Concepts (242)
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?
|
|---|
| Microscopy, Fluorescence, Multiphoton | 14 | 2019 | 61 | 3.730 |
Why?
|
| Microscopy, Confocal | 15 | 2016 | 659 | 2.470 |
Why?
|
| Neurons | 27 | 2019 | 2451 | 2.410 |
Why?
|
| Hippocampus | 29 | 2015 | 973 | 1.990 |
Why?
|
| Calcium | 22 | 2019 | 1593 | 1.650 |
Why?
|
| Acoustics | 5 | 2010 | 40 | 1.320 |
Why?
|
| Microscopy, Fluorescence | 8 | 2009 | 766 | 1.270 |
Why?
|
| Synaptic Transmission | 13 | 2014 | 476 | 1.080 |
Why?
|
| Nerve Net | 8 | 2016 | 273 | 1.080 |
Why?
|
| Imaging, Three-Dimensional | 7 | 2017 | 907 | 1.060 |
Why?
|
| Membrane Potentials | 13 | 2015 | 452 | 1.030 |
Why?
|
| Action Potentials | 10 | 2014 | 598 | 0.980 |
Why?
|
| Presynaptic Terminals | 8 | 2014 | 121 | 0.970 |
Why?
|
| Synapses | 12 | 2015 | 556 | 0.860 |
Why?
|
| Visual Cortex | 3 | 2019 | 131 | 0.780 |
Why?
|
| Calcium Signaling | 5 | 2015 | 282 | 0.710 |
Why?
|
| Image Processing, Computer-Assisted | 6 | 2015 | 1689 | 0.710 |
Why?
|
| Neurotransmitter Agents | 5 | 2010 | 171 | 0.660 |
Why?
|
| Fluorescent Dyes | 12 | 2015 | 469 | 0.600 |
Why?
|
| In Vitro Techniques | 20 | 2016 | 1716 | 0.590 |
Why?
|
| Image Enhancement | 4 | 2007 | 553 | 0.590 |
Why?
|
| Neural Inhibition | 4 | 2016 | 160 | 0.570 |
Why?
|
| Molecular Imaging | 1 | 2019 | 186 | 0.570 |
Why?
|
| Calcium Channels | 6 | 1999 | 215 | 0.550 |
Why?
|
| Voltage-Sensitive Dye Imaging | 2 | 2015 | 7 | 0.530 |
Why?
|
| Rats, Sprague-Dawley | 14 | 2010 | 2211 | 0.490 |
Why?
|
| Nervous System | 1 | 2015 | 183 | 0.470 |
Why?
|
| Optical Imaging | 2 | 2015 | 158 | 0.470 |
Why?
|
| Equipment Design | 10 | 2010 | 1203 | 0.470 |
Why?
|
| Rats | 18 | 2010 | 6522 | 0.460 |
Why?
|
| Photic Stimulation | 2 | 2014 | 271 | 0.430 |
Why?
|
| Cytological Techniques | 1 | 2013 | 69 | 0.410 |
Why?
|
| Models, Neurological | 5 | 2009 | 240 | 0.410 |
Why?
|
| Equipment Failure Analysis | 7 | 2010 | 327 | 0.410 |
Why?
|
| Microscopy | 1 | 2013 | 188 | 0.400 |
Why?
|
| Animals | 50 | 2019 | 62021 | 0.400 |
Why?
|
| Calcium Channel Blockers | 8 | 2004 | 145 | 0.380 |
Why?
|
| Acoustic Stimulation | 2 | 2010 | 121 | 0.370 |
Why?
|
| Fura-2 | 5 | 2002 | 19 | 0.360 |
Why?
|
| Photolysis | 1 | 2009 | 14 | 0.350 |
Why?
|
| Microscopy, Video | 2 | 2006 | 32 | 0.340 |
Why?
|
| Guinea Pigs | 11 | 2006 | 252 | 0.340 |
Why?
|
| Refractometry | 1 | 2009 | 15 | 0.330 |
Why?
|
| Lenses | 1 | 2009 | 11 | 0.330 |
Why?
|
| Brain Mapping | 3 | 2016 | 624 | 0.330 |
Why?
|
| Lighting | 1 | 2009 | 25 | 0.330 |
Why?
|
| Pyramidal Cells | 5 | 2010 | 172 | 0.330 |
Why?
|
| 4-Aminopyridine | 4 | 2001 | 43 | 0.320 |
Why?
