Relationship Between Bilirubin UDP-Glucuronosyl Transferase 1A1 Gene and Neonatal Hyperbilirubinemia-Reference-Cited by-同舟云学术

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Relationship Between Bilirubin UDP-Glucuronosyl Transferase 1A1 Gene and Neonatal Hyperbilirubinemia

Published:2002-10 Issue:4 Volume:52 Page:601-605
ISSN:0031-3998
Container-title:Pediatric Research
language:
Short-container-title:Pediatr Res

Author:

Huang Ching-Shan,Chang Pi-Feng,Huang May-Jen,Chen En-Sung,Hung Kun-Long,Tsou Kuo-Inn

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference28 articles.

1. Cloning of two human liver bilirubin UDP-glucuronosyltransferase cDNAs with expression in COS-1 cells.

2. Mechanisms of inherited deficiencies of multiple UDP‐glucuronosyltransferase isoforms in two patients with Crigler‐Najjar syndrome, type I

3. Identification of Defect in the Genes for Bilirubin UDP-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type II

4. The Genetic Basis of the Reduced Expression of Bilirubin UDP-Glucuronosyltransferase 1 in Gilbert's Syndrome

5. Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias

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1. Neonatal Hyperbilirubinemia and Kernicterus;Avery's Diseases of the Newborn;2024

2. UGT1A1 variants in Chinese Uighur and Han newborns and its correlation with neonatal hyperbilirubinemia;PLOS ONE;2022-12-15

3. Bilirubin metabolism and UDP ‐glucuronosyltransferase 1A1 variants in Asians: Pathogenic implications and therapeutic response;The Kaohsiung Journal of Medical Sciences;2022-08

4. Contribution of genetic factors to high rates of neonatal hyperbilirubinaemia on the Thailand-Myanmar border;PLOS Global Public Health;2022-06-17

5. Underestimation of the contribution of 211 G to A variation in UGT1A1 to neonatal hyperbilirubinemia in China;The Journal of Pediatrics;2022-06

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