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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Proc Natl Acad Sci U S A
Päätekijät: Reddy, M K, Usuda, N, Reddy, M N, Kuczmarski, E R, Rao, M S, Reddy, J K
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: National Academy of Sciences 1987
Aiheet:
Research Article
Linkit: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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