Severe deficiency of cystic fibrosis transmembrane conductance regulator messenger RNA carrying nonsense mutations R553X and W1316X in respiratory epithelial cells of patients with cystic fibrosis.

Gelijkaardige items

• A cystic fibrosis patient homozygous for the nonsense mutation R553X.
  door: Bal, J, et al.
  Gepubliceerd in: (1991)
• Nonsense mutation R1162X of the cystic fibrosis transmembrane conductance regulator gene does not reduce messenger RNA expression in nasal epithelial tissue.
  door: Rolfini, R, et al.
  Gepubliceerd in: (1993)
• Extensive posttranscriptional deletion of the coding sequences for part of nucleotide-binding fold 1 in respiratory epithelial mRNA transcripts of the cystic fibrosis transmembrane conductance regulator gene is not associated with the clinical manifestations of cystic fibrosis.
  door: Chu, C S, et al.
  Gepubliceerd in: (1992)
• Expression of the cystic fibrosis transmembrane conductance regulator gene in the respiratory tract of normal individuals and individuals with cystic fibrosis.
  door: Trapnell, B C, et al.
  Gepubliceerd in: (1991)
• A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosis.
  door: Will, K, et al.
  Gepubliceerd in: (1994)