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P L Herrling

Showing results (21-30 of 28) with videos related to

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Neuroscience|January 1, 1989
Differential effects of (D)- and (L)-homocysteic acid on the membrane potential of cat caudate neurons in situP L Herrling, J Maeder, C L Meier, et al.
Neuroscience Letters|August 31, 1988
6,7-Dichloro-3-hydroxy-2-quinoxalinecarboxylic acid is a relatively potent antagonist at NMDA and kainate receptorsP Frey, D Berney, P L Herrling, et al.
Neuroscience Letters|January 14, 1987
Muscle relaxant and anticonvulsant activity of 3-((+/-)-2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid, a novel N-methyl-D-aspartate antagonist, in rodentsL Turski, T Klockgether, K H Sontag, et al.
Journal of Ethnopharmacology|November 1, 1996
Extracts from rhizomes of Cyperus articulatus (Cyperaceae) displace [3H]CGP39653 and [3H]glycine binding from cortical membranes and selectively inhibit NMDA receptor-mediated neurotransmissionE N Bum, C L Meier, S Urwyler, et al.
Neuroscience|January 1, 1995
Thalamocortical and corticocortical excitatory postsynaptic potentials mediated by excitatory amino acid receptors in the cat motor cortex in vivoT E Salt, C L Meier, N Seno, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 1, 1986
In vitro release and electrophysiological effects in situ of homocysteic acid, an endogenous N-methyl-(D)-aspartic acid agonist, in the mammalian striatumK Q Do, P L Herrling, P Streit, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
Homocysteic acid, an endogenous agonist of NMDA-receptor: release, neuroactivity and localizationM Cuénod, K Q Do, P L Herrling, et al.
Brain Research|September 10, 1986
CPP, a new potent and selective NMDA antagonist. Depression of central neuron responses, affinity for [3H]D-AP5 binding sites on brain membranes and anticonvulsant activityJ Davies, R H Evans, P L Herrling, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Neuroscience|January 1, 1989
Differential effects of (D)- and (L)-homocysteic acid on the membrane potential of cat caudate neurons in situP L Herrling, J Maeder, C L Meier, et al.
Neuroscience Letters|August 31, 1988
6,7-Dichloro-3-hydroxy-2-quinoxalinecarboxylic acid is a relatively potent antagonist at NMDA and kainate receptorsP Frey, D Berney, P L Herrling, et al.
Neuroscience Letters|January 14, 1987
Muscle relaxant and anticonvulsant activity of 3-((+/-)-2-carboxypiperazin-4-yl)-propyl-1-phosphonic acid, a novel N-methyl-D-aspartate antagonist, in rodentsL Turski, T Klockgether, K H Sontag, et al.
Journal of Ethnopharmacology|November 1, 1996
Extracts from rhizomes of Cyperus articulatus (Cyperaceae) displace [3H]CGP39653 and [3H]glycine binding from cortical membranes and selectively inhibit NMDA receptor-mediated neurotransmissionE N Bum, C L Meier, S Urwyler, et al.
Neuroscience|January 1, 1995
Thalamocortical and corticocortical excitatory postsynaptic potentials mediated by excitatory amino acid receptors in the cat motor cortex in vivoT E Salt, C L Meier, N Seno, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 1, 1986
In vitro release and electrophysiological effects in situ of homocysteic acid, an endogenous N-methyl-(D)-aspartic acid agonist, in the mammalian striatumK Q Do, P L Herrling, P Streit, et al.
Advances in Experimental Medicine and Biology|January 1, 1986
Homocysteic acid, an endogenous agonist of NMDA-receptor: release, neuroactivity and localizationM Cuénod, K Q Do, P L Herrling, et al.
Brain Research|September 10, 1986
CPP, a new potent and selective NMDA antagonist. Depression of central neuron responses, affinity for [3H]D-AP5 binding sites on brain membranes and anticonvulsant activityJ Davies, R H Evans, P L Herrling, et al.
Pageof 3