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Items: 1 to 20 of 103

1.

5-HTT, BMPR2, EDN1, ENG, KCNA5 gene polymorphisms and susceptibility to pulmonary arterial hypertension: A meta-analysis.

Jiao YR, Wang W, Lei PC, Jia HP, Dong J, Gou YQ, Chen CL, Cao J, Wang YF, Zhu YK.

Gene. 2019 Jan 5;680:34-42. doi: 10.1016/j.gene.2018.09.020. Epub 2018 Sep 12. Review.

PMID:
30218748
2.

Association between serotonin transporter (SERT) gene polymorphism and idiopathic pulmonary arterial hypertension: a meta-analysis and review of the literature.

Zhang H, Xu M, Xia J, Qin RY.

Metabolism. 2013 Dec;62(12):1867-75. doi: 10.1016/j.metabol.2013.08.012. Epub 2013 Sep 24. Review.

PMID:
24075737
3.

Genetic variants in a Polish population of patients with pulmonary arterial hypertension: sequencing of BMPR2, ALK1, and ENG genes.

Uznańska-Loch B, Wikło K, Kulczycka-Wojdala D, Szymańska B, Chrzanowski Ł, Wierzbowska-Drabik K, Trzos E, Kasprzak JD, Kurpesa M.

Kardiol Pol. 2018;76(5):852-859. doi: 10.5603/KP.a2018.0034. Epub 2018 Jan 19.

4.

Serotonin transporter polymorphisms in familial and idiopathic pulmonary arterial hypertension.

Willers ED, Newman JH, Loyd JE, Robbins IM, Wheeler LA, Prince MA, Stanton KC, Cogan JA, Runo JR, Byrne D, Humbert M, Simonneau G, Sztrymf B, Morse JA, Knowles JA, Roberts KE, McElroy JJ, Barst RJ, Phillips JA 3rd.

Am J Respir Crit Care Med. 2006 Apr 1;173(7):798-802. Epub 2005 Dec 9.

5.

Novel mutations in BMPR2, ACVRL1 and KCNA5 genes and hemodynamic parameters in patients with pulmonary arterial hypertension.

Pousada G, Baloira A, Vilariño C, Cifrian JM, Valverde D.

PLoS One. 2014 Jun 17;9(6):e100261. doi: 10.1371/journal.pone.0100261. eCollection 2014.

6.

Sequence variants in BMPR2 and genes involved in the serotonin and nitric oxide pathways in idiopathic pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension: relation to clinical parameters and comparison with left heart disease.

Ulrich S, Szamalek-Hoegel J, Hersberger M, Fischler M, Garcia JS, Huber LC, Grünig E, Janssen B, Speich R.

Respiration. 2010;79(4):279-87. doi: 10.1159/000250322. Epub 2009 Oct 17.

7.

[K198N polymorphism in the EDN1 gene in patients with pulmonary arterial hypertension].

Pousada G, Baloira A, Vilariño C, Valverde D.

Med Clin (Barc). 2015 Apr 20;144(8):348-52. doi: 10.1016/j.medcli.2013.11.037. Epub 2014 Feb 14. Spanish.

PMID:
24529882
8.

KCNA5 gene is not confirmed as a systemic sclerosis-related pulmonary arterial hypertension genetic susceptibility factor.

Bossini-Castillo L, Simeon CP, Beretta L, Broen J, Vonk MC, Callejas JL, Carreira P, Rodríguez-Rodríguez L, García-Portales R, González-Gay MA, Castellví I, Camps MT, Tolosa C, Vicente-Rabaneda E, Egurbide MV; Spanish Scleroderma Group, Schuerwegh AJ, Hesselstrand R, Lunardi C, van Laar JM, Shiels P, Herrick A, Worthington J, Denton C, Radstake TR, Fonseca C, Martin J.

Arthritis Res Ther. 2012 Dec 27;14(6):R273. doi: 10.1186/ar4124.

9.

Mutational and clinical analysis of the ENG gene in patients with pulmonary arterial hypertension.

Pousada G, Baloira A, Fontán D, Núñez M, Valverde D.

BMC Genet. 2016 Jun 4;17(1):72. doi: 10.1186/s12863-016-0384-3.

10.

Associations between endothelial nitric oxide synthase A/B, angiotensin converting enzyme I/D and serotonin transporter L/S gene polymorphisms with pulmonary hypertension in COPD patients.

Ulasli SS, Eyuboglu FO, Verdi H, Atac FB.

Mol Biol Rep. 2013 Oct;40(10):5625-33. doi: 10.1007/s11033-013-2664-6. Epub 2013 Sep 21.

