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Mutations in either gene impair this surveillance, allowing damaged mitochondria to persist and propagate oxidative stress ( 2.2 Mitochondrial dysfunction and oxidative stress Mitochondrial complex I deficiency is consistently observed in PD, leading to impaired ATP synthesis and overproduction of reactive oxygen species (ROS) ( Furthermore, LRRK2 mutationsparticularly G2019Sare linked to disrupted mitochondrial dynamics, altered kinase activity, and aberrant autophagy ( 2.3 Ferroptosis: iron-mediated cell death Ferroptosis is an emerging mechanism in PD, characterized by iron-dependent lipid peroxidation

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Proteomic analysis of mesenchymal stem-like cells derived from ovarian teratoma: potential role of glutathione S-transferase M2 in ovarian teratoma

Contribution of oral triamcinolone to treating proliferative and necrotising otitis externa in a 14-year-old Persian cat