Dominant optic atrophy (DOA) is an inherited mitochondrial disease leading to specific
degeneration of retinal ganglion cells (RGCs), thus compromising transmission of visual …

Duchenne muscular dystrophy (DMD), myotonic dystrophy type 1 (DM1), and spinal
muscular atrophy (SMA) are the most prevalent neuromuscular disorders (NMDs) in children …

Hepatocellular carcinoma (HCC) is the most common primary malignancy of the liver and
the third-leading cause of cancer-related mortality. Currently, the global burden of …

Autosomal dominant optic atrophy (DOA) is the most common inherited optic neuropathy in
the United Kingdom. DOA has an insidious onset in early childhood, typically presenting …

The dynamic nature of mitochondria, which can fuse, divide and move throughout the cell,
allows these critical organelles to adapt their function in response to cellular demands, and …

Aim Myotonic dystrophy type 1 (DM1) is the second most common muscular dystrophy after
Duchenne and is the most prevalent muscular dystrophy in adults. DM1 patients that …

Autosomal dominant optic atrophy (DOA) is the most common inherited optic neuropathy,
characterized by the preferential loss of retinal ganglion cells (RGCs), resulting in optic …

Mitochondrial dysfunction contributes to cardiovascular disorders, especially post-infarction
cardiac injury, through incompletely characterized mechanisms. Among the latter, increasing …

Immune activation has been widely recognized to promote anti‐tumor effects in vivo.
However, in previous anti‐tumor studies of combined photo/immunotherapy, the tumor …

Mitochondria are dynamic and plastic, undergoing continuous fission and fusion and
rearrangement of their bioenergetic sub‐compartments called cristae. These fascinating …