Showing 1- [6] of [7] Publications
Author: | Fernandez-Vizarra Erika E | |
Pubmed ID: | 17403714 | |
Journal: | Hum Mol Genet | |
Title: | Impaired complex III assembly associated with BCS1L gene mutations in isolated mitochondrial encephalopathy. | |
Application: | WB | |
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Species: | human |
Author: | Fernández-Vizarra Erika E | |
Pubmed ID: | 18620006 | |
Journal: | Biochim Biophys Acta | |
Title: | Assembly of the oxidative phosphorylation system in humans: what we have learned by studying its defects. | |
Application: | WB | |
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Species: | human |
Author: | Mineri Rossana R | |
Pubmed ID: | 19492094 | |
Journal: | PLoS One | |
Title: | How do human cells react to the absence of mitochondrial DNA? | |
Application: | WB | |
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Species: | human |
Author: | Morán María M | |
Pubmed ID: | 20518024 | |
Journal: | Hum Mutat | |
Title: | Cellular pathophysiological consequences of BCS1L mutations in mitochondrial complex III enzyme deficiency. | |
Application: | WB | |
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Species: | human |
Author: | Sánchez Ester E | |
Pubmed ID: | 23168492 | |
Journal: | Biochim Biophys Acta | |
Title: | LYRM7/MZM1L is a UQCRFS1 chaperone involved in the last steps of mitochondrial Complex III assembly in human cells. | |
Application: | WB | |
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Species: | human |
Author: | Sarah E Calvo | |
Pubmed ID: | 22277967 | |
Journal: | Sci Transl Med | |
Title: | Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing. | |
Application: | WB | |
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Species: | human |