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Items: 12

1.

Crigler-Najjar syndrome in The Netherlands: identification of four novel UGT1A1 alleles, genotype-phenotype correlation, and functional analysis of 10 missense mutants.

Sneitz N, Bakker CT, de Knegt RJ, Halley DJ, Finel M, Bosma PJ.

Hum Mutat. 2010 Jan;31(1):52-9. doi: 10.1002/humu.21133.

PMID:
19830808
2.

Genetic lesions of bilirubin uridine-diphosphoglucuronate glucuronosyltransferase (UGT1A1) causing Crigler-Najjar and Gilbert syndromes: correlation of genotype to phenotype.

Kadakol A, Ghosh SS, Sappal BS, Sharma G, Chowdhury JR, Chowdhury NR.

Hum Mutat. 2000 Oct;16(4):297-306. Review.

PMID:
11013440
3.

[From gene to disease; unconjugated hyperbilirubinemia: Gilbert's syndrome and Crigler-Najjar types I and II].

Drenth JP, Peters WH, Jansen JB.

Ned Tijdschr Geneeskd. 2002 Aug 10;146(32):1488-90. Review. Dutch.

PMID:
12198827
4.

[Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus].

Kraemer D, Scheurlen M.

Med Klin (Munich). 2002 Sep 15;97(9):528-32. Review. German.

PMID:
12371080
5.

Function, genetic polymorphism, and transcriptional regulation of human UDP-glucuronosyltransferase (UGT) 1A1.

Sugatani J.

Drug Metab Pharmacokinet. 2013;28(2):83-92. Epub 2012 Oct 23. Review.

6.
7.

Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes.

Sampietro M, Iolascon A.

Haematologica. 1999 Feb;84(2):150-7. Review.

8.

[Inherited disorders of bilirubin metabolism].

Rossi F, Francese M, Iodice RM, Falcone E, Vetrella S, Punzo F, De Vita S, Perrotta S.

Minerva Pediatr. 2005 Apr;57(2):53-63. Review. Italian.

PMID:
15985997
9.

Molecular genetics of unconjugated hyperbilirubinemia in Taiwanese.

Huang CS.

J Biomed Sci. 2005;12(3):445-50. Review.

PMID:
15965581
10.

Effect of the UGT1A1*28 allele on unconjugated hyperbilirubinemia in HIV-positive patients receiving Atazanavir: a systematic review.

Culley CL, Kiang TK, Gilchrist SE, Ensom MH.

Ann Pharmacother. 2013 Apr;47(4):561-72. doi: 10.1345/aph.1R550. Epub 2013 Apr 2. Review.

PMID:
23548653
11.

Genetic factors in neonatal hyperbilirubinemia and kernicterus.

Sarici SU, Saldir M.

Turk J Pediatr. 2007 Jul-Sep;49(3):245-9. Review.

12.

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for UGT1A1 and Atazanavir Prescribing.

Gammal RS, Court MH, Haidar CE, Iwuchukwu OF, Gaur AH, Alvarellos M, Guillemette C, Lennox JL, Whirl-Carrillo M, Brummel SS, Ratain MJ, Klein TE, Schackman BR, Caudle KE, Haas DW; Clinical Pharmacogenetics Implementation Consortium.

Clin Pharmacol Ther. 2016 Apr;99(4):363-9. doi: 10.1002/cpt.269. Epub 2015 Nov 9. Review.

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