摘要 : Pulmonary arterial hypertension (PAH) is a chronic disease characterized by a progressive elevation in mean pulmonary arterial pressure. This occurs due to abnormal remodeling of small peripheral lung vasculature resulting in prog... 展开
作者 | Xin~ Zhihong Wang~ Junfu Li~ Susu Sun~ Chao Jiang~ Wan Xin~ Qian Wang~ Jue Qi~ Tonggnag Li~ Kailin Zhang~ Zhaohua Luan~ Yun |
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作者单位 | |
期刊名称 | 《Clinical and experimental hypertension: CEH》 |
总页数 | 6 |
语种/中图分类号 | 英语 / R54 |
关键词 | PAH BMP Wnt5A PASMCs right ventricular failure MUSCLE-CELL PROLIFERATION VE-CADHERIN HYPOXIA EXPRESSION RECEPTOR CATENIN ANGIOGENESIS DYSFUNCTION INHIBITION SURVIVAL |
馆藏号 | N2007EPST0000246 |