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Journal Abstract Search

158 related items for PubMed ID: 16288871

  • 1. The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice.
    von der Hagen M, Laval SH, Cree LM, Haldane F, Pocock M, Wappler I, Peters H, Reitsamer HA, Hoger H, Wiedner M, Oberndorfer F, Anderson LV, Straub V, Bittner RE, Bushby KM.
    Neuromuscul Disord; 2005 Dec; 15(12):863-77. PubMed ID: 16288871
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  • 2. 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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  • 3. Disruption of muscle membrane and phenotype divergence in two novel mouse models of dysferlin deficiency.
    Ho M, Post CM, Donahue LR, Lidov HG, Bronson RT, Goolsby H, Watkins SC, Cox GA, Brown RH.
    Hum Mol Genet; 2004 Sep 15; 13(18):1999-2010. PubMed ID: 15254015
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  • 4. 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 15; 20(1):127-9. PubMed ID: 16306063
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  • 5. 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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  • 6. Role of thrombospondin 1 in macrophage inflammation in dysferlin myopathy.
    De Luna N, Gallardo E, Sonnet C, Chazaud B, Dominguez-Perles R, Suarez-Calvet X, Gherardi RK, Illa I.
    J Neuropathol Exp Neurol; 2010 Jun 08; 69(6):643-53. PubMed ID: 20467328
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  • 7. Novel sequence variants in dysferlin-deficient muscular dystrophy leading to mRNA decay and possible C2-domain misfolding.
    Wenzel K, Carl M, Perrot A, Zabojszcza J, Assadi M, Ebeling M, Geier C, Robinson PN, Kress W, Osterziel KJ, Spuler S.
    Hum Mutat; 2006 Jun 08; 27(6):599-600. PubMed ID: 16705711
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  • 8. Dysferlin expression in monocytes: a source of mRNA for mutation analysis.
    De Luna N, Freixas A, Gallano P, Caselles L, Rojas-García R, Paradas C, Nogales G, Dominguez-Perles R, Gonzalez-Quereda L, Vílchez JJ, Márquez C, Bautista J, Guerrero A, Salazar JA, Pou A, Illa I, Gallardo E.
    Neuromuscul Disord; 2007 Jan 08; 17(1):69-76. PubMed ID: 17070050
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  • 11. Variable reduction of caveolin-3 in patients with LGMD2B/MM.
    Walter MC, Braun C, Vorgerd M, Poppe M, Thirion C, Schmidt C, Schreiber H, Knirsch UI, Brummer D, Müller-Felber W, Pongratz D, Müller-Höcker J, Huebner A, Lochmüller H.
    J Neurol; 2003 Dec 08; 250(12):1431-8. PubMed ID: 14673575
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  • 12. Severe respiratory and skeletal muscles involvement in a carrier of dysferlinopathy with chronic obstructive pulmonary disease.
    Fuschillo S, Torrente Y, Balzano G.
    Respir Care; 2010 Aug 08; 55(8):1091-3. PubMed ID: 20667157
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  • 14. Distal anterior compartment myopathy: a dysferlin mutation causing a new muscular dystrophy phenotype.
    Illa I, Serrano-Munuera C, Gallardo E, Lasa A, Rojas-García R, Palmer J, Gallano P, Baiget M, Matsuda C, Brown RH.
    Ann Neurol; 2001 Jan 08; 49(1):130-4. PubMed ID: 11198284
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  • 19. Murine central and peripheral nervous system transcriptomes: comparative gene expression.
    LeDoux MS, Xu L, Xiao J, Ferrell B, Menkes DL, Homayouni R.
    Brain Res; 2006 Aug 30; 1107(1):24-41. PubMed ID: 16824496
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  • 20. The effects of neuronal induction on gene expression profile in bone marrow stromal cells (BMSC)--a preliminary study using microarray analysis.
    Yamaguchi S, Kuroda S, Kobayashi H, Shichinohe H, Yano S, Hida K, Shinpo K, Kikuchi S, Iwasaki Y.
    Brain Res; 2006 May 04; 1087(1):15-27. PubMed ID: 16626644
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