MRC Mitochondrial Biology Unit
Mitochondrial complex I: An intricate energy-converting machine, a cornerstone of mitochondrial metabolism, and a locus of mitochondrial dysfunction and disease
Mitochondrial Genomics: Inherited and acquired variants of nuclear and mitochondrial DNA in human health and disease
Mitochondrial transport proteins: Highly dynamic integral membrane proteins required for the translocation of metabolites and cofactors, key to the function of the mitochondrion
Mitochondrial genetics: Mitochondrial genome engineering to unravel the genetic links between mitochondrial gene regulation and human disease for future therapies
Mitochondrial ROS production: Central to many pathologies and signalling processes and a key target for novel therapies
Mitochondrial phospholipids: Understanding the regulation and the biological importance of mitochondrial phospholipid composition
Mitochondrial cell biology: Mitochondrial dynamics and membrane contact sites as key regulators of cell fate decisions
Mitochondrial metabolism: Metabolic reprogramming and metabolite signalling as regulators of inflammatory disease
Mitochondria in development: Neural stem cell-niche interactions that protect the developing and aging brain against mitochondrial dysfunction
Mitochondrial ATP synthase: cellular power generator, determinant of mitochondrial cristae formation, a site linked to human diseases
Mitochondria in neurodegeneration: Investigating the role of mitochondria and metabolism in the cause and therapeutic targeting of neurodegenerative diseases