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L Ornstein

Showing results (161-170 of 233) with videos related to

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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.
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.
Journal of Medicinal Chemistry|December 8, 1995
(3SR,4aRS,6SR,8aRS)-6-(1H-tetrazol-5-yl)decahydroisoquinoline-3-carboxylic acid, a novel, competitive, systemically active NMDA and AMPA receptor antagonistP L Ornstein, M B Arnold, N K Allen, et al.
Neuropharmacology|December 16, 1998
Actions of kainate and AMPA selective glutamate receptor ligands on nociceptive processing in the spinal cordM J Procter, A K Houghton, E S Faber, et al.
Journal of Medicinal Chemistry|August 21, 1992
NMDA antagonist activity of (+/-)-(2SR,4RS)-4-(1H-tetrazol-5-ylmethyl)piperidine-2-carboxylic acid resides with the (-)-2R,4S-isomerP L Ornstein, D D Schoepp, M B Arnold, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Heteroatom-substitution as a strategy for increasing the potency of competitive NMDA antagonistsP L Ornstein, M B Arnold, W H Lunn, et al.
Neuropharmacology|December 16, 1998
Decahydroisoquinolines: novel competitive AMPA/kainate antagonists with neuroprotective effects in global cerebral ischaemiaM J O'Neill, A Bond, P L Ornstein, et al.
Molecular Pharmacology|April 1, 1996
Pharmacological discrimination of GluR5 and GluR6 kainate receptor subtypes by (3S,4aR,6R,8aR)-6-[2-(1(2)H-tetrazole-5-yl)ethyl]decahyd roisdoquinoline-3 carboxylic-acidR Bleakman, D D Schoepp, B Ballyk, et al.
Military Medicine|March 27, 2001
Treatment of severe thrombocytopenia in alloimmunized, transfusion-refractory patientsD L Ornstein, K L Mortara, M B Smith, et al.
Pageof 24

Showing results (161-170 of 233) with videos related to

Sort By:
Pageof 24
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.
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.
Journal of Medicinal Chemistry|December 8, 1995
(3SR,4aRS,6SR,8aRS)-6-(1H-tetrazol-5-yl)decahydroisoquinoline-3-carboxylic acid, a novel, competitive, systemically active NMDA and AMPA receptor antagonistP L Ornstein, M B Arnold, N K Allen, et al.
Neuropharmacology|December 16, 1998
Actions of kainate and AMPA selective glutamate receptor ligands on nociceptive processing in the spinal cordM J Procter, A K Houghton, E S Faber, et al.
Journal of Medicinal Chemistry|August 21, 1992
NMDA antagonist activity of (+/-)-(2SR,4RS)-4-(1H-tetrazol-5-ylmethyl)piperidine-2-carboxylic acid resides with the (-)-2R,4S-isomerP L Ornstein, D D Schoepp, M B Arnold, et al.
Bioorganic & Medicinal Chemistry Letters|January 1, 1999
Heteroatom-substitution as a strategy for increasing the potency of competitive NMDA antagonistsP L Ornstein, M B Arnold, W H Lunn, et al.
Neuropharmacology|December 16, 1998
Decahydroisoquinolines: novel competitive AMPA/kainate antagonists with neuroprotective effects in global cerebral ischaemiaM J O'Neill, A Bond, P L Ornstein, et al.
Molecular Pharmacology|April 1, 1996
Pharmacological discrimination of GluR5 and GluR6 kainate receptor subtypes by (3S,4aR,6R,8aR)-6-[2-(1(2)H-tetrazole-5-yl)ethyl]decahyd roisdoquinoline-3 carboxylic-acidR Bleakman, D D Schoepp, B Ballyk, et al.
Military Medicine|March 27, 2001
Treatment of severe thrombocytopenia in alloimmunized, transfusion-refractory patientsD L Ornstein, K L Mortara, M B Smith, et al.
Pageof 24