Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Kou-Yi Tserng"'
Autor:
William C. Stanley, Eric E. Morgan, Brian D. Hoit, Martin E. Young, Margaret P. Chandler, Tracy A. McElfresh, Kou Yi Tserng, Theodore A. Kung, Julie H. Rennison
Publikováno v:
European Journal of Heart Failure. 8:687-693
Studies in advanced heart failure show down-regulation of fatty acid oxidation genes, possibly due to decreased expression of the nuclear transcription factors peroxisome proliferator activated receptor alpha (PPARalpha) and retinoid X receptor alpha
Autor:
Martin E. Young, Julie H. Rennison, Hani N. Sabbah, William C. Stanley, Kou Yi Tserng, Tracy A. McElfresh, Isidore C. Okere, Brian D. Hoit, Paul Ernsberger, Margaret P. Chandler, Victor G. Sharov
Publikováno v:
American Journal of Physiology-Heart and Circulatory Physiology. 291:H38-H44
Fatty acids are the primary fuel for the heart and are ligands for peroxisome proliferator-activated receptors (PPARs), which regulate the expression of genes encoding proteins involved in fatty acid metabolism. Saturated fatty acids, particularly pa
Autor:
Matthew M. Cooney, Keith R. McCrae, R. Jeff McPeak, Afshin Dowlati, Pamela Ksenich, Vinit Makar, Pierre Lavertu, Kou Yi Tserng, Beth Overmoyer, Charles L. Hoppel, Percy Ivy, Scot C. Remick, Stephen T. Ingalls
Publikováno v:
Cancer Chemotherapy and Pharmacology. 55:295-300
SU5416 is a novel small organic molecule that non-competitively inhibits the phosphorylation of the VEGF tyrosine kinase receptor, Flk-1. This phase IB study was performed to determine the safety, pharmacokinetics, and preliminary efficacy of the com
Autor:
Stephen T. Ingalls, Stanton Gerson, Timothy P. Spiro, Charles L. Hoppel, Xiaolin Li, Susan M. Majka, Kou Yi Tserng, James K. V. Willson, Erik M. Boczko
Publikováno v:
The Journal of Clinical Pharmacology. 43:881-893
O 6 -Benzylguanine and its metabolite, 8-oxo-O 6 -benzylguanine, are equally potent inhibitors of the DNA repair enzyme, O 6 -alkylguanine-DNA alkyltransferase. Pharmacokinetic values are derived from cancer patients participating in a phase I trial
Autor:
Ronald L. Horst, Jeffrey W. Clark, Kou-Yi Tserng, D Balkundi, G. Satyanarayana Reddy, D.Sunita Rao, Milan R. Uskokovic
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 78:167-176
1alpha,25-Dihydroxyvitamin D(3) [1alpha,25(OH)(2)D(3)] is mainly metabolized via the C-24 oxidation pathway and undergoes several side chain modifications which include C-24 hydroxylation, C-24 ketonization, C-23 hydroxylation and side chain cleavage
Autor:
Mei-Ling Siu-Caldera, Kou-Yi Tserng, G. Satyanarayana Reddy, D.Sunita Rao, Seiichi Ishizuka, Edward A. Weinstein, Milan R. Uskokovic
Publikováno v:
Biochemical Pharmacology. 58:1965-1973
1alpha,24(R)-Dihydroxyvitamin D3 [1alpha,24(R)(OH)2D3], a synthetic vitamin D3 analog, has been developed as a drug for topical use in the treatment of psoriasis. At present, the target tissue metabolism of 1alpha,24(R)(OH)2D3 is not understood compl
Autor:
Kou-Yi Tserng, Mei-Ling Siu-Caldera, Milan R. Uskokovic, G. Satyanarayana Reddy, Ronald L. Horst, Ramesh Dayal, D.Sunita Rao
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 71:63-70
Vitamin D 2 is less toxic in rats when compared to vitamin D 3 . Our laboratory has been involved in research projects which were directed towards identifying the possible mechanisms responsible for the toxicity differences between vitamins D 2 and D
Autor:
Jeffrey W. Hazey, D. W. Kirschenbaum, J. Koshy, Kou-Yi Tserng, M. V. Soloviev, D. Lucas, Henri Brunengraber, Stephen F. Previs, A. P. Keating, S. K. Martin, F. David
Publikováno v:
American Journal of Physiology-Endocrinology and Metabolism. 271:E1118-E1124
The classical concept holds that liver and kidneys are the main sinks of glycerol released by adipose tissue. However, rates of glycerol appearance (Ra) exceed the rate of glycerol delivery to liver and kidneys. We measured the hepatic and renal cont
Publikováno v:
Biochemical Journal. 313:581-588
Besides the conventional isomerase-mediated pathway, unsaturated fatty acids with odd-numbered double bonds are also metabolized by reduction pathways with NADPH as cofactor. The relative contributions of these pathways were measured in intact rat-li
Publikováno v:
Biochemistry. 33:10527-10534
A new enzyme, i.e., delta 3,delta 5-t-2,t-4-dienoyl-CoA isomerase, required in the NADPH-dependent metabolic pathway of odd-numbered double bond, unsaturated fatty acids, was isolated and purified to apparent homogeneity from rat liver. In the oxidat