|
| Receptors, Metabotropic Glutamate | 2 | 2014 | 64 | 0.320 |
Why?
|
| Excitatory Postsynaptic Potentials | 4 | 2003 | 253 | 0.320 |
Why?
|
| Interneurons | 2 | 2016 | 151 | 0.300 |
Why?
|
| Sensitivity and Specificity | 10 | 2010 | 5159 | 0.290 |
Why?
|
| Evoked Potentials | 7 | 2001 | 229 | 0.290 |
Why?
|
| Microscopy, Interference | 1 | 2006 | 16 | 0.280 |
Why?
|
| Electric Stimulation | 9 | 2010 | 492 | 0.280 |
Why?
|
| Microvilli | 1 | 2006 | 87 | 0.280 |
Why?
|
| Electrophysiology | 6 | 1999 | 363 | 0.280 |
Why?
|
| Subcellular Fractions | 1 | 2006 | 210 | 0.270 |
Why?
|
| Nanostructures | 1 | 2006 | 101 | 0.260 |
Why?
|
| Olfactory Bulb | 2 | 2016 | 121 | 0.250 |
Why?
|
| Brain | 4 | 2007 | 4209 | 0.250 |
Why?
|
| Dendrites | 5 | 2015 | 206 | 0.240 |
Why?
|
| Dendritic Spines | 1 | 2004 | 58 | 0.230 |
Why?
|
| Optics and Photonics | 3 | 2005 | 165 | 0.230 |
Why?
|
| Calcium Channels, L-Type | 1 | 2004 | 78 | 0.230 |
Why?
|
| Receptors, Adrenergic, beta-2 | 1 | 2004 | 125 | 0.230 |
Why?
|
| Reproducibility of Results | 8 | 2010 | 6188 | 0.230 |
Why?
|
| Receptors, GABA-A | 2 | 2001 | 83 | 0.220 |
Why?
|
| Receptors, Presynaptic | 2 | 1999 | 27 | 0.210 |
Why?
|
| Cells, Cultured | 7 | 2010 | 5690 | 0.210 |
Why?
|
| Receptors, Opioid, mu | 1 | 2003 | 96 | 0.210 |
Why?
|
| Indicators and Reagents | 2 | 1998 | 137 | 0.190 |
Why?
|
| Phantoms, Imaging | 3 | 2019 | 1330 | 0.190 |
Why?
|
| Zinc | 2 | 2014 | 195 | 0.190 |
Why?
|
| Optogenetics | 3 | 2016 | 52 | 0.190 |
Why?
|
| Pattern Recognition, Automated | 2 | 2015 | 122 | 0.190 |
Why?
|
| Neuronal Plasticity | 2 | 2016 | 328 | 0.180 |
Why?
|
| Potassium Channels | 2 | 1999 | 194 | 0.180 |
Why?
|
| Artifacts | 1 | 2003 | 538 | 0.180 |
Why?
|
| Intracellular Fluid | 2 | 2000 | 49 | 0.170 |
Why?
|
| Peptides | 5 | 1997 | 1504 | 0.170 |
Why?
|
| Patch-Clamp Techniques | 4 | 2016 | 398 | 0.170 |
Why?
|
| omega-Conotoxin GVIA | 5 | 1997 | 10 | 0.170 |
Why?
|
| Adenosine | 3 | 1999 | 297 | 0.170 |
Why?
|
| Receptors, GABA-B | 2 | 1997 | 32 | 0.160 |
Why?
|
| Receptors, Neuropeptide Y | 1 | 1997 | 6 | 0.150 |
Why?
|
| Neuropeptide Y | 1 | 1997 | 49 | 0.150 |
Why?
|
| Hair Cells, Auditory, Outer | 2 | 2009 | 69 | 0.150 |
Why?
|
| Organic Chemicals | 4 | 1999 | 104 | 0.150 |
Why?
|
| Calcium Channels, N-Type | 1 | 1997 | 40 | 0.150 |
Why?
|
| Glycine | 2 | 2014 | 319 | 0.150 |
Why?
|
| Receptors, Muscarinic | 1 | 1997 | 72 | 0.150 |
Why?
|
| Spectrometry, Fluorescence | 3 | 2006 | 206 | 0.140 |
Why?
|
| Association Learning | 1 | 2016 | 27 | 0.140 |
Why?
|
| Computer-Aided Design | 2 | 2009 | 76 | 0.130 |
Why?
|
| Pyridinium Compounds | 4 | 2006 | 64 | 0.130 |
Why?
