Search Results - "Luthin, David R"
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Anti-obesity effects of small molecule melanin-concentrating hormone receptor1 (MCHR1) antagonists
Published in Life sciences (1973) (19-07-2007)“…Over the past ten years, tremendous advances in our understanding of the role of the hypothalamic neurohormone, melanin-concentrating hormone (MCH), and its…”
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Current and Emerging Treatments for Irritable Bowel Syndrome with Constipation and Chronic Idiopathic Constipation: Focus on Prosecretory Agents
Published in Pharmacotherapy (01-06-2015)“…Irritable bowel syndrome with constipation (IBS‐C) and chronic idiopathic constipation (CIC) are two common functional gastrointestinal disorders that impair…”
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Biological characterization of a novel, orally active small molecule gonadotropin-releasing hormone (GnRH) antagonist using castrated and intact rats
Published in The Journal of pharmacology and experimental therapeutics (01-05-2003)“…Gonadotropin-releasing hormone (GnRH) receptor antagonists have potential in treating numerous hormone-dependent pathologies including cancers of the prostate,…”
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Impact of an inter-professional concussion awareness program for intramural athletes on students’ readiness for inter-professional learning
Published in Journal of interprofessional education & practice (01-03-2020)“…AbstractSports-related concussions are the third leading cause of traumatic brain injuries in student athletes throughout the country. In a survey of all NCAA…”
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Linaclotide: A Novel Approach to the Treatment of Irritable Bowel Syndrome
Published in The Annals of pharmacotherapy (01-12-2011)“…Objective: To review the pharmacology, pharmacokinetics, efficacy, and safety of linaclotide for irritable bowel syndrome (IBS). Data Sources: A literature…”
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Wheel access does not attenuate weight gain in mice fed high-fat or high-CHO diets
Published in Medicine and science in sports and exercise (01-02-2010)“…To determine the effect of a high-fat or high-carbohydrate diet and running wheel activity on body composition, body mass, and caloric intake in C57Bl/6 mice…”
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D-cycloserine in the treatment of posttraumatic stress disorder
Published in The mental health clinician (01-03-2017)“…Posttraumatic stress disorder (PTSD) is a common and serious psychiatric illness. Exposure therapy is a type of cognitive behavioral therapy that is considered…”
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Parental perspectives of diabetes management in Alabama public schools
Published in Southern medical journal (Birmingham, Ala.) (01-04-2013)“…The purpose of this study was to assess parental perceptions of the current state of care for children with diabetes in the Alabama public school system,…”
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Discovery of a Novel, Orally Active, Small Molecule Gonadotropin-Releasing Hormone (GnRH) Receptor Antagonist
Published in Journal of medicinal chemistry (01-06-2006)“…Gonadotropin releasing hormone (GnRH) plays an important role in the biology of reproduction. The use of GnRH receptor antagonists has been reported in the…”
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Discovery of a Novel, Orally Active, Small Molecule Gonadotropin-Releasing Hormone (GnRH) Receptor Antagonist
Published in Journal of medicinal chemistry (21-09-2006)Get full text
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Characterization of mono- and diaminopyrimidine derivatives as novel, nonpeptide gonadotropin releasing hormone (GnRH) receptor antagonists
Published in Bioorganic & medicinal chemistry letters (16-12-2002)“…A novel series of derivatives of mono- and diaminopyrimidines 1 potently displaced binding of a radiolabeled GnRH analogue to human and rat GnRH receptors…”
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The discovery of novel small molecule non-peptide gonadotropin releasing hormone (GnRH) receptor antagonists
Published in Bioorganic & medicinal chemistry letters (02-12-2002)“…A novel series of non-peptide derivatives 1, 14, and 15 that bind with high affinity to the human GnRH receptors is discussed. The discovery was made from…”
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Synthesis and biological activity of oxo-7H-benzo[E]perimidine-4-carboxylic acid derivatives as potent, nonpeptide corticotropin releasing factor (CRF) receptor antagonists
Published in Bioorganic & medicinal chemistry letters (08-03-1999)“…A novel series of derivatives of oxo-7H-benzo[e]perimidine-4-carboxylic acid (I) potently displaced radioligand binding of 125I-CRF to both CRF1 and CRF2…”
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Genomic Analysis and Expression Patterns Reveal Distinct Genes for Endothelial and Brain Nitric Oxide Synthase
Published in Hypertension (Dallas, Tex. 1979) (01-06-1993)“…Constitutively active nitric oxide synthases (NOS) are a unique class of NADPH-dependent, calcium/ caimodulin-dependent enzymes that catalyze the conversion of…”
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Anti-obesity effects of small molecule melanin-concentrating hormone receptor 1 (MCHR1) antagonists
Published in Life sciences (1973) (19-07-2007)“…Over the past ten years, tremendous advances in our understanding of the role of the hypothalamic neurohormone, melanin-concentrating hormone (MCH), and its…”
Get full text
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Relationship between pharmacy students' knowledge about, attitudes toward, and intention to provide pharmacy-based immunization services
Published in Currents in pharmacy teaching and learning (01-07-2011)“…The purpose of this study was to examine pharmacy students' knowledge about, attitudes toward, and intention to provide pharmacy-based immunization services…”
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Double tagging recombinant A1- and A2A-adenosine receptors with hexahistidine and the FLAG epitope : Development of an efficient generic protein purification procedure
Published in Biochemical pharmacology (23-02-1996)“…An expression plasmid for mammalian cells (CLDN10B) has been modified to add nucleotides encoding hexahistidine and the FLAG peptide (H/F) to cDNAs. The new…”
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Effect of testosterone suppression on the pharmacokinetics of a potent GnRH receptor antagonist
Published in Pharmaceutical research (01-02-2002)“…The expression of cytochrome P450 enzymes (CYPs) in animals and humans is under complex hormonal regulation. Chronic treatment with drugs that alter sex…”
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Characterization of two affinity states of adenosine A2a receptors with a new radioligand, 2-[2-(4-amino-3-[125I]iodophenyl)ethylamino]adenosine
Published in Molecular pharmacology (01-02-1995)“…Adenosine analogs substituted in the 2-position with arylamino groups have been found to have high affinity and selectivity for A2a adenosine receptors. Two…”
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