BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 21070126)

  • 1. A novel BMPR2 gene mutation associated with exercise-induced pulmonary hypertension in septal defects.
    Möller T; Leren TP; Eiklid KL; Holmstrøm H; Fredriksen PM; Thaulow E
    Scand Cardiovasc J; 2010 Dec; 44(6):331-6. PubMed ID: 21070126
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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. PubMed ID: 29350394
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Transforming growth factor-beta receptor mutations and pulmonary arterial hypertension in childhood.
    Harrison RE; Berger R; Haworth SG; Tulloh R; Mache CJ; Morrell NW; Aldred MA; Trembath RC
    Circulation; 2005 Feb; 111(4):435-41. PubMed ID: 15687131
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 133(18):1747-60. PubMed ID: 26984938
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Implications of mutations of activin receptor-like kinase 1 gene (ALK1) in addition to bone morphogenetic protein receptor II gene (BMPR2) in children with pulmonary arterial hypertension.
    Fujiwara M; Yagi H; Matsuoka R; Akimoto K; Furutani M; Imamura S; Uehara R; Nakayama T; Takao A; Nakazawa M; Saji T
    Circ J; 2008 Jan; 72(1):127-33. PubMed ID: 18159113
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic counselling in a national referral centre for pulmonary hypertension.
    Girerd B; Montani D; Jaïs X; Eyries M; Yaici A; Sztrymf B; Savale L; Parent F; Coulet F; Godinas L; Lau EM; Tamura Y; Sitbon O; Soubrier F; Simonneau G; Humbert M
    Eur Respir J; 2016 Feb; 47(2):541-52. PubMed ID: 26699722
    [TBL] [Abstract][Full Text] [Related]  

  • 7. BMPR2 mutations in pulmonary arterial hypertension with congenital heart disease.
    Roberts KE; McElroy JJ; Wong WP; Yen E; Widlitz A; Barst RJ; Knowles JA; Morse JH
    Eur Respir J; 2004 Sep; 24(3):371-4. PubMed ID: 15358693
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Hemodynamic and genetic analysis in children with idiopathic, heritable, and congenital heart disease associated pulmonary arterial hypertension.
    Pfarr N; Fischer C; Ehlken N; Becker-Grünig T; López-González V; Gorenflo M; Hager A; Hinderhofer K; Miera O; Nagel C; Schranz D; Grünig E
    Respir Res; 2013 Jan; 14(1):3. PubMed ID: 23298310
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Outcomes of childhood pulmonary arterial hypertension in BMPR2 and ALK1 mutation carriers.
    Chida A; Shintani M; Yagi H; Fujiwara M; Kojima Y; Sato H; Imamura S; Yokozawa M; Onodera N; Horigome H; Kobayashi T; Hatai Y; Nakayama T; Fukushima H; Nishiyama M; Doi S; Ono Y; Yasukouchi S; Ichida F; Fujimoto K; Ohtsuki S; Teshima H; Kawano T; Nomura Y; Gu H; Ishiwata T; Furutani Y; Inai K; Saji T; Matsuoka R; Nonoyama S; Nakanishi T
    Am J Cardiol; 2012 Aug; 110(4):586-93. PubMed ID: 22632830
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and molecular genetic features of pulmonary hypertension in patients with hereditary hemorrhagic telangiectasia.
    Trembath RC; Thomson JR; Machado RD; Morgan NV; Atkinson C; Winship I; Simonneau G; Galie N; Loyd JE; Humbert M; Nichols WC; Morrell NW; Berg J; Manes A; McGaughran J; Pauciulo M; Wheeler L
    N Engl J Med; 2001 Aug; 345(5):325-34. PubMed ID: 11484689
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mutation in BMPR2 Promoter: A 'Second Hit' for Manifestation of Pulmonary Arterial Hypertension?
    Viales RR; Eichstaedt CA; Ehlken N; Fischer C; Lichtblau M; Grünig E; Hinderhofer K
    PLoS One; 2015; 10(7):e0133042. PubMed ID: 26167679
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Identification of a new intronic BMPR2-mutation and early diagnosis of heritable pulmonary arterial hypertension in a large family with mean clinical follow-up of 12 years.
    Hinderhofer K; Fischer C; Pfarr N; Szamalek-Hoegel J; Lichtblau M; Nagel C; Egenlauf B; Ehlken N; Grünig E
    PLoS One; 2014; 9(3):e91374. PubMed ID: 24621962
    [TBL] [Abstract][Full Text] [Related]  

  • 13. BMPR2 gene delivery reduces mutation-related PAH and counteracts TGF-β-mediated pulmonary cell signalling.
    Feng F; Harper RL; Reynolds PN
    Respirology; 2016 Apr; 21(3):526-32. PubMed ID: 26689975
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and genetic characteristics of Chinese patients with hereditary haemorrhagic telangiectasia-associated pulmonary hypertension.
    Chen YJ; Yang QH; Liu D; Liu QQ; Eyries M; Wen L; Wu WH; Jiang X; Yuan P; Zhang R; Soubrier F; Jing ZC
    Eur J Clin Invest; 2013 Oct; 43(10):1016-24. PubMed ID: 23919827
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The Efficacy of a Genetic Analysis of the BMPR2 Gene in a Patient with Severe Pulmonary Arterial Hypertension and an Atrial Septal Defect Treated with Bilateral Lung Transplantation.
    Tatebe S; Sugimura K; Aoki T; Yamamoto S; Yaoita N; Suzuki H; Sato H; Kozu K; Konno R; Satoh K; Fukuda K; Adachi O; Saito R; Nakanishi N; Morisaki H; Oyama K; Saiki Y; Okada Y; Shimokawa H
    Intern Med; 2017 Dec; 56(23):3193-3197. PubMed ID: 29021450
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Genetic, cellular and molecular mechanisms of pulmonary arterial hypertension].
    Alan B; Nalbantgil S
    Anadolu Kardiyol Derg; 2010 Aug; 10 Suppl 1():9-13. PubMed ID: 20819762
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Pulmonary arterial hypertension and portal hypertension in a patient with hereditary hemorrhagic telangiectasia.
    Pousada G; Baloira A; Valverde D
    Med Clin (Barc); 2015 Mar; 144(6):261-4. PubMed ID: 25543221
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Eisenmenger syndrome and atrial septal defect: nature or nurture?
    Therrien J; Rambihar S; Newman B; Siminovitch K; Langleben D; Webb G; Granton J
    Can J Cardiol; 2006 Nov; 22(13):1133-6. PubMed ID: 17102831
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia.
    Harrison RE; Flanagan JA; Sankelo M; Abdalla SA; Rowell J; Machado RD; Elliott CG; Robbins IM; Olschewski H; McLaughlin V; Gruenig E; Kermeen F; Halme M; Räisänen-Sokolowski A; Laitinen T; Morrell NW; Trembath RC
    J Med Genet; 2003 Dec; 40(12):865-71. PubMed ID: 14684682
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Right ventricular and pulmonary vascular reserve in asymptomatic BMPR2 mutation carriers.
    Claessen G; La Gerche A; Petit T; Gillijns H; Bogaert J; Claeys M; Dymarkowski S; Claus P; Delcroix M; Heidbuchel H
    J Heart Lung Transplant; 2017 Feb; 36(2):148-156. PubMed ID: 27475894
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.