|
| Smell | 1 | 2016 | 133 | 0.130 |
Why?
|
| Mossy Fibers, Hippocampal | 1 | 2014 | 10 | 0.120 |
Why?
|
| Mice | 11 | 2019 | 35592 | 0.120 |
Why?
|
| Neurogenesis | 1 | 2016 | 240 | 0.120 |
Why?
|
| Time Factors | 8 | 2015 | 12991 | 0.120 |
Why?
|
| Cyclopropanes | 1 | 2014 | 90 | 0.120 |
Why?
|
| Microelectrodes | 3 | 2010 | 55 | 0.120 |
Why?
|
| Light | 2 | 2016 | 279 | 0.110 |
Why?
|
| Pyramidal Tracts | 1 | 1994 | 64 | 0.110 |
Why?
|
| Excitatory Amino Acid Antagonists | 3 | 2014 | 163 | 0.110 |
Why?
|
| Cerebral Cortex | 1 | 2017 | 629 | 0.110 |
Why?
|
| 6-Cyano-7-nitroquinoxaline-2,3-dione | 3 | 2014 | 49 | 0.110 |
Why?
|
| Visual Perception | 1 | 2014 | 150 | 0.110 |
Why?
|
| omega-Agatoxin IVA | 3 | 1997 | 4 | 0.110 |
Why?
|
| Feasibility Studies | 1 | 2019 | 2364 | 0.110 |
Why?
|
| Spider Venoms | 3 | 1997 | 11 | 0.110 |
Why?
|
| Long-Term Potentiation | 1 | 1994 | 180 | 0.100 |
Why?
|
| Image Interpretation, Computer-Assisted | 2 | 2007 | 584 | 0.100 |
Why?
|
| Green Fluorescent Proteins | 2 | 2016 | 692 | 0.100 |
Why?
|
| Anticonvulsants | 1 | 2014 | 443 | 0.100 |
Why?
|
| Epilepsy | 2 | 1999 | 946 | 0.090 |
Why?
|
| KATP Channels | 1 | 2010 | 12 | 0.090 |
Why?
|
| Hair Cells, Auditory, Inner | 1 | 2010 | 24 | 0.090 |
Why?
|
| CA3 Region, Hippocampal | 1 | 2010 | 16 | 0.090 |
Why?
|
| Nerve Tissue Proteins | 1 | 1997 | 1582 | 0.090 |
Why?
|
| Mice, Transgenic | 3 | 2016 | 4222 | 0.090 |
Why?
|
| Biopolymers | 1 | 2009 | 37 | 0.090 |
Why?
|
| Optical Fibers | 1 | 2009 | 39 | 0.080 |
Why?
|
| Cochlea | 1 | 2010 | 118 | 0.080 |
Why?
|
| Models, Chemical | 1 | 2009 | 179 | 0.080 |
Why?
|
| Rhodopsin | 1 | 2009 | 72 | 0.080 |
Why?
|
| Pollen | 1 | 2009 | 46 | 0.080 |
Why?
|
| Electroencephalography | 1 | 1994 | 979 | 0.080 |
Why?
|
| GABA Antagonists | 2 | 2001 | 56 | 0.080 |
Why?
|
| 2-Amino-5-phosphonovalerate | 2 | 2001 | 27 | 0.080 |
Why?
|
| Ion Channel Gating | 2 | 1999 | 151 | 0.070 |
Why?
|
| Computer Simulation | 3 | 2009 | 1573 | 0.070 |
Why?
|
| Mammals | 2 | 1999 | 368 | 0.070 |
Why?
|
| Baclofen | 2 | 1997 | 57 | 0.070 |
Why?
|
| Particle Size | 1 | 2006 | 187 | 0.070 |
Why?
|
| Receptors, Purinergic P1 | 2 | 1997 | 29 | 0.070 |
Why?
|
| Odorants | 2 | 2016 | 80 | 0.070 |
Why?
|
| Channelrhodopsins | 2 | 2016 | 13 | 0.070 |
Why?
|
| Systems Integration | 1 | 2006 | 79 | 0.060 |
Why?
|
| Luminescent Measurements | 1 | 2006 | 158 | 0.060 |
Why?
|
| Retina | 1 | 2009 | 538 | 0.060 |
Why?
|
| Protein Isoforms | 2 | 2004 | 848 | 0.060 |
Why?
|
| Calcium Channel Agonists | 1 | 2004 | 15 | 0.060 |
Why?
