Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage-Reference-Cited by-同舟云学术

Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage

Published:2005-10-13 Issue:23 Volume:14 Page:3565-3577
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Ferrer Isidre,Kapfhammer Josef P.,Hindelang Colette,Kemp Stephan,Troffer-Charlier Nathalie,Broccoli Vania,Callyzot Noëlle,Mooyer Petra,Selhorst Jacqueline,Vreken Peter,Wanders Ronald J.A.,Mandel Jean Louis,Pujol Aurora

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/14/23/3565/1489986/ddi384.pdf

Reference56 articles.

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2. Wanders, R.J. and Tager, J.M. (1998) Lipid metabolism in peroxisomes in relation to human disease. Mol. Aspects Med., 19, 69–154.

3. Subramani, S. (1998) Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement. Physiol. Rev., 78, 171–188.

4. Gould, S.J. and Valle, D. (2000) Peroxisome biogenesis disorders: genetics and cell biology. Trends Genet., 16, 340–345.

5. Citkowitz, E. and Holtzman, E. (1973) Peroxisomes in dorsal root ganglia. J. Histochem. Cytochem., 21, 34–41.

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