Peroxisomal disorders
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Pediatrics, Perinatology and Child Health
Reference54 articles.
1. Peroxisomal and mitochondrial defects in the cerebro-hepatorenal syndrome;Goldfischer;Science,1973
2. Microbodies: constituent organelles of animal cells;Hruban;Lab Invest,1972
3. Microperoxisomes in the central nervous system of the postnatal rat;Arnold;Brain Res,1978
4. Biogenesis of peroxisomes;Lazarow;Ann Rev Cell Biol,1985
5. Protein import into peroxisomes and biogenesis of the organelle;Subramani;Ann Rev Cell Biol,1993
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2. PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress;Disease Models & Mechanisms;2011-01-01
3. Modulation of peroxisome proliferator-activated receptor-α activity by N-acetyl cysteine attenuates inhibition of oligodendrocyte development in lipopolysaccharide stimulated mixed glial cultures;Journal of Neurochemistry;2008-05
4. Lipopolysaccharide-induced peroxisomal dysfunction exacerbates cerebral white matter injury: Attenuation by N-acetyl cysteine;Experimental Neurology;2008-04
5. First identification of a 2-ketoglutarate/isocitrate transport system in mammalian peroxisomes and its characterization;Biochemical and Biophysical Research Communications;2006-10
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