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4. Genetic ablation of the BMPR2 gene in pulmonary endothelium is sufficient to predispose to pulmonary arterial hypertension. Hong KH; Lee YJ; Lee E; Park SO; Han C; Beppu H; Li E; Raizada MK; Bloch KD; Oh SP Circulation; 2008 Aug; 118(7):722-30. PubMed ID: 18663089 [TBL] [Abstract][Full Text] [Related]
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17. Heterozygous null bone morphogenetic protein receptor type 2 mutations promote SRC kinase-dependent caveolar trafficking defects and endothelial dysfunction in pulmonary arterial hypertension. Prewitt AR; Ghose S; Frump AL; Datta A; Austin ED; Kenworthy AK; de Caestecker MP J Biol Chem; 2015 Jan; 290(2):960-71. PubMed ID: 25411245 [TBL] [Abstract][Full Text] [Related]
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