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 | 42 | 3.320 |
Why?
|
| Microscopy, Confocal | 15 | 2016 | 335 | 2.390 |
Why?
|
| Neurons | 27 | 2019 | 1979 | 2.350 |
Why?
|
| Hippocampus | 29 | 2015 | 806 | 1.870 |
Why?
|
| Calcium | 22 | 2019 | 1010 | 1.620 |
Why?
|
| Microscopy, Fluorescence | 8 | 2009 | 303 | 1.260 |
Why?
|
| Acoustics | 5 | 2010 | 20 | 1.170 |
Why?
|
| Imaging, Three-Dimensional | 7 | 2017 | 371 | 1.120 |
Why?
|
| Synaptic Transmission | 13 | 2014 | 299 | 1.040 |
Why?
|
| Nerve Net | 8 | 2016 | 254 | 0.970 |
Why?
|
| Membrane Potentials | 13 | 2015 | 293 | 0.940 |
Why?
|
| Action Potentials | 10 | 2014 | 476 | 0.910 |
Why?
|
| Presynaptic Terminals | 8 | 2014 | 74 | 0.890 |
Why?
|
| Image Processing, Computer-Assisted | 6 | 2015 | 587 | 0.850 |
Why?
|
| Synapses | 12 | 2015 | 425 | 0.820 |
Why?
|
| Visual Cortex | 3 | 2019 | 125 | 0.690 |
Why?
|
| Calcium Signaling | 5 | 2015 | 243 | 0.640 |
Why?
|
| Image Enhancement | 4 | 2007 | 159 | 0.640 |
Why?
|
| Neurotransmitter Agents | 5 | 2010 | 134 | 0.600 |
Why?
|
| In Vitro Techniques | 20 | 2016 | 808 | 0.590 |
Why?
|
| Fluorescent Dyes | 12 | 2015 | 246 | 0.580 |
Why?
|
| Molecular Imaging | 1 | 2019 | 58 | 0.560 |
Why?
|
| Neural Inhibition | 4 | 2016 | 107 | 0.510 |
Why?
|
| Rats, Sprague-Dawley | 14 | 2010 | 1105 | 0.510 |
Why?
|
| Calcium Channels | 6 | 1999 | 143 | 0.510 |
Why?
|
| Rats | 18 | 2010 | 3370 | 0.500 |
Why?
|
| Equipment Design | 10 | 2010 | 512 | 0.470 |
Why?
|
| Voltage-Sensitive Dye Imaging | 2 | 2015 | 8 | 0.470 |
Why?
|
| Animals | 50 | 2019 | 33912 | 0.460 |
Why?
|
| Optical Imaging | 2 | 2015 | 76 | 0.440 |
Why?
|
| Nervous System | 1 | 2015 | 114 | 0.430 |
Why?
|
| Photic Stimulation | 2 | 2014 | 227 | 0.390 |
Why?
|
| Equipment Failure Analysis | 7 | 2010 | 79 | 0.390 |
Why?
|
| Cytological Techniques | 1 | 2013 | 18 | 0.380 |
Why?
|
| Models, Neurological | 5 | 2009 | 212 | 0.370 |
Why?
|
| Microscopy | 1 | 2013 | 118 | 0.370 |
Why?
|
| Calcium Channel Blockers | 8 | 2004 | 107 | 0.350 |
Why?
|
| Sensitivity and Specificity | 10 | 2010 | 2085 | 0.340 |
Why?
|
| Acoustic Stimulation | 2 | 2010 | 91 | 0.330 |
Why?
|
| Brain Mapping | 3 | 2016 | 384 | 0.320 |
Why?
|
| Fura-2 | 5 | 2002 | 10 | 0.320 |
Why?
|
| Photolysis | 1 | 2009 | 10 | 0.310 |
Why?
|
| Guinea Pigs | 11 | 2006 | 147 | 0.300 |
Why?
|
| Excitatory Postsynaptic Potentials | 4 | 2003 | 101 | 0.300 |
Why?
|
| Microscopy, Video | 2 | 2006 | 15 | 0.300 |
Why?
|
| Pyramidal Cells | 5 | 2010 | 151 | 0.300 |
Why?
|
| Lenses | 1 | 2009 | 5 | 0.300 |
Why?
|
| Refractometry | 1 | 2009 | 9 | 0.290 |
Why?
|
| Lighting | 1 | 2009 | 19 | 0.290 |
Why?
