BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

190 related articles for article (PubMed ID: 11734539)

  • 1. Suppression of revertant fibers in mdx mice by expression of a functional dystrophin.
    Crawford GE; Lu QL; Partridge TA; Chamberlain JS
    Hum Mol Genet; 2001 Nov; 10(24):2745-50. PubMed ID: 11734539
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Morpholino-induced exon skipping stimulates cell-mediated and humoral responses to dystrophin in mdx mice.
    Vila MC; Novak JS; Benny Klimek M; Li N; Morales M; Fritz AG; Edwards K; Boehler JF; Hogarth MW; Kinder TB; Zhang A; Mazala D; Fiorillo AA; Douglas B; Chen YW; van den Anker J; Lu QL; Hathout Y; Hoffman EP; Partridge TA; Nagaraju K
    J Pathol; 2019 Jul; 248(3):339-351. PubMed ID: 30883742
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Massive idiosyncratic exon skipping corrects the nonsense mutation in dystrophic mouse muscle and produces functional revertant fibers by clonal expansion.
    Lu QL; Morris GE; Wilton SD; Ly T; Artem'yeva OV; Strong P; Partridge TA
    J Cell Biol; 2000 Mar; 148(5):985-96. PubMed ID: 10704448
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Revertant fibers in the mdx murine model of Duchenne muscular dystrophy: an age- and muscle-related reappraisal.
    Pigozzo SR; Da Re L; Romualdi C; Mazzara PG; Galletta E; Fletcher S; Wilton SD; Vitiello L
    PLoS One; 2013; 8(8):e72147. PubMed ID: 24015212
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutation types and aging differently affect revertant fiber expansion in dystrophic mdx and mdx52 mice.
    Echigoya Y; Lee J; Rodrigues M; Nagata T; Tanihata J; Nozohourmehrabad A; Panesar D; Miskew B; Aoki Y; Yokota T
    PLoS One; 2013; 8(7):e69194. PubMed ID: 23894429
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Live-imaging of revertant and therapeutically restored dystrophin in the Dmd
    Petkova MV; Stantzou A; Morin A; Petrova O; Morales-Gonzalez S; Seifert F; Bellec-Dyevre J; Manoliu T; Goyenvalle A; Garcia L; Richard I; Laplace-Builhé C; Schuelke M; Amthor H
    Neuropathol Appl Neurobiol; 2020 Oct; 46(6):602-614. PubMed ID: 32573804
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Impaired regenerative capacity and lower revertant fibre expansion in dystrophin-deficient mdx muscles on DBA/2 background.
    Rodrigues M; Echigoya Y; Maruyama R; Lim KR; Fukada SI; Yokota T
    Sci Rep; 2016 Dec; 6():38371. PubMed ID: 27924830
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Prevention of dystrophic pathology in mdx mice by a truncated dystrophin isoform.
    Rafael JA; Sunada Y; Cole NM; Campbell KP; Faulkner JA; Chamberlain JS
    Hum Mol Genet; 1994 Oct; 3(10):1725-33. PubMed ID: 7849695
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Expansion of revertant fibers in dystrophic mdx muscles reflects activity of muscle precursor cells and serves as an index of muscle regeneration.
    Yokota T; Lu QL; Morgan JE; Davies KE; Fisher R; Takeda S; Partridge TA
    J Cell Sci; 2006 Jul; 119(Pt 13):2679-87. PubMed ID: 16757519
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Matrix metalloproteinase-2 ablation in dystrophin-deficient mdx muscles reduces angiogenesis resulting in impaired growth of regenerated muscle fibers.
    Miyazaki D; Nakamura A; Fukushima K; Yoshida K; Takeda S; Ikeda S
    Hum Mol Genet; 2011 May; 20(9):1787-99. PubMed ID: 21320869
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Towards a therapeutic inhibition of dystrophin exon 23 splicing in mdx mouse muscle induced by antisense oligoribonucleotides (splicomers): target sequence optimisation using oligonucleotide arrays.
    Graham IR; Hill VJ; Manoharan M; Inamati GB; Dickson G
    J Gene Med; 2004 Oct; 6(10):1149-58. PubMed ID: 15386737
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Revertant fibres: a possible genetic therapy for Duchenne muscular dystrophy?
    Wilton SD; Dye DE; Blechynden LM; Laing NG
    Neuromuscul Disord; 1997 Jul; 7(5):329-35. PubMed ID: 9267847
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alterations in Notch signalling in skeletal muscles from mdx and dko dystrophic mice and patients with Duchenne muscular dystrophy.
    Church JE; Trieu J; Chee A; Naim T; Gehrig SM; Lamon S; Angelini C; Russell AP; Lynch GS
    Exp Physiol; 2014 Apr; 99(4):675-87. PubMed ID: 24443351
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Enhanced expression of the alpha 7 beta 1 integrin reduces muscular dystrophy and restores viability in dystrophic mice.
    Burkin DJ; Wallace GQ; Nicol KJ; Kaufman DJ; Kaufman SJ
    J Cell Biol; 2001 Mar; 152(6):1207-18. PubMed ID: 11257121
    [TBL] [Abstract][Full Text] [Related]  

  • 15. L-type Ca2+ channel function is linked to dystrophin expression in mammalian muscle.
    Friedrich O; von Wegner F; Chamberlain JS; Fink RH; Rohrbach P
    PLoS One; 2008 Mar; 3(3):e1762. PubMed ID: 18516256
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Inhibitory control over Ca(2+) sparks via mechanosensitive channels is disrupted in dystrophin deficient muscle but restored by mini-dystrophin expression.
    Teichmann MD; Wegner FV; Fink RH; Chamberlain JS; Launikonis BS; Martinac B; Friedrich O
    PLoS One; 2008; 3(11):e3644. PubMed ID: 18982068
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Expression of a NOS transgene in dystrophin-deficient muscle reduces muscle membrane damage without increasing the expression of membrane-associated cytoskeletal proteins.
    Tidball JG; Wehling-Henricks M
    Mol Genet Metab; 2004 Aug; 82(4):312-20. PubMed ID: 15308129
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Differential expression of myosin heavy chain isoforms in the masticatory muscles of dystrophin-deficient mice.
    Spassov A; Gredes T; Gedrange T; Lucke S; Morgenstern S; Pavlovic D; Kunert-Keil C
    Eur J Orthod; 2011 Dec; 33(6):613-9. PubMed ID: 21187529
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Rescue of dystrophin expression in mdx mouse muscle by RNA/DNA oligonucleotides.
    Rando TA; Disatnik MH; Zhou LZ
    Proc Natl Acad Sci U S A; 2000 May; 97(10):5363-8. PubMed ID: 10805797
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mdx mice inducibly expressing dystrophin provide insights into the potential of gene therapy for duchenne muscular dystrophy.
    Ahmad A; Brinson M; Hodges BL; Chamberlain JS; Amalfitano A
    Hum Mol Genet; 2000 Oct; 9(17):2507-15. PubMed ID: 11030755
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.