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a putative membrane glycerophosphodiester phosphodiesterase\; may mediate lipid metabolism and G protein signaling [RGD, Feb 2006].. Additionally we are shipping GDE1 Antibodies (58) and GDE1 Kits (7) and many more products for this protein.
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Our outcomes suggest that miR (show MLXIP Proteins)-15a/16 maintain the retinal endothelial cell barrier by reducing TGFbeta3/VEGF (show VEGFA Proteins) signaling and increasing levels of key tight junction proteins.
The mRNA of TYRP1 (show TYRP1 Proteins) is now found to sequester the tumour suppressor miR-16.
we identified cyclin J and far upstream element-binding protein 1 (FUBP1 (show FUBP1 Proteins)) as novel miR-16 targets, which mediate miR-16 antiproliferative effects.
miR (show MLXIP Proteins)-15a/16 may function as a tumor suppressor in MM through multiple regulatory mechanisms
The expression levels of two target genes, Myb (show MYB Proteins) and VEGFR2 (show KDR Proteins), were affected significantly by miR-16, while glucose administration inhibited miR-16 expression and enhanced tumor cell proliferation and migration.
Quercetin decreases claudin-2 (show CLDN2 Proteins) expression mediated by up-regulation of miR-16 expression and instability of claudin-2 (show CLDN2 Proteins) mRNA in lung adenocarcinoma cells.
Our data indicate differential concentrations of plasma miR-16, miR (show MLXIP Proteins)-107, miR (show MLXIP Proteins)-130a and miR (show MLXIP Proteins)-146a in different breast cancer subtypes, suggesting a potential role of these miRs in breast cancer biology and tumor progression.
YAP1 (show YAP1 Proteins) was confirmed to be a functional target of miR (show MLXIP Proteins)-15a and miR-16-1 in GAC (show GLS Proteins).
miR-16 and miR (show MLXIP Proteins)-26a target checkpoint kinases Wee1 (show WEE1 Proteins) and Chk1 (show CHEK1 Proteins) in response to p53 (show TP53 Proteins) activation by genotoxic stress.
Up-regulation of miR-16 is associated with triple negative breast cancer.
The authors confirmed the role of Gde1 in NAFLD by in vivo hepatic over-expression and shRNA knockdown studies.
findings designate GroPSer as a previously unappreciated reservoir for free serine in the nervous system and suggest that GDE1, through recycling serine from GroPSer, may impact D-serine-dependent neural signaling processes in vivo
regulation by by stimulation of G protein-coupled receptors
a multistep pathway for the production of anandamide in the nervous system by the sequential actions of Abh4 (show ABHD4 Proteins) and GDE1.
a putative membrane glycerophosphodiester phosphodiesterase\; may mediate lipid metabolism and G protein signaling
RGS16-interacting membrane protein
, membrane interacting protein of RGS16
, membrane-interacting protein of RGS16