Open AccessDysfunctional BMPR2 signaling drives an abnormal endothelial requirement for glutamine in pulmonary arterial hypertension
Author(s) -
Robert A. Egnatchik,
Evan L. Brittain,
Amy T. Shah,
Wassim H. Fares,
H. James Ford,
Kevin Monahan,
Christie Kang,
Emily G. Kocurek,
Shiqun Zhu,
Thong Luong,
Thùy Nguyễn,
Erik B. Hysinger,
Eric D. Austin,
Melissa C. Skala,
Jamey D. Young,
L. Jackson Roberts,
Anna R. Hemnes,
James E. West,
Joshua P. Fessel
Publication year - 2017
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/vn0p-d114
Subject(s) - bmpr2 , dysfunctional family , pulmonary hypertension , cardiology , medicine , endothelial dysfunction , chemistry , biochemistry , psychiatry , gene , bone morphogenetic protein