Similar articles for PMID: 18024717

Year	Number of Results
2002	1
2004	2
2005	7
2006	7
2007	6
2008	9
2009	8
2010	7
2011	6
2012	7
2013	7
2014	9
2015	14
2016	10
2017	7
2018	6
2019	3
2020	6
2021	6
2022	11
2023	2
2024	0

1

Increased susceptibility to hypoxic pulmonary hypertension in Bmpr2 mutant mice is associated with endothelial dysfunction in the pulmonary vasculature.

Frank DB, Lowery J, Anderson L, Brink M, Reese J, de Caestecker M. Frank DB, et al. Am J Physiol Lung Cell Mol Physiol. 2008 Jan;294(1):L98-109. doi: 10.1152/ajplung.00034.2007. Epub 2007 Nov 16. Am J Physiol Lung Cell Mol Physiol. 2008. PMID: 18024717 Free article.

2

Bmpr2 Mutant Rats Develop Pulmonary and Cardiac Characteristics of Pulmonary Arterial Hypertension.

Hautefort A, Mendes-Ferreira P, Sabourin J, Manaud G, Bertero T, Rucker-Martin C, Riou M, Adão R, Manoury B, Lambert M, Boet A, Lecerf F, Domergue V, Brás-Silva C, Gomez AM, Montani D, Girerd B, Humbert M, Antigny F, Perros F. Hautefort A, et al. Circulation. 2019 Feb 12;139(7):932-948. doi: 10.1161/CIRCULATIONAHA.118.033744. Circulation. 2019. PMID: 30586714

3

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. Hwangbo C, et al. Circulation. 2017 Jun 6;135(23):2288-2298. doi: 10.1161/CIRCULATIONAHA.116.025390. Epub 2017 Mar 29. Circulation. 2017. PMID: 28356442 Free PMC article.

4

Inflammation, endothelial injury, and persistent pulmonary hypertension in heterozygous BMPR2-mutant mice.

Song Y, Coleman L, Shi J, Beppu H, Sato K, Walsh K, Loscalzo J, Zhang YY. Song Y, et al. Am J Physiol Heart Circ Physiol. 2008 Aug;295(2):H677-90. doi: 10.1152/ajpheart.91519.2007. Epub 2008 Jun 13. Am J Physiol Heart Circ Physiol. 2008. PMID: 18552156 Free PMC article.

5

Serotonin increases susceptibility to pulmonary hypertension in BMPR2-deficient mice.

Long L, MacLean MR, Jeffery TK, Morecroft I, Yang X, Rudarakanchana N, Southwood M, James V, Trembath RC, Morrell NW. Long L, et al. Circ Res. 2006 Mar 31;98(6):818-27. doi: 10.1161/01.RES.0000215809.47923.fd. Epub 2006 Feb 23. Circ Res. 2006. PMID: 16497988

6

Codependence of Bone Morphogenetic Protein Receptor 2 and Transforming Growth Factor-β in Elastic Fiber Assembly and Its Perturbation in Pulmonary Arterial Hypertension.

Tojais NF, Cao A, Lai YJ, Wang L, Chen PI, Alcazar MAA, de Jesus Perez VA, Hopper RK, Rhodes CJ, Bill MA, Sakai LY, Rabinovitch M. Tojais NF, et al. Arterioscler Thromb Vasc Biol. 2017 Aug;37(8):1559-1569. doi: 10.1161/ATVBAHA.117.309696. Epub 2017 Jun 15. Arterioscler Thromb Vasc Biol. 2017. PMID: 28619995 Free PMC article.

7

CCL5 deficiency rescues pulmonary vascular dysfunction, and reverses pulmonary hypertension via caveolin-1-dependent BMPR2 activation.

Nie X, Tan J, Dai Y, Liu Y, Zou J, Sun J, Ye S, Shen C, Fan L, Chen J, Bian JS. Nie X, et al. J Mol Cell Cardiol. 2018 Mar;116:41-56. doi: 10.1016/j.yjmcc.2018.01.016. Epub 2018 Jan 31. J Mol Cell Cardiol. 2018. PMID: 29374556

8

Bone morphogenetic protein type 2 receptor gene therapy attenuates hypoxic pulmonary hypertension.

Reynolds AM, Xia W, Holmes MD, Hodge SJ, Danilov S, Curiel DT, Morrell NW, Reynolds PN. Reynolds AM, et al. Am J Physiol Lung Cell Mol Physiol. 2007 May;292(5):L1182-92. doi: 10.1152/ajplung.00020.2006. Epub 2007 Feb 2. Am J Physiol Lung Cell Mol Physiol. 2007. PMID: 17277049 Free article.

9

Endothelial BMPR2 Loss Drives a Proliferative Response to BMP (Bone Morphogenetic Protein) 9 via Prolonged Canonical Signaling.

Theilmann AL, Hawke LG, Hilton LR, Whitford MKM, Cole DV, Mackeil JL, Dunham-Snary KJ, Mewburn J, James PD, Maurice DH, Archer SL, Ormiston ML. Theilmann AL, et al. Arterioscler Thromb Vasc Biol. 2020 Nov;40(11):2605-2618. doi: 10.1161/ATVBAHA.119.313357. Epub 2020 Oct 1. Arterioscler Thromb Vasc Biol. 2020. PMID: 32998516 Free PMC article.

10

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. Hong KH, et al. Circulation. 2008 Aug 12;118(7):722-30. doi: 10.1161/CIRCULATIONAHA.107.736801. Epub 2008 Jul 28. Circulation. 2008. PMID: 18663089 Free PMC article.

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