?
|
| Neuroglia | 2 | 1996 | 133 | 0.050 |
Why?
|
| Dendrites | 2 | 2001 | 57 | 0.050 |
Why?
|
| Drug Interactions | 1 | 2003 | 150 | 0.050 |
Why?
|
| Chloride Channels | 1 | 2002 | 4 | 0.050 |
Why?
|
| Microscopy, Interference | 1 | 2001 | 1 | 0.050 |
Why?
|
| Isoquinolines | 1 | 2001 | 55 | 0.040 |
Why?
|
| Cell Separation | 1 | 2001 | 94 | 0.040 |
Why?
|
| Cell Membrane | 4 | 2004 | 403 | 0.040 |
Why?
|
| Neuroprotective Agents | 1 | 2003 | 269 | 0.040 |
Why?
|
| Electric Fish | 2 | 1989 | 9 | 0.040 |
Why?
|
| Mice, Inbred C57BL | 1 | 2004 | 1869 | 0.040 |
Why?
|
| Photic Stimulation | 4 | 1989 | 125 | 0.040 |
Why?
|
| Pargyline | 1 | 1998 | 11 | 0.040 |
Why?
|
| Fluoxetine | 1 | 1998 | 15 | 0.040 |
Why?
|
| Monoamine Oxidase Inhibitors | 1 | 1998 | 28 | 0.040 |
Why?
|
| Aspartic Acid | 1 | 1998 | 51 | 0.040 |
Why?
|
| Organ Culture Techniques | 1 | 1998 | 101 | 0.040 |
Why?
|
| Evoked Potentials | 1 | 1997 | 91 | 0.030 |
Why?
|
| Kynurenic Acid | 1 | 1996 | 9 | 0.030 |
Why?
|
| Protein Kinase C | 1 | 1996 | 124 | 0.030 |
Why?
|
| Female | 2 | 2005 | 24698 | 0.030 |
Why?
|
| Nerve Tissue Proteins | 1 | 1996 | 386 | 0.030 |
Why?
|
| Exocytosis | 1 | 1991 | 49 | 0.020 |
Why?
|
| Sensory Thresholds | 1 | 1991 | 13 | 0.020 |
Why?
|
| Catfishes | 1 | 1991 | 10 | 0.020 |
Why?
|
| Mathematics | 1 | 1991 | 57 | 0.020 |
Why?
|
| Feedback | 2 | 1981 | 56 | 0.020 |
Why?
|
| Humans | 1 | 2014 | 43102 | 0.020 |
Why?
|
| Cytoplasm | 2 | 1981 | 154 | 0.020 |
Why?
|
| Receptors, GABA-A | 2 | 1997 | 65 | 0.020 |
Why?
|
| Action Potentials | 2 | 1989 | 246 | 0.020 |
Why?
|
| Reaction Time | 1 | 1987 | 157 | 0.020 |
Why?
|
| Physiology | 1 | 1985 | 17 | 0.010 |
Why?
|
| Tetraethylammonium | 1 | 2004 | 6 | 0.010 |
Why?
|
| Biological Transport, Active | 1 | 2004 | 27 | 0.010 |
Why?
|
| Male | 1 | 2004 | 23409 | 0.010 |
Why?
|
| Time Factors | 2 | 1984 | 1857 | 0.010 |
Why?
|
| Models, Biological | 1 | 1985 | 712 | 0.010 |
Why?
|
| Curare | 1 | 1981 | 1 | 0.010 |
Why?
|
| Signal Transduction | 2 | 2004 | 2157 | 0.010 |
Why?
|
| Electric Stimulation | 1 | 1981 | 186 | 0.010 |
Why?
|
| Tubocurarine | 1 | 1978 | 3 | 0.010 |
Why?
|
| Cockroaches | 1 | 1978 | 8 | 0.010 |
Why?
|
| Synaptic Transmission | 1 | 1978 | 149 | 0.010 |
Why?
|
| Axons | 1 | 1997 | 117 | 0.010 |
Why?
|
| Models, Neurological | 1 | 1978 | 136 | 0.010 |
Why?
|
| Ion Transport | 1 | 1996 | 23 | 0.010 |
Why?
|
| Electric Conductivity | 1 | 1994 | 55 | 0.010 |
Why?
|
| Microelectrodes | 1 | 1972 | 22 | 0.010 |
Why?
|
| Tetrodotoxin | 1 | 1972 | 22 | 0.010 |
Why?
|
| Microscopy, Electron | 1 | 1972 | 210 | 0.010 |
Why?
|
| Electrodes | 1 | 1989 | 59 | 0.000 |
Why?
|
| Electrophysiology | 1 | 1988 | 138 | 0.000 |
Why?
|
| Electron Probe Microanalysis | 1 | 1979 | 13 | 0.000 |
Why?
|