PMID:
24057178
11.

Genetic analyses in a cohort of 191 pulmonary arterial hypertension patients.

Yang H, Zeng Q, Ma Y, Liu B, Chen Q, Li W, Xiong C, Zhou Z.

Respir Res. 2018 May 9;19(1):87. doi: 10.1186/s12931-018-0789-9.

12.

Association of a KCNA5 gene polymorphism with systemic sclerosis-associated pulmonary arterial hypertension in the European Caucasian population.

Wipff J, Dieudé P, Guedj M, Ruiz B, Riemekasten G, Cracowski JL, Matucci-Cerinic M, Melchers I, Humbert M, Hachulla E, Airo P, Diot E, Hunzelmann N, Caramaschi P, Sibilia J, Valentini G, Tiev K, Girerd B, Mouthon L, Riccieri V, Carpentier PH, Distler J, Amoura Z, Tarner I, Degano B, Avouac J, Meyer O, Kahan A, Boileau C, Allanore Y.

Arthritis Rheum. 2010 Oct;62(10):3093-100. doi: 10.1002/art.27607.

13.

Early onset severe pulmonary arterial hypertension with 'two-hit' digenic mutations in both BMPR2 and KCNA5 genes.

Wang G, Knight L, Ji R, Lawrence P, Kanaan U, Li L, Das A, Cui B, Zou W, Penny DJ, Fan Y.

Int J Cardiol. 2014 Dec 20;177(3):e167-9. doi: 10.1016/j.ijcard.2014.08.124. Epub 2014 Aug 28. No abstract available.

PMID:
25189502
14.

BMPR2 mutations and survival in pulmonary arterial hypertension: an individual participant data meta-analysis.

Evans JD, Girerd B, Montani D, Wang XJ, Galiè N, Austin ED, Elliott G, Asano K, Grünig E, Yan Y, Jing ZC, Manes A, Palazzini M, Wheeler LA, Nakayama I, Satoh T, Eichstaedt C, Hinderhofer K, Wolf M, Rosenzweig EB, Chung WK, Soubrier F, Simonneau G, Sitbon O, Gräf S, Kaptoge S, Di Angelantonio E, Humbert M, Morrell NW.

Lancet Respir Med. 2016 Feb;4(2):129-37. doi: 10.1016/S2213-2600(15)00544-5. Epub 2016 Jan 19.

15.

Function of Kv1.5 channels and genetic variations of KCNA5 in patients with idiopathic pulmonary arterial hypertension.

Remillard CV, Tigno DD, Platoshyn O, Burg ED, Brevnova EE, Conger D, Nicholson A, Rana BK, Channick RN, Rubin LJ, O'connor DT, Yuan JX.

Am J Physiol Cell Physiol. 2007 May;292(5):C1837-53. Epub 2007 Jan 31.

16.

Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects.

Machado RD, Southgate L, Eichstaedt CA, Aldred MA, Austin ED, Best DH, Chung WK, Benjamin N, Elliott CG, Eyries M, Fischer C, Gräf S, Hinderhofer K, Humbert M, Keiles SB, Loyd JE, Morrell NW, Newman JH, Soubrier F, Trembath RC, Viales RR, Grünig E.

Hum Mutat. 2015 Dec;36(12):1113-27. doi: 10.1002/humu.22904. Epub 2015 Oct 12. Review.

17.
18.

Genetics and genomics of pulmonary arterial hypertension.

Machado RD, Eickelberg O, Elliott CG, Geraci MW, Hanaoka M, Loyd JE, Newman JH, Phillips JA 3rd, Soubrier F, Trembath RC, Chung WK.

J Am Coll Cardiol. 2009 Jun 30;54(1 Suppl):S32-42. doi: 10.1016/j.jacc.2009.04.015. Review.

19.

Polymorphisms in the serotonin transporter protein (SERT) gene in patients with pulmonary arterial hypertension.

Baloira A, Núñez M, Cifrian J, Vilariño C, Ojeda M, Valverde D.

Arch Bronconeumol. 2012 Mar;48(3):77-80. doi: 10.1016/j.arbres.2011.10.008. Epub 2011 Dec 16. English, Spanish.

20.

Hemodynamic and clinical onset in patients with hereditary pulmonary arterial hypertension and BMPR2 mutations.

Pfarr N, Szamalek-Hoegel J, Fischer C, Hinderhofer K, Nagel C, Ehlken N, Tiede H, Olschewski H, Reichenberger F, Ghofrani AH, Seeger W, Grünig E.

Respir Res. 2011 Jul 29;12:99. doi: 10.1186/1465-9921-12-99.

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