|
| Receptors, Metabotropic Glutamate | 2 | 2014 | 47 | 0.290 |
Why?
|
| 4-Aminopyridine | 4 | 2001 | 28 | 0.280 |
Why?
|
| Evoked Potentials | 7 | 2001 | 113 | 0.270 |
Why?
|
| Electric Stimulation | 9 | 2010 | 234 | 0.270 |
Why?
|
| Interneurons | 2 | 2016 | 146 | 0.260 |
Why?
|
| Reproducibility of Results | 8 | 2010 | 2904 | 0.260 |
Why?
|
| Microscopy, Interference | 1 | 2006 | 5 | 0.250 |
Why?
|
| Electrophysiology | 6 | 1999 | 241 | 0.250 |
Why?
|
| Microvilli | 1 | 2006 | 61 | 0.250 |
Why?
|
| Subcellular Fractions | 1 | 2006 | 89 | 0.250 |
Why?
|
| Phantoms, Imaging | 3 | 2019 | 142 | 0.250 |
Why?
|
| Brain | 4 | 2007 | 3175 | 0.240 |
Why?
|
| Nanostructures | 1 | 2006 | 69 | 0.240 |
Why?
|
| Olfactory Bulb | 2 | 2016 | 82 | 0.230 |
Why?
|
| Cells, Cultured | 7 | 2010 | 2885 | 0.230 |
Why?
|
| Dendrites | 5 | 2015 | 180 | 0.220 |
Why?
|
| Optics and Photonics | 3 | 2005 | 107 | 0.210 |
Why?
|
| Receptors, Adrenergic, beta-2 | 1 | 2004 | 57 | 0.210 |
Why?
|
| Calcium Channels, L-Type | 1 | 2004 | 50 | 0.210 |
Why?
|
| Dendritic Spines | 1 | 2004 | 56 | 0.210 |
Why?
|
| Receptors, GABA-A | 2 | 2001 | 57 | 0.190 |
Why?
|
| Receptors, Opioid, mu | 1 | 2003 | 34 | 0.190 |
Why?
|
| Receptors, Presynaptic | 2 | 1999 | 4 | 0.190 |
Why?
|
| Artifacts | 1 | 2003 | 100 | 0.180 |
Why?
|
| Peptides | 5 | 1997 | 708 | 0.180 |
Why?
|
| Zinc | 2 | 2014 | 128 | 0.180 |
Why?
|
| Indicators and Reagents | 2 | 1998 | 43 | 0.170 |
Why?
|
| Pattern Recognition, Automated | 2 | 2015 | 40 | 0.170 |
Why?
|
| Neuronal Plasticity | 2 | 2016 | 283 | 0.170 |
Why?
|
| Potassium Channels | 2 | 1999 | 154 | 0.160 |
Why?
|
| Optogenetics | 3 | 2016 | 71 | 0.160 |
Why?
|
| Adenosine | 3 | 1999 | 116 | 0.160 |
Why?
|
| Patch-Clamp Techniques | 4 | 2016 | 271 | 0.160 |
Why?
|
| Intracellular Fluid | 2 | 2000 | 19 | 0.150 |
Why?
|
| omega-Conotoxin GVIA | 5 | 1997 | 7 | 0.150 |
Why?
|
| Receptors, GABA-B | 2 | 1997 | 10 | 0.150 |
Why?
|
| Glycine | 2 | 2014 | 156 | 0.140 |
Why?
|
| Mice | 11 | 2019 | 18301 | 0.140 |
Why?
|
| Time Factors | 8 | 2015 | 6196 | 0.140 |
Why?
|
| Receptors, Neuropeptide Y | 1 | 1997 | 8 | 0.130 |
Why?
|
| Receptors, Muscarinic | 1 | 1997 | 10 | 0.130 |
Why?
|
| Organic Chemicals | 4 | 1999 | 58 | 0.130 |
Why?
|
| Neuropeptide Y | 1 | 1997 | 34 | 0.130 |
Why?
|
| Hair Cells, Auditory, Outer | 2 | 2009 | 67 | 0.130 |
Why?
|
| Calcium Channels, N-Type | 1 | 1997 | 47 | 0.130 |
Why?
|
| Spectrometry, Fluorescence | 3 | 2006 | 79 | 0.130 |
Why?
|
| Computer-Aided Design | 2 | 2009 | 18 | 0.120 |
Why?
