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The Role of I₁-Imidazoline and α₂-Adrenergic Receptors in the Modulation of Glucose Metabolism in the Spontaneously Hypertensive Obese Rat Model of Metabolic Syndrome X
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Journal of Pharmacology and Experimental Therapeutics August 2003, 306 (2) 646-657; DOI: https://doi.org/10.1124/jpet.103.050468
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Pharmacology of (2S,4Z)-N-[(2S)-2-Hydroxy-2-phenylethyl]-4-(methoxyimino) -1-[(2′-methyl[1,1′-biphenyl]-4-yl)carbonyl]-2-pyrrolidinecarboxamide, a New Potent and Selective Nonpeptide Antagonist of the Oxytocin Receptor
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Journal of Pharmacology and Experimental Therapeutics July 2003, 306 (1) 253-261; DOI: https://doi.org/10.1124/jpet.103.049395
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Effect of Ursodeoxycholic Acid on the Impairment Induced by Maternal Cholestasis in the Rat Placenta-Maternal Liver Tandem Excretory Pathway
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Journal of Pharmacology and Experimental Therapeutics May 2003, 305 (2) 515-524; DOI: https://doi.org/10.1124/jpet.102.047977
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Structure-Activity Relations of Successful Pharmacologic Chaperones for Rescue of Naturally Occurring and Manufactured Mutants of the Gonadotropin-Releasing Hormone Receptor
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Journal of Pharmacology and Experimental Therapeutics May 2003, 305 (2) 608-614; DOI: https://doi.org/10.1124/jpet.102.048454
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Biological Characterization of a Novel, Orally Active Small Molecule Gonadotropin-Releasing Hormone (GnRH) Antagonist Using Castrated and Intact Rats
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Journal of Pharmacology and Experimental Therapeutics May 2003, 305 (2) 688-695; DOI: https://doi.org/10.1124/jpet.102.046656
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Structure-Activity Study of LVV-Hemorphin-7: Angiotensin AT₄ Receptor Ligand and Inhibitor of Insulin-Regulated Aminopeptidase
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Ca_v1.3 Is Preferentially Coupled to Glucose-Stimulated Insulin Secretion in the Pancreatic β-Cell Line INS-1
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Journal of Pharmacology and Experimental Therapeutics April 2003, 305 (1) 271-278; DOI: https://doi.org/10.1124/jpet.102.046334
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Is 11β-Hydroxysteroid Dehydrogenase Type 1 a Therapeutic Target? Effects of Carbenoxolone in Lean and Obese Zucker Rats
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Pharmacodynamics of Selective Androgen Receptor Modulators
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Identification of a Peptide Antagonist to the Peripheral-Type Benzodiazepine Receptor That Inhibits Hormone-Stimulated Leydig Cell Steroid Formation
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