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In this issue (p 74), Hyung Chun and his * X. z, J' D2 o) a+ E* w) F
coworkers uncover an apelin–miRNA–fibroblast growth factor signaling axis in - D, n& b6 V% J4 e
endothelial cells that is disrupted in pulmonary arterial hypertension. The / g3 E2 v4 H) `7 d1 L) F M+ W Q
cover shows a remodeled pulmonary blood vessel from an individual with pulmonary
6 y% B. ^7 M. X- U( Tarterial hypertension. Red, smooth muscle actin; cyan, von Willebrand factor;
! k5 d9 n& u0 l# yblue, DAPI. : X0 Y" v4 L t! g
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