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Journal Abstract Search

253 related items for PubMed ID: 2261642

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  • 2. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion.
    Koenig M, Beggs AH, Moyer M, Scherpf S, Heindrich K, Bettecken T, Meng G, Müller CR, Lindlöf M, Kaariainen H, de la Chapellet A, Kiuru A, Savontaus ML, Gilgenkrantz H, Récan D, Chelly J, Kaplan JC, Covone AE, Archidiacono N, Romeo G, Liechti-Gailati S, Schneider V, Braga S, Moser H, Darras BT, Murphy P, Francke U, Chen JD, Morgan G, Denton M, Greenberg CR, Wrogemann K, Blonden LA, van Paassen MB, van Ommen GJ, Kunkel LM.
    Am J Hum Genet; 1989 Oct; 45(4):498-506. PubMed ID: 2491009
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  • 3. Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to exon 44 or 45 skipping.
    Anthony K, Arechavala-Gomeza V, Ricotti V, Torelli S, Feng L, Janghra N, Tasca G, Guglieri M, Barresi R, Armaroli A, Ferlini A, Bushby K, Straub V, Ricci E, Sewry C, Morgan J, Muntoni F.
    JAMA Neurol; 2014 Jan; 71(1):32-40. PubMed ID: 24217213
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  • 4. 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
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  • 7. Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients.
    Chelly J, Gilgenkrantz H, Hugnot JP, Hamard G, Lambert M, Récan D, Akli S, Cometto M, Kahn A, Kaplan JC.
    J Clin Invest; 1991 Oct; 88(4):1161-6. PubMed ID: 1918370
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  • 8. Deletions in the 5' region of dystrophin and resulting phenotypes.
    Muntoni F, Gobbi P, Sewry C, Sherratt T, Taylor J, Sandhu SK, Abbs S, Roberts R, Hodgson SV, Bobrow M.
    J Med Genet; 1994 Nov; 31(11):843-7. PubMed ID: 7853367
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  • 11. Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.
    Malhotra SB, Hart KA, Klamut HJ, Thomas NS, Bodrug SE, Burghes AH, Bobrow M, Harper PS, Thompson MW, Ray PN.
    Science; 1988 Nov 04; 242(4879):755-9. PubMed ID: 3055295
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  • 12. Dystrophin in frameshift deletion patients with Becker muscular dystrophy.
    Gangopadhyay SB, Sherratt TG, Heckmatt JZ, Dubowitz V, Miller G, Shokeir M, Ray PN, Strong PN, Worton RG.
    Am J Hum Genet; 1992 Sep 04; 51(3):562-70. PubMed ID: 1496988
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  • 18. Transcription of the dystrophin gene in Duchenne muscular dystrophy muscle.
    Muntoni F, Strong PN.
    FEBS Lett; 1989 Jul 31; 252(1-2):95-8. PubMed ID: 2668030
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  • 20. Molecular deletion patterns in families from southern France with Duchenne/Becker muscular dystrophies.
    Claustres M, Tuffery S, Chevron MP, Jozelon MP, Martinez P, Echenne B, Demaille J.
    Hum Genet; 1991 Dec 31; 88(2):179-84. PubMed ID: 1684565
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