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Torcetrapib Induces Aldosterone and Cortisol Production by an Intracellular Calcium-Mediated Mechanism Independently of Cholesteryl Ester Transfer Protein Inhibition

Endocrinology (Philadelphia), 2009-05, Vol.150 (5), p.2211-2219

2009

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Effects of age on noninvasive assessments of vascular function in nonhuman primates: implications for translational drug discovery

Journal of translational medicine, 2013-04, Vol.11 (1), p.101-101, Article 101

2013

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CCR2 receptor blockade alters blood monocyte subpopulations but does not affect atherosclerotic lesions in apoE−/− mice

Atherosclerosis, 2010-02, Vol.208 (2), p.370-375

2010

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Zoniporide: a potent and highly selective inhibitor of human Na +/H + exchanger-1

European journal of pharmacology, 2002-09, Vol.451 (1), p.37-41

2002

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Cardioprotective effects of ingliforib, a novel glycogen phosphorylase inhibitor

American journal of physiology. Heart and circulatory physiology, 2004-03, Vol.286 (3), p.H1177-H1184

2004

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3‘-Aminoadenosine-5‘-uronamides: Discovery of the First Highly Selective Agonist at the Human Adenosine A3 Receptor

Journal of medicinal chemistry, 2003-01, Vol.46 (3), p.353-355

2003

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Editorial overview: cardioprotective drugs for myocardial ischemic injury--a therapeutic area at risk

Current opinion in investigational drugs (London, England : 2000), 2007-03, Vol.8 (3), p.190

Knight, Delvin R

2007

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Discovery of zoniporide: A potent and selective sodium–hydrogen exchanger type 1 (NHE-1) inhibitor with high aqueous solubility

Bioorganic & medicinal chemistry letters, 2001-03, Vol.11 (6), p.803-807

2001

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The synthesis of highly potent, selective, and water-soluble agonists at the human adenosine A3 receptor

Bioorganic & medicinal chemistry letters, 2006-05, Vol.16 (9), p.2525-2527

2006

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Aldose reductase inhibition alone or combined with an adenosine A3 agonist reduces ischemic myocardial injury

American journal of physiology. Heart and circulatory physiology, 2000-10, Vol.279 (4), p.H1447

2000

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Treatment of peripheral artery disease: an unmet medical need

Current opinion in investigational drugs (London, England : 2000), 2009-09, Vol.10 (9), p.899

2009

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Novel variants in human and monkey CETP

Biochimica et biophysica acta, 2005-10, Vol.1737 (1), p.69-75

2005

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Comparisons between electromagnetic and X-beam transit-time flow measurements for evaluating drug actions on cardiac output in the conscious dog

Journal of pharmacological and toxicological methods, 2006-11, Vol.54 (3), p.296-306

2006

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The sulfonylurea glipizide does not inhibit ischemic preconditioning in anesthetized rabbits

Cardiovascular drugs and therapy, 2005-10, Vol.19 (5), p.337-346

2005

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Cloning, expression and pharmacological characterization of rabbit adenosine A1 and A3 receptors

The Journal of pharmacology and experimental therapeutics, 1997-01, Vol.280 (1), p.122

1997

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NO modulates myocardial O2 consumption in the nonhuman primate: an additional mechanism of action of amlodipine

American journal of physiology. Heart and circulatory physiology, 1999-06, Vol.276 (6), p.H2069

1999

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NO modulates myocardial O 2 consumption in the nonhuman primate: an additional mechanism of action of amlodipine

American journal of physiology. Heart and circulatory physiology, 1999-06, Vol.276 (6), p.H2069-H2075

1999

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Abstract 8926: Rosiglitazone Acutely Improves Flow Mediated Dilation and Favorably Alters Endothelial Microparticle and Progenitor Cell Numbers in Euglycemic, Senescent Monkeys

Circulation (New York, N.Y.), 2011-11, Vol.124 (suppl_21)

2011

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Abstract 16821: Reductions in Vascular Function Correlate with Age in a Novel Non-Human Primate Model for Assessment of Vascular Health

Circulation (New York, N.Y.), 2011-11, Vol.124 (suppl_21)