|
| Association Learning | 1 | 2016 | 20 | 0.120 |
Why?
|
| Smell | 1 | 2016 | 70 | 0.120 |
Why?
|
| Pyridinium Compounds | 4 | 2006 | 27 | 0.120 |
Why?
|
| Feasibility Studies | 1 | 2019 | 824 | 0.120 |
Why?
|
| Mossy Fibers, Hippocampal | 1 | 2014 | 9 | 0.110 |
Why?
|
| Neurogenesis | 1 | 2016 | 206 | 0.110 |
Why?
|
| Image Interpretation, Computer-Assisted | 2 | 2007 | 229 | 0.110 |
Why?
|
| Cyclopropanes | 1 | 2014 | 70 | 0.110 |
Why?
|
| Light | 2 | 2016 | 166 | 0.110 |
Why?
|
| Cerebral Cortex | 1 | 2017 | 445 | 0.100 |
Why?
|
| Excitatory Amino Acid Antagonists | 3 | 2014 | 83 | 0.100 |
Why?
|
| Microelectrodes | 3 | 2010 | 37 | 0.100 |
Why?
|
| Pyramidal Tracts | 1 | 1994 | 33 | 0.100 |
Why?
|
| Long-Term Potentiation | 1 | 1994 | 103 | 0.100 |
Why?
|
| 6-Cyano-7-nitroquinoxaline-2,3-dione | 3 | 2014 | 15 | 0.100 |
Why?
|
| Visual Perception | 1 | 2014 | 128 | 0.100 |
Why?
|
| Green Fluorescent Proteins | 2 | 2016 | 358 | 0.100 |
Why?
|
| omega-Agatoxin IVA | 3 | 1997 | 4 | 0.090 |
Why?
|
| Spider Venoms | 3 | 1997 | 6 | 0.090 |
Why?
|
| Mice, Transgenic | 3 | 2016 | 2326 | 0.090 |
Why?
|
| Anticonvulsants | 1 | 2014 | 363 | 0.090 |
Why?
|
| Nerve Tissue Proteins | 1 | 1997 | 1075 | 0.090 |
Why?
|
| Epilepsy | 2 | 1999 | 876 | 0.080 |
Why?
|
| KATP Channels | 1 | 2010 | 11 | 0.080 |
Why?
|
| Hair Cells, Auditory, Inner | 1 | 2010 | 18 | 0.080 |
Why?
|
| CA3 Region, Hippocampal | 1 | 2010 | 17 | 0.080 |
Why?
|
| Biopolymers | 1 | 2009 | 17 | 0.080 |
Why?
|
| Computer Simulation | 3 | 2009 | 674 | 0.080 |
Why?
|
| Cochlea | 1 | 2010 | 85 | 0.070 |
Why?
|
| Models, Chemical | 1 | 2009 | 78 | 0.070 |
Why?
|
| Optical Fibers | 1 | 2009 | 17 | 0.070 |
Why?
|
| Electroencephalography | 1 | 1994 | 863 | 0.070 |
Why?
|
| Pollen | 1 | 2009 | 39 | 0.070 |
Why?
|
| Rhodopsin | 1 | 2009 | 60 | 0.070 |
Why?
|
| GABA Antagonists | 2 | 2001 | 17 | 0.070 |
Why?
|
| 2-Amino-5-phosphonovalerate | 2 | 2001 | 14 | 0.070 |
Why?
|
| Ion Channel Gating | 2 | 1999 | 119 | 0.070 |
Why?
|
| Mammals | 2 | 1999 | 253 | 0.060 |
Why?
|
| Recombinant Fusion Proteins | 1 | 2009 | 688 | 0.060 |
Why?
|
| Baclofen | 2 | 1997 | 44 | 0.060 |
Why?
|
| Odorants | 2 | 2016 | 43 | 0.060 |
Why?
|
| Particle Size | 1 | 2006 | 135 | 0.060 |
Why?
|
| Protein Isoforms | 2 | 2004 | 423 | 0.060 |
Why?
|
| Receptors, Purinergic P1 | 2 | 1997 | 12 | 0.060 |
Why?
|
| Luminescent Measurements | 1 | 2006 | 55 | 0.060 |
Why?
|
| Systems Integration | 1 | 2006 | 24 | 0.060 |
Why?
|
| Channelrhodopsins | 2 | 2016 | 10 | 0.060 |
Why?
|
| Retina | 1 | 2009 | 425 | 0.060 |
Why?
