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Journal Abstract Search

407 related items for PubMed ID: 8240311

  • 1. The fibrillin-Marfan syndrome connection.
    Ramirez F, Pereira L, Zhang H, Lee B.
    Bioessays; 1993 Sep; 15(9):589-94. PubMed ID: 8240311
    [Abstract] [Full Text] [Related]

  • 2. Microfibrils: a cornerstone of extracellular matrix and a key to understand Marfan syndrome.
    Bonetti MI.
    Ital J Anat Embryol; 2009 Sep; 114(4):201-24. PubMed ID: 20578676
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  • 4. Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders.
    Dietz HC, Pyeritz RE.
    Hum Mol Genet; 1995 Sep; 4 Spec No():1799-809. PubMed ID: 8541880
    [Abstract] [Full Text] [Related]

  • 5. 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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  • 7. The molecular basis of Marfan syndrome.
    Maslen CL, Glanville RW.
    DNA Cell Biol; 1993 Sep 01; 12(7):561-72. PubMed ID: 8397814
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  • 10. The fibrillins.
    Ramirez F, Pereira L.
    Int J Biochem Cell Biol; 1999 Feb 01; 31(2):255-9. PubMed ID: 10216958
    [Abstract] [Full Text] [Related]

  • 11. Fibrillin microfibrils.
    Kielty CM, Sherratt MJ, Marson A, Baldock C.
    Adv Protein Chem; 2005 Feb 01; 70():405-36. PubMed ID: 15837522
    [Abstract] [Full Text] [Related]

  • 12. Partial sequence of a candidate gene for the Marfan syndrome.
    Maslen CL, Corson GM, Maddox BK, Glanville RW, Sakai LY.
    Nature; 1991 Jul 25; 352(6333):334-7. PubMed ID: 1852207
    [Abstract] [Full Text] [Related]

  • 13. Fibrillin-rich microfibrils: Structural determinants of morphogenetic and homeostatic events.
    Ramirez F, Dietz HC.
    J Cell Physiol; 2007 Nov 25; 213(2):326-30. PubMed ID: 17708531
    [Abstract] [Full Text] [Related]

  • 14. Fibrillin-1 mutations in Marfan syndrome and other type-1 fibrillinopathies.
    Hayward C, Brock DJ.
    Hum Mutat; 1997 Nov 25; 10(6):415-23. PubMed ID: 9401003
    [Abstract] [Full Text] [Related]

  • 15. The molecular genetics of Marfan syndrome and related microfibrillopathies.
    Robinson PN, Godfrey M.
    J Med Genet; 2000 Jan 25; 37(1):9-25. PubMed ID: 10633129
    [Abstract] [Full Text] [Related]

  • 16. Fibrillin-1, a calcium binding protein of extracellular matrix.
    Handford PA.
    Biochim Biophys Acta; 2000 Dec 20; 1498(2-3):84-90. PubMed ID: 11108952
    [Abstract] [Full Text] [Related]

  • 17. Identification of defects in the fibrillin gene and protein in individuals with the Marfan syndrome and related disorders.
    Milewicz DM.
    Tex Heart Inst J; 1994 Dec 20; 21(1):22-9. PubMed ID: 8180508
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  • 18. Basic Components of Connective Tissues and Extracellular Matrix: Fibronectin, Fibrinogen, Laminin, Elastin, Fibrillins, Fibulins, Matrilins, Tenascins and Thrombospondins.
    Halper J.
    Adv Exp Med Biol; 2021 Dec 20; 1348():105-126. PubMed ID: 34807416
    [Abstract] [Full Text] [Related]

  • 19. 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 20; 9(3):191-205. PubMed ID: 9263339
    [Abstract] [Full Text] [Related]

  • 20. Fibrillln mutations in Marfan syndrome and related phenotypes.
    Ramirez F.
    Curr Opin Genet Dev; 1996 Jun 20; 6(3):309-15. PubMed ID: 8791520
    [Abstract] [Full Text] [Related]

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