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Volumn 11, Issue 6, 2005, Pages 797-802

Polymorphisms of uridine-diphosphoglucuronosyltransferase 1A7 gene in Taiwan Chinese

Author keywords

Genotype; Single nucleotide polymorphisms; Taiwan chinese; UGT1A7 gene

Indexed keywords

ADENINE; CYTOSINE; GLUCURONOSYLTRANSFERASE; GLUCURONOSYLTRANSFERASE 1A7; GUANINE; NUCLEOTIDE; PRIMER DNA; RESTRICTION ENDONUCLEASE; THYMINE; UNCLASSIFIED DRUG;

EID: 14544300089     PISSN: 10079327     EISSN: None     Source Type: Journal    
DOI: 10.3748/wjg.v11.i6.797     Document Type: Article
Times cited : (22)

References (32)
  • 1
    • 0032959531 scopus 로고    scopus 로고
    • Genetic epidemiology of environmental toxicity and cancer susceptibility: Human allelic polymorphisms in drug-metabolizing enzyme genes, their functional importance, and nomenclature issues
    • Nebert D, Ingelman-Sundberg M, Daly A. Genetic epidemiology of environmental toxicity and cancer susceptibility: Human allelic polymorphisms in drug-metabolizing enzyme genes, their functional importance, and nomenclature issues. Drug Metab Rev 1999; 31: 467-487
    • (1999) Drug Metab. Rev. , vol.31 , pp. 467-487
    • Nebert, D.1    Ingelman-Sundberg, M.2    Daly, A.3
  • 5
    • 0030699360 scopus 로고    scopus 로고
    • Genetic polymorphism in the human UGT1A6 (plnnar phenol) UDP-glucuronosyltransferase: Pharmacological implications
    • Ciotti M, Marrone A, Potter C, Owens IS. Genetic polymorphism in the human UGT1A6 (plnnar phenol) UDP-glucuronosyltransferase: Pharmacological implications. Pharmacogenetics 1997; 7: 485-495
    • (1997) Pharmacogenetics , vol.7 , pp. 485-495
    • Ciotti, M.1    Marrone, A.2    Potter, C.3    Owens, I.S.4
  • 6
    • 0033789766 scopus 로고    scopus 로고
    • Structural heterogeneity at the UDP-glucuronosyltransferase 1 locus: Functional consequences of three novel missense mutations in the human UGT1A7 gene
    • Guillemette C, Ritter JK, Auyeung DJ, Kessler FK, Housman DE. Structural heterogeneity at the UDP-glucuronosyltransferase 1 locus: Functional consequences of three novel missense mutations in the human UGT1A7 gene. Pharmacogenetics 2000; 10: 629-644
    • (2000) Pharmacogenetics , vol.10 , pp. 629-644
    • Guillemette, C.1    Ritter, J.K.2    Auyeung, D.J.3    Kessler, F.K.4    Housman, D.E.5
  • 8
    • 0033816138 scopus 로고    scopus 로고
    • Variations of the bilirubin uridine-diphosphoglucuronosyltransferase 1A1 gene in healthy Taiwanese
    • Huang CS, Luo GA, Huang MJ, Yu SC, Yang SS. Variations of the bilirubin uridine-diphosphoglucuronosyltransferase 1A1 gene in healthy Taiwanese. Pharmacogenetics 2000; 10: 539-544
    • (2000) Pharmacogenetics , vol.10 , pp. 539-544
    • Huang, C.S.1    Luo, G.A.2    Huang, M.J.3    Yu, S.C.4    Yang, S.S.5
  • 9
    • 0036157862 scopus 로고    scopus 로고
    • Genetic polymorphisms of UDP-glucuronosyltransferase in Asians: UGT1A1 *28 is a common allele in Indians
    • Balram C, Sabapathy K, Fei G, Khoo KS, Lee EJ. Genetic polymorphisms of UDP-glucuronosyltransferase in Asians: UGT1A1 *28 is a common allele in Indians. Pharmacogenetics 2002; 12: 81-83
    • (2002) Pharmacogenetics , vol.12 , pp. 81-83
    • Balram, C.1    Sabapathy, K.2    Fei, G.3    Khoo, K.S.4    Lee, E.J.5
  • 10
    • 0030053274 scopus 로고    scopus 로고
    • The genetic basis of Gilbert's syndrome
    • Sato H, Adachi Y, Koiwai O. The genetic basis of Gilbert's syndrome. Lancet 1996; 347: 557-558
    • (1996) Lancet , vol.347 , pp. 557-558
    • Sato, H.1    Adachi, Y.2    Koiwai, O.3
  • 12
  • 14
    • 0030030762 scopus 로고    scopus 로고
    • Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
    • Monaghan G, Ryan M, Seddon R, Hume R, Burchell B. Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome. Lancet 1996; 347: 578-581
    • (1996) Lancet , vol.347 , pp. 578-581
    • Monaghan, G.1    Ryan, M.2    Seddon, R.3    Hume, R.4    Burchell, B.5
  • 16
