Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase. - Wikidata - wikimedia - TriplyDB

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

http://www.wikidata.org/entity/Q33911448

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ATP1A2 Mutations in Migraine: Seeing through the Facets of an Ion Pump onto the Neurobiology of Disease Specialized Functional Diversity and Interactions of the Na,K-ATPase Cardiotonic Steroids as Modulators of Neuroinflammation Crystal structure of the high-affinity Na+,K+-ATPase-ouabain complex with Mg2+ bound in the cation binding site Regulation of Cardiac Remodeling by Cardiac Na(+)/K(+)-ATPase Isoforms Natriuretic hormone: the ultimate determinant of the preservation of external sodium balance Novel stereoselective bufadienolides reveal new insights into the requirements for Na(+), K(+)-ATPase inhibition by cardiotonic steroids Sodium potassium adenosine triphosphatase (Na/K-ATPase) as a therapeutic target for uremic cardiomyopathy.Cardiac Glycosides Activate the Tumor Suppressor and Viral Restriction Factor Promyelocytic Leukemia Protein (PML)Cellular Na+ handling mechanisms involved in airway smooth muscle contraction (Review)Spherical Oligo-Silicic Acid SOSA Disclosed as Possible Endogenous Digitalis-Like Factor.Explaining intraspecific diversity in plant secondary metabolites in an ecological context.Structures and characterization of digoxin- and bufalin-bound Na+,K+-ATPase compared with the ouabain-bound complex Widespread convergence in toxin resistance by predictable molecular evolution Digoxin derivatives with selectivity for the α2β3 isoform of Na,K-ATPase potently reduce intraocular pressure.Importance of the Voltage Dependence of Cardiac Na/K ATPase Isozymes.Probing the regiospecificity of enzyme-catalyzed steroid glycosylation.Epi-reevesioside F inhibits Na+/K+-ATPase, causing cytosolic acidification, Bak activation and apoptosis in glioblastoma Arenobufagin intercalates with DNA leading to G2 cell cycle arrest via ATM/ATR pathway.Hellebrin and its aglycone form hellebrigenin display similar in vitro growth inhibitory effects in cancer cells and binding profiles to the alpha subunits of the Na+/K+-ATPase Cardiac glycosides display selective efficacy for STK11 mutant lung cancer.Ouabain-induced internalization and lysosomal degradation of the Na+/K+-ATPase.Digoxin-induced retinal degeneration depends on rhodopsin.Functional characterization of drug uptake and metabolism in the heart.Modulators of Na/K-ATPase: a patent review.A perspective on re-evaluating digoxin's role in the current management of patients with chronic systolic heart failure: targeting serum concentration to reduce hospitalization and improve safety profile.Metal fluoride complexes of Na,K-ATPase: characterization of fluoride-stabilized phosphoenzyme analogues and their interaction with cardiotonic steroids.Cardiac glycosides induced toxicity in human cells expressing α1-, α2-, or α3-isoforms of Na-K-ATPase.Modulation of cell polarization by the Na+-K+-ATPase-associated protein FXYD5 (dysadherin).Na⁺i,K⁺i-Dependent and -Independent Signaling Triggered by Cardiotonic Steroids: Facts and Artifacts.Na/K Pump and Beyond: Na/K-ATPase as a Modulator of Apoptosis and Autophagy.Neutral phospholipids stimulate Na,K-ATPase activity: a specific lipid-protein interaction.Stabilization of the α2 isoform of Na,K-ATPase by mutations in a phospholipid binding pocket.Digitoxin analogues with improved anticytomegalovirus activity.Comparison of Digitalis Sensitivities of Na+/K+-ATPases from Human and Pig Kidneys.Time- and dose dependent actions of cardiotonic steroids on transcriptome and intracellular content of Na+ and K+: a comparative analysis.A structural view on the functional importance of the sugar moiety and steroid hydroxyls of cardiotonic steroids in binding to Na,K-ATPase.Istaroxime stimulates SERCA2a and accelerates calcium cycling in heart failure by relieving phospholamban inhibition.C5'-Alkyl Substitution Effects on Digitoxigenin α-l-Glycoside Cancer Cytotoxicity.Selective Assembly of Na,K-ATPase α2β2 Heterodimers in the Heart: DISTINCT FUNCTIONAL PROPERTIES AND ISOFORM-SELECTIVE INHIBITORS.

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P2860

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

http://www.wikidata.org/entity/Q33911448

description

2010 nî lūn-bûn

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2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

@ast

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

@en

type

label

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

@ast

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

@en

prefLabel

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

@ast

Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

@en

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JBC.M110.119248

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Journal of Biological Chemistry

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Selectivity of digitalis glycosides for isoforms of human Na,K-ATPase.

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Adriana Katz

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Daniel M Tal

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Einat Kapri-Pardes

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Elizabeta Bab-Dinitz

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Rivka Goldshleger

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Steven J D Karlish

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Yael Lifshitz

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P2860

Transport and pharmacological properties of nine different human Na, K-ATPase isozymes

All human Na(+)-K(+)-ATPase alpha-subunit isoforms have a similar affinity for cardiac glycosides

Crystal structure of the sodium-potassium pump at 2.4 A resolution

Crystal structure of the sodium-potassium pump (Na+,K+-ATPase) with bound potassium and ouabain

Differentiation between isoforms of Na+/K+-transporting atpase from human and guinea-pig muscle through use of digitalis derivatives as analytical probes.

Structure-activity relationships for the hypertensinogenic activity of ouabain: role of the sugar and lactone ring.

Ouabain, a steroid hormone that signals with slow calcium oscillations.

Digoxin and reduction in mortality and hospitalization in heart failure: a comprehensive post hoc analysis of the DIG trial.

Endogenous cardiotonic steroids: physiology, pharmacology, and novel therapeutic targets.

Na+ pump low and high ouabain affinity alpha subunit isoforms are differently distributed in cells

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10.1074/JBC.M110.119248

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25

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285

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20388710

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2885237

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