These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

116 related articles for article (PubMed ID: 15714930)

  • 1. Radiotherapy and Marfan syndrome: a report of two cases.
    Finlay M; Laperriere N; Bristow RG
    Clin Oncol (R Coll Radiol); 2005 Feb; 17(1):54-6. PubMed ID: 15714930
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Molecular biological aspects of Marfan syndromes].
    Belsing TZ; Lund AM; Abildstrøm SZ; Søndergaard L; Friis-Hansen L
    Ugeskr Laeger; 2011 Jan; 173(5):333-7. PubMed ID: 21276395
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Interactions between fibrillin-1 and tgf-beta: consequences and human pathology].
    Wipff J; Allanore Y; Boileau C
    Med Sci (Paris); 2009 Feb; 25(2):161-7. PubMed ID: 19239848
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic analysis of the contribution of LTBP-3 to thoracic aneurysm in Marfan syndrome.
    Zilberberg L; Phoon CK; Robertson I; Dabovic B; Ramirez F; Rifkin DB
    Proc Natl Acad Sci U S A; 2015 Nov; 112(45):14012-7. PubMed ID: 26494287
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular pathogenesis of Marfan syndrome.
    Ramachandra CJ; Mehta A; Guo KW; Wong P; Tan JL; Shim W
    Int J Cardiol; 2015; 187():585-91. PubMed ID: 25863307
    [TBL] [Abstract][Full Text] [Related]  

  • 6. TGF-beta-dependent pathogenesis of mitral valve prolapse in a mouse model of Marfan syndrome.
    Ng CM; Cheng A; Myers LA; Martinez-Murillo F; Jie C; Bedja D; Gabrielson KL; Hausladen JM; Mecham RP; Judge DP; Dietz HC
    J Clin Invest; 2004 Dec; 114(11):1586-92. PubMed ID: 15546004
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Exogenous activation of BMP-2 signaling overcomes TGFβ-mediated inhibition of osteogenesis in Marfan embryonic stem cells and Marfan patient-specific induced pluripotent stem cells.
    Quarto N; Li S; Renda A; Longaker MT
    Stem Cells; 2012 Dec; 30(12):2709-19. PubMed ID: 23037987
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 110(2):312-24. PubMed ID: 22116819
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome.
    Loeys B; Nuytinck L; Delvaux I; De Bie S; De Paepe A
    Arch Intern Med; 2001 Nov; 161(20):2447-54. PubMed ID: 11700157
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Antagonism of GxxPG fragments ameliorates manifestations of aortic disease in Marfan syndrome mice.
    Guo G; Muñoz-García B; Ott CE; Grünhagen J; Mousa SA; Pletschacher A; von Kodolitsch Y; Knaus P; Robinson PN
    Hum Mol Genet; 2013 Feb; 22(3):433-43. PubMed ID: 23100322
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Recent progress towards a molecular understanding of Marfan syndrome.
    Dietz HC; Loeys B; Carta L; Ramirez F
    Am J Med Genet C Semin Med Genet; 2005 Nov; 139C(1):4-9. PubMed ID: 16273535
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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; 18(6):582-7. PubMed ID: 17053502
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Cardiac remodeling in the mouse model of Marfan syndrome develops into two distinctive phenotypes.
    Tae HJ; Petrashevskaya N; Marshall S; Krawczyk M; Talan M
    Am J Physiol Heart Circ Physiol; 2016 Jan; 310(2):H290-9. PubMed ID: 26566724
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fibrillin abnormalities and prognosis in Marfan syndrome and related disorders.
    Aoyama T; Francke U; Gasner C; Furthmayr H
    Am J Med Genet; 1995 Aug; 58(2):169-76. PubMed ID: 8533811
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutations of FBN1 and genotype-phenotype correlations in Marfan syndrome and related fibrillinopathies.
    Robinson PN; Booms P; Katzke S; Ladewig M; Neumann L; Palz M; Pregla R; Tiecke F; Rosenberg T
    Hum Mutat; 2002 Sep; 20(3):153-61. PubMed ID: 12203987
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Antagonistic effect of the matricellular signaling protein CCN3 on TGF-beta- and Wnt-mediated fibrillinogenesis in systemic sclerosis and Marfan syndrome.
    Lemaire R; Farina G; Bayle J; Dimarzio M; Pendergrass SA; Milano A; Perbal B; Whitfield ML; Lafyatis R
    J Invest Dermatol; 2010 Jun; 130(6):1514-23. PubMed ID: 20182440
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Fibrillin-1 gene mutation in Chinese patients with Marfan syndrome and its gene diagnosis by haplotype analysis].
    Wang B; Hu DX; Xia JH; Li Q; Lu GH
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2003 Feb; 20(1):1-4. PubMed ID: 12579488
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Marfan syndrome: from gene to therapy.
    Bolar N; Van Laer L; Loeys BL
    Curr Opin Pediatr; 2012 Aug; 24(4):498-504. PubMed ID: 22705998
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Muscle and Bone Impairment in Children With Marfan Syndrome: Correlation With Age and FBN1 Genotype.
    Haine E; Salles JP; Khau Van Kien P; Conte-Auriol F; Gennero I; Plancke A; Julia S; Dulac Y; Tauber M; Edouard T
    J Bone Miner Res; 2015 Aug; 30(8):1369-76. PubMed ID: 25656438
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypes.
    Cook JR; Carta L; Galatioto J; Ramirez F
    Clin Genet; 2015; 87(1):11-20. PubMed ID: 24867163
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.