Polymorphism in the promoter region of the bilirubin UDP-glucuronosyltransferase (Gilbert's syndrome) in healthy Dutch subjects [2]

Hepatology

Volumn 33, Issue 3, 2001, Pages 765-

  Te Morsche, R H M ^a   Zusterzeel, P L M ^a   Raijmakers, M T M ^a   Roes, E M ^a   Steegers, E A P ^a   Peters, W H M ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; GLUCURONOSYLTRANSFERASE;

ADULT; BILIRUBIN BLOOD LEVEL; ENERGY TRANSFER; FEMALE; GENETIC POLYMORPHISM; GILBERT DISEASE; HOMOZYGOSITY; HUMAN; HUMAN EXPERIMENT; LETTER; MALE; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL; SCREENING TEST; TATA BOX;

FEMALE; GILBERT DISEASE; GLUCURONOSYLTRANSFERASE; HUMANS; MALE; NETHERLANDS; POLYMORPHISM, GENETIC; PROMOTER REGIONS (GENETICS);

EID: 17744374081     PISSN: 02709139     EISSN: None     Source Type: Journal    
DOI: 10.1053/jhep.2001.0103303le03     Document Type: Letter

References (10)

1. Molecular diagnosis of a familial nonhemolytic hyperbilirubinemia (Gilbert's syndrome) in healthy subjects
2. Genetic variation in bilirubin UDP-glucuronosyltranferase gene promoter and Gilbert's syndrome
3. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyltransferase 1 in Gilbert's Syndrome
4. Die pravalenz des Gilbert-syndroms in Deutschland
5. Association of human liver bilirubin UDP-glucuronyltransferase activity with a polymorphism in the promotor region of the UGT1A1 gene
6. Effect of sex and sex steroid hormones on bilirubin conjugation and secretion
7. Contribution of the TATA-box genotype (Gilbert syndrome) to serum bilirubin concentrations in the Italian population
8. Gilbert syndrome accelerates development of neonatal jaundice
9. Racial variability in the UDP glucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
10. Hyperbilirubinaemia in heterozygous B-thalassaemia is related to coinherited Gilbert's syndrome