The 3-methylcholanthrene-inducible UDP-glucuronosyltransferase deficiency in the hyperbilirubinemic rat (Gunn rat) is caused by a −1 frameshift mutation
Open Access
- 1 December 1989
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 264 (35) , 21302-21307
- https://doi.org/10.1016/s0021-9258(19)30079-1
Abstract
No abstract availableThis publication has 43 references indexed in Scilit:
- Characterization of the common genetic defect in humans deficient in debrisoquine metabolismNature, 1988
- Genetic deficiency of bilirubin glucuronidation in rats and humansMolecular Aspects of Medicine, 1987
- The molecular basis of the inherited deficiency of androsterone UDP‐glucuronyltransferase in Wistar ratsFEBS Letters, 1987
- Isolation of multiple normal and functionally defective forms of uridine diphosphate-glucuronosyltransferase from inbred Gunn rats.Journal of Clinical Investigation, 1987
- A comparison of uridine diphosphate-glucuronosyltransferase and other drug metabolizing enzyme activities between two mutant strains of Wistar rats with a genetic deficiency in bilirubin or androsterone glucuronidation.Journal of Pharmacobio-Dynamics, 1987
- Congenital jaundice in rats due to the absence of hepatic bilirubin UDP‐glucuronyltransferase enzyme proteinFEBS Letters, 1985
- Isolation of stable mouse cell lines that express cell surface and secreted forms of the vesicular stomatitis virus glycoprotein.The Journal of cell biology, 1983
- Construction of influenza haemagglutinin genes that code for intracellular and secreted forms of the proteinNature, 1982
- Isolation of biologically active ribonucleic acid from sources enriched in ribonucleaseBiochemistry, 1979
- Reactivation of a pure defective UDP‐glucuronyltransferase from homozygous gunn rat liverFEBS Letters, 1978