Mouse Models with Peroxisome Biogenesis Defects
Author:
Publisher
Springer Vienna
Link
http://link.springer.com/content/pdf/10.1007/978-3-7091-1788-0_2
Reference60 articles.
1. Ahlemeyer B, Gottwald M, Baumgart-Vogt E (2012) Deletion of a single allele of the Pex11β gene is sufficient to cause oxidative stress, delayed differentiation and neuronal death in mouse brain. Dis Model Mech 5:125–140
2. Baes M, Gressens P, Baumgart E et al (1997) A mouse model for Zellweger syndrome. Nat Genet 17:49–57
3. Baes M, Dewerchin M, Janssen A, Collen D, Carmeliet P (2002) Generation of Pex5-IoxP mice allowing the conditional elimination of peroxisomes. Genesis 32:177–178
4. Baumgart E, Vanhorebeek I, Grabenbauer M et al (2001) Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (PEX5 knockout mouse). Am J Pathol 159:1477–1494
5. Bjorkman J, Tonks I, Maxwell MA, Paterson C, Kay GF, Crane DI (2002) Conditional inactivation of the peroxisome biogenesis Pex13 gene by Cre-IoxP excision. Genesis 32:179–180
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