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MEF2D is a member of the myocyte-specific enhancer factor 2 (MEF2) family of transcription factors. Additionally we are shipping MEF2D Antibodies (147) and MEF2D Kits (1) and many more products for this protein.
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Our study suggests that the MEF2D, PRDM16 (show PRDM16 Proteins) and ASTN2 (show ASTN2 Proteins) genes from GWAS are associated with migraine susceptibility, especially migraine without aura (show AURKA Proteins) , among Chinese patients. It appears that there is no association with serotonin receptor (show HTR1B Proteins) related genes.
In summary, we found that miR (show MLXIP Proteins)-1244 affected cisplatin-treated non-small cell lung cancer via MEF2D expression.
MEF2d mRNA level is up-regulated in both sporadic and SOD1 + ALS patients.
MEF2D might be a potential biomarker during chronic inflammation-lung cancer transition, predicting the risk of lung cancer among patients with chronic respiratory diseases.
HIF-1alpha (show HIF1A Proteins) transactivates MEF2D expression by binding to the MEF2D gene promoter to induce angiogenesis in colorectal tumors.
MEF2D directly regulated transcription of the epithelial-mesenchymal transition driver gene ZEB1 and facilitated histone acetylation at the ZEB1 promoter in colorectal cancer cells
MEF2D-BCL9 (show BCL9 Proteins)-positive patients had B-cell precursor immunophenotype and were characterized as being older in age, being resistant to chemotherapy, having very early relapse, and having leukemic blasts that mimic morphologically mature B-cell leukemia with markedly high expression of HDAC9 (show HDAC9 Proteins).
These results suggest that PPARgamma (show PPARG Proteins) may exert its antiproliferative effects by negatively regulating the MEF2D in CM cells, which through upregulation of miR (show MLXIP Proteins)-122, and PPARgamma (show PPARG Proteins)/miR (show MLXIP Proteins)-122/MEF2D signaling pathway may be a novel target for treatment of CM.
MEF2D overexpression participated in the growth of lung cancers and its aberrant expression may result from the reduction of tumor suppressor miR (show MLXIP Proteins)-218.
MEF2D is a direct target of miR (show MLXIP Proteins)-19.
Both synapse silencing and elimination required de novo transcription, but only silencing required the activity-dependent transcription factors MEF2A (show MEF2A Proteins)/D.
In the Mef2d heterozygous retina, NRF2 (show NFE2L2 Proteins) is not up-regulated to a normal degree in the face of light-induced oxidative stress, contributing to accelerated photoreceptor cell death.
These findings uncover a novel role for Mef2c (show MEF2C Proteins)/d in coordinating the transcriptional network that promotes early B-cell development.
This study identifies MEF2D as a critical regulator of IL-10 (show IL10 Proteins) gene expression that negatively controls microglia inflammation response and prevents inflammation-mediated cytotoxicity.
Mef2d is essential for the maturation and integrity of retinal photoreceptor and bipolar cells
miR (show MLXIP Proteins)-103 worked through activating AKT (show AKT1 Proteins)/mTOR (show FRAP1 Proteins) signal pathway and impairing target gene MEF2D.
These findings demonstrate that broadly expressed TFs acquire specific functions through competitive recruitment to enhancers by tissue-specific Mef2d and through selective activation of these enhancers to regulate tissue-specific genes.
Whereas MEF2A (show MEF2A Proteins) is absolutely required for proper myoblast differentiation, MEF2B (show MEF2B Proteins), -C, and -D were found to be dispensable for this process.
A role for endogenous MEF2 (show MEF2C Proteins) factors exclusively in hormone/Fsk/cAMP-induced Nr4a1 (show NR4A1 Proteins) gene expression in mouse MA-10 Leydig cells.
Oxidation of survival factor MEF2D inhibits its function, underlies oxidative stress-induced (show SQSTM1 Proteins) neurotoxicity, and may be a part of the Parkinson disease pathogenic process.
Expression analysis showed that the MEF2D polymorphisms were highly correlated with MEF2D mRNA and protein levels in the longissimus dorsi muscle of Polish Holstein-Friesian bulls carrying the three different combined genotypes.
This gene is a member of the myocyte-specific enhancer factor 2 (MEF2) family of transcription factors. Members of this family are involved in control of muscle and neuronal cell differentiation and development, and are regulated by class II histone deacetylases. Fusions of the encoded protein with Deleted in Azoospermia-Associated Protein 1 (DAZAP1) due to a translocation have been found in an acute lymphoblastic leukemia cell line, suggesting a role in leukemogenesis. The encoded protein may also be involved in Parkinson disease and myotonic dystrophy. Alternative splicing results in multiple transcript variants.
myocyte enhancer factor 2D
, MADS box transcription enhancer factor 2, polypeptide D (myocyte enhancer factor 2D)
, myocyte-specific enhancer factor 2D-like
, MADS box transcription enhancer factor 2, polypeptide D
, myocyte-specific enhancer factor 2D