 Nathan Schoppa
Concepts (157)
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?
|
|---|
| Olfactory Bulb | 28 | 2025 | 98 | 9.920 |
Why?
| | Neural Inhibition | 11 | 2019 | 177 | 2.100 |
Why?
| | Smell | 6 | 2025 | 128 | 1.920 |
Why?
| | Neurons | 13 | 2019 | 1619 | 1.850 |
Why?
| | Synapses | 6 | 2025 | 428 | 1.760 |
Why?
| | Gap Junctions | 3 | 2025 | 63 | 1.550 |
Why?
| | Glutamic Acid | 6 | 2025 | 256 | 1.480 |
Why?
| | Action Potentials | 10 | 2021 | 499 | 1.390 |
Why?
| | Olfactory Receptor Neurons | 5 | 2021 | 42 | 1.380 |
Why?
| | Receptors, Metabotropic Glutamate | 3 | 2021 | 38 | 1.280 |
Why?
| | Olfactory Pathways | 5 | 2013 | 39 | 1.120 |
Why?
| | Dendrites | 7 | 2025 | 104 | 1.110 |
Why?
| | Connexins | 2 | 2025 | 52 | 1.050 |
Why?
| | Rats, Sprague-Dawley | 18 | 2025 | 2520 | 1.040 |
Why?
| | Excitatory Postsynaptic Potentials | 6 | 2014 | 124 | 0.950 |
Why?
| | Rats | 21 | 2025 | 5629 | 0.940 |
Why?
| | Nerve Net | 6 | 2013 | 281 | 0.900 |
Why?
| | gamma-Aminobutyric Acid | 6 | 2014 | 198 | 0.780 |
Why?
| | Patch-Clamp Techniques | 14 | 2016 | 293 | 0.770 |
Why?
| | Fragile X Syndrome | 1 | 2023 | 118 | 0.770 |
Why?
| | Odorants | 7 | 2025 | 116 | 0.750 |
Why?
| | Synaptic Transmission | 5 | 2015 | 295 | 0.700 |
Why?
| | Potassium Channels | 6 | 2001 | 149 | 0.680 |
Why?
| | Animals | 38 | 2025 | 37663 | 0.660 |
Why?
| | Sensory Receptor Cells | 3 | 2021 | 101 | 0.660 |
Why?
| | Receptors, Adrenergic | 2 | 2010 | 21 | 0.610 |
Why?
| | Interneurons | 6 | 2019 | 124 | 0.590 |
Why?
| | Adrenergic alpha-Agonists | 3 | 2012 | 28 | 0.540 |
Why?
| | In Vitro Techniques | 10 | 2017 | 1093 | 0.530 |
Why?
| | Signal Transduction | 3 | 2025 | 5144 | 0.510 |
Why?
| | Norepinephrine | 3 | 2012 | 193 | 0.500 |
Why?
| | Receptors, AMPA | 4 | 2006 | 143 | 0.450 |
Why?
| | Piriform Cortex | 1 | 2014 | 3 | 0.440 |
Why?
| | Mice, Knockout | 4 | 2025 | 3068 | 0.410 |
Why?
| | Ion Channel Gating | 6 | 2001 | 92 | 0.370 |
Why?
| | Receptors, N-Methyl-D-Aspartate | 4 | 2001 | 222 | 0.350 |
Why?
| | Electric Stimulation | 7 | 2010 | 281 | 0.340 |
Why?
| | Membrane Potentials | 10 | 2009 | 284 | 0.330 |
Why?
| | Biological Clocks | 1 | 2010 | 46 | 0.320 |
Why?
| | Olfactory Perception | 1 | 2009 | 16 | 0.310 |
Why?
| | Inhibitory Postsynaptic Potentials | 3 | 2017 | 47 | 0.310 |
Why?
| | Excitatory Amino Acid Antagonists | 6 | 2010 | 105 | 0.280 |
Why?
| | Receptors, Kainic Acid | 1 | 2006 | 10 | 0.260 |
Why?
| | Cerebral Cortex | 2 | 2015 | 461 | 0.250 |
Why?
| | Axons | 2 | 2006 | 198 | 0.250 |
Why?
| | Male | 12 | 2025 | 69789 | 0.240 |
Why?
| | Brain Mapping | 1 | 2009 | 532 | 0.240 |
Why?
| | Mice | 8 | 2025 | 18055 | 0.230 |
Why?
| | GABA Antagonists | 4 | 2010 | 35 | 0.230 |
Why?
| | Electrophysiology | 5 | 2008 | 217 | 0.230 |
Why?
| | Quinoxalines | 4 | 2010 | 67 | 0.230 |
Why?
| | Models, Neurological | 4 | 2009 | 251 | 0.220 |
Why?