|
| Kinetics | 3 | 2000 | 2220 | 0.060 |
Why?
|
| Cyclic AMP-Dependent Protein Kinases | 1 | 2004 | 240 | 0.060 |
Why?
|
| Recombinant Fusion Proteins | 1 | 2009 | 1641 | 0.060 |
Why?
|
| Adrenergic beta-2 Receptor Agonists | 1 | 2004 | 107 | 0.060 |
Why?
|
| Glutamic Acid | 2 | 2015 | 333 | 0.050 |
Why?
|
| Receptor, Metabotropic Glutamate 5 | 1 | 2002 | 21 | 0.050 |
Why?
|
| Microinjections | 1 | 2002 | 107 | 0.050 |
Why?
|
| Resorcinols | 1 | 2002 | 27 | 0.050 |
Why?
|
| Scattering, Radiation | 1 | 2003 | 334 | 0.050 |
Why?
|
| Time | 1 | 2002 | 183 | 0.050 |
Why?
|
| Artificial Intelligence | 1 | 2007 | 435 | 0.050 |
Why?
|
| Picrotoxin | 1 | 2001 | 18 | 0.050 |
Why?
|
| Rats, Wistar | 2 | 2014 | 598 | 0.050 |
Why?
|
| Neural Pathways | 2 | 2001 | 312 | 0.050 |
Why?
|
| Polyethyleneimine | 1 | 2000 | 22 | 0.050 |
Why?
|
| Organ Culture Techniques | 1 | 2001 | 229 | 0.050 |
Why?
|
| Male | 9 | 2016 | 128105 | 0.040 |
Why?
|
| Tetraethylammonium Compounds | 1 | 1999 | 9 | 0.040 |
Why?
|
| Biocompatible Materials | 1 | 2000 | 201 | 0.040 |
Why?
|
| Electrochemistry | 1 | 1999 | 39 | 0.040 |
Why?
|
| Biophysical Phenomena | 1 | 1999 | 117 | 0.040 |
Why?
|
| Styrenes | 1 | 1998 | 6 | 0.040 |
Why?
|
| Biophysics | 1 | 1999 | 117 | 0.040 |
Why?
|
| Software | 2 | 1997 | 1389 | 0.040 |
Why?
|
| Evaluation Studies as Topic | 1 | 1999 | 453 | 0.040 |
Why?
|
| Peptide YY | 1 | 1997 | 21 | 0.040 |
Why?
|
| Lasers | 1 | 1999 | 235 | 0.040 |
Why?
|
| Carbachol | 1 | 1997 | 33 | 0.040 |
Why?
|
| Atropine | 1 | 1997 | 44 | 0.040 |
Why?
|
| Ion Transport | 1 | 1997 | 69 | 0.040 |
Why?
|
| Automation, Laboratory | 1 | 2017 | 21 | 0.040 |
Why?
|
| Coloring Agents | 1 | 1998 | 229 | 0.040 |
Why?
|
| Ions | 1 | 1997 | 58 | 0.040 |
Why?
|
| Receptors, Neurotransmitter | 1 | 1997 | 33 | 0.040 |
Why?
|
| Cadmium | 1 | 1997 | 47 | 0.040 |
Why?
|
| Thy-1 Antigens | 1 | 2016 | 52 | 0.030 |
Why?
|
| LIM-Homeodomain Proteins | 1 | 2016 | 94 | 0.030 |
Why?
|
| Inhibitory Postsynaptic Potentials | 1 | 2016 | 48 | 0.030 |
Why?
|
| GTP-Binding Proteins | 1 | 1997 | 342 | 0.030 |
Why?
|
| Mitochondria | 1 | 2003 | 1300 | 0.030 |
Why?
|
| Humans | 8 | 2017 | 270457 | 0.030 |
Why?
|
| Ion Channels | 1 | 1997 | 238 | 0.030 |
Why?
|
| Fluorometry | 1 | 1995 | 35 | 0.030 |
Why?
|
| Forecasting | 1 | 1998 | 704 | 0.030 |
Why?
|
| Transfection | 1 | 2000 | 3118 | 0.030 |
Why?
|
| Nifedipine | 1 | 1994 | 26 | 0.030 |
Why?
|
| Synaptic Vesicles | 1 | 2014 | 72 | 0.030 |
Why?
|
| CA1 Region, Hippocampal | 1 | 2015 | 77 | 0.030 |
Why?
