Human Cockayne syndrome B protein reciprocally communicates with mitochondrial proteins and promotes transcriptional elongation

Cockayne syndrome (CS) is a rare human disorder characterized by pathologies of premature aging, neurological abnormalities, sensorineural hearing loss and cachectic dwarfism. With recent data identifying CS proteins as physical components of mitochondria, we sought to identify protein partners and...

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Detalles Bibliográficos
Autores principales: Berquist, Brian R., Canugovi, Chandrika, Sykora, Peter, Wilson, David M., Bohr, Vilhelm A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Genome Integrity, Repair and Replication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458532/
https://www.ncbi.nlm.nih.gov/pubmed/22743267
http://dx.doi.org/10.1093/nar/gks565

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458532/
https://www.ncbi.nlm.nih.gov/pubmed/22743267
http://dx.doi.org/10.1093/nar/gks565

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