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Defective DNA Ligation during Short-Patch Single-Strand Break Repair in Ataxia Oculomotor Apraxia 1

Ataxia oculomotor apraxia 1 (AOA1) results from mutations in aprataxin, a component of DNA strand break repair that removes AMP from 5′ termini. Despite this, global rates of chromosomal strand break repair are normal in a variety of AOA1 and other aprataxin-defective cells. Here we show that short-...

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Detalhes bibliográficos
Main Authors: Reynolds, John J., El-Khamisy, Sherif F., Katyal, Sachin, Clements, Paula, McKinnon, Peter J., Caldecott, Keith W.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Microbiology (ASM) 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2643831/
https://ncbi.nlm.nih.gov/pubmed/19103743
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.01471-08
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