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Site-specific non-covalent interaction of the biopolymer poly(ADP-ribose) with the Werner syndrome protein regulates protein functions

Werner syndrome is a premature aging disorder that is caused by defects in the Werner protein (WRN). WRN is a member of the RecQ helicase family and possesses helicase and exonuclease activities. It is involved in various aspects of DNA metabolism such as DNA repair, telomere maintenance, and replic...

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Autors principals: Popp, Oliver, Veith, Sebastian, Fahrer, Jörg, Bohr, Vilhelm A., Bürkle, Alexander, Mangerich, Aswin
Format: Artigo
Idioma:Inglês
Publicat: 2012
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3549037/
https://ncbi.nlm.nih.gov/pubmed/23082994
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/cb300363g
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