Protein BANP (BANP) Kits ELISA

Human Protein BANP (BANP) interaction partners

1. Cdc20 functions as an important negative regulator of SMAR1 in higher grades of cancer

2. Dysregulated circ-BANP appears to have an important role in colorectal cancer cells.

3. results reveal the complex molecular mechanism underlying SMAR1-mediated signal-dependent and -independent regulation of alternative splicing via Sam68 deacetylation

4. SMAR1-mediated regulation of repair and apoptosis via a complex crosstalk involving Ku70, HDAC6 and Bax.

5. Data indicate the role of SMAR1 protein in NF-kappaappa B dependent transcriptional regulation of pro-angiogenic chemokine interleukin-8 (IL-8).

6. indicate a crucial role for SMAR1 in restraining breast cancer cell migration and suggest the candidature of this scaffold matrix-associated region-binding protein as a tumor suppressor.

7. SMAR1 has a role in repressing c-Fos-mediated HPV18 E6 transcription through alteration of chromatin histone deacetylation

8. During hemin-induced erythroid differentiation, enhanced expression of SMAR1 negatively correlates with miR-320a expression.

9. TCF-4, beta-catenin, and SMAR1 tether at the -143-nucleotide site on the HIV LTR to inhibit HIV promoter activity.

10. Results indicate that SMAR1 is an important player in p300-p53 regulated DNA damage signalling pathway and can exert its effect on apoptosis in a transcription independent manner.

11. multiple roles of nuclear matrix associated protein SMAR1 in regulating various cellular target genes involved in cell growth, apoptosis and tumorigenesis.(REVIEW)

12. A novel mechanism of regulation of oxidative stress by ATM through modulation of SMAR1-AKR1a4 complex, is proposed.

13. SMAR1 plays a central role in coordinating p53 and TGFbeta pathways in human breast cancer.

14. report Prostaglandin A2 (PGA2) induced binding of HSP70 to a novel site on phi1 SMAR1 5' UTR which stabilizes the wild type transcript and leads to subsequent increase in SMAR1 protein levels.

15. On mild DNA damage, SMAR1 selectively represses BAX and PUMA through binding to the MAR independently of inducing p53 deacetylation through HDAC1.

16. Human breast cancer tissue sections that showed reduced SMAR1 expression exhibited increased surface roughness.

17. SMAR1 plays an important role in the regulation of T cell development as well as V(D)J recombination

18. SMAR1 regulates cyclin D1 by modification of chromatin through the SIN3/histone deacetylase 1 complex

19. tumor suppressor SMAR1 downregulates Cytokeratin 8 gene expression by modulating p53-mediated transactivation of this gene

20. tumor suppressor protein SMAR1 can modulate NF-kappaB transactivation and inhibit tumorigenesis by regulating NF-kappaB target genes

Mouse (Murine) Protein BANP (BANP) interaction partners

1. SMAR1 downregulation enhances the tumor killing effect of CD8+T cells by activating T-bet and down-regulating PD-1.

2. SMAR1 transgenic mice exhibited susceptibility to M. tuberculosis infection in vivo irrespective of genetic background. This susceptibility was attributed to downregulation of Th1 response and its hallmark cytokine IFN-gamma

3. This study reveals a critical role of SMAR1 in maintaining the proinflammatory immune responses by repressing Th1 and Th17 cell function and it gives the novel insight into immune regulatory mechanisms.

4. we report an essential role of the matrix attachment region (MAR)-binding protein SMAR1 in regulating immune response during allergic airway disease

5. SMAR1, a known transcription factor and tumor suppressor, is directly involved in maintaining regulatory T cell fate decision

6. Glucose deprivation can induce p53 internal ribosome entry sites (IRESs) and also increases cytoplasmic abundance of SMAR1 that in turn binds to p53 IRESs, indicating the role of SMAR1 in controlling translation of p53 isoforms.

7. combined action of Foxp3 and SMAR1 restricts effector cytokine production and enhance the production of IL-10 by colonic Treg cells that controls acute colitis

8. SMAR1 and p53 act synergistically to up-regulate GAD65 expression upon Streptozotocin treatment.

9. A novel mechanism of regulation of oxidative stress by ATM through modulation of SMAR1-AKR1a4 complex, is proposed.

10. C/EBPbeta may regulate preadipocyte proliferation through activation of banp and trim35.

11. TNFalpha mediated regulation of CD40 expression occurs by dual phosphorylation of SMAR1 and STAT1.

12. SMAR1 modulates the roughness of cell surface.

13. SMAR1-mediated stabilization of p53 is brought about by inhibiting Mdm2-mediated degradation of p53

14. A short SMAR1 peptide efficiently activates p53 protein by mediating its phosphorylation at serine 15, resulting in the activation of p21 and in effect regulating cell cycle checkpoint.