Latest papers

The soluble form of Bax regulates mitochondrial fusion via MFN2 homotypic complexes.

Antigenically dominant proteins within the human liver mitochondrial proteome identified by monoclonal antibodies.

Reduction of N(ω)-hydroxy-L-arginine by the mitochondrial amidoxime reducing component (mARC).

Neurodegeneration in mnd2 mutant mice is not prevented by parkin transgene.

Quantification and identification of mitochondrial proteins containing vicinal dithiols.

Functional annotation of heart enriched mitochondrial genes GBAS and CHCHD10 through guilt by association.

Identification of protein-protein and protein-ribosome interacting regions of the C-terminal tail of human mitochondrial inner membrane protein Oxa1L.

The transcriptional coregulators TIF2 and SRC-1 regulate energy homeostasis by modulating mitochondrial respiration in skeletal muscles.

Trichoplein/mitostatin regulates endoplasmic reticulum-mitochondria juxtaposition.

Why barcode? High-throughput multiplex sequencing of mitochondrial genomes for molecular systematics.

Loss of Nix in Pdx1-deficient mice prevents apoptotic and necrotic β cell death and diabetes.

Parallel loss of nuclear-encoded mitochondrial aminoacyl-tRNA synthetases and mtDNA-encoded tRNAs in Cnidaria.

Mitochondrial dysfunction in obesity.

Tissue-specific distribution of uncoupling proteins in normal rats and rats with high-fat-diet-induced obesity.

The complete mitochondrial genome of the yellow coaster, Acraea issoria (Lepidoptera: Nymphalidae: Heliconiinae: Acraeini): sequence, gene organization and a unique tRNA translocation event.

Subsarcolemmal and intermyofibrillar mitochondria proteome differences disclose functional specializations in skeletal muscle.

Mechanisms of non-apoptotic programmed cell death in diabetes and heart failure.

Mdm35p imports Ups proteins into the mitochondrial intermembrane space by functional complex formation.

Human ERAL1 is a mitochondrial RNA chaperone involved in the assembly of the 28S small mitochondrial ribosomal subunit.

The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations