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Journal Abstract Search

253 related items for PubMed ID: 2261642

  • 21. Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy.
    Arahata K, Beggs AH, Honda H, Ito S, Ishiura S, Tsukahara T, Ishiguro T, Eguchi C, Orimo S, Arikawa E.
    J Neurol Sci; 1991 Feb; 101(2):148-56. PubMed ID: 2033400
    [Abstract] [Full Text] [Related]

  • 22. Molecular deletion patterns in Turkish Duchenne and Becker muscular dystrophy patients.
    Dinçer P, Topaloğlu H, Ayter S, Ozgüç M, Taşdemir HA, Renda Y.
    Brain Dev; 1996 Feb; 18(2):91-4. PubMed ID: 8733896
    [Abstract] [Full Text] [Related]

  • 23. [Molecular pathology of Duchenne and Becker muscular dystrophy].
    Gilgenkrantz H, Chelly J, Récan D, Chafey P, Kaplan JC.
    C R Seances Soc Biol Fil; 1992 Feb; 186(4):349-53. PubMed ID: 1301222
    [Abstract] [Full Text] [Related]

  • 24. [Deletions within the gene of dystrophin in Duchenne and Becker muscular dystrophy].
    Zimowski JG, Bisko M, Fidziańska E, Hausmanowa-Petrusewicz I, Badurska B, Borkowska J, Lusakowska A, Fidziańska A, Jezuita J, Zaremba J.
    Neurol Neurochir Pol; 1993 Feb; 27(4):469-78. PubMed ID: 8247234
    [Abstract] [Full Text] [Related]

  • 25. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection.
    Asano J, Tomatsu S, Sukegawa K, Ikedo Y, Minami R, Iida M, Nishimura M, Nakagawa M, Ohshiro M, Orii T.
    Clin Genet; 1991 Jun; 39(6):419-24. PubMed ID: 1863988
    [Abstract] [Full Text] [Related]

  • 26. Exon skipping and translation in patients with frameshift deletions in the dystrophin gene.
    Sherratt TG, Vulliamy T, Dubowitz V, Sewry CA, Strong PN.
    Am J Hum Genet; 1993 Nov; 53(5):1007-15. PubMed ID: 8213828
    [Abstract] [Full Text] [Related]

  • 27. Frameshift deletions of exons 3-7 and revertant fibers in Duchenne muscular dystrophy: mechanisms of dystrophin production.
    Winnard AV, Mendell JR, Prior TW, Florence J, Burghes AH.
    Am J Hum Genet; 1995 Jan; 56(1):158-66. PubMed ID: 7825572
    [Abstract] [Full Text] [Related]

  • 28. [Genetic diagnosis of Duchenne/Becker muscular dystrophy; clinical application and problems].
    Takeshima Y.
    No To Hattatsu; 1998 Mar; 30(2):141-7. PubMed ID: 9545779
    [Abstract] [Full Text] [Related]

  • 29. Normal dystrophin transcripts detected in Duchenne muscular dystrophy patients after myoblast transplantation.
    Gussoni E, Pavlath GK, Lanctot AM, Sharma KR, Miller RG, Steinman L, Blau HM.
    Nature; 1992 Apr 02; 356(6368):435-8. PubMed ID: 1557125
    [Abstract] [Full Text] [Related]

  • 30. Direct Reprogramming of Human DMD Fibroblasts into Myotubes for In Vitro Evaluation of Antisense-Mediated Exon Skipping and Exons 45-55 Skipping Accompanied by Rescue of Dystrophin Expression.
    Lee JJA, Saito T, Duddy W, Takeda S, Yokota T.
    Methods Mol Biol; 2018 Apr 02; 1828():141-150. PubMed ID: 30171539
    [Abstract] [Full Text] [Related]

  • 31. Deletion of Dystrophin In-Frame Exon 5 Leads to a Severe Phenotype: Guidance for Exon Skipping Strategies.
    Toh ZY, Thandar Aung-Htut M, Pinniger G, Adams AM, Krishnaswarmy S, Wong BL, Fletcher S, Wilton SD.
    PLoS One; 2016 Apr 02; 11(1):e0145620. PubMed ID: 26745801
    [Abstract] [Full Text] [Related]

  • 32. A novel splice site mutation in a Becker muscular dystrophy patient.
    Bartolo C, Papp AC, Snyder PJ, Sedra MS, Burghes AH, Hall CD, Mendell JR, Prior TW.
    J Med Genet; 1996 Apr 02; 33(4):324-7. PubMed ID: 8730289
    [Abstract] [Full Text] [Related]

  • 33. Characterization of revertant muscle fibers in Duchenne muscular dystrophy, using exon-specific monoclonal antibodies against dystrophin.
    Thanh LT, Nguyen TM, Helliwell TR, Morris GE.
    Am J Hum Genet; 1995 Mar 02; 56(3):725-31. PubMed ID: 7887428
    [Abstract] [Full Text] [Related]

  • 34. [Molecular genetic analysis of deletions in the Duchenne and Becker types of progressive muscular dystrophy].
    Kádasi L, Gécz J, Saksová L, Thurzová M.
    Bratisl Lek Listy; 1993 May 02; 94(5):249-53. PubMed ID: 8173987
    [Abstract] [Full Text] [Related]

  • 35. A TaqI map of the dystrophin gene useful for deletion and carrier status analysis.
    Walker AP, Laing NG, Yamada T, Chandler DC, Kakulas BA, Bartlett RJ.
    J Med Genet; 1992 Jan 02; 29(1):14-9. PubMed ID: 1552537
    [Abstract] [Full Text] [Related]

  • 36. Genetic abnormalities in Duchenne and Becker dystrophies: clinical correlations.
    Medori R, Brooke MH, Waterston RH.
    Neurology; 1989 Apr 02; 39(4):461-5. PubMed ID: 2648185
    [Abstract] [Full Text] [Related]

  • 37. Antisense-induced exon skipping restores dystrophin expression in DMD patient derived muscle cells.
    van Deutekom JC, Bremmer-Bout M, Janson AA, Ginjaar IB, Baas F, den Dunnen JT, van Ommen GJ.
    Hum Mol Genet; 2001 Jul 15; 10(15):1547-54. PubMed ID: 11468272
    [Abstract] [Full Text] [Related]

  • 38. Large in-frame deletions of the rod-shaped domain of the dystrophin gene resulting in severe phenotype.
    Nevo Y, Muntoni F, Sewry C, Legum C, Kutai M, Harel S, Dubowitz V.
    Isr Med Assoc J; 2003 Feb 15; 5(2):94-7. PubMed ID: 12674656
    [Abstract] [Full Text] [Related]

  • 39. A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation.
    Patria SY, Alimsardjono H, Nishio H, Takeshima Y, Nakamura H, Matsuo M.
    Proc Assoc Am Physicians; 1996 Jul 15; 108(4):308-14. PubMed ID: 8863344
    [Abstract] [Full Text] [Related]

  • 40. Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies.
    Le Rumeur E.
    Bosn J Basic Med Sci; 2015 Jul 20; 15(3):14-20. PubMed ID: 26295289
    [Abstract] [Full Text] [Related]

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