A microglial cell model for acyl-CoA oxidase 1 deficiency

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

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology

Reference64 articles.

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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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