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Journal Abstract Search

244 related items for PubMed ID: 14610243

  • 1. Cat red blood cell thiopurine S-methyltransferase: companion animal pharmacogenetics.
    Salavaggione OE, Yang C, Kidd LB, Thomae BA, Pankratz VS, Trepanier LA, Weinshilboum RM.
    J Pharmacol Exp Ther; 2004 Feb; 308(2):617-26. PubMed ID: 14610243
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  • 2. Canine red blood cell thiopurine S-methyltransferase: companion animal pharmacogenetics.
    Salavaggione OE, Kidd L, Prondzinski JL, Szumlanski CL, Pankratz VS, Wang L, Trepanier L, Weinshilboum RM.
    Pharmacogenetics; 2002 Dec; 12(9):713-24. PubMed ID: 12464800
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  • 3. Human liver thiopurine methyltransferase pharmacogenetics: biochemical properties, liver-erythrocyte correlation and presence of isozymes.
    Szumlanski CL, Honchel R, Scott MC, Weinshilboum RM.
    Pharmacogenetics; 1992 Aug; 2(4):148-59. PubMed ID: 1306116
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  • 5. Functional characterization of 23 allelic variants of thiopurine S-methyltransferase gene (TPMT*2 - *24).
    Ujiie S, Sasaki T, Mizugaki M, Ishikawa M, Hiratsuka M.
    Pharmacogenet Genomics; 2008 Oct; 18(10):887-93. PubMed ID: 18708949
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  • 6. Thiopurine S-methyltransferase pharmacogenetics: genotype to phenotype correlation in the Slovenian population.
    Milek M, Murn J, Jaksic Z, Lukac Bajalo J, Jazbec J, Mlinaric Rascan I.
    Pharmacology; 2006 Oct; 77(3):105-14. PubMed ID: 16691038
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  • 9. Isolation of a human thiopurine S-methyltransferase (TPMT) complementary DNA with a single nucleotide transition A719G (TPMT*3C) and its association with loss of TPMT protein and catalytic activity in humans.
    Loennechen T, Yates CR, Fessing MY, Relling MV, Krynetski EY, Evans WE.
    Clin Pharmacol Ther; 1998 Jul; 64(1):46-51. PubMed ID: 9695718
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  • 10. Human pharmacogenetics of methyl conjugation.
    Weinshilboum RM.
    Fed Proc; 1984 May 15; 43(8):2303-7. PubMed ID: 6714437
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  • 11. Segregation analysis of human red blood cell thiopurine methyltransferase activity.
    Vuchetich JP, Weinshilboum RM, Price RA.
    Genet Epidemiol; 1995 May 15; 12(1):1-11. PubMed ID: 7713396
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  • 14. The role of genetic variation in thiopurine methyltransferase activity and the efficacy and/or side effects of azathioprine therapy in dermatologic patients.
    Snow JL, Gibson LE.
    Arch Dermatol; 1995 Feb 15; 131(2):193-7. PubMed ID: 7857117
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  • 15. Thiopurine methyltransferase activity in a Korean population sample of children.
    Park-Hah JO, Klemetsdal B, Lysaa R, Choi KH, Aarbakke J.
    Clin Pharmacol Ther; 1996 Jul 15; 60(1):68-74. PubMed ID: 8689814
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  • 18. Genetic determinants of the pre- and post-azathioprine therapy thiopurine methyltransferase activity phenotype.
    Arenas M, Duley JA, Ansari A, Shobowale-Bakre EA, Fairbanks L, Soon SY, Sanderson J, Marinaki AM.
    Nucleosides Nucleotides Nucleic Acids; 2004 Oct 15; 23(8-9):1403-5. PubMed ID: 15571267
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  • 19. Detection of known and new mutations in the thiopurine S-methyltransferase gene by single-strand conformation polymorphism analysis.
    Spire-Vayron de la Moureyre C, Debuysère H, Sabbagh N, Marez D, Vinner E, Chevalier ED, Lo Guidice JM, Broly F.
    Hum Mutat; 1998 Oct 15; 12(3):177-85. PubMed ID: 9711875
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  • 20. High prevalence of polymorphism and low activity of thiopurine methyltransferase in patients with inflammatory bowel disease.
    Larussa T, Suraci E, Lentini M, Nazionale I, Gallo L, Abenavoli L, Imeneo M, Costanzo FS, Cuda G, Luzza F.
    Eur J Intern Med; 2012 Apr 15; 23(3):273-7. PubMed ID: 22385887
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