Mitochondria possess their own DNA (mtDNA), which plays important roles in cellular respiration and energy consumption.

Researchers used mitochondrial gene editing to model genetic disorders in mice, revealing profound impacts on brain function, ...

Mitochondrial diseases are among the most prevalent hereditary metabolic disorders, known to occur in 1 out of every 5,000 ...

Animal models expressing loss-of-function mutations in mitochondrial DNA enable the investigation of mitochondrial gene function and related disorders. In a recent study, scientists from Korea ...

Explore the role of cell-free DNA biomarkers in differentiating Parkinson’s disease and multiple system atrophy (MSA).

Mitochondrial diseases are among the most prevalent hereditary metabolic disorders, known to occur in one out every 5000 births. Single nucleotide variations, indels, and structural variations are ...

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 ...

Mitochondrial disease can be inherited through mutations in DNA that specifically affect mitochondrial function. About 50 ...

Mitochondrial diseases are among the most prevalent hereditary metabolic disorders, known to occur in one out every 5000 ...

Mitophagy dynamics change with age, particularly during midlife, influencing brain health and aging. These findings offer ...