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Mitochondrial permeability transition pore contributes to mitochondrial dysfunction in fibroblasts of patients with sporadic Alzheimer's disease.
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The role of mitochondrial dysfunction in psychiatric disease.
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Cyclosporine A prevents apoptosis-related mitochondrial dysfunction after neonatal cardioplegic arrest.
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Apoptosis-related mitochondrial dysfunction in the early postoperative neonatal lamb heart.
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KIF5A mutations cause an infantile onset phenotype including severe myoclonus with evidence of mitochondrial dysfunction.
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The hallmarks of mitochondrial dysfunction in chronic kidney disease.
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Impact of Age-Related Mitochondrial Dysfunction and Exercise on Intestinal Microbiota Composition.
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Mitochondrial dysfunction in human breast cancer cells and their transmitochondrial cybrids.
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VACTERL association and mitochondrial dysfunction.
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De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction.
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DNA double-strand breaks activate ATM independent of mitochondrial dysfunction in A549 cells.
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Mitochondrial dysfunction in human immunodeficiency virus-1 transgenic mouse cardiac myocytes.
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BMI1 Silencing Induces Mitochondrial Dysfunction in Lung Epithelial Cells Exposed to Hyperoxia.
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Cancer mutational burden is shaped by G4 DNA, replication stress and mitochondrial dysfunction.
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Increased superoxide in vivo accelerates age-associated muscle atrophy through mitochondrial dysfunction and neuromuscular junction degeneration.
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