Works matching IS 09697128 AND DT 2001 AND VI 8 AND IP 16
Results: 10
Human myeloid dendritic cells transduced with an adenoviral interleukin-10 gene construct inhibit human skin graft rejection in humanized NOD-scid chimeric mice.
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- Gene Therapy, 2001, v. 8, n. 16, p. 1224, doi. 10.1038/sj.gt.3301513
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- Article
Liver-targeted gene transfer into a human hepatoblastoma cell line and in vivo by sterylglucoside-containing cationic liposomes.
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- Gene Therapy, 2001, v. 8, n. 16, p. 1276, doi. 10.1038/sj.gt.3301510
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- Article
A novel system for mitigation of ectopic transgene expression induced by adenoviral vectors.
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- Gene Therapy, 2001, v. 8, n. 16, p. 1271, doi. 10.1038/sj.gt.3301511
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- Article
Self-complementary recombinant adeno-associated virus (scAAV) vectors promote efficient transduction independently of DNA synthesis.
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- Gene Therapy, 2001, v. 8, n. 16, p. 1248, doi. 10.1038/sj.gt.3301514
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- Article
Rat marrow stromal cells rapidly transduced with a self-inactivating retrovirus synthesize L-DOPA in vitro.
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- Gene Therapy, 2001, v. 8, n. 16, p. 1214, doi. 10.1038/sj.gt.3301517
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- Article
Hepatic intra-arterial delivery of a retroviral vector expressing the cytosine deaminase gene, controlled by the CEA promoter and intraperitoneal treatment with 5-fluorocytosine suppresses growth of colorectal liver metastases.
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- Gene Therapy, 2001, v. 8, n. 16, p. 1241, doi. 10.1038/sj.gt.3301518
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- Article
In vivo electroporation-mediated transfer of interleukin-12 and interleukin-18 genes induces significant antitumor effects against melanoma in mice.
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- Gene Therapy, 2001, v. 8, n. 16, p. 1234, doi. 10.1038/sj.gt.3301519
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- Article
Adenovirus-transduced dendritic cells stimulate cellular immunity to melanoma via a CD4<sup>+</sup> T cell-dependent mechanism.
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- Gene Therapy, 2001, v. 8, n. 16, p. 1255, doi. 10.1038/sj.gt.3301521
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- Article
Optimisation of electrotransfer of plasmid into skeletal muscle by pretreatment with hyaluronidase – increased expression with reduced muscle damage.
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- Gene Therapy, 2001, v. 8, n. 16, p. 1264, doi. 10.1038/sj.gt.3301522
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- Article
Fibroblast growth factor-II gene therapy reverts the clinical course and the pathological signs of chronic experimental autoimmune encephalomyelitis in C57BL/6 mice.
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- Gene Therapy, 2001, v. 8, n. 16, p. 1207, doi. 10.1038/sj.gt.3301523
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- Article