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Volumn 115, Issue 14, 2000, Pages 540-541

Variability in the UGT-1 gene promoter and Gilbert's syndrome;Distribución del genotipo A(TA)7TAA asociado al síndrome de Gilbert en la población española

Author keywords

Gilbert's syndrome; TA repeat; UGT 1 gene

Indexed keywords

GLUCURONOSYLTRANSFERASE;

EID: 0034727348     PISSN: 00257753     EISSN: None     Source Type: Journal    
DOI: 10.1016/s0025-7753(00)71617-4     Document Type: Article
Times cited : (21)

References (10)
  • 2
    • 0028276410 scopus 로고
    • Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man
    • Bosma PJ, Seppen J, Goldhoorn B. Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man. J Biol Chem 1994; 269: 17960-17964.
    • (1994) J Biol Chem , vol.269 , pp. 17960-17964
    • Bosma, P.J.1    Seppen, J.2    Goldhoorn, B.3
  • 3
    • 0028867826 scopus 로고
    • The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome
    • Bosma PJ, Chowdhury JR, Bakker C, Gantla S, de Boer A, Oostra B et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome. N Engl J Med 1995; 333: 1171-1175.
    • (1995) N Engl J Med , vol.333 , pp. 1171-1175
    • Bosma, P.J.1    Chowdhury, J.R.2    Bakker, C.3    Gantla, S.4    De Boer, A.5    Oostra, B.6
  • 4
    • 0030030762 scopus 로고    scopus 로고
    • Genetic variation in bilirubin UDP-glucoronosyltransferase gen promoter and Gilbert's syndrome
    • Monaghan G, Ryan M, Seddon R, Hume R, Burchell B. Genetic variation in bilirubin UDP-glucoronosyltransferase gen 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
  • 5
    • 0032860652 scopus 로고    scopus 로고
    • Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndrome
    • Sampietro M, Iolascon A. Molecular pathology of Crigler-Najjar type I and II and Gilbert's Syndrome. Haematologica 1999; 84: 150-157.
    • (1999) Haematologica , vol.84 , pp. 150-157
    • Sampietro, M.1    Iolascon, A.2
  • 6
    • 0032852420 scopus 로고    scopus 로고
    • Co-inherited Gilbert's syndrome: A factor determining hyperbilirubinemia in homozygous beta-thalassaemia
    • Galanello R, Cipollina MD, Dessi C, Giagu N, Lai E, Cao A. Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassaemia. Haematologica 1999; 84: 103-105.
    • (1999) Haematologica , vol.84 , pp. 103-105
    • Galanello, R.1    Cipollina, M.D.2    Dessi, C.3    Giagu, N.4    Lai, E.5    Cao, A.6
  • 7
    • 0030663191 scopus 로고    scopus 로고
    • The expression of uridine diphosphate glucoronosyltransferase gene is a major determinant of bilirrubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenese deficiency
    • Sampietro M, Lupica L, Perrero L, Comino A, Martínez F, Cappellini D et al. The expression of uridine diphosphate glucoronosyltransferase gene is a major determinant of bilirrubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenese deficiency. Br J Haematol 1997; 99: 437-439.
    • (1997) Br J Haematol , vol.99 , pp. 437-439
    • Sampietro, M.1    Lupica, L.2    Perrero, L.3    Comino, A.4    Martínez, F.5    Cappellini, D.6
  • 8
    • 0008435402 scopus 로고    scopus 로고
    • Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis
    • Miraglia del Giudice E, Perrotta S, Nobili B, Specchia C, d'Urzo G, Iolascon A. Coinheritance of Gilbert Syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis. Blood 1999; 94: 2259-2262.
    • (1999) Blood , vol.94 , pp. 2259-2262
    • Miraglia Del Giudice, E.1    Perrotta, S.2    Nobili, B.3    Specchia, C.4    D'Urzo, G.5    Iolascon, A.6
  • 9
    • 0033510908 scopus 로고    scopus 로고
    • Gilbert's syndrome is a contributory factor in prolonged uncongugated hyperbilirubinemia of the newborn
    • Monaghan G, McLellan A, McGeehan A, Li Volti S, Mollica F, Salemi I et al. Gilbert's syndrome is a contributory factor in prolonged uncongugated hyperbilirubinemia of the newborn. J Pediatr 1999; 134: 441-446.
    • (1999) J Pediatr , vol.134 , pp. 441-446
    • Monaghan, G.1    McLellan, A.2    McGeehan, A.3    Li Volti, S.4    Mollica, F.5    Salemi, I.6
  • 10
    • 0032493441 scopus 로고    scopus 로고
    • Racial variability in the UDP-glucuronosyltransferase 1 (UGT-1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
    • Beutler E, Gelbart T, Demina A. Racial variability in the UDP-glucuronosyltransferase 1 (UGT-1A1) 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.