메뉴 건너뛰기




Volumn 2, Issue 1, 2000, Pages 39-47

Vectors for gene therapy of cardiovascular disease

Author keywords

[No Author keywords available]

Indexed keywords

ADENO ASSOCIATED VIRUS; ADENOVIRUS; CARDIOVASCULAR DISEASE; GENE EXPRESSION REGULATION; GENE THERAPY; GENE TRANSFER; GENE VECTOR; GENETIC TRANSDUCTION; GENETICS; HUMAN; LENTIVIRINAE; MURINE LEUKEMIA VIRUS; PLASMID; REVIEW;

EID: 0033650681     PISSN: 15233782     EISSN: 15343170     Source Type: Journal    
DOI: 10.1007/s11886-000-0024-3     Document Type: Article
Times cited : (5)

References (51)
  • 1
    • 0031580712 scopus 로고    scopus 로고
    • Gene transfer into the carotid artery using an adventitial collar: Comparison of the effectiveness of the plasmid-liposome complexes, retroviruses, pseudotyped retroviruses and adenoviruses
    • Laitinen M, Pakkanen T, Donetti E, et al. : Gene transfer into the carotid artery using an adventitial collar: comparison of the effectiveness of the plasmid-liposome complexes, retroviruses, pseudotyped retroviruses and adenoviruses. Hum Gene Ther 1997, 8:1645 1650.
    • (1997) Hum Gene Ther , vol.8 , pp. 1645-1650
    • Laitinen, M.1    Pakkanen, T.2    Donetti, E.3
  • 2
    • 0032770333 scopus 로고    scopus 로고
    • Gene therapy for myocardial angiogenesis
    • Losordo DW, Vale PR, Isner JM: Gene therapy for myocardial angiogenesis. Am Heart J 1999, 138:132-141.
    • (1999) Am Heart J , vol.138 , pp. 132-141
    • Losordo, D.W.1    Vale, P.R.2    Isner, J.M.3
  • 3
    • 0033520056 scopus 로고    scopus 로고
    • Angiogenesis gene therapy: Phase i assessment of direct intramyocardial administration of an adenovirus vector expressing VEGF121 cDNA to individuals with clinically significant severe coronary artery disease
    • Rosengart T, Lee L, Patel S, et al. : Angiogenesis gene therapy: phase I assessment of direct intramyocardial administration of an adenovirus vector expressing VEGF121 cDNA to individuals with clinically significant severe coronary artery disease. Circulation 1999, 100:468 474.
    • (1999) Circulation , vol.100 , pp. 468-474
    • Rosengart, T.1    Lee, L.2    Patel, S.3
  • 4
    • 0032890904 scopus 로고    scopus 로고
    • Is gene therapy for hypertension possible?
    • Phillips M: Is gene therapy for hypertension possible? Hypertension 1999, 33:8-13.
    • (1999) Hypertension , vol.33 , pp. 8-13
    • Phillips, M.1
  • 5
    • 0031731473 scopus 로고    scopus 로고
    • Vascular gene transfer for th treatment of restenosis and atherosclerosis
    • Laitinen M , Yla-Herttuala S: Vascular gene transfer for th treatment of restenosis and atherosclerosis. Curr Opin Lipidol 1998, 9:465-469.
    • (1998) Curr Opin Lipidol , vol.9 , pp. 465-469
    • Laitinen, M.1    Yla-Herttuala, S.2
  • 6
    • 0032813559 scopus 로고    scopus 로고
    • Variability of human systemic humoral immune responses to adenovirus gene transfer vectors administered to different organs
    • Harvey BG, Hackett NR, El-Sawy T, et al. : Variability of human systemic humoral immune responses to adenovirus gene transfer vectors administered to different organs. J Virol 1999, 73:6729-6742.
    • (1999) J Virol , vol.73 , pp. 6729-6742
    • Harvey, B.G.1    Hackett, N.R.2    El-Sawy, T.3
  • 7
    • 16944367354 scopus 로고    scopus 로고
    • Circumvention of antiadenovirus neutralizing immunity by administration of an adenoviral vector of an alternate serotype
    • Mack C, Song W, Carpenter H, et al. : Circumvention of antiadenovirus neutralizing immunity by administration of an adenoviral vector of an alternate serotype. Hum Gene Ther 1997, 8:99-109.
