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Bioorganic & Medicinal Chemistry Letters
|
August 22, 2001
Discovery of (R)-1-[2-hydroxy-3-(4-hydroxy-phenyl)-propyl]-4-(4-methyl-benzyl)-piperidin-4-ol: a novel NR1/2B subtype selective NMDA receptor antagonist
E Pinard, A Alanine, A Bourson, et al.
Journal of Neurochemistry
|
July 2, 1998
Binding characteristics of a potent AMPA receptor antagonist [3H]Ro 48-8587 in rat brain
V Mutel, G Trube, A Klingelschmidt, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 20, 2000
Functional consequences of reduction in NMDA receptor glycine affinity in mice carrying targeted point mutations in the glycine binding site
J N Kew, A Koester, J L Moreau, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
August 17, 2002
Pharmacological characterization of Ro 63-1908 (1-[2-(4-hydroxy-phenoxy)-ethyl]-4-(4-methyl-benzyl)-piperidin-4-ol), a novel subtype-selective N-methyl-D-aspartate antagonist
R Gill, A Alanine, A Bourson, et al.
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Search research articles
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Showing results (41-50 of 44) with videos related to
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Page
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This site can display upto 44 results.
Bioorganic & Medicinal Chemistry Letters
|
August 22, 2001
Discovery of (R)-1-[2-hydroxy-3-(4-hydroxy-phenyl)-propyl]-4-(4-methyl-benzyl)-piperidin-4-ol: a novel NR1/2B subtype selective NMDA receptor antagonist
E Pinard, A Alanine, A Bourson, et al.
Journal of Neurochemistry
|
July 2, 1998
Binding characteristics of a potent AMPA receptor antagonist [3H]Ro 48-8587 in rat brain
V Mutel, G Trube, A Klingelschmidt, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
May 20, 2000
Functional consequences of reduction in NMDA receptor glycine affinity in mice carrying targeted point mutations in the glycine binding site
J N Kew, A Koester, J L Moreau, et al.
The Journal of Pharmacology and Experimental Therapeutics
|
August 17, 2002
Pharmacological characterization of Ro 63-1908 (1-[2-(4-hydroxy-phenoxy)-ethyl]-4-(4-methyl-benzyl)-piperidin-4-ol), a novel subtype-selective N-methyl-D-aspartate antagonist
R Gill, A Alanine, A Bourson, et al.
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of 5