-
1
-
-
0014215065
-
Idiopathic unconjugated hyperbilirubinemia (Gilbert's syndrome). A study of 42 families
-
Powell LW, Hemingway E, Billing BH, Sherlock S. Idiopathic unconjugated hyperbilirubinemia (Gilbert's syndrome). A study of 42 families. N Engl J Med 1967; 277: 1108-1112
-
(1967)
N Engl J Med
, vol.277
, pp. 1108-1112
-
-
Powell, L.W.1
Hemingway, E.2
Billing, B.H.3
Sherlock, S.4
-
2
-
-
0037230622
-
Inherited disorders of bilirubin metabolism
-
Bosma PJ. Inherited disorders of bilirubin metabolism. J Hepatol 2003; 38: 107-117
-
(2003)
J Hepatol
, vol.38
, pp. 107-117
-
-
Bosma, P.J.1
-
3
-
-
0030663191
-
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency
-
Sampietro M, Lupica L, Perrero L, Comino A, Martinez di Montemuros F, Cappellini MD, Fiorelli G. The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase 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
Martinez di Montemuros, F.5
Cappellini, M.D.6
Fiorelli, G.7
-
4
-
-
0033849474
-
Effect of bilirubin UDP glucuronosyltransferase 1 gene TATA box genotypes on serum bilirubin concentrations in chronic liver injuries
-
Doyama H, Okada T, Kobayashi T, Suzuki A, Takeda Y, Mabuchi H. Effect of bilirubin UDP glucuronosyltransferase 1 gene TATA box genotypes on serum bilirubin concentrations in chronic liver injuries. Hepatology 2000; 32: 563-568
-
(2000)
Hepatology
, vol.32
, pp. 563-568
-
-
Doyama, H.1
Okada, T.2
Kobayashi, T.3
Suzuki, A.4
Takeda, Y.5
Mabuchi, H.6
-
5
-
-
0030745309
-
Persistent unconjugated hyperbilirubinemia after liver transplantation due to an abnormal bilirubin UDP-glucuronosyltransferase gene promoter sequence in the donor
-
Jansen PL, Bosma PJ, Bakker C, Lems SP, Slooff MJ, Haagsma EB. Persistent unconjugated hyperbilirubinemia after liver transplantation due to an abnormal bilirubin UDP-glucuronosyltransferase gene promoter sequence in the donor. J Hepatol 1997; 27: 1-5
-
(1997)
J Hepatol
, vol.27
, pp. 1-5
-
-
Jansen, P.L.1
Bosma, P.J.2
Bakker, C.3
Lems, S.P.4
Slooff, M.J.5
Haagsma, E.B.6
-
6
-
-
0028867826
-
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 BA, Lindhout D, Tytgat GN, Jansen PL, Oude Elferink RP. 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.A.6
Lindhout, D.7
Tytgat, G.N.8
Jansen, P.L.9
Oude Elferink, R.P.10
-
7
-
-
0029015847
-
Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase
-
Koiwai O, Nishizawa M, Hasada K, Aono S, Adachi Y, Mamiya N, Sato H. Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase. Hum Mol Genet 1995; 4: 1183-1186
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1183-1186
-
-
Koiwai, O.1
Nishizawa, M.2
Hasada, K.3
Aono, S.4
Adachi, Y.5
Mamiya, N.6
Sato, H.7
-
8
-
-
0032847365
-
Molecular genetic basis of Gilbert's syndrome
-
Burchell B, Hume R. Molecular genetic basis of Gilbert's syndrome. J Gastroenterol Hepatol 1999; 14: 960-966
-
(1999)
J Gastroenterol Hepatol
, vol.14
, pp. 960-966
-
-
Burchell, B.1
Hume, R.2
-
9
-
-
0030728222
-
Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias
-
Clarke DJ, Moghrabi N, Monaghan G, Cassidy A, Boxer M, Hume R, Burchell B. Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias. Clin Chim Acta 1997; 266: 63-74
-
(1997)
Clin Chim Acta
, vol.266
, pp. 63-74
-
