Dysferlin is a newly identified binding partner of AβPP and it co-aggregates with amyloid-β42 within sporadic inclusion-body myositis (s-IBM) muscle fibers-Reference-Cited by-同舟云学术

Dysferlin is a newly identified binding partner of AβPP and it co-aggregates with amyloid-β42 within sporadic inclusion-body myositis (s-IBM) muscle fibers

Published:2013-10-04 Issue:5 Volume:126 Page:781-783
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Cacciottolo Mafalda,Nogalska Anna,D’Agostino Carla,Engel W. King,Askanas Valerie

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Neurology (clinical),Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-013-1186-6.pdf

Reference7 articles.

1. Askanas V, Engel WK, Nogalska A (2012) Pathogenic considerations in sporadic inclusion-body myositis, a degenerative muscle disease associated with aging and abnormalities of myoproteostasis. J Neuropathol Exp Neurol 71:680–693

2. Barthélémy F, Wein N, Krahn M, Lévy N, Bartoli M (2011) Translational research and therapeutic perspectives in dysferlinopathies. Mol Med 17:875–882

3. Cacciottolo M, Belcastro V, Laval S, Bushby K, Di Bernardo D, Nigro V (2011) Reverse engineering gene network identifies new dysferlin-interacting proteins. J Biol Chem 286:5404–5413

4. Dalakas MC (2011) Review: an update on inflammatory and autoimmune myopathies. Neuropathol Appl Neurobiol 37:226–242

5. Gallardo E, de Luna N, Diaz-Manera J et al (2011) Comparison of dysferlin expression in human skeletal muscle with that in monocytes for the diagnosis of dysferlin myopathy. PLoS ONE 6:e29061

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