메뉴 건너뛰기




Volumn 68, Issue 4, 2004, Pages 313-323

Tracing the origin of the most common thiopurine methyltransferase (TPMT) variants: Preliminary data from the patterns of haplotypic association with two CA repeats

Author keywords

[No Author keywords available]

Indexed keywords

THIOPURINE METHYLTRANSFERASE;

EID: 4444268912     PISSN: 00034800     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1529-8817.2004.00104.x     Document Type: Article
Times cited : (21)

References (32)
  • 1
    • 0035377554 scopus 로고    scopus 로고
    • STR data (AmpFlSTR Profiler Plus and GenePrint CTTv) from Mozambique
    • Alves, C., Gusmao, L. & Amorim, A. (2001a) STR data (AmpFlSTR Profiler Plus and GenePrint CTTv) from Mozambique. Forensic Sci Int 1119, 131-3.
    • (2001) Forensic Sci. Int. , vol.1119 , pp. 131-133
    • Alves, C.1    Gusmao, L.2    Amorim, A.3
  • 2
    • 0034050713 scopus 로고    scopus 로고
    • Screening of thiopurine S-methyltransferase mutations by horizontal conformation-sensitive gel electrophoresis
    • Alves, S., Prata, M. J., Ferreira, F. & Amorim, A. (2000) Screening of thiopurine S-methyltransferase mutations by horizontal conformation-sensitive gel electrophoresis. Hum Mutat 15, 246-53.
    • (2000) Hum. Mutat. , vol.15 , pp. 246-253
    • Alves, S.1    Prata, M.J.2    Ferreira, F.3    Amorim, A.4
  • 3
    • 0034889535 scopus 로고    scopus 로고
    • Influence of the variable number of tandem repeats located in the promoter region of the thiopurine methyltransferase gene on enzymatic activity
    • Alves, S., Amorim, A., Ferreira, F. & Prata, M. J. (2001b) Influence of the variable number of tandem repeats located in the promoter region of the thiopurine methyltransferase gene on enzymatic activity. Clin Pharmacol Ther 70, 165-74.
    • (2001) Clin. Pharmacol. Ther. , vol.70 , pp. 165-174
    • Alves, S.1    Amorim, A.2    Ferreira, F.3    Prata, M.J.4
  • 5
    • 0019732410 scopus 로고
    • Measuring the strength of associations between HLA antigens and diseases
    • Bengtsson, B. O. & Thomson, G. (1981) Measuring the strength of associations between HLA antigens and diseases. Tissue Antigens 18, 356-63.
    • (1981) Tissue Antigens , vol.18 , pp. 356-363
    • Bengtsson, B.O.1    Thomson, G.2
  • 6
    • 0033866345 scopus 로고    scopus 로고
    • Age and origin of the PRNP E200K mutation causing familial Creutzfeldt-Jacob disease in Libyan Jews
    • Colombo, R. (2000) Age and origin of the PRNP E200K mutation causing familial Creutzfeldt-Jacob disease in Libyan Jews. Am J Hum Genet 67, 528-31.
    • (2000) Am. J. Hum. Genet. , vol.67 , pp. 528-531
    • Colombo, R.1
  • 7
    • 0031981271 scopus 로고    scopus 로고
    • Heterogeneity of microsatellite mutations within and between loci, and implications for human demographic histories
    • Di Rienzo, A., Donnelly, P., Toomajian, C., Sisk, B., Hill, A., Petzl-Erler, M. L., Haines, G. K. & Barch, D. H. (1998) Heterogeneity of microsatellite mutations within and between loci, and implications for human demographic histories. Genetics 148, 1269-84.
    • (1998) Genetics , vol.148 , pp. 1269-1284
    • Di Rienzo, A.1    Donnelly, P.2    Toomajian, C.3    Sisk, B.4    Hill, A.5    Petzl-Erler, M.L.6    Haines, G.K.7    Barch, D.H.8
  • 11
    • 0025837127 scopus 로고
    • Altered mercaptopurine metabolism, toxic effects, and dosage requirement in a thiopurine methyltransferase-deficient child with acute lymphocytic leukemia
    • Evans, W. E., Horner, M., Chu, Y. Q., Kalwinsky, D. & Roberts, W. M. (1991) Altered mercaptopurine metabolism, toxic effects, and dosage requirement in a thiopurine methyltransferase-deficient child with acute lymphocytic leukemia. J Pediatr 119, 985-9.
    • (1991) J. Pediatr. , vol.119 , pp. 985-989
    • Evans, W.E.1    Horner, M.2    Chu, Y.Q.3    Kalwinsky, D.4    Roberts, W.M.5
  • 12
    • 0033358085 scopus 로고    scopus 로고
    • Age estimates of two common mutations causing factor XI deficiency: Recent genetic drift is not necessary for elevated disease incidence among Ashkenazi Jews
    • Goldstein, D. B., Reich, D. E., Bradman, N., Usher, S., Seligsohn, U. & Peretz, H. (1999) Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi Jews. Am J Hum Genet 64, 1071-5.
    • (1999) Am. J. Hum. Genet. , vol.64 , pp. 1071-1075
    • Goldstein, D.B.1    Reich, D.E.2    Bradman, N.3    Usher, S.4    Seligsohn, U.5    Peretz, H.6
  • 15
    • 0036066914 scopus 로고    scopus 로고
    • Thiopurine methyltransferase polymorphisms in a multiracial asian population and children with acute lymphoblastic leukemia
    • Kham, S. K., Tan, P. L., Tay, A. H., Heng, C. K., Yeoh, A. E. & Quah, T. C. (2002) Thiopurine methyltransferase polymorphisms in a multiracial asian population and children with acute lymphoblastic leukemia. J Pediatr Hematol Oncol 24, 353-9.
