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EZH1 is a component of a noncanonical Polycomb repressive complex-2 (PRC2) that mediates methylation of histone H3 (see MIM 602812) lys27 (H3K27) and functions in the maintenance of embryonic stem cell pluripotency and plasticity (Shen et al., 2008 [PubMed 19026780]).[supplied by OMIM, Mar 2009].. Additionally we are shipping EZH1 Antibodies (121) and EZH1 Proteins (7) and many more products for this protein.
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identification of EZH1 as a repressor of haematopoietic multipotency in the early mammalian embryo
pVHL (show VHL ELISA Kits) loss causes the transcriptional activation of hypoxia-inducible factor (HIF) target genes, including many genes that encode histone lysine demethylases.
Data show that embryonic stem cells with deletion of EZH1 or EZH2 (show EZH2 ELISA Kits) fail to differentiate into ectoderm lineages.
Expression of the EZH2 (show EZH2 ELISA Kits) homolog EZH1 is reduced in EZH2 (show EZH2 ELISA Kits)-deficient CML (show BCR ELISA Kits) LICs, creating a scenario resembling complete loss of PRC2. EZH2 (show EZH2 ELISA Kits) dependence of CML (show BCR ELISA Kits) LICs raises prospects for improved therapy of TKI-resistant CML (show BCR ELISA Kits) and/or eradication of disease by addition of EZH2 (show EZH2 ELISA Kits) inhibitors
a hot-spot mutation in EZH1 is the second most frequent genetic alteration in autonomous thyroid adenomas; the association between EZH1 and TSHR (show TSHR ELISA Kits) mutations suggests a 2-hit model for the pathogenesis of these tumors, whereby constitutive activation of the cAMP pathway and EZH1 mutations cooperate to induce the hyperproliferation of thyroid cells
EZH1, SUZ12 and UXT work synergistically to regulate pathway activation in the nucleus.
The authors report a novel PRC2-Ezh1 function that utilizes Ezh1beta as an adaptive stress sensor in the cytoplasm, thus allowing postmitotic cells to maintain tissue integrity in response to environmental changes.
These evidences suggest that EZH2 (show EZH2 ELISA Kits) and EZH1 are important in the counter-balancing mechanisms controlling proliferation/resting of lymphoid cells. The disruption of the balanced EZH2/EZH1 (show EZH2 ELISA Kits) ratio may play important roles in the pathogenesis of lymphomas
The related enzymatic subunits EZH1 and EZH2 (show EZH2 ELISA Kits) undergo an expression switch during blood cell development.
EZH1 maintains repressive chromatin through different mechanisms.
The combined loss of Ezh1 and Ezh2 (show EZH2 ELISA Kits) in chondrocytes severely impairs skeletal growth in mice.
Suggest that EZH1 and -2 are novel targets of miR (show MLXIP ELISA Kits)-214-3p, and miR (show MLXIP ELISA Kits)-214-3p might be one potential miRNA for the prevention of cardiac fibrosis.
Ezh1 is required for neonatal heart regeneration and development.
in the skin epithelium, EED (show EED ELISA Kits), Suz12, and Ezh1/2 function largely as subunits of the PRC2 complex and have roles in skin development
the expression level of Ezh1 determines the restoration of H3K27 methylation in the absence of the canonical EZH2 (show EZH2 ELISA Kits)-PRC2.
These results clearly demonstrated an essential role of Ezh1 in the pathogenesis of hematopoietic malignancies induced by Ezh2 (show EZH2 ELISA Kits) insufficiency, and highlighted the differential functions of Ezh1 and Ezh2 (show EZH2 ELISA Kits) in hematopoiesis.
Loss of EZH1 is associated with increased liver injury and a blunted regenerative response.
Data show that histone lysine methyltransferase Ezh1 promotes toll (show TLR4 ELISA Kits)-like receptor (TLR)-triggered inflammatory cytokine production by suppressing the Toll-interacting protein (Tollip (show TOLLIP ELISA Kits)), contributing to full activation of the innate immunity.
presence of Ezh1 helps to maintain PRC2 occupancy on its target genes in myoblasts where Jarid2 (show JARID2 ELISA Kits) is not expressed.
EZH1 is a component of a noncanonical Polycomb repressive complex-2 (PRC2) that mediates methylation of histone H3 (see MIM 602812) lys27 (H3K27) and functions in the maintenance of embryonic stem cell pluripotency and plasticity (Shen et al., 2008
, histone-lysine N-methyltransferase EZH1
, enhancer of zeste 1
, enhancer of zeste homolog 1 (Drosophila)
, enhancer of zeste homolog 1-like
, histone-lysine N-methyltransferase EZH1-like
, enhancer of zeste homolog 1