-
2
-
-
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; 347:578-81.
-
(1996)
Lancet
, vol.347
, pp. 578-581
-
-
Monaghan, G.1
Ryan, M.2
Seddon, R.3
Hume, R.4
Burchell, B.5
-
3
-
-
85040025033
-
Hepatic bilirubin UDP-glucuronosyltransferase activity in liver disease and Gilbert's syndrome
-
Black M, Billing BH. Hepatic bilirubin UDP-glucuronosyltransferase activity in liver disease and Gilbert's syndrome. N Engl J Med 1969; 280:166-71.
-
(1969)
N Engl J Med
, vol.280
, pp. 166-171
-
-
Black, M.1
Billing, B.H.2
-
4
-
-
0006264039
-
Diagnosis of Gilbert's syndrome: Role of reduced caloric intake test
-
Owens D, Sherlock S. Diagnosis of Gilbert's syndrome: Role of reduced caloric intake test. Br Med J 1973; 559:1973-6.
-
(1973)
Br Med J
, vol.559
, pp. 1973-1976
-
-
Owens, D.1
Sherlock, S.2
-
5
-
-
0026008487
-
Cloning of two human liver bilirubin UDP glucuronosyltransferase cDNAs with expression in COS1 cells
-
Ritter JK, Crawford JM, Owens IS. Cloning of two human liver bilirubin UDP glucuronosyltransferase cDNAs with expression in COS1 cells. J Biol Chem 1991; 266:1043-7.
-
(1991)
J Biol Chem
, vol.266
, pp. 1043-1047
-
-
Ritter, J.K.1
Crawford, J.M.2
Owens, I.S.3
-
6
-
-
0026701911
-
A novel complex locus UGT1 encodes human bilirubin, phenol, and others UDP glucuronosyltransferase isoenzymes with identical carboxyl termini
-
Ritter JK, Chen F, Sheene YY, et al. A novel complex locus UGT1 encodes human bilirubin, phenol, and others UDP glucuronosyltransferase isoenzymes with identical carboxyl termini. J Biol Chem 1992; 267: 3257-61.
-
(1992)
J Biol Chem
, vol.267
, pp. 3257-3261
-
-
Ritter, J.K.1
Chen, F.2
Sheene, Y.Y.3
-
7
-
-
0343924387
-
Regulation of the human bilirubin UDP-glucuronosyltransferase gene
-
Brierley CH, Senafi SB, Clarke D, Hsu MH, Johnson EF, Burchell B. Regulation of the human bilirubin UDP-glucuronosyltransferase gene. Adv Enzyme Regul 1996; 36:85-97.
-
(1996)
Adv Enzyme Regul
, vol.36
, pp. 85-97
-
-
Brierley, C.H.1
Senafi, S.B.2
Clarke, D.3
Hsu, M.H.4
Johnson, E.F.5
Burchell, B.6
-
8
-
-
0028904620
-
Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
-
Aono S, Adachi Y, Uyama E, et al. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome. Lancet 1995; 345:958-9.
-
(1995)
Lancet
, vol.345
, pp. 958-959
-
-
Aono, S.1
Adachi, Y.2
Uyama, E.3
-
9
-
-
0029015847
-
Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase
-
Koiwai O, Nishizawa M, Hasada K, et al. Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase. Hum Mol Genet 1995; 4:1183-6.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1183-1186
-
-
Koiwai, O.1
Nishizawa, M.2
Hasada, K.3
-
10
-
-
0028867826
-
The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
-
Bosma PJ, Chowdhury JR, Bakker C, et al. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase in Gilbert's 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
-
11
-
-
0030698230
-
Hyperbilirubinaemia in heterozygous β-thalassaemia is related to co-inherited Gilbert's syndrome
-
Galanello R, Perseu L, Melis MA, et al. Hyperbilirubinaemia in heterozygous β-thalassaemia is related to co-inherited Gilbert's syndrome. Br J Haematol 1997; 99:433-6.
-
(1997)
Br J Haematol
, vol.99
, pp. 433-436
-
-
Galanello, R.1
Perseu, L.2
Melis, M.A.3
-
12
-
-
0030663191
-
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency
-
Sampietro M, Lupica L, Perrero L, et al. The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous β-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency. Br J Haematol 1997; 99:-437-9.
