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S1PR3 encodes a member of the EDG family of receptors, which are G protein-coupled receptors. Additionally we are shipping S1PR3 Kits (19) and S1PR3 Proteins (6) and many more products for this protein.
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in breast cancer cells overexpression of S1P3 and its activation by S1P (show MBTPS1 Antibodies) has pro-inflammatory and pro-metastatic potential by inducing COX-2 (show COX2 Antibodies) expression and PGE2 signaling via EP2 (show SPAG11B Antibodies) and EP4 (show PTGER4 Antibodies).
S1PR1 (show S1PR1 Antibodies)/3 silencing alters proliferation, adhesion, viability and lateral motility in estrogen receptor (show ESR1 Antibodies)-negative MCF-7 and estrogen receptor (show ESR1 Antibodies)-positive MDA-MB-231 breast cancer cells.
High S1PR3 expression is associated with increased lung adenocarcinoma.
The S1P1,3 activation results in Akt (show AKT1 Antibodies) phosphorylation and subsequent activation of eNOS (show NOS3 Antibodies) via phosphorylation at serine(1177) and dephosphorylation at threonine(495).
HDL (show HSD11B1 Antibodies)-associated ApoM (show APOM Antibodies) is anti-apoptotic by delivering sphingosine 1-phosphate to S1P1 (show S1PR1 Antibodies) and S1P3 receptors on vascular endothelium.
The study shows that S1P receptor 3 (S1PR3) mRNA is overexpressed in EBV-positive NPC (show NPC1 Antibodies) patient-derived xenografts and a subset of primary NPC (show NPC1 Antibodies) tissues, and that knockdown of S1PR3 suppressed the activation of AKT (show AKT1 Antibodies) and the S1P (show MBTPS1 Antibodies)-induced migration of NPC (show NPC1 Antibodies) cells.
S1pr3 promotes leukocyte rolling by mobilization of endothelial P-selectin (show SELP Antibodies).
Stimulation with sphingosine-1-phosphate enhances cancer stem cells via S1PR3 and subsequent Notch1 (show NOTCH1 Antibodies) activation.
TRPC1 (show TRPC1 Antibodies) functions as a major regulator of S1P3 and VEGFR2 (show KDR Antibodies) expression.
Data show that sphingosine kinase SphK1 (show SPHK1 Antibodies) and sphingosine-1-phosphate (S1P (show MBTPS1 Antibodies)) receptors S1P1 (show S1PR1 Antibodies), S1P2 (show S1PR2 Antibodies), S1P3, and S1P5 (show S1PR5 Antibodies) were expressed from primary, up to recurrent and secondary glioblastomas, with sphingosine kinase SphK2 (show SPHK2 Antibodies) levels were highest in primary tumors.
S1P3 deletion protects mouse soleus from age-related drop in muscle mass, force, and regenerative capacity.
The finding that S1P3 receptor- and Galpha13 (show GNA13 Antibodies)-mediated RhoA (show RHOA Antibodies) activation is responsible for protection against ischemia/reperfusion suggests that selective targeting of S1P3 receptors could provide therapeutic benefits in ischemic heart disease.
The role of the S1PR3/PDGFR-beta (show PDGFRB Antibodies)/Akt (show AKT1 Antibodies) pathway in sphingosine-1-phosphate -induced endothelial progenitor cells migration and angiogenesis
P2RY8 promotes clustering of activated B cells within follicles in a follicular dendritic cell (FDC)-dependent manner.
Smad3 (show SMAD3 Antibodies) deficiency leads to mandibular condyle degradation via the sphingosine 1-phosphate (S1P (show S1PR1 Antibodies))/S1P3 signaling axis
CTGF (show CTGF Antibodies) exerts profibrotic action in myoblasts via the up-regulation of sphingosine kinase-1 (show SPHK1 Antibodies)/S1P3 signaling axis in TGF-beta (show TGFB1 Antibodies) dependent manner.
results indicate that S1P3 receptor signaling plays an important role in pulmonary inflammation and fibrosis and that this signaling occurs via CTGF (show CTGF Antibodies) expression
key role of Sphk1 (show SPHK1 Antibodies), S1PR1 (show S1PR1 Antibodies) and S1PR3 in angiogenesis underlying the liver fibrosis process
Data show that two S1P (show S1PR1 Antibodies) receptors, S1P2 (show S1PR2 Antibodies) and S1P3, are collectively essential mediators of eyelid closure during murine development.
This gene encodes a member of the EDG family of receptors, which are G protein-coupled receptors. This protein has been identified as a functional receptor for sphingosine 1-phosphate and likely contributes to the regulation of angiogenesis and vascular endothelial cell function.
sphingosine-1-phosphate receptor 3
, sphingosine 1-phosphate receptor 3-like
, G protein-coupled receptor, endothelial differentiation gene-3
, S1P receptor 3
, S1P receptor EDG3
, S1P receptor Edg-3
, endothelial differentiation G-protein coupled receptor 3
, endothelial differentiation, sphingolipid G-protein-coupled receptor, 3
, sphingosine 1-phosphate receptor 3
, sphingosine 1-phosphate receptor Edg-3
, S1p receptor 3
, endothelial differentiation sphingolipid G-protein-coupled receptor 3
, lysophospholipid receptor B3