Pregnane-x-receptor controls hepatic glucuronidation during pregnancy and neonatal development in humanized UGT1 mice

Developmental hyperbilirubinemia and CNS toxicity in mice humanized with the UDP glucuronosyltransferase 1 (UGT1) locus

(2010) R. Fujiwara et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Evolution of transcriptional control in mammals

(2009) Michael D Wilson et al.   CURRENT OPINION IN GENETICS & DEVELOPMENT

Up-Regulation of UDP-Glucuronosyltransferase (UGT) 1A4 by 17 -Estradiol: A Potential Mechanism of Increased Lamotrigine Elimination in Pregnancy

(2009) H. Chen et al.   DRUG METABOLISM AND DISPOSITION

Biological risks for neurological abnormalities associated with hyperbilirubinemia

(2009) D Brites et al.   Journal of Perinatology

Homozygous variant ofUGT1A1gene mutation and severe neonatal hyperbilirubinemia

(2009) Nem-Yun Boo et al.   PEDIATRICS INTERNATIONAL

Exploring the genetic architecture of neonatal hyperbilirubinemia

(2009) Jon F. Watchko et al.   Seminars in Fetal & Neonatal Medicine

Disruption of theUgt1Locus in Mice Resembles Human Crigler-Najjar Type I Disease

(2008) Nghia Nguyen et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Preferential Physical and Functional Interaction of Pregnane X Receptor with the SMRT  Isoform

(2008) C.-W. Li et al.   MOLECULAR PHARMACOLOGY

Species-Specific Transcription in Mice Carrying Human Chromosome 21

(2008) M. D. Wilson et al.   SCIENCE

Regulation of UDP-glucuronosyltransferase (UGT) 1A1 by progesterone and its impact on labetalol elimination

(2007) H. Jeong et al.   XENOBIOTICA