Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

D Lodge

Showing results (101-110 of 135) with videos related to

Pageof 14
Sort By:
Science (New York, N.Y.)|August 5, 1988
Quinoxalinediones: potent competitive non-NMDA glutamate receptor antagonistsT Honoré, S N Davies, J Drejer, et al.
Neuropharmacology|December 16, 1998
The GluR5 subtype of kainate receptor regulates excitatory synaptic transmission in areas CA1 and CA3 of the rat hippocampusM Vignes, V R Clarke, M J Parry, et al.
Journal of Neuroscience Methods|October 12, 1999
Measurement of calcium flux through ionotropic glutamate receptors using Cytostar-T scintillating microplatesA Cushing, M J Price-Jones, R Graves, et al.
Neuroscience Letters|October 9, 1999
LY379268, a potent and selective Group II metabotropic glutamate receptor agonist, is neuroprotective in gerbil global, but not focal, cerebral ischaemiaA Bond, N Ragumoorthy, J A Monn, et al.
Life Sciences|June 30, 1986
Is Metaphit a phencyclidine antagonist? Studies with ketamine, phencyclidine and N-methylaspartateS N Davies, J Church, J Blake, et al.
Neurochemical Research|April 1, 1980
Cyclobutane analogs of GABAR D Allan, D R Curtis, P M Headley, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1990
Pharmacological characterization of LY233053: a structurally novel tetrazole-substituted competitive N-methyl-D-aspartic acid antagonist with a short duration of actionD D Schoepp, P L Ornstein, J D Leander, et al.
Journal of Neurochemistry|April 1, 1997
Irreversible inhibition of high-affinity [3H]kainate binding by a novel photoactivatable analogue: (2'S,3'S,4'R)-2'-carboxy-4'-(2-diazo-1-oxo-3, 3,3-trifluoropropyl)-3'-pyrrolidinyl acetateC L Willis, D A Wacker, R D Bartlett, et al.
Neuron|November 24, 2001
A critical role of a facilitatory presynaptic kainate receptor in mossy fiber LTPS E Lauri, Z A Bortolotto, D Bleakman, et al.
Journal of Medicinal Chemistry|January 1, 1991
4-(Tetrazolylalkyl)piperidine-2-carboxylic acids. Potent and selective N-methyl-D-aspartic acid receptor antagonists with a short duration of actionP L Ornstein, D D Schoepp, M B Arnold, et al.
Pageof 14

Showing results (101-110 of 135) with videos related to

Sort By:
Pageof 14
Science (New York, N.Y.)|August 5, 1988
Quinoxalinediones: potent competitive non-NMDA glutamate receptor antagonistsT Honoré, S N Davies, J Drejer, et al.
Neuropharmacology|December 16, 1998
The GluR5 subtype of kainate receptor regulates excitatory synaptic transmission in areas CA1 and CA3 of the rat hippocampusM Vignes, V R Clarke, M J Parry, et al.
Journal of Neuroscience Methods|October 12, 1999
Measurement of calcium flux through ionotropic glutamate receptors using Cytostar-T scintillating microplatesA Cushing, M J Price-Jones, R Graves, et al.
Neuroscience Letters|October 9, 1999
LY379268, a potent and selective Group II metabotropic glutamate receptor agonist, is neuroprotective in gerbil global, but not focal, cerebral ischaemiaA Bond, N Ragumoorthy, J A Monn, et al.
Life Sciences|June 30, 1986
Is Metaphit a phencyclidine antagonist? Studies with ketamine, phencyclidine and N-methylaspartateS N Davies, J Church, J Blake, et al.
Neurochemical Research|April 1, 1980
Cyclobutane analogs of GABAR D Allan, D R Curtis, P M Headley, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 1, 1990
Pharmacological characterization of LY233053: a structurally novel tetrazole-substituted competitive N-methyl-D-aspartic acid antagonist with a short duration of actionD D Schoepp, P L Ornstein, J D Leander, et al.
Journal of Neurochemistry|April 1, 1997
Irreversible inhibition of high-affinity [3H]kainate binding by a novel photoactivatable analogue: (2'S,3'S,4'R)-2'-carboxy-4'-(2-diazo-1-oxo-3, 3,3-trifluoropropyl)-3'-pyrrolidinyl acetateC L Willis, D A Wacker, R D Bartlett, et al.
Neuron|November 24, 2001
A critical role of a facilitatory presynaptic kainate receptor in mossy fiber LTPS E Lauri, Z A Bortolotto, D Bleakman, et al.
Journal of Medicinal Chemistry|January 1, 1991
4-(Tetrazolylalkyl)piperidine-2-carboxylic acids. Potent and selective N-methyl-D-aspartic acid receptor antagonists with a short duration of actionP L Ornstein, D D Schoepp, M B Arnold, et al.
Pageof 14