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American Journal of Respiratory and Critical Care Medicine|December 10, 2015
Bone Marrow-derived Cells Contribute to the Pathogenesis of Pulmonary Arterial HypertensionLing Yan, Xinping Chen, Megha Talati, et al.
Pulmonary Circulation|July 14, 2017
Pulmonary vascular effect of insulin in a rodent model of pulmonary arterial hypertensionAaron W Trammell, Megha Talati, Thomas R Blackwell, et al.
Pulmonary Circulation|August 1, 2022
l-Carnitine therapy improves right heart dysfunction through Cpt1-dependent fatty acid oxidationVineet Agrawal, Anna R Hemnes, Nicholas J Shelburne, et al.
Pulmonary Circulation|April 18, 2025
Mas1 Receptor Activation is Necessary and Sufficient to Transduce ACE2 Effect in PAH, But Ang(1-7) Alone is InsufficientJames West, Megha Talati, Erica Carrier, et al.
American Journal of Respiratory and Critical Care Medicine|November 27, 2013
Evidence for right ventricular lipotoxicity in heritable pulmonary arterial hypertensionAnna R Hemnes, Evan L Brittain, Aaron W Trammell, et al.
Pulmonary Circulation|September 10, 2011
Oxidative injury is a common consequence of BMPR2 mutationsKirk L Lane, Megha Talati, Eric Austin, et al.
American Journal of Respiratory and Critical Care Medicine|April 17, 2002
Selective cyclooxygenase-1 and -2 inhibitors each increase allergic inflammation and airway hyperresponsiveness in miceR Stokes Peebles, Koichi Hashimoto, Jason D Morrow, et al.
Pulmonary Circulation|December 6, 2011
Idiopathic and heritable PAH perturb common molecular pathways, correlated with increased MSX1 expressionEric D Austin, Swapna Menon, Anna R Hemnes, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|December 20, 2011
Cytoskeletal defects in Bmpr2-associated pulmonary arterial hypertensionJennifer A Johnson, Anna R Hemnes, Daniel S Perrien, et al.
Circulation|March 24, 2016
Fatty Acid Metabolic Defects and Right Ventricular Lipotoxicity in Human Pulmonary Arterial HypertensionEvan L Brittain, Megha Talati, Joshua P Fessel, et al.
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