Author:
Raas Q.,Saih F.-E.,Gondcaille C.,Trompier D.,Hamon Y.,Leoni V.,Caccia C.,Nasser B.,Jadot M.,Ménétrier F.,Lizard G.,Cherkaoui-Malki M.,Andreoletti P.,Savary S.
Funder
Ministère de l'Education Nationale, de l'Enseignement Superieur et de la Recherche
Inserm
CNRS
Aix-Marseille University
French National Research Agency
Subject
Cell Biology,Molecular Biology
Reference64 articles.
1. The human peroxisome in health and disease: the story of an oddity becoming a vital organelle;Vamecq;Biochimie,2014
2. Biochemistry of mammalian peroxisomes revisited;Wanders;Annu. Rev. Biochem.,2006
3. Molecular characterization of the human peroxisomal branched-chain acyl-CoA oxidase: cDNA cloning, chromosomal assignment, tissue distribution, and evidence for the absence of the protein in Zellweger syndrome;Baumgart;Proc. Natl. Acad. Sci. U. S. A.,1996
4. A novel case of ACOX2 deficiency leads to recognition of a third human peroxisomal acyl-CoA oxidase;Ferdinandusse;Biochim. Biophys. Acta,2018
5. Presence of three acyl-CoA oxidases in rat liver peroxisomes. An inducible fatty acyl-CoA oxidase, a noninducible fatty acyl-CoA oxidase, and a noninducible trihydroxycoprostanoyl-CoA oxidase;Schepers;J. Biol. Chem.,1990
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