| | Neuronal Plasticity | 2 | 2012 | 304 | 0.220 |
Why?
| | Fragile X Mental Retardation Protein | 1 | 2023 | 86 | 0.200 |
Why?
| | GABAergic Neurons | 2 | 2014 | 36 | 0.200 |
Why?
| | Autoreceptors | 1 | 2002 | 4 | 0.200 |
Why?
| | Cholecystokinin | 1 | 2021 | 15 | 0.180 |
Why?
| | Potassium Channels, Calcium-Activated | 1 | 2001 | 11 | 0.180 |
Why?
| | Neurotransmitter Agents | 1 | 2021 | 81 | 0.180 |
Why?
| | Lysine | 2 | 2016 | 292 | 0.170 |
Why?
| | Animals, Newborn | 3 | 2010 | 863 | 0.160 |
Why?
| | Bicuculline | 2 | 2010 | 22 | 0.160 |
Why?
| | Mutation | 4 | 2015 | 4013 | 0.160 |
Why?
| | GABA-A Receptor Antagonists | 3 | 2010 | 19 | 0.160 |
Why?
| | Calcium Signaling | 1 | 2001 | 250 | 0.150 |
Why?
| | Mice, Inbred C57BL | 2 | 2025 | 5887 | 0.150 |
Why?
| | Potassium | 1 | 1999 | 148 | 0.150 |
Why?
| | Female | 8 | 2025 | 75522 | 0.150 |
Why?
| | Kinetics | 5 | 2001 | 1652 | 0.150 |
Why?
| | Organ Culture Techniques | 2 | 2013 | 157 | 0.140 |
Why?
| | Ion Channels | 3 | 1998 | 130 | 0.140 |
Why?
| | Microscopy, Electron | 2 | 2016 | 441 | 0.140 |
Why?
| | Nerve Tissue Proteins | 1 | 2001 | 601 | 0.140 |
Why?
| | 3,3'-Diaminobenzidine | 1 | 2016 | 3 | 0.130 |
Why?
| | N-Methylaspartate | 2 | 2010 | 43 | 0.130 |
Why?
| | Vesicle-Associated Membrane Protein 2 | 1 | 2015 | 14 | 0.120 |
Why?
| | Munc18 Proteins | 1 | 2015 | 24 | 0.120 |
Why?
| | Models, Biological | 3 | 2017 | 1828 | 0.120 |
Why?
| | Oocytes | 4 | 1998 | 179 | 0.120 |
Why?
| | Reproducibility of Results | 1 | 2023 | 3348 | 0.120 |
Why?
| | Exocytosis | 1 | 2015 | 88 | 0.120 |
Why?
| | Microscopy, Fluorescence | 1 | 2016 | 417 | 0.110 |
Why?
| | Mice, Neurologic Mutants | 3 | 1998 | 21 | 0.110 |
Why?
| | Biotransformation | 3 | 1998 | 62 | 0.100 |
Why?
| | Xenopus laevis | 3 | 1998 | 107 | 0.100 |
Why?
| | Disease Models, Animal | 1 | 2023 | 4405 | 0.100 |
Why?
| | Imaging, Three-Dimensional | 1 | 2016 | 567 | 0.100 |
Why?
| | In Situ Hybridization | 1 | 2013 | 320 | 0.090 |
Why?
| | Mice, 129 Strain | 1 | 2012 | 86 | 0.090 |
Why?
| | Brain Waves | 1 | 2012 | 45 | 0.090 |
Why?
| | 2-Amino-5-phosphonovalerate | 2 | 2001 | 10 | 0.080 |
Why?
| | Biophysical Phenomena | 1 | 2010 | 68 | 0.080 |
Why?
| | Valine | 1 | 2010 | 77 | 0.080 |
Why?
| | Pyridazines | 1 | 2010 | 56 | 0.080 |
Why?
| | Calcium | 2 | 2009 | 1187 | 0.080 |
Why?
| | Excitatory Amino Acid Agonists | 2 | 2001 | 41 | 0.080 |
Why?
| | Mice, Transgenic | 1 | 2014 | 2181 | 0.070 |
Why?
| | Probability | 1 | 2009 | 309 | 0.070 |
Why?
| | Electric Conductivity | 2 | 2002 | 86 | 0.070 |
Why?
| | Dose-Response Relationship, Radiation | 1 | 2008 | 144 | 0.070 |
Why?
| | Triazines | 1 | 2008 | 45 | 0.070 |
Why?
| | Chlorides | 1 | 1989 | 138 | 0.070 |
Why?
| | Learning | 1 | 2012 | 437 | 0.070 |
Why?
| | Trachea | 1 | 1989 | 255 | 0.070 |
Why?
