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Can I read Human UDP‐glucuronosyl transferases: Chemical defence, jaundice and gene therapy on EtoBox?

Human UDP‐glucuronosyl transferases: Chemical defence, jaundice and gene therapy by Catherine H. Brierley; Brian Burchell is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

What is Human UDP‐glucuronosyl transferases: Chemical defence, jaundice and gene therapy about?

Human UDP-glucuronosyltransferases (UDPGTs) are a family of enzymes which detoxify many hundreds of compounds by their conjugation to glucuronic acid, rendering them both harmless and more water soluble, hence, excretable. The level of expression of each UDPGT isoform in the body is the result of interplay between temporal, tissue-specific and environmental regulators. This complexity contributes to the difficulty in predicting the metabolic fate of compounds. Genetic defects and polymorphisms affecting individual isoform activities have deleterious and potentially lethal effects, as exemplified by the severe hyperbilirubinaemia observed in Crigler-Najjar Syndrome. Such severe genetic defects in bilirubin glucuronidation are obvious candidates for antenatal screening and gene therapy.

Who reads Human UDP‐glucuronosyl transferases: Chemical defence, jaundice and gene therapy?

It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.

Author
Catherine H. Brierley; Brian Burchell
Publisher
John Wiley and Sons; Wiley (John Wiley & Sons); John Wiley & Sons Inc.; Wiley (ISSN 0265-9247)
Published
1993
Language
EN
Field
Biochemistry, Genetics and Molecular Biology (Life Sciences)

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