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Direct Gene Transfer for the Understanding and Treatment of Human Disease

dc.contributor.authorPlautz, Gregory E.en_US
dc.contributor.authorNabel, Elizabeth G.en_US
dc.contributor.authorFox, Bernard A.en_US
dc.contributor.authorYang, Zhi-Yongen_US
dc.contributor.authorJaffe, Michele L.en_US
dc.contributor.authorGordon, Daviden_US
dc.contributor.authorChang, Alfreden_US
dc.contributor.authorNabel, Gary J.en_US
dc.date.accessioned2010-06-01T22:47:54Z
dc.date.available2010-06-01T22:47:54Z
dc.date.issued1994-05en_US
dc.identifier.citationPLAUTZ, GREGORY E.; NABEL, ELIZABETH G.; FOX, BERNARD; YANG, ZHI-YONG; JAFFE, MICHELE; GORDON, DAVID; CHANG, ALFRED; NABEL, GARY J. (1994). "Direct Gene Transfer for the Understanding and Treatment of Human Disease." Annals of the New York Academy of Sciences 716(1 Gene Therapy for Neoplastic Diseases ): 144-153. <http://hdl.handle.net/2027.42/75762>en_US
dc.identifier.issn0077-8923en_US
dc.identifier.issn1749-6632en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/75762
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8024191&dopt=citationen_US
dc.format.extent681739 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Ltden_US
dc.rights1994 The New York Academy of Sciencesen_US
dc.titleDirect Gene Transfer for the Understanding and Treatment of Human Diseaseen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelScience (General)en_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Pediatrics and Communicable Diseases, University of Michigan Medical Center, Ann Arbor, Michigan 48109–0684en_US
dc.contributor.affiliationumDepartment of Internal Medicine, University of Michigan Medical Center, Ann Arbor, Michigan 48109–0684en_US
dc.contributor.affiliationumDepartment of Biologial Chemistry, University of Michigan Medical Center, Ann Arbor, Michigan 48109–0684en_US
dc.contributor.affiliationumDepartment of Surgery, University of Michigan Medical Center, Ann Arbor, Michigan 48109–0684en_US
dc.contributor.affiliationumDepartment of Pathology, University of Michigan Medical Center, Ann Arbor, Michigan 48109–0684en_US
dc.contributor.affiliationumHoward Hughes Medical Institute, University of Michigan Medical Center, Ann Arbor, Michigan 48109–0684en_US
dc.identifier.pmid8024191en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/75762/1/j.1749-6632.1994.tb21709.x.pdf
dc.identifier.doi10.1111/j.1749-6632.1994.tb21709.xen_US
dc.identifier.sourceAnnals of the New York Academy of Sciencesen_US
dc.identifier.citedreferencePrice, J., D. Turner & C. Cepko. 1987. Lineage analysis in the vertebrate nervous system by retrovirus-mediated gene transfer. Proc. Natl. Acad. Sci. USA 84: 156 – 160.en_US
dc.identifier.citedreferenceNabel, E. G., G. Plautz & G. J. Nabel. 1990. Site-specific gene expression in vivo by direct gene transfer into the arterial wall. Science 249: 1285 – 1288.en_US
dc.identifier.citedreferenceCulver, K. W., Z. Ram, S. Wallbridge, H. Ishii, E. H. Oldfield & R. M. Blaese. 1992. In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors. Science 256: 1550 – 1552.en_US
dc.identifier.citedreferenceRosenfeld, M. A., W. Siegfried, K. Yoshimura, K. Yoneyama, M. Fukayama, L. E. Stier, P. K. Paakko, P. Gilardi, L. D. Stratford-Perricaudet, M. Perricaudet et al. 1991. Adenovirus-mediated transfer of a recombinant alpha 1-antitrypsin gene to the lung epithelium in vivo. Science 252: 431 – 434.en_US
