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2. 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; 112 ( Pt 6)():867-76. PubMed ID: 10036236 [Abstract] [Full Text] [Related]
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7. Immunogold EM reveals a close association of plectin and the desmin cytoskeleton in human skeletal muscle. Schröder R, Warlo I, Herrmann H, van der Ven PF, Klasen C, Blümcke I, Mundegar RR, Fürst DO, Goebel HH, Magin TM. Eur J Cell Biol; 1999 Apr; 78(4):288-95. PubMed ID: 10350217 [Abstract] [Full Text] [Related]
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10. Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy. Winter L, Türk M, Harter PN, Mittelbronn M, Kornblum C, Norwood F, Jungbluth H, Thiel CT, Schlötzer-Schrehardt U, Schröder R. Acta Neuropathol Commun; 2016 Apr 27; 4(1):44. PubMed ID: 27121971 [Abstract] [Full Text] [Related]
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12. Altered distribution of plectin/HD1 in dystrophinopathies. Schröder R, Mundegar RR, Treusch M, Schlegel U, Blümcke I, Owaribe K, Magin TM. Eur J Cell Biol; 1997 Oct 27; 74(2):165-71. PubMed ID: 9352221 [Abstract] [Full Text] [Related]
15. 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 [Abstract] [Full Text] [Related]
19. 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 [Abstract] [Full Text] [Related]
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