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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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Bibliografske podrobnosti
izdano v:Proc Natl Acad Sci U S A
Principais autores: Reddy, M K, Usuda, N, Reddy, M N, Kuczmarski, E R, Rao, M S, Reddy, J K
Format: Artigo
Jezik:Inglês
Izdano: National Academy of Sciences 1987
Teme:
Online dostop: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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