Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Show all synonyms
Select your origin of interest
This is the first patient with documented refractory epilepsy caused by a novel homozygous pathogenic variant in MED23 expanding the phenotypic spectrum. Identification of the underlying genetic defect in MED23 sheds light on the possible mechanism of complete response to the ketogenic diet in this child.
a 7-gene signature was identified which correctly predicted the primary prefibrotic myelofibrosis group with a sensitivity of 100% and a specificity of 89%. The 7 genes included MPO (show MPO Proteins), CEACAM8, CRISP3 (show CRISP3 Proteins), MS4A3 (show MS4A3 Proteins), CEACAM6, HEMGN, and MMP8 (show MMP8 Proteins)
Higher l-arginine (show GATM Proteins) was associated with higher risk of Ischemic heart disease (odds ratio and of myocardial infarction, based on 2 SNPs from MED23.
MED23-associated intellectual disability has been found in two brothers from a non-consanguineous family.
MED23 plays an important role in hepatocarcinogenesis, and it may be a novel target for HCC (show FAM126A Proteins) therapy.
Upregulation of mediator MED23 in non-small-cell lung cancer promotes the growth, migration, and metastasis of cancer cells.
Mediator MED23 regulates basal transcription in vivo via an interaction with P-TEFb (show CCNT1 Proteins).
Data show that Med23 RNAi specifically inhibits the proliferation and tumorigenicity of lung cancer cells with hyperactive Ras activity.
missense mutation (p. R617Q) in MED23 that cosegregates with nonsyndromic autosomal recessive intellectual disability; mutation impaired response of JUN and FOS to mitogens by altering interaction between enhancer-bound transcription factors and Mediator
DRIP130 regulates HER2 (show ERBB2 Proteins) expression by binding to ESX (show ELF3 Proteins)
MED23 constitutes a molecular node in the regulatory network of anabolic bone formation and related diseases.
Med23 contributes to controlling T-cell activation at the transcriptional level and prevents the development of autoimmunity.
The hepatic Med23 deletion impaired the Mediator and RNAPII recruitment and attenuated the expression of FOXO1 (show FOXO1 Proteins) target genes.
Data show that Kruppel-like transcription factors KLF2 (show KLF2 Proteins) expression is decreased in mediator complex Med23 null thymocytes.
Mediator Med23 deficiency enhances neural differentiation of murine embryonic stem cells through modulating BMP signaling.
Reduced expression of MED23 inhibits cell apoptosis by downregulation of Bax (show BAX Proteins), activated Caspase 3 (show CASP3 Proteins), activated Caspase 9 (show CASP9 Proteins) and upregulation of cyclinD1 and Bcl2 (show BCL2 Proteins).
Data show tha tMed23 deficiency in fibroblasts selectively inhibited the oncogenic transformation induced by Ras.
Mediator MED23 controls the cell fate preference that directs differentiation into smooth muscle cells (SMCs) or adipocytes
MED23 regulates a subset of hnRNP L (show HNRNPL Proteins)-targeted alternative splicing (AS) and alternative cleavage and polyadenylation (APA (show ENPEP Proteins)) events.
MED23 Mediator controls Egr1 gene and stimulates Pol II initiation at a step subsequent to preinitiation complex assembly
we investigate orthologs of a transcription complex that acts in mammalian EGFR (show EGFR Proteins) signaling-lin-1/Elk1 (show ELK1 Proteins), sur-2/Med23, and the Cdk8 (show CDK8 Proteins) Kinase module (CKM (show CKM Proteins)).our analysis using cell fate reporters reveals that both EGFR (show EGFR Proteins) and LIN-12/Notch (show NOTCH1 Proteins) signal transduction pathways are active in all VPCs in lin-1/Elk1 (show ELK1 Proteins) mutants
Study shows that sur-2 mutation affects the Cbr (show CNR1 Proteins)-sur-2/MED23 gene that is orthologous to a C. elegans gene critical for the normal response to the EGF (show EGF Proteins) signal. whereas Cel-sur-2 mutants exhibit a reduced vulval development because of defects in the VPC immediately adjacent to the anchor cell (the P6.p cell), similar defects in Caenorhabditis briggsae -sur-2 mutants do not have the same impact.
The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. This protein also acts as a metastasis suppressor. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.
, mediator complex subunit 23
, mediator complex subunit n23
, cofactor required for Sp1 transcriptional activation, subunit 3, 130kDa
, Sp1 transcriptional activation cofactor subunit 3
, mediator of RNA polymerase II transcription subunit 23-like
, mediator of RNA polymerase II transcription subunit 23
, 130 kDa transcriptional co-activator
, 133 kDa transcriptional co-activator
, activator-recruited cofactor 130 kDa component
, cofactor required for Sp1 transcriptional activation subunit 3
, vitamin D3 receptor interacting protein
, CRSP complex subunit 3
, cofactor required for Sp1 transcriptional activation, subunit 3 (130kD)
, protein sur-2 homolog
, cofactor required for Sp1 transcriptional activation, subunit 3