Trans-complementation of E1-deleted adenovirus: a new vector to reduce the possibility of codissemination of wild-type and recombinant adenoviruses.
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M. Mehtali | A. Bout | A. Pavirani | J. Imler | D. Valerio | D. Dreyer | A. Dieterlé | H. Schultz
[1] M. Perricaudet,et al. In vivo adenovirus-mediated transfer of human CFTR cDNA to rhesus monkey airway epithelium: efficacy, toxicity and safety. , 1994, Gene therapy.
[2] R. Crystal,et al. Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis , 1994, Nature Genetics.
[3] R. Crystal,et al. Acute responses of non-human primates to airway delivery of an adenovirus vector containing the human cystic fibrosis transmembrane conductance regulator cDNA. , 1994, Human gene therapy.
[4] J. Wilson,et al. Ablation of E2A in recombinant adenoviruses improves transgene persistence and decreases inflammatory response in mouse liver. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[5] E. Furth,et al. Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[6] B. Trapnell,et al. Adenovirus-mediated gene transfer for cystic fibrosis: quantitative evaluation of repeated in vivo vector administration to the lung. , 1994, Gene therapy.
[7] R. Crystal,et al. Gene transfer to freshly isolated human respiratory epithelial cells in vitro using a replication-deficient adenovirus containing the human cystic fibrosis transmembrane conductance regulator cDNA. , 1994, Human gene therapy.
[8] J. Wilson,et al. Adenovirus-mediated transfer of the CFTR gene to lung of nonhuman primates: toxicity study. , 1993, Human gene therapy.
[9] J. Wilson,et al. Adenovirus-mediated transfer of the CFTR gene to lung of nonhuman primates: biological efficacy study. , 1993, Human gene therapy.
[10] Joseph Zabner,et al. Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis , 1993, Cell.
[11] F. Graham,et al. Packaging capacity and stability of human adenovirus type 5 vectors , 1993, Journal of virology.
[12] J. Olsen,et al. Functional consequences of heterologous expression of the cystic fibrosis transmembrane conductance regulator in fibroblasts. , 1993, The Journal of biological chemistry.
[13] M. Kay,et al. Assessment of recombinant adenoviral vectors for hepatic gene therapy. , 1993, Human gene therapy.
[14] B. Davidson,et al. Adenoviral-mediated gene transfer to rabbit synovium in vivo. , 1993, The Journal of clinical investigation.
[15] M. Welsh,et al. Development and analysis of recombinant adenoviruses for gene therapy of cystic fibrosis. , 1993, Human gene therapy.
[16] A. Barkan,et al. Suppression of growth hormone (GH) secretion by a selective GH-releasing hormone (GHRH) antagonist. Direct evidence for involvement of endogenous GHRH in the generation of GH pulses. , 1993, The Journal of clinical investigation.
[17] P. C. van der Vliet,et al. The adenovirus terminal protein influences binding of replication proteins and changes the origin structure. , 1993, Nucleic acids research.
[18] R. Mulligan,et al. The basic science of gene therapy. , 1993, Science.
[19] Sanford H. Feldman,et al. Direct in vivo gene transfer to ependymal cells in the central nervous system using recombinant adenovirus vectors , 1993, Nature Genetics.
[20] P. Briand,et al. Efficient adenovirus-mediated transfer of a human minidystrophin gene to skeletal muscle of mdx mice , 1993, Nature.
[21] M. Perricaudet,et al. An adenovirus vector for gene transfer into neurons and glia in the brain , 1993, Science.
[22] S. Thorgeirsson,et al. Adenovirus–mediated in vivo gene transfer and expression in normal rat liver , 1992, Nature Genetics.
[23] E. Bikoff,et al. Developmental failure of chimeric embryos expressing high levels of H-2Dd transplantation antigens. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[24] F. Collins,et al. Cystic fibrosis: molecular biology and therapeutic implications. , 1992, Science.
[25] J. Mandel,et al. Adenovirus as an expression vector in muscle cells in vivo. , 1992, Proceedings of the National Academy of Sciences of the United States of America.
[26] P. Hearing,et al. cis and trans requirements for the selective packaging of adenovirus type 5 DNA , 1992, Journal of virology.
[27] M. Perricaudet,et al. In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium , 1992, Cell.
[28] Pascal Barbry,et al. Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutation , 1991, Nature.
[29] M. Perricaudet,et al. Defective and nondefective adenovirus vectors for expressing foreign genes in vitro and in vivo. , 1991, Gene.
[30] P. Hearing,et al. Adenovirus type 5 packaging domain is composed of a repeated element that is functionally redundant , 1990, Journal of virology.
[31] L. Tsui,et al. Erratum: Identification of the Cystic Fibrosis Gene: Cloning and Characterization of Complementary DNA , 1989, Science.
[32] K. Münger,et al. The human papillomavirus type 16 E7 gene encodes transactivation and transformation functions similar to those of adenovirus E1A , 1988, Cell.
[33] M. Stinski,et al. Participation of two human cytomegalovirus immediate early gene regions in transcriptional activation of adenovirus promoters. , 1987, Virology.
[34] Samulski,et al. Identification of a repeated sequence element required for efficient encapsidation of the adenovirus type 5 chromosome , 1987, Journal of virology.
[35] C. Tibbetts,et al. Polar encapsidation of adenovirus DNA: evolutionary variants reveal dispensable sequences near the left ends of Ad3 genomes. , 1984, Virology.
[36] E. Dubovi,et al. A new animal model for human respiratory tract disease due to adenovirus. , 1984, The Journal of infectious diseases.
[37] N. Stow,et al. Replication of adenovirus mini-chromosomes. , 1984, Journal of molecular biology.
[38] R. Lathe,et al. New versatile cloning and sequencing vectors based on bacteriophage M13. , 1983, Gene.
[39] T. Shenk,et al. Adenovirus VAI RNA is required for efficient translation of viral mRNAs at late times after infection , 1982, Cell.
[40] N. Stow. The infectivity of adenovirus genomes lacking DNA sequences from their left-hand termini. , 1982, Nucleic acids research.
[41] G. Winberg,et al. Encapsidation of adenovirus 16 DNA is directed by a small DNA sequence at the left end of the genome , 1980, Cell.
[42] B. Hirt. Selective extraction of polyoma DNA from infected mouse cell cultures. , 1967, Journal of molecular biology.
[43] M. Perricaudet,et al. Lung gene therapy: in vivo adenovirus-mediated gene transfer to rhesus monkey airway epithelium. , 1994, Human gene therapy.
[44] M. Welsh,et al. Safety and efficacy of repetitive adenovirus–mediated transfer of CFTR cDNA to airway epithelia of primates and cotton rats , 1994, Nature Genetics.
[45] M. Perricaudet,et al. Diversity of airway epithelial cell targets for in vivo recombinant adenovirus-mediated gene transfer. , 1993, The Journal of clinical investigation.
[46] J. Chroboczek,et al. The sequence of the genome of adenovirus type 5 and its comparison with the genome of adenovirus type 2. , 1992, Virology.