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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

491 related items for PubMed ID: 8397814

  • 1. The molecular basis of Marfan syndrome.
    Maslen CL, Glanville RW.
    DNA Cell Biol; 1993 Sep; 12(7):561-72. PubMed ID: 8397814
    [Abstract] [Full Text] [Related]

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

  • 3. 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 Sep; 765():7-18. PubMed ID: 26281765
    [Abstract] [Full Text] [Related]

  • 4. 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 Sep; 21(1):22-9. PubMed ID: 8180508
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Fibrillin: from microfibril assembly to biomechanical function.
    Kielty CM, Baldock C, Lee D, Rock MJ, Ashworth JL, Shuttleworth CA.
    Philos Trans R Soc Lond B Biol Sci; 2002 Feb 28; 357(1418):207-17. PubMed ID: 11911778
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders.
    Dietz HC, Pyeritz RE.
    Hum Mol Genet; 1995 Feb 28; 4 Spec No():1799-809. PubMed ID: 8541880
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes.
    Lee B, Godfrey M, Vitale E, Hori H, Mattei MG, Sarfarazi M, Tsipouras P, Ramirez F, Hollister DW.
    Nature; 1991 Jul 25; 352(6333):330-4. PubMed ID: 1852206
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 25.