-
1
-
-
0031580712
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
|