    • (1997) Hum Gene Ther , vol.8 , pp. 99-109
    • Mack, C.1    Song, W.2    Carpenter, H.3
  • 8
    • 0344780779 scopus 로고    scopus 로고
    • Ovine adenovirus vectors overcome preexisting humoral immunity against human adenoviruses in vivo
    • Hofmann C, Löser P, Cichon G, et al. : Ovine adenovirus vectors overcome preexisting humoral immunity against human adenoviruses in vivo. J Virol 1999, 73:6930-6936.
    • (1999) J Virol , vol.73 , pp. 6930-6936
    • Hofmann, C.1    Löser, P.2    Cichon, G.3
  • 9
    • 0033587174 scopus 로고    scopus 로고
    • PEGylation of adenovirus with retention of infectivity and protection from neutralizing antibody in vitro and in vivo
    • O'Riordan CR, Lachapelle A, Delgado C, et al. : PEGylation of adenovirus with retention of infectivity and protection from neutralizing antibody in vitro and in vivo. Hum Gene Ther 1999, 10:1349-1358.
    • (1999) Hum Gene Ther , vol.10 , pp. 1349-1358
    • O'Riordan, C.R.1    Lachapelle, A.2    Delgado, C.3
  • 10
    • 0029936764 scopus 로고    scopus 로고
    • Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors
    • Tripathy S, Black H, Goldwasser E, Leiden J: Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors. Nat Med 1996, 2:545-550.
    • (1996) Nat Med , vol.2 , pp. 545-550
    • Tripathy, S.1    Black, H.2    Goldwasser, E.3    Leiden, J.4
  • 11
    • 0030923808 scopus 로고    scopus 로고
    • Long-term gene delivery into the livers of immunocompetent mice with E1/E4-defective adenoviruses
    • Dedieu JF, Vigne E, Torrent C, et al. : Long-term gene delivery into the livers of immunocompetent mice with E1/E4-defective adenoviruses. J Virol 1997, 71: 4626 4637.
    • (1997) J Virol , vol.71 , pp. 4626-4637
    • Dedieu, J.F.1    Vigne, E.2    Torrent, C.3
  • 12
    • 0029959867 scopus 로고    scopus 로고
    • Biology of adenovirus vectors with E1 and E4 deletions for liver-directed gene therapy
    • Gao GP, Yang YP, Wilson JM: Biology of adenovirus vectors with E1 and E4 deletions for liver-directed gene therapy. J Virol 1996, 70:8934-8943.
    • (1996) J Virol , vol.70 , pp. 8934-8943
    • Gao, G.P.1    Yang, Y.P.2    Wilson, J.M.3
  • 13
    • 0032991720 scopus 로고    scopus 로고
    • Generation of an adenovirus vector lacking E1, e2a, E3, and all of E4 except open reading frame 3
    • Gorziglia M, Lapcevich C, Roy S, et al. : Generation of an adenovirus vector lacking E1, e2a, E3, and all of E4 except open reading frame 3. J Virol 1999, 73 6048-6055.
    • (1999) J Virol , vol.73 , pp. 6048-6055
    • Gorziglia, M.1    Lapcevich, C.2    Roy, S.3
  • 14
    • 0031008929 scopus 로고    scopus 로고
    • Persistent transgene expression in mouse liver following in vivo gene transfer with a delta E1/delta E4 adenovirus vector
    • Wang Q, Greenburg G, Bunch D, Farson D, Finer M: Persistent transgene expression in mouse liver following in vivo gene transfer with a delta E1/delta E4 adenovirus vector. Gene Ther 1997, 4:393-400.
    • (1997) Gene Ther , vol.4 , pp. 393-400
    • Wang, Q.1    Greenburg, G.2    Bunch, D.3    Farson, D.4    Finer, M.5
  • 15
    • 13144283616 scopus 로고    scopus 로고
    • An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene
    • Morsy M, Gu M, Motzel S, et al. : An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene. Proc Natl Acad Sci U S A 1998, 95 7866-7871.
    • (1998) Proc Natl Acad Sci U S A , vol.95 , pp. 7866-7871
    • Morsy, M.1    Gu, M.2    Motzel, S.3
  • 16
    • 0033540620 scopus 로고    scopus 로고
    • DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscle
    • Chen H, Mack L, Choi S, Ontell M, et al. : DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscle. Hum Gene Ther 1999, 10:365-373.