    • 0032493441 scopus 로고    scopus 로고
    • Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
    • Beutler E, Gelbart T, Demina. A. Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism? Proc Natl Acad Sci USA 1998; 95: 8170-8174
    • (1998) Proc. Natl. Acad. Sci. USA , vol.95 , pp. 8170-8174
    • Beutler, E.1    Gelbart, T.2    Demina, A.3
  • 17
    • 0036305499 scopus 로고    scopus 로고
    • Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia
    • Huang CS, Chang PF, Huang MJ, Chen ES, Chen WC. Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia. Gastroenterology 2002; 123: 127-133
    • (2002) Gastroenterology , vol.123 , pp. 127-133
    • Huang, C.S.1    Chang, P.F.2    Huang, M.J.3    Chen, E.S.4    Chen, W.C.5
  • 18
    • 0036787116 scopus 로고    scopus 로고
    • Relationship between UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia
    • Huang CS, Chang PF, Huang MJ, Chen ES, Hung KL, Tsou KI. Relationship between UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia. Pediatr Res 2002; 52; 601-605
    • (2002) Pediatr. Res. , vol.52 , pp. 601-605
    • Huang, C.S.1    Chang, P.F.2    Huang, M.J.3    Chen, E.S.4    Hung, K.L.5    Tsou, K.I.6
  • 19
    • 0030691028 scopus 로고    scopus 로고
    • Gilbert's syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose- dependent genetic interaction crucial to neonatal hyperbilirubinemia
    • Kaplan M, Renbaum P, Levy-Lahad E, Hammerman C, Lahad A, Beutler E. Gilbert's syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose- dependent genetic interaction crucial to neonatal hyperbilirubinemia. Proc Natl Acad Sci USA 1997; 94: 12128-12132
    • (1997) Proc. Natl. Acad. Sci. USA , vol.94 , pp. 12128-12132
    • Kaplan, M.1    Renbaum, P.2    Levy-Lahad, E.3    Hammerman, C.4    Lahad, A.5    Beutler, E.6
  • 20
    • 0031949264 scopus 로고    scopus 로고
    • Gilbert's syndrome accelerates development of neonatal jaundice
    • Bancroft JD, Kreamer B, Gourley GR. Gilbert's syndrome accelerates development of neonatal jaundice. J Pediatr 1998; 132: 656-660
    • (1998) J. Pediatr. , vol.132 , pp. 656-660
    • Bancroft, J.D.1    Kreamer, B.2    Gourley, G.R.3
  • 21
    • 0034797873 scopus 로고    scopus 로고
    • A novel compound heterozygous variation of the uridine-diphosphoglucuronosyl transferase 1A1 gene that causes crigler-najjar syndrome type II
    • Huang CS, Luo GA, Huang MJ, Chen ES, Young TH, Chao YC. A novel compound heterozygous variation of the uridine-diphosphoglucuronosyl transferase 1A1 gene that causes crigler-najjar syndrome type II. Pharmacogenetics 2001; 11: 639-642
    • (2001) Pharmacogenetics , vol.11 , pp. 639-642
    • Huang, C.S.1    Luo, G.A.2    Huang, M.J.3    Chen, E.S.4    Young, T.H.5    Chao, Y.C.6
  • 22
    • 0036313887 scopus 로고    scopus 로고
    • Genetic polymorphisms of the UDP-glucuronosyltransferase 1A7 gene and irinotecan toxicity in Japanese cancer patients
    • Ando M, Ando Y, Sekido Y, Ando M, Shimokata K, Hasegawa Y. Genetic polymorphisms of the UDP-glucuronosyltransferase 1A7 gene and irinotecan toxicity in Japanese cancer patients. Jpn J Cancer Res 2002; 93: 591-597
    • (2002) Jpn. J. Cancer Res. , vol.93 , pp. 591-597
    • Ando, M.1    Ando, Y.2    Sekido, Y.3    Ando, M.4    Shimokata, K.5    Hasegawa, Y.6
  • 23
    • 0035053747 scopus 로고    scopus 로고
    • Correlation of mutational analysis to clinical features in Taiwanese patients with Gilbert's syndrome
    • Hsieh SY, Wu YH, Lin DY, Chu CM, Wu M, Liaw YF. Correlation of mutational analysis to clinical features in Taiwanese patients with Gilbert's syndrome. Am J Gastroenterol 2001; 96 1188-1193
    • (2001) Am. J. Gastroenterol. , vol.96 , pp. 1188-1193
    • Hsieh, S.Y.1    Wu, Y.H.2    Lin, D.Y.3    Chu, C.M.4    Wu, M.5    Liaw, Y.F.6
  • 24
    • 12244254497 scopus 로고    scopus 로고
    • Co-inheritance of variant UDP-glucuronosyltransferase 1A1 gene and glucose-6-phosphate dehydrogenase deficiency in adults with hyperbilirubinemia
