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Showing 1 to 20 of 94 for “"Health Sciences, Pharmacology."”.

  1. Zyxin signaling: Protease-activated receptor-1 and Rho guanine nucleotide exchange factor p114.

    Zyxin signaling: Protease-activated receptor-1 and Rho guanine nucleotide exchange factor p114.

    uic

  2. Selective modulation of the platelet thromboxane A2/prostaglandin H2 receptor by omega-3 fatty acids.

    Selective modulation of the platelet thromboxane A2/prostaglandin H2 receptor by omega-3 fatty acids.

    uic

  3. BIOCHEMICAL BASIS OF IMPAIRED HEPATIC MICROSOMAL DRUG METABOLISM IN THE NEONATE.

    BIOCHEMICAL BASIS OF IMPAIRED HEPATIC MICROSOMAL DRUG METABOLISM IN THE NEONATE.

    uic

  4. MORPHOLOGY AND PHYTOCHEMISTRY OF DATURA INOXIA MILL.

    MORPHOLOGY AND PHYTOCHEMISTRY OF DATURA INOXIA MILL.

    uic

  5. Investigation of resveratrol metabolism using liquid chromatography-mass spectrometry.

    Investigation of resveratrol metabolism using liquid chromatography-mass spectrometry.

    uic

  6. Design and synthesis of novel factor Xa inhibitors.

    Design and synthesis of novel factor Xa inhibitors.

    uic

  7. ENZYME INDUCTION BY THE PORPHYRINOGENIC DRUG ALLYLISOPROPYLACETAMIDE.

    ENZYME INDUCTION BY THE PORPHYRINOGENIC DRUG ALLYLISOPROPYLACETAMIDE.

    uic

  8. Clinical pharmacology of camptothecins: Model based population pharmacokinetic and pharmacodynamic analysis.

    Clinical pharmacology of camptothecins: Model based population pharmacokinetic and pharmacodynamic analysis.

    uic

  9. Regulation of p115RhoGEF by Galpha13.

    Regulation of p115RhoGEF by Galpha13.

    uic

  10. Neuroprotective effects of overexpression of the inhibitor of apoptosis proteins in the quinolinic acid model of excitotoxic injury.

    Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder which results in the selective loss of the medium spiny neurons in the striatum. The neuropathological and behavioural deficits of HD can be modeled in rats by injection of the NMDA receptor agonist quinolinic acid (2,3 …

    ottawa-retro Repository record for Neuroprotective effects of overexpression of the inhibitor of apoptosis proteins in the quinolinic acid model of excitotoxic injury. (opens in a new tab)

  11. Non-steriodal anti-inflammatory drug-mediated regulation of COX-2 and EP3 receptor expression in the M-1 murine cortical collecting duct cell line.

    The cortical collecting duct (CCD) is a major site of intrarenal prostaglandin E2 (PGE2) synthesis. By indirect immunofluorescence using isoform specific antibodies, we have localized COX-1 and -2 immunoreactivity to all cell types of the murine M-1 CCD cell line. By, immunohistochemistry, both …

    ottawa-retro Repository record for Non-steriodal anti-inflammatory drug-mediated regulation of COX-2 and EP3 receptor expression in the M-1 murine cortical collecting duct cell line. (opens in a new tab)

  12. The FP prostanoid receptor: Isoforms and functional studies

    Prostaglandin F₂(α) (PGF₂(α)) is a locally acting hormone derived from arachidonic acid that is involved in a diverse range of physiological functions including regulation of the corpus luteum and regulation of intraocular pressure. The goal of this research has been to characterize the signaling …

    arizona-thes Repository record for The FP prostanoid receptor: Isoforms and functional studies (opens in a new tab)

  13. In vivo and in vitro toxicity of M-741 (3,15 di-(5,5-dimethyl-3-N(-(cyclopropylmethylinium)-(N-propylinium));-1-cyclohex-1-enyl);-7,11,18,21-tetraoxa-3,15-diazatrispiro (5.2.2.5.2.2); heneicosane)

