Molecular basis of Diamond–Blackfan anemia: structure and function analysis of RPS19

Diamond–Blackfan anemia (DBA) is a rare congenital disease linked to mutations in the ribosomal protein genes rps19, rps24 and rps17. It belongs to the emerging class of ribosomal disorders. To understand the impact of DBA mutations on RPS19 function, we have solved the crystal structure of RPS19 fr...

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Detaylı Bibliyografya
Asıl Yazarlar: Gregory, Lynn A., Aguissa-Touré, Almass-Houd, Pinaud, Noël, Legrand, Pierre, Gleizes, Pierre-Emmanuel, Fribourg, Sébastien
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2007
Konular:
Structural Biology
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2034476/
https://ncbi.nlm.nih.gov/pubmed/17726054
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkm626
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