PEX13-knockout mice model Zellweger syndrome

Samankaltaisia teoksia

• Mitochondrial Alterations Caused by Defective Peroxisomal Biogenesis in a Mouse Model for Zellweger Syndrome (PEX5 Knockout Mouse)
  Tekijä: Baumgart, Eveline, et al.
  Julkaistu: (2001)
• PEX13 deficiency in mouse brain as a model of Zellweger syndrome: abnormal cerebellum formation, reactive gliosis and oxidative stress
  Tekijä: Müller, C. Catharina, et al.
  Julkaistu: (2011)
• Pex13 Inactivation in the Mouse Disrupts Peroxisome Biogenesis and Leads to a Zellweger Syndrome Phenotype
  Tekijä: Maxwell, Megan, et al.
  Julkaistu: (2003)
• Drosophila Carrying Pex3 or Pex16 Mutations Are Models of Zellweger Syndrome That Reflect Its Symptoms Associated with the Absence of Peroxisomes
  Tekijä: Nakayama, Minoru, et al.
  Julkaistu: (2011)
• Zellweger syndrome; identification of mutations in PEX19 and PEX26 gene in Saudi families
  Tekijä: Abdulfatah M. Alayoubi, et al.
  Julkaistu: (2025-12-01)