-
1
-
-
0023703969
-
Comparison of bilirubin production in Japanese and Caucasian infants
-
Fischer AF, Nakamura H, Uetani Y, Vreman HJ, Stevenson DK: Comparison of bilirubin production in Japanese and Caucasian infants. J Pediatr Gastroenterol Nutr 1988;7:27-29.
-
(1988)
J Pediatr Gastroenterol Nutr
, vol.7
, pp. 27-29
-
-
Fischer, A.F.1
Nakamura, H.2
Uetani, Y.3
Vreman, H.J.4
Stevenson, D.K.5
-
2
-
-
0036195126
-
Neonatal jaundice in Asian, white, and mixed-race infants
-
Setia S, Villaveces A, Dhillon P, Mueller BA: Neonatal jaundice in Asian, white, and mixed-race infants. Arch Pediatr Adolesc Med 2002;156:276-279.
-
(2002)
Arch Pediatr Adolesc Med
, vol.156
, pp. 276-279
-
-
Setia, S.1
Villaveces, A.2
Dhillon, P.3
Mueller, B.A.4
-
3
-
-
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, 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.A.6
Lindhout, D.7
Tytgat, G.N.8
Jansen, P.L.9
Oude Elferink, R.P.10
-
4
-
-
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
-
5
-
-
0031949264
-
Gilbert syndrome accelerates development of neonatal jaundice
-
Bancroft JD, Kreamer B, Gourley GR: Gilbert syndrome accelerates development of neonatal jaundice. J Pediatr 1998;132:656-660.
-
(1998)
J Pediatr
, vol.132
, pp. 656-660
-
-
Bancroft, J.D.1
Kreamer, B.2
Gourley, G.R.3
-
6
-
-
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, Umeda H, Yoshida H, Umetsu K, Chiba H, Yuasa I, Hayasaka K: 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
Umeda, H.7
Yoshida, H.8
Umetsu, K.9
Chiba, H.10
Yuasa, I.11
Hayasaka, K.12
-
7
-
-
0033001454
-
Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism
-
Maruo Y, Nishizawa K, Sato H, Doida Y, Shimada M: Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism. Pediatrics 1999;103:1224-1227.
-
(1999)
Pediatrics
, vol.103
, pp. 1224-1227
-
-
Maruo, Y.1
Nishizawa, K.2
Sato, H.3
Doida, Y.4
Shimada, M.5
-
8
-
-
0034324675
-
Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate-glucuronosyltransferase gene
-
Maruo Y, Nishizawa K, Sato H, Sawa H, Shimada M: Prolonged unconjugated hyperbilirubinemia associated with breast milk and mutations of the bilirubin uridine diphosphate-glucuronosyltransferase gene. Pediatrics 2000;106:E59.
-
(2000)
Pediatrics
, vol.106
-
-
Maruo, Y.1
Nishizawa, K.2
Sato, H.3
Sawa, H.4
Shimada, M.5
-
10
-
-
0036943127
-
Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population
-
Yamamoto A, Nishio H, Waku S, Yokoyama N, Yonetani M, Uetani Y, Nakamura H: Gly71Arg mutation of the bilirubin UDP-glucuronosyltransferase 1A1 gene is associated with neonatal hyperbilirubinemia in the Japanese population. Kobe J Med Sci 2002;48:73-77.
-
(2002)
Kobe J Med Sci
, vol.48
, pp. 73-77
-
-
Yamamoto, A.1
Nishio, H.2
Waku, S.3
Yokoyama, N.4
Yonetani, M.5
Uetani, Y.6
Nakamura, H.7
-
11
-
-
7044269611
-
Screening for G71R mutation of the UGT1A1 gene in the Javanese-Indonesian and Malay-Malaysian populations
-
Sutomo R, Talib NA, Yusoff NM, Van Rostenberghe H, Sadewa AH, Sunarti, Sofro AS, Yokoyama N, Lee MJ, Matsuo M, Nishio H: Screening for G71R mutation of the UGT1A1 gene in the Javanese-Indonesian and Malay-Malaysian populations. Pediatr Int 2004;46:565-569.
-
(2004)
Pediatr Int
, vol.46
, pp. 565-569
-
-
Sutomo, R.1
Talib, N.A.2
Yusoff, N.M.3
Van Rostenberghe, H.4
Sadewa, A.H.5
Sunarti6
Sofro, A.S.7
Yokoyama, N.8
Lee, M.J.9
Matsuo, M.10
Nishio, H.11
-
12
-
-
0036039396
-
Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome
-
Sutomo R, Laosombat V, Sadewa AH, Yokoyama N, Nakamura H, Matsuo M, Nishio H: Novel missense mutation of the UGT1A1 gene in Thai siblings with Gilbert's syndrome. Pediatr Int 2002:44:427-432.
