-
1
-
-
0032860652
-
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;84:150-7.
-
(1999)
Haematologica
, vol.84
, pp. 150-157
-
-
Sampietro, M.1
Iolascon, A.2
-
2
-
-
0033802568
-
Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert syndrome) in healthy subjects
-
Borlak J, Thum T, Landt O, Erb K, Hermann R. Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert syndrome) in healthy subjects. Hepatology 2000;32:792-5.
-
(2000)
Hepatology
, vol.32
, pp. 792-795
-
-
Borlak, J.1
Thum, T.2
Landt, O.3
Erb, K.4
Hermann, R.5
-
3
-
-
0033054393
-
Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in Italian population
-
Biondi ML, Turri O, Dilillo D, Stival G, Guagnellini E. Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in Italian population. Clin Chem 1999;45:897-8.
-
(1999)
Clin Chem
, vol.45
, pp. 897-898
-
-
Biondi, M.L.1
Turri, O.2
Dilillo, D.3
Stival, G.4
Guagnellini, E.5
-
4
-
-
0028867826
-
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert syndrome
-
Bosma PJ, Chowdhury JR, Bakker C, Gantla S, Boer A, Oostra BA, et al. The genetic basis of the reduced expression of bilirubin UDP- glucuronosyltransferase 1 in Gilbert syndrome. N Engl J Med 1995;333:1171-5.
-
(1995)
N Engl J Med
, vol.333
, pp. 1171-1175
-
-
Bosma, P.J.1
Chowdhury, J.R.2
Bakker, C.3
Gantla, S.4
Boer, A.5
Oostra, B.A.6
-
5
-
-
0033961560
-
Rapid method for detection of extra (TA) in the promoter of the bilirubin-UDP-glucoronosyl transferase 1 gene associated with Gilbert syndrome
-
Pirulli D, Giordano M, Puzzer D, Crovella S, Rigato I, Tiribelli C, et al. Rapid method for detection of extra (TA) in the promoter of the bilirubin-UDP-glucoronosyl transferase 1 gene associated with Gilbert syndrome. Clin Chem 2000;46:129-31.
-
(2000)
Clin Chem
, vol.46
, pp. 129-131
-
-
Pirulli, D.1
Giordano, M.2
Puzzer, D.3
Crovella, S.4
Rigato, I.5
Tiribelli, C.6
-
6
-
-
0036546068
-
TATA-box polymorphism in the uridine diphosphate glucuronosyl transferase gene in Portuguese patients with a clinical diagnosis of Gilbert's syndrome
-
Costa E, Vieira E, Santos-Silva E, Barbot J, dos Santos R. TATA-box polymorphism in the uridine diphosphate glucuronosyl transferase gene in Portuguese patients with a clinical diagnosis of Gilbert's syndrome. Haematologica 2002;87:ELT21.
-
(2002)
Haematologica
, vol.87
-
-
Costa, E.1
Vieira, E.2
Santos-Silva, E.3
Barbot, J.4
Dos Santos, R.5
-
7
-
-
0032493441
-
Racial variability in the UDP-glucuronosyl-transferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
-
Beutler E, Gelbart T, Demina A. Racial variability in the UDP-glucuronosyl-transferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism? Proc Natl Acad Sci U S A 1998;95:8170-4.
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 8170-8174
-
-
Beutler, E.1
Gelbart, T.2
Demina, A.3
-
8
-
-
0035029401
-
The phenobarbital response enhancer module in the human bilirubin UDP-glucuronosyltransferase UGT1A1 gene and regulation by the nuclear receptor CAR
-
Sugatani J, Kojima H, Ueda A, Kakizaki S, Yoshinari K, Gong QH, et al. The phenobarbital response enhancer module in the human bilirubin UDP-glucuronosyltransferase UGT1A1 gene and regulation by the nuclear receptor CAR. Hepatology 2001;33:1232-8.
-
(2001)
Hepatology
, vol.33
, pp. 1232-1238
-
-
Sugatani, J.1
Kojima, H.2
Ueda, A.3
Kakizaki, S.4
Yoshinari, K.5
Gong, Q.H.6
-
9
-
-
18444399926
-
Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia
-
Sugatani J, Yamakawa K, Yoshinari K, Machida T, Takagi H, Mori M, et al. Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia. Biochem Biophys Res Commun 2002;292:492-7.
-
(2002)
Biochem Biophys Res Commun
, vol.292
, pp. 492-497
-
-
Sugatani, J.1
Yamakawa, K.2
Yoshinari, K.3
Machida, T.4
Takagi, H.5
Mori, M.6
-
10
-
-
9544252947
-
Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert Syndrome
-
Maruo Y, D'Addario C, Mori A, Iwai M, Takahashi H, Sato H, et al. Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert Syndrome. Hum Genet 2004;115:525-6.
-
(2004)
Hum Genet
, vol.115
, pp. 525-526
-
-
Maruo, Y.1
D'Addario, C.2
Mori, A.3
Iwai, M.4
Takahashi, H.5
Sato, H.6
-
11
-
-
21944434407
-
Genetic polymorphism in the phenobarbital-responsive enhancer module of the UDP-glucuronosyltransferase 1A1 gene and irinotecan toxicity
-
Kitagawa C, Ando M, Ando Y, Sekido Y, Wakai K, Imaizumi K, et al. Genetic polymorphism in the phenobarbital-responsive enhancer module of the UDP-glucuronosyltransferase 1A1 gene and irinotecan toxicity. Pharmacogenet Genomics 2005;15:35-41.
-
(2005)
Pharmacogenet Genomics
, vol.15
, pp. 35-41
-
-
Kitagawa, C.1
Ando, M.2
Ando, Y.3
Sekido, Y.4
Wakai, K.5
Imaizumi, K.6
-
12
-
-
0031949264
-
Gilbert syndrome accelerates development of neonatal jaundice
-
Bancroft JD, Kreamer B, Gourley GR. Gilbert syndrome accelerates development of neonatal jaundice. J Pediatr 1998;132:656-60.
-
(1998)
J Pediatr
, vol.132
, pp. 656-660
-
-
Bancroft, J.D.1
Kreamer, B.2
Gourley, G.R.3
-
13
-
-
0031423835
-
Analysis of the promoter of human bilirubin UDP-glucuronosyltransferase gene (UGT1*1) in relevance to Gilbert's syndrome
-
Ueyama H, Koiwai O, Soeda Y, Sato H, Satoh Y, Ohkubo I, et al. Analysis of the promoter of human bilirubin UDP-glucuronosyltransferase gene (UGT1*1) in relevance to Gilbert's syndrome. Hepatol Res 1997;9:152-63.
-
(1997)
Hepatol Res
, vol.9
, pp. 152-163
-
-
Ueyama, H.1
Koiwai, O.2
Soeda, Y.3
Sato, H.4
Satoh, Y.5
Ohkubo, I.6
-
14
-
-
18744373338
-
Haplotypes of variants in the UDP-glucuronosyltransferase1A9 and 1A1 genes
-
Innocenti F, Liu W, Chen P, Desai AA, Das S, Ratain MJ. Haplotypes of variants in the UDP-glucuronosyltransferase1A9 and 1A1 genes. Pharmacogenet Genomics 2005;15:295-301.
-
(2005)
Pharmacogenet Genomics
, vol.15
, pp. 295-301
-
-
Innocenti, F.1
Liu, W.2
Chen, P.3
Desai, A.A.4
Das, S.5
Ratain, M.J.6
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