D D Schoepp

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Comparison of Excitatory Amino Acid‐Stimulated Phosphoinositide Hydrolysis and N‐[3H]Acetylaspartylglutamate Binding in Rat Brain: Selective Inhibition of Phosphoinositide Hydrolysis by 2‐Amino‐3‐Phosphonopropionate

D. Schoepp, D D Schoepp, B G Johnson, 1989, Journal of neurochemistry.

Cloning and expression of a human metabotropic glutamate receptor 1 alpha: enhanced coupling on co-transfection with a glutamate transporter.

D. Schoepp, M. A. Desai, D D Schoepp, 1995, Molecular pharmacology.

Inhibition of Cyclic AMP Formation by a Selective Metabotropic Glutamate Receptor Agonist

D. Schoepp, D D Schoepp, B G Johnson, 1992, Journal of neurochemistry.

Guinea Pig Striatum as a Model of Human Dopamine Deamination: The Role of Monoamine Oxidase Isozyme Ratio, Localization, and Affinity for Substrate in Synaptic Dopamine Metabolism

J Frost, D. Schoepp, A. Azzaro, 1985, Journal of neurochemistry.

Alteration of Dopamine Synthesis in Rat Striatum Subsequent to Selective Type A Monoamine Oxidase Inhibition

D. Schoepp, A. Azzaro, D D Schoepp, 1981, Journal of neurochemistry.

3,5‐Dihydroxyphenylglycine Is a Highly Selective Agonist for Phosphoinositide‐Linked Metabotropic Glutamate Receptors in the Rat Hippocampus

D. Schoepp, D D Schoepp, B G Johnson, 1994, Journal of neurochemistry.

A novel, competitive mGlu(5) receptor antagonist (LY344545) blocks DHPG-induced potentiation of NMDA responses but not the induction of LTP in rat hippocampal slices.

D D Schoepp, Z A Bortolotto, G L Collingridge, 2000, British journal of pharmacology.

2-substituted (2SR)-2-amino-2-((1SR,2SR)-2-carboxycycloprop-1-yl)glycines as potent and selective antagonists of group II metabotropic glutamate receptors. 2. Effects of aromatic substitution, pharmacological characterization, and bioavailability.

P. Ornstein, D. Schoepp, D D Schoepp, 1998, Journal of medicinal chemistry.

Pharmacological characterization of LY233053: a structurally novel tetrazole-substituted competitive N-methyl-D-aspartic acid antagonist with a short duration of action.

P. Ornstein, D. Schoepp, D. Lodge, 1990, The Journal of pharmacology and experimental therapeutics.

6-substituted decahydroisoquinoline-3-carboxylic acids as potent and selective conformationally constrained NMDA receptor antagonists.

P. Ornstein, D. Schoepp, D. Lodge, 1992, Journal of medicinal chemistry.