-
Clarke, D.J.1
Moghrabi, N.2
Monaghan, G.3
Cassidy, A.4
Boxer, M.5
Hume, R.6
Burchell, B.7
-
10
-
-
0026545451
-
Decreased glucuronidation and increased bioactivation of acetaminophen in Gilbert's syndrome
-
de Morais SM, Uetrecht JP, Wells PG. Decreased glucuronidation and increased bioactivation of acetaminophen in Gilbert's syndrome. Gastroenterology 1992; 102: 577-586
-
(1992)
Gastroenterology
, vol.102
, pp. 577-586
-
-
de Morais, S.M.1
Uetrecht, J.P.2
Wells, P.G.3
-
11
-
-
0032055273
-
Drug glucuronidation by human renal UDP-glucuronosyltransferases
-
McGurk KA, Brierley CH, Burchell B. Drug glucuronidation by human renal UDP-glucuronosyltransferases. Biochem Pharmacol 1998; 55: 1005-1012
-
(1998)
Biochem Pharmacol
, vol.55
, pp. 1005-1012
-
-
McGurk, K.A.1
Brierley, C.H.2
Burchell, B.3
-
12
-
-
0016784220
-
Population studies on Gilbert's syndrome
-
Owens D, Evans J. Population studies on Gilbert's syndrome. J Med Genet 1975; 12: 152-156
-
(1975)
J Med Genet
, vol.12
, pp. 152-156
-
-
Owens, D.1
Evans, J.2
-
13
-
-
0023217260
-
Prevalence of Gilbert's syndrome in Germany
-
Sieg A, Arab L, Schlierf G, Stiehl A, Kommerell B. Prevalence of Gilbert's syndrome in Germany. Dtsch Med Wochenschr 1987; 112: 1206-1208
-
(1987)
Dtsch Med Wochenschr
, vol.112
, pp. 1206-1208
-
-
Sieg, A.1
Arab, L.2
Schlierf, G.3
Stiehl, A.4
Kommerell, B.5
-
14
-
-
0032493441
-
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
-
15
-
-
0030030762
-
Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome
-
Monaghan G, Ryan M, Seddon R, Hume R, Burchell B. Genetic variation in bilirubin UPD-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
-
-
0032767352
-
UDP-glucuronosyltransferase (UGT1A1*28 and UGT1A6*2) polymorphisms in Caucasians and Asians: Relationships to serum bilirubin concentrations
-
Lampe JW, Bigler J, Horner NK, Potter JD. UDP-glucuronosyltransferase (UGT1A1*28 and UGT1A6*2) polymorphisms in Caucasians and Asians: relationships to serum bilirubin concentrations. Pharmacogenetics 1999; 9: 341-349
-
(1999)
Pharmacogenetics
, vol.9
, pp. 341-349
-
-
Lampe, J.W.1
Bigler, J.2
Horner, N.K.3
Potter, J.D.4
-
17
-
-
0031595660
-
The UGT1A1*28 allele is relatively rare in a Japanese population
-
Ando Y, Chida M, Nakayama K, Saka H, Kamataki T. The UGT1A1*28 allele is relatively rare in a Japanese population. Pharmacogenetics 1998; 8: 357-360
-
(1998)
Pharmacogenetics
, vol.8
, pp. 357-360
-
-
Ando, Y.1
Chida, M.2
Nakayama, K.3
Saka, H.4
Kamataki, T.5
-
18
-
-
0033054393
-
Contribution of the TATA-box genotype (Gilbert syndrome) to serum biliubin concentrations in the Italian population
-
Biondi ML, Turri O, Dilillo D, Stival G, Guagnellini E. Contribution of the TATA-box genotype (Gilbert syndrome) to serum biliubin concentrations in the Italian population. Clin Chem 1999; 45: 897-898
-
(1999)
Clin Chem
, vol.45
, pp. 897-898
-
-
Biondi, M.L.1
Turri, O.2
Dilillo, D.3
Stival, G.4
Guagnellini, E.5
-
19
-
-
4544326498
-
Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects
-
Takeuchi K, Kobayashi Y, Tamaki S, Ishihara T, Maruo Y, Araki J, Mifuji R, Itani T, Kuroda M, Sato H, Kaito M, Adachi Y. Genetic polymorphisms of bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese patients with Crigler-Najjar syndrome or Gilbert's syndrome as well as in healthy Japanese subjects. J Gastroenterol Hepatol 2004; 19: 1023-1028
