Pathogenesis of Sporadic Inclusion-Body Myositis: Role of Aging and Muscle-Fiber Degeneration, and Accumulation of the Same Proteins as in Alzheimer and Parkinson Brains
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Wiley-Blackwell
Reference260 articles.
1. Inclusion-body myositis: muscle-fiber molecular pathology and possible pathogenic significance of its similarity to Alzheimer's and Parkinson's disease brains;Askanas;Acta Neuropathol,2008
2. Inclusion body myositis: a degenerative muscle disease associated with intra-muscle fiber multi-protein aggregates, proteasome inhibition, endoplasmic reticulum stress and decreased lysosomal degradation;Askanas;Brain Pathol,2009
3. Inclusion-body myositis, a multifactorial muscle disease associated with aging: current concepts of pathogenesis;Askanas;Curr Opin Rheumatol,2007
4. Inclusion-body myositis: a myodegenerative conformational disorder associated with Abeta, protein misfolding, and proteasome inhibition;Askanas;Neurology,2006
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Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Sporadic inclusion-body myositis: Conformational multifactorial ageing-related degenerative muscle disease associated with proteasomal and lysosomal inhibition, endoplasmic reticulum stress, and accumulation of amyloid-β42 oligomers and phosphorylated tau;La Presse Médicale;2011-04
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