    • (1999) Hum Gene Ther , vol.10 , pp. 365-373
    • Chen, H.1    Mack, L.2    Choi, S.3    Ontell, M.4
  • 17
    • 0033055017 scopus 로고    scopus 로고
    • Adenovirus-mediated delivery of the Gax transcription factor to rat carotid arteries inhibits smooth muscle proliferation and induces apoptosis
    • Perlman H, Luo Z, Krasinski K, et al. : Adenovirus-mediated delivery of the Gax transcription factor to rat carotid arteries inhibits smooth muscle proliferation and induces apoptosis. Gene Ther 1999, 6:758-763.
    • (1999) Gene Ther , vol.6 , pp. 758-763
    • Perlman, H.1    Luo, Z.2    Krasinski, K.3
  • 18
    • 0032577954 scopus 로고    scopus 로고
    • Gene transfer into normal and atherosclerotic human blood vessels
    • Rekhter M, Simari R, Work C, et al. : Gene transfer into normal and atherosclerotic human blood vessels. Circ Res 1998, 82:1243 1252.
    • (1998) Circ Res , vol.82 , pp. 1243-1252
    • Rekhter, M.1    Simari, R.2    Work, C.3
  • 19
    • 0033061221 scopus 로고    scopus 로고
    • RGD inclusion in the hexon monomer provides adenovirus type 5-based vectors with a fiber knob-independent pathway for infection
    • Vigne E, Mahfouz I, Dedieu JF, et al. : RGD inclusion in the hexon monomer provides adenovirus type 5-based vectors with a fiber knob-independent pathway for infection. J Virol 1999, 73 5156-5161.
    • (1999) J Virol , vol.73 , pp. 5156-5161
    • Vigne, E.1    Mahfouz, I.2    Dedieu, J.F.3
  • 20
    • 0030768124 scopus 로고    scopus 로고
    • Increased in vitro and in vivo gene transfer by adenovirus vectors containing chimeric fiber proteins
    • Wickham T, Tzen E, Shears LN, et al. : Increased in vitro and in vivo gene transfer by adenovirus vectors containing chimeric fiber proteins. J Virol 1997, 71:8221-8229.
    • (1997) J Virol , vol.71 , pp. 8221-8229
    • Wickham, T.1    Tzen, E.2    Shears, L.N.3
  • 21
    • 0032896334 scopus 로고    scopus 로고
    • Hepatic gene therapy using adeno-associated virus vectors
    • Patijn GA , Kay MA: Hepatic gene therapy using adeno-associated virus vectors. Semin Liver Dis 1999, 19:61-69.
    • (1999) Semin Liver Dis , vol.19 , pp. 61-69
    • Patijn, G.A.1    Kay, M.A.2
  • 22
    • 0032104430 scopus 로고    scopus 로고
    • Recent advances in skeletal-musclebased gene therapy
    • Marshall DJ , Leiden JM: Recent advances in skeletal-musclebased gene therapy. Curr Opin Genet Dev 1998, 8:360-365.
    • (1998) Curr Opin Genet Dev , vol.8 , pp. 360-365
    • Marshall, D.J.1    Leiden, J.M.2
  • 23
    • 0032990410 scopus 로고    scopus 로고
    • Isolation of recombinant adeno-associated virus vector-cellular DNA junctions from mouse liver
    • Nakai H, Iwaki Y, Kay MA, Couto LB: Isolation of recombinant adeno-associated virus vector-cellular DNA junctions from mouse liver. J Virol 1999, 73:5438-5447.
    • (1999) J Virol , vol.73 , pp. 5438-5447
    • Nakai, H.1    Iwaki, Y.2    Kay, M.A.3    Couto, L.B.4
  • 24
    • 0031969428 scopus 로고    scopus 로고
    • Transduction of dendritic cells by DNA viral vectors directs the immune response to transgene products in muscle fibers
    • Jooss K, Yang Y, Fisher KJ, Wilson JM: Transduction of dendritic cells by DNA viral vectors directs the immune response to transgene products in muscle fibers. J Virol 1998, 72:4212-4223
    • (1998) J Virol , vol.72 , pp. 4212-4223
    • Jooss, K.1    Yang, Y.2    Fisher, K.J.3    Wilson, J.M.4
  • 25
    • 0031471130 scopus 로고    scopus 로고
    • Long-term correction of obesity and diabetes in genetically obese mice by a single intramuscular injection of recombinant adeno-associated virus encoding mouse leptin
    • Murphy JE, Zhou S, Giese K, et al. : Long-term correction of obesity and diabetes in genetically obese mice by a single intramuscular injection of recombinant adeno-associated virus encoding mouse leptin. Proc Natl Acad Sci U S A 1997, 94:13921-13926.
