Introduction to the mini-review series on mitochondrial matters in epilepsy
Mitochondrial dysfunction in neurological disorders with epileptic phenotypes
Mitochondrial dysfunction and oxidative stress: a contributing link to acquired epilepsy?
Mitochondrial matters of the brain: mitochondrial dysfunction and oxidative status in epilepsy
The potential role of mitochondrial dysfunction in seizure-associated cell death in the hippocampus and epileptogenesis
Mitochondria and neonatal epileptic encephalopathies with suppression burst
Functioning of the mitochondrial ATP-dependent potassium channel in rats varying in their resistance to hypoxia. Involvement of the channel in the process of animal’s adaptation to hypoxia
VDAC contributes to mRNA levels in Saccharomyces cerevisiae cells by the intracellular reduction/oxidation state dependent and independent mechanisms
Brain mitochondria from rats treated with sulforaphane are resistant to redox-regulated permeability transition
Dehydrosilybin attenuates the production of ROS in rat cardiomyocyte mitochondria with an uncoupler-like mechanism
Transmembrane topology of subunit N of complex I (NADH:ubiquinone oxidoreductase) from Escherichia coli
Characterization of two cytochrome b6 proteins from the cyanobacterium Gloeobacter violaceus PCC 7421