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May 14, 2024Frontiers in Cell and Developmental BiologyOpen Access

Mitochondrial defects in sporadic inclusion body myositis—causes and consequences

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Authors

EIElsie Chit Yu IuHSHo SoCCChi Bun Chan

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Cite This Study

Iu et al. (2024) studied this question.

synapsesocial.com/papers/68e6a3bcb6db643587627681https://doi.org/10.3389/fcell.2024.1403463
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Proteomics of rimmed vacuoles define new risk allele in inclusion body myositis2016 · 83 citations
  2. 2New Evidence of Premature Oxidative DNA Damage: Mitochondrial DNA Deletion in Gingival Tissue of Patients With Periodontitis2006 · 60 citations
  3. 3Mitochondrial DNA variants in inclusion body myositis characterized by deep sequencing2020 · 38 citations
  4. 4Influence of Inflammatory Cytokines IL-1β and IFNγ on Sarcoplasmic Aggregation of p62 and TDP-43 in Myotubes2023 · 4 citations
  5. 5Pathogenic Considerations in Sporadic Inclusion-Body Myositis, a Degenerative Muscle Disease Associated With Aging and Abnormalities of Myoproteostasis2012 · 74 citations