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Length-dependent degradation of single-stranded 3' ends by the Werner syndrome protein (WRN): implications for spatial orientation and coordinated 3' to 5' movement of its ATPase/helicase and exonuclease domains

BACKGROUND: The cancer-prone and accelerated aging disease Werner syndrome is caused by loss of function of the WRN gene product that possesses ATPase, 3' to 5' helicase and 3' to 5' exonuclease activities. Although WRN has been most prominently suggested to function in telomere...

Täydet tiedot

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Bibliografiset tiedot
Päätekijät: Machwe, Amrita, Xiao, Liren, Orren, David K
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2006
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1435914/
https://ncbi.nlm.nih.gov/pubmed/16503984
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2199-7-6
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