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NFATc1 controls the cytotoxicity and metabolic switching of activated CD8 (zeige CD8A Proteine)(+) T cells required for optimal response to bacteria and tumor cells.
ATF3 (zeige ATF3 Proteine) is a new co-factor of c-Fos and NFATc1 to activate osteoclast differentiation and activity.
NFAT is activated through calcineurin and interacts with NFsmall ka, CyrillicB after P. aeruginosa lung infection, and contributes to the host inflammatory response.
IKKepsilon (zeige IKBKE Proteine) promotes NFATc1 phosphorylation and inhibits T cell responses, identifying IKKepsilon (zeige IKBKE Proteine) as a crucial negative regulator of T cell activation and a potential target for immunotherapy.
Transplantation from GRIM19 (zeige NDUFA13 Proteine)-overexpressing cells downregulated the expression of nuclear factor of activated T cells (NFATc1) but promoted the expression of regulator of calcineurin (RCAN)3 (zeige RCAN3 Proteine) while downregulating NFAT-dependent cytokine gene expression.
These results suggest that the Keap1 (zeige KEAP1 Proteine)/Nrf2 (zeige NFE2L2 Proteine) axis plays a critical role in NFATc1 expression and osteoclastogenic progression.
Inhibition of calcineurin activity with FK506 or blockage of L-type calcium channels with nifedipine significantly suppressed NFATc1 mRNA expression and CTSK (zeige CTSK Proteine) protein expression.
astrocytes were strongly associated with proteolysis of the protein phosphatase calcineurin (CN) and the elevated expression of the CN-dependent transcription factor nuclear factor of activated T cells 4 (NFAT4 (zeige NFATC3 Proteine)
In studies of human and mouse pancreatic cells and tissue, we identified context-specific epigenetic regulation of NFATc1 activity as an important mechanism of pancreatic cell plasticity.
Immunoreceptor tyrosine-based inhibitory motif DC-STAMP is a functional motif that regulates osteoclast differentiation through the NFATc1/Ca(2 (zeige CA2 Proteine)+) axis.
Exposure to UVB radiation induces nuclear translocation and stimulates binding between NFAT5 (zeige NFAT5 Proteine) and NF-kappaB (zeige NFKB1 Proteine) proteins in HLE (zeige ELANE Proteine)-B3 cells. These interactions may form part of the biochemical mechanism of cataractogenesis in UVB-irradiated HLECs.
data identified a novel role of SFKs in preventing aberrant NFAT1 (zeige NFAT1 Proteine) activation in resting T cells, and suggest that maintaining this pool of active SFKs in therapeutic T cells may increase the efficacy of T cell therapies
Pathway analysis of the genes associated with the 46 CpG sites revealed an enrichment of immune system process genes, including LYST (cg16962115, FDR = 1.24E-04), CADM1 (zeige CADM1 Proteine) (cg21933078, FDR = 1.22E-02) and NFATC1 (cg06784563, FDR = 1.46E-02)
there is an NFATc1/ABCA1 (zeige ABCA1 Proteine)-dependent mechanism in which local TNF (zeige TNF Proteine) is sufficient to cause free cholesterol-dependent podocyte injury irrespective of TNF (zeige TNF Proteine), TNFR1 (zeige TNFRSF1A Proteine), or TNFR2 (zeige TNFRSF1B Proteine) serum levels
NFATC1 transcription factor (NFATc1) expression is detected in prostate cancer (PCa (zeige FLVCR1 Proteine)) specimens and PCa (zeige FLVCR1 Proteine) cells but is absent in non-neoplastic human prostates and non-tumorigenic prostatic cells
DYRK1A phosphorylation of NFATc1/alphaA at S261, S278, S403 and S409 interfered with NFATc1 ubiquitination and ubiquitin-proteasome degradation.
NFATC1 rs3894049 GC was a risk factor for acute rejection in renal transplant recipients compared with CC carriers.
revealed more than 170 NFAT-associated proteins, half of which are involved in transcriptional regulation. Among them are many hitherto unknown interaction partners of NFATc1 and NFATc2 (zeige NFAT1 Proteine) in T cells, such as Raptor (zeige RPTOR Proteine), CHEK1 (zeige CHEK1 Proteine), CREB1 (zeige CREB1 Proteine), RUNX1 (zeige RUNX1 Proteine), SATB1 (zeige SATB1 Proteine), Ikaros (zeige IKZF1 Proteine), and Helios (zeige ZNFN1A2 Proteine).
NFATc1 silencing regulates the cell cycle.
In calf pulmonary artery endothelial cells, extracellular application of vasoactive agonist ATP or calcium ionophore ionomycin generates a rise in intracellular calcium that induces nuclear localization of NFATc1.
regulation of nuclear localization of NFAT is isoform-specific and dependent on nuclear export processes
The product of this gene is a component of the nuclear factor of activated T cells DNA-binding transcription complex. This complex consists of at least two components: a preexisting cytosolic component that translocates to the nucleus upon T cell receptor (TCR) stimulation, and an inducible nuclear component. Proteins belonging to this family of transcription factors play a central role in inducible gene transcription during immune response. The product of this gene is an inducible nuclear component. It functions as a major molecular target for the immunosuppressive drugs such as cyclosporin A. Five transcript variants encoding distinct isoforms have been identified for this gene. Different isoforms of this protein may regulate inducible expression of different cytokine genes.
nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 1
, nuclear factor of activated T-cells, cytosolic component 1
, nuclear factor of activated T-cells calcineurin-dependent 1
, nuclear factor of activated T-cells, cytoplasmic 1
, nuclear factor of activated T-cells, cytoplasmic 1-like
, NFAT transcription complex cytosolic component
, transcription factor NF-ATc
, transcription factor NFATmac