Last Updated: 09/26/2026
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Found 18 publications
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition).
Journal: Autophagy
Published: January 23, 2016
Activation of the Unfolded Protein Response in Sporadic Inclusion-Body Myositis but Not in Hereditary GNE Inclusion-Body Myopathy.
Journal: Journal of neuropathology and experimental neurology
Published: May 16, 2015
Update on neuromuscular diseases: Pathology and molecular pathogenesis.
Journal: Biochimica et biophysica acta
Published: January 14, 2015
Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy.
Journal: Biochimica et biophysica acta
Published: August 07, 2014
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.
Journal: Acta neuropathologica
Published: September 04, 2013
Sodium phenylbutyrate reverses lysosomal dysfunction and decreases amyloid-β42 in an in vitro-model of inclusion-body myositis.
Journal: Neurobiology of disease
Published: August 23, 2013
Luminescent conjugated oligothiophenes for sensitive fluorescent assignment of protein inclusion bodies.
Journal: Chembiochem : a European journal of chemical biology
Published: November 22, 2012
Chaperone-mediated autophagy components are upregulated in sporadic inclusion-body myositis muscle fibres.
Journal: Neuropathology and applied neurobiology
Published: October 23, 2012
Guidelines for the use and interpretation of assays for monitoring autophagy.
Journal: Autophagy
Published: September 12, 2012
Pathogenic considerations in sporadic inclusion-body myositis, a degenerative muscle disease associated with aging and abnormalities of myoproteostasis.
Journal: Journal of neuropathology and experimental neurology
Published: July 19, 2012
Activation of the γ-secretase complex and presence of γ-secretase-activating protein may contribute to Aβ42 production in sporadic inclusion-body myositis muscle fibers.
Journal: Neurobiology of disease
Published: February 09, 2012
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.
Journal: Presse medicale (Paris, France : 1983)
Published: October 29, 2010
Last Updated: 09/26/2026