dc.identifier.citedreferenceRosenfeld, M. A., K. Yoshimura, B. C. Trapnell, K. Yoneyama, E. R. Rosenthal, W. Dalemans, M. Fukayama, J. Bargon, L. E. Stier, L. Stratford-Perricaudet et al. 1992. In vivo transfer of the human cystic fibrosis trans-membrane conductance regulator gene to the airway epithelium. Cell 68: 143 – 155.en_US
dc.identifier.citedreferenceJaffe, H. A., C. Danel, G. Longenecker, M. Metzger, Y. Setoguchi, M. A. Rosenfeld, T. W. Gant, S. S. Thorgeirsson, L. D. Stratford-Perricaudet, M. Perricaudet, A. Pavirani, J. P. Lecocq & R. G. Crystal. 1992. Adenovirus-mediated in vivo gene transfer and expression in normal rat liver. Nature Genet. 1: 372 – 378.en_US
dc.identifier.citedreferenceSamulski, R. J., X. Zhu, X. Xiao, J. D. Brook, D. E. Housman, N. Epstein & L. A. Hunter. 1991. Targeted integration of adeno-associated virus (AAV) into human chromosome 19 [ published erratum appears in EMBO J. 1992. Mar; 11(3): 1228 ]. EMBO J. 10: 3941 – 3950.en_US
dc.identifier.citedreferencePalella, T. D., L. J. Silverman, C. T. Schroll, F. L. Homa, M. Levine & W. N. Kelley. 1988. Herpes simplex virus-mediated human hypoxanthine-guanine phosphoribosyltransrase gene transfer into neuronal cells. Mol. Cell. Biol. 8: 457 – 460.en_US
dc.identifier.citedreferenceChiocca, E. A., B. B. Choi, W. Z. Cai, N. A. De Luce, P. A. Schaffer, M. De Figlia, X. O. Breakfield & R. L. Martuza. 1990. Transfer and expression of the lacZ gene in rat brain neurons mediated by herpes simplex virus mutants. New Biol. 2: 739 – 746.en_US
dc.identifier.citedreferenceBreakefield, X. O. & N. A. De Luca. 1991. Herpes simplex virus for gene delivery to neurons. New Biol. 3: 203 – 218.en_US
dc.identifier.citedreferenceWolff, J. A., R. W. Malone, P. Williams, G. Chong, G. Ascadi, A. Jani & P. Felgner. 1990. Direct gene transfer into mouse muscle in vivo. Science 247: 1465 – 1468.en_US
dc.identifier.citedreferenceLin, H., M. S. Parmacek, G. Morle, S. Bolling & J. M. Leiden. 1990. Expression of recombinant genes in myocardium in vivo after direct injection of DNA. Circulation 82: 2217 – 2221.en_US
dc.identifier.citedreferenceAcsadi, G., S. S. Jiao, A. Jani, D. Duke, P. Williams, W. Chong & J. A. Wolff. 1991. Direct gene transfer and expression into rat heart in vivo. New Biol. 3: 71 – 81.en_US
dc.identifier.citedreferenceVile, R. G. & I. R. Hart. 1993 In Vitro and in vivo Targeting of gene expression to melanoma cells. Cancer Res. 53: 962 – 967.en_US
dc.identifier.citedreferenceBrigham, K. L., B. Meyrick, B. Christman, M. Magnuson, G. King & L. C. Berry. 1989. In vivo transfection of murine lungs with a functioning prokaryotic gene using a liposome vehicle. Am. J. Med. Sci. 298: 278 – 281.en_US
dc.identifier.citedreferenceHolt, C. I., N. Garlick & E. Cornel. 1990. Lipofection of cDNAs in the embryonic vertebrate central nervous system. Neuron 4: 203 – 214.en_US
dc.identifier.citedreferencePlautz, G. E., Z. Y. Yang, B. Wu, X. Gao, L. Huang & G. J. Nabel. 1993. Immunotherapy of malignancy by in vivo gene transfer into tumors. Proc. Natl. Acad. Sci. USA 90: 4645 – 4649.en_US
