Drosophila Carrying Pex3 or Pex16 Mutations Are Models of Zellweger Syndrome That Reflect Its Symptoms Associated with the Absence of Peroxisomes-Reference-Cited by-同舟云学术

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Drosophila Carrying Pex3 or Pex16 Mutations Are Models of Zellweger Syndrome That Reflect Its Symptoms Associated with the Absence of Peroxisomes

Published:2011-08-03 Issue:8 Volume:6 Page:e22984
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Nakayama Minoru,Sato Hiroyasu,Okuda Takayuki,Fujisawa Nao,Kono Nozomu,Arai Hiroyuki,Suzuki Emiko,Umeda Masato,Ishikawa Hiroyuki O.,Matsuno Kenji

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference57 articles.

1. Peroxisome biogenesis disorders.;SJ Steinberg;Biochim Biophys Acta,2006

2. Molecular and clinical aspects of peroxisomal diseases.;N Shimozawa;J Inherit Metab Dis,2007

3. Disorders of peroxisome biogenesis.;PW Lazarow,1994

4. Targeted deletion of the PEX2 peroxisome assembly gene in mice provides a model for Zellweger syndrome, a human neuronal migration disorder.;PL Faust;J Cell Biol,1997

5. A mouse model for Zellweger syndrome.;M Baes;Nat Genet,1997

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