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354 related items for PubMed ID: 9326947

  • 1. Targetting of the gene encoding fibrillin-1 recapitulates the vascular aspect of Marfan syndrome.
    Pereira L, Andrikopoulos K, Tian J, Lee SY, Keene DR, Ono R, Reinhardt DP, Sakai LY, Biery NJ, Bunton T, Dietz HC, Ramirez F.
    Nat Genet; 1997 Oct; 17(2):218-22. PubMed ID: 9326947
    [Abstract] [Full Text] [Related]

  • 2. Pathogenetic sequence for aneurysm revealed in mice underexpressing fibrillin-1.
    Pereira L, Lee SY, Gayraud B, Andrikopoulos K, Shapiro SD, Bunton T, Biery NJ, Dietz HC, Sakai LY, Ramirez F.
    Proc Natl Acad Sci U S A; 1999 Mar 30; 96(7):3819-23. PubMed ID: 10097121
    [Abstract] [Full Text] [Related]

  • 3. Marfan syndrome: new clues to genotype-phenotype correlations.
    Ramirez F, Gayraud B, Pereira L.
    Ann Med; 1999 Jun 30; 31(3):202-7. PubMed ID: 10442675
    [Abstract] [Full Text] [Related]

  • 4. miR-29b participates in early aneurysm development in Marfan syndrome.
    Merk DR, Chin JT, Dake BA, Maegdefessel L, Miller MO, Kimura N, Tsao PS, Iosef C, Berry GJ, Mohr FW, Spin JM, Alvira CM, Robbins RC, Fischbein MP.
    Circ Res; 2012 Jan 20; 110(2):312-24. PubMed ID: 22116819
    [Abstract] [Full Text] [Related]

  • 5. Therapy insight: aortic aneurysm and dissection in Marfan's syndrome.
    Ramirez F, Dietz HC.
    Nat Clin Pract Cardiovasc Med; 2004 Nov 20; 1(1):31-6. PubMed ID: 16265257
    [Abstract] [Full Text] [Related]

  • 6. Phenotypic alteration of vascular smooth muscle cells precedes elastolysis in a mouse model of Marfan syndrome.
    Bunton TE, Biery NJ, Myers L, Gayraud B, Ramirez F, Dietz HC.
    Circ Res; 2001 Jan 19; 88(1):37-43. PubMed ID: 11139471
    [Abstract] [Full Text] [Related]

  • 7. Mutations of extracellular matrix components in vascular disease.
    Ramirez F, Pereira L.
    Ann Thorac Surg; 1999 Jun 19; 67(6):1857-8; discussion 1868-70. PubMed ID: 10391325
    [Abstract] [Full Text] [Related]

  • 8. Ascending aortic aneurysm with or without features of Marfan syndrome and other fibrillinopathies: new insights.
    Furthmayr H, Francke U.
    Semin Thorac Cardiovasc Surg; 1997 Jul 19; 9(3):191-205. PubMed ID: 9263339
    [Abstract] [Full Text] [Related]

  • 9. Fibrillin-1 genetic deficiency leads to pathological ageing of arteries in mice.
    Mariko B, Pezet M, Escoubet B, Bouillot S, Andrieu JP, Starcher B, Quaglino D, Jacob MP, Huber P, Ramirez F, Faury G.
    J Pathol; 2011 May 19; 224(1):33-44. PubMed ID: 21432852
    [Abstract] [Full Text] [Related]

  • 10. Nanoscale Structural Comparison of Fibrillin-1 Microfibrils Isolated from Marfan and Non-Marfan Syndrome Human Aorta.
    Șulea CM, Mártonfalvi Z, Csányi C, Haluszka D, Pólos M, Ágg B, Stengl R, Benke K, Szabolcs Z, Kellermayer MSZ.
    Int J Mol Sci; 2023 Apr 20; 24(8):. PubMed ID: 37108724
    [Abstract] [Full Text] [Related]