dc.identifier.citedreferenceNabel, E. G., Z. Yang, G. Plautz, R. Forough, X. Zhan, C. C. Haudenschild, T. Maciag & G. J. Nabel. 1993. Recombinant fibroblast growth factor-1 promotes intimal hyperplasia and angiogenesis in arteries in vivo. Nature 362: 844 – 846.en_US
dc.identifier.citedreferenceNabel, E. G., Z. Yang, S. Liptay, H. San, D. Gordon, C. C. Haudenschild & G. J. Nabel. 1993. Recombinant platelet-derived growth factor B gene expression in porcine arteries induces intimal hyperplasia in vivo. J. Clin. Invest. 91: 1822 – 1829.en_US
dc.identifier.citedreferenceFelgner, P. L. & G. M. Ringold. 1989. Cationic liposome-mediated transfection. Nature 337: 387 – 388.en_US
dc.identifier.citedreferenceFelgner, P. L., M. Holm & H. Chan. 1989. Cationic liposome mediated transfection. Proc. West. Pharmacol. Soc. 32: 115 – 121.en_US
dc.identifier.citedreferenceFelgner, P. L., T. R. Gadek, M. Holm, R. Roman, H. W. Chan, M. Wenz, J. P. Northrop, G. M. Ringold & M. Danielsen. 1987. Lipofection: A highly efficient lipid-mediated DNA-transfection procedure. Proc. Natl. Acad. Sci. USA 84: 7413 – 7417.en_US
dc.identifier.citedreferenceNabel, E. G., G. Plautz & G. J. Nabel. 1992. Transduction of a foreign histocompatibility gene into the arterial wall induces vasculitis. Proc. Natl. Acad. Sci. USA 89: 5157 – 5161.en_US
dc.identifier.citedreferenceLim, C. S., G. D. Chapman, R. S. Gammon, J. B. Muhlestein, R. P. Bauman, R. S. Stack & J. L. Swain. 1991. Direct in vivo gene transfer into the coronary and peripheral vasculatures of the intact dog. Circulation 83: 2007 – 2011.en_US
dc.identifier.citedreferenceGao, X. & L. Huang. 1991. A novel cationic liposome reagent for efficient transfection of mammalian cells. Biochem. Biophys. Res. Commun. 179: 280 – 285.en_US
dc.identifier.citedreferenceStewart, M. J., G. E. Plautz, L. Del Buono, Z. Y. Yang, L. Xu, X. Gao, L. Huang, E. G. Nabel & G. J. Nabel. 1992. Gene transfer in vivo with DNA-liposome complexes: Safety and acute toxicity in mice. Hum. Gene Ther. 3: 267 – 275.en_US
dc.identifier.citedreferenceNabel, E. G., D. Gordon, Z.-Y. Xang, L. Xu, H. San, G. E. Plautz, X. Gao, L. Huang & G. J. Nabel. 1992. Gene transfer in vivo with DNA-liposome complexes: Lack of autoimmunity and gonadal localization. Hum. Gene Ther. 3: 649 – 656.en_US
dc.identifier.citedreferenceFearon, E. R., D. M. Pardoll, T. Itaya, P. Golumbek, H. I. Levitsky, J. W. Simons, H. Karasuyama, B. Vogelstein & P. Frost. 1990. Interleukin-2 production by tumor cells bypasses T helper function in the generation of an antitumor response. Cell 60: 397 – 403.en_US
dc.identifier.citedreferenceGansbacher, B., K. Zier, B. Daniels, K. Cronin, R. Bannerji & E. Gilboa. 1990. Interleukin 2 gene transfer into tumor cells abrogates tumorigenicity and induces protective immunity. J. Exp. Med. 172: 1217 – 1224.en_US
dc.identifier.citedreferenceTepper, R. I., P. K. Pattengale & P. Leder. 1989. Murine interleukin-4 displays potent antitumor activity in vivo. Cell 57: 503 – 512.en_US
dc.identifier.citedreferenceLi, W., T. Diamantstein & T. Blankenstein. 1990. Lack of tumorienicity of interleukin 4 autocrine growing cells seems related to the anti-tumor function of interleukin 4. Mol. Immunol. 27: 1331 – 1337.en_US
