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Myeloid neoplasms with isolated isochromosome 17q demonstrate a high frequency of mutations in SETBP1, SRSF2, ASXL1 and NRAS

Isolated isochromosome 17q, i(17q), accounts for less than 1% of myeloid neoplasms that are commonly classified as myelodysplastic/myeloproliferative neoplasms, acute myeloid leukemia (AML), myelodysplastic syndrome (MDS) or myeloproliferative neoplasms (MPN). We have shown previously that these cas...

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Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Oncotarget
Prif Awduron: Kanagal-Shamanna, Rashmi, Luthra, Rajyalakshmi, Yin, Cameron C., Patel, Keyur P., Takahashi, Koichi, Lu, Xinyan, Lee, John, Zhao, Chong, Stingo, Francesco, Zuo, Zhuang, Routbort, Mark J., Singh, Rajesh R., Fox, Patricia, Ravandi, Farhad, Garcia-Manero, Guillermo, Medeiros, L. Jeffrey, Bueso-Ramos, Carlos E.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Impact Journals LLC 2016
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC4924712/
https://ncbi.nlm.nih.gov/pubmed/26883102
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.7350
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