-
(2004)
J Gastroenterol Hepatol
, vol.19
, pp. 1023-1028
-
-
Takeuchi, K.1
Kobayashi, Y.2
Tamaki, S.3
Ishihara, T.4
Maruo, Y.5
Araki, J.6
Mifuji, R.7
Itani, T.8
Kuroda, M.9
Sato, H.10
Kaito, M.11
Adachi, Y.12
-
20
-
-
4544385348
-
What is Gilbert's syndrome? Lesson from genetic polymorphisms of UGT1A1 in Gilbert's syndrome from Asia
-
Kamisako T. What is Gilbert's syndrome? Lesson from genetic polymorphisms of UGT1A1 in Gilbert's syndrome from Asia. J Gastroenterol Hepatol 2004; 19: 955-957
-
(2004)
J Gastroenterol Hepatol
, vol.19
, pp. 955-957
-
-
Kamisako, T.1
-
21
-
-
0036204931
-
Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism
-
Kaplan M, Hammerman C, Rubaltelli FF, Vilei MT, Levy-Lahad E, Renbaum P, Vreman HJ, Stevenson DK, Muraca M. Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism. Hepatology 2002; 35: 905-911
-
(2002)
Hepatology
, vol.35
, pp. 905-911
-
-
Kaplan, M.1
Hammerman, C.2
Rubaltelli, F.F.3
Vilei, M.T.4
Levy-Lahad, E.5
Renbaum, P.6
Vreman, H.J.7
Stevenson, D.K.8
Muraca, M.9
-
22
-
-
0028862469
-
Predicted homozygous mis-sense mutation in Gilbert's syndrome
-
Soeda Y, Yamamoto K, Adachi Y, Hori T, Aono S, Koiwai O, Sato H. Predicted homozygous mis-sense mutation in Gilbert's syndrome. Lancet 1995; 346: 1494
-
(1995)
Lancet
, vol.346
, pp. 1494
-
-
Soeda, Y.1
Yamamoto, K.2
Adachi, Y.3
Hori, T.4
Aono, S.5
Koiwai, O.6
Sato, H.7
-
23
-
-
0030053274
-
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
-
24
-
-
0028904620
-
Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
-
Aono S, Adachi Y, Uyama E, Yamada Y, Keino H, Nanno T, Koiwai O, Sato H. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome. Lancet 1995; 345: 958-959
-
(1995)
Lancet
, vol.345
, pp. 958-959
-
-
Aono, S.1
Adachi, Y.2
Uyama, E.3
Yamada, Y.4
Keino, H.5
Nanno, T.6
Koiwai, O.7
Sato, H.8
-
25
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988; 16: 1215
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
26
-
-
0031955116
-
Consed: A graphical tool for sequence finishing
-
Gordon D, Abajian C, Green P. Consed: a graphical tool for sequence finishing. Genome Res 1998; 8: 195-202
-
(1998)
Genome Res
, vol.8
, pp. 195-202
-
-
Gordon, D.1
Abajian, C.2
Green, P.3
-
28
-
-
0033841077
-
Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene
-
Raijmakers MT, Jansen PL, Steegers EA, Peters WH. Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene. J Hepatol 2000; 33: 348-351
-
(2000)
J Hepatol
, vol.33
, pp. 348-351
-
-
Raijmakers, M.T.1
Jansen, P.L.2
Steegers, E.A.3
Peters, W.H.4
-
29
-
-
0035055199
-
Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus
-
Kadakol A, Sappal BS, Ghosh SS, Lowenheim M, Chowdhury A, Chowdhury S, Santra A, Arias IM, Chowdhury JR, Chowdhury NR. Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus. J Med Genet 2001; 38: 244-249
-
(2001)
J Med Genet
, vol.38
, pp. 244-249
-
-
Kadakol, A.1
Sappal, B.S.2
Ghosh, S.S.3
Lowenheim, M.4
Chowdhury, A.5
Chowdhury, S.6
Santra, A.7
Arias, I.M.8
Chowdhury, J.R.9
Chowdhury, N.R.10
-
30
-
-
33646266837
-
