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Article

Mutations of the HIPK2 gene in acute myeloid leukemia and myelodysplastic syndrome impair AML1- and p53-mediated transcription

28 May 2007

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

Identifiers

PMID: 17533375
DOI: 10.1038/sj.onc.1210523

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Related research

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Mutations of the HIPK2 gene in acute myeloid leukemia and myelodysplastic syndrome impair AML1- and p53-mediated transcriptionPMID 17533375Read ↗

Regulation of p53 activity by HIPK2: molecular mechanisms and therapeutical implications in human cancer cellsSemantic proximity Read ↗

HIPK2 deficiency causes chromosomal instability by cytokinesis failure and increases tumorigenicitySemantic proximity Read ↗

PRKCH regulates hematopoietic stem cell function and predicts poor prognosis in acute myeloid leukemia.Semantic proximity Read ↗

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Regulation of p21 by TWIST2 contributes to its tumor-suppressor function in human acute myeloid leukemiaSemantic proximity Read ↗

Posttranslational modifications regulate HIPK2, a driver of proliferative diseasesSemantic proximity Read ↗

Heterogeneous nuclear ribonucleoprotein K is overexpressed in acute myeloid leukemia and causes myeloproliferative disease in mice via altered <i>Runx1</i> splicingSemantic proximity Read ↗

Tumor Suppressor HIPK2 Regulates Malignant Growth via Phosphorylation of Notch1.Semantic proximity Read ↗

JARID2 Functions as a Tumor Suppressor in Myeloid Neoplasms by Repressing Self-Renewal in Hematopoietic Progenitor CellsSemantic proximity Read ↗

Splicing factor YBX1 mediates persistence of JAK2-mutated neoplasms.Semantic proximity Read ↗

Requirement for LIM kinases in acute myeloid leukemia.Semantic proximity Read ↗

Tribbles-1 and -2 are tumour suppressors, down-regulated in human acute myeloid leukaemiaSemantic proximity Read ↗

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