Works matching IS 09697128 AND DT 1997 AND VI 4 AND IP 11
Results: 19
Retrovirus-mediated transfer of the human α- L-iduronidase cDNA into human hematopoietic progenitor cells leads to correction in trans of Hurler fibroblasts.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1150, doi. 10.1038/sj.gt.3300504
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- Article
Ability of a chimeric cAMP-responsive promoter to confer pharmacologic control of CFTR cDNA expression and cAMP-mediated Cl<sup>-</sup> secretion.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1195, doi. 10.1038/sj.gt.3300512
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- Article
Integrin-mediated transfection with peptides containing arginine-glycine-aspartic acid domains.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1225, doi. 10.1038/sj.gt.3300513
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- Article
In vitro packaging of an infectious recombinant adeno-associated virus 2.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1167, doi. 10.1038/sj.gt.3300514
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- Article
A second dose of a CFTR cDNA–liposome complex is as effective as the first dose in restoring cAMP-dependent chloride secretion to null CF mice trachea.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1231, doi. 10.1038/sj.gt.3300515
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- Article
Long-term survival of immunocompetent rats with intraperitoneal colon carcinoma tumors using herpes simplex thymidine kinase/ganciclovir and IL-2 treatments.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1160, doi. 10.1038/sj.gt.3300516
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- Article
Local and systemic antitumor response after combined therapy of mouse metastatic tumors with tumor cells expressing IFN-α and HSVtk: perspectives for the generation of cancer vaccines.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1246, doi. 10.1038/sj.gt.3300518
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- Article
Rapid identification of viable retrovirus-transduced cells using the green fluorescent protein as a marker.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1256, doi. 10.1038/sj.gt.3300519
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- Article
HSV-1 thymidine kinase gene therapy for colorectal adenocarcinoma-derived peritoneal carcinomatosis.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1189, doi. 10.1038/sj.gt.3300520
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- Article
Adenovirus-mediated transfer of a functional GAD gene into nerve cells: potential for the treatment of neurological diseases.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1237, doi. 10.1038/sj.gt.3300521
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- Article
Inhibition of HIV-1 replication by a Tat transdominant negative mutant in human peripheral blood lymphocytes from healthy donors and HIV-1-infected patients.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1261, doi. 10.1038/sj.gt.3300522
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- Article
A novel herpesvirus amplicon system for in vivo gene delivery.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1132, doi. 10.1038/sj.gt.3300523
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- Article
A low rate of cell proliferation and reduced DNA uptake limit cationic lipid-mediated gene transfer to primary cultures of ciliated human airway epithelia.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1173, doi. 10.1038/sj.gt.3300524
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- Article
Adenovirus-mediated gene transfer during initial organogenesis in the mammalian embryo is promoter-dependent and tissue-specific.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1142, doi. 10.1038/sj.gt.3300525
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- Article
Gene therapy of diabetes: glucose-stimulated insulin secretion in a human hepatoma cell line (HEP G2ins/g).
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- Gene Therapy, 1997, v. 4, n. 11, p. 1202, doi. 10.1038/sj.gt.3300527
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- Article
Tumour immunotherapy using an adenoviral vector expressing a membrane-bound mutant of murine TNFα.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1181, doi. 10.1038/sj.gt.3300528
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- Article
Immuno gene therapy comes into its own.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1129, doi. 10.1038/sj.gt.3300552
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- Article
Foamy virus vectors for suicide gene therapy.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1270, doi. 10.1038/sj.gt.3300561
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- Article
Anti-HIV genetic treatment of antigen-specific human CD4 lymphocytes for adoptive immunotherapy of opportunistic infections in AIDS.
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- Gene Therapy, 1997, v. 4, n. 11, p. 1216, doi. 10.1038/sj.gt.3300539
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- Article