Papers 4

  1. Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice.
    Alton EW et al., Nat Genet. 1993 Oct;5(2):135-42.
  2. Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis.
    Caplen NJ et al., Nat Med. 1995 Jan;1(1):39-46.
  3. Laboratory and clinical studies in support of cystic fibrosis gene therapy using pCMV-CFTR-DOTAP.
    McLachlan G et al., Gene Ther. 1996 Dec;3(12):1113-23.
  4. A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis.
    Gill DR et al., Gene Ther. 1997 Mar;4(3):199-209.

 

Pellets of DNA following precipitation.