Hereditary spastic paraplegia-causing mutations in atlastin-1 interfere with BMPRII trafficking

Author:

Zhao Jiali,Hedera Peter

Publisher

Elsevier BV

Subject

Cell Biology,Cellular and Molecular Neuroscience,Molecular Biology

Reference40 articles.

1. Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A;Abel;Neurogenetics,2004

2. Troyer syndrome protein spartin is mono-ubiquitinated and functions in EGF receptor trafficking;Bakowska;Mol. Biol. Cell,2007

3. The BMP signaling pathway at the Drosophila neuromuscular junction and its links to neurodegenerative diseases;Bayat;Curr. Opin. Neurobiol.,2010

4. Hereditary spastic paraplegias: membrane traffic and the motor pathway;Blackstone;Nat. Rev. Neurosci.,2011

5. The effect of HSP-causing mutations in SPG3A and NIPA1 on the assembly, trafficking, and interaction between atlastin-1 and NIPA1;Botzolakis;Mol. Cell. Neurosci.,2011

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