Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene (Q33920356)

30 July 2017

title

Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promoter region of the UGT1A1 gene (English)

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30 July 2017

3

E A Steegers

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30 July 2017

M T Raijmakers

1

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30 July 2017

P L Jansen

series ordinal

2

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30 July 2017

W H Peters

series ordinal

4

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30 July 2017

language of work or name

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1 September 2000

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30 July 2017

published in

Journal of Hepatology

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30 July 2017

volume

33

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issue

3

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30 July 2017

page(s)

348-351

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The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome

30 July 2017

cites work

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Genetic variation in bilirubin UPD-glucuronosyltransferase gene promoter and Gilbert's syndrome

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Hepatic Bilirubin UDP-Glucuronyl Transferase Activity in Liver Disease and Gilbert's Syndrome

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Decreased glucuronidation and increased bioactivation of acetaminophen in Gilbert's syndrome

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Drug glucuronidation by human renal UDP-glucuronosyltransferases.

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Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes

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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

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Gilbert syndrome accelerates development of neonatal jaundice

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Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: a balanced polymorphism for regulation of bilirubin metabolism?

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Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome

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Microsomal UDP-glucuronyltransferase-catalyzed bilirubin diglucuronide formation in human liver

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Coding defect and a TATA box mutation at the bilirubin UDP-glucuronosyltransferase gene cause Crigler-Najjar type I disease

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The genetic basis of Gilbert's syndrome

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Identifiers

DOI

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30 July 2017

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