9 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 29448836 | AAV8 Gene Therapy Rescues the Newborn Phenotype of a Mouse Model of Crigler-Najjar. | 2018 Jul | 3 |
2 | 28025333 | Modulation of bilirubin neurotoxicity by the Abcb1 transporter in the Ugt1-/- lethal mouse model of neonatal hyperbilirubinemia. | 2017 Jan 1 | 2 |
3 | 28805798 | Repeated AAV-mediated gene transfer by serotype switching enables long-lasting therapeutic levels of hUgt1a1 enzyme in a mouse model of Crigler-Najjar Syndrome Type I. | 2017 Oct | 1 |
4 | 29399656 | Severe Neonatal Hyperbilirubinemia in Crigler-Najjar Syndrome Model Mice Can Be Reversed With Zinc Protoporphyrin. | 2017 Oct | 1 |
5 | 25950469 | Impairment of enzymatic antioxidant defenses is associated with bilirubin-induced neuronal cell death in the cerebellum of Ugt1 KO mice. | 2015 May 7 | 2 |
6 | 23950218 | Importance of UDP-glucuronosyltransferase 1A1 expression in skin and its induction by UVB in neonatal hyperbilirubinemia. | 2013 Nov | 1 |
7 | 20194756 | Developmental hyperbilirubinemia and CNS toxicity in mice humanized with the UDP glucuronosyltransferase 1 (UGT1) locus. | 2010 Mar 16 | 3 |
8 | 18180294 | Disruption of the ugt1 locus in mice resembles human Crigler-Najjar type I disease. | 2008 Mar 21 | 2 |
9 | 12814968 | Nuclear receptor, pregname X receptor, is required for induction of UDP-glucuronosyltranferases in mouse liver by pregnenolone-16 alpha-carbonitrile. | 2003 Jul | 1 |