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The objective of this study was to characterize the profiles of Ang-(1-7), MAS receptor, ACE(2), NEP and PEP during the ovulatory process in cattle.
Ang-(1 (show ANGPT1 ELISA Kits)-7) downregulated AT1R (show AGTR1 ELISA Kits) mRNA, upregulated mRNA levels of Ang II (show AGT ELISA Kits) type 2 receptor (AT2R (show AGTR2 ELISA Kits)) and Mas receptor (MasR) and p38-MAPK (show MAPK14 ELISA Kits) phosphorylation and suppressed H22 cell-endothelial cell communication
MAS1 might act as an inhibitory regulator of breast cancer.
Data show that MAS receptor exhibited constitutive activity that was inhibited by the non-peptide inverse agonist.
Data suggest that angiotensin converting enzyme 2 (show ACE2 ELISA Kits)/angiotensin II-(1-7)/MAS1 axis regulates leukocyte recruitment/activation, cell proliferation, and inflammation/fibrosis; main topic here is kidney/inflammatory renal disease. [REVIEW]
Up-regulation of the ACE2 (show ACE2 ELISA Kits)/Ang-(1 (show ANGPT1 ELISA Kits)-7)/Mas axis protected against pulmonary fibrosis by inhibiting the MAPK (show MAPK1 ELISA Kits)/NF-kappaB (show NFKB1 ELISA Kits) pathway.
A proximal promoter construct for the MAS gene was repressed by the SOX (show PIPOX ELISA Kits) [SRY (show SRY ELISA Kits) (sex-determining region on the Y chromosome) box] proteins SRY (show SRY ELISA Kits), SOX2 (show SOX2 ELISA Kits), SOX3 (show SOX3 ELISA Kits) and SOX14 (show SOX14 ELISA Kits), of which SRY (show SRY ELISA Kits) is known to interact with the KRAB domain.
Mas appears to be a critical component required for NO-mediated vasodilatation induced by renin angiotensin system-dependent and RAS-independent agonists and therefore arises as a key pharmacological target to modulate endothelial function
Control of adipogenesis by the autocrine interplays between angiotensin 1-7/Mas receptor and angiotensin II/AT1 receptor (show AGTRAP ELISA Kits) signaling pathways.
MasR was significantly upregulated in colon adenocarcinoma compared with non-neoplastic colon mucosa, which showed little or no expression of it. ACE (show ACE ELISA Kits) gene expression and enzymatic activity were also increased in the tumors.
Activation of Mas during myocardial infarction contributes to ischemia-reperfusion injury and suggest that inhibition of Mas-G(q) signaling may provide a new therapeutic strategy directed at cardioprotection.
MAS receptors mediate vasoprotective and atheroprotective effects of candesartan upon the recovery of vascular ACE2 (show ACE2 ELISA Kits)-angiotensin-(1-7)-MAS axis functionality
Mas receptor deficiency results in exacerbated inflammation in LPS (show TLR4 ELISA Kits)-challenged mice, which suggest a potential role for the Mas receptor as a regulator of systemic and brain inflammatory response induced by LPS (show TLR4 ELISA Kits).
a Mas receptor-mediated mechanism may stimulate pancreatic cell development
Hydronephrosis led to an increase of ACE (show ACE ELISA Kits) level and a decrease of ACE2 (show ACE2 ELISA Kits) and Mas receptor in the heart.
TGF-beta (show TGFB1 ELISA Kits) inhibits Mas receptor expression in fibroblasts but not in myoblasts or differentiated myotubes in animal model of muscular distrophy.
Deletion of the MasR causes marked increase in the aortic intima:media ratio, which is not due to generalized cellular proliferation.
The complete mouse Mas gene structure and organization.
Participation of AT1 (show SLC33A1 ELISA Kits) and Mas receptors in the modulation of inflammatory pain.
Klkb1 (show KLKB1 ELISA Kits)(-/-) mice have a novel mechanism for thrombosis protection in addition to reduced contact activation. This pathway arises when bradykinin delivery to vasculature is compromised and mediated by increased receptor Mas, prostacyclin, Sirt1 (show SIRT1 ELISA Kits), and KLF4 (show KLF4 ELISA Kits)
Ang-(1 (show ANGPT1 ELISA Kits)-7) counteracts the skeletal muscle atrophy induced by AngII through a mechanism dependent on the Mas receptor, which involves AKT (show AKT1 ELISA Kits) activity.
oncogene\; may be involved in function or development of neural tissues
, proto-oncogene Mas
, MAS proto-oncogene
, angiotensin-(1-7) receptor