Pharmacogenetics as a molecular basis for individualized drug therapy: the thiopurine S-methyltransferase paradigm.
- 1 January 1999
- journal article
- review article
- Published by Springer Nature in Pharmaceutical Research
- Vol. 16 (3) , 342-349
- https://doi.org/10.1023/a:1011909315614
Abstract
No abstract availableKeywords
This publication has 53 references indexed in Scilit:
- Racial variability in the UDP-glucuronosyltransferase 1 ( UGT1A1 ) promoter: A balanced polymorphism for regulation of bilirubin metabolism?Proceedings of the National Academy of Sciences, 1998
- A tellurite-resistance genetic determinant from phytopathogenic pseudomonads encodes a thiopurine methyltransferase: evidence of a widely-conserved family of methyltransferasesBiochimica et Biophysica Acta (BBA) - Gene Structure and Expression, 1998
- Conventional Compared with Individualized Chemotherapy for Childhood Acute Lymphoblastic LeukemiaNew England Journal of Medicine, 1998
- Detection of known and new mutations in the thiopurineS-methyltransferase gene by single-strand conformation polymorphism analysisHuman Mutation, 1998
- Human thiopurine methyltransferase pharmacogenetics: Gene sequence polymorphisms*Clinical Pharmacology & Therapeutics, 1997
- Methylation of mercaptopurine, thioguanine, and their nucleotide metabolites by heterologously expressed human thiopurine S-methyltransferase.1995
- Beneficial effects of conversion from cyclosporin to azathioprine after kidney transplantationThe Lancet, 1995
- Human thiopurine methyltransferase: molecular cloning and expression of T84 colon carcinoma cell cDNA.1993
- Genetic basis for a lower prevalence of deficient CYP2D6 oxidative drug metabolism phenotypes in black Americans.Journal of Clinical Investigation, 1993
- Human erythrocyte thiopurine methyltransferase: Radiochemical microassay and biochemical propertiesClinica Chimica Acta; International Journal of Clinical Chemistry, 1978