-
(2002)
Pediatr Int
, vol.44
, pp. 427-432
-
-
Sutomo, R.1
Laosombat, V.2
Sadewa, A.H.3
Yokoyama, N.4
Nakamura, H.5
Matsuo, M.6
Nishio, H.7
-
13
-
-
0032766238
-
A variant TATA box in the bilirubin UDP-glucuronosyltransferase 1 gene promoter does not contribute to neonatal jaundice in the Japanese population
-
Waku S, Takeshima Y, Nakamura H, Nishio H, Sumino K: A variant TATA box in the bilirubin UDP-glucuronosyltransferase 1 gene promoter does not contribute to neonatal jaundice in the Japanese population. Arch Dis Child Fetal Neonatal Ed 1999;81:F159.
-
(1999)
Arch Dis Child Fetal Neonatal Ed
, vol.81
-
-
Waku, S.1
Takeshima, Y.2
Nakamura, H.3
Nishio, H.4
Sumino, K.5
-
14
-
-
0028287482
-
A new type of defect in the gene for bilirubin uridine 5′-diphosphate-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type I
-
Aono S, Yamada Y, Keino H, Sasaoka Y, Nakagawa T, Onishi S, Mimura S, Koiwai O, Sato H: A new type of defect in the gene for bilirubin uridine 5′-diphosphate-glucuronosyltransferase in a patient with Crigler-Najjar syndrome type I. Pediatr Res 1994;35:629-632.
-
(1994)
Pediatr Res
, vol.35
, pp. 629-632
-
-
Aono, S.1
Yamada, Y.2
Keino, H.3
Sasaoka, Y.4
Nakagawa, T.5
Onishi, S.6
Mimura, S.7
Koiwai, O.8
Sato, H.9
-
15
-
-
0032005254
-
UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis
-
Iolascon A, Faienza MF, Moretti A, Perrotta S, Miraglia del Giudice E: UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis. Blood 1998;91:1093.
-
(1998)
Blood
, vol.91
, pp. 1093
-
-
Iolascon, A.1
Faienza, M.F.2
Moretti, A.3
Perrotta, S.4
Miraglia Del Giudice, E.5
-
16
-
-
0033063940
-
The interaction between Gilbert's syndrome and G6PD deficiency influences bilirubin levels
-
Cappellini M, Sampieto M, Tarazzi D, Fiorelli G: The interaction between Gilbert's syndrome and G6PD deficiency influences bilirubin levels. Br J Haematol 1999;104:928.
-
(1999)
Br J Haematol
, vol.104
, pp. 928
-
-
Cappellini, M.1
Sampieto, M.2
Tarazzi, D.3
Fiorelli, G.4
-
17
-
-
0033510908
-
Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn
-
Monaghan G, McLellan A, McGeehan A, Li Volti S, Mollica F, Salemi I, Din Z, Cassidy A, Hume R, Burchell B: Gilbert's syndrome is a contributory factor in prolonged unconjugated 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
Din, Z.7
Cassidy, A.8
Hume, R.9
Burchell, B.10
-
18
-
-
0036787116
-
Relationship between bilirubin UDP-glucuronosyl transferase 1A1 gene and neonatal hyperbilirubinemia
-
Huang CS, Chang PF, Huang MJ, Chen ES, Hung KL, Tsou KI: Relationship between bilirubin 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
-
-
0032845453
-
Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome
-
Galanello R, Cipollina MD, Carboni G, Perseu L, Barella S, Corrias A, Cao A: Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome. Eur J Pediatr 1999;158:914-916.
-
(1999)
Eur J Pediatr
, vol.158
, pp. 914-916
-
-
Galanello, R.1
Cipollina, M.D.2
Carboni, G.3
Perseu, L.4
Barella, S.5
Corrias, A.6
Cao, A.7
-
20
-
-
0032859356
-
Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates
-
Iolascon A, Faienza MF, Perrotta S, Meloni GF, Ruggiu G, del Giudice EM: Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates. Haematologica 1999;84:99-102.
-
(1999)
Haematologica
, vol.84
, pp. 99-102
-
-
Iolascon, A.1
Faienza, M.F.2
Perrotta, S.3
Meloni, G.F.4
Ruggiu, G.5
Del Giudice, E.M.6
-
21
-
-
0033961560
-
Rapid method for detection of extra (TA) in the promoter of the bilirubin-UDP-glucuronosyl transferase 1 gene associated with Gilbert syndrome
-
Pirulli D, Giordano M, Puzzer D, Crovella S, Rigato I, Tiribelli C, Momigliano-Richiardi P, Amoroso A: Rapid method for detection of extra (TA) in the promoter of the bilirubin-UDP-glucuronosyl transferase 1 gene associated with Gilbert syndrome. Clin Chem 2000;46:129-131.
