A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia. (Q44675167)

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21 December 2019

title

A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia (English)

1 reference

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bilirubin metabolic disorder

21 December 2019

main subject

1 reference

10

1 reference

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21 December 2019

6

A M Saunders

1 reference

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21 December 2019

author name string

T M Danoff

1

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21 December 2019

D A Campbell

2

1 reference

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21 December 2019

L C McCarthy

3

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21 December 2019

K F Lewis

4

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21 December 2019

M H Repasch

5

1 reference

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21 December 2019

N K Spurr

7

1 reference

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21 December 2019

I J Purvis

8

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21 December 2019

A D Roses

9

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21 December 2019

publication date

1 January 2004

1 reference

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The Pharmacogenomics Journal

21 December 2019

language of work or name

English

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published in

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21 December 2019

volume

4

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21 December 2019

issue

1

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21 December 2019

page(s)

49-53

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Discrimination between Crigler-Najjar type I and II by expression of mutant bilirubin uridine diphosphate-glucuronosyltransferase

21 December 2019

cites work

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Human UDP-glucuronosyltransferases: metabolism, expression, and disease

21 January 2018

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Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype

21 January 2018

1 reference

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Does Gilbert's disease exist?

21 January 2018

1 reference

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

21 January 2018

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

21 January 2018

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Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome

21 January 2018

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

21 January 2018

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

21 January 2018

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

21 January 2018

1 reference

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Gilbert's syndrome is caused by a heterozygous missense mutation in the gene for bilirubin UDP-glucuronosyltransferase

21 January 2018

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Power calculations for genetic association studies using estimated probability distributions

21 January 2018

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Mechanism of indinavir-induced hyperbilirubinemia

21 January 2018

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UGT1A1*28 polymorphism as a determinant of irinotecan disposition and toxicity

21 January 2018

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Results of Prevention of REStenosis with Tranilast and its Outcomes (PRESTO) trial

21 January 2018

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Restenosis after successful percutaneous transluminal coronary angioplasty: serial angiographic follow-up of 229 patients

21 January 2018

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7 January 2021

Impact of tranilast on restenosis after coronary angioplasty: tranilast restenosis following angioplasty trial (TREAT)

1 reference

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7 January 2021

The PRESTO (Prevention of restenosis with tranilast and its outcomes) protocol: a double-blind, placebo-controlled trial

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7 January 2021

Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects

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7 January 2021

Predicting the risk of sporadic elevated bilirubin levels and diagnosing Gilbert's syndrome by genotyping UGT1A1*28 promoter polymorphism

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7 January 2021

The UGT1A1*28 allele is relatively rare in a Japanese population

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7 January 2021

Predicted homozygous mis-sense mutation in Gilbert's syndrome

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7 January 2021

The genetic basis of Gilbert's syndrome

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7 January 2021