-
(1997)
Br J Haematol
, vol.99
, pp. 437-439
-
-
Sampietro, M.1
Lupica, L.2
Perrero, L.3
-
13
-
-
0030691028
-
Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
-
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: 12128-32.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 12128-12132
-
-
Kaplan, M.1
Renbaum, P.2
Levy-Lahad, E.3
Hammerman, C.4
Lahad, A.5
Beutler, E.6
-
14
-
-
85069127338
-
UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocitosis
-
Iolascon A, Faienza MF, Moretti A, Perrotta S, Miraglia del Giudice E. UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocitosis. Blood 1997; 91:1093.
-
(1997)
Blood
, vol.91
, pp. 1093
-
-
Iolascon, A.1
Faienza, M.F.2
Moretti, A.3
Perrotta, S.4
Miraglia Del Giudice, E.5
-
15
-
-
0032493441
-
Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
-
Beutler E, Geleart 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; 95:8170-4.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 8170-8174
-
-
Beutler, E.1
Geleart, T.2
Demina, A.3
-
18
-
-
0020724929
-
Three regions upstream from the cap site are required for efficient and accurate transcription of the rabbit β-globin gene in mouse 3TS cells
-
Dierks P, van Ooyen A, Cochran MD, Dobkin C, Reiser J, Wessemann C. Three regions upstream from the cap site are required for efficient and accurate transcription of the rabbit β-globin gene in mouse 3TS cells. Cell 1983; 32:695-706.
-
(1983)
Cell
, vol.32
, pp. 695-706
-
-
Dierks, P.1
Van Ooyen, A.2
Cochran, M.D.3
Dobkin, C.4
Reiser, J.5
Wessemann, C.6
-
19
-
-
0023645070
-
Regulation of inducible and tissue-specific gene expression
-
Maniatis T, Goodbourn S, Fischer JA. Regulation of inducible and tissue-specific gene expression. Science 1977; 236:1237-45.
-
(1977)
Science
, vol.236
, pp. 1237-1245
-
-
Maniatis, T.1
Goodbourn, S.2
Fischer, J.A.3
-
20
-
-
0020031458
-
DNA sequences necessary for transcription of the rabbit β-globin gene in vivo
-
Grosveld GC, de Boer E, Shewmaker CK, Flavell RA. DNA sequences necessary for transcription of the rabbit β-globin gene in vivo. Nature 1982; 295:120-6.
-
(1982)
Nature
, vol.295
, pp. 120-126
-
-
Grosveld, G.C.1
De Boer, E.2
Shewmaker, C.K.3
Flavell, R.A.4
-
21
-
-
0026633346
-
DNA sequences at and between the GC and TATA boxes: Potential DNA looping and spatial juxtapositioning of the protein factors
-
Nussinov R. DNA sequences at and between the GC and TATA boxes: potential DNA looping and spatial juxtapositioning of the protein factors. J Biomol Struct Dynamics 1992; 9:1213-37.
-
(1992)
J Biomol Struct Dynamics
, vol.9
, pp. 1213-1237
-
-
Nussinov, R.1
-
22
-
-
0026505255
-
Sequence of exons and the flankmg regions of human bilirubin UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I
-
Bosma PJ, Roy-Chowdhur N, Goldhoorn B, et al. Sequence of exons and the flankmg regions of human bilirubin UDP-glucuronosyltransferase gene complex and identification of a genetic mutation in a patient with Crigler-Najjar syndrome, type I. Hepatology 1992; 15:941-7.
-
(1992)
Hepatology
, vol.15
, pp. 941-947
-
-
Bosma, P.J.1
Roy-Chowdhur, N.2
Goldhoorn, B.3
-
23
-
-
0032168989
-
Equilibrium distribuitions of microsatellite repeat length resulting from a balance between slippage events and point mutations
-
Kruglyak S, Durrett RT, Schug MD, Aonadro CF. Equilibrium distribuitions of microsatellite repeat length resulting from a balance between slippage events and point mutations. Proc Natl Acad Sci USA 1998; 95:10774-8.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 10774-10778
-
-
Kruglyak, S.1
Durrett, R.T.2
Schug, M.D.3
Aonadro, C.F.4
|