NCOR2 Antibody

1. this report tried to address the molecular basis for the direct interaction between CSL and SMRT. PMID: 30157580
2. The pregnane X receptor (PXR) and the nuclear receptor corepressor 2 (NCoR2) modulate cell growth in head and neck squamous cell carcinoma PMID: 29470550
3. Cellular Differentiation of Human Monocytes Is Regulated by Time-Dependent Interleukin-4 Signaling and the Transcriptional Regulator NCOR2. PMID: 29262348
4. this study identifies NCOR2 as a new gene for FVC, indicating the importance of further research into the role of vitamin A intake/supplementation and its interactions with related genes in the regulation of FVC. PMID: 26836265
5. Molecular basis for the specific interactions between HDAC4 and the SMRT corepressor. PMID: 26161557
6. SNPs in Notch pathway genes may be predictors of cutaneous melanoma disease-specific survival. PMID: 25953768
7. Significant methylation changes in the SLC23A2 and NCOR2 regulatory regions. PMID: 25821969
8. A repeated peptide motif present in both SMRT and NCoR is sufficient to mediate specific interaction, with micromolar affinity, with all the Class IIa Histone Deacetylases (HDACs 4, 5, 7, and 9). PMID: 26055705
9. SMRT enhances cell growth of estrogen receptor-alpha-positive breast cancer cells by promotion of cell cycle progression and inhibition of apoptosis. PMID: 24971610
10. Phosphorylation of the CK2 site on SMRT significantly increased affinity for SHARP. PMID: 24268649
11. SMRT is responsible for basal repression of Wip1,a phosphatase that de-phosphorylates and inactivates Chk2, thus affecting a feedback loop responsible for licensing the correct timing of Chk2 activation and the proper execution of the DNA repair process. PMID: 23690919
12. SMRT may be recruited in the SXR-cofactor complex even in the presence of ligand; SMRTmay be involved not only in SXR-mediated suppression without ligand, but also in ligand-activated transcription to suppress the overactivation of transcription PMID: 23562850
13. There was no association between SMRT expression and overall survival for patients, regardless of whether they received tamoxifen PMID: 23015261
14. expression of the transcriptional corepressor complex subunits GPS2 and SMRT was significantly reduced in obese adipose tissue, inversely correlated to inflammatory status PMID: 23221346
15. Both MEK1 and SMRT bind to the c-Fos promoter and regulate its transcription; SMRT knockdown results in early-phase stimulation followed by a late-phase inhibition of T cell activation. PMID: 23225884
16. Thyroid hormone receptors induce TRAIL expression, and TRAIL thus synthesized acts in concert with simultaneously synthesized Bcl-xL to promote metastasis PMID: 22576662
17. Our findings highlight a novel splice variant of NCOR2 as a candidate biomarker in breast cancer that not only predicts tamoxifen response but may be targeted to overcome tamoxifen resistance PMID: 23117886
18. SMRT and GR act in a consistent manner with steroid hormones PMID: 23055525
19. altered recruitment and loss of corepressors SMRT/NCoR may provide a mechanism that changes the response of AR function to ligands and contributes to the progression of the advanced stages of human prostate cancer. PMID: 22695118
20. miR-16 targets SMRT and modulates NF-kappaB-regulated transactivation of the IL-8 gene. PMID: 22292036
21. An equilibrium dissociation constant obtained for SMRT in the presence and absence of rifampicin indicates that the ligand does not enhance the affinity of the pregnane X receptor or its corepressor. PMID: 22185585
22. Data report that SMRT interacts with itself to form a protein dimer, and that Erk2, a mitogen-activated protein (MAP) kinase, disrupts this SMRT self-dimerization in vitro and in vivo. PMID: 20965228
23. The crystal structure of the tetrameric oligomerization domain of TBL1, which interacts with both SMRT and GPS2, and the NMR structure of the interface complex between GPS2 and SMRT. PMID: 21240272
24. This study independently verifies the influence of NCOR2 and IDH1 on HIV transmission, and its findings suggest that variation in these genes affects susceptibility to HIV infection in exposed individuals. PMID: 21083371
