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Journal Abstract Search

129 related items for PubMed ID: 9352221

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  • 2. Defective expression of plectin/HD1 in epidermolysis bullosa simplex with muscular dystrophy.
    Gache Y, Chavanas S, Lacour JP, Wiche G, Owaribe K, Meneguzzi G, Ortonne JP.
    J Clin Invest; 1996 May 15; 97(10):2289-98. PubMed ID: 8636409
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  • 4. Primary longitudinal adhesion structures: plectin-containing precursors of costameres in differentiating human skeletal muscle cells.
    Schröder R, Pacholsky D, Reimann J, Matten J, Wiche G, Fürst DO, van der Ven PF.
    Histochem Cell Biol; 2002 Oct 15; 118(4):301-10. PubMed ID: 12376826
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  • 5. Association of mitochondria with plectin and desmin intermediate filaments in striated muscle.
    Reipert S, Steinböck F, Fischer I, Bittner RE, Zeöld A, Wiche G.
    Exp Cell Res; 1999 Nov 01; 252(2):479-91. PubMed ID: 10527638
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  • 7. A homozygous nonsense mutation in the PLEC1 gene in patients with epidermolysis bullosa simplex with muscular dystrophy.
    Chavanas S, Pulkkinen L, Gache Y, Smith FJ, McLean WH, Uitto J, Ortonne JP, Meneguzzi G.
    J Clin Invest; 1996 Nov 15; 98(10):2196-200. PubMed ID: 8941634
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  • 10. Plectin tethers desmin intermediate filaments onto subsarcolemmal dense plaques containing dystrophin and vinculin.
    Hijikata T, Murakami T, Ishikawa H, Yorifuji H.
    Histochem Cell Biol; 2003 Feb 15; 119(2):109-23. PubMed ID: 12610730
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  • 12. Plectin is a linker of intermediate filaments to Z-discs in skeletal muscle fibers.
    Hijikata T, Murakami T, Imamura M, Fujimaki N, Ishikawa H.
    J Cell Sci; 1999 Mar 15; 112 ( Pt 6)():867-76. PubMed ID: 10036236
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  • 14. Disorganization of the desmin cytoskeleton and mitochondrial dysfunction in plectin-related epidermolysis bullosa simplex with muscular dystrophy.
    Schröder R, Kunz WS, Rouan F, Pfendner E, Tolksdorf K, Kappes-Horn K, Altenschmidt-Mehring M, Knoblich R, van der Ven PF, Reimann J, Fürst DO, Blümcke I, Vielhaber S, Zillikens D, Eming S, Klockgether T, Uitto J, Wiche G, Rolfs A.
    J Neuropathol Exp Neurol; 2002 Jun 15; 61(6):520-30. PubMed ID: 12071635
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  • 20. Homozygous deletion mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophy.
    Pulkkinen L, Smith FJ, Shimizu H, Murata S, Yaoita H, Hachisuka H, Nishikawa T, McLean WH, Uitto J.
    Hum Mol Genet; 1996 Oct 15; 5(10):1539-46. PubMed ID: 8894687
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