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Results show an essential role of NumbL during Xenopus primary neurogenesis and provide evidence for a Notch (show NOTCH1 Proteins)-independent function of NumbL.
NumbL can act as an independent tumor suppressor inhibiting the Notch (show NOTCH1 Proteins) pathway and regulating the cancer stem cell pool
let-7c inhibits Notch (show NOTCH1 Proteins) and progression markers but up-regulates Numbl in pancreatic cancer treated with quercetin
investigations revealed that NUMB (show NUMB Proteins) and NUMBL interacted with small GTPase (show RACGAP1 Proteins) Rab7 (show RAB7B Proteins) to transition ERBB2 (show ERBB2 Proteins) from early to late endosome for degradation.
These findings highlight the importance of Numb (show NUMB Proteins) and Numbl in the control of myoepithelial cell fate determination, epithelial identity, and lactogenesis
Numb/Numbl control VEGF receptor (show FLT1 Proteins) endocytosis, signaling, and recycling in endothelial cells, which promotes the angiogenic growth of blood vessels.
Numbl might be involved in the inhibition of growth, proliferation, and invasion of 95-D lung cancer cells.
Numbl-Klf4 (show KLF4 Proteins) signaling is critical to maintain multiple nodes of metastatic progression, including persistence of cancer-initiating cells.
data suggest that Numbl regulates glioma cell migration and invasion by abrogating TRAF5 (show TRAF5 Proteins)-induced activation of NF-KappaB (show NFKB1 Proteins)
NUMBL interacts with TRAF6 (show TRAF6 Proteins) and promotes the degradation of TRAF6 (show TRAF6 Proteins) in vivo, leading to the inhibition of NF-kappaB (show NFKB1 Proteins) signaling pathway.
Both gene sequence alterations and amplifications of LNX1 (show LNX1 Proteins) and Numbl are present in a subset of human gliomas.
investigations revealed that NUMB (show NUMB Proteins) and NUMBL interacted with small GTPase (show RACGAP1 Proteins) Rab7 (show RAB7A Proteins) to transition ERBB2 (show ERBB2 Proteins) from early to late endosome for degradation.
findings demonstrate that Nb and Nbl are intrinsic factors crucial for the renewal of CPCs in the PA2 and that the PA2 serves as a microenvironment for their expansion
By ablating Numb (show NUMB Proteins) and Numbl in different cardiac populations followed by lineage tracing, we determined that Numb (show NUMB Proteins) and Numbl in the second heart field are required for outflow tract (OFT) and atrioventricular septation and OFT alignment.
Concomitant but not separate ablation of Numb (show NUMB Proteins) and Numblike in the developing heart leads to increased Notch2 (show NOTCH2 Proteins) activity along with hypertrabeculation, reduced compaction, and ventricular septum defects.
Numbl is a physiologically relevant target of miR (show MLXIP Proteins)-34a in neural progenitor cells, allowing for enhanced Notch (show NOTCH1 Proteins) signaling and inhibition of neuronal differentiation.
the data demonstrate that Numb (show NUMB Proteins) and Numblike have evolved to acquire at least partially distinct functions.
mouse numb (show NUMB Proteins) and numblike play redundant but critical roles in maintaining neural progenitor cells during embryogenesis, by allowing their progenies to choose progenitor over neuronal fates
Numblike plays an essential role in the control of cortical morphogenesis, a process requiring precise regulation of neural progenitor cell proliferation, differentiation, and apoptosis.
Plays a role in the process of neurogenesis. Required throughout embryonic neurogenesis to maintain neural progenitor cells, also called radial glial cells (RGCs), by allowing their daughter cells to choose progenitor over neuronal cell fate. Not required for the proliferation of neural progenitor cells before the onset of embryonic neurogenesis. Also required postnatally in the subventricular zone (SVZ) neurogenesis by regulating SVZ neuroblasts survival and ependymal wall integrity. Negative regulator of NF-kappa-B signaling pathway. The inhibition of NF- kappa-B activation is mediated at least in part, by preventing MAP3K7IP2 to interact with polyubiquitin chains of TRAF6 and RIPK1 and by stimulating the 'Lys-48'-linked polyubiquitination and degradation of TRAF6 in cortical neurons.
, numb-like protein
, numb-related protein