NO-independent regulatory site on soluble guanylate cyclase.
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NO-independent stimulators and activators of soluble guanylate cyclase: discovery and therapeutic potentialNO-independent regulatory site of direct sGC stimulators like YC-1 and BAY 41-2272Ancient conserved domains shared by animal soluble guanylyl cyclases and bacterial signaling proteinsPlatelet-derived NO slows thrombus growth on a collagen type III surfaceComparison of the properties of the five soluble guanylyl cyclase subunits in Drosophila melanogaster.Is enhancing cGMP-PKG signalling a promising therapeutic target for heart failure with preserved ejection fraction?Breakthrough in heart failure with preserved ejection fraction: are we there yet?Cardiac endothelium-myocyte interaction: clinical opportunities for new heart failure therapies regardless of ejection fractionDrug treatment of pulmonary hypertension in childrenPAS-mediated Dimerization of Soluble Guanylyl Cyclase Revealed by Signal Transduction Histidine Kinase Domain Crystal StructureHeme-dependent and independent soluble guanylate cyclase activators and vasodilation.Effects of stimulation of soluble guanylate cyclase on diabetic nephropathy in diabetic eNOS knockout mice on top of angiotensin II receptor blockadeSpare guanylyl cyclase NO receptors ensure high NO sensitivity in the vascular systemDissociation of nitric oxide from soluble guanylate cyclase and heme-nitric oxide/oxygen binding domain constructsThe Concise Guide to PHARMACOLOGY 2013/14: enzymes.Thrombospondin-1 and angiotensin II inhibit soluble guanylyl cyclase through an increase in intracellular calcium concentration.Stimulation of soluble guanylyl cyclase inhibits mesangial cell proliferation and matrix accumulation in experimental glomerulonephritis.Vericiguat in patients with worsening chronic heart failure and preserved ejection fraction: results of the SOluble guanylate Cyclase stimulatoR in heArT failurE patientS with PRESERVED EF (SOCRATES-PRESERVED) studyProtective effects of YC-1 against glutamate induced PC12 cell apoptosis.Thrombospondin-1 is an inhibitor of pharmacological activation of soluble guanylate cyclase.Incorporation of tyrosine and glutamine residues into the soluble guanylate cyclase heme distal pocket alters NO and O2 binding.Nitric oxide/cGMP pathway signaling actively down-regulates α4β1-integrin affinity: an unexpected mechanism for inducing cell de-adhesion.YC-1 activation of human soluble guanylyl cyclase has both heme-dependent and heme-independent componentsDrugs of abuse and stress impair LTP at inhibitory synapses in the ventral tegmental area.Future prospects in the treatment of erectile dysfunction: focus on avanafil.Targeting soluble guanylate cyclase for the treatment of pulmonary hypertension.Pulmonary and systemic vasodilator responses to the soluble guanylyl cyclase stimulator, BAY 41-8543, are modulated by nitric oxide.Heme oxygenase-1 deficiency leads to alteration of soluble guanylate cyclase redox regulation.The anti-aggregating effect of BAY 41-2272, a stimulator of soluble guanylyl cyclase, requires the presence of nitric oxide.Oxidative stress impairs vasorelaxation induced by the soluble guanylyl cyclase activator BAY 41-2272 in spontaneously hypertensive rats.Activators of soluble guanylate cyclase for the treatment of male erectile dysfunction.Cellular targets of nitric oxide in the hippocampus.Nitric oxide donor drugs: current status and future trends.The soluble guanylate cyclase activator BAY 58-2667 protects against morbidity and mortality in endotoxic shock by recoupling organ systemsEffects of different pulmonary vasodilators on arterial saturation in a model of pulmonary hypertension.Involvement of beta 3-adrenergic receptor activation via cyclic GMP- but not NO-dependent mechanisms in human corpus cavernosum function.A Rho-kinase inhibitor, soluble guanylate cyclase activator and nitric oxide-releasing PDE5 inhibitor: novel approaches to erectile dysfunction.Soluble guanylate cyclase as an emerging therapeutic target in cardiopulmonary disease.Cardiovascular actions of a novel NO-independent guanylyl cyclase stimulator, BAY 41-8543: in vivo studiesPharmacological actions of a novel NO-independent guanylyl cyclase stimulator, BAY 41-8543: in vitro studies
P2860
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P2860
NO-independent regulatory site on soluble guanylate cyclase.
description
2001 nî lūn-bûn
@nan
2001 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի մարտին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年論文
@yue
2001年論文
@zh-hant
2001年論文
@zh-hk
2001年論文
@zh-mo
2001年論文
@zh-tw
2001年论文
@wuu
name
NO-independent regulatory site on soluble guanylate cyclase.
@ast
NO-independent regulatory site on soluble guanylate cyclase.
@en
type
label
NO-independent regulatory site on soluble guanylate cyclase.
@ast
NO-independent regulatory site on soluble guanylate cyclase.
@en
prefLabel
NO-independent regulatory site on soluble guanylate cyclase.
@ast
NO-independent regulatory site on soluble guanylate cyclase.
@en
P2093
P2860
P356
P1433
P1476
NO-independent regulatory site on soluble guanylate cyclase.
@en
P2093
Alonso-Alija C
Dembowsky K
Perzborn E
P2860
P2888
P304
P356
10.1038/35065611
P407
P577
2001-03-01T00:00:00Z
P6179
1049910466