    • (1997) Proc Natl Acad Sci U S A , vol.94 , pp. 13921-13926
    • Murphy, J.E.1    Zhou, S.2    Giese, K.3
  • 26
    • 17444387438 scopus 로고    scopus 로고
    • Long-term correction of canine hemophilia B by gene transfer of blood coagulation factor IX mediated by adeno-associated viral vector
    • Herzog RW, Yang EY, Couto LB, et al. : Long-term correction of canine hemophilia B by gene transfer of blood coagulation factor IX mediated by adeno-associated viral vector. Nat Genet 1999, 5:56-63.
    • (1999) Nat Genet , vol.5 , pp. 56-63
    • Herzog, R.W.1    Yang, E.Y.2    Couto, L.B.3
  • 27
    • 0030540970 scopus 로고    scopus 로고
    • Long-term gene transfer in porcine myocardium after coronary infusion of an adenoassociated virus vector
    • Kaplitt MG, Xiao X, Samulski RJ, et al. : Long-term gene transfer in porcine myocardium after coronary infusion of an adenoassociated virus vector. Ann Thorac Sur 1996, 62:1669 1676.
    • (1996) Ann Thorac sur , vol.62 , pp. 1669-1676
    • Kaplitt, M.G.1    Xiao, X.2    Samulski, R.J.3
  • 28
    • 0032902054 scopus 로고    scopus 로고
    • Efficient and stable transduction of cardiomyocytes after intramyocardial injection or intracoronary perfusion with recombinant adeno-associated virus vectors
    • Svensson EC, Marshall DJ, Woodard K, et al. : Efficient and stable transduction of cardiomyocytes after intramyocardial injection or intracoronary perfusion with recombinant adeno-associated virus vectors. Circulation 1999, 99:201-205.
    • (1999) Circulation , vol.99 , pp. 201-205
    • Svensson, E.C.1    Marshall, D.J.2    Woodard, K.3
  • 29
    • 0030866312 scopus 로고    scopus 로고
    • Adeno-associated virusmediated gene transfer into rat carotid arteries
    • Rolling F, Nong Z, Pisvin S, Collen D: Adeno-associated virusmediated gene transfer into rat carotid arteries. Gene Ther 1997, 4:757-761.
    • (1997) Gene Ther , vol.4 , pp. 757-761
    • Rolling, F.1    Nong, Z.2    Pisvin, S.3    Collen, D.4
  • 30
    • 0030912001 scopus 로고    scopus 로고
    • Adeno-associated virus vectors for vascular gene delivery
    • Lynch CM, Hara PS, Leonard JC, et al. : Adeno-associated virus vectors for vascular gene delivery. Circ Res 1997, 80:497-505.
    • (1997) Circ Res , vol.80 , pp. 497-505
    • Lynch, C.M.1    Hara, P.S.2    Leonard, J.C.3
  • 31
    • 0032549488 scopus 로고    scopus 로고
    • Factors influencing recombinant adeno-associated virus production
    • Salvetti A, Oreve S, Chadeuf G, et al. : Factors influencing recombinant adeno-associated virus production. Hum Gene Ther 1998, 9:695 706.
    • (1998) Hum Gene Ther , vol.9 , pp. 695-706
    • Salvetti, A.1    Oreve, S.2    Chadeuf, G.3
  • 32
    • 0032212276 scopus 로고    scopus 로고
    • High-titer adeno-associated viral vectors from a Rep/Cap cell line and hybrid shuttle virus
    • Gao GP, Qu G, Faust LZ, et al. : High-titer adeno-associated viral vectors from a Rep/Cap cell line and hybrid shuttle virus. Hum Gene Ther 1998, 9:2353-2362.
