(Q50169464)

English

UDP-glucuronosyltransferase 1 gene promoter polymorphism is associated with increased serum bilirubin levels and cholecystectomy in patients with sickle cell anemia.

scientific article published in August 2003

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scholarly article

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

UDP-glucuronosyltransferase 1 gene promoter polymorphism is associated with increased serum bilirubin levels and cholecystectomy in patients with sickle cell anemia. (English)

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

Kleber Yotsumoto Fertrin

1

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

author name string

Melo MB

2

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

Assis AM

3

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

Saad ST

4

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

Costa FF

5

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

publication date

1 August 2003

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

Clinical Genetics

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

64

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

2

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

160-162

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Hyperbilirubinaemia in heterozygous beta-thalassaemia is related to co-inherited Gilbert's syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Gilbert syndrome accelerates development of neonatal jaundice

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Neonatal hyperbilirubinemia and a common mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene in Japanese

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Cholelithiasis and Gilbert's syndrome in homozygous beta-thalassaemia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic determinants of jaundice and gallstones in haemoglobin E beta thalassaemia

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Sickle cell disease in a Brazilian population from Sao Paulo: a study of the beta s haplotypes.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Influence of bilirubin uridine diphosphate-glucuronosyltransferase 1A promoter polymorphisms on serum bilirubin levels and cholelithiasis in children with sickle cell anemia.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Sickle cell disease: no longer a single gene disorder

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00113.X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1034/J.1399-0004.2003.00113.X

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

1 reference

Europe PubMed Central

26 February 2018

http://europepmc.org/abstract/MED/12859413

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