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

Lignende værker

• Molecular cloning and further characterization of rat peroxisomal trihydroxycoprostanoyl-CoA oxidase.
  af: Baumgart, E, et al.
  Udgivet: (1996)
• Evidence that peroxisomal acyl-CoA synthetase is located at the cytoplasmic side of the peroxisomal membrane.
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• Mitochondrial Alterations Caused by Defective Peroxisomal Biogenesis in a Mouse Model for Zellweger Syndrome (PEX5 Knockout Mouse)
  af: Baumgart, Eveline, et al.
  Udgivet: (2001)
• Purification and further characterization of peroxisomal trihydroxycoprostanoyl-CoA oxidase from rat liver.
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  Udgivet: (1994)
• Evidence for the existence of a pristanoyl-CoA oxidase gene in man.
  af: Vanhooren, J C, et al.
  Udgivet: (1997)