to edit your profile (add a photo, awards, links to other websites, etc.)
Edit My Profile
My Person List (
Return to Top
Search Result Details
Back to Search Results
This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to
Angiotensin-(1-7) inhibits growth of cardiac myocytes through activation of the mas receptor.
Mineralocorticoid receptor blockade attenuates chronic overexpression of the renin-angiotensin-aldosterone system stimulation of reduced nicotinamide adenine dinucleotide phosphate oxidase and cardiac remodeling.
Localization of the novel angiotensin peptide, angiotensin-(1-12), in heart and kidney of hypertensive and normotensive rats.
Regulation of ACE2 in cardiac myocytes and fibroblasts.
Uptake and metabolism of the novel peptide angiotensin-(1-12) by neonatal cardiac myocytes.
Chymase-dependent generation of angiotensin II from angiotensin-(1-12) in human atrial tissue.
Cardiac angiotensin-(1-7) in ischemic cardiomyopathy.
Renin inhibition and AT(1)R blockade improve metabolic signaling, oxidant stress and myocardial tissue remodeling.
Chymase mediates injury and mitochondrial damage in cardiomyocytes during acute ischemia/reperfusion in the dog.
Modulation of cardiac L-type Ca2+ current by angiotensin-(1-7): normal versus heart failure.
Cardiomyocyte-specific deletion of the G protein-coupled estrogen receptor (GPER) leads to left ventricular dysfunction and adverse remodeling: A sex-specific gene profiling analysis.
Cellular basis of angiotensin-(1-7)-induced augmentation of left ventricular functional performance in heart failure.
Inflammatory and mitochondrial gene expression data in GPER-deficient cardiomyocytes from male and female mice.
Vaso-Hormonal Mechanisms in Hypertension
Blunting of estrogen modulation of cardiac cellular chymase/RAS activity and function in SHR.
Critical role of the chymase/angiotensin-(1-12) axis in modulating cardiomyocyte contractility.
Estrogen modulates the differential expression of cardiac myocyte chymase isoforms and diastolic function.