-
1
-
-
0035971239
-
Hepatic uptake of bilirubin and its conjugates by the human organic anion transporter SLC21A6
-
Cui Y, Konig J, Leier I, Buchholz U, Keppler D. Hepatic uptake of bilirubin and its conjugates by the human organic anion transporter SLC21A6. J Biol Chem 2001; 276:9626-9630.
-
(2001)
J Biol Chem
, vol.276
, pp. 9626-9630
-
-
Cui, Y.1
Konig, J.2
Leier, I.3
Buchholz, U.4
Keppler, D.5
-
2
-
-
0030728222
-
Genetic defects of the UDP-glucuronosyltransferase 1 (UGT1) gene that cause familial non-hemolytic unconjugated hyperbilirubinaemias
-
Clarke DJ, Moghrabi N, Monaghan G, Cassidy A, Boxer M, Hume R, et al. Genetic defects of the UDP-glucuronosyltransferase 1 (UGT1) gene that cause familial non-hemolytic 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
-
3
-
-
0028867826
-
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome
-
Bosma PJ, Chowdhury JR, Bakker CT, Gantla S, de Boer A, Oostra BA, 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.T.3
Gantla, S.4
De Boer, A.5
Oostra, B.A.6
-
4
-
-
0030030762
-
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
-
5
-
-
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
-
6
-
-
0035053747
-
Correlation of mutation 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 mutation 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
-
7
-
-
0033816138
-
Variations of the bilirubin uridine-diphosphoglucuronosyl transferase 1 A1 gene in healthy Taiwanese
-
Huang CS, Luo GA, Huang MJ, Yu SC, Yang SS. Variations of the bilirubin uridine-diphosphoglucuronosyl transferase 1 A1 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
-
8
-
-
0036157862
-
Genetic polymorphisms of UDP-glucuronosyltransferase in Asians: UGT1A1*28 is a common allele in Indians
-
Chowbay B, Kanaga S, Gao F, Kei SK, Edmund JDL. 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
-
-
Chowbay, B.1
Kanaga, S.2
Gao, F.3
Kei, S.K.4
Edmund, J.5
-
9
-
-
0031719562
-
Neonatal hyperbilirubinemia and mutation of the bilirubin uridine-diphosphate-glucuronosyltransferase gene: A common missense mutation among Japanese, Koreans and Chinese
-
Akaba K, Kimura T, Sasaki A, Tanabe S, Ikegami T, Hashimoto M, et al. Neonatal hyperbilirubinemia and mutation of the bilirubin uridine-diphosphate-glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese. Biochem Mol Biol Int 1998; 46:21-26.
-
(1998)
Biochem Mol Biol Int
, vol.46
, pp. 21-26
-
-
Akaba, K.1
Kimura, T.2
Sasaki, A.3
Tanabe, S.4
Ikegami, T.5
Hashimoto, M.6
-
10
-
-
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
-
11
-
-
0038271981
-
Comprehensive UGT1A1 genotyping in a Japanese population by pyrosequencing
-
Saeki M, Saito Y, Jinno H, Tohkin M, Kurose K, Kaniwa S, et al. Comprehensive UGT1A1 genotyping in a Japanese population by pyrosequencing. Clin Chem 2003; 49:1182-1185.
-
(2003)
Clin Chem
, vol.49
, pp. 1182-1185
-
-
Saeki, M.1
Saito, Y.2
Jinno, H.3
Tohkin, M.4
Kurose, K.5
Kaniwa, S.6
-
12
-
-
0030610807
-
UGT1 *1 genotyping in a Canadian Inuit population
-
Monaghan G, Foster B, Jurima-Romet M, Hume R, Burchell B, Owens IS. UGT1 *1 genotyping in a Canadian Inuit population. Pharmacogenetics 1997; 7:153-156.
-
(1997)
Pharmacogenetics
, vol.7
, pp. 153-156
-
-
Monaghan, G.1
Foster, B.2
Jurima-Romet, M.3
Hume, R.4
Burchell, B.5
Owens, I.S.6
-
13
-
-
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 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
-
-
0035929574
-
Polymorphisms in OATP-C: Identification of multiple allele variants associated with altered transport activity among European- and African-Americans
-
Tirona RG, Leake BF, Merino G, Kim RB. Polymorphisms in OATP-C: identification of multiple allele variants associated with altered transport activity among European- and African-Americans. J Biol Chem 2001; 276:35669-35675.
-
(2001)
J Biol Chem
, vol.276
, pp. 35669-35675
-
-
Tirona, R.G.1
Leake, B.F.2
Merino, G.3
Kim, R.B.4
-
16
-
-
0036073404
-
Genetic polymorphisms of human organic anion transporter OATP-C (SLC21A6) and OATP-B (SLC21A9): Allele frequencies in the Japanese population and functional analysis
-
Nozawa T, Nakajima M, Tami I, Noda K, Nezu J, Sai Y, et al. Genetic polymorphisms of human organic anion transporter OATP-C (SLC21A6) and OATP-B (SLC21A9): allele frequencies in the Japanese population and functional analysis. J Pharmacol Exp Ther 2002; 302:804-813.
