(Q57499954)

1

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Paul Renbaum

2

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Hendrik J Vreman

3

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Ronald J Wong

4

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Cathy Hammerman

6

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David K Stevenson

https://scigraph.springernature.com/pub.10.1203/pdr.0b013e31805365c5

7

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language of work or name

English

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publication date

June 2007

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published in

Pediatric Research

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volume

61

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issue

6

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page(s)

727-731

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exact match

0 references

cites work

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

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

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/10.1203%2FPDR.0B013E31805365C5

Molecular genetic basis of Gilbert's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

Onset of jaundice in glucose-6-phosphate dehydrogenase-deficient neonates

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

Hyperbilirubinemia among African American, glucose-6-phosphate dehydrogenase-deficient neonates

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

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/10.1203%2FPDR.0B013E31805365C5

Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5

Hematologically important mutations: bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler-Najjar syndromes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1203%2FPDR.0B013E31805365C5