| | Piperidines | 1 | 2008 | 216 | 0.060 |
Why?
| | Cytoplasmic Granules | 1 | 2006 | 93 | 0.060 |
Why?
| | Age Factors | 1 | 2012 | 3292 | 0.060 |
Why?
| | Membrane Proteins | 1 | 1989 | 1155 | 0.050 |
Why?
| | Receptors, Odorant | 1 | 2002 | 32 | 0.050 |
Why?
| | Large-Conductance Calcium-Activated Potassium Channels | 1 | 2001 | 11 | 0.050 |
Why?
| | Calcium Channels, N-Type | 1 | 2001 | 10 | 0.050 |
Why?
| | Periodicity | 1 | 2001 | 57 | 0.040 |
Why?
| | Ion Transport | 1 | 2001 | 62 | 0.040 |
Why?
| | Time Factors | 2 | 2009 | 6956 | 0.040 |
Why?
| | Aspartic Acid | 1 | 2001 | 81 | 0.040 |
Why?
| | Macromolecular Substances | 1 | 2001 | 226 | 0.040 |
Why?
| | Neural Pathways | 1 | 2002 | 308 | 0.040 |
Why?
| | Sodium Channel Blockers | 1 | 1999 | 25 | 0.040 |
Why?
| | 4-Aminopyridine | 1 | 1999 | 30 | 0.040 |
Why?
| | Potassium Channel Blockers | 1 | 1999 | 47 | 0.040 |
Why?
| | Sodium Channels | 1 | 1999 | 63 | 0.040 |
Why?
| | Feedback | 1 | 1999 | 179 | 0.040 |
Why?
| | Dizocilpine Maleate | 1 | 1998 | 24 | 0.040 |
Why?
| | Magnesium | 1 | 1998 | 157 | 0.030 |
Why?
| | Cycloleucine | 1 | 1997 | 4 | 0.030 |
Why?
| | alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid | 1 | 1997 | 15 | 0.030 |
Why?
| | Tetrodotoxin | 1 | 1997 | 41 | 0.030 |
Why?
| | Adenylyl Cyclases | 1 | 1997 | 63 | 0.030 |
Why?
| | Cadmium | 1 | 1997 | 68 | 0.030 |
Why?
| | Calcium Channels | 1 | 1997 | 156 | 0.030 |
Why?
| | Neuroprotective Agents | 1 | 1997 | 139 | 0.030 |
Why?
| | Cells, Cultured | 2 | 1997 | 4208 | 0.030 |
Why?
| | Membrane Fusion | 1 | 2015 | 41 | 0.030 |
Why?
| | SNARE Proteins | 1 | 2015 | 40 | 0.030 |
Why?
| | Immunoblotting | 1 | 2015 | 310 | 0.030 |
Why?
| | Receptors, Glycine | 1 | 1993 | 5 | 0.030 |
Why?
| | Liposomes | 1 | 2015 | 224 | 0.030 |
Why?
| | Baculoviridae | 1 | 1993 | 44 | 0.030 |
Why?
| | Binding Sites | 1 | 2015 | 1316 | 0.020 |
Why?
| | Epilepsy | 1 | 2015 | 349 | 0.020 |
Why?
| | Humans | 2 | 2023 | 141197 | 0.020 |
Why?
| | DNA Mutational Analysis | 1 | 1992 | 398 | 0.020 |
Why?
| | Structure-Activity Relationship | 1 | 1992 | 579 | 0.020 |
Why?
| | Drosophila melanogaster | 1 | 1992 | 237 | 0.020 |
Why?
| | Chloride Channels | 1 | 1989 | 35 | 0.020 |
Why?
| | Dogs | 1 | 1989 | 427 | 0.020 |
Why?
| | Receptors, GABA-A | 1 | 2001 | 141 | 0.010 |
Why?
| | Chromatography, Affinity | 1 | 1993 | 86 | 0.010 |
Why?
| | DNA, Complementary | 1 | 1993 | 274 | 0.010 |
Why?
| | Electrophoresis, Polyacrylamide Gel | 1 | 1993 | 336 | 0.010 |
Why?
| | Moths | 1 | 1993 | 52 | 0.010 |
Why?
| | Cloning, Molecular | 1 | 1993 | 533 | 0.010 |
Why?
| | Blotting, Western | 1 | 1993 | 1234 | 0.010 |
Why?
| | Cell Membrane | 1 | 1993 | 724 | 0.000 |
Why?
| | Amino Acid Sequence | 1 | 1993 | 2158 | 0.000 |
Why?
| | Molecular Sequence Data | 1 | 1993 | 2929 | 0.000 |
Why?
| | Cell Line | 1 | 1993 | 2885 | 0.000 |
Why?
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