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Distinct Functional Domains of Nibrin Mediate Mre11 Binding, Focus Formation, and Nuclear Localization

The inherited chromosomal instability disorder Nijmegen breakage syndrome (NBS) results from truncating mutations in the NBS1 gene, which encodes the protein nibrin. Nibrin is part of a nuclear multiprotein complex that also contains the DNA repair proteins Mre11 and Rad50. Upon irradiation, this co...

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Detaylı Bibliyografya
Asıl Yazarlar: Desai-Mehta, Ami, Cerosaletti, Karen M., Concannon, Patrick
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society for Microbiology 2001
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC86852/
https://ncbi.nlm.nih.gov/pubmed/11238951
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1128/MCB.21.6.2184-2191.2001
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