Cockayne syndrome group B protein has novel strand annealing and exchange activities

Cockayne syndrome (CS) is a rare inherited human genetic disorder characterized by UV sensitivity, severe neurological abnormalities and prageroid symptoms. The CS complementation group B (CSB) protein is involved in UV-induced transcription coupled repair (TCR), base excision repair and general tra...

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Detalles Bibliográficos
Autores principales: Muftuoglu, Meltem, Sharma, Sudha, Thorslund, Tina, Stevnsner, Tinna, Soerensen, Martin M., Brosh, Robert M., Bohr, Vilhelm A.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2006
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1331990/
https://www.ncbi.nlm.nih.gov/pubmed/16410611
http://dx.doi.org/10.1093/nar/gkj410

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1331990/
https://www.ncbi.nlm.nih.gov/pubmed/16410611
http://dx.doi.org/10.1093/nar/gkj410

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