Id proteins are critical downstream effectors of BMPR-Ⅱ in pulmonary arterial smooth muscle cells

来源 :The 12th Meeting of the Asia Pacific Federation of Pharmacol | 被引量 : 0次 | 上传用户:bpsend
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Aim: Bone morphogenetic protein type Ⅱ receptor (BMPR-Ⅱ) mutations are responsible for over 70% of cases of heritable pulmonary arterial hypertension (PAH) and up to 15%-40% of sporadic idiopathic disease.Loss of BMP signalling promotes pulmonary vascular remodelling via modulation of pulmonary artery smooth muscle cell (PASMC) migration, differentiation and proliferation.
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