20 results on '"Fernandez-Vizarra, Erika"'
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2. Measurement of mitochondrial respiratory chain enzymatic activities in Drosophila melanogaster samples
3. CEDAR, an online resource for the reporting and exploration of complexome profiling data
4. NDUFS3 depletion permits complex I maturation and reveals TMEM126A/OPA7 as an assembly factor binding the ND4-module intermediate
5. A homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assembly
6. Bioenergetic consequences from xenotopic expression of a tunicate AOX in mouse mitochondria: Switch from RET and ROS to FET
7. Biogenesis of NDUFS3-Less Complex I Indicates TMEM126A/OPA7 as an Assembly Factor of the ND4-Module
8. TTC19 Plays a Husbandry Role on UQCRFS1 Turnover in the Biogenesis of Mitochondrial Respiratory Complex III
9. Bioenergetic consequences of xenotopic expression of Ciona intestinalis alternative oxidase (AOX) in the mouse
10. TTC19 Plays a Husbandry Role on UQCRFS1 Turnover in the Biogenesis of Mitochondrial Respiratory Complex III
11. Novel mutation in mitochondrial Elongation Factor EF-Tu associated to dysplastic leukoencephalopathy and defective mitochondrial DNA translation
12. MR-1S Interacts with PET100 and PET117 in Module-Based Assembly of Human Cytochrome c Oxidase
13. Exome sequencing coupled with mRNA analysis identifies NDUFAF6 as a Leigh gene
14. Mutations in NDUFB11, Encoding a Complex I Component of the Mitochondrial Respiratory Chain, Cause Microphthalmia with Linear Skin Defects Syndrome
15. Mutations in APOPT1, Encoding a Mitochondrial Protein, Cause Cavitating Leukoencephalopathy with Cytochrome c Oxidase Deficiency
16. Partial tandem duplication of mtDNA–tRNAPhe impairs mtDNA translation in late-onset mitochondrial myopathy
17. FASTKD2 Nonsense Mutation in an Infantile Mitochondrial Encephalomyopathy Associated with Cytochrome C Oxidase Deficiency
18. Severe Infantile Encephalomyopathy Caused by a Mutation in COX6B1, a Nucleus-Encoded Subunit of Cytochrome C Oxidase
19. Infantile Encephalopathy and Defective Mitochondrial DNA Translation in Patients with Mutations of Mitochondrial Elongation Factors EFG1 and EFTu
20. In vitro transcription termination activity of the Drosophila mitochondrial DNA-binding protein DmTTF
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