Gerald T. Miwa - Concepedia

Author

Gerald T. Miwa

Merck & Co., Inc., Rahway, NJ, USA (United States)

Also Known As

G MIWA, G Miwa, G T Miwa, G. Miwa, G. T. MIWA, G. T. Miwa, G.T. Miwa, GERALD T. MIWA, Gerald Miwa, Gerald T Miwa

Publications

6.2K

Citations

H-Index

Concepts

All Affiliations

Merck & Co., Inc., Rahway, NJ, USA (United States)Millennium Engineering and Integration (United States)La Roche College Research Triangle Park Foundation Procter & Gamble (United States)

About

Gerald T. Miwa is an author at Merck & Co., Inc., Rahway, NJ, USA (United States) specializing in biochemistry, medicine, and pharmacology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Biochemistry	23	31	2.9K
2	Medicine	20	30	2.7K
3	Natural Sciences	15	17	1.9K
4	Health Sciences	3	3	236
5	Engineering	1	1	16

Gerald T. Miwa

Publications

5.3K

Citations

H-Index

Page 1

	Year	Citations
N-acetyl-p-benzoquinone imine: a cytochrome P-450-mediated oxidation product of acetaminophen. David C. Dahlin, Gerald T. Miwa, Albert Lu, Proceedings of the National Academy of Sciences PharmacotherapyRedox BiologyPharmaceutical ChemistryToxicological MechanismOxidative Stress	1984	1.1K
THE CONDUCT OF IN VITRO AND IN VIVO DRUG-DRUG INTERACTION STUDIES: A PHARMACEUTICAL RESEARCH AND MANUFACTURERS OF AMERICA (PhRMA) PERSPECTIVE Thorir D. Bjornsson, John T. Callaghan, Heidi J. Einolf, Drug Metabolism and Disposition	2003	781
The Conduct of In Vitro and In Vivo Drug‐Drug Interaction Studies: A PhRMA Perspective Thorir D. Bjornsson, John T. Callaghan, Heidi J. Einolf, The Journal of Clinical Pharmacology Drug InteractionsPreclinical Drug EvaluationBiochemistryPharmacological StudyMedicine	2003	309
A simple and rapid procedure for the purification of phenobarbitalinducible cytochrome P-450 from rat liver microsomes Susan West, Mou‐Tuan Huang, Gerald T. Miwa, Archives of Biochemistry and Biophysics Molecular PharmacologyRat Liver MicrosomesBiochemistryMedicineLiver Physiology	1979	163
The use of intramolecular isotope effects to distinguish between deprotonation and hydrogen atom abstraction mechanisms in cytochrome P-450- and peroxidase-catalyzed N-demethylation reactions. Gerald T. Miwa, John Walsh, G.L. Kedderis, Journal of Biological Chemistry	1983	161
Comparison of Intrinsic Clearance in Liver Microsomes and Hepatocytes from Rats and Humans: Evaluation of Free Fraction and Uptake in Hepatocytes Chuang Lu, Ping Li, Richard Gallegos, Drug Metabolism and Disposition	2006	141
RELATIVE CONTRIBUTIONS OF THE FIVE MAJOR HUMAN CYTOCHROMES P450, 1A2, 2C9, 2C19, 2D6, AND 3A4, TO THE HEPATIC METABOLISM OF THE PROTEASOME INHIBITOR BORTEZOMIB Vinita Uttamsingh, Chuang Lu, Gerald T. Miwa, Drug Metabolism and Disposition	2005	136
Studies on the association of cytochrome P-450 and NADPH-cytochrome c reductase during catalysis in a reconstituted hydroxylating system. Gerald T. Miwa, S.B. West, Mou‐Tuan Huang, Journal of Biological Chemistry Aldehyde DehydrogenaseBinary ComplexBiochemistryAldo-keto ReductaseBioenergetics	1979	134
HUMAN METABOLISM OF THE PROTEASOME INHIBITOR BORTEZOMIB: IDENTIFICATION OF CIRCULATING METABOLITES Teresa Pekol, J. Scott Daniels, Jason Labutti, Drug Metabolism and Disposition	2005	131
EXPRESSION, LOCALIZATION, AND FUNCTIONAL CHARACTERISTICS OF BREAST CANCER RESISTANCE PROTEIN IN CACO-2 CELLS Cindy Q. Xia, Ning Liu, David Yang, Drug Metabolism and Disposition	2005	127

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