dc.identifier.citedreferenceGolumbek, P. T., A. J. Lazenby, H. I. Levitsky, L. M. Jaffee, H. Karasuyama, M. Baker & D. M. Pardoll. 1991. Treatment of established renal cancer by tumor cells engineered to secrete interleukin-4. Science 254: 713 – 716.en_US
dc.identifier.citedreferenceGansbacher, B., R. Bannerji, B. Daniels, K. Zier, K. Cronin & E. Gilboa. 1990. Retroviral vector-mediated Γ-interferon gene transfer into tumor cells generates potent and long lasting antitumor immunity. Cancer Res. 50: 7820 – 7825.en_US
dc.identifier.citedreferenceChen, L., S. Ashe, W. A. Brady, I. Hellstrom, K. E. Hellstrom, J. A. Ledbetter, P. McGowan & P. S. Linsley. 1992. Costimulation of antitumor immunity by the B7 counterreceptor for the T lymphocyte molecule CD28 and CTLA-4. Cell 71: 1093 – 1102.en_US
dc.identifier.citedreferenceTownsend, S. & J. P. Allison. 1993. Tumor rejection after direct costimulation of CD8+ T cells by B7-transfected melanoma cells. Science 259: 368 – 370.en_US
dc.identifier.citedreferenceBlankenstein, Th., Z. Qin, K. Überla, W. MÜller, H. Rosen, H.-D. Volk & T. Diamanstein. 1991. Tumor suppression after tumor cell-targeted tumor necrosis factor a gene transfer. J. Exp. Med. 173: 1047 – 1052.en_US
dc.identifier.citedreferenceTeng, M. N., B. H. Park, H. K. Koeppen, K. J. Tracey, B. M. Fendly & H. Schreiber. 1991. Long-term inhibition of tumor growth by tumor necrosis factor in the absence of cachexia or T-cell immunity. Proc. Natl. Acad. Sci. USA 88: 3535 – 3539.en_US
dc.identifier.citedreferenceAsher, A. L., J. J. Mule, A. Kasid, N. P. Restifo, J. C. Salo, C. M. Reichert, G. Jaffe, B. Fendly, M. Kriegler & S. A. Rosenberg. 1991. Murine tumor cells transduced with the gene for tumor necrosis factor-Α. J. Immunol. 146: 3227 – 3234.en_US
dc.identifier.citedreferenceParham, P., C. E. Lomen, D. A. Lawlor, J. P. Ways, N. Holmes, H. L. Coppin, R. D. Salter, A. M. Wan & P. D. Ennis. 1988. Nature of polymorphism in HLA-A, -B, and -C molecules. Proc. Natl. Acad. Sci. USA 85: 4005 – 4009.en_US
dc.identifier.citedreferenceSkinner, M. A. & J. Marbrook. 1976. An estimation of the frequency of precursor cells which generate cytotoxic lymhocytes. J. Exp. Med. 143: 1562 – 1567.en_US
dc.identifier.citedreferenceLindahl, K. E. & D. B. Wilson. 1977. Histocomatibility antigen-activated cytotoxic T lymhocytes I Estimates of the absolute frequency of killer cells generated in vitro. J. Exp. Med. 145: 500 – 522.en_US
dc.identifier.citedreferenceWahl, W. L., G. E. Plautz, B. A. Fox, G. J. Nabel, S. Shu & A. E. Chang. 1992. Generation of therapeutic lymphocytes after in vivo transfection of tumor with a gene encoding allogeneic class I MHC antigen. Surg. Forum 63: 476 – 478.en_US
dc.identifier.citedreferenceNabel, G. J., A. Chang, E. G. Nabel, G. Plautz, B. A. Fox, L. Huang & S. Shu. 1992. Clinical protocol. Immunotherapy of malignancy by in vivo gene transfer into tumors. Hum. Gene Ther. 3: 399 – 410.en_US
dc.identifier.citedreferenceNabel, G. J., E. G. Nabel, Z. Yang, B. Fox, G. Plautz, X. Gao, L. Huang, S. Shu, D. Gordon & A. E. Chang. 1993. Direct gene transfer with DNA liposome complexes in humans: Expression, lack of toxicity and therapeutic potential in melanoma. Proc. Natl. Acad. Sci. USA 90: 10759 – 10763.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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