Biochemical Features of a Patient with Zellweger-like Syndrome with Normal PTS-1 and PTS-2 Peroxisomal Protein Import Systems: A New Peroxisomal Disease-Reference-Cited by-同舟云学术

Biochemical Features of a Patient with Zellweger-like Syndrome with Normal PTS-1 and PTS-2 Peroxisomal Protein Import Systems: A New Peroxisomal Disease

Published:1997-08 Issue:2 Volume:61 Page:198-207
ISSN:1077-3150
Container-title:Biochemical and Molecular Medicine
language:en
Short-container-title:Biochemical and Molecular Medicine

Author:

Singh Inderjit,Voigt Robert G.,Sheikh Faruk G.,Kremser Karl,Brown Frank R.

Publisher

Elsevier BV

Subject

Biochemistry

Reference31 articles.

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3. Pseudo infantile Refsum disease: Catalase-negative peroxisomal particles with partial plasmalogen synthesis and oxidation of fatty acids;Aubourg;Pediatr Res,1993

4. Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: Similarities in phenotype and accumulation of very long chain fatty acids;Brown;Johns Hopkins Med. J,1982

5. Synthesis of cerebronic acid from lignoceric acid by rat brain preparation. Some properties and distribution of the hydroxylation system;Hoshi;J Biol Chem,1973

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1. Peroxisomal Dysfunction in Inflammatory Childhood White Matter Disorders: An Unexpected Contributor to Neuropathology;Journal of Child Neurology;2009-07-15

2. Molecular organization of peroxisomal enzymes: Protein–protein interactions in the membrane and in the matrix;Archives of Biochemistry and Biophysics;2006-07

3. Inhibition of peroxisomal functions due to oxidative imbalance induced by mistargeting of catalase to cytoplasm is restored by vitamin E treatment in skin fibroblasts from Zellweger syndrome-like patients;Molecular Genetics and Metabolism;2004-12

4. Impaired peroxisomal function in the central nervous system with inflammatory disease of experimental autoimmune encephalomyelitis animals and protection by lovastatin treatment;Brain Research;2004-10

5. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003