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JM Humphrey

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Hans P Koch; Michael P Kavanaugh; C Sean Esslinger; N Zerangue; JM Humphrey; Susan Amara; A Richard Chamberlin; Richard J Bridges
Differentiation of substrate and nonsubstrate inhibitors of the high-affinity, sodium-dependent glutamate transporters.
James B Aggen; JM Humphrey; CM Gauss; Hsien-Bin Huang; Angus Nairn; A Richard Chamberlin
The design, synthesis, and biological evaluation of analogues of the serine-threonine protein phosphatase 1 and 2A selective inhibitor microcystin LA: rational modifications imparting PP1 selectivity.
C L Willis; D L Dauenhauer; JM Humphrey; A Richard Chamberlin; AL Buller; Daniel T Monaghan; Richard J Bridges
Methylation of the NMDA receptor agonist L-trans-2,3-pyrrolidine-dicarboxylate: enhanced excitotoxic potency and selectivity.

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All Publications

1999: Hans P Koch; Michael P Kavanaugh; C Sean Esslinger; N Zerangue; JM Humphrey; Susan Amara; A Richard Chamberlin; Richard J Bridges
Differentiation of substrate and nonsubstrate inhibitors of the high-affinity, sodium-dependent glutamate transporters.
Molecular pharmacology 1999;56(6):1095-104.
1999: James B Aggen; JM Humphrey; CM Gauss; Hsien-Bin Huang; Angus Nairn; A Richard Chamberlin
The design, synthesis, and biological evaluation of analogues of the serine-threonine protein phosphatase 1 and 2A selective inhibitor microcystin LA: rational modifications imparting PP1 selectivity.
Bioorganic & medicinal chemistry 1999;7(3):543-64.
1997: C L Willis; D L Dauenhauer; JM Humphrey; A Richard Chamberlin; AL Buller; Daniel T Monaghan; Richard J Bridges
Methylation of the NMDA receptor agonist L-trans-2,3-pyrrolidine-dicarboxylate: enhanced excitotoxic potency and selectivity.
Toxicology and applied pharmacology 1997;144(1):45-55.

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