RUNX1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes. - Wikidata - wikimedia - TriplyDB

RUNX1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes.

RUNX1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes.

http://www.wikidata.org/entity/Q38118553

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Aberrant nuclear factor-kappa B activity in acute myeloid leukemia: from molecular pathogenesis to therapeutic target High frequency of additional gene mutations in acute myeloid leukemia with MLL partial tandem duplication: DNMT3A mutation is associated with poor prognosis.Aberrant AML1 gene expression in the diagnosis of childhood leukemias not characterized by AML1-involved cytogenetic abnormalities.Dynamic Gene Regulatory Networks of Human Myeloid Differentiation.Clinical Relevance of RUNX1 and CBFB Alterations in Acute Myeloid Leukemia and Other Hematological Disorders.Histone Chaperone HIRA in Regulation of Transcription Factor RUNX1.Sensitivity of MLL-rearranged AML cells to all-trans retinoic acid is associated with the level of H3K4me2 in the RARα promoter region.Expression of RKIP in chronic myelogenous leukemia K562 cell and inhibits cell proliferation by regulating the ERK/MAPK pathway.Covalent Modifications of RUNX Proteins: Structure Affects Function.AML suppresses hematopoiesis by releasing exosomes that contain microRNAs targeting c-MYB.RUNX3 is a novel negative regulator of oncogenic TEAD-YAP complex in gastric cancer.Protein arginine methyltransferase 6 controls erythroid gene expression and differentiation of human CD34+ progenitor cells.RUNX1 contributes to higher-order chromatin organization and gene regulation in breast cancer cells.Modelling of a genetically diverse evolution of Systemic Mastocytosis with Chronic Myelomonocytic Leukemia (SM-CMML) by Next Generation Sequencing.Stabilization of NF-κB-Inducing Kinase Suppresses MLL-AF9-Induced Acute Myeloid Leukemia.Respecifying human iPSC-derived blood cells into highly engraftable hematopoietic stem and progenitor cells with a single factor.Heterogeneity of Abnormal RUNX1 Leading to Clinicopathologic Variations in Childhood B-Lymphoblastic Leukemia.

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RUNX1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes.

http://www.wikidata.org/entity/Q38118553

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RUNX1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes.

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RUNX1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes.

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RUNX1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes.

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RUNX1 meets MLL: epigenetic regulation of hematopoiesis by two leukemia genes.

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C E L Ng

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C P Koh

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C Q Wang

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G Huang

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M Araki

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M Osato

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V Tergaonkar

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Y Ito

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P2860

Activation of AML1-mediated transcription by MOZ and inhibition by the MOZ-CBP fusion protein

Leukemia proto-oncoprotein MLL forms a SET1-like histone methyltransferase complex with menin to regulate Hox gene expression

Physical association and coordinate function of the H3 K4 methyltransferase MLL1 and the H4 K16 acetyltransferase MOF

Genes on chromosomes 4, 9, and 19 involved in 11q23 abnormalities in acute leukemia share sequence homology and/or common motifs

Fusion between transcription factor CBF beta/PEBP2 beta and a myosin heavy chain in acute myeloid leukemia

Transcriptional repression by AML1 and LEF-1 is mediated by the TLE/Groucho corepressors

Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia

Structural basis for the requirement of additional factors for MLL1 SET domain activity and recognition of epigenetic marks

The 3;21 translocation in myelodysplasia results in a fusion transcript between the AML1 gene and the gene for EAP, a highly conserved protein associated with the Epstein-Barr virus small RNA EBER 1

The genetic basis of early T-cell precursor acute lymphoblastic leukaemia.

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1793-1802

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scholarly article

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10.1038/LEU.2013.200

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9

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27

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2013-07-02T00:00:00Z

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1051326917

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