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Ribosomal lesions promote oncogenic mutagenesis

Ribosomopathies are congenital disorders caused by mutations in ribosomal proteins (RP) or assembly factors and are characterized by cellular hypo-proliferation at an early stage. Paradoxically, many of these disorders have an elevated risk to progress to hyper-proliferative cancer at a later stage....

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Detalhes bibliográficos
Publicado no:Cancer Res
Main Authors: Sulima, Sergey O., Kampen, Kim R., Vereecke, Stijn, Pepe, Daniele, Fancello, Laura, Verbeeck, Jelle, Dinman, Jonathan D., De Keersmaecker, Kim
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7116100/
https://ncbi.nlm.nih.gov/pubmed/30482776
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1158/0008-5472.CAN-18-1987
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