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Pediatric Pulmonology|October 11, 2024
Outpatient clinical care for bronchopulmonary dysplasia: A survey of the BPD collaborativePaul E Moore, Lystra P Hayden, Natalie M Villafranco, et al.
The Journal of Clinical Investigation|December 7, 2007
In vivo blockade of OX40 ligand inhibits thymic stromal lymphopoietin driven atopic inflammationDhaya Seshasayee, Wyne P Lee, Meijuan Zhou, et al.
Biorxiv : the Preprint Server for Biology|February 12, 2026
A Large Animal Model of Heritable Pulmonary Arterial Hypertension Using Gene-edited BMPR2 SheepSanjeev A Datar, Nicholas Werry, Austin R Brown, et al.
Circulation. Genomic and Precision Medicine|April 11, 2018
Exome Sequencing in Children With Pulmonary Arterial Hypertension Demonstrates Differences Compared With AdultsNa Zhu, Claudia Gonzaga-Jauregui, Carrie L Welch, et al.
Nature Communications|June 4, 2026
Myosin light chain proteins cooperatively promote sarcomere growth in fast-twitch muscleTayo E Adekeye, Troy E Hupper, Teresa E Easterbrooks, et al.
JCI Insight|July 14, 2026
A large animal model of heritable pulmonary arterial hypertension using gene-edited BMPR2 sheepSanjeev A Datar, Nicholas Werry, Austin R Brown, et al.
Science Translational Medicine|April 20, 2022
Steroid-induced fibroblast growth factors drive an epithelial-mesenchymal inflammatory axis in severe asthmaRiccardo Guidi, Daqi Xu, David F Choy, et al.
Hepatology (Baltimore, Md.)|May 15, 2020
Estrogen Signaling and Portopulmonary Hypertension: The Pulmonary Vascular Complications of Liver Disease Study (PVCLD2)Nadine Al-Naamani, Michael J Krowka, Kimberly A Forde, et al.
American Journal of Respiratory and Critical Care Medicine|December 10, 2014
Serum endostatin is a genetically determined predictor of survival in pulmonary arterial hypertensionRachel Damico, Todd M Kolb, Lidenys Valera, et al.
Pulmonary Circulation|April 3, 2025
Cellular Communication Network Protein 2 in the Right Ventricle of Pulmonary Arterial HypertensionCarly E Byrd, Jennifer E Schramm, Jun Yang, et al.
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