Phospho-NFATC1 (S294) Antibody

1. A novel role of HPV oncoprotein in facilitating NFAT2 dependent cell proliferation. PMID:29129565
2. There is a correlation between NFATC1 genes and the incidence of congenital heart disease in children, and a correlation between different genotypes and allele frequency and the incidence of the disease. PMID:28829497
3. Increased expression of nuclear factor of activated T cells 1 drives IL-9-mediated allergic asthma. PMID:26993036
4. NFATc1 knockdown strongly reduced the number and the surface area of myotubes, NFATc4 knockdown increased the surface area of myotubes and reduced the pool of reserve cells. PMID:28760926
5. APC defines Treg differentiation and anti-inflammatory function through microtubule-mediated NFAT localization. PMID:28978472
6. Our results were first found that NFATC1rs9518 closely associated with the risk and the development of Osteonecrosis of the Femoral Head, while OPGrs2073617 statistically correlated with the etiological classification of Osteonecrosis of the Femoral Head PMID:28824302
7. NFAT2 is an important regulator for the anergic phenotype of chronic lymphocytic leukaemia. PMID:28970470
8. Exposure to UVB radiation induces nuclear translocation and stimulates binding between NFAT5 and NF-kappaB proteins in HLE-B3 cells. These interactions may form part of the biochemical mechanism of cataractogenesis in UVB-irradiated HLECs. PMID:28632030
9. data identified a novel role of SFKs in preventing aberrant NFAT1 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 PMID:29073235
10. 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 (cg21933078, FDR = 1.22E-02) and NFATC1 (cg06784563, FDR = 1.46E-02) PMID:28637314
11. there is an NFATc1/ABCA1-dependent mechanism in which local TNF is sufficient to cause free cholesterol-dependent podocyte injury irrespective of TNF, TNFR1, or TNFR2 serum levels PMID:27482889
12. NFATC1 transcription factor (NFATc1) expression is detected in prostate cancer (PCa) specimens and PCa cells but is absent in non-neoplastic human prostates and non-tumorigenic prostatic cells PMID:26477312
13. TRAP activity and NFTAc1 nuclear localization are associated with aggressive cherubism and therefore could be added to routine pathologic examination to aid in prognosis and management of the disease. PMID:27498064
14. DYRK1A phosphorylation of NFATc1/alphaA at S261, S278, S403 and S409 interfered with NFATc1 ubiquitination and ubiquitin-proteasome degradation. PMID:28235034
15. 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. PMID:28188746
16. NFATC1 rs3894049 GC was a risk factor for acute rejection in renal transplant recipients compared with CC carriers. PMID:28244807
17. 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 in T cells, such as Raptor, CHEK1, CREB1, RUNX1, SATB1, Ikaros, and Helios. PMID:27637333
18. NFATc1 silencing regulates the cell cycle. PMID:27350254
19. Study showed that luteolin and apigenin effectively maintain pluripotency of PDLCs through activation of Oct-4/Sox2 signal via NFATc1. PMID:27449921
20. The enhanced osteoclast formation by TECK was mediated by NFATc1, but not by NF-kB signaling. PMID:26921718
21. The results demonstrate the importance of NFAT activation during PMA-induced mesenchymal stem cells differentiation. PMID:27405982
22. it was shown that NFATc1 siRNA significantly suppresses the growth and vascular generation of SKOV3 human ovarian carcinoma cell-transplanted tumors subcutaneously xenografted into nude mice. PMID:26820075
23. Data indicate that RNA interference of NFAT isoforms NFATc1, NFATc2, NFATc3 and NFATc4 regulate gene expression differentially in human retinal microvascular endothelial cells (HRMEC). PMID:26527057
24. NFATc1binds the GLI1 promoter and represses its transcription. PMID:26601952
25. InB may exhibit growth-inhibitory activity through the activation of PKCalpha, followed by an increase in NFAT transactivation ability. PMID:26398575
