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Opa1 Is Required for Proper Mitochondrial Metabolism in Early Development

Opa1 catalyzes fusion of inner mitochondrial membranes and formation of the cristae. OPA1 mutations in humans lead to autosomal dominant optic atrophy. OPA1 knockout mice lose viability around embryonic day 9 from unknown reasons, indicating that OPA1 is essential for embryonic development. Zebrafis...

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Detalles Bibliográficos
Autores principales: Rahn, Jennifer J., Stackley, Krista D., Chan, Sherine S. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3597633/
https://www.ncbi.nlm.nih.gov/pubmed/23516612
http://dx.doi.org/10.1371/journal.pone.0059218