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PUBMED FOR HANDHELDS

Journal Abstract Search


587 related items for PubMed ID: 24433082

  • 1. Loss of bone morphogenetic protein receptor 2 is associated with abnormal DNA repair in pulmonary arterial hypertension.
    Li M, Vattulainen S, Aho J, Orcholski M, Rojas V, Yuan K, Helenius M, Taimen P, Myllykangas S, De Jesus Perez V, Koskenvuo JW, Alastalo TP.
    Am J Respir Cell Mol Biol; 2014 Jun; 50(6):1118-28. PubMed ID: 24433082
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  • 2. Endothelin-Bone morphogenetic protein type 2 receptor interaction induces pulmonary artery smooth muscle cell hyperplasia in pulmonary arterial hypertension.
    Maruyama H, Dewachter C, Belhaj A, Rondelet B, Sakai S, Remmelink M, Vachiery JL, Naeije R, Dewachter L.
    J Heart Lung Transplant; 2015 Mar; 34(3):468-78. PubMed ID: 25447587
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  • 3. BMPR2 Loss Activates AKT by Disrupting DLL4/NOTCH1 and PPARγ Signaling in Pulmonary Arterial Hypertension.
    Awad KS, Wang S, Dougherty EJ, Keshavarz A, Demirkale CY, Yu ZX, Miller L, Elinoff JM, Danner RL.
    Int J Mol Sci; 2024 May 15; 25(10):. PubMed ID: 38791441
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  • 5. Bone morphogenetic protein receptor-2 signaling promotes pulmonary arterial endothelial cell survival: implications for loss-of-function mutations in the pathogenesis of pulmonary hypertension.
    Teichert-Kuliszewska K, Kutryk MJ, Kuliszewski MA, Karoubi G, Courtman DW, Zucco L, Granton J, Stewart DJ.
    Circ Res; 2006 Feb 03; 98(2):209-17. PubMed ID: 16357305
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  • 7. [Bone morphogenetic protein type II receptor gene promoter mutation-142G > A in a patient with familial pulmonary arterial hypertension].
    Li W, Hu H.
    Zhonghua Yi Xue Za Zhi; 2009 Feb 03; 89(4):230-4. PubMed ID: 19552837
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  • 12. In Pulmonary Arterial Hypertension, Reduced BMPR2 Promotes Endothelial-to-Mesenchymal Transition via HMGA1 and Its Target Slug.
    Hopper RK, Moonen JR, Diebold I, Cao A, Rhodes CJ, Tojais NF, Hennigs JK, Gu M, Wang L, Rabinovitch M.
    Circulation; 2016 May 03; 133(18):1783-94. PubMed ID: 27045138
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  • 14. MED1 Regulates BMP/TGF-β in Endothelium: Implication for Pulmonary Hypertension.
    Wang C, Xing Y, Zhang J, He M, Dong J, Chen S, Wu H, Huang HY, Chou CH, Bai L, He F, She J, Su A, Wang Y, Thistlethwaite PA, Huang HD, Yuan JX, Yuan ZY, Shyy JY.
    Circ Res; 2022 Oct 28; 131(10):828-841. PubMed ID: 36252121
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  • 15. Targeted gene delivery of BMPR2 attenuates pulmonary hypertension.
    Reynolds AM, Holmes MD, Danilov SM, Reynolds PN.
    Eur Respir J; 2012 Feb 28; 39(2):329-43. PubMed ID: 21737550
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  • 18. Autophagy contributes to BMP type 2 receptor degradation and development of pulmonary arterial hypertension.
    Gomez-Puerto MC, van Zuijen I, Huang CJ, Szulcek R, Pan X, van Dinther MA, Kurakula K, Wiesmeijer CC, Goumans MJ, Bogaard HJ, Morrell NW, Rana AA, Ten Dijke P.
    J Pathol; 2019 Nov 28; 249(3):356-367. PubMed ID: 31257577
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  • 20. 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 12; 118(7):722-30. PubMed ID: 18663089
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