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Journal Abstract Search

340 related items for PubMed ID: 9436421

  • 1. [Molecular genetics and problems found in genetic diagnosis of Duchenne Becker muscular dystrophy].
    Takeshima Y, Matsuo M.
    Nihon Rinsho; 1997 Dec; 55(12):3120-5. PubMed ID: 9436421
    [Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA resulting from deletion mutations.
    Kitoh Y, Matsuo M, Nishio H, Nakamura H.
    Kobe J Med Sci; 1994 Apr; 40(2):39-48. PubMed ID: 7823533
    [Abstract] [Full Text] [Related]

  • 4. [Molecular genetics of Duchenne/Becker muscular dystrophy].
    Saito K, Ikeya K, Kondo E, Yamauchi A, Komine S, Fukuyama Y.
    Nihon Rinsho; 1993 Sep; 51(9):2420-7. PubMed ID: 8411723
    [Abstract] [Full Text] [Related]

  • 5. Multiexon skipping leading to an artificial DMD protein lacking amino acids from exons 45 through 55 could rescue up to 63% of patients with Duchenne muscular dystrophy.
    Béroud C, Tuffery-Giraud S, Matsuo M, Hamroun D, Humbertclaude V, Monnier N, Moizard MP, Voelckel MA, Calemard LM, Boisseau P, Blayau M, Philippe C, Cossée M, Pagès M, Rivier F, Danos O, Garcia L, Claustres M.
    Hum Mutat; 2007 Feb; 28(2):196-202. PubMed ID: 17041910
    [Abstract] [Full Text] [Related]

  • 6. [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]

  • 7. Re-evaluation of reading frame-shift hypothesis in Duchenne and Becker muscular dystrophy.
    Pandey GS, Kesari A, Mukherjee M, Mittal RD, Mittal B.
    Neurol India; 2003 Sep; 51(3):367-9. PubMed ID: 14652441
    [Abstract] [Full Text] [Related]

  • 8. PGD for dystrophin gene deletions using fluorescence in situ hybridization.
    Malmgren H, White I, Johansson S, Levkov L, Iwarsson E, Fridström M, Blennow E.
    Mol Hum Reprod; 2006 May; 12(5):353-6. PubMed ID: 16608904
    [Abstract] [Full Text] [Related]

  • 9. Bioinformatic and functional optimization of antisense phosphorodiamidate morpholino oligomers (PMOs) for therapeutic modulation of RNA splicing in muscle.
    Popplewell LJ, Graham IR, Malerba A, Dickson G.
    Methods Mol Biol; 2011 May; 709():153-78. PubMed ID: 21194027
    [Abstract] [Full Text] [Related]

  • 10. Genotype-phenotype correlation in Duchenne/Becker muscular dystrophy patients seen at Lucknow.
    Mittal B, Singh V, Mishra S, Sinha S, Mittal RD, Chaturvedi LS, Danda S, Pradhan S, Agarwal SS.
    Indian J Med Res; 1997 Jan; 105():32-8. PubMed ID: 9029833
    [Abstract] [Full Text] [Related]

  • 11. Dystrophin expression in Duchenne patients with "in-frame" gene deletions.
    Nicholson LV, Bushby KM, Johnson MA, Gardner-Medwin D, Ginjaar IB.
    Neuropediatrics; 1993 Apr; 24(2):93-7. PubMed ID: 8327067
    [Abstract] [Full Text] [Related]

  • 12. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R, Gluck E, Legum C, Shiloh Y.
    Am J Med Genet; 1994 Feb 15; 49(4):369-73. PubMed ID: 8160727
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  • 15. 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]

  • 16. [Genotypic diagnosis of Duchenne and Becker muscular dystrophies].
    Tuffery-Giraud S, Chambert S, Demaille J, Claustres M.
    Ann Biol Clin (Paris); 1999 Jul 15; 57(4):417-26. PubMed ID: 10432364
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  • 18. [Deletions in the dystrophin gene and its phenotype expression].
    Lalić T, Guć-Sćekić M, Djurisić M, Radivojević D, Zamurović D, Todorović S.
    Srp Arh Celok Lek; 2001 Jul 15; 129 Suppl 1():3-5. PubMed ID: 15637982
    [Abstract] [Full Text] [Related]

  • 19. Characterization of translational frame exception patients in Duchenne/Becker muscular dystrophy.
    Winnard AV, Klein CJ, Coovert DD, Prior T, Papp A, Snyder P, Bulman DE, Ray PN, McAndrew P, King W.
    Hum Mol Genet; 1993 Jun 15; 2(6):737-44. PubMed ID: 8353493
    [Abstract] [Full Text] [Related]

  • 20. Deletion screening of the Duchenne/Becker muscular dystrophy gene in Croatian population.
    Sertić J, Barisić N, Sostarko M, Brzović Z, Stavljenić-Rukavina A.
    Coll Antropol; 1997 Jun 15; 21(1):151-6. PubMed ID: 9225508
    [Abstract] [Full Text] [Related]

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