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Items: 1 to 20 of 100

1.

Understanding the low penetrance of bone morphogenetic protein receptor 2 gene mutations: another needle in the haystack.

White RJ, Morrell NW.

Circulation. 2012 Oct 9;126(15):1818-20. doi: 10.1161/CIRCULATIONAHA.112.135004. No abstract available.

2.

Role of BMPR2 alternative splicing in heritable pulmonary arterial hypertension penetrance.

Cogan J, Austin E, Hedges L, Womack B, West J, Loyd J, Hamid R.

Circulation. 2012 Oct 9;126(15):1907-16. doi: 10.1161/CIRCULATIONAHA.112.106245. Epub 2012 Aug 24.

3.

Waiting in anticipation: the genetics of pulmonary arterial hypertension.

Aldred MA, Morrell NW.

Am J Respir Crit Care Med. 2012 Nov 1;186(9):820-1. doi: 10.1164/rccm.201209-1666ED. No abstract available.

4.

Letter by Kataoka et al Regarding Article, "Bone Morphogenetic Protein Receptor Type 2 Mutation in Pulmonary Arterial Hypertension: A View on the Right Ventricle".

Kataoka M, Satoh T, Fukuda K.

Circulation. 2016 Aug 30;134(9):e115-6. doi: 10.1161/CIRCULATIONAHA.116.022841. No abstract available.

5.

Response by van der Bruggen et al to Letter Regarding Article, "Bone Morphogenetic Protein Receptor Type 2 Mutation in Pulmonary Arterial Hypertension: A View on the Right Ventricle".

van der Bruggen CE, Happé CM, Goumans MJ, Bogaard HJ, Vonk Noordegraaf A, de Man FS.

Circulation. 2016 Aug 30;134(9):e117-8. doi: 10.1161/CIRCULATIONAHA.116.024173. No abstract available.

6.

Fat and cardiotoxicity in hereditary pulmonary hypertension.

Tuder RM, Robinson JC, Graham BB.

Am J Respir Crit Care Med. 2014 Feb 1;189(3):247-9. doi: 10.1164/rccm.201312-2240ED. No abstract available.

7.

Heritable forms of pulmonary arterial hypertension.

Austin ED, Loyd JE.

Semin Respir Crit Care Med. 2013 Oct;34(5):568-80. doi: 10.1055/s-0033-1355443. Epub 2013 Sep 13.

8.

Heritable pulmonary arterial hypertension with elevated pulmonary wedge pressure.

Digne F, Sablayrolles JL, Montani D, Laperche T, Rousseau J, Guyon P, Stratiev V, Royer T, Attias D.

Circulation. 2012 Aug 28;126(9):e124-7. doi: 10.1161/CIRCULATIONAHA.112.096271. No abstract available.

9.

Mutations in bone morphogenetic protein type II receptor cause dysregulation of Id gene expression in pulmonary artery smooth muscle cells: implications for familial pulmonary arterial hypertension.

Yang J, Davies RJ, Southwood M, Long L, Yang X, Sobolewski A, Upton PD, Trembath RC, Morrell NW.

Circ Res. 2008 May 23;102(10):1212-21. doi: 10.1161/CIRCRESAHA.108.173567. Epub 2008 Apr 24.

10.

Deletion of the sequence encoding the tail domain of the bone morphogenetic protein type 2 receptor reveals a bone morphogenetic protein 7-specific gain of function.

Leyton PA, Beppu H, Pappas A, Martyn TM, Derwall M, Baron DM, Galdos R, Bloch DB, Bloch KD.

PLoS One. 2013 Oct 8;8(10):e76947. doi: 10.1371/journal.pone.0076947. eCollection 2013.

11.

Connectivity map analysis of nonsense-mediated decay-positive BMPR2-related hereditary pulmonary arterial hypertension provides insights into disease penetrance.

Flynn C, Zheng S, Yan L, Hedges L, Womack B, Fessel J, Cogan J, Austin E, Loyd J, West J, Zhao Z, Hamid R.

Am J Respir Cell Mol Biol. 2012 Jul;47(1):20-7. doi: 10.1165/rcmb.2011-0251OC. Epub 2012 Feb 3.

12.

Synergistic heterozygosity for TGFbeta1 SNPs and BMPR2 mutations modulates the age at diagnosis and penetrance of familial pulmonary arterial hypertension.

Phillips JA 3rd, Poling JS, Phillips CA, Stanton KC, Austin ED, Cogan JD, Wheeler L, Yu C, Newman JH, Dietz HC, Loyd JE.

Genet Med. 2008 May;10(5):359-65. doi: 10.1097/GIM.0b013e318172dcdf.

PMID:
18496036
13.

Bone morphogenetic protein receptor 2 mutations in adults and children with idiopathic pulmonary arterial hypertension: association with thyroid disease.

Roberts KE, Barst RJ, McElroy JJ, Widlitz A, Chada K, Knowles JA, Morse JH.

Chest. 2005 Dec;128(6 Suppl):618S. No abstract available.

PMID:
16373874
14.

Bone morphogenetic protein type II receptor mutations causing protein misfolding in heritable pulmonary arterial hypertension.

Li W, Dunmore BJ, Morrell NW.

Proc Am Thorac Soc. 2010 Nov;7(6):395-8. doi: 10.1513/pats.201002-024AW. Review.

PMID:
21030519
15.

Molecular Genetic Diagnosis of Pulmonary Arterial Hypertension: An Increased Complexity.

Eyries M, Soubrier F.

Rev Esp Cardiol (Engl Ed). 2016 Nov;69(11):1003-1004. doi: 10.1016/j.rec.2016.05.026. Epub 2016 Sep 12. English, Spanish. No abstract available.

PMID:
27634583
16.

Somatic mutations in pulmonary arterial hypertension: primary or secondary events?

Austin ED, Hamid R, Ahmad F.

Am J Respir Crit Care Med. 2010 Nov 1;182(9):1094-6. doi: 10.1164/rccm.201007-1147ED. No abstract available.

PMID:
21041561
17.

Better off blue: BMPR-2 mutation, arteriovenous malformation, and pulmonary arterial hypertension.

Soon E, Southwood M, Sheares K, Pepke-Zaba J, Morrell NW.

Am J Respir Crit Care Med. 2014 Jun 1;189(11):1435-6. doi: 10.1164/rccm.201311-2019IM. No abstract available.

PMID:
24881940
18.

Genetics of pulmonary arterial hypertension.

Austin ED, Loyd JE, Phillips JA 3rd.

Semin Respir Crit Care Med. 2009 Aug;30(4):386-98. doi: 10.1055/s-0029-1233308. Epub 2009 Jul 24. Review.

19.

Bone Morphogenetic Protein Receptor Type 2 Mutation in Pulmonary Arterial Hypertension: A View on the Right Ventricle.

van der Bruggen CE, Happé CM, Dorfmüller P, Trip P, Spruijt OA, Rol N, Hoevenaars FP, Houweling AC, Girerd B, Marcus JT, Mercier O, Humbert M, Handoko ML, van der Velden J, Vonk Noordegraaf A, Bogaard HJ, Goumans MJ, de Man FS.

Circulation. 2016 May 3;133(18):1747-60. doi: 10.1161/CIRCULATIONAHA.115.020696. Epub 2016 Mar 16.

20.

The genetics of pulmonary arterial hypertension.

Austin ED, Loyd JE.

Circ Res. 2014 Jun 20;115(1):189-202. doi: 10.1161/CIRCRESAHA.115.303404. Review.

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