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Peroxisomal Diseases

Keywords

Zellweger Syndrome Mitochondrial Respiratory Chain Complex Peroxisomal Disorder Peroxisomal Matrix Peroxisomal Membrane Protein 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Baumgart E, Vanhoorebeek I, Grabenbauer M, Borgers M, Declerq P, Fahimi HD, and Baes M (2001) Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (PEX5 knockout mouse). Am J Pathol 159: 1477PubMedGoogle Scholar
  2. Chang C, South S, Warren D, Jones J, and Moser A (1999) Metabolic control of peroxisome abundance. J Cell Sci 112: 1579PubMedGoogle Scholar
  3. Gould SJ, Raymond GV, and Valle D (2001) The peroxisome biogenesis disorders. In: The metabolic and molecular bases of inherited disease (Scriver C, Beaudet A, Valle D, Sly WS, Childs B, Kinzler K, and Vogelstein B, eds). New York: McGraw-Hill, pp 3181Google Scholar
  4. Wanders R, Barth P, and Heymans H (2001) Single peroxisomal enzyme deficiencies. In: The metabolic and molecular bases of inherited disease (Scriver C, Beaudet A, D. Valle D, Sly WS, Childs B, Kinzler K, and Vogelstein B, eds). New York: McGraw-Hill, pp 3219Google Scholar
  5. Wiemer E, Nuttley W, Bertolaet B, Li X, Franke U, Wheelock M, Anné U, Johnson K, and Subramani S (1995) Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders. J Cell Biol 130: 51 Peroxisome website: www.peroxisome.orgCrossRefPubMedGoogle Scholar

Copyright information

© Springer-Verlag/Wien 2005

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