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Ribosomal protein L11 mutation in zebrafish leads to haematopoietic and metabolic defects

Mutations in ribosomal proteins are associated with a congenital syndrome, Diamond–Blackfan anaemia (DBA), manifested by red blood cell aplasia, developmental abnormalities and increased risk of malignancy. Recent studies suggest the involvement of p53 activation in DBA. However, which pathways are...

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Bibliografiske detaljer
Main Authors: Danilova, Nadia, Sakamoto, Kathleen M., Lin, Shuo
Format: Artigo
Sprog:Inglês
Udgivet: 2010
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3457809/
https://ncbi.nlm.nih.gov/pubmed/21114664
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2141.2010.08396.x
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