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The role of Cockayne Syndrome group B (CSB) protein in base excision repair and aging

Cockayne Syndrome (CS) is a rare human genetic disorder characterized by progressive multisystem degeneration and segmental premature aging. The CS complementation group B (CSB) protein is engaged in transcription coupled and global nucleotide excision repair, base excision repair and general transc...

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Bibliographic Details
Main Authors: Stevnsner, Tinna, Muftuoglu, Meltem, Aamann, Maria Diget, Bohr, Vilhelm A.
Format: Artigo
Language:Inglês
Published: 2008
Subjects:
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC2538557/
https://ncbi.nlm.nih.gov/pubmed/18541289
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mad.2008.04.009
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