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Journal Abstract Search

265 related items for PubMed ID: 18723761

  • 1. Mice expressing BMPR2R899X transgene in smooth muscle develop pulmonary vascular lesions.
    West J, Harral J, Lane K, Deng Y, Ickes B, Crona D, Albu S, Stewart D, Fagan K.
    Am J Physiol Lung Cell Mol Physiol; 2008 Nov; 295(5):L744-55. PubMed ID: 18723761
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  • 2. Rho-kinase inhibition alleviates pulmonary hypertension in transgenic mice expressing a dominant-negative type II bone morphogenetic protein receptor gene.
    Yasuda T, Tada Y, Tanabe N, Tatsumi K, West J.
    Am J Physiol Lung Cell Mol Physiol; 2011 Nov; 301(5):L667-74. PubMed ID: 21856816
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  • 3. Physiologic and molecular consequences of endothelial Bmpr2 mutation.
    Majka S, Hagen M, Blackwell T, Harral J, Johnson JA, Gendron R, Paradis H, Crona D, Loyd JE, Nozik-Grayck E, Stenmark KR, West J.
    Respir Res; 2011 Jun 22; 12(1):84. PubMed ID: 21696628
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  • 4. Cytoskeletal defects in Bmpr2-associated pulmonary arterial hypertension.
    Johnson JA, Hemnes AR, Perrien DS, Schuster M, Robinson LJ, Gladson S, Loibner H, Bai S, Blackwell TR, Tada Y, Harral JW, Talati M, Lane KB, Fagan KA, West J.
    Am J Physiol Lung Cell Mol Physiol; 2012 Mar 01; 302(5):L474-84. PubMed ID: 22180660
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  • 5. Molecular effects of loss of BMPR2 signaling in smooth muscle in a transgenic mouse model of PAH.
    Tada Y, Majka S, Carr M, Harral J, Crona D, Kuriyama T, West J.
    Am J Physiol Lung Cell Mol Physiol; 2007 Jun 01; 292(6):L1556-63. PubMed ID: 17369292
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  • 6. Dysfunctional Smad signaling contributes to abnormal smooth muscle cell proliferation in familial pulmonary arterial hypertension.
    Yang X, Long L, Southwood M, Rudarakanchana N, Upton PD, Jeffery TK, Atkinson C, Chen H, Trembath RC, Morrell NW.
    Circ Res; 2005 May 27; 96(10):1053-63. PubMed ID: 15845886
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  • 7. BMPR2 gene delivery reduces mutation-related PAH and counteracts TGF-β-mediated pulmonary cell signalling.
    Feng F, Harper RL, Reynolds PN.
    Respirology; 2016 Apr 27; 21(3):526-32. PubMed ID: 26689975
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  • 8. Serotonin 2B Receptor Antagonism Prevents Heritable Pulmonary Arterial Hypertension.
    West JD, Carrier EJ, Bloodworth NC, Schroer AK, Chen P, Ryzhova LM, Gladson S, Shay S, Hutcheson JD, Merryman WD.
    PLoS One; 2016 Apr 27; 11(2):e0148657. PubMed ID: 26863209
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  • 16. Let-7a-transfected mesenchymal stem cells ameliorate monocrotaline-induced pulmonary hypertension by suppressing pulmonary artery smooth muscle cell growth through STAT3-BMPR2 signaling.
    Cheng G, Wang X, Li Y, He L.
    Stem Cell Res Ther; 2017 Feb 10; 8(1):34. PubMed ID: 28187784
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  • 17. Evidence for right ventricular lipotoxicity in heritable pulmonary arterial hypertension.
    Hemnes AR, Brittain EL, Trammell AW, Fessel JP, Austin ED, Penner N, Maynard KB, Gleaves L, Talati M, Absi T, Disalvo T, West J.
    Am J Respir Crit Care Med; 2014 Feb 01; 189(3):325-34. PubMed ID: 24274756
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  • 18. BMPR2 gene therapy for PAH acts via Smad and non-Smad signalling.
    Harper RL, Reynolds AM, Bonder CS, Reynolds PN.
    Respirology; 2016 May 01; 21(4):727-33. PubMed ID: 26809239
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  • 19. BMP pathway regulation of and by macrophages.
    Talati M, West J, Zaynagetdinov R, Hong CC, Han W, Blackwell T, Robinson L, Blackwell TS, Lane K.
    PLoS One; 2014 May 01; 9(4):e94119. PubMed ID: 24713633
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  • 20. Modulation of Endothelial Bone Morphogenetic Protein Receptor Type 2 Activity by Vascular Endothelial Growth Factor Receptor 3 in Pulmonary Arterial Hypertension.
    Hwangbo C, Lee HW, Kang H, Ju H, Wiley DS, Papangeli I, Han J, Kim JD, Dunworth WP, Hu X, Lee S, El-Hely O, Sofer A, Pak B, Peterson L, Comhair S, Hwang EM, Park JY, Thomas JL, Bautch VL, Erzurum SC, Chun HJ, Jin SW.
    Circulation; 2017 Jun 06; 135(23):2288-2298. PubMed ID: 28356442
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