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

scientific article published on 01 February 2005

Association of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia is …
instance of (P31):
scholarly articleQ13442814

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P698PubMed publication ID15710570

P50authorMarc RomanaQ57566069
Jacques ElionQ59198601
P2093author name stringJohn Clayton
Rajagopal Krishnamoorthy
Vicky Chaar
Jean Pierre Diara
Lysiane Kéclard
Claudine Leturdu
P433issue2
P921main subjectgallstoneQ272714
P304page(s)188-199
P577publication date2005-02-01
P1433published inHaematologicaQ5638209
P1476titleAssociation of UGT1A1 polymorphism with prevalence and age at onset of cholelithiasis in sickle cell anemia
P478volume90

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cites work (P2860)
Q34256214A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia
Q36368068Differences of microparticle patterns between sickle cell anemia and hemoglobin SC patients
Q54117269Do Alpha Thalassemia, Fetal Hemoglobin, and the UGT1A1 Polymorphism have an Influence on Serum Bilirubin Levels and Cholelithiasis in Patients with Sickle Cell Disease?
Q30448607Early complication in sickle cell anemia children due to A(TA)nTAA polymorphism at the promoter of UGT1A1 gene
Q50185437Early modification of sickle cell disease clinical course by UDP-glucuronosyltransferase 1A1 gene promoter polymorphism
Q37687064High rates of recurrent biliary tract obstruction in children with sickle cell disease
Q36913577Minireview: Clinical severity in sickle cell disease: the challenges of definition and prognostication
Q26826934New pathophysiological concepts underlying pathogenesis of pigment gallstones
Q36208312Serum Total Bilirubin, not Cholelithiasis, is Influenced by UGT1A1 Polymorphism, Alpha Thalassemia and β(s) Haplotype: First Report on Comparison between Arab-Indian and African β(s) Genes
Q33791764Sickle Cell Disease in the Post Genomic Era: A Monogenic Disease with a Polygenic Phenotype
Q38048766The search for genetic modifiers of disease severity in the β-hemoglobinopathies
Q85987864UGT1A1 promoter polymorphism associated with serum bilirubin level in Saudi patients with sickle cell disease
Q90751255Uridine diphosphate glucuronosyl transferase 1A (UGT1A1) promoter polymorphism in young patients with sickle cell anaemia: report of the first cohort study from Nigeria

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