Genetic and molecular bases of peroxisome biogenesis disorders

This publication has 52 references indexed in Scilit:

• Peroxisomal protein targeting and identification of peroxisomal targeting signals in cholesterol biosynthetic enzymes
  Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids, 2000
• Lipid metabolism in peroxisomes: enzymology, functions and dysfunctions of the fatty acid α- and β-oxidation systems in humans
  Biochemical Society Transactions, 2000
• Variable peroxisomal and mitochondrial targeting of alanine: Glyoxylate aminotransferase in mammalian evolution and disease
  BioEssays, 1997
• Severe deficiency of docosahexaenoic acid in peroxisomal disorders
  Neurology, 1990
• Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome)
  Nature, 1983
• Infantile phytanic acid storage disease, a possible variant of Refsum's disease: Three cases, including ultrastructural studies of the liver
  Journal of Inherited Metabolic Disease, 1982
• Adrenoleukodystrophy
  Acta Neuropathologica, 1978
• A fatty acyl-CoA oxidizing system in rat liver peroxisomes; enhancement by clofibrate, a hypolipidemic drug.
  Proceedings of the National Academy of Sciences, 1976
• Peroxisomal and Mitochondrial Defects in the Cerebro-Hepato-Renal Syndrome
  Science, 1973
• Peroxisomes (microbodies and related particles).
  Physiological Reviews, 1966