-
(2002)
J Pharmacol Exp Ther
, vol.302
, pp. 804-813
-
-
Nozawa, T.1
Nakajima, M.2
Tami, I.3
Noda, K.4
Nezu, J.5
Sai, Y.6
-
17
-
-
0038209381
-
Polymorphisms of OATP-C (SLC21A6) and OAT3 (SLC22A8) genes: Consequences for pravastatin pharmacokinetics
-
Yohei N, Ichiro I, Hiroshi S, Miyuki K, Kiyoshi K, Takeshi H, et al. Polymorphisms of OATP-C (SLC21A6) and OAT3 (SLC22A8) genes: consequences for pravastatin pharmacokinetics. Clin Pharmacol Ther 2003; 73:554-565.
-
(2003)
Clin Pharmacol Ther
, vol.73
, pp. 554-565
-
-
Yohei, N.1
Ichiro, I.2
Hiroshi, S.3
Miyuki, K.4
Kiyoshi, K.5
Takeshi, H.6
-
18
-
-
12244254497
-
Coinheritance of variant UDP-glucuronosyl transferase 1A1 gene and glucose-6-phosphate dehydrogenase deficiency in adults with hyperbilirubinemia
-
Huang MJ, Yang YC, Yang SS, Lin MS, Chen ES, Huang CS. Coinheritance of variant UDP-glucuronosyl transferase 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
-
19
-
-
0030031242
-
Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants
-
Huang CS, Hung KL, Huang MJ, Li YC, Liu TH, Tang TK. Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants. Am J Hematol 1996; 51:19-25.
-
(1996)
Am J Hematol
, vol.51
, pp. 19-25
-
-
Huang, C.S.1
Hung, K.L.2
Huang, M.J.3
Li, Y.C.4
Liu, T.H.5
Tang, T.K.6
-
20
-
-
0036305499
-
Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyltransferase 1A1 gene and neonatal hyperbilirubinemia
-
Huang CS, Chang PF, Huang MJ, Chen ES, Chen WC. Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyltransferase 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
-
21
-
-
6344289138
-
Risk factors for severe hyperbilirubinemia in neonates
-
Huang MJ, Kua KE, Teng HC, Tang KS, Weng HW, Huang CS. Risk factors for severe hyperbilirubinemia in neonates. Pediatr Res 2004; 56:682-689.
-
(2004)
Pediatr Res
, vol.56
, pp. 682-689
-
-
Huang, M.J.1
Kua, K.E.2
Teng, H.C.3
Tang, K.S.4
Weng, H.W.5
Huang, C.S.6
-
22
-
-
0026643947
-
Diverse point mutations result in glucose-6-phosphate dehydrogenase (G6PD) polymorphism in Taiwan
-
Tang TK, Huang CS, Huang MJ, Tam KB, Yen CH, Tang CJC. Diverse point mutations result in glucose-6-phosphate dehydrogenase (G6PD) polymorphism in Taiwan. Blood 1992; 79:2135-2140.
-
(1992)
Blood
, vol.79
, pp. 2135-2140
-
-
Tang, T.K.1
Huang, C.S.2
Huang, M.J.3
Tam, K.B.4
Yen, C.H.5
Tang, C.J.C.6
-
24
-
-
0034709561
-
Molecular identification and characterization of novel members of the human organic anion transporter (OATP) family
-
Tamai I, Nezu J, Uchino H, Sai Y, Oku A, Shimane M, et al. Molecular identification and characterization of novel members of the human organic anion transporter (OATP) family. Biochem Biophys Res Commun 2000; 273:251-260.
-
(2000)
Biochem Biophys Res Commun
, vol.273
, pp. 251-260
-
-
Tamai, I.1
Nezu, J.2
Uchino, H.3
Sai, Y.4
Oku, A.5
Shimane, M.6
-
25
-
-
0031864410
-
Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II
-
Yamamoto K, Sato H, Fujiyama Y, Doida YU, Bamba T. Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert's syndrome and Crigler-Najjar syndrome type II. Biochem Biophys Acta 1998; 1406:267-273.
-
(1998)
Biochem Biophys Acta
, vol.1406
, pp. 267-273
-
-
Yamamoto, K.1
Sato, H.2
Fujiyama, Y.3
Doida, Y.U.4
Bamba, T.5
-
26
-
-
0028337574
-
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Chinese infants with or without severe neonatal hyperbilirubinemia
-
Lo YS, Lu CC, Chiou SS, Chen BH, Chang JG. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Chinese infants with or without severe neonatal hyperbilirubinemia. Br J Hematol 1993; 86:858-862.
