Glucose-6-phosphate dehydrogenase deficiency, the UDP-glucuronosyl transferase 1A1 gene, and neonatal hyperbilirubinemia

Gastroenterology

Volumn 123, Issue 1, 2002, Pages 127-133

  Huang, ChingShan ^a   Chang, PiFeng ^b   Huang, MayJen ^a   Chen, EnSung ^a   Chen, WuCharng ^b  

^a Departments of Laboratory Medicine   (United States)

^b Cathay General Hospital   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUCURONOSYLTRANSFERASE;

ARTICLE; BILIRUBIN BLOOD LEVEL; CAUCASIAN; CLINICAL ARTICLE; CONTROLLED STUDY; GENETIC VARIABILITY; GENOTYPE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN CELL; HYPERBILIRUBINEMIA; MALE; NEWBORN; NEWBORN JAUNDICE; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; RISK FACTOR; SEQUENCE ANALYSIS; TAIWAN;

EID: 0036305499     PISSN: 00165085     EISSN: None     Source Type: Journal    
DOI: 10.1053/gast.2002.34173     Document Type: Article

References (30)

1. Genetic defects of the UDP-glucuronosyltransferase 1 (UGT1) gene that cause familial non-hemolytic unconjugated hyperbilirubinaemia
2. Jaundice
3. Gastroenterology part 1. Neonatal jaundice
4. G6PD deficiency
5. Neonatal hyperbilirubinemia associated with glucose-6-phosphate dehydrogenase deficiency in Sephardic-Jewish infants: Incidence, severity and the effect of phototherapy
6. Neonatal hyperbilirubinemia and mutation of the bilirubin uridinediphosphate glucuronosyltransferase gene: A common missense mutation among Japanese, Koreans and Chinese
7. Gilbert’s syndrome accelerates development of neonatal jaundice
8. Association of neonatal hyperbilirubinemia with bilirubin UDP-glucuronosyltransferase polymorphism
9. Gilbert’s syndrome is a contributory factor in prolonged unconjugated hyperbilirubinemia of the newborn
10. Relationship between bilirubin UDP-glucuronosyl transferase1A1 gene and neonatal hyperbilirubinemia
11. The genetic basis of the reduced expression of bilirubin UDP-glucuronosyl transferase 1 in Gilbert’s syndrome
12. Molecular pathology of Crigler-Najjar type I and II and Gilbert’s syndromes
13. Gilbert’s syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
14. Hyperbilirubinemia, glucose-6-phosphate dehydrogenase deficiency and Gilbert’s syndrome
15. Gilbert’s syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates
16. The expression of uridine diphosphate glucuronosyl-transferase gene is a major determinant of bilirubin level in heterozygous β-thalassemia and glucose6-phosphate dehydrogenase deficiency
17. The interaction between Gilbert’s syndrome and G6PD deficiency influences bilirubin levels
18. Diverse point mutations result in glucose-6-phosphate dehydrogenase (G6PD) polymorphism in Taiwan
19. Association between glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice
20. Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Chinese infants with or without severe neonatal hyperbilirubinemia
21. Neonatal jaundice and molecular mutations in glucose-6-phosphate dehydrogenase deficient newborn infants
22. Two novel glucose-6-phosphate dehydrogenase deficiency mutations and association of such mutations with F8C/G6PD haplotype in Chinese
23. Free radical theory of erythrocyte aging
24. Association of glucose-6-phosphate dehydrogenase (G6PD) deficiency and F8C/G6PD hapoltypes in Taiwan
25. Variations of the bilirubin uridine-diphosphoglucuronosyl transferase 1A1 gene in healthy Taiwanese
26. A novel compound heterozygous variation of the uridine-diphosphoglucuronosyl transferase 1A1 gene that causes Crigler-Najjar syndrome type II
27. The clinical application of glucose-6-phosphate dehydrogenase quantitation test
28. Can severe neonatal jaundice be prevented by neonatal screening for glucose-6-phosphate dehydrogenase deficiency?-a review of evidence
29. Contribution of two missense mutations (G71R and Y486D) of the bilirubin UDP glycosyltransferase (UGT1A1) gene to phenotypes of Gilbert’s syndrome and Crigler-Najjar syndrome type II
30. G6PD Nankang (517T→C; 173 Phe→Leu): A new G6PD variant identified in a Chinese associated with neonatal jaundice