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Article

Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia

25 Feb 2010

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Share to Acute Myeloid Leukemia Research
Share to Epigenetics and DNA Methylation
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 20182461
DOI: 10.1038/leu.2010.20

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Related research

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Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemiaPMID 20182461Read ↗

Epigenetic regulation by ASXL1 in myeloid malignancies.Semantic proximity Read ↗

Mutations of polycomb-associated gene ASXL1 in myelodysplastic syndromes and chronic myelomonocytic leukaemia.Semantic proximity Read ↗

[Role of ASXL1 mutation in myeloid malignancies].Semantic proximity Read ↗

ASXL1/2 mutations and myeloid malignancies.Semantic proximity Read ↗

Mutations in ASXL1 are associated with poor prognosis across the spectrum of malignant myeloid diseases.Semantic proximity Read ↗

Frequent ASXL1 mutations in children and young adults with chronic myeloid leukemia.Semantic proximity Read ↗

Aberrant histone modifications induced by mutant ASXL1 in myeloid neoplasmsSemantic proximity Read ↗

ASXL1 mutations promote myeloid transformation through loss of PRC2-mediated gene repression.Semantic proximity Read ↗

Loss of Asxl1 leads to myelodysplastic syndrome-like disease in mice.Semantic proximity Read ↗

Deletion of Asxl1 results in myelodysplasia and severe developmental defects in vivo.Semantic proximity Read ↗

The role of ASXL1 in hematopoiesis and myeloid malignanciesSemantic proximity Read ↗

The role of ASXL1 mutations and ASXL1 CircRNAs in cancer.Semantic proximity Read ↗

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