Modulation of in vitro splicing of the upstream intron by modifying an intra-exon sequence which is deleted from the dystrophin gene in dystrophin Kobe.

Samankaltaisia teoksia

• Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.
  Tekijä: Matsuo, M, et al.
  Julkaistu: (1991)
• A novel point mutation (G-1 to T) in a 5' splice donor site of intron 13 of the dystrophin gene results in exon skipping and is responsible for Becker muscular dystrophy.
  Tekijä: Hagiwara, Y., et al.
  Julkaistu: (1994)
• Splicing of constitutive upstream introns is essential for the recognition of intra-exonic suboptimal splice sites in the thrombopoietin gene
  Tekijä: Romano, Maurizio, et al.
  Julkaistu: (2001)
• Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy.
  Tekijä: Shiga, N, et al.
  Julkaistu: (1997)
• Identification of a novel first exon in the human dystrophin gene and of a new promoter located more than 500 kb upstream of the nearest known promoter.
  Tekijä: Nishio, H, et al.
  Julkaistu: (1994)