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Journal Abstract Search

674 related items for PubMed ID: 12833158

  • 1. A negative element in SMN2 exon 7 inhibits splicing in spinal muscular atrophy.
    Kashima T, Manley JL.
    Nat Genet; 2003 Aug; 34(4):460-3. PubMed ID: 12833158
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  • 4. Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2.
    Cartegni L, Hastings ML, Calarco JA, de Stanchina E, Krainer AR.
    Am J Hum Genet; 2006 Jan; 78(1):63-77. PubMed ID: 16385450
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  • 5. Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1.
    Cartegni L, Krainer AR.
    Nat Genet; 2002 Apr; 30(4):377-84. PubMed ID: 11925564
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  • 7. hnRNP A1 functions with specificity in repression of SMN2 exon 7 splicing.
    Kashima T, Rao N, David CJ, Manley JL.
    Hum Mol Genet; 2007 Dec 15; 16(24):3149-59. PubMed ID: 17884807
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  • 10. A non-sequence-specific requirement for SMN protein activity: the role of aminoglycosides in inducing elevated SMN protein levels.
    Wolstencroft EC, Mattis V, Bajer AA, Young PJ, Lorson CL.
    Hum Mol Genet; 2005 May 01; 14(9):1199-210. PubMed ID: 15790598
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  • 11. Genetic conversion of an SMN2 gene to SMN1: a novel approach to the treatment of spinal muscular atrophy.
    DiMatteo D, Callahan S, Kmiec EB.
    Exp Cell Res; 2008 Feb 15; 314(4):878-86. PubMed ID: 18078930
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  • 15. Splicing of a critical exon of human Survival Motor Neuron is regulated by a unique silencer element located in the last intron.
    Singh NK, Singh NN, Androphy EJ, Singh RN.
    Mol Cell Biol; 2006 Feb 15; 26(4):1333-46. PubMed ID: 16449646
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