Literature DB >> 3306240

Genetic deficiency of bilirubin glucuronidation in rats and humans.

B Burchell, M W Coughtrie, M R Jackson, S R Shepherd, D Harding, R Hume.   

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Year:  1987        PMID： 3306240     DOI： 10.1016/0098-2997(87)90007-0

Source DB:  PubMed          Journal:  Mol Aspects Med        ISSN： 0098-2997


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  4 in total

1.  Immunochemical analysis of uridine diphosphate-glucuronosyltransferase in four patients with the Crigler-Najjar syndrome type I.

Authors:  H H van Es; B G Goldhoorn; M Paul-Abrahamse; R P Elferink; P L Jansen
Journal:  J Clin Invest       Date:  1990-04       Impact factor: 14.808

2.  Cloning and substrate specificity of a human phenol UDP-glucuronosyltransferase expressed in COS-7 cells.

Authors:  D Harding; S Fournel-Gigleux; M R Jackson; B Burchell
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

Review 3.  Investigation of the molecular basis of the genetic deficiency of UDP-glucuronosyltransferase in Crigler-Najjar syndrome.

Authors:  K J Robertson; D Clarke; L Sutherland; R Wooster; M W Coughtrie; B Burchell
Journal:  J Inherit Metab Dis       Date:  1991       Impact factor: 4.982

Review 4.  Genetic and environmental factors associated with variation of human xenobiotic glucuronidation and sulfation.

Authors:  B Burchell; M W Coughtrie
Journal:  Environ Health Perspect       Date:  1997-06       Impact factor: 9.031
  4 in total

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