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  1. Jul 2026
  2. www.nature.com www.nature.com
    Hypoxia rescues complex 1-associated disease caused by proteostatic defects
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    nature.com/articles/s42255-026-01566-0
  3. Jul 2025
  4. www.sciencedirect.com www.sciencedirect.com
    An updated inventory of genes essential for oxidative phosphorylation identifies a mitochondrial origin in familial Ménière’s disease
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    sciencedirect.com/science/article/pii/S221112472500840X
  5. Sep 2023
  6. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Mitochondrial defects caused by PARL deficiency lead to arrested spermatogenesis and ferroptosis
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    ncbi.nlm.nih.gov/pmc/articles/PMC10519710/
  7. Sep 2020
  8. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Skd3 (human ClpB) is a potent mitochondrial protein disaggregase that is inactivated by 3-methylglutaconic aciduria-linked mutations
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    ncbi.nlm.nih.gov/pmc/articles/PMC7343390/