(Q44675167)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

title

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

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

bilirubin metabolic disorder

21 December 2019

main subject

1 reference

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

author name string

T M Danoff

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

D A Campbell

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

L C McCarthy

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

K F Lewis

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

M H Repasch

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

A M Saunders

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

N K Spurr

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

I J Purvis

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

A D Roses

9

1 reference

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21 December 2019

publication date

1 January 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

The Pharmacogenomics Journal

21 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14647407%20AND%20SRC:MED&resulttype=core&format=json

21 December 2019

volume

4

1 reference

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21 December 2019

issue

1

1 reference

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21 December 2019

page(s)

49-53

1 reference

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https://scigraph.springernature.com/pub.10.1038/sj.tpj.6500221

21 December 2019

exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

Human UDP-glucuronosyltransferases: metabolism, expression, and disease

21 January 2018

1 reference

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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

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

Does Gilbert's disease exist?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

Power calculations for genetic association studies using estimated probability distributions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

Mechanism of indinavir-induced hyperbilirubinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

7 January 2021

Predicted homozygous mis-sense mutation in Gilbert's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

7 January 2021

The genetic basis of Gilbert's syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.TPJ.6500221

7 January 2021