    • Huang MJ, Yang YC, Yang SS, Lin MS, Chen ES, Huang CS. Co-inheritance of variant UDP-glucuronosyltransferase 1A1 gene and glucose-6-phosphate dehydrogenase deficiency in adults with hyperbilirubinemia. Pharmacogenetics 2002; 12: 663-666
    • (2002) Pharmacogenetics , vol.12 , pp. 663-666
    • Huang, M.J.1    Yang, Y.C.2    Yang, S.S.3    Lin, M.S.4    Chen, E.S.5    Huang, C.S.6
  • 25
    • 0030800075 scopus 로고    scopus 로고
    • Differential expression of the UGT1A locus in human liver, biliary, and gastric tissue: Identification of UGT1A7 and UGT1A10 transcripts in extrahepatic tissue
    • Strassburg CP, Oldhafer K, Manns MP, Tukey RH. Differential expression of the UGT1A locus in human liver, biliary, and gastric tissue: Identification of UGT1A7 and UGT1A10 transcripts in extrahepatic tissue. Mol Pharmacol 1997; 52: 212-220
    • (1997) Mol. Pharmacol. , vol.52 , pp. 212-220
    • Strassburg, C.P.1    Oldhafer, K.2    Manns, M.P.3    Tukey, R.H.4
  • 26
    • 0033104667 scopus 로고    scopus 로고
    • Regulation and function of family 1 and family 2 UDP-glucuronosyltransferase gene (UGT1A, UGT2B) in human oesophagus
    • Strassburg CP, Strassburg A, Nguyen N, Li Q, Manns MP, Tukey RH. Regulation and function of family 1 and family 2 UDP-glucuronosyltransferase gene (UGT1A, UGT2B) in human oesophagus. Biochem J 1999; 338(Pt 2): 489-498
    • (1999) Biochem. J. , vol.338 , Issue.PART 2 , pp. 489-498
    • Strassburg, C.P.1    Strassburg, A.2    Nguyen, N.3    Li, Q.4    Manns, M.P.5    Tukey, R.H.6
  • 27
    • 0036101804 scopus 로고    scopus 로고
    • Polymorphisms of human UDP-glucuronosyltransferase 1A7 gene in colorectal cancer
    • Strassburg CP, Vogel A, Kneip S, Tukey RH, Mann MP. Polymorphisms of human UDP-glucuronosyltransferase 1A7 gene in colorectal cancer. Gut 2002; 50: 851-856
    • (2002) Gut , vol.50 , pp. 851-856
    • Strassburg, C.P.1    Vogel, A.2    Kneip, S.3    Tukey, R.H.4    Mann, M.P.5
  • 28
    • 0032502764 scopus 로고    scopus 로고
    • Expression of the UDP-glucuronosyltransferase 1A locus in human colon
    • Strassburg CP, Mann MP, Tukey RH. Expression of the UDP-glucuronosyltransferase 1A locus in human colon. J Biol Chem 1998; 273: 8719-8726
    • (1998) J. Biol. Chem. , vol.273 , pp. 8719-8726
    • Strassburg, C.P.1    Mann, M.P.2    Tukey, R.H.3
  • 29
    • 0033600191 scopus 로고    scopus 로고
    • Glucuronidation of 7-ethyl-10-hydroxycamptothecin (SN-38) by the human UDP-glucuronosyltransferases encoded at the UGT1 locus
    • Ciotti M, Basu N, Brangi M, Owens I. Glucuronidation of 7-ethyl-10-hydroxycamptothecin (SN-38) by the human UDP-glucuronosyltransferases encoded at the UGT1 locus. Biochem Biophys Res Commun 1999; 260: 199-202
    • (1999) Biochem. Biophys. Res. Commun. , vol.260 , pp. 199-202
    • Ciotti, M.1    Basu, N.2    Brangi, M.3    Owens, I.4
  • 30
    • 0035913673 scopus 로고    scopus 로고
    • Tobacco carcinogen-detoxifying enzyme UGT1A7 and its association with orolaryngeal cancer risk
    • Zheng Z, Park JY, Guillemette C, Schantz SP, Lazarus P. Tobacco carcinogen-detoxifying enzyme UGT1A7 and its association with orolaryngeal cancer risk. J Natl Cancer Inst 2001; 93: 1411-1418
    • (2001) J. Natl. Cancer Inst. , vol.93 , pp. 1411-1418
    • Zheng, Z.1    Park, J.Y.2    Guillemette, C.3    Schantz, S.P.4    Lazarus, P.5
  • 31
    • 0034765595 scopus 로고    scopus 로고
    • Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene
    • Vogel A, Kneip S, Barut A, Ehmer U, Tukey RH, Mann MP, Strassburg CP. Genetic link of hepatocellular carcinoma with polymorphisms of the UDP-glucuronosyltransferase UGT1A7 gene. Gastroenterology 2001; 121: 1136-1144
    • (2001) Gastroenterology , vol.121 , pp. 1136-1144
    • Vogel, A.1    Kneip, S.2    Barut, A.3    Ehmer, U.4    Tukey, R.H.5    Mann, M.P.6    Strassburg, C.P.7


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