    • (1998) Hum Gene Ther , vol.9 , pp. 2353-2362
    • Gao, G.P.1    Qu, G.2    Faust, L.Z.3
  • 33
    • 0031846518 scopus 로고    scopus 로고
    • Packaging cells based on inducible gene amplification for the production of adeno-associated virus vector
    • Inoue N , Russell DW: Packaging cells based on inducible gene amplification for the production of adeno-associated virus vector. J Virol 1998, 72:7024-7031.
    • (1998) J Virol , vol.72 , pp. 7024-7031
    • Inoue, N.1    Russell, D.W.2
  • 34
    • 0031875874 scopus 로고    scopus 로고
    • Adeno-associated virus vectors can be efficiently produced without helper virus
    • Matsushita T, Elliger S, Elliger C, et al. : Adeno-associated virus vectors can be efficiently produced without helper virus. Gene Ther 1998, 5:938 945.
    • (1998) Gene Ther , vol.5 , pp. 938-945
    • Matsushita, T.1    Elliger, S.2    Elliger, C.3
  • 35
    • 2642642141 scopus 로고    scopus 로고
    • Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirus
    • Xiao X, Li J, Samulski RJ: Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirus. J Virol 1998 72:2224-2232.
    • (1998) J Virol , vol.72 , pp. 2224-2232
    • Xiao, X.1    Li, J.2    Samulski, R.J.3
  • 36
    • 0032031816 scopus 로고    scopus 로고
    • Transient immunosuppression allows transgene expression following readministration of adeno-associated viral vectors
    • Manning WC, Zhou S, Bland MP, et al. : Transient immunosuppression allows transgene expression following readministration of adeno-associated viral vectors. Hum Gene Ther 1998, 19:477-485.
    • (1998) Hum Gene Ther , vol.19 , pp. 477-485
    • Manning, W.C.1    Zhou, S.2    Bland, M.P.3
  • 37
    • 0032924185 scopus 로고    scopus 로고
    • Gene therapy vectors based on adeno-associated virus type 1
    • Xiao W, Chirmule N, Berta SC, et al. : Gene therapy vectors based on adeno-associated virus type 1. J Virol 1999, 73:3994-4003.
    • (1999) J Virol , vol.73 , pp. 3994-4003
    • Xiao, W.1    Chirmule, N.2    Berta, S.C.3
  • 38
    • 0032170592 scopus 로고    scopus 로고
    • Control of erythropoietin delivery by doxycycline in mice after intramuscular injection of adeno-associated vector
    • Bohl D, Salvetti A, Moullier P, Heard J: Control of erythropoietin delivery by doxycycline in mice after intramuscular injection of adeno-associated vector. Blood 1998, 92:1512-1517.
    • (1998) Blood , vol.92 , pp. 1512-1517
    • Bohl, D.1    Salvetti, A.2    Moullier, P.3    Heard, J.4
  • 39
    • 0032949030 scopus 로고    scopus 로고
    • Regulated delivery of therapeutic proteins after in vivo somatic cell gene transfer
    • Ye X, Rivera VM, Zoltick P, et al. : Regulated delivery of therapeutic proteins after in vivo somatic cell gene transfer. Science 1999, 283:88-91.
    • (1999) Science , vol.283 , pp. 88-91
    • Ye, X.1    Rivera, V.M.2    Zoltick, P.3
  • 40
    • 0029924681 scopus 로고    scopus 로고
    • Ischemic/reperfused myocardium can express recombinant protein following direct DNA or retroviral injection
    • Prentice H, Kloner RA, Li Y, et al. : Ischemic/reperfused myocardium can express recombinant protein following direct DNA or retroviral injection. J Mol Cell Cardiol 1996, 28:133-140.
    • (1996) J Mol Cell Cardiol , vol.28 , pp. 133-140
    • Prentice, H.1    Kloner, R.A.2    Li, Y.3
  • 41
    • 0012299086 scopus 로고    scopus 로고
    • Downregulation of cyclin G1 expression by retrovirus-mediated antisense gene transfer inhibits vascular smooth muscle cell proliferation and neointima formation
    • Zhu NL, Wu L, Liu PX, et al. : Downregulation of cyclin G1 expression by retrovirus-mediated antisense gene transfer inhibits vascular smooth muscle cell proliferation and neointima formation Circulation 1997, 96:628-635.