    M-741 (3,15 di-[5,5-dimethyl-3-N[-(cyclopropylmethylinium)-(N-propylinium]-1-cyclohex-1-enyl]-7,11,18,21-tetraoxa-3,15-diazatrispiro [5.2.2.5.2.2] heneicosane produces hepatotoxicity in rats following intravenous administration. Hepatocellular pathology is characterized by parenchymal cell necrosis …

    arizona-thes Repository record for In vivo and in vitro toxicity of M-741 (3,15 di-(5,5-dimethyl-3-N(-(cyclopropylmethylinium)-(N-propylinium));-1-cyclohex-1-enyl);-7,11,18,21-tetraoxa-3,15-diazatrispiro (5.2.2.5.2.2); heneicosane) (opens in a new tab)

  14. The human cannabinoid CB(1) receptor stably expressed in Chinese hamster ovary cells provides a model system to predict the pharmacological effects of cannabinoids in man

    Since the cloning of the only known cannabinoid receptor in the human brain, CB₁, scientists have been trying to elucidate the mechanisms of action of this receptor. The possibility of yet unidentified cannabinoid receptors in human brain makes it important to be certain that any results obtained …

    arizona-thes Repository record for The human cannabinoid CB(1) receptor stably expressed in Chinese hamster ovary cells provides a model system to predict the pharmacological effects of cannabinoids in man (opens in a new tab)

  15. Supramolecular Architectures in Molecular Medicine: Visualizing and Manipulating the Structure of Protein-Lipid Surfaces

    In separate studies, myoglobin has been used to study the fluorescence lifetime behavior of oriented biomolecular surfaces. These studies have revealed differences in lifetime between differentially oriented myoglobin molecules, consistent with differential accessibility of the heme pocket to …

    uiuc Repository record for Supramolecular Architectures in Molecular Medicine: Visualizing and Manipulating the Structure of Protein-Lipid Surfaces (opens in a new tab)

  16. Single-Channel Studies of Agonist Interactions With the Neurotransmitter-Binding and Pore Domains of the Muscle Nicotinic Acetylcholine Receptor

    The nicotinic acetylcholine receptor, a ligand-gated ion channel, is activated by a variety of naturally occurring and synthetic ligands. The overall 'response' elicited by any ligand of the nicotinic receptor is not only a consequence of its binding to the extracellular neurotransmitter-binding …

    uiuc Repository record for Single-Channel Studies of Agonist Interactions With the Neurotransmitter-Binding and Pore Domains of the Muscle Nicotinic Acetylcholine Receptor (opens in a new tab)

  17. Clinical Globalization: Pharmaceutical Research in the Global South

    … the United States, an uneven global gradient of health care access, and changing health demographics in the Global South---have prompted the development of an extensive international infrastructure for conducting clinical trials. This infrastructure is not only technical and physical, but also …

    uiuc Repository record for Clinical Globalization: Pharmaceutical Research in the Global South (opens in a new tab)

  18. A Structural and Functional Analysis of the Human Angiotensin II Type-2 Receptor

    In the third series of experiments we used synthetic peptides derived from the amino acid sequence of the cytoplasmic loops and tail of the AT 2 receptor are used to determine what regions are important to G-protein activation. These studies will map the G-protein coupling regions of the human AT2 …

    uiuc Repository record for A Structural and Functional Analysis of the Human Angiotensin II Type-2 Receptor (opens in a new tab)

  19. NMR, Crystallographic and Computational Investigations of Peptides, Proteins and Bisphosphonates: New Paradigms for Rational Drug Design

    "The standard approaches to lead identification and optimization involve a long and expensive process including random and nonrandom (targeted or focused) screening. Given the limited success of these standard approaches, an alternate route to develop a new drug would be to start with an existing …

    uiuc Repository record for NMR, Crystallographic and Computational Investigations of Peptides, Proteins and Bisphosphonates: New Paradigms for Rational Drug Design (opens in a new tab)

  20. Synthetic Studies in the Didemnin Series

    Semi-synthetic studies directed toward didemnin analogues in which structural modifications were introduced in the side chain for investigating structure-activity relationships have been performed. The syntheses of several known didemnins including didemnin M, dehydrodidemnin B, and pyroglutamyl …

    uiuc Repository record for Synthetic Studies in the Didemnin Series (opens in a new tab)

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