26. The low socioeconomic status (SES) were associated with DNA methylation of genes involved in inflammation. NFATC1, in particular, was consistently found to be less methylated in individuals with low vs high SES, in a dose-dependent manner. PMID:25889032
27. Synergistic interactions between NFAT and Foxp3 determine Treg-specific GARP expression. PMID:26584734
28. analysis of information transfer via gonadotropin-releasing hormone receptors to extracellular signal-regulated kinase or nuclear factor of activated T-cells PMID:26644469
29. Tmem178 localizes to the ER membrane and regulates RANKL-induced Ca(2+) fluxes, thus controlling NFATc1 induction PMID:26644563
30. DDIAS is a target of NFATc1 and is associated with cisplatin resistance in lung cancer cells. PMID:26493727
31. that alternative N-terminal domains of NFAT2 could provide differential mechanisms for the control of cellular functions PMID:26483414
32. This study suggested that development of specific NFAT inhibitors may offer promise as an effective strategy for attenuating the microgliosis and Abeta plaque deposition that occur in Alzheimer's disease. PMID:25889879
33. NFATc1 participation in osteogenic differentiation through its direct involvement in the regulatory machinery of mitochondria suggests a new role for this transcription factor. PMID:25952151
34. A channel chimera of Orai3 with the N terminus of Orai1 was able to couple local Ca(2+) entry to NFAT activation, identifying the N-terminal domain of Orai1 as central to Ca(2+) nanodomain-transcription coupling. PMID:24909327
35. A meta-analysis of the replication study data demonstrated that three chromosome 18 SNPs were associated with AAD, including a non-synonymous variant in the NFATC1 gene. PMID:26042420
36. NFATc1 activation promotes the invasion of U251 human glioblastoma multiforme cells through COX-2. PMID:25738651
37. The effects of NRON on HIV-1 replication are shown to be mediated by NFAT, and the viral Nef and Vpu proteins to modulate NFAT activity through their effects on NRON. PMID:25728138
38. NFAT polymorphisms are associated with Kawasaki disease. PMID:24903211
39. High NFATc1 expression is associated with acute myeloid leukemia. PMID:25976987
40. NFATc1 plays a important role in prostate cancer outgrowth. PMID:25631176
41. Data indicate that both nuclear factors of activated T cells (NFATs) motifs partially compete for binding but do not fully displace each other on the calcineurin (Cn) epitope. PMID:24954618
42. Authors report a role for the human herpesvirus 6B (HHV-6B) U54 tegument protein in inhibiting MCF-7 breast cancer cell proliferation by inhibiting NFAT activation. PMID:25122795
43. VEGF regulates NFATc1 binding to angiogenesis-related genes in the endothelium PMID:25157100
44. this study identified two crucial immune-related molecules-CD28 and NFATc1, as putative targets of miR-145 in human and experimental myasthenia gravis PMID:24043548
45. NFAT2 mediates VEGF-induced upregulation of integrin subunit synthesis by providing a constant supply of newly synthesized "refreshed" mature integrin receptors, which are involved at different stages of angiogenesis. PMID:24657343
46. ITPR2 and hypertrophy specific gene expression is regulated, in part, by a positive feedback regulation between InsP3R2 and calcineurin-NFATc signaling pathways. PMID:24415751
47. The expression of NFATc1CA promoted cancer cell invasion in association with changes in cell morphology. PMID:23811942
48. High NFAT expression is associated with metastasis in breast cancer. PMID:23832742
49. NFATc1 is associated with the occurrence of ventricular septal defect (VSD) and it may be a predisposing gene to Congenital heart disease in Han Chinese. PMID:23286482
50. Data indicate that depletion of NFATc1, cyclin D1, CDK6, or CDK4 levels attenuated MCP1-induced Pak1 phosphorylation/activation and resulted in decreased aortic smooth muscle cells (HASMCs) F-actin stress fiber formation, migration, and proliferation. PMID:23737530

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HGNC: 7775

UNIGENE: Hs.534074

KEGG: hsa:4772

STRING: 9606.ENSP00000327850

OMIM: 600489