Characterization of right ventricular remodeling and failure in a chronic pulmonary hypertension model. - Wikidata - awgldk - TriplyDB

Characterization of right ventricular remodeling and failure in a chronic pulmonary hypertension model.

Characterization of right ventricular remodeling and failure in a chronic pulmonary hypertension model.

http://www.wikidata.org/entity/Q34356167

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Molecular Mechanisms of Pulmonary Vascular Remodeling in Pulmonary Arterial Hypertension Emerging Concepts in the Molecular Basis of Pulmonary Arterial Hypertension: Part II: Neurohormonal Signaling Contributes to the Pulmonary Vascular and Right Ventricular Pathophenotype of Pulmonary Arterial Hypertension A Zero-Dimensional Model and Protocol for Simulating Patient-Specific Pulmonary Hemodynamics From Limited Clinical Data.Genetic ablation of interleukin-18 does not attenuate hypobaric hypoxia-induced right ventricular hypertrophy Right Ventricular Longitudinal Strain Is Depressed in a Bovine Model of Pulmonary Hypertension.Limiting collagen turnover via collagenase-resistance attenuates right ventricular dysfunction and fibrosis in pulmonary arterial hypertension.Pulmonary vascular and ventricular dysfunction in the susceptible patient (2015 Grover Conference series).Adaptive capacity of the right ventricle: why does it fail?Inhaled Gene Transfer for Pulmonary Circulation.Intratracheal Gene Delivery of SERCA2a Ameliorates Chronic Post-Capillary Pulmonary Hypertension: A Large Animal Model.Influence of periostin-positive cell-specific Klf5 deletion on aortic thickening in DOCA-salt hypertensive mice.Novel Therapeutic Strategies for Reducing Right Heart Failure Associated Mortality in Fibrotic Lung Diseases.Trimedazidine alleviates pulmonary artery banding-induced acute right heart dysfunction and activates PRAS40 in rats.Maternal-pup interaction disturbances induce long-lasting changes in the newborn rat pulmonary vasculature.Right ventricular end-diastolic stiffness heralds right ventricular failure in monocrotaline-induced pulmonary hypertension.Persistence and proliferation of human mesenchymal stromal cells in the right ventricular myocardium after intracoronary injection in a large animal model of pulmonary hypertension.Lipopolysaccharide acutely suppresses right-ventricular strain in rats with pulmonary artery hypertension.Distinct right ventricle remodeling in response to pressure overload in the rat.Right ventricular recovery after bilateral lung transplantation for pulmonary arterial hypertension†.Pulmonary Arterial Hypertension in Women.

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P2860

Characterization of right ventricular remodeling and failure in a chronic pulmonary hypertension model.

http://www.wikidata.org/entity/Q34356167

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2014 nî lūn-bûn

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2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

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2014 թվականի օգոստոսին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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AJPHEART.00246.2014

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American Journal of Physiology - Heart and Circulatory Physiology

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Characterization of right vent ...... pulmonary hypertension model.

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P2093

Ana García-Alvarez

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Antoine Chaanine

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Jane A Leopold

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Kenneth Fish

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Kiyotake Ishikawa

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Lahouaria Hadri

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Partho P Sengupta

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Roger J Hajjar

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Samantha Torquato

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P2860

3D Echo systematically underestimates right ventricular volumes compared to cardiovascular magnetic resonance in adult congenital heart disease patients with moderate or severe RV dilatation.

A brief overview of mouse models of pulmonary arterial hypertension: problems and prospects.

Guidelines for the echocardiographic assessment of the right heart in adults: a report from the American Society of Echocardiography endorsed by the European Association of Echocardiography, a registered branch of the European Society of Cardiology,

Guidelines for the diagnosis and treatment of pulmonary hypertension: the Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS), endorsed by the In

Swine model of chronic postcapillary pulmonary hypertension with right ventricular remodeling: long-term characterization by cardiac catheterization, magnetic resonance, and pathology.

Molecular signature of a right heart failure program in chronic severe pulmonary hypertension.

Assessment of systolic and diastolic ventricular properties via pressure-volume analysis: a guide for clinical, translational, and basic researchers.

Differential calcium handling in two canine models of right ventricular pressure overload.

Aldosterone inactivates the endothelin-B receptor via a cysteinyl thiol redox switch to decrease pulmonary endothelial nitric oxide levels and modulate pulmonary arterial hypertension.

Plasma aldosterone levels are elevated in patients with pulmonary arterial hypertension in the absence of left ventricular heart failure: a pilot study

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8

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307

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Carlos G Santos-Gallego

Nadjib Hammoudi

Valentín Fuster Carulla

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