Myeloid neoplasms with isolated isochromosome 17q demonstrate a high frequency of mutations in SETBP1, SRSF2, ASXL1 and NRAS.
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Bone marrow pathologic abnormalities in familial platelet disorder with propensity for myeloid malignancy and germline RUNX1 mutation.Genetics and Epigenetics of Myelodysplastic Syndromes and Response to Drug Therapy: New Insights.An exploratory clinical trial of bortezomib in patients with lower risk myelodysplastic syndromes.TP53 mutation does not confer a poor outcome in adult patients with acute lymphoblastic leukemia who are treated with frontline hyper-CVAD-based regimens.SETBP1 mutations as a biomarker for myelodysplasia /myeloproliferative neoplasm overlap syndrome.Myeloid Neoplasms with Isolated Isochromosome 17q: a yet to be Defined Entity.Recurrent Cytogenetic Abnormalities in Myelodysplastic Syndromes.Bone marrow findings in blast phase of polycythemia vera.
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P2860
Myeloid neoplasms with isolated isochromosome 17q demonstrate a high frequency of mutations in SETBP1, SRSF2, ASXL1 and NRAS.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 12 February 2016
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Myeloid neoplasms with isolate ...... SETBP1, SRSF2, ASXL1 and NRAS.
@en
Myeloid neoplasms with isolate ...... SETBP1, SRSF2, ASXL1 and NRAS.
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type
label
Myeloid neoplasms with isolate ...... SETBP1, SRSF2, ASXL1 and NRAS.
@en
Myeloid neoplasms with isolate ...... SETBP1, SRSF2, ASXL1 and NRAS.
@nl
prefLabel
Myeloid neoplasms with isolate ...... SETBP1, SRSF2, ASXL1 and NRAS.
@en
Myeloid neoplasms with isolate ...... SETBP1, SRSF2, ASXL1 and NRAS.
@nl
P2093
P2860
P356
P1433
P1476
Myeloid neoplasms with isolate ...... SETBP1, SRSF2, ASXL1 and NRAS.
@en
P2093
Cameron C Yin
Carlos E Bueso-Ramos
Chong Zhao
Francesco Stingo
Keyur P Patel
Koichi Takahashi
L Jeffrey Medeiros
Mark J Routbort
Patricia Fox
P2860
P304
14251-14258
P356
10.18632/ONCOTARGET.7350
P407
P577
2016-02-12T00:00:00Z