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Pulmonary Circulation|January 17, 2017
Macrophage migration inhibitory factor as a novel biomarker of portopulmonary hypertensionHilary M DuBrock, Josanna M Rodriguez-Lopez, Barbara L LeVarge, et al.
Nature Medicine|January 9, 2026
The NOTCH3 extracellular domain is a serum biomarker for pulmonary arterial hypertensionMoises Hernandez, Nolan M Winicki, Cristian D Puerta, et al.
Nature Medicine|November 26, 2008
BMP type I receptor inhibition reduces heterotopic [corrected] ossificationPaul B Yu, Donna Y Deng, Carol S Lai, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 24, 2016
Up-regulation of the mammalian target of rapamycin complex 1 subunit Raptor by aldosterone induces abnormal pulmonary artery smooth muscle cell survival patterns to promote pulmonary arterial hypertensionReza Aghamohammadzadeh, Ying-Yi Zhang, Thomas E Stephens, et al.
Scientific Reports|February 21, 2020
Inhibition of bone morphogenetic protein 6 receptors ameliorates Sjögren's syndrome in miceHongen Yin, Lovika Kalra, Zhennan Lai, et al.
JCI Insight|March 11, 2021
Saracatinib is an efficacious clinical candidate for fibrodysplasia ossificans progressivaEleanor Williams, Jana Bagarova, Georgina Kerr, et al.
Nature Medicine|June 16, 2015
Selective enhancement of endothelial BMPR-II with BMP9 reverses pulmonary arterial hypertensionLu Long, Mark L Ormiston, Xudong Yang, et al.
Science Translational Medicine|November 25, 2016
Two tissue-resident progenitor lineages drive distinct phenotypes of heterotopic ossificationDevaveena Dey, Jana Bagarova, Sarah J Hatsell, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|July 19, 2017
Strategic Targeting of Multiple BMP Receptors Prevents Trauma-Induced Heterotopic OssificationShailesh Agarwal, Shawn J Loder, Christopher Breuler, et al.
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