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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Pubblicato in:	Proc Natl Acad Sci U S A
Autori principali:	Reddy, M K, Usuda, N, Reddy, M N, Kuczmarski, E R, Rao, M S, Reddy, J K
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	National Academy of Sciences 1987
Soggetti:	Research Article
Accesso online:	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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