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Accumulation of (5′S)-8,5′-cyclo-2′-deoxyadenosine in organs of Cockayne syndrome complementation group B gene knockout mice

Cockayne syndrome (CS) is a human genetic disorder characterized by sensitivity to UV radiation, neurodegeneration, premature aging among other phenotypes. CS complementation group B (CS-B) gene (csb) encodes the CSB protein (CSB) that is involved in base excision repair of a number of oxidatively i...

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Autori principali: Kirkali, Güldal, de Souza-Pinto, Nadja C., Jaruga, Pawel, Bohr, Vilhelm A., Dizdaroglu, Miral
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2008
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2693312/
https://ncbi.nlm.nih.gov/pubmed/18992371
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.dnarep.2008.09.009
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