(FM) Hematología
Departamento académico
John Radcliffe Hospital
Oxford, Reino UnidoJohn Radcliffe Hospital-ko ikertzaileekin lankidetzan egindako argitalpenak (7)
2013
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Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression
British Journal of Haematology, Vol. 163, Núm. 2, pp. 235-239
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Silencing of ASXL1 impairs the granulomonocytic lineage potential of human CD34+ progenitor cells
British Journal of Haematology, Vol. 160, Núm. 6, pp. 842-850
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Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes
Haematologica, Vol. 98, Núm. 12, pp. 1856-1864
2012
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Mutation patterns of 16 genes in primary and secondary acute myeloid leukemia (AML) with normal cytogenetics
PLoS ONE, Vol. 7, Núm. 8
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TET2 mutations are associated with specific 5-methylcytosine and 5-hydroxymethylcytosine profiles in patients with chronic myelomonocytic leukemia
PLoS ONE, Vol. 7, Núm. 2