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High-throughput sequencing screen reveals novel, transforming RAS mutations in myeloid leukemia patients

Transforming mutations in NRAS and KRAS are thought to play a causative role in the development of numerous cancers, including myeloid malignancies. Although mutations at amino acids 12, 13, or 61 account for the majority of oncogenic Ras variants, we hypothesized that less frequent mutations at alt...

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Detalhes bibliográficos
Main Authors: Tyner, Jeffrey W., Erickson, Heidi, Deininger, Michael W. N., Willis, Stephanie G., Eide, Christopher A., Levine, Ross L., Heinrich, Michael C., Gattermann, Norbert, Gilliland, D. Gary, Druker, Brian J., Loriaux, Marc M.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Hematology 2009
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2647674/
https://ncbi.nlm.nih.gov/pubmed/19075190
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2008-04-152157
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