|
| Kinetics | 3 | 2000 | 1088 | 0.060 |
Why?
|
| Calcium Channel Agonists | 1 | 2004 | 11 | 0.050 |
Why?
|
| Adrenergic beta-2 Receptor Agonists | 1 | 2004 | 50 | 0.050 |
Why?
|
| Male | 9 | 2016 | 64957 | 0.050 |
Why?
|
| Cyclic AMP-Dependent Protein Kinases | 1 | 2004 | 157 | 0.050 |
Why?
|
| Glutamic Acid | 2 | 2015 | 200 | 0.050 |
Why?
|
| Scattering, Radiation | 1 | 2003 | 52 | 0.050 |
Why?
|
| Resorcinols | 1 | 2002 | 7 | 0.050 |
Why?
|
| Receptor, Metabotropic Glutamate 5 | 1 | 2002 | 11 | 0.050 |
Why?
|
| Microinjections | 1 | 2002 | 38 | 0.050 |
Why?
|
| Time | 1 | 2002 | 92 | 0.050 |
Why?
|
| Rats, Wistar | 2 | 2014 | 299 | 0.040 |
Why?
|
| Picrotoxin | 1 | 2001 | 14 | 0.040 |
Why?
|
| Artificial Intelligence | 1 | 2007 | 369 | 0.040 |
Why?
|
| Software | 2 | 1997 | 733 | 0.040 |
Why?
|
| Neural Pathways | 2 | 2001 | 270 | 0.040 |
Why?
|
| Organ Culture Techniques | 1 | 2001 | 140 | 0.040 |
Why?
|
| Polyethyleneimine | 1 | 2000 | 10 | 0.040 |
Why?
|
| Humans | 8 | 2017 | 131163 | 0.040 |
Why?
|
| Biocompatible Materials | 1 | 2000 | 108 | 0.040 |
Why?
|
| Tetraethylammonium Compounds | 1 | 1999 | 3 | 0.040 |
Why?
|
| Electrochemistry | 1 | 1999 | 25 | 0.040 |
Why?
|
| Biophysical Phenomena | 1 | 1999 | 39 | 0.040 |
Why?
|
| Biophysics | 1 | 1999 | 47 | 0.040 |
Why?
|
| Radiometry | 1 | 1999 | 49 | 0.040 |
Why?
|
| Evaluation Studies as Topic | 1 | 1999 | 225 | 0.040 |
Why?
|
| Styrenes | 1 | 1998 | 5 | 0.040 |
Why?
|
| Lasers | 1 | 1999 | 111 | 0.040 |
Why?
|
| Transfection | 1 | 2000 | 962 | 0.040 |
Why?
|
| Coloring Agents | 1 | 1998 | 71 | 0.030 |
Why?
|
| Peptide YY | 1 | 1997 | 20 | 0.030 |
Why?
|
| Carbachol | 1 | 1997 | 12 | 0.030 |
Why?
|
| Ion Transport | 1 | 1997 | 48 | 0.030 |
Why?
|
| Atropine | 1 | 1997 | 28 | 0.030 |
Why?
|
| Automation, Laboratory | 1 | 2017 | 17 | 0.030 |
Why?
|
| Ions | 1 | 1997 | 25 | 0.030 |
Why?
|
| Receptors, Neurotransmitter | 1 | 1997 | 20 | 0.030 |
Why?
|
| Mitochondria | 1 | 2003 | 785 | 0.030 |
Why?
|
| GTP-Binding Proteins | 1 | 1997 | 156 | 0.030 |
Why?
|
| Cadmium | 1 | 1997 | 33 | 0.030 |
Why?
|
| Forecasting | 1 | 1998 | 351 | 0.030 |
Why?
|
| LIM-Homeodomain Proteins | 1 | 2016 | 28 | 0.030 |
Why?
|
| Thy-1 Antigens | 1 | 2016 | 18 | 0.030 |
Why?
|
| Inhibitory Postsynaptic Potentials | 1 | 2016 | 29 | 0.030 |
Why?
|
| Ion Channels | 1 | 1997 | 195 | 0.030 |
Why?
|
| Fluorometry | 1 | 1995 | 27 | 0.030 |
Why?
|
| Nifedipine | 1 | 1994 | 22 | 0.030 |
Why?
|
| Synaptic Vesicles | 1 | 2014 | 63 | 0.030 |
Why?
