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In this issue (p 74), Hyung Chun and his & _& g+ `6 Q: d w- |
coworkers uncover an apelin–miRNA–fibroblast growth factor signaling axis in
+ e) U1 H, c3 kendothelial cells that is disrupted in pulmonary arterial hypertension. The
: \* D9 ?. O+ l6 `( o8 ?cover shows a remodeled pulmonary blood vessel from an individual with pulmonary
5 J" s5 \ Z- ~6 d( ^# i# harterial hypertension. Red, smooth muscle actin; cyan, von Willebrand factor;
& y$ Y$ c7 C* C/ E3 [blue, DAPI. 9 S/ z- o, ]& j9 z) P# V& |
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