Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
Show all synonyms
Select your origin of interest
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.
Here, we review the role and effects of ACE2 (show ACE2 Proteins), ACE2 (show ACE2 Proteins) activators, Ang-(1 (show ANGPT1 Proteins)-7) and synthetic Mas receptor agonists in the control of inflammation and fibrosis in cardiovascular and renal diseases and as counter-regulators of the ACE (show ACE Proteins)-Ang II (show AGT Proteins)-AT1 (show AGTR1 Proteins) axis.
Downregulation of ACE2 (show ACE2 Proteins)/Ang-(1 (show ANGPT1 Proteins)-7)/Mas axis stimulates breast cancer metastasis through the activation of store-operated calcium entry and PAK1 (show PAK1 Proteins)/NF-kappaB (show NFKB1 Proteins)/Snail1 (show SNAI1 Proteins) pathways.
These results indicated that angiotensin-(1-7)/ACE2 (show ACE2 Proteins)/Mas axis may reduce liver lipid accumulation partly by regulating lipid-metabolizing genes through ATP/P2 receptor/CaM (show CALM1 Proteins) signaling pathway.
Ang-(1 (show ANGPT1 Proteins)-7) downregulated AT1R (show AGTR1 Proteins) mRNA, upregulated mRNA levels of Ang II (show AGT Proteins) type 2 receptor (AT2R (show AGTR2 Proteins)) and Mas receptor (MasR) and p38-MAPK (show MAPK14 Proteins) 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 Proteins)/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 Proteins)/Ang-(1 (show ANGPT1 Proteins)-7)/Mas axis protected against pulmonary fibrosis by inhibiting the MAPK (show MAPK1 Proteins)/NF-kappaB (show NFKB1 Proteins) pathway.
A proximal promoter construct for the MAS gene was repressed by the SOX (show PIPOX Proteins) [SRY (show SRY Proteins) (sex-determining region on the Y chromosome) box] proteins SRY (show SRY Proteins), SOX2 (show SOX2 Proteins), SOX3 (show SOX3 Proteins) and SOX14 (show SOX14 Proteins), of which SRY (show SRY Proteins) 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
Results suggest that angiotensin converting enzyme 2 (show ACE2 Proteins) may reduce anxiety-like behavior by activating central Mas receptor that facilitate GABA release onto pyramidal neurons within the basolateral amygdala.
impairment of the ANG-(1 (show ANGPT1 Proteins)-7)/Mas receptor pathway may lead to worsening of the pathophysiological changes of asthma.
The data indicate a significant function of Ang-(1 (show ANGPT1 Proteins)-7) in the regulation of insulin (show INS Proteins) secretion from mouse islets in vitro and in vivo, mainly, but not exclusively, by Mas-dependent signaling, modulating the accessory pathway of insulin (show INS Proteins) secretion via increase in cAMP.
This study suggests that deletion of AT2R decreases the expression of the beneficial ACE2/Ang-(1-7)/MasR.
Ang-(1 (show ANGPT1 Proteins)-7)/Mas axis seems more important in autonomic modulation of arterial pressure than heart rate.
Mas receptor mediates cardioprotection of angiotensin-(1-7) against Ang II (show AGT Proteins)-induced cardiomyocyte autophagy and cardiac remodelling through inhibition of oxidative stress.
MAS receptors mediate vasoprotective and atheroprotective effects of candesartan upon the recovery of vascular ACE2 (show ACE2 Proteins)-angiotensin-(1-7)-MAS axis functionality
Mas receptor deficiency results in exacerbated inflammation in LPS (show TLR4 Proteins)-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 Proteins).
a Mas receptor-mediated mechanism may stimulate pancreatic cell development
Hydronephrosis led to an increase of ACE (show ACE Proteins) level and a decrease of ACE2 (show ACE2 Proteins) and Mas receptor in the heart.
oncogene\; may be involved in function or development of neural tissues
, proto-oncogene Mas
, MAS proto-oncogene
, angiotensin-(1-7) receptor