    • (1997) Circulation , vol.96 , pp. 628-635
    • Zhu, N.L.1    Wu, L.2    Liu, P.X.3
  • 42
    • 0029091741 scopus 로고
    • Inhibition of intravascular thrombosis and vascular smooth muscle cell proliferation by gene therapy
    • Flugelman MY: Inhibition of intravascular thrombosis and vascular smooth muscle cell proliferation by gene therapy. Thromb Haemost 1995, 74:406-410.
    • (1995) Thromb Haemost , vol.74 , pp. 406-410
    • Flugelman, M.Y.1
  • 43
    • 0032798686 scopus 로고    scopus 로고
    • The resistance of retroviral vectors produced from human cells to serum inactivation in vivo and in vitro is primate species dependent
    • DePolo NJ, Harkleroad CE, Bodner M, et al. : The resistance of retroviral vectors produced from human cells to serum inactivation in vivo and in vitro is primate species dependent. J Virol 1999, 73 6708-6714.
    • (1999) J Virol , vol.73 , pp. 6708-6714
    • Depolo, N.J.1    Harkleroad, C.E.2    Bodner, M.3
  • 44
    • 0031564336 scopus 로고    scopus 로고
    • Targeting retroviral vectors to vascular lesions by genetic engineering of the MoML gp70 envelope protein
    • Hall FL, Gordon EM, Wu L, et al. : Targeting retroviral vectors to vascular lesions by genetic engineering of the MoML gp70 envelope protein. Hum Gene Ther 1997, 8:2183-2192.
    • (1997) Hum Gene Ther , vol.8 , pp. 2183-2192
    • Hall, F.L.1    Gordon, E.M.2    Wu, L.3
  • 45
    • 0033616561 scopus 로고    scopus 로고
    • Identification of the block in targeted retroviral-mediated gene transfer
    • Zhao Y, Zhu L, Lee S, et al. : Identification of the block in targeted retroviral-mediated gene transfer Proc Natl Acad Sci U S A 1999, 96 4005-4010.
    • (1999) Proc Natl Acad Sci U S A , vol.96 , pp. 4005-4010
    • Zhao, Y.1    Zhu, L.2    Lee, S.3
  • 46
    • 0032775219 scopus 로고    scopus 로고
    • Retrovirus targeting by tropism restriction to melanoma cells
    • Martin F, Neil S, Kupsch J, et al. : Retrovirus targeting by tropism restriction to melanoma cells. J Virol 1999, 73:6923 6929.
    • (1999) J Virol , vol.73 , pp. 6923-6929
    • Martin, F.1    Neil, S.2    Kupsch, J.3
  • 47
    • 0033104799 scopus 로고    scopus 로고
    • Tissue-engineered human bioartificial muscles expressing a foreign recombinant protein for gene therapy
    • Powell C, Shansky J, Del Tatto M, et al. : Tissue-engineered human bioartificial muscles expressing a foreign recombinant protein for gene therapy. Hum Gene Ther 1999, 10:565-577
    • (1999) Hum Gene Ther , vol.10 , pp. 565-577
    • Powell, C.1    Shansky, J.2    Del Tatto, M.3
  • 49
    • 0032191380 scopus 로고    scopus 로고
    • Lentiviruses as gene transfer agents for delivery to non-dividing cells
    • Naldini L: Lentiviruses as gene transfer agents for delivery to non-dividing cells. Curr Opin Biotechnol 1998, 9:457-463.
    • (1998) Curr Opin Biotechnol , vol.9 , pp. 457-463
    • Naldini, L.1
  • 50
    • 0030716959 scopus 로고    scopus 로고
    • Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors
    • Kafri T, Blömer U, Peterson DA, et al. : Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors. Nat Genet 1997, 17 314-317.
    • (1997) Nat Genet , vol.17 , pp. 314-317
    • Kafri, T.1    Blömer, U.2    Peterson, D.A.3
  • 51
    • 0031686754 scopus 로고    scopus 로고
    • High-titer human immunodeficiency virus type 1-based vector system for gene delivery into nondividing cells
    • Mochizuki H, Schwartz JP, Tanaka K, et al. : High-titer human immunodeficiency virus type 1-based vector system for gene delivery into nondividing cells. J Virol 1998, 72:8873-8883.
    • (1998) J Virol , vol.72 , pp. 8873-8883
    • Mochizuki, H.1    Schwartz, J.P.2    Tanaka, K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.