    • (2002) J. Pediatr. Hematol. Oncol. , vol.24 , pp. 353-359
    • Kham, S.K.1    Tan, P.L.2    Tay, A.H.3    Heng, C.K.4    Yeoh, A.E.5    Quah, T.C.6
  • 18
    • 0033434009 scopus 로고    scopus 로고
    • Ethnic differences in thiopurine methyltransferase pharmacogenetics: Evidence for allele specificity in Caucasian and Kenyan individuals
    • McLeod, H. L., Pritchard, S. C. Githang'a, J., Indalo, A., Ameyaw, M. M., Powrie, R. H., Booth, L. & Collie-Duguid, E. S. (1999) Ethnic differences in thiopurine methyltransferase pharmacogenetics: evidence for allele specificity in Caucasian and Kenyan individuals. Pharmacogenetics 9, 773-6.
    • (1999) Pharmacogenetics , vol.9 , pp. 773-776
    • McLeod, H.L.1    Pritchard, S.C.2    Githang'a, J.3    Indalo, A.4    Ameyaw, M.M.5    Powrie, R.H.6    Booth, L.7    Collie-Duguid, E.S.8
  • 19
    • 0034034158 scopus 로고    scopus 로고
    • Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia
    • McLeod, H. L., Krynetski, E. Y., Relling, M. V. & Evans, W. E. (2000) Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia. Leukemia 14, 567-72.
    • (2000) Leukemia , vol.14 , pp. 567-572
    • McLeod, H.L.1    Krynetski, E.Y.2    Relling, M.V.3    Evans, W.E.4
  • 21
  • 23
    • 0028819262 scopus 로고
    • Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population
    • Risch, N., de Leon, D. Ozelius, L., Kramr, P., Almasy, L., Singer, B., Fahn, S., Breakefield, X. & Bressman, S. (1995) Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population. Nat Genet 9, 152-159.
    • (1995) Nat. Genet. , vol.9 , pp. 152-159
    • Risch, N.1    de Leon, D.2    Ozelius, L.3    Kramr, P.4    Almasy, L.5    Singer, B.6    Fahn, S.7    Breakefield, X.8    Bressman, S.9
  • 24
    • 0003300707 scopus 로고    scopus 로고
    • Arlequin ver 2.000: A software for population genetics data analysis
    • University of Geneva, Switerzland
    • Scheneider, S., Roessli, D. & Excoffier, L. (2000) Arlequin ver 2.000: a software for population genetics data analysis. Genetics and Biometry laboratory, University of Geneva, Switerzland.
    • (2000) Genetics and Biometry Laboratory
    • Scheneider, S.1    Roessli, D.2    Excoffier, L.3
  • 25
    • 0035129485 scopus 로고    scopus 로고
    • Patterns of haplotype diversity within the serpin gene cluster at 14q32.1: Insights into the natural history of the alpha1-antitrypsin polymorphism
    • Seixas, S., Garcia, O., Trovoada, M.J., Santos, M. T., Amorim, A. & Rocha, J. (2001) Patterns of haplotype diversity within the serpin gene cluster at 14q32.1: insights into the natural history of the alpha1-antitrypsin polymorphism. Hum Genet 108, 20-30.
    • (2001) Hum. Genet. , vol.108 , pp. 20-30
    • Seixas, S.1    Garcia, O.2    Trovoada, M.J.3    Santos, M.T.4    Amorim, A.5    Rocha, J.6
  • 29
    • 0033910668 scopus 로고    scopus 로고
    • New estimates of intergenerational time intervals for the calculation of age and origins mutations
    • Tremblay, M. & Vézina, H. (2000) New estimates of intergenerational time intervals for the calculation of age and origins mutations. Am J Hum Genet 66, 651-658.
    • (2000) Am. J. Hum. Genet. , vol.66 , pp. 651-658
    • Tremblay, M.1    Vézina, H.2
  • 30
    • 0018822866 scopus 로고
    • Mercaptopurine Pharmacogenetics: Monogenic inheritance of erythrocyte thiopurine methyltransferase activity
    • Weinshilboum, R. M. & Sladek, S. L. (1980) Mercaptopurine Pharmacogenetics: Monogenic inheritance of erythrocyte thiopurine methyltransferase activity. Am J Hum Genet 32, 651-662.
    • (1980) Am. J. Hum. Genet. , vol.32 , pp. 651-662
    • Weinshilboum, R.M.1    Sladek, S.L.2
  • 31
    • 0034891467 scopus 로고    scopus 로고
    • Do delta F508 heterozygotes have a selective advantage?
    • Wiuf C. (2001) Do delta F508 heterozygotes have a selective advantage? Genet Res 78, 41-7.
    • (2001) Genet. Res. , vol.78 , pp. 41-47
    • Wiuf, C.1
  • 32
    • 0030934850 scopus 로고    scopus 로고
    • Molecular diagnosis of thiopurine S-methyltransterase deficiency: Genetic basis for azathioprine and mercaptopurine intolerance
    • Yates, C. R., Krynetski, E. Y., Loennechen, T., Fessing, M. Y., Tai, H. L., Pui, C. H., Relling, M. V. & Evans, W. E. (1997) Molecular diagnosis of thiopurine S-methyltransterase deficiency: genetic basis for azathioprine and mercaptopurine intolerance. Ann Intern Med 126, 608-14.
    • (1997) Ann. Intern. Med. , vol.126 , pp. 608-614
    • Yates, C.R.1    Krynetski, E.Y.2    Loennechen, T.3    Fessing, M.Y.4    Tai, H.L.5    Pui, C.H.6    Relling, M.V.7    Evans, W.E.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.