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The protein encoded by EGR2 is a transcription factor with three tandem C2H2-type zinc fingers. Additionally we are shipping EGR2 Antibodies (117) and EGR2 Proteins (12) and many more products for this protein.
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Low EGR2 expression is associated with hepatocellular carcinoma.
The study suggests that acetylation of EGR2 is regulated independently of nucleosome remodeling and deacetylase.
Egr2-driven cell surface proteins LAG-3 (show LAG3 ELISA Kits) and 4-1BB (show TNFRSF9 ELISA Kits) can identify dysfunctional tumor antigen-specific CD8 (show CD8A ELISA Kits)(+) TIL (show TLR1 ELISA Kits).
Egr2 and Egr3 (show EGR3 ELISA Kits) have emerged as regulatory molecules that suppress excessive immune responses. Mice deficient for Egr2 and Egr3 (show EGR3 ELISA Kits) develop a lupus-like disease with dysregulated activation of effector T cells. Egr2 and Egr3 (show EGR3 ELISA Kits) confer suppressive activity to CD4 (show CD4 ELISA Kits)(+) T cells and regulate the production of inhibitory cytokines such as IL-10 (show IL10 ELISA Kits) and TGF-beta1 (show TGFB1 ELISA Kits).
Analysis of consensus EGR (show EGR1 ELISA Kits)-binding elements (EBEs) showed that the immediate early response 3 (show IER3 ELISA Kits) gene (IER3 (show IER3 ELISA Kits)) is a novel transcriptional target gene of EGR2 as confirmed by the luciferase assay, electrophoretic mobility-shift assay (EMSA), chromatin immunoprecipitation (ChIP), and western blot analysis.
In the PPI network, genes may be involved in Down syndrome (DS) by interacting with others, including nuclear receptor subfamily 4 group A member 2 (NR4A2 (show NR4A2 ELISA Kits))early growth response (EGR)2 and NR4A2EGR3. Therefore, RUNX1 (show RUNX1 ELISA Kits), NR4A2 (show NR4A2 ELISA Kits), EGR2, EGR3 (show EGR3 ELISA Kits) and ID4 (show ID4 ELISA Kits) may be key genes associated with the pathogenesis of DS.
EGR2 mutation presents as an axonal Charcot-Marie-Tooth phenotype with variable severity.
MicroRNA20a promotes the proliferation and cell cycle of human osteosarcoma cells by suppressing EGR2 expression.
These results suggested that EGR2 overexpression has a pivotal role in the downregulation of cytokines implicated in the pathophysiology of Guillain-Barre syndrome
A recurrent mutation was identified in EGR2 which appears to be associated with the pathogenesis of schizophrenia.
Egr2 and Egr3 (show EGR3 ELISA Kits) expressed in T cells cooperatively prevent humoral immune responses by supporting TGF-beta3 (show TGFB3 ELISA Kits) secretion.
study revealed GCN5-mediated EGR2 acetylation as a molecular mechanism that regulates iNKT development.
findings demonstrate a crucial role for Krox20 in arterial valve development and reveal that an excess of neural crest cells may be associated with bicuspid aortic valve.
these results suggested that the basal promoter activity of the mIRF-3 gene is regulated by transcription factors Egr2 and YY1 (show YY1 ELISA Kits) in NIH3T3 cells
Prss56 expression was regulated by Egr2 during mouse decidualization.
Egr2 and 3 are upstream regulators of effector CD4 (show CD4 ELISA Kits) and CD8 (show CD8A ELISA Kits) T cells that are essential for optimal responses with limited immunopathology.
Egr2 and 3 are antagonists of T-bet function in effector T cells and are important for the control of inflammatory responses of T cells.
We discovered that Tead1 (show TEAD1 ELISA Kits) and co-activators Yap (show YAP1 ELISA Kits) and Taz (show TAZ ELISA Kits) are required for Pmp22 (show PMP22 ELISA Kits) expression, as well as for the expression of Egr2 Tead1 (show TEAD1 ELISA Kits) directly binds Pmp22 (show PMP22 ELISA Kits) and Egr2 enhancers early in development and Tead1 (show TEAD1 ELISA Kits) binding is induced during myelination, correlating with Pmp22 (show PMP22 ELISA Kits) expression. The data identify Tead1 (show TEAD1 ELISA Kits) as a novel regulator of Pmp22 (show PMP22 ELISA Kits) expression during development in concert with Sox10 (show SOX10 ELISA Kits) and Egr2
endogenous KLF4 (show KLF4 ELISA Kits) and Krox20 are dispensable for adipogenesis in culture and for brown adipose tissue development in mice. In contrast, the master adipogenic transcription factor peroxisome proliferator-activated receptor gamma (PPARgamma (show PPARG ELISA Kits)) is essential.
Decreased expression of Krox20 in mice causes degeneration of the aortic leaflets and disorganization of the extracellular matrix, causing valvular dysfunction.
A direct, positive autoregulatory loop amplifies and maintains the expression of Krox20, a transcription factor governing vertebrate hindbrain segmentation.
Hindbrain patterning requires fine-tuning of early krox20 transcription by Sprouty 4.
Data show that Irx7 and Irx1b are required for the proper formation and specification of rhombomeres 1 to 4, and that Irx7 functionally interacts with Meis1.1 (show MEIS1 ELISA Kits) to activate the expression of anterior hindbrain markers, such as krox20.
The protein encoded by this gene is a transcription factor with three tandem C2H2-type zinc fingers. Defects in this gene are associated with Charcot-Marie-Tooth disease type 1D (CMT1D), Charcot-Marie-Tooth disease type 4E (CMT4E), and with Dejerine-Sottas syndrome (DSS). Multiple transcript variants encoding two different isoforms have been found for this gene.
E3 SUMO-protein ligase EGR2
, KROX-20, Drosophila, homolog (early growth response-2)
, early growth response protein 2
, zinc finger protein Krox-20
, early growth response 2 (Krox-20 homolog, Drosophila)
, early growth response protein 2b
, protein krx-20