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High affinity receptor for urotensin-2 and urotensin-2B. 再加上，我们可以发Urotensin 2 Receptor 试剂盒 (7) 和 和数多这个蛋白质的别的产品。
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ligand-induced activation of the chemokine receptor CXCR4 (显示 CXCR4 抗体) and the urotensin 2 receptor UTS2R, triggers a marked reduction in the biogenesis of autophagosomes.
The role of Urotensin-II receptor in vasoconstriction and in the development of digestive tract cancers
UII (显示 UTS2 抗体)/GPR14 signaling was involved in the DSS (显示 NR0B1 抗体)-induced colonic inflammation and its inhibition may serve as a potential therapeutic target, which may be associated with the NF-kappaB (显示 NFKB1 抗体) signaling pathway.
Urotensin II (显示 UTS2 抗体) can induce the proliferation of BEL (显示 LHX2 抗体)-7402 cells via the urotensin receptor mediated PKC (显示 PRRT2 抗体)/ERK/p38 MAPK (显示 MAPK1 抗体) signaling pathways.
Report interaction of urantide with urotensin II receptor.
UTR protein and mRNA levels were increased in colon cancer cell lines and in colon adenoma and adenocarcinoma. UTR appears to be involved in the regulation of colon cancer cell invasion and motility.
High UTR expression is an independent prognostic factor of good prognosis for non muscle invasive bladder transitional cancer.
family-based analysis of association between blood pressure, glomerular filtration and genes of the urotensin-II (显示 UTS2 抗体) pathway (urotensin-II (显示 UTS2 抗体), urotensin-II related peptide, urotensin-II receptor) saturated with 28 tagging single nucleotide polymorphisms
Data suggest that UTS2R in aortic endothelium is involved in development of diabetes-associated atherosclerosis; diabetes-associated plaque development is attenuated by urotensin II (显示 UTS2 抗体)/UTS2R antagonism in in vitro setting.
Data show that vasoactive peptide urotensin II receptor and GABA(A)R are co-expressed in cerebellar glial cells from rat brain slices, in human native astrocytes and in glioma cell line.
UII (显示 UTS2 抗体)/UTR system plays a role in lipopolysaccharide (LPS (显示 TLR4 抗体))/D-galactosamine (GalN (显示 GAL 抗体))-induced acute liver failure.
findings demonstrate an important role for UII (显示 UTS2 抗体) in the pathogenesis of the metabolic syndrome and suggest that the use of UT receptor antagonists may provide a new therapeutic tool for the treatment of this syndrome
a new urotensin II receptor signalling pathway which is mediated by EGFR (显示 EGFR 抗体) trans-activation, dependent by beta-arrestin 1 (显示 ARRB1 抗体)/2, promoting cell survival and cardioprotection.
In addition to its role at the neuromuscular junction, urotensin II (显示 UTS2 抗体) may control motor function through the modulation of motoneuron activity within the spinal cord.
the up-regulation of vascular U-II (显示 UTS2 抗体) receptor (UT), GPR14 might be involved in the pathogenesis of atherosclerosis.
Elevated expression of Uts2r in skeletal muscle of diabetic mouse is repoted.
Urotensin II receptor knockout mice on an ApoE (显示 APOE 抗体) knockout background fed a high-fat diet exhibit an enhanced hyperlipidemic and atherosclerotic phenotype.
The role of urotensin 2 (显示 UTS2 抗体) and urotensin 2 (显示 UTS2 抗体) receptors in the skeletal muscle fat accumulation and fatty acid metabolism, thus indicating their potential pathological functions related to obesity and type 2 diabetes in humans.
High affinity receptor for urotensin-2 and urotensin-2B. The activity of this receptor is mediated by a G-protein that activate a phosphatidylinositol-calcium second messenger system.
urotensin 2 receptor
, G protein-coupled receptor
, urotensin II receptor
, urotensin-2 receptor
, G protein-coupled receptor 14
, G-protein coupled receptor 14
, G-protein coupled sensory epithelial neuropeptide-like receptor
, putative G protein-coupled receptor (SENR)
, urotensin receptor
, UT receptor