Characterization of liposome-mediated gene delivery: expression, stability and pharmacokinetics of plasmid DNA.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 226, doi. 10.1038/sj.gt.3300350
- By:
- Publication type:
- Article
Works matching IS 09697128 AND DT 1997 AND VI 4 AND IP 3
Results: 13
1
2
Combined strategies for gene therapy of AIDS.
- Published in:
- 1997
- By:
- Publication type:
- Editorial
3
Use of SV40-based vectors to transduce foreign genes to normal human peripheral blood mononuclear cells.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 219, doi. 10.1038/sj.gt.3300368
- By:
- Publication type:
- Article
4
Safety studies of the intraperitoneal injection of E1A–liposome complex in mice.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 238, doi. 10.1038/sj.gt.3300376
- By:
- Publication type:
- Article
5
Isolation and characterization of packaging cell lines that coexpress the adenovirus E1, DNA polymerase, and preterminal proteins: implications for gene therapy.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 258, doi. 10.1038/sj.gt.3300378
- By:
- Publication type:
- Article
6
Mechanism of ‘bystander effect’ killing in the herpes simplex thymidine kinase gene therapy model of cancer treatment.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 244, doi. 10.1038/sj.gt.3300379
- By:
- Publication type:
- Article
7
Immune-mediated destruction of transfected muscle fibers after direct gene transfer with antigen-expressing plasmid DNA.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 181, doi. 10.1038/sj.gt.3300380
- By:
- Publication type:
- Article
8
Human CD34<sup>+</sup> cells do not express glutathione S-transferases alpha.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 268, doi. 10.1038/sj.gt.3300381
- By:
- Publication type:
- Article
9
Improved efficiency of arterial gene transfer by use of poloxamer 407 as a vehicle for adenoviral vectors.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 189, doi. 10.1038/sj.gt.3300382
- By:
- Publication type:
- Article
10
Constitutive systemic expression of IL-1Ra or soluble TNF receptor by genetically modified hematopoietic cells suppresses LPS induction of IL-6 and IL-10.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 252, doi. 10.1038/sj.gt.3300387
- By:
- Publication type:
- Article
11
Evidence for safety and efficacy of DOTAP cationic liposome mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 210, doi. 10.1038/sj.gt.3300390
- By:
- Publication type:
- Article
12
A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 199, doi. 10.1038/sj.gt.3300391
- By:
- Publication type:
- Article
13
A strategy for specific targeting of therapeutic agents to tumour cells of virus-associated cancers.
- Published in:
- Gene Therapy, 1997, v. 4, n. 3, p. 264, doi. 10.1038/sj.gt.3300392
- By:
- Publication type:
- Article