  • 11. New insights into the structure, assembly and biological roles of 10-12 nm connective tissue microfibrils from fibrillin-1 studies.
    Jensen SA, Handford PA.
    Biochem J; 2016 Apr 01; 473(7):827-38. PubMed ID: 27026396
    [Abstract] [Full Text] [Related]

  • 12. Genetic fibrillinopathies: new insights in molecular diagnosis and clinical management.
    Loeys BL, Matthys DM, de Paepe AM.
    Acta Clin Belg; 2003 Apr 01; 58(1):3-11. PubMed ID: 12723256
    [Abstract] [Full Text] [Related]

  • 13. Elastic and collagenous networks in vascular diseases.
    Arteaga-Solis E, Gayraud B, Ramirez F.
    Cell Struct Funct; 2000 Apr 01; 25(2):69-72. PubMed ID: 10885576
    [Abstract] [Full Text] [Related]

  • 14. A Gly1127Ser mutation in an EGF-like domain of the fibrillin-1 gene is a risk factor for ascending aortic aneurysm and dissection.
    Francke U, Berg MA, Tynan K, Brenn T, Liu W, Aoyama T, Gasner C, Miller DC, Furthmayr H.
    Am J Hum Genet; 1995 Jun 01; 56(6):1287-96. PubMed ID: 7762551
    [Abstract] [Full Text] [Related]

  • 15. Relationship between fibrillin-1 genotype and severity of cardiovascular involvement in Marfan syndrome.
    Franken R, Teixido-Tura G, Brion M, Forteza A, Rodriguez-Palomares J, Gutierrez L, Garcia Dorado D, Pals G, Mulder BJ, Evangelista A.
    Heart; 2017 Nov 01; 103(22):1795-1799. PubMed ID: 28468757
    [Abstract] [Full Text] [Related]

  • 16. Rationale and design of a trial evaluating the effects of losartan vs. nebivolol vs. the association of both on the progression of aortic root dilation in Marfan syndrome with FBN1 gene mutations.
    Gambarin FI, Favalli V, Serio A, Regazzi M, Pasotti M, Klersy C, Dore R, Mannarino S, Viganò M, Odero A, Amato S, Tavazzi L, Arbustini E.
    J Cardiovasc Med (Hagerstown); 2009 Apr 01; 10(4):354-62. PubMed ID: 19430350
    [Abstract] [Full Text] [Related]

  • 17. The molecular pathogenesis of the Marfan syndrome.
    Robinson PN, Booms P.
    Cell Mol Life Sci; 2001 Oct 01; 58(11):1698-707. PubMed ID: 11706995
    [Abstract] [Full Text] [Related]

  • 18. Ciprofloxacin accelerates aortic enlargement and promotes dissection and rupture in Marfan mice.
    LeMaire SA, Zhang L, Zhang NS, Luo W, Barrish JP, Zhang Q, Coselli JS, Shen YH.
    J Thorac Cardiovasc Surg; 2022 Mar 01; 163(3):e215-e226. PubMed ID: 34586071
    [Abstract] [Full Text] [Related]

  • 19. Identification of fibrillin 1 gene mutations in patients with bicuspid aortic valve (BAV) without Marfan syndrome.
    Pepe G, Nistri S, Giusti B, Sticchi E, Attanasio M, Porciani C, Abbate R, Bonow RO, Yacoub M, Gensini GF.
    BMC Med Genet; 2014 Feb 24; 15():23. PubMed ID: 24564502
    [Abstract] [Full Text] [Related]

  • 20. Fibrillin in Marfan syndrome and tight skin mice provides new insights into transforming growth factor-beta regulation and systemic sclerosis.
    Lemaire R, Bayle J, Lafyatis R.
    Curr Opin Rheumatol; 2006 Nov 24; 18(6):582-7. PubMed ID: 17053502
    [Abstract] [Full Text] [Related]

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