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Journal Abstract Search


381 related items for PubMed ID: 15254580

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  • 7. Engineered mutations in fibrillin-1 leading to Marfan syndrome act at the protein, cellular and organismal levels.
    Zeyer KA, Reinhardt DP.
    Mutat Res Rev Mutat Res; 2015; 765():7-18. PubMed ID: 26281765
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  • 10. 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
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  • 12. [Molecular biological aspects of Marfan syndromes].
    Belsing TZ, Lund AM, Abildstrøm SZ, Søndergaard L, Friis-Hansen L.
    Ugeskr Laeger; 2011 Jan 31; 173(5):333-7. PubMed ID: 21276395
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  • 13. Fibrillin-rich microfibrils: Structural determinants of morphogenetic and homeostatic events.
    Ramirez F, Dietz HC.
    J Cell Physiol; 2007 Nov 31; 213(2):326-30. PubMed ID: 17708531
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  • 14. 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 15; 139C(1):4-9. PubMed ID: 16273535
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  • 16. Evidence for a critical contribution of haploinsufficiency in the complex pathogenesis of Marfan syndrome.
    Judge DP, Biery NJ, Keene DR, Geubtner J, Myers L, Huso DL, Sakai LY, Dietz HC.
    J Clin Invest; 2004 Jul 15; 114(2):172-81. PubMed ID: 15254584
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  • 19. 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 15; 30(12):2709-19. PubMed ID: 23037987
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