|
| Analysis of Variance | 1 | 2016 | 928 | 0.030 |
Why?
|
| CA1 Region, Hippocampal | 1 | 2015 | 68 | 0.030 |
Why?
|
| Xanthines | 1 | 1994 | 10 | 0.030 |
Why?
|
| Seizures | 1 | 2000 | 890 | 0.030 |
Why?
|
| Culture Techniques | 1 | 1994 | 73 | 0.030 |
Why?
|
| Peptide Fragments | 1 | 1997 | 687 | 0.030 |
Why?
|
| Statistics, Nonparametric | 1 | 2014 | 423 | 0.030 |
Why?
|
| Quinoxalines | 1 | 1994 | 39 | 0.030 |
Why?
|
| Signal Transduction | 2 | 2014 | 4686 | 0.030 |
Why?
|
| Species Specificity | 1 | 1994 | 470 | 0.020 |
Why?
|
| Wakefulness | 1 | 2014 | 103 | 0.020 |
Why?
|
| Homeodomain Proteins | 1 | 2016 | 555 | 0.020 |
Why?
|
| Regression Analysis | 1 | 1994 | 761 | 0.020 |
Why?
|
| Single-Cell Analysis | 1 | 2015 | 350 | 0.020 |
Why?
|
| Machine Learning | 1 | 2015 | 387 | 0.020 |
Why?
|
| Databases, Factual | 1 | 2015 | 1240 | 0.020 |
Why?
|
| Tolbutamide | 1 | 2010 | 5 | 0.020 |
Why?
|
| Muscle Spindles | 1 | 1989 | 5 | 0.020 |
Why?
|
| Forelimb | 1 | 1989 | 11 | 0.020 |
Why?
|
| Fluoresceins | 1 | 2010 | 30 | 0.020 |
Why?
|
| Cell Membrane Permeability | 1 | 2010 | 64 | 0.020 |
Why?
|
| Diffusion | 1 | 2009 | 56 | 0.020 |
Why?
|
| Hydrogen-Ion Concentration | 2 | 2000 | 437 | 0.020 |
Why?
|
| Motor Neurons | 1 | 1989 | 131 | 0.020 |
Why?
|
| Capillaries | 1 | 2008 | 63 | 0.020 |
Why?
|
| Transcription Factors | 1 | 2016 | 2406 | 0.020 |
Why?
|
| Neurophysiology | 1 | 1986 | 22 | 0.010 |
Why?
|
| Data Interpretation, Statistical | 1 | 2007 | 226 | 0.010 |
Why?
|
| Research Design | 1 | 2010 | 716 | 0.010 |
Why?
|
| Mice, Inbred C57BL | 1 | 2014 | 4738 | 0.010 |
Why?
|
| Monitoring, Physiologic | 1 | 1986 | 376 | 0.010 |
Why?
|
| Synapsins | 1 | 2003 | 6 | 0.010 |
Why?
|
| Anions | 1 | 2003 | 15 | 0.010 |
Why?
|
| Microscopy, Electron | 1 | 2003 | 305 | 0.010 |
Why?
|
| Cyclosporine | 1 | 2003 | 132 | 0.010 |
Why?
|
| Female | 3 | 2016 | 70963 | 0.010 |
Why?
|
| Buffers | 1 | 2000 | 27 | 0.010 |
Why?
|
| DNA, Recombinant | 1 | 2000 | 71 | 0.010 |
Why?
|
| Deoxyribonucleases | 1 | 2000 | 22 | 0.010 |
Why?
|
| Materials Testing | 1 | 2000 | 73 | 0.010 |
Why?
|
| Ammonium Chloride | 1 | 2000 | 9 | 0.010 |
Why?
|
| Benzopyrans | 1 | 2000 | 19 | 0.010 |
Why?
|
| Rhodamines | 1 | 2000 | 22 | 0.010 |
Why?
|
| Naphthols | 1 | 2000 | 11 | 0.010 |
Why?
|
| Propionates | 1 | 2000 | 31 | 0.010 |
Why?
|
| Dentate Gyrus | 1 | 2000 | 37 | 0.010 |
Why?
|
| Algorithms | 1 | 2007 | 1680 | 0.010 |
Why?
|
| Lysosomes | 1 | 2000 | 268 | 0.010 |
Why?
|
| Cell Line | 1 | 2000 | 2552 | 0.010 |
Why?
|
| Cats | 1 | 1989 | 117 | 0.000 |
Why?
|