(Q50185437)

26 February 2018

title

Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism. (English)

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9

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Lígia Braga

Lígia Braga

7

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Paula Faustino

Paula Faustino

13

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Luísa Romão

Luísa Romão

11

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João Lavinha

João Lavinha

12

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author name string

Rute Martins

1

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26 February 2018

Anabela Morais

2

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Alexandra Dias

3

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Isabel Soares

4

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Cristiana Rolão

5

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J L Ducla-Soares

6

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Teresa Seixas

8

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Gabriel Olim

10

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publication date

5 April 2008

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Journal of Human Genetics

published in

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volume

53

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issue

6

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page(s)

524-528

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https://scigraph.springernature.com/pub.10.1007/s10038-008-0281-3

exact match

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cites work

UGT1A1 variation and gallstone formation in sickle cell disease

1 reference

12 December 2020

Rapid analysis of -alpha 3.7 thalassaemia and alpha alpha alpha anti 3.7 triplication by enzymatic amplification analysis

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12 December 2020

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

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12 December 2020

Influence of alpha-thalassemia on cholelithiasis in SS patients with elevated Hb F.

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12 December 2020

Modifier genes and sickle cell anemia

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12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome

1 reference

12 December 2020

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

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12 December 2020

The influence of uridine diphosphate glucuronosyl transferase 1A promoter polymorphisms, beta-globin gene haplotype, co-inherited alpha-thalassemia trait and Hb F on steady-state serum bilirubin levels in sickle cell anemia

1 reference

12 December 2020

Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster.

1 reference

12 December 2020

The emerging understanding of sickle cell disease

1 reference

12 December 2020

Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia

1 reference

12 December 2020

Co-inherited Gilbert's syndrome: a factor determining hyperbilirubinemia in homozygous beta-thalassemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Overlapping PCR for bidirectional PCR amplification of specific alleles: a rapid one-tube method for simultaneously differentiating homozygotes and heterozygotes

1 reference

12 December 2020

UGT1A1 polymorphism outweighs the modest effect of deletional (-3.7 kb) alpha-thalassemia on cholelithogenesis in sickle cell anemia

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12 December 2020

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

1 reference

12 December 2020

The linear effects of alpha-thalassaemia, the UGT1A1 and HMOX1 polymorphisms on cholelithiasis in sickle cell disease

1 reference

12 December 2020

10.1007/S10038-008-0281-3

Identifiers

DOI

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26 February 2018

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26 February 2018