Latest papers

Modification of radiation damage to mitochondrial system in vivo by Podophyllum hexandrum: mechanistic aspects.

coq7/clk-1 regulates mitochondrial respiration and the generation of reactive oxygen species via coenzyme Q.

Effect of some cardiac and respiratory drugs on succinate-cytochrome c reductase.

Increased heme oxygenase-1 expression during copper deficiency in rats results from increased mitochondrial generation of hydrogen peroxide.

The operation of the alternative electron-leak pathways mediated by cytochrome c in mitochondria.

99mTc-HMPAO distribution at SPECT is associated with succinate-cytochrome c reductase (SCR) activity in subjects with psychiatric disorders.

Cytochrome c oxidase is decreased in Alzheimer's disease platelets.

Effect of streptozotocin-induced diabetes on rat brain mitochondria.

Inhibition of brain energy metabolism by the alpha-keto acids accumulating in maple syrup urine disease.

Alpha-synuclein expression in HEK293 cells enhances the mitochondrial sensitivity to rotenone.

Heat shock pretreatment prevents cardiac mitochondrial dysfunction during sepsis.

The herbicide dicamba (2-methoxy-3,6-dichlorobenzoic acid) interacts with mitochondrial bioenergetic functions.

Cytochrome C is a hydrogen peroxide scavenger in mitochondria.

Coenzyme Q releases the inhibitory effect of free fatty acids on mitochondrial glycerophosphate dehydrogenase.

Blood mononuclear cell coenzyme Q10 concentration and mitochondrial respiratory chain succinate cytochrome-c reductase activity in phenylketonuric patients.

Insecticidal 2-hydroxy-3-alkyl-1,4-naphthoquinones: correlation of inhibition of ubiquinol cytochrome c oxidoreductase (complex III) with insecticidal activity.

Nitric oxide inhibits mitochondrial NADH:ubiquinone reductase activity through peroxynitrite formation.

Biomolecular and biochemical response of myocardial cell to ischemia and reperfusion in the course of heart surgery.

Inhibition of succinate-cytochrome C reductase by a ferromacrocyclic complex.

Navajo neurohepatopathy: A mitochondrial DNA depletion syndrome?