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Journal Abstract Search

141 related items for PubMed ID: 15811552

  • 1. Expression profiling with progression of dystrophic change in dysferlin-deficient mice (SJL).
    Suzuki N, Aoki M, Hinuma Y, Takahashi T, Onodera Y, Ishigaki A, Kato M, Warita H, Tateyama M, Itoyama Y.
    Neurosci Res; 2005 May; 52(1):47-60. PubMed ID: 15811552
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  • 4. Efficient recovery of dysferlin deficiency by dual adeno-associated vector-mediated gene transfer.
    Lostal W, Bartoli M, Bourg N, Roudaut C, Bentaïb A, Miyake K, Guerchet N, Fougerousse F, McNeil P, Richard I.
    Hum Mol Genet; 2010 May 15; 19(10):1897-907. PubMed ID: 20154340
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  • 6. Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients.
    Au CG, Butler TL, Egan JR, Cooper ST, Lo HP, Compton AG, North KN, Winlaw DS.
    Acta Neuropathol; 2008 Sep 15; 116(3):235-46. PubMed ID: 18392839
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  • 7. Defective membrane repair in dysferlin-deficient muscular dystrophy.
    Bansal D, Miyake K, Vogel SS, Groh S, Chen CC, Williamson R, McNeil PL, Campbell KP.
    Nature; 2003 May 08; 423(6936):168-72. PubMed ID: 12736685
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  • 11. Characterisation of the dysferlin skeletal muscle promoter.
    Foxton RM, Laval SH, Bushby KM.
    Eur J Hum Genet; 2004 Feb 08; 12(2):127-31. PubMed ID: 14560310
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  • 12. Common pathological mechanisms in mouse models for muscular dystrophies.
    Turk R, Sterrenburg E, van der Wees CG, de Meijer EJ, de Menezes RX, Groh S, Campbell KP, Noguchi S, van Ommen GJ, den Dunnen JT, 't Hoen PA.
    FASEB J; 2006 Jan 08; 20(1):127-9. PubMed ID: 16306063
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  • 15. Loss of podocyte dysferlin expression is associated with minimal change nephropathy.
    Izzedine H, Brocheriou I, Eymard B, Le Charpentier M, Romero NB, Lenaour G, Bourry E, Deray G.
    Am J Kidney Dis; 2006 Jul 08; 48(1):143-50. PubMed ID: 16797397
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  • 16. Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B.
    Bittner RE, Anderson LV, Burkhardt E, Bashir R, Vafiadaki E, Ivanova S, Raffelsberger T, Maerk I, Höger H, Jung M, Karbasiyan M, Storch M, Lassmann H, Moss JA, Davison K, Harrison R, Bushby KM, Reis A.
    Nat Genet; 1999 Oct 08; 23(2):141-2. PubMed ID: 10508505
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  • 18. Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice.
    Leriche-Guérin K, Anderson LV, Wrogemann K, Roy B, Goulet M, Tremblay JP.
    Neuromuscul Disord; 2002 Feb 08; 12(2):167-73. PubMed ID: 11738359
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  • 19. Painful enlargement of the calf muscles in limb girdle muscular dystrophy type 2B (LGMD2B) with a novel compound heterozygous mutation in DYSF.
    Diers A, Carl M, Stoltenburg-Didinger G, Vorgerd M, Spuler S.
    Neuromuscul Disord; 2007 Feb 08; 17(2):157-62. PubMed ID: 17129727
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  • 20. Dysferlin mutations in LGMD2B, Miyoshi myopathy, and atypical dysferlinopathies.
    Nguyen K, Bassez G, Bernard R, Krahn M, Labelle V, Figarella-Branger D, Pouget J, Hammouda el H, Béroud C, Urtizberea A, Eymard B, Leturcq F, Lévy N.
    Hum Mutat; 2005 Aug 08; 26(2):165. PubMed ID: 16010686
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