Export byl úspěšný — 

Molecular characterization of the human peroxisomal branchedchain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome

Peroxisomes in human liver contain two distinct acyl-CoA oxidases with different substrate specificities: (i) palmitoyl-CoA oxidase, oxidizing very long straight-chain fatty acids and eicosanoids, and (ii) a branched-chain acyl-CoA oxidase (hBRCACox), involved in the degradation of long branched fat...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Baumgart, Eveline, Vanhooren, Johannes C. T., Fransen, Mark, Marynen, Peter, Puype, Magda, Vandekerckhove, Joël, Leunissen, Jack A. M., Fahimi, H. Dariush, Mannaerts, Guy P., Van Veldhoven, Paul P.
Médium: Artigo
Jazyk:Inglês
Vydáno: The National Academy of Sciences of the USA 1996
Témata:
Biological Sciences
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC19413/
https://ncbi.nlm.nih.gov/pubmed/8943006
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!

Podobné jednotky