M. S. McIntyre

发表

CNS 7056: A Novel Ultra–short-acting Benzodiazepine

Gavin Kilpatrick, J. Stafford, G. J. Pacofsky, 2007, Anesthesiology.

Endoplasmic reticulum calcium store regulates membrane potential in mouse islet beta-cells.

I. Dukes, M. Roe, J. Worley, 1994, The Journal of biological chemistry.

Discovery of a highly potent, nonabsorbable apical sodium-dependent bile acid transporter inhibitor (GSK2330672) for treatment of type 2 diabetes.

M. J. Bishop, J. Ambroso, J. Collins, 2013, Journal of medicinal chemistry.

Dependence on NADH produced during glycolysis for beta-cell glucose signaling.

L. Philipson, I. Dukes, M. Roe, 1994, The Journal of biological chemistry.

Interaction between neurotransmitters and exogenous norepinephrine in isolated rat anococcygeus muscle.

M. S. McIntyre, R. Mudumbi, H. Leighton, 1996, General pharmacology.

Relating the structure, activity, and physical properties of ultrashort-acting benzodiazepine receptor agonists.

J. Stafford, G. J. Pacofsky, P. Feldman, 2002, Bioorganic & medicinal chemistry letters.

Identification and structure-activity studies of novel ultrashort-acting benzodiazepine receptor agonists.

J. Stafford, G. J. Pacofsky, P. Feldman, 2002, Bioorganic & medicinal chemistry letters.

Expression and function of pancreatic beta-cell delayed rectifier K+ channels. Role in stimulus-secretion coupling.

A. Kuznetsov, L. Philipson, W. Shehee, 1996, The Journal of biological chemistry.

Novel 4,4-disubstituted piperidine-based C-C chemokine receptor-5 inhibitors with high potency against human immunodeficiency virus-1 and an improved human ether-a-go-go related gene (hERG) profile.

Brian A. Chauder, W. Kazmierski, B. Chauder, 2011, Journal of medicinal chemistry.

6-(4-chlorophenyl)-3-substituted-thieno[3,2-d]pyrimidin-4(3H)-one-based melanin-concentrating hormone receptor 1 antagonist.

M. J. Bishop, A. Goetz, F. Tavares, 2006, Journal of medicinal chemistry.

Predicting QT prolongation in humans during early drug development using hERG inhibition and an anaesthetized guinea-pig model

X Yao, D L Anderson, S A Ross, 2008, British journal of pharmacology.

Depletion of intracellular Ca2+ stores activates a maitotoxin-sensitive nonselective cationic current in beta-cells.

I. Dukes, J F Worley, M S McIntyre, 1994, The Journal of biological chemistry.

Discovery of a highly potent, nonabsorbable apical sodium-dependent bile acid transporter inhibitor (GSK2330672) for treatment of type 2 diabetes.

M. J. Bishop, J. Ambroso, J. Collins, 2013, Journal of medicinal chemistry.