Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders-Reference-Cited by-同舟云学术

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Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

Published:1997-12 Issue:4 Volume:17 Page:445-448
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Reuber Bernadette E.,Germain-Lee Emily,Collins Cynthia S.,Morrell James C.,Ameritunga Rohan,Moser Hugo W.,Valle David,Gould Stephen J.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng1297-445.pdf

Reference26 articles.

1. van den Bosch, H., Schutgens, R.B.H., Wanders, R.J.A. & Tager, J.M. Biochemistry of peroxisomes. Annu. Rev. Biochem. 61, 157–197 (1992).

2. Gould, S.J., Keller, G.A., Hosken, N., Wilkinson, J. & Subramani, S. A conserved tripeptide sorts proteins to peroxisomes. J. Cell Biol. 108, 1657–166 (1989).

3. Swinkels, B.W., Gould, S.J., Bodnar, A.G., Rachubinski, R.A. & Subramani, S. A novel, cleavable peroxisomal targeting signal at the ammo-terminus of the rat 3-ketoacyl-CoAthiolase. EMBO J. 10, 3255–3262 (1991).

4. Dyer, J.M., McNew, J.A. & Goodman, J.M. The sorting sequence of the peroxisomal integral membrane protein PMP47 is contained within a short hydrophilic loop. J. Cell Biol. 133, 269–280 (1996).

5. Lazarow, P.B. & Fujiki, Y. Biogenesis of peroxisomes. Annu. Rev. Cell. Biol. 1, 489–530 (1985).

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