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51. Mutant ubiquitin UBB1is accumulated in sporadic inclusion-body myositis muscle fibers

56. Expression of muscle-gene-specific isozymes of phosphorylase and creatine kinase in innervated cultured human muscle.

57. X-linked Recessive Congenital Muscle Fiber Hypotrophy With Central Nuclei: Abnormalities of Growth and Adenylate Cyclase in Muscle Tissue Cultures

88. Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)

90. Activation of the Unfolded Protein Response in Sporadic Inclusion-Body Myositis but Not in Hereditary GNE Inclusion-Body Myopathy.

91. Sporadic inclusion-body myositis: A degenerative muscle disease associated with aging, impaired muscle protein homeostasis and abnormal mitophagy.

93. Sodium phenylbutyrate reverses lysosomal dysfunction and decreases amyloid-β42 in an in vitro-model of inclusion-body myositis.

94. 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.

95. Luminescent conjugated oligothiophenes for sensitive fluorescent assignment of protein inclusion bodies.

96. 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.

97. Pathogenic considerations in sporadic inclusion-body myositis, a degenerative muscle disease associated with aging and abnormalities of myoproteostasis.

98. Guidelines for the use and interpretation of assays for monitoring autophagy.

99. Abnormalities of NBR1, a novel autophagy-associated protein, in muscle fibers of sporadic inclusion-body myositis.

100. Novel demonstration of conformationally modified tau in sporadic inclusion-body myositis muscle fibers.

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