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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Publicado en:	Proc Natl Acad Sci U S A
Autores principales:	Reddy, M K, Usuda, N, Reddy, M N, Kuczmarski, E R, Rao, M S, Reddy, J K
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	National Academy of Sciences 1987
Materias:	Research Article
Acceso en línea:	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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