Purification, properties, and immunocytochemical localization of human liver peroxisomal enoyl-CoA hydratase/3-hydroxyacyl-CoA dehydrogenase.

A molecular understanding of genetic disease in which peroxisomal functions are impaired depends on analysis of the structure of normal and mutant enzymes of peroxisomes. We report experiments describing the isolation, characterization, and immunocytochemical localization of enoyl-CoA hydratase/3-hy...

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Vydáno v:Proc Natl Acad Sci U S A
Hlavní autoři: Reddy, M K, Usuda, N, Reddy, M N, Kuczmarski, E R, Rao, M S, Reddy, J K
Médium: Artigo
Jazyk:Inglês
Vydáno: National Academy of Sciences 1987
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Research Article
On-line přístup:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC304839/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3106963/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.84.10.3214
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