[Pharmacogenetic study of thiopurine S-methyltransferase (TPMT) and thiopurine toxicity].
H, Corominas +3 more
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The role of pharmacogenetics in the therapy regimen of acute lymphoblastic leukemia in children: recent discoveries and future perspectives. [PDF]
Szoszkiewicz A +5 more
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An Ambiguous NUDT15 Signal in a Child with B-cell Acute Lymphoblastic Leukemia. [PDF]
Sterner RM +4 more
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Bone Marrow Aplasia and Neutropenic Fever Following Azathioprine Dose Escalation in a TPMT-Deficient Patient with Crohn's Disease and Psoriatic Arthritis-A CARE-Compliant Case. [PDF]
Wroński K +4 more
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Severe myelosuppression and alopecia after thiopurine initiation in a patient with NUDT15 deficiency. [PDF]
Wu AS, Mozessohn L, Kim RB, Zipursky JS.
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Knowledge, attitudes, and practices of healthcare providers toward ADR reporting regarding thiopurine drugs for the treatment of acute lymphoblastic leukemia at the University of Gondar Comprehensive Specialized Hospital, Northwest Ethiopia. [PDF]
Kassa E +10 more
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Examination of the TPMT and NUDT15*3 Variants to Predict the Response to Thiopurines in an Italian Cohort of Patients with Inflammatory Bowel Disease. [PDF]
Tavano F +10 more
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Purine substrates for human thiopurine methyltransferase
Biochemical Pharmacology, 1994Thiopurine methyltransferase (TPMT) catalyzes the S-methylation of thiopurine drugs such as 6-mercaptopurine (6-MP) and 6-thioguanine (6-TG). A genetic polymorphism regulating TPMT activity in human tissue is an important factor responsible for individual differences in the toxicity and therapeutic efficacy of these drugs.
M, Deininger +5 more
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▪ Abstract Methyl conjugation is an important pathway in the biotransformation of many exogenous and endogenous compounds. Pharmacogenetic studies of methyltransferase enzymes have resulted in the identification and characterization of functionally important common genetic polymorphisms for catechol O-methyltransferase, thiopurine methyltransferase ...
R M, Weinshilboum +2 more
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