181 related articles for article (PubMed ID: 18482735)
21. Thiopurine S-methyltransferase pharmacogenetics: autophagy as a mechanism for variant allozyme degradation.
Li F; Wang L; Burgess RJ; Weinshilboum RM
Pharmacogenet Genomics; 2008 Dec; 18(12):1083-94. PubMed ID: 18820593
[TBL] [Abstract][Full Text] [Related]
22. Polymorphisms of the thiopurine S-methyltransferase gene among the Libyan population.
Zeglam HB; Benhamer A; Aboud A; Rtemi H; Mattardi M; Saleh SS; Bashein A; Enattah N
Libyan J Med; 2015; 10(1):27053. PubMed ID: 25819542
[TBL] [Abstract][Full Text] [Related]
23. Frequencies of thiopurine S-methyltransferase mutant alleles (TPMT*2, *3A, *3B and *3C) in 151 healthy Japanese subjects and the inheritance of TPMT*3C in the family of a propositus.
Kubota T; Chiba K
Br J Clin Pharmacol; 2001 May; 51(5):475-7. PubMed ID: 11422006
[TBL] [Abstract][Full Text] [Related]
24. Thiopurine S-methyltransferase pharmacogenetics: chaperone protein association and allozyme degradation.
Wang L; Sullivan W; Toft D; Weinshilboum R
Pharmacogenetics; 2003 Sep; 13(9):555-64. PubMed ID: 12972954
[TBL] [Abstract][Full Text] [Related]
25. [Frequency of thiopurine S-methyltransferase alleles in different ethnic groups living in Spain].
Corominas H; Domènech M; del Río E; Gich I; Domingo P; Baiget M
Med Clin (Barc); 2006 Mar; 126(11):410-2. PubMed ID: 16595084
[TBL] [Abstract][Full Text] [Related]
26. Molecular analysis of the thiopurine S-methyltransferase alleles in Bolivians and Tibetans.
Lu HF; Shih MC; Hsueh SC; Chen CM; Chang JY; Chang JG
J Clin Pharm Ther; 2005 Oct; 30(5):491-6. PubMed ID: 16164497
[TBL] [Abstract][Full Text] [Related]
27. Human thiopurine methyltransferase pharmacogenetics: gene sequence polymorphisms.
Otterness D; Szumlanski C; Lennard L; Klemetsdal B; Aarbakke J; Park-Hah JO; Iven H; Schmiegelow K; Branum E; O'Brien J; Weinshilboum R
Clin Pharmacol Ther; 1997 Jul; 62(1):60-73. PubMed ID: 9246020
[TBL] [Abstract][Full Text] [Related]
28. Human thiopurine methyltransferase pharmacogenetics. Kindred with a terminal exon splice junction mutation that results in loss of activity.
Otterness DM; Szumlanski CL; Wood TC; Weinshilboum RM
J Clin Invest; 1998 Mar; 101(5):1036-44. PubMed ID: 9486974
[TBL] [Abstract][Full Text] [Related]
29. Thiopurine S-methyltransferase (TPMT) pharmacogenetics: three new mutations and haplotype analysis in the Estonian population.
Tamm R; Oselin K; Kallassalu K; Magi R; Anier K; Remm M; Metspalu A
Clin Chem Lab Med; 2008; 46(7):974-9. PubMed ID: 18605963
[TBL] [Abstract][Full Text] [Related]
30. Frequency of thiopurine S-methyltransferase (TPMT) alleles in southeast Iranian population.
Bahari A; Hashemi M; Bari Z; Moazeni-Roodi A; Kaykhaei MA; Narouie B
Nucleosides Nucleotides Nucleic Acids; 2010 Mar; 29(3):237-44. PubMed ID: 20408054
[TBL] [Abstract][Full Text] [Related]
31. Genetic polymorphism of thiopurine S-methyltransferase: molecular mechanisms and clinical importance.
Krynetski EY; Evans WE
Pharmacology; 2000 Sep; 61(3):136-46. PubMed ID: 10971199
[TBL] [Abstract][Full Text] [Related]
32. Molecular analysis of thiopurine S-methyltransferase alleles in Taiwan aborigines and Taiwanese.
Lu HF; Shih MC; Chang YS; Chang JY; Ko YC; Chang SJ; Chang JG
J Clin Pharm Ther; 2006 Feb; 31(1):93-8. PubMed ID: 16476125
[TBL] [Abstract][Full Text] [Related]
33. Thiopurine S-methyltransferase (TPMT) genetic polymorphisms in Mexican newborns.
González-Del Angel A; Bermúdez-López C; Alcántara-Ortigoza MA; Vela-Amieva M; Castillo-Cruz RA; Martínez V; Torres-Espíndola L
J Clin Pharm Ther; 2009 Dec; 34(6):703-8. PubMed ID: 20175804
[TBL] [Abstract][Full Text] [Related]
34. Determination of intra-ethnic differences in the polymorphisms of thiopurine S-methyltransferase in Chinese.
Zhang JP; Zhou SF; Chen X; Huang M
Clin Chim Acta; 2006 Mar; 365(1-2):337-41. PubMed ID: 16223474
[TBL] [Abstract][Full Text] [Related]
35. [Mutant thiopurine S-methyltransferase alleles among Jing Chinese in Guangxi province].
Zhang JP; Huang M; Guan YY; Xu AL; Wu JH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Aug; 20(4):303-6. PubMed ID: 12903038
[TBL] [Abstract][Full Text] [Related]
36. Pyrosequencing of TPMT alleles in a general Swedish population and in patients with inflammatory bowel disease.
Haglund S; Lindqvist M; Almer S; Peterson C; Taipalensuu J
Clin Chem; 2004 Feb; 50(2):288-95. PubMed ID: 14656901
[TBL] [Abstract][Full Text] [Related]
37. Enhanced proteolysis of thiopurine S-methyltransferase (TPMT) encoded by mutant alleles in humans (TPMT*3A, TPMT*2): mechanisms for the genetic polymorphism of TPMT activity.
Tai HL; Krynetski EY; Schuetz EG; Yanishevski Y; Evans WE
Proc Natl Acad Sci U S A; 1997 Jun; 94(12):6444-9. PubMed ID: 9177237
[TBL] [Abstract][Full Text] [Related]
38. Comprehensive study of thiopurine methyltransferase genotype, phenotype, and genotype-phenotype discrepancies in Sweden.
Zimdahl Kahlin A; Helander S; Skoglund K; Söderkvist P; Mårtensson LG; Appell ML
Biochem Pharmacol; 2019 Jun; 164():263-272. PubMed ID: 31005613
[TBL] [Abstract][Full Text] [Related]
39. Structural basis of substrate recognition in thiopurine s-methyltransferase.
Peng Y; Feng Q; Wilk D; Adjei AA; Salavaggione OE; Weinshilboum RM; Yee VC
Biochemistry; 2008 Jun; 47(23):6216-25. PubMed ID: 18484748
[TBL] [Abstract][Full Text] [Related]
40. [Genetic polymorphism of the thiopurine S-methyltransferase of healthy Han Chinese].
Zhang JP; Guan YY; Wu JH; Jiang WQ; Huang M
Ai Zheng; 2003 Apr; 22(4):385-8. PubMed ID: 12703994
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