|
| Xanthines | 1 | 1994 | 31 | 0.030 |
Why?
|
| Culture Techniques | 1 | 1994 | 146 | 0.030 |
Why?
|
| Seizures | 1 | 2000 | 1032 | 0.030 |
Why?
|
| Quinoxalines | 1 | 1994 | 98 | 0.030 |
Why?
|
| Radiometry | 1 | 1999 | 1017 | 0.030 |
Why?
|
| Wakefulness | 1 | 2014 | 157 | 0.030 |
Why?
|
| Species Specificity | 1 | 1994 | 793 | 0.030 |
Why?
|
| Statistics, Nonparametric | 1 | 2014 | 983 | 0.030 |
Why?
|
| Analysis of Variance | 1 | 2016 | 2321 | 0.030 |
Why?
|
| Peptide Fragments | 1 | 1997 | 1309 | 0.020 |
Why?
|
| Machine Learning | 1 | 2015 | 366 | 0.020 |
Why?
|
| Homeodomain Proteins | 1 | 2016 | 1122 | 0.020 |
Why?
|
| Single-Cell Analysis | 1 | 2015 | 553 | 0.020 |
Why?
|
| Regression Analysis | 1 | 1994 | 1570 | 0.020 |
Why?
|
| Tolbutamide | 1 | 2010 | 8 | 0.020 |
Why?
|
| Muscle Spindles | 1 | 1989 | 9 | 0.020 |
Why?
|
| Forelimb | 1 | 1989 | 23 | 0.020 |
Why?
|
| Fluoresceins | 1 | 2010 | 74 | 0.020 |
Why?
|
| Cell Membrane Permeability | 1 | 2010 | 124 | 0.020 |
Why?
|
| Diffusion | 1 | 2009 | 96 | 0.020 |
Why?
|
| Motor Neurons | 1 | 1989 | 146 | 0.020 |
Why?
|
| Hydrogen-Ion Concentration | 2 | 2000 | 613 | 0.020 |
Why?
|
| Capillaries | 1 | 2008 | 98 | 0.020 |
Why?
|
| Signal Transduction | 2 | 2014 | 12104 | 0.020 |
Why?
|
| Databases, Factual | 1 | 2015 | 2234 | 0.020 |
Why?
|
| Neurophysiology | 1 | 1986 | 22 | 0.020 |
Why?
|
| Data Interpretation, Statistical | 1 | 2007 | 485 | 0.010 |
Why?
|
| Synapsins | 1 | 2003 | 7 | 0.010 |
Why?
|
| Anions | 1 | 2003 | 35 | 0.010 |
Why?
|
| Monitoring, Physiologic | 1 | 1986 | 533 | 0.010 |
Why?
|
| Mice, Inbred C57BL | 1 | 2014 | 7093 | 0.010 |
Why?
|
| Research Design | 1 | 2010 | 1573 | 0.010 |
Why?
|
| Transcription Factors | 1 | 2016 | 5438 | 0.010 |
Why?
|
| Microscopy, Electron | 1 | 2003 | 703 | 0.010 |
Why?
|
| Cyclosporine | 1 | 2003 | 292 | 0.010 |
Why?
|
| Buffers | 1 | 2000 | 43 | 0.010 |
Why?
|
| Deoxyribonucleases | 1 | 2000 | 55 | 0.010 |
Why?
|
| DNA, Recombinant | 1 | 2000 | 161 | 0.010 |
Why?
|
| Ammonium Chloride | 1 | 2000 | 14 | 0.010 |
Why?
|
| Materials Testing | 1 | 2000 | 119 | 0.010 |
Why?
|
| Rhodamines | 1 | 2000 | 48 | 0.010 |
Why?
|
| Benzopyrans | 1 | 2000 | 42 | 0.010 |
Why?
|
| Propionates | 1 | 2000 | 78 | 0.010 |
Why?
|
| Naphthols | 1 | 2000 | 27 | 0.010 |
Why?
|
| Dentate Gyrus | 1 | 2000 | 78 | 0.010 |
Why?
|
| Lysosomes | 1 | 2000 | 345 | 0.010 |
Why?
|
| Female | 3 | 2016 | 148644 | 0.010 |
Why?
|
| Algorithms | 1 | 2007 | 3919 | 0.010 |
Why?
|
| Cell Line | 1 | 2000 | 5339 | 0.010 |
Why?
|
| Cats | 1 | 1989 | 167 | 0.010 |
Why?
|