Use your antibodies-online credentials, if available.
Keine Produkte auf Ihrer Vergleichsliste.
Ihr Warenkorb ist leer.
Weitere Synonyme anzeigen
Wählen Sie die gewünschte Spezies
loss-of-function mutation (crb) in bmyb causes defects in mitotic progression and spindle formation and genome instability in embryos, and cancer susceptibility in adult crb heterozygotes
Downregulation of B-myb induced senescence by upregulation of p22(phox (zeige CYBA Proteine)) and activation of the ROS (zeige ROS1 Proteine)/p53 (zeige TP53 Proteine)/p21 pathway
B-myb is an essential regulator of hematopoietic stem cell and myeloid progenitor cell development.
MYBL2 haploinsufficiency increases susceptibility to age-related haematopoietic neoplasia.
Results coupled with functional studies demonstrate that B-MYB not only controls and accelerates cell cycle progression in ESCs (zeige NR2E3 Proteine) it contributes to fate decisions and maintenance of pluripotent stem cell identity.
Our data suggest that B-Myb is required as a pioneer factor to enable FoxM1 (zeige FOXM1 Proteine) binding to G2/M gene promoters and explains how these transcription factors may collaborate to induce mitosis.
Mybl2 upregulation induces fast growth and progression of premalignant and malignant liver, through cell cycle deregulation and activation of genes and pathways related to tumor progression.
The transcription factor B-Myb is maintained in an inhibited state in target cells through its interaction with the nuclear corepressors N-CoR and SMRT.
Results describe the characterization of a corepressor site (downstream repression site (DRS (zeige SRPX Proteine))) required for transcriptional regulation of the B-myb (MybL2 gene) promoter.
B-Myb repressor function is regulated by cyclin A phosph (zeige CCNA2 Proteine)orylation and sequences within the C-terminal domain.
B-Myb has a role in regulation of c-Myc (zeige MYC Proteine) expression by cytosolic phospholipase A2 (zeige PLA2G4A Proteine)
B-Myb is an independent prognostic marker and serves as a potential target in the diagnosis and/or treatment of NSCLC, and that B-Myb functions as a tumor-promoting gene by targeting IGFBP3 (zeige IGFBP3 Proteine) in NSCLC cells.
MYBL2 is a key downstream factor of Akt (zeige AKT1 Proteine)/FoxM1 (zeige FOXM1 Proteine) signaling to promote progression of human glioma, and could be a new candidate gene for molecular targeting therapy and biomarker for radiotherapy of glioma.
These results suggested that overexpression of MYBL2 might serve as a novel prognostic biomarker in pancreatic ductal adenocarcinoma patients
A total of 41 differentially expressed genes, such as SOCS3 (zeige SOCS3 Proteine), VAPA (zeige VAPA Proteine), and COL5A2 (zeige COL5A2 Proteine), are speculated to have roles in the pathogenesis of acute myocardial infarction; 2 transcription factors FOXO3 (zeige FOXO3 Proteine) and MYBL2, and 2 miRNAs hsa (zeige CD24 Proteine)-miR (zeige MLXIP Proteine)-21-5p and hsa (zeige CD24 Proteine)-miR (zeige MLXIP Proteine)-30c-5p may be involved in the regulation of the expression of these differentially expressed genes.
Results suggested that the oncogenic transcription factor HIF-2alpha (zeige EPAS1 Proteine) stabilized VHL (zeige VHL Proteine) disease suppressor B-Myb, which is also a transcription factor, by physical interaction. Some B-Myb-dependent gene expression was similarly affected by B-Myb or HIF-2alpha (zeige EPAS1 Proteine) knockdown, suggesting that stabilization of B-Myb by HIF-2alpha (zeige EPAS1 Proteine) may play a role in specific gene expressions.
The MuvB multiprotein complex, together with B-MYB and FOXM1 (zeige FOXM1 Proteine) (MMB-FOXM1 (zeige FOXM1 Proteine)) regulate the expression of mitotic kinesins in breast cancer cells.
MYBL2 overexpression promotes Gallbladder Cancer cell proliferation through the regulation of the cell cycle at the S and G2/M phase transitions. Thus, MYBL2 could serve as a potential prognostic and therapeutic biomarker in Gallbladder Cancer patients.
Study identified B-Myb as a substrate of the pVHL (zeige VHL Proteine) ubiquitin ligase complex, which targets it for degradation via the ubiquitin-proteasome pathway. It also, provide evidence that the regulation of B-Myb by pVHL (zeige VHL Proteine) plays a critical role in von Hippel-Lindau disease.
Data indicate that gene expression alterations in endometrial carcinoma samples with high ATAD2 (zeige ATAD2 Proteine) expression showed upregulation of several cancer-related genes including B-MYB gene.
We found that B-Myb upregulated expression of the key epithelial-to-mesenchymal transition regulator snail (zeige SNAI1 Proteine) and that it mediated epithelial-to-mesenchymal transition activation and cell invasion by B-Myb.
B-Myb (MYBL2)repressor function is regulated by cyclin A (zeige CCNA2 Proteine) phosphorylation and sequences within the C-terminal domain.
B-Myb represses SMC (zeige DYM Proteine) elastin (zeige ELN Proteine) gene expression and cyclin A (zeige CCNA2 Proteine) plays a role in the developmental regulation of elastin (zeige ELN Proteine) gene expression in the aorta
The protein encoded by this gene, a member of the MYB family of transcription factor genes, is a nuclear protein involved in cell cycle progression. The encoded protein is phosphorylated by cyclin A/cyclin-dependent kinase 2 during the S-phase of the cell cycle and possesses both activator and repressor activities. It has been shown to activate the cell division cycle 2, cyclin D1, and insulin-like growth factor-binding protein 5 genes. Transcript variants may exist for this gene, but their full-length natures have not been determined.
v-myb myeloblastosis viral oncogene homolog (avian)-like 2
, myb-related protein B
, v-myb myeloblastosis viral oncogene homolog-like 2
, myb-like protein 2
, myb-related protein 1
, myeloblastosis oncogene-like 2