Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism (Q34120603)

31 July 2017

title

Hemolysis and bilirubin conjugation in association with UDP-glucuronosyltransferase 1A1 promoter polymorphism (English)

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31 July 2017

Ephrat Levy-Lahad

5

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Maurizio Muraca

object named as

Maurizio Muraca

9

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Hendrik J Vreman

7

object named as

Hendrik J Vreman

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31 July 2017

Michael Kaplan

1

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31 July 2017

Cathy Hammerman

2

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31 July 2017

Firmino F Rubaltelli

3

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31 July 2017

Maria T Vilei

4

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31 July 2017

Paul Renbaum

6

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David K Stevenson

8

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31 July 2017

language of work or name

English

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publication date

1 April 2002

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31 July 2017

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31 July 2017

volume

35

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31 July 2017

issue

4

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31 July 2017

page(s)

905-911

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Molecular genetic basis of Gilbert's syndrome

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

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/10.1053%2FJHEP.2002.32526

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

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/10.1053%2FJHEP.2002.32526

Chronic unconjugated hyperbilirubinemia without overt signs of hemolysis in adolescents and adults

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

Detection of Gilbert's syndrome in patients with hemolysis. A method using radioactive chromium.

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

Carbon monoxide and bilirubin production in neonates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

A simple salting out procedure for extracting DNA from human nucleated cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

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/10.1053%2FJHEP.2002.32526

Gilbert's syndrome: diagnosis by typical serum bilirubin pattern

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

Antioxidant and cytotoxic effects of bilirubin on neonatal erythrocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

Diagnosis and management of Crigler-Najjar syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

What can we learn from analysis of serum bilirubin?

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

Gilbert syndrome accelerates development of neonatal jaundice

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

Differing pathogenesis of perinatal bilirubinemia in glucose-6-phosphate dehydrogenase-deficient versus-normal neonates.

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

Neonatal hyperbilirubinemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1053%2FJHEP.2002.32526

21 January 2018

Identifiers

DOI

10.1053/JHEP.2002.32526

1 reference

31 July 2017

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