Disruption of the Ugt1 Locus in Mice Resembles Human Crigler-Najjar Type I Disease-Reference-Cited by-同舟云学术

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Disruption of the Ugt1 Locus in Mice Resembles Human Crigler-Najjar Type I Disease

Published:2008-03 Issue:12 Volume:283 Page:7901-7911
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Nguyen Nghia,Bonzo Jessica A.,Chen Shujuan,Chouinard Sarah,Kelner Michael J.,Hardiman Gary,Bélanger Alain,Tukey Robert H.

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference71 articles.

1. Inherited disorders of bilirubin metabolism

2. Bilirubin UDP-glucuronosyltransferase 1 is the only relevant bilirubin glucuronidating isoform in man.

3. Genetic variation in bilirubin UDP-glucuronosyltransferase gene promoter and Gilbert's syndrome

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

5. Gilbert's disease and atazanavir: From phenotype to UDP-glucuronosyltransferase haplotype

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2. Triclosan administration to humanized UDP-glucuronosyltransferase 1 neonatal mice induces UGT1A1 through a dependence on PPARα and ATF4;Journal of Biological Chemistry;2024-06

3. Molecular events in brain bilirubin toxicity revisited;Pediatric Research;2024-02-20

4. La maladie de Crigler-Najjar : un nouveau succès pour la thérapie génique;médecine/sciences;2023-11

5. Bilirubin induces microglial NLRP3 inflammasome activation in vitro and in vivo;Molecular and Cellular Neuroscience;2023-06

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