Literature DB >> 10778488

[Peroxisomal disorders: classification and overview of biochemical abnormalities].

H W Moser1.   

Abstract

The peroxisomal disorders are subdivided into two major categories: those in which the organelle is not formed normally (disorders of peroxisome biogenesis), and those that are associated with defects of single peroxisomal proteins. The Zellweger cerebrohepatorenal syndrome is the prototype of the peroxisome biogenesis disorders. It has been shown to be due to defective import of proteins into the organelle. Ten distinct molecular defects can lead to the failure of import.

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Year:  1999        PMID: 10778488

Source DB:  PubMed          Journal:  Rev Neurol        ISSN: 0210-0010            Impact factor:   0.870


  3 in total

1.  Modulation of peroxisome proliferator-activated receptor-alpha activity by N-acetyl cysteine attenuates inhibition of oligodendrocyte development in lipopolysaccharide stimulated mixed glial cultures.

Authors:  Manjeet K Paintlia; Ajaib S Paintlia; Mushfiquddin Khan; Inderjit Singh; Avtar K Singh
Journal:  J Neurochem       Date:  2008-01-12       Impact factor: 5.372

2.  Lipopolysaccharide-induced peroxisomal dysfunction exacerbates cerebral white matter injury: attenuation by N-acetyl cysteine.

Authors:  Manjeet K Paintlia; Ajaib S Paintlia; Miguel A Contreras; Inderjit Singh; Avtar K Singh
Journal:  Exp Neurol       Date:  2007-12-23       Impact factor: 5.330

3.  Pex13 inactivation in the mouse disrupts peroxisome biogenesis and leads to a Zellweger syndrome phenotype.

Authors:  Megan Maxwell; Jonas Bjorkman; Tam Nguyen; Peter Sharp; John Finnie; Carol Paterson; Ian Tonks; Barbara C Paton; Graham F Kay; Denis I Crane
Journal:  Mol Cell Biol       Date:  2003-08       Impact factor: 4.272

  3 in total

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