HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
about
Functional cloning and characterization of a novel nonhomeodomain protein that inhibits the binding of PBX1-HOX complexes to DNAHOXA9 methylation by PRMT5 is essential for endothelial cell expression of leukocyte adhesion moleculesRegulation of EphA8 gene expression by TALE homeobox transcription factors during development of the mesencephalonHomeodomain protein DLX4 counteracts key transcriptional control mechanisms of the TGF-β cytostatic program and blocks the antiproliferative effect of TGF-βCharacterization of PREP2, a paralog of PREP1, which defines a novel sub-family of the MEINOX TALE homeodomain transcription factorsTranscriptional repression of peri-implantation EMX2 expression in mammalian reproduction by HOXA10The HOX homeodomain proteins block CBP histone acetyltransferase activityPBX and MEIS as non-DNA-binding partners in trimeric complexes with HOX proteinsHoxa9 and Meis1 are key targets for MLL-ENL-mediated cellular immortalizationDifferential and common leukemogenic potentials of multiple NUP98-Hox fusion proteins alone or with Meis1HOXA9 regulates miR-155 in hematopoietic cellsA genomic approach to the identification and characterization of HOXA13 functional binding elementsGenome-wide analysis of histidine repeats reveals their role in the localization of human proteins to the nuclear speckles compartmentRole of HOXA9 in leukemia: dysregulation, cofactors and essential targetsTyrosine phosphorylation of HoxA10 decreases DNA binding and transcriptional repression during interferon gamma -induced differentiation of myeloid leukemia cell linesTALE homeoproteins as HOX11-interacting partners in T-cell leukemiaB-cell development in the presence of the MLL/AF4 oncoprotein proceeds in the absence of HOX A7 and HOX A9 expressionHigh levels of the adhesion molecule CD44 on leukemic cells generate acute myeloid leukemia relapse after withdrawal of the initial transforming eventHematopoietic, angiogenic and eye defects in Meis1 mutant animals.Changes in HOXB6 homeodomain protein structure and localization during human epidermal development and differentiationp21 is a transcriptional target of HOXA10 in differentiating myelomonocytic cells.An Abd-B class HOX.PBX recognition sequence is required for expression from the mouse Ren-1c gene.Homeotic proteins participate in the function of human-DNA replication origins.Epigenetic stress responses induce muscle stem-cell ageing by Hoxa9 developmental signals.The pancreatic and duodenal homeobox protein PDX-1 regulates the ductal specific keratin 19 through the degradation of MEIS1 and DNA bindingNUP98-HOXD13 transgenic mice develop a highly penetrant, severe myelodysplastic syndrome that progresses to acute leukemia.Meis1a suppresses differentiation by G-CSF and promotes proliferation by SCF: potential mechanisms of cooperativity with Hoxa9 in myeloid leukemia.Regulation of CCL2 expression by an upstream TALE homeodomain protein-binding site that synergizes with the site created by the A-2578G SNP.Hoxa9 immortalizes a granulocyte-macrophage colony-stimulating factor-dependent promyelocyte capable of biphenotypic differentiation to neutrophils or macrophages, independent of enforced meis expression.Defining roles for HOX and MEIS1 genes in induction of acute myeloid leukemiaMolecular biology of leukemia.NUP98-HOXA9 expression in hemopoietic stem cells induces chronic and acute myeloid leukemias in mice.Hox genes and their candidate downstream targets in the developing central nervous system.Identification of homeodomain proteins, PBX1 and PREP1, involved in the transcription of murine leukemia virus.TGFbeta/BMP inhibits the bone marrow transformation capability of Hoxa9 by repressing its DNA-binding ability.Cdx4 dysregulates Hox gene expression and generates acute myeloid leukemia alone and in cooperation with Meis1a in a murine model.Antagonism versus cooperativity with TALE cofactors at the base of the functional diversification of Hox protein functionHOX and non-HOX homeobox genes in leukemic hematopoiesis.Down-regulation of homeobox genes MEIS1 and HOXA in MLL-rearranged acute leukemia impairs engraftment and reduces proliferationDelayed biosynthesis of varicella-zoster virus glycoprotein C: upregulation by hexamethylene bisacetamide and retinoic acid treatment of infected cells.
P2860
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P2860
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
@ast
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
@en
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
@nl
type
label
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
@ast
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
@en
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
@nl
prefLabel
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
@ast
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
@en
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
@nl
P2093
P2860
P3181
P356
P1476
HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells
@en
P2093
P2860
P304
P3181
P356
10.1128/MCB.19.4.3051
P407
P577
1999-04-01T00:00:00Z