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403 related items for PubMed ID: 16519886

  • 1. Forced expression of desmin and desmin mutants in cultured cells: impact of myopathic missense mutations in the central coiled-coil domain on network formation.
    Bär H, Kostareva A, Sjöberg G, Sejersen T, Katus HA, Herrmann H.
    Exp Cell Res; 2006 May 15; 312(9):1554-65. PubMed ID: 16519886
    [Abstract] [Full Text] [Related]

  • 2. Pathogenic effects of a novel heterozygous R350P desmin mutation on the assembly of desmin intermediate filaments in vivo and in vitro.
    Bär H, Fischer D, Goudeau B, Kley RA, Clemen CS, Vicart P, Herrmann H, Vorgerd M, Schröder R.
    Hum Mol Genet; 2005 May 15; 14(10):1251-60. PubMed ID: 15800015
    [Abstract] [Full Text] [Related]

  • 3. Severe muscle disease-causing desmin mutations interfere with in vitro filament assembly at distinct stages.
    Bär H, Mücke N, Kostareva A, Sjöberg G, Aebi U, Herrmann H.
    Proc Natl Acad Sci U S A; 2005 Oct 18; 102(42):15099-104. PubMed ID: 16217025
    [Abstract] [Full Text] [Related]

  • 4. Assembly of carboxy-terminally deleted desmin in vimentin-free cells.
    Raats JM, Henderik JB, Verdijk M, van Oort FL, Gerards WL, Ramaekers FC, Bloemendal H.
    Eur J Cell Biol; 1991 Oct 18; 56(1):84-103. PubMed ID: 1724756
    [Abstract] [Full Text] [Related]

  • 5. Impact of disease mutations on the desmin filament assembly process.
    Bär H, Mücke N, Ringler P, Müller SA, Kreplak L, Katus HA, Aebi U, Herrmann H.
    J Mol Biol; 2006 Jul 28; 360(5):1031-42. PubMed ID: 16828798
    [Abstract] [Full Text] [Related]

  • 6. Biochemical and structural aspects of transiently and stably expressed mutant desmin in vimentin-free and vimentin-containing cells.
    Raats JM, Gerards WL, Schreuder MI, Grund C, Henderik JB, Hendriks IL, Ramaekers FC, Bloemendal H.
    Eur J Cell Biol; 1992 Jun 28; 58(1):108-27. PubMed ID: 1644057
    [Abstract] [Full Text] [Related]

  • 7. Desmin myopathy, a skeletal myopathy with cardiomyopathy caused by mutations in the desmin gene.
    Dalakas MC, Park KY, Semino-Mora C, Lee HS, Sivakumar K, Goldfarb LG.
    N Engl J Med; 2000 Mar 16; 342(11):770-80. PubMed ID: 10717012
    [Abstract] [Full Text] [Related]

  • 8. Truncation mutagenesis of the non-alpha-helical carboxyterminal tail domain of vimentin reveals contributions to cellular localization but not to filament assembly.
    Rogers KR, Eckelt A, Nimmrich V, Janssen KP, Schliwa M, Herrmann H, Franke WW.
    Eur J Cell Biol; 1995 Feb 16; 66(2):136-50. PubMed ID: 7774600
    [Abstract] [Full Text] [Related]

  • 9. Disruption of vimentin intermediate filaments in transgenic mice by expression of a dominant negative mutant desmin subunit.
    Pieper FR, Raats JM, Schaart G, Dunia I, van der Kemp A, Benedetti EL, Ramaekers FC, Bloemendal H.
    Eur J Cell Biol; 1995 Dec 16; 68(4):355-68. PubMed ID: 8690015
    [Abstract] [Full Text] [Related]

  • 10. Colocalization of nestin and vimentin/desmin in skeletal muscle cells demonstrated by three-dimensional fluorescence digital imaging microscopy.
    Sjöberg G, Jiang WQ, Ringertz NR, Lendahl U, Sejersen T.
    Exp Cell Res; 1994 Oct 16; 214(2):447-58. PubMed ID: 7925640
    [Abstract] [Full Text] [Related]

  • 11. Interaction of surfactant protein A with the intermediate filaments desmin and vimentin.
    Garcia-Verdugo I, Synguelakis M, Degrouard J, Franco CA, Valot B, Zivy M, Chaby R, Tanfin Z.
    Biochemistry; 2008 May 06; 47(18):5127-38. PubMed ID: 18407667
    [Abstract] [Full Text] [Related]

  • 12. Mutations in desmin's carboxy-terminal "tail" domain severely modify filament and network mechanics.
    Bär H, Schopferer M, Sharma S, Hochstein B, Mücke N, Herrmann H, Willenbacher N.
    J Mol Biol; 2010 Apr 16; 397(5):1188-98. PubMed ID: 20171226
    [Abstract] [Full Text] [Related]

  • 13. Interference of amino-terminal desmin fragments with desmin filament formation.
    Bär H, Sharma S, Kleiner H, Mücke N, Zentgraf H, Katus HA, Aebi U, Herrmann H.
    Cell Motil Cytoskeleton; 2009 Nov 16; 66(11):986-99. PubMed ID: 19530175
    [Abstract] [Full Text] [Related]

  • 14. Expression of desmin cDNA in PtK2 cells results in assembly of desmin filaments from multiple sites throughout the cytoplasm.
    Mittal B, Danowski BA, Sanger JM, Sanger JW.
    Cell Motil Cytoskeleton; 1992 Nov 16; 23(3):188-200. PubMed ID: 1292875
    [Abstract] [Full Text] [Related]

  • 15. Plectin interacts with the rod domain of type III intermediate filament proteins desmin and vimentin.
    Favre B, Schneider Y, Lingasamy P, Bouameur JE, Begré N, Gontier Y, Steiner-Champliaud MF, Frias MA, Borradori L, Fontao L.
    Eur J Cell Biol; 2011 May 16; 90(5):390-400. PubMed ID: 21296452
    [Abstract] [Full Text] [Related]

  • 16. Severe myopathy mutations modify the nanomechanics of desmin intermediate filaments.
    Kreplak L, Bär H.
    J Mol Biol; 2009 Jan 30; 385(4):1043-51. PubMed ID: 19026658
    [Abstract] [Full Text] [Related]

  • 17. Characterization of distinct early assembly units of different intermediate filament proteins.
    Herrmann H, Häner M, Brettel M, Ku NO, Aebi U.
    J Mol Biol; 1999 Mar 12; 286(5):1403-20. PubMed ID: 10064706
    [Abstract] [Full Text] [Related]

  • 18. Network incorporation of intermediate filament molecules differs between preexisting and newly assembling filaments.
    Lu X, Quinlan RA, Steel JB, Lane EB.
    Exp Cell Res; 1993 Sep 12; 208(1):218-25. PubMed ID: 7689477
    [Abstract] [Full Text] [Related]

  • 19. Assembly defects of desmin disease mutants carrying deletions in the alpha-helical rod domain are rescued by wild type protein.
    Bär H, Mücke N, Katus HA, Aebi U, Herrmann H.
    J Struct Biol; 2007 Apr 12; 158(1):107-15. PubMed ID: 17188893
    [Abstract] [Full Text] [Related]

  • 20. Structural and functional analysis of a new desmin variant causing desmin-related myopathy.
    Goudeau B, Dagvadorj A, Rodrigues-Lima F, Nédellec P, Casteras-Simon M, Perret E, Langlois S, Goldfarb L, Vicart P.
    Hum Mutat; 2001 Nov 12; 18(5):388-96. PubMed ID: 11668632
    [Abstract] [Full Text] [Related]

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