Title : Investigation of the molecular basis of the genetic deficiency of UDP-glucuronosyltransferase in Crigler-Najjar syndrome.

Pub. Date : 1991

PMID : 1749222






2 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 1-Naphthol UDPGT activity was normal in most patients, where membrane integrity was maintained by correct sample procurement and preparation. 1-naphthol UDP glucuronosyltransferase family 1 member A4 Homo sapiens
2 Analysis of four patient liver samples by immunoblot analysis revealed the heterogeneous nature of this inherited disease within the patient population, and one sample where 1-naphthol UDPGT activity was considerably reduced appeared to correlate with the non-detection of a phenol UDPGT protein. 1-naphthol UDP glucuronosyltransferase family 1 member A4 Homo sapiens