2011

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Impact of Delayed Reperfusion of Myocardial Hibernation on Myocardial Ultrastructure and Function and Their Recoveries After Reperfusion in a Pig Model of Myocardial Hibernation

Cardiovascular pathology, 2000-03, Vol.9 (2), p.67-84

2000

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Zoniporide: A Potent and Selective Inhibitor of the Human Sodium‐Hydrogen Exchanger Isoform 1 (NHE‐1)

Cardiovascular drug reviews, 2003-03, Vol.21 (1), p.17-32

2003

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Vasoconstrictor Action of Angiotensin I–Convertase and the Synthetic Substrate (Pro11,D-Ala12)-Angiotensin I

Hypertension (Dallas, Tex. 1979), 1994-06, Vol.23 (6, Part 2), p.857-860

1994

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Measurement of organ blood flow with coloured microspheres in the rat

Cardiovascular research, 1995, Vol.29 (1), p.74-79

1995

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A novel sodium-hydrogen exchanger isoform-1 inhibitor, zoniporide, reduces ischemic myocardial injury in vitro and in vivo

The Journal of pharmacology and experimental therapeutics, 2001-04, Vol.297 (1), p.254

2001

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Autonomic control of large coronary arteries and resistance vessels

Progress in cardiovascular diseases, 1987-11, Vol.30 (3), p.211-234

1987

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Torcetrapib Induces Aldosterone and Cortisol Production by an Intracellular Calcium-Mediated Mechanism Independently of Cholesteryl Ester Transfer Protein Inhibition

Effects of age on noninvasive assessments of vascular function in nonhuman primates: implications for translational drug discovery

CCR2 receptor blockade alters blood monocyte subpopulations but does not affect atherosclerotic lesions in apoE−/− mice

Zoniporide: a potent and highly selective inhibitor of human Na +/H + exchanger-1

Cardioprotective effects of ingliforib, a novel glycogen phosphorylase inhibitor

3‘-Aminoadenosine-5‘-uronamides: Discovery of the First Highly Selective Agonist at the Human Adenosine A3 Receptor

Editorial overview: cardioprotective drugs for myocardial ischemic injury--a therapeutic area at risk

Discovery of zoniporide: A potent and selective sodium–hydrogen exchanger type 1 (NHE-1) inhibitor with high aqueous solubility

The synthesis of highly potent, selective, and water-soluble agonists at the human adenosine A3 receptor

Aldose reductase inhibition alone or combined with an adenosine A3 agonist reduces ischemic myocardial injury

Treatment of peripheral artery disease: an unmet medical need

Novel variants in human and monkey CETP

Comparisons between electromagnetic and X-beam transit-time flow measurements for evaluating drug actions on cardiac output in the conscious dog

The sulfonylurea glipizide does not inhibit ischemic preconditioning in anesthetized rabbits

Cloning, expression and pharmacological characterization of rabbit adenosine A1 and A3 receptors

NO modulates myocardial O2 consumption in the nonhuman primate: an additional mechanism of action of amlodipine

NO modulates myocardial O 2 consumption in the nonhuman primate: an additional mechanism of action of amlodipine

Abstract 8926: Rosiglitazone Acutely Improves Flow Mediated Dilation and Favorably Alters Endothelial Microparticle and Progenitor Cell Numbers in Euglycemic, Senescent Monkeys

Abstract 16821: Reductions in Vascular Function Correlate with Age in a Novel Non-Human Primate Model for Assessment of Vascular Health

Impact of Delayed Reperfusion of Myocardial Hibernation on Myocardial Ultrastructure and Function and Their Recoveries After Reperfusion in a Pig Model of Myocardial Hibernation

Zoniporide: A Potent and Selective Inhibitor of the Human Sodium‐Hydrogen Exchanger Isoform 1 (NHE‐1)

Vasoconstrictor Action of Angiotensin I–Convertase and the Synthetic Substrate (Pro11,D-Ala12)-Angiotensin I

Measurement of organ blood flow with coloured microspheres in the rat

A novel sodium-hydrogen exchanger isoform-1 inhibitor, zoniporide, reduces ischemic myocardial injury in vitro and in vivo

Autonomic control of large coronary arteries and resistance vessels

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