Interrogating Mitochondrial Biology and Disease Using CRISPR/Cas9 Gene Editing

Mitochondrial disease originates from genetic changes that impact human bodily functions by disrupting the mitochondrial oxidative phosphorylation system. MitoCarta is a curated and published inventory that sheds light on the mitochondrial proteome, but the function of some mitochondrially-localised...

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Detalles Bibliográficos
Autores principales: Tang, Jia-Xin, Pyle, Angela, Taylor, Robert W., Oláhová, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536160/
https://www.ncbi.nlm.nih.gov/pubmed/34680998
http://dx.doi.org/10.3390/genes12101604

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536160/
https://www.ncbi.nlm.nih.gov/pubmed/34680998
http://dx.doi.org/10.3390/genes12101604

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