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The various novel mechanisms are described by which Dab2 mediates an array of signaling events with vast physiological consequences.
In conclusion, DAB2 and Intelectin-1 (show ITLN1 ELISA Kits) are newly identified positive markers of mesothelioma and have potential to be included in future immunohistochemical marker panels for differentiation of epithelioid mesothelioma from pulmonary adenocarcinoma
cathepsin B (CTSB (show CTSB ELISA Kits)) inhibition or expression of a CTSB (show CTSB ELISA Kits)-resistant Dab2 mutant maintains Dab2 expression and shifts long-term TGF-beta (show TGFB1 ELISA Kits)-treated cells from autophagy to apoptosis
abundances of megalin (show LRP2 ELISA Kits) and Dab2 (p = 0.046) were reduced in infected placentas from women with LBW deliveries
Data show that miR106b was frequently up-regulated in human cervical carcinoma tumors and cell lines and inversely correlated with DAB2 expression. Its regulation in under TGF-beta1 (show TGFB1 ELISA Kits) which contributes to cell migration by targeting DAB2 in cervical carcinoma.
these findings reveal that DAB2 is critical for controlling inflammatory signaling during phenotypic polarization of macrophages
inhibition of WNT (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) signaling by DAB2 is essential for establishing the correct number of cardiomyocytes in the developing heart.
DAB2 regulated the cell migration associated genes in PC3 (show PCSK1 ELISA Kits) cells, and the differential DAB2 expression between LNCaP and PC3 (show PCSK1 ELISA Kits) cells was partly regulated by histone 4 acetylation.
Dab2 depletion also increases the rescued protein half-life of DeltaF508 CFTR (show CFTR ELISA Kits) by ~18% and ~91%, respectively
These results indicated that miR (show MLXIP ELISA Kits)-93 plays an important role in the initiation and progression of NPC (show NPC1 ELISA Kits) by targeting Dab2 and the miR (show MLXIP ELISA Kits)-93/Dab2 pathway may contribute to the development of novel therapeutic strategies for NPC (show NPC1 ELISA Kits) in the future.
The combination of Arh (show LDLRAP1 ELISA Kits) and Dab2 is responsible for the majority of adaptor function in LDLR (show LDLR ELISA Kits) endocytosis and LDLR (show LDLR ELISA Kits)-mediated cholesterol homeostasis.
Results identified a novel activation marker, DAB2, which expression is significantly different between microglia activation stages M2a and either M1 or M2b.
Dab2 expression is induced by hormones
Results suggest that endogenous Dab2 exacerbates central nervous system inflammation, potentially acting to up-regulate reactive oxygen species expression in macrophages and microglia, and that it is of potential pathogenic relevance in multiple sclerosis
Disabled-2 is required for efficient hemostasis and platelet activation by thrombin (show F2 ELISA Kits) in mice.
Akt1 (show AKT1 ELISA Kits) and Akt2 (show AKT2 ELISA Kits) are involved in albumin (show ALB ELISA Kits) endocytosis, and phosphorylation of Dab2 by Akt (show AKT1 ELISA Kits) induces albumin (show ALB ELISA Kits) endocytosis in proximal tubule epithelial cells.
Study of dab2 mutant allele in embryos and embryoid bodies confirms a role for Dab2 in extraembryonic endoderm development and epithelial organization. Also, Dab2 has a physiological role in the endocytosis of lipoproteins and cholesterol metabolism.
Exposure to follicular fluid transiently increased the transcript levels of IL8 (show IL8 ELISA Kits) and PTGS2 (show PTGS2 ELISA Kits), and decreased the expression of SOD2 (show SOD2 ELISA Kits), GPX3 (show GPX3 ELISA Kits), DAB2, and NR3C1 (show NR3C1 ELISA Kits). TNF (show TNF ELISA Kits) and IL6 (show IL6 ELISA Kits) levels were also decreased while those of NAMPT (show NAMPT ELISA Kits) were unaffected.
This gene encodes a mitogen-responsive phosphoprotein. It is expressed in normal ovarian epithelial cells, but is down-regulated or absent from ovarian carcinoma cell lines, suggesting its role as a tumor suppressor. This protein binds to the SH3 domains of GRB2, an adaptor protein that couples tyrosine kinase receptors to SOS (a guanine nucleotide exchange factor for Ras), via its C-terminal proline-rich sequences, and may thus modulate growth factor/Ras pathways by competing with SOS for binding to GRB2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
disabled homolog 2, mitogen-responsive phosphoprotein (Drosophila)
, disabled homolog 2
, disabled homolog 2, mitogen-responsive phosphoprotein
, disabled homolog 2-like
, differentially-expressed protein 2
, mitogen-responsive phosphoprotein
, DOC-2 p82 isoform
, disabled homolog 2 mitogen-responsive phosphoprotein