25. Aberrant expression and modification of SMRT might be involved in the pathogenesis of tumoral cortisol resistance. PMID: 20555024
26. Tamoxifen treatment of breast cancer cells reduced the expression of ER-alpha and increased the expression of SMRT. PMID: 18546531
27. SMRT decreased with oestradiol treatment in human skeletal muscle cells PMID: 19432593
28. Sstable binding of the Stat5-RARalpha fusion protein to corepressor SMRT is accompanied by an impaired response to differentiation signals in hematopoietic cells PMID: 11929749
29. Interactions that determine the assembly of a retinoid X receptor/corepressor complex PMID: 11972046
30. The silencing mediator of retinoic acid and thyroid hormone receptors can interact with the aryl hydrocarbon (Ah) receptor but fails to repress Ah receptor-dependent gene expression. PMID: 12139968
31. SMRT has a role as a coactivator for thyroid hormone receptor T3Ralpha from a negative hormone response element PMID: 12388540
32. a significant role of SMRT in modulating androgen receptor transcriptional activity PMID: 12441355
33. Differing transcriptional properties appear to reflect the differing abilities of the three RAR isotypes to interact with the SMRT corepressor protein. PMID: 12554770
34. SMRT and DAX-1 repress agonist-dependent activity of both androgen and progesterone receptors PMID: 12771131
35. SANT motif interprets the histone code and promotes histone deacetylation PMID: 12840002
36. Data describe a 17 residue fragment from SMRT that binds to the BCL6 BTB domain, and report the crystal structure of the complex to 2.2 angstroms. PMID: 14690607
37. Elevated SMRT levels are common in prostate cancer cells, resulting in suppression of target genes associated with antiproliferative action. PMID: 15300237
38. SMRTbeta expression may influence the binding and transcriptional capacities of nuclear receptors in tumor cells (SMRTbeta) PMID: 15319284
39. differential mRNA splicing of SMRT serves to customize corepressor function in different cells, allowing the transcriptional properties of nuclear receptors to be adapted to different contexts PMID: 15632172
40. No significant allelic/genotypic association between any of the five mutations in SMRT/N-CoR2 and bipolar phenotype and the CAG repeat did not demonstrate allelic instability. PMID: 15635693
41. the subnuclear positioning of SMRT is influenced by the ligand-bound ERalpha, and this activity is dependent on the ratio of the co-expressed ERalpha and SMRT PMID: 15713534
42. TRAC-1 (T cell RING protein identified in activation screen)is the first E3 ubiquitin ligase that serves a positive regulatory role in T cell activation. PMID: 15843525
43. The aryl hydrocarbon receptor activates the retinoic acid receptoralpha through SMRT antagonism PMID: 16480812
44. expression of the silencing mediator of retinoid and thyroid receptor (SMRT) & histone deacetylase4 (HDAC4) enhances formation of Bach2 foci in nuclear matrix. SMRT mediates HDAC4 binding to Bach2, & HDAC4 facilitates retention of Bach2 in the foci. PMID: 17383980
45. NCOR2/SMRT is associated with poor patient outcome in breast cancer PMID: 17902051
46. These results would shed new insights for the molecular mechanisms of PML-RARalpha-associated leukemogenesis. PMID: 17991421
47. CD40 signaling rapidly disrupts the ability of BCL6 to recruit the SMRT corepressor complex by excluding it from the nucleus, leading to histone acetylation, RNA polymerase II processivity, and activation of BCL6 target genes PMID: 18487509
48. SMRT protein stability is regulated by Pin1 and Cdk2. PMID: 18838553
49. Activated MEK signaling cascade inhibits functional recruitment of corepressor SMRT to cyproterone acetate-bound AR in prostate cancer cells. PMID: 19223455
50. SMRT function restoration induces JAG2 down-regulation as well as multipe myeloma apoptosis. PMID: 19417136

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HGNC: 7673

OMIM: 600848

KEGG: hsa:9612

STRING: 9606.ENSP00000384018

UniGene: Hs.137510