Pages that link to "Q40914646"
Jump to navigation
Jump to search
The following pages link to Long-term analysis of differentiation in human myoblasts repopulated with mitochondria harboring mtDNA mutations. (Q40914646):
Displaying 8 items.
- M19 modulates skeletal muscle differentiation and insulin secretion in pancreatic β-cells through modulation of respiratory chain activity (Q24306087) (← links)
- Evidence for nuclear modifier gene in mitochondrial cardiomyopathy (Q37340280) (← links)
- RNA-mediated restoration of mitochondrial function in cells harboring a Kearns Sayre Syndrome mutation (Q39575848) (← links)
- The m.3243A>G mtDNA mutation is pathogenic in an in vitro model of the human blood brain barrier (Q39812451) (← links)
- Correction of translational defects in patient-derived mutant mitochondria by complex-mediated import of a cytoplasmic tRNA. (Q40477028) (← links)
- Vesicular transport of a ribonucleoprotein to mitochondria (Q42175742) (← links)
- Pathogenesis of the deafness-associated A1555G mitochondrial DNA mutation. (Q44020891) (← links)
- Mitochondria as a potential regulator of myogenesis. (Q55619121) (← links)