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Mitochondrial heteroplasmy disrupts osteoclast differentiation and bone resorption by impairing respiratory complex I

2025-05-02

Abstract excerpt

Mitochondrial heteroplasmy, the co-existence of different mitochondrial genomes within a cell, is linked to aging and disease. Patients with heteroplasmy due to mitochondrial mutations experience multiple organ complications, particularly poor bone health and bone structure defects. However, the mechanisms involved are generally unknown, due largely to the difficulty of manipulating mtDNA in vivo. To overcome this...

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Literature Corpus work
d2a61042-d02c-5f61-ab09-1f22f8d24476
DOI
10.1101/2025.05.02.651799
Open publication

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Mitochondrial heteroplasmy disrupts osteoclast differentiation and bone resorption by impairing respiratory complex IDOI 10.1101/2025.05.02.651799
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