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HES5 encodes a member of a family of basic helix-loop-helix transcriptional repressors. Additionally we are shipping HES5 Proteins (5) and many more products for this protein.
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Over-expression of her12, her15 or her7 disrupts cyclic gene expression and somite border formation, and structure function analysis of Her7 indicates that DNA binding, but not Groucho-recruitment seems to be important in this process.
that suppression of the HES5 leading to inhibition of proliferation may be one of the mechanisms against Hepatocellular carcinoma
HES5 silencing is an early and recurrent change in prostate tumourigenesis
these data identify HES5 as a key mediator of the Wnt-3a (show WNT3A Antibodies) proneurogenic effect occurring independently of the classical Wnt (show WNT2 Antibodies)/beta-catenin (show CTNNB1 Antibodies) signaling cascade thus further deciphering crosstalk mechanisms of Wnt (show WNT2 Antibodies) and Notch (show NOTCH1 Antibodies) signaling pathways regulating cell fate
the downstream Notch (show NOTCH1 Antibodies) signalling effector HES5 directly represses transcription of the E3 ligase Fbw7beta.
Notch3 (show NOTCH3 Antibodies) and Hes5 are hypermethylated in human B cell acute lymphoblastic leukemia (ALL).
Hes5 overactivation is associated with cell differentiation, thereby resulting in uterine carcinogenesis.
In this study, HES 5 transcription factor was detected in the lining epithelium of human periapical cysts with limited inflammation, showing Notch (show NOTCH1 Antibodies) pathway activation in those cells.
The expression of HES5 in adenocarcinoma was significantly higher than those in adenoma and normal control
For marking and purifying neural stem cells to ascertain whether differences exist, we generated transgenic mice using promoters from Hes (show RRBP1 Antibodies) genes (pHes1 or pHes5) to drive expression of destabilized enhanced green fluorescent protein.
Notch protein binding to Hes5-GFP is extinguished fast and recovered slowly, whereas Hes1-GFP is inhibited late and recovered quickly
This study demonstrated that Hes1 and Hes5 modulate not only maintenance of progenitor cells but also pituicyte versus neuron fate specification during neurohypophysis development.
delivery of siRNA to Hes1 and Hes5 using a transfection reagent or siRNA to Hes1 encapsulated within nanoparticles increased hair cell numbers in non-toxin treated organotypic cultures of cochleae and maculae
The transcription and expression patterns of Notch (show NOTCH1 Antibodies) pathway components (Notch 1 (show NOTCH1 Antibodies)-3, Delta1 and 4, Jagged1 (show JAG1 Antibodies)) and effectors (Hes1, Hes2 (show HES2 Antibodies), Hes5 and Nrarp (show NRARP Antibodies)) were evaluated in the mouse testis
Hes1 and Hes5 regulate vascular remodeling and arterial fate specification of endothelial cells in the development of the brain; they are critical transducers of Notch (show NOTCH1 Antibodies) signals in brain vascular development.
Data demonstrate that Hes5 levels in the utricle decreased after the application of siRNA and that the number of hair cells in these utricles was significantly larger than following control treatment.
Epigenetic silencing of Hes5 leads to neuronal differentiation despite active Notch (show NOTCH1 Antibodies) signaling.
Simultaneous overexpression of Hes5 and Sox21 (show SOX21 Antibodies) reveals Hes5 as a downstream effector of Sox21 (show SOX21 Antibodies) in adult hippocampus neurogenesis.
This study suggested that Hes5 expression is serially activated first by Gcms and later by the canonical Notch (show NOTCH1 Antibodies) pathway
Hes1, Hes5 and Hey1 (show HEY1 Antibodies) cooperatively inhibit hair cell formation, and one allele of Hes1, Hes5 or Hey1 (show HEY1 Antibodies) is sufficient for supporting cell (show PTPRJ Antibodies) production probably by lateral inhibition in the sensory epithelium.
This gene encodes a member of a family of basic helix-loop-helix transcriptional repressors. The protein product of this gene, which is activated downstream of the Notch pathway, regulates cell differentiation in multiple tissues. Disruptions in the normal expression of this gene have been associated with developmental diseases and cancer.
hairy and enhancer of split 5
, transcription factor HES-5
, Transcription factor HES-5
, class B basic helix-loop-helix protein 38