Combined effect of regulatory polymorphisms on transcription of UGT1A1 as a cause of Gilbert syndrome (Q33597058)

28 July 2017

title

Combined effect of regulatory polymorphisms on transcription of UGT1A1 as a cause of Gilbert syndrome (English)

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28 July 2017

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Katsuyuki Matsui

1

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28 July 2017

Yoshihiro Maruo

series ordinal

2

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28 July 2017

Hiroshi Sato

series ordinal

3

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28 July 2017

Yoshihiro Takeuchi

series ordinal

4

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28 July 2017

publication date

8 June 2010

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28 July 2017

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28 July 2017

volume

10

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28 July 2017

page(s)

57

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Haploview: analysis and visualization of LD and haplotype maps

28 July 2017

cites work

1 reference

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Alternatively spliced isoforms of the human constitutive androstane receptor

14 July 2018

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Induction of bilirubin clearance by the constitutive androstane receptor (CAR)

14 July 2018

1 reference

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Haplotype structure of the UDP-glucuronosyltransferase 1A1 promoter in different ethnic groups

14 July 2018

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Dual effect of dexamethasone on CYP3A4 gene expression in human hepatocytes. Sequential role of glucocorticoid receptor and pregnane X receptor.

14 July 2018

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

14 July 2018

1 reference

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Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion

14 July 2018

1 reference

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

14 July 2018

1 reference

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

14 July 2018

1 reference

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Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man

14 July 2018

1 reference

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

14 July 2018

1 reference

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

14 July 2018

1 reference

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[Prevalence of Gilbert's syndrome in Germany]

14 July 2018

1 reference

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Molecular analysis of five independent Japanese mutant genes responsible for hypoxanthine guanine phosphoribosyltransferase (HPRT) deficiency

14 July 2018

1 reference

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A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini

14 July 2018

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Population studies on Gilbert's syndrome

14 July 2018

1 reference

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The phenobarbital response enhancer module in the human bilirubin UDP-glucuronosyltransferase UGT1A1 gene and regulation by the nuclear receptor CAR.

14 July 2018

1 reference

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Identification of a defect in the UGT1A1 gene promoter and its association with hyperbilirubinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1186/1471-230X-10-57

Correlation between the UDP-glucuronosyltransferase (UGT1A1) TATAA box polymorphism and carcinogen detoxification phenotype: significantly decreased glucuronidating activity against benzo(a)pyrene-7,8-dihydrodiol(-) in liver microsomes from subjects

21 January 2018

1 reference

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UGT1A1 polymorphisms are important determinants of dietary carcinogen detoxification in the liver

21 January 2018

1 reference

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UGT1A1 haplotypes associated with reduced glucuronidation and increased serum bilirubin in irinotecan-administered Japanese patients with cancer

21 January 2018

1 reference

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Transcriptional regulation of human UGT1A1 gene expression through distal and proximal promoter motifs: implication of defects in the UGT1A1 gene promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1186/1471-230X-10-57

Variations in the UDP-glucuronosyltransferase 1A1 gene for the development of unconjugated hyperbilirubinemia in Taiwanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1186/1471-230X-10-57

The genetic basis of Gilbert's syndrome

21 January 2018

1 reference

12 December 2020

Regulation of the human bilirubin UDP-glucuronosyltransferase gene

1 reference

12 December 2020

Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism

1 reference

12 December 2020

Two linked polymorphic mutations (A(TA)7TAA and T-3279G) of UGT1A1 as the principal cause of Gilbert syndrome

1 reference

12 December 2020

The Polymorphism c.-3279T>G in the Phenobarbital-Responsive Enhancer Module of the Bilirubin UDP-Glucuronosyltransferase Gene Is Associated with Gilbert Syndrome

1 reference

12 December 2020

Linkage between A(TA)7TAA and -3279T>G mutations in UGT1A1 is not essential for pathogenesis of Gilbert syndrome

1 reference

12 December 2020

Haplotypes in the UGT1A1 gene and their role as genetic determinants of bilirubin concentration in healthy German volunteers

1 reference

12 December 2020

Hepatic bilirubin-conjugating enzymes of man in the normal state and in liver disease

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-230X-10-57

1 reference

Dimensions Publication ID

28 July 2017

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28 July 2017

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