(Q44506208)

English

The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): hematologic and evolutionary implications

scientific article published in July 2003

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scholarly article

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Europe PubMed Central

PubMed publication ID

3 December 2017

The global distribution of length polymorphisms of the promoters of the glucuronosyltransferase 1 gene (UGT1A1): hematologic and evolutionary implications (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

author name string

A Premawardhena

1

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

C A Fisher

2

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

Y T Liu

3

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

I C Verma

4

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

S de Silva

5

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

M Arambepola

6

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

J B Clegg

7

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

D J Weatherall

8

1 reference

Europe PubMed Central

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3 December 2017

publication date

1 July 2003

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Europe PubMed Central

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3 December 2017

Blood Cells, Molecules and Diseases

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Europe PubMed Central

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3 December 2017

31

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Europe PubMed Central

PubMed publication ID

3 December 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

98-101

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

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

1 reference

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

1 reference

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The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency

1 reference

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

1 reference

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Gilbert's syndrome accounts for the phenotypic variability of congenital dyserythropoietic anemia type II (CDA-II).

1 reference

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

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Genetic determinants of jaundice and gallstones in haemoglobin E beta thalassaemia

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

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UGT1*1 genotyping in a Canadian Inuit population

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UGT1A1 genotypes and glucuronidation of SN-38, the active metabolite of irinotecan

1 reference

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Microsatellite diversity and the demographic history of modern humans

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Microsatellite data support an early population expansion in Africa

1 reference

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Genetic evidence of an early exit of Homo sapiens sapiens from Africa through eastern Africa

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Ascertainment bias cannot entirely account for human microsatellites being longer than their chimpanzee homologues.

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Identifiers

10.1016/S1079-9796(03)00071-8

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 December 2017

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