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Hunter C. Champion

Researcher at Johns Hopkins University

Publications -  275
Citations -  23191

Hunter C. Champion is an academic researcher from Johns Hopkins University. The author has contributed to research in topics: Pulmonary hypertension & Adrenomedullin. The author has an hindex of 74, co-authored 275 publications receiving 21959 citations. Previous affiliations of Hunter C. Champion include Johns Hopkins University School of Medicine & National Institutes of Health.

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PDE5A Inhibitor Treatment of Persistent Pulmonary Hypertension After Mechanical Circulatory Support

TL;DR: In patients with persistent PH after recent LVAD placement, phosphodiesterase type 5A inhibition in this open-label trial resulted in a significant decrease in PVR when compared with control patients.
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FIZZ1/RELMα, a Novel Hypoxia-Induced Mitogenic Factor in Lung With Vasoconstrictive and Angiogenic Properties

TL;DR: The PI3K/Akt pathway, at least in part, mediates the proliferative effect of HIMF, which increased pulmonary arterial pressure and vascular resistance more potently than either endothelin-1 or angiotensin II.
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Compartmentalization of Cardiac β-Adrenergic Inotropy Modulation by Phosphodiesterase Type 5

TL;DR: Regulation of cardiac &bgr;-adrenergic response by cGMP is specifically linked to a nitric oxide–synthesis/PDE-5–hydrolyzed pool signaling via protein kinase G.
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Phosphodiesterase regulation of nitric oxide signaling

TL;DR: Growing evidence supports an important role of several PDEs, including PDE1, PDE2, and PDE5, in the regulation of cGMP in both vascular smooth muscle and cardiac myocytes, and cross-signaling with NO-cGMP synthetic pathways that may be particularly helpful in treating certain disease states.
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PDE5A inhibition attenuates bleomycin-induced pulmonary fibrosis and pulmonary hypertension through inhibition of ROS generation and RhoA/Rho kinase activation.

TL;DR: It is demonstrated that PDE5 inhibition ameliorates RV hypertrophy and pulmonary fibrosis associated with intratracheal bleomycin in a manner that is associated with improved NOS coupling and a reduction in reactive oxygen species signaling.