A team led by the UAB Institut de Neurociències (INc-UAB) has for the first time identified the mechanism behind a ...

A team led by the UAB Institut de Neurociències (INc-UAB) has for the first time identified the mechanism behind a potentially fatal type of epilepsy, a symptom of mitochondrial diseases.

Mitochondria are incredible organelles. They not only provide crucial power to our cells, these little machines also have ...

New research reveals that NAD+ supplements may slow aging and boost cellular health, but experts urge caution and more ...

More than half of people with mitochondrial disease can be diagnosed via genomic sequencing, a finding that will revolutionise care for families, according to a new study. And the Melbourne ...

A groundbreaking investigation from the Technical University of Munich has uncovered a crucial link between mitochondrial dysfunction and Crohn’s disease. This revelation could transform the ...

A study published in Science reveals a cellular mechanism involved in the inheritance of genetic mutations. The study also ...

Mitochondrial DNA depletion syndrome (MTDPS) is a rare genetic disorder characterized by a marked decrease in mitochondrial DNA (mtDNA). This condition can cause symptoms including muscle weakness, ...

Prince Frederik of Luxembourg died from a genetic disease called PolG, but experts hope his passing could bring more awareness to the rare condition that impacted his life. Prince Frederik, 22, died ...

Andrew Joseph covers health, medicine, and the biopharma industry in Europe. You can reach Andrew on Signal at drewqjoseph.45. Megan Molteni reports on discoveries from the frontiers of genomic ...

Researchers from the Mitochondrial Medicine Program at Children's Hospital of Philadelphia (CHOP) have better characterized a spectrum of what were classically considered discrete mitochondrial DNA ...