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In a cohort of youth at risk for bipolar disorder, pathway analysis showed an enrichment of the glucocorticoid receptor (GR (Montrer NR3C1 Protéines)) pathway with the genes MED1, HSPA1L (Montrer HSPA1L Protéines), GTF2A1 (Montrer GTF2A1 Protéines) and TAF15 (Montrer TAF15 Protéines), which might underlie the previously reported role of stress response in the risk for bipolar disorder in vulnerable populations.
modulation of ESR1 (Montrer ESR1 Protéines)-MED1 interactions by cAMP signaling plays a critical role in human decidualization.
Our data indicate that MED1 serves as a key mediator in ARv567es induced gene expression
Results show that miR-1 (Montrer FSD1 Protéines) is downregulated in osteosarcoma cells but both of its targets Med1 and Med31 (Montrer MED31 Protéines) were overexpressed suggesting that MiR-1 (Montrer FSD1 Protéines) plays an important role on the proliferation of osteosarcoma cells through regulation of Med1 and Med31 (Montrer MED31 Protéines).
MED1 is required for optimal PRDM16 (Montrer PRDM16 Protéines)-induced Ucp1 (Montrer UCP1 Protéines) expression
no association between SCZ and the SNPs of VDR, suggesting that VDR is not a major gene for SCZ in Chinese Han population. However, our data indicate a potential involvement of VDR SNPs in the susceptibility of risperidone-treated patients to MetS
hyperactivated ERK (Montrer EPHB2 Protéines) and/or AKT (Montrer AKT1 Protéines) signaling pathways promoted MED1 overexpression in prostate cancer cells.
These results demonstrate a role for MED1 in mediating resistance to the pure anti-estrogen fulvestrant both in vitro and in vivo.
multiple modes of the GATA1 (Montrer GATA1 Protéines)-MED1 axis may help to fine-tune GATA1 (Montrer GATA1 Protéines) function during GATA1 (Montrer GATA1 Protéines)-mediated homeostasis events.
Data concluded that those of VDR ff genotype may be regarded as "low responders" to vitamin D intake in terms of response of circulating 25(OH)D and certain inflammatory biomarkers.
Data, including data from studies using cells from transgenic/knockout mice, suggest that Med1 (Montrer MBD4 Protéines) plays role in enamel formation; Med1 (Montrer MBD4 Protéines) induces Alpl (Montrer ALPL Protéines) via stimulation of Notch1 (Montrer NOTCH1 Protéines) signaling by forming Notch1 (Montrer NOTCH1 Protéines)-RBP-Jk (Montrer RBPJ Protéines) complex on Alpl (Montrer ALPL Protéines) promoter. (Med1 (Montrer MBD4 Protéines) = mediator complex subunit 1; Alpl (Montrer ALPL Protéines) = alkaline phosphatase, liver-bone-kidney; Notch1 (Montrer NOTCH1 Protéines) = Notch gene homolog 1 (Montrer NOTCH1 Protéines); RBP-Jk (Montrer RBPJ Protéines) = kappa J region recombining binding protein suppressor of hairless (Montrer RBPJ Protéines))
MED1 (Montrer MBD4 Protéines) in macrophages has an antiatherosclerotic role via PPARgamma (Montrer PPARG Protéines)-regulated transactivation.
Cardiomyocyte-specific ablation of Med1 (Montrer MBD4 Protéines) causes lethal dilated cardiomyopathy in mice.
Med1 (Montrer MBD4 Protéines) deletion disrupted cardiac mitochondrial and metabolic gene expression patterns
Med1 and Med12, two subunits of the mediator complex implicated in transcription initiation and long-range enhancer/promoter loop formation, are dynamically recruited to the IgH locus enhancers.
We conclude that MED1 (Montrer MBD4 Protéines) regulates the temporal progression of primary spermatocytes through meiosis, with its absence resulting in abbreviated pre-leptotene, leptotene, and zygotene stages, and a prolonged pachytene stage.
These results demonstrate that Med1 (Montrer MBD4 Protéines) is a master regulator in adult stem cells to govern epithelial cell fate
The novel function of MED1 (Montrer MBD4 Protéines) in keratinocytes.
PRDM16 (Montrer PRDM16 Protéines) deficiency in BAT (Montrer BAAT Protéines) reduces MED1 (Montrer MBD4 Protéines) binding at PRDM16 (Montrer PRDM16 Protéines) target sites and causes a fundamental change in chromatin architecture at key brown fat-selective genes
Collectively, these observations strongly suggest that MED1 (Montrer MBD4 Protéines) has an important affect on mitochondrial function.
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. It also regulates p53-dependent apoptosis and it is essential for adipogenesis. This protein is known to have the ability to self-oligomerize.
, PPAR binding protein
, PPAR-binding protein
, PPARG binding protein
, TR-interacting protein 2
, activator-recruited cofactor 205 kDa component
, mediator of RNA polymerase II transcription subunit 1
, p53 regulatory protein RB18A
, peroxisome proliferator-activated receptor-binding protein
, thyroid hormone receptor-associated protein complex 220 kDa component
, thyroid hormone receptor-associated protein complex component TRAP220
, thyroid receptor interacting protein 2
, thyroid receptor-interacting protein 2
, vitamin D receptor-interacting protein 230 kD
, vitamin D receptor-interacting protein complex component DRIP205
, mediator complex subunit 1
, peroxisome proliferator-activated receptor binding protein
, membrane component, chromosome 17, surface marker 2
, Ppar binding protein
, peroxisome proliferator activated receptor binding protein