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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.
JCI Insight|October 5, 2016
Depletion of major pathogenic cells in asthma by targeting CRTh2Tao Huang, Meredith Hazen, Yonglei Shang, et al.
Genome Medicine|July 22, 2018
Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart diseaseNa Zhu, Carrie L Welch, Jiayao Wang, et al.
Human Mutation|September 22, 2015
Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic DefectsRajiv D Machado, Laura Southgate, Christina A Eichstaedt, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 11, 2013
Polyclonal hyper-IgE mouse model reveals mechanistic insights into antibody class switch recombinationShahram Misaghi, Kate Senger, Tao Sai, et al.
Bioorganic & Medicinal Chemistry Letters|March 3, 2015
Structure-based design of inhibitors of coagulation factor XIa with novel P1 moietiesDonald J P Pinto, Joanne M Smallheer, James R Corte, et al.
Pediatric Pulmonology|November 8, 2023
Number of children in the household influences respiratory morbidities in children with bronchopulmonary dysplasia in the outpatient settingJoseph M Collaco, Katharine R Tsukahara, Michael C Tracy, et al.
The Journal of Pediatrics|July 8, 2022
Daycare Attendance is Linked to Increased Risk of Respiratory Morbidities in Children Born Preterm with Bronchopulmonary DysplasiaSharon A McGrath-Morrow, Amit Agarwal, Stamatia Alexiou, et al.
Nature Communications|November 6, 2024
Induction of a distinct macrophage population and protection from lung injury and fibrosis by Notch2 blockadeMayra Cruz Tleugabulova, Sandra P Melo, Aaron Wong, et al.
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