TA insertion mutation in bilirubin UDP- glucoronyl transferase gene (UGT1A1) promoter in Indian patients with Gilbert's syndrome
-
Parvez MK, Goyal A, Kazim N, Hasnain SE, Sarin SK. TA insertion mutation in bilirubin UDP- glucoronyl transferase gene (UGT1A1) promoter in Indian patients with Gilbert's syndrome. J Hepatol 2002; 36(S1): 159-160
-
(2002)
J Hepatol
, vol.36
, Issue.S1
, pp. 159-160
-
-
Parvez, M.K.1
Goyal, A.2
Kazim, N.3
Hasnain, S.E.4
Sarin, S.K.5
-
31
-
-
0033802568
-
Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects
-
Borlak J, Thum T, Landt O, Erb K, Hermann R. Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects. Hepatology 2000; 32: 792-725
-
(2000)
Hepatology
, vol.32
, pp. 725-792
-
-
Borlak, J.1
Thum, T.2
Landt, O.3
Erb, K.4
Hermann, R.5
-
32
-
-
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, Kakizaki S, Sueyoshi T, Negishi M, Miwa M. Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia. Biochem Biophys Res Commun 2002; 292: 492-497
-
(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
Kakizaki, S.7
Sueyoshi, T.8
Negishi, M.9
Miwa, M.10
-
33
-
-
0035075564
-
New concepts in bilirubin neurotoxicity and the need for studies at clinically relevant bilirubin concentrations
-
Ostrow JD, Tiribelli C. New concepts in bilirubin neurotoxicity and the need for studies at clinically relevant bilirubin concentrations. J Hepatol 2001; 34: 467-470
-
(2001)
J Hepatol
, vol.34
, pp. 467-470
-
-
Ostrow, J.D.1
Tiribelli, C.2
-
34
-
-
0345211459
-
Heterogeneity of paracetamol metabolism in Gilbert's syndrome
-
Esteban A, Perez-Mateo M. Heterogeneity of paracetamol metabolism in Gilbert's syndrome. Eur J Drug Metab Pharmacokinet 1999; 24: 9-13
-
(1999)
Eur J Drug Metab Pharmacokinet
, vol.24
, pp. 9-13
-
-
Esteban, A.1
Perez-Mateo, M.2
-
35
-
-
0029089659
-
Glucuronidation of propofol in microsomal fractions from various tissues and species including humans: Effect of different drugs
-
Le Guellec C, Lacarelle B, Villard PH, Point H, Catalin J, Durand A. Glucuronidation of propofol in microsomal fractions from various tissues and species including humans: effect of different drugs. Anesth Analg 1995; 81: 855-861
-
(1995)
Anesth Analg
, vol.81
, pp. 855-861
-
-
Le Guellec, C.1
Lacarelle, B.2
Villard, P.H.3
Point, H.4
Catalin, J.5
Durand, A.6
-
36
-
-
0034671387
-
Polymorphisms of UDP-glucuronosyltransferase gene and irinotecan toxicity: A pharmacogenetic analysis
-
Ando Y, Saka H, Ando M, Sawa T, Muro K, Ueoka H, Yokoyama A, Saitoh S, Shimokata K, Hasegawa Y. Polymorphisms of UDP-glucuronosyltransferase gene and irinotecan toxicity: a pharmacogenetic analysis. Cancer Res 2000; 60: 6921-6926
-
(2000)
Cancer Res
, vol.60
, pp. 6921-6926
-
-
Ando, Y.1
Saka, H.2
Ando, M.3
Sawa, T.4
Muro, K.5
Ueoka, H.6
Yokoyama, A.7
Saitoh, S.8
Shimokata, K.9
Hasegawa, Y.10
-
37
-
-
0035940414
-
Mechanism of indinavir-induced hyperbilirubinemia
-
Zucker SD, Qin X, Rouster SD, Yu F, Green RM, Keshavan P, Feinberg J, Sherman KE. Mechanism of indinavir-induced hyperbilirubinemia. Proc Natl Acad Sci USA 2001; 98: 12671-12676
-
(2001)
Proc Natl Acad Sci USA
, vol.98
, pp. 12671-12676
-
-
Zucker, S.D.1
Qin, X.2
Rouster, S.D.3
Yu, F.4
Green, R.M.5
Keshavan, P.6
Feinberg, J.7
Sherman, K.E.8
|