Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Jeffrey N. Masters"'
Publikováno v:
Xenobiotica. 42:863-871
We describe the usability of human pooled hepatocytes for non-CYP metabolism evaluation and an in vivo-in vitro correlation analysis for aldehyde oxidase (AO) substrate compounds using pooled hepatocytes. By comparing intrinsic clearance values of 18
Autor:
Earl J. Gubbins, Loan N. Miller, Marc A. Terranova, Robert B. Moreland, Jeffrey N. Masters, Odile F. El-Kouhen, Diana L. Donnelly-Roberts, Marie E. Uchic, Jorge D. Brioni, Marian T. Namovic, Rosalind J. Helfrich, Renjie Chang, Masaki Nakane
Publikováno v:
Biochemical Pharmacology. 68:761-772
The goal of this study was to develop a new approach to study the pharmacology of the dopamine D 4 receptor that could be used in comparative studies with dopamine D 2 and D 3 receptors. Stable HEK-293 cell lines co-expressing recombinant human D 2L
Autor:
Robert B. Moreland, Usha Warrior, Diana L. Donnelly-Roberts, Jennifer McGowen, Jeffrey N. Masters, Jorge D. Brioni, James L. Kofron, Rosalind J. Helfrich, David J. Burns, Earl J. Gubbins, Sujatha M. Gopalakrishnan
Publikováno v:
Analytical Biochemistry. 321:192-201
The identification of agonist and antagonist leads for G-protein-coupled receptors (GPCRs) is of critical importance to the pharmaceutical and biotechnology industries. We report on the utilization of a novel, high-density, well-less screening platfo
Publikováno v:
Pharmacology Research & Perspectives
Metabolism and sinusoidal/canalicular efflux of mycophenolic acid (MPA) was investigated using sandwich-cultured hepatocytes (SCHs). After applying MPA to SCHs from humans, wild-type rats, and multidrug resistance-associated protein (Mrp) 2-deficient
Publikováno v:
Drug metabolism and pharmacokinetics. 29(2)
Rat sandwich-cultured hepatocytes (SCH) were used to correlate the in vitro hepatic disposition of mycophenolic acid (MPA) with published in vivo data, as well as mechanistic studies on drug-drug interaction. The major metabolite of MPA in SCH was 7-
Publikováno v:
Journal of Molecular Neuroscience. 7:203-215
CR16 is a glucocorticoid-regulated gene expressed in subpopulations of neurons in the brain, including the hippocampus. The CR16 open reading frame encodes a 45 kDa protein containing 32% proline. To begin characterizing the CR16 protein, a rabbit po
Publikováno v:
Neuroendocrinology. 63:28-38
A novel cDNA clone, CR16, was isolated from a rat hippocampal cDNA library and characterized for responses to corticosteroids and regional expression. The 4-kb RNA was increased 3-fold by treatment of adrenalectomized (ADX) rats with corticosterone (
Publikováno v:
Neuroendocrinology. 60:23-35
Twenty-five years ago, glycerol phosphate dehydrogenase (GPDH, EC 1.1.1.8) was described as a hormonally dependent enzyme in the brain, and since then has been characterized for its developmental regulation and as a marker for oligodendrocytes. These
Publikováno v:
Drug metabolism and pharmacokinetics. 27(2)
Human hepatocytes are a physiologically relevant tool useful in evaluating liver-related pharmacokinetics, including non-cytochrome P-450 (CYP) metabolism, due to their broad spectrum of metabolic enzyme activity. To verify the usefulness of human he
Publikováno v:
Developmental Brain Research. 73:253-259
Mechanisms controlling the synthesis of corticotropin releasing hormone (CRH) in neonatal rats, and the ontogeny of glucocorticoid (GC) feedback control of hypothalamic CRH remain unknown. Specific issues are whether stress induces up-regulation of C