Peroxisomes, lipid metabolism, and peroxisomal disorders-Reference-Cited by-同舟云学术

Peroxisomes, lipid metabolism, and peroxisomal disorders

Published:2004-09 Issue:1-2 Volume:83 Page:16-27
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Wanders R.J.A.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference56 articles.

1. Peroxisome biogenesis disorders: genetics and cell biology;Gould;Trends Genet.,2000

2. Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene;Shimozawa;Hum. Mutat.,2004

3. 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

4. Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome);Heymans;Nature,1983

5. Dihydroxyacetone phosphate acyltransferase and alkyldihydroxyacetone phosphate synthase activities in rat liver subcellular fractions and human skin fibroblasts;Singh;Arch. Biochem. Biophys.,1989

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