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.

Benzer Materyaller

• Exon skipping during splicing of dystrophin mRNA precursor due to an intraexon deletion in the dystrophin gene of Duchenne muscular dystrophy kobe.
  Yazar:: Matsuo, M, ve diğerleri
  Baskı/Yayın Bilgisi: (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.
  Yazar:: Hagiwara, Y., ve diğerleri
  Baskı/Yayın Bilgisi: (1994)
• Splicing of constitutive upstream introns is essential for the recognition of intra-exonic suboptimal splice sites in the thrombopoietin gene
  Yazar:: Romano, Maurizio, ve diğerleri
  Baskı/Yayın Bilgisi: (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.
  Yazar:: Shiga, N, ve diğerleri
  Baskı/Yayın Bilgisi: (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.
  Yazar:: Nishio, H, ve diğerleri
  Baskı/Yayın Bilgisi: (1994)