Načítá se...

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...

Celý popis

Uloženo v:
Podrobná bibliografie
Hlavní autoři: Gregory, Lynn A., Aguissa-Touré, Almass-Houd, Pinaud, Noël, Legrand, Pierre, Gleizes, Pierre-Emmanuel, Fribourg, Sébastien
Médium: Artigo
Jazyk:Inglês
Vydáno: Oxford University Press 2007
Témata:
On-line přístup: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
Tagy: Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!