Cargando…
Ultrasensitive deletion detection links mitochondrial DNA replication, disease, and aging
BACKGROUND: Acquired human mitochondrial genome (mtDNA) deletions are symptoms and drivers of focal mitochondrial respiratory deficiency, a pathological hallmark of aging and late-onset mitochondrial disease. RESULTS: To decipher connections between these processes, we create LostArc, an ultrasensit...
Autores principales: | Lujan, Scott A., Longley, Matthew J., Humble, Margaret H., Lavender, Christopher A., Burkholder, Adam, Blakely, Emma L., Alston, Charlotte L., Gorman, Grainne S., Turnbull, Doug M., McFarland, Robert, Taylor, Robert W., Kunkel, Thomas A., Copeland, William C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7500033/ https://www.ncbi.nlm.nih.gov/pubmed/32943091 http://dx.doi.org/10.1186/s13059-020-02138-5 |
Ejemplares similares
-
Disease progression in patients with single, large-scale mitochondrial DNA deletions
por: Grady, John P., et al.
Publicado: (2014) -
Pathological mechanisms underlying single large‐scale mitochondrial DNA deletions
por: Rocha, Mariana C., et al.
Publicado: (2018) -
Scientific and Ethical Issues in Mitochondrial Donation
por: Craven, Lyndsey, et al.
Publicado: (2018) -
Natural History of Leigh Syndrome: A Study of Disease Burden and Progression
por: Lim, Albert Z., et al.
Publicado: (2021) -
Mitochondrial DNA deletions in muscle satellite cells: implications for therapies
por: Spendiff, Sally, et al.
Publicado: (2013)