Interest in the study of genetic variants of the promoter region of the UGT1A1 gene in neonatal jaundice;Interés del estudio de las variantes genéticas del promotor del gen UGT1A1 en la ictericia neonatal

Anales Espanoles de Pediatria

Volumn 56, Issue 2, 2002, Pages 139-143

  Seco, M L ^a   Del Rio E ^a   Barcelo M J ^a   Remacha, A ^a   Ginovart, G ^a   Moliner, E ^a   Baiget, M ^a  

^a HOSPITAL DE LA SANTA CREU I SANT PAU   (Spain)

Author keywords

Gilbert's syndrome; Neonatal jaundice; TA repeats; UGT1A1 gene

Indexed keywords

ARTICLE; DNA POLYMORPHISM; GENE; GENETIC SCREENING; GENETIC VARIABILITY; GILBERT DISEASE; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; NEWBORN; NEWBORN JAUNDICE; POLYMERASE CHAIN REACTION; PREVALENCE; PROMOTER REGION; TATA BOX; UGT1A1 GENE;

GILBERT DISEASE; GLUCURONOSYLTRANSFERASE; HUMANS; INFANT, NEWBORN; JAUNDICE, NEONATAL; POLYMORPHISM, GENETIC; PROMOTER REGIONS (GENETICS);

EID: 0036325238     PISSN: 03024342     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)

1. Heme and bile pigment metabolism
2. Bilirrubin metabolism and its disorders
3. The genetic basis of the reduced expression of bilirrubin UDP-glucuronosyltransferase 1 in Gilbert's syndrome
4. Analysis of genes for bilirubin UDP-glucuronosyltransferase in Gilbert's syndrome
5. Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome
6. Molecular pathology of Crigler-Najjar type I and II and Gilbert's syndromes
7. Neonatal jaundice
8. Distribución del genotipo A(TA)7TAA asociado al síndrome de Gilbert en la población española
9. Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
10. Bilirrubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome
11. Co-inherited Gilbert's syndrome: A factor determining hyperbilirrubinemia in homozygous beta-thalassemia
12. Coinheritence of Gilbert's syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis
13. Determinants of iron status and bilirrubin levels in congenital dyseritropoietic anaemia type I
14. UGT1 promoter plymorphism accounts for increased neonatal appearence of hereditary spherocytosis
15. Gilbert's syndrome and jaundice in glucosa-6-phosphate dehydrogenase deficient neonates
16. Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
17. Early discharge. In the end, it is judgement
18. Gilbert syndrome accelerates development of neonatal jaundice
19. Gilbert's syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn
20. Association of neonatal hyperbilirrubinemia with bilirrubin UDP-glucoronosyltransferase polymorphism