-
(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
Momigliano-Richiardi, P.7
Amoroso, A.8
-
22
-
-
0030691028
-
Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
-
USA
-
Kaplan M, Renbaum P, Levy-Lahad E, Hammerman C, Lahad A, Beutler E: Gilbert 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
, vol.94
, pp. 12128-12132
-
-
Kaplan, M.1
Renbaum, P.2
Levy-Lahad, E.3
Hammerman, C.4
Lahad, A.5
Beutler, E.6
-
23
-
-
0034686969
-
Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates
-
Kaplan M, Hammerman C, Renbaum P, Klein G, Levy-Lahad E: Gilbert's syndrome and hyperbilirubinaemia in ABO-incompatible neonates. Lancet 2000;356:652-653.
-
(2000)
Lancet
, vol.356
, pp. 652-653
-
-
Kaplan, M.1
Hammerman, C.2
Renbaum, P.3
Klein, G.4
Levy-Lahad, E.5
-
24
-
-
2942527225
-
UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancer
-
Sai K, Saeki M, Saito Y, Ozawa S, Katori N, Jinno H, Hasegawa R, Kaniwa N, Sawada J, Komamura K, Ueno K, Kamakura S, Kitakaze M, Kitamura Y, Kamatani N, Minami H, Ohtsu A, Shirao K, Yoshida T, Saijo N: UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancer. Clin Pharmacol Ther 2004;75:501-515.
-
(2004)
Clin Pharmacol Ther
, vol.75
, pp. 501-515
-
-
Sai, K.1
Saeki, M.2
Saito, Y.3
Ozawa, S.4
Katori, N.5
Jinno, H.6
Hasegawa, R.7
Kaniwa, N.8
Sawada, J.9
Komamura, K.10
Ueno, K.11
Kamakura, S.12
Kitakaze, M.13
Kitamura, Y.14
Kamatani, N.15
Minami, H.16
Ohtsu, A.17
Shirao, K.18
Yoshida, T.19
Saijo, N.20
more..
-
25
-
-
18444399926
-
Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia
-
Sugatani J, 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
Yoshinari, K.2
Machida, T.3
Takagi, H.4
Mori, M.5
Kakizaki, S.6
Sueyoshi, T.7
Negishi, M.8
Miwa, M.9
-
26
-
-
12244271026
-
Haplotype structure of the UDP-glucuronosyltransferase 1A1 promoter in different ethnic groups
-
Innocenti F, Grimsley C, Das S, Ramirez J, Cheng C, Kuttab-Boulos H, Ratain MJ, Di Rienzo A: Haplotype structure of the UDP-glucuronosyltransferase 1A1 promoter in different ethnic groups. Pharmacogenetics 2002;12:725-733.
-
(2002)
Pharmacogenetics
, vol.12
, pp. 725-733
-
-
Innocenti, F.1
Grimsley, C.2
Das, S.3
Ramirez, J.4
Cheng, C.5
Kuttab-Boulos, H.6
Ratain, M.J.7
Di Rienzo, A.8
-
27
-
-
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, Takeuchi Y: Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome. Hum Genet 2004;115:525-526.
-
(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
Takeuchi, Y.7
-
28
-
-
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
-
29
-
-
0035053747
-
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
-
30
-
-
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 Y, 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. Biochim Biophys Acta 1998;1406:267-273.
-
(1998)
Biochim Biophys Acta
, vol.1406
, pp. 267-273
-
-
Yamamoto, K.1
Sato, H.2
Fujiyama, Y.3
Doida, Y.4
Bamba, T.5
-
31
-
-
33645565998
-
Identification of uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) gene mutation in babies with early onset of neonatal jaundice (NNJ)
-
Norlelawati A, Van Rostenberghe H, Sutomo R, Selamah G, Matsuo M, Nishio H, Narazah Y: Identification of uridine diphosphate glucuronosyltransferase 1A1 (UGT1A1) gene mutation in babies with early onset of neonatal jaundice (NNJ). Abstract book of 9th National Conference on Medical Sciences 2004;9:92.
-
(2004)
Abstract Book of 9th National Conference on Medical Sciences
, vol.9
, pp. 92
-
-
Norlelawati, A.1
Van Rostenberghe, H.2
Sutomo, R.3
Selamah, G.4
Matsuo, M.5
Nishio, H.6
Narazah, Y.7
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