-
(1993)
Br J Hematol
, vol.86
, pp. 858-862
-
-
Lo, Y.S.1
Lu, C.C.2
Chiou, S.S.3
Chen, B.H.4
Chang, J.G.5
-
27
-
-
0031417640
-
Two novel glucose-6-phosphate dehydrogenase deficiency mutations and association of such mutations with F8C/G6PD haplotype in Chinese
-
Chen HL, Huang MJ, Huang CS, Tang TK. Two novel glucose-6-phosphate dehydrogenase deficiency mutations and association of such mutations with F8C/G6PD haplotype in Chinese. J Formosan Med Assoc 1997; 96:779-783.
-
(1997)
J Formosan Med Assoc
, vol.96
, pp. 779-783
-
-
Chen, H.L.1
Huang, M.J.2
Huang, C.S.3
Tang, T.K.4
-
28
-
-
0026451162
-
Association between glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice
-
Yu MW, Hsiao KJ, Wuu KD, Chen CJ. Association between glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice. Int J Epidemiol 1992; 21:947-952.
-
(1992)
Int J Epidemiol
, vol.21
, pp. 947-952
-
-
Yu, M.W.1
Hsiao, K.J.2
Wuu, K.D.3
Chen, C.J.4
-
29
-
-
0033063940
-
The interaction between Gilbert's syndrome and G6PD deficiency influences bilirubin levels
-
Cappellini MD, Di Montemuros FM, Sampietro M, Tavazzi D, Fiorelli G. The interaction between Gilbert's syndrome and G6PD deficiency influences bilirubin levels. Br J Haematol 1999; 104:928-929.
-
(1999)
Br J Haematol
, vol.104
, pp. 928-929
-
-
Cappellini, M.D.1
Di Montemuros, F.M.2
Sampietro, M.3
Tavazzi, D.4
Fiorelli, G.5
-
30
-
-
0038081033
-
The human organic anion transport protein SLC21A6 is not sufficient for bilirubin transport
-
Wang P, Kim RB, Chowdhury R, Wolkoff AW. The human organic anion transport protein SLC21A6 is not sufficient for bilirubin transport. J Biol Chem 2003; 278:20695-20699.
-
(2003)
J Biol Chem
, vol.278
, pp. 20695-20699
-
-
Wang, P.1
Kim, R.B.2
Chowdhury, R.3
Wolkoff, A.W.4
-
31
-
-
3242808852
-
High plasma pravastatin concentrations are associated with single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide-C (OATP-C, SLCO1B1)
-
Mikko N, Elke S, Thomas L, Martin FF, Mikko N, Carl K, et al. High plasma pravastatin concentrations are associated with single nucleotide polymorphisms and haplotypes of organic anion transporting polypeptide-C (OATP-C, SLCO1B1). Pharmacogenetics 2004; 14:429-440.
-
(2004)
Pharmacogenetics
, vol.14
, pp. 429-440
-
-
Mikko, N.1
Elke, S.2
Thomas, L.3
Martin, F.F.4
Mikko, N.5
Carl, K.6
-
32
-
-
6344265401
-
Genetics and the risk of neonatal hyperbilirubinemia
-
Watchko JF. Genetics and the risk of neonatal hyperbilirubinemia. Pediatr Res 2004; 56:677-678.
-
(2004)
Pediatr Res
, vol.56
, pp. 677-678
-
-
Watchko, J.F.1
-
33
-
-
0035127524
-
Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1
-
Persico M, Persico E, Bakker CTM, Rigato I, Amoroso A, Torella R, et al. Hepatic uptake of organic anions affects the plasma bilirubin level in subjects with Gilbert's syndrome mutations in UGT1A1. Hepatology 2001; 33:627-632.
-
(2001)
Hepatology
, vol.33
, pp. 627-632
-
-
Persico, M.1
Persico, E.2
Bakker, C.3
Rigato, I.4
Amoroso, A.5
Torella, R.6
-
34
-
-
0037223551
-
Genetic variation of human UDP-glucuronosyltransferase: Implications in disease and drug glucuronidation
-
Burchell B. Genetic variation of human UDP-glucuronosyltransferase: implications in disease and drug glucuronidation. Am J Pharmacogenomics 2003; 3:37-52.
-
(2003)
Am J Pharmacogenomics
, vol.3
, pp. 37-52
-
-
Burchell, B.1
-
35
-
-
0037819284
-
Pharmacogenomics of human UDP-glucuronosyltransferase enzymes
-
Guillemette C. Pharmacogenomics of human UDP-glucuronosyltransferase enzymes. Pharmacogenomics J 2003; 3:136-158.
-
(2003)
Pharmacogenomics J
, vol.3
, pp. 136-158
-
-
Guillemette, C.1
-
36
-
-
0242469240
-
Organic anion-transporting polypeptide (OATP) transporter family and drug disposition
-
Kim RB. Organic anion-transporting polypeptide (OATP) transporter family and drug disposition. Eur J Clin Invest 2003; 33(suppl 2):1-5.
-
(2003)
Eur J Clin Invest
, vol.33
, pp. 1-5
-
-
Kim, R.B.1
|