Ratings
0
Nobody has rated this yet. Be the first!
Works
7
Mutations in the UQCC1-interacting protein, UQCC2, cause human complex III deficiency associated with perturbed cytochrome b protein expression
Complex fate of paralogs
Mosaic origin of the mitochondrial proteome
WeGET: predicting new genes for molecular systems by weighted co-expression.
SHOT: a web server for the construction of genome phylogenies
Mitochondrial proteome evolution and genetic disease.
BOLA1 is an aerobic protein that prevents mitochondrial morphology changes induced by glutathione depletion
