-
1
-
-
0001957609
-
Adenoviridae and their replication
-
Horwitz MS. Adenoviridae and their replication. Virology 1990; 2: 1679-1720.
-
(1990)
Virology
, vol.2
, pp. 1679-1720
-
-
Horwitz, M.S.1
-
2
-
-
0033759405
-
Production of first generation adenovirus vectors: A review
-
Danthinne X, Imperiale MJ. Production of first generation adenovirus vectors: a review. Gene Therapy 2000; 7: 1707-1714.
-
(2000)
Gene Therapy
, vol.7
, pp. 1707-1714
-
-
Danthinne, X.1
Imperiale, M.J.2
-
3
-
-
0017710978
-
Characteristics of a human cell line transformed by dna from human adenovirus type 5
-
Graham FL, Smiley J, Russell WC, Nairn R. Characteristics of a human cell line transformed by DNA from human adenovirus type 5. J Gen Virol 1977; 36: 59-74.
-
(1977)
J Gen Virol
, vol.36
, pp. 59-74
-
-
Graham, F.L.1
Smiley, J.2
Russell, W.C.3
Nairn, R.4
-
4
-
-
0030024402
-
Characterization of 911: A new helper cell line for the titration and propagation of early region 1-deleted adenoviral vectors
-
Fallaux FJ et al. Characterization of 911: a new helper cell line for the titration and propagation of early region 1-deleted adenoviral vectors. Hum Gene Ther 1996; 7: 215-222.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 215-222
-
-
Fallaux, F.J.1
-
5
-
-
0034633740
-
Efficient transformation of primary human amniocytes by e1 functions of ad5: Generation of new cell lines for adenoviral vector production
-
Schiedner G, Hertel S, Kochanek S. Efficient transformation of primary human amniocytes by E1 functions of Ad5: generation of new cell lines for adenoviral vector production. Hum Gene Ther 2000; 11: 2105-2116.
-
(2000)
Hum Gene Ther
, vol.11
, pp. 2105-2116
-
-
Schiedner, G.1
Hertel, S.2
Kochanek, S.3
-
6
-
-
17344373287
-
New helper cells and matched early region 1-deleted adenovirus vectors prevent generation of replication- competent adenoviruses
-
Fallaux FJ et al. New helper cells and matched early region 1-deleted adenovirus vectors prevent generation of replication- competent adenoviruses. Hum Gene Ther 1998; 9: 1909-1917.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 1909-1917
-
-
Fallaux, F.J.1
-
7
-
-
0028328261
-
Cellular immunity to viral antigens limits e1-deleted adenoviruses for gene therapy
-
Yang Y et al. Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy. Proc Natl Acad Sci USA 1994; 91: 4407-4411.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 4407-4411
-
-
Yang, Y.1
-
8
-
-
0031883829
-
Production and characterization of improved adenovirus vectors with the e1, e2b, and e3 genes deleted
-
Amalfitano A et al. Production and characterization of improved adenovirus vectors with the E1, E2b, and E3 genes deleted. J Virol 1998; 72: 926-933.
-
(1998)
J Virol
, vol.72
, pp. 926-933
-
-
Amalfitano, A.1
-
9
-
-
0031041586
-
Effect of the e4 region on the persistence of transgene expression from adenovirus vectors
-
Armentano D et al. Effect of the E4 region on the persistence of transgene expression from adenovirus vectors. J Virol 1997; 71: 2408-2416.
-
(1997)
J Virol
, vol.71
, pp. 2408-2416
-
-
Armentano, D.1
-
10
-
-
0030809684
-
Complementation of helper-dependent adenoviral vectors: Size effects and titer fluctuations
-
Alemany R et al. Complementation of helper-dependent adenoviral vectors: size effects and titer fluctuations. J Virol Methods 1997; 68: 147-159.
-
(1997)
J Virol Methods
, vol.68
, pp. 147-159
-
-
Alemany, R.1
-
11
-
-
0027260609
-
Packaging capacity and stability of human adenovirus type 5 vectors
-
Bett AJ, Prevec L, Graham FL. Packaging capacity and stability of human adenovirus type 5 vectors. J Virol 1993; 67: 5911-5921.
-
(1993)
J Virol
, vol.67
, pp. 5911-5921
-
-
Bett, A.J.1
Prevec, L.2
Graham, F.L.3
-
12
-
-
0023230477
-
Stable transfer of a mouse dihydrofolate reductase gene into a deficient cell line using human adenovirus vector
-
Ghosh-Choudhury G, Graham FL. Stable transfer of a mouse dihydrofolate reductase gene into a deficient cell line using human adenovirus vector. Biochem Biophys Res Commun 1987; 147: 964-973.
-
(1987)
Biochem Biophys Res Commun
, vol.147
, pp. 964-973
-
-
Ghosh-Choudhury, G.1
Graham, F.L.2
-
13
-
-
0029054932
-
Rescue, propagation, and partial purification of a helper virus- dependent adenovirus vector
-
Mitani K, Graham FL, Caskey CT, Kochanek S. Rescue, propagation, and partial purification of a helper virus- dependent adenovirus vector. Proc Natl Acad Sci USA 1995; 92: 3854-3858.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 3854-3858
-
-
Mitani, K.1
Graham, F.L.2
Caskey, C.T.3
Kochanek, S.4
-
14
-
-
0030900511
-
A helper-dependent system for adenovirus vector production helps define a lower limit for efficient dna packaging
-
Parks RJ, Graham FL. A helper-dependent system for adenovirus vector production helps define a lower limit for efficient DNA packaging. J Virol 1997; 71: 3293-3298.
-
(1997)
J Virol
, vol.71
, pp. 3293-3298
-
-
Parks, R.J.1
Graham, F.L.2
-
15
-
-
0032827780
-
Use of helper-dependent adenoviral vectors of alternative serotypes permits repeat vector administration
-
Parks R, Evelegh C, Graham F. Use of helper-dependent adenoviral vectors of alternative serotypes permits repeat vector administration. Gene Therapy 1999; 6: 1565-1573.
-
(1999)
Gene Therapy
, vol.6
, pp. 1565-1573
-
-
Parks, R.1
Evelegh, C.2
Graham, F.3
-
16
-
-
0036148167
-
Variables affecting in vivo performance of high-capacity adenovirus vectors
-
Schiedner G et al. Variables affecting in vivo performance of high-capacity adenovirus vectors. J Virol 2002; 76: 1600-1609.
-
(2002)
J Virol
, vol.76
, pp. 1600-1609
-
-
Schiedner, G.1
-
17
-
-
12944315064
-
Optimization of the helper-dependent adenovirus system for production and potency in vivo
-
Sandig V et al. Optimization of the helper-dependent adenovirus system for production and potency in vivo. Proc Natl Acad Sci USA 2000; 97: 1002-1007.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 1002-1007
-
-
Sandig, V.1
-
18
-
-
0346872991
-
Improved system for helper-dependent adenoviral vector production
-
Palmer D, Ng P. Improved system for helper-dependent adenoviral vector production. Mol Ther 2003; 8: 846-852.
-
(2003)
Mol Ther
, vol.8
, pp. 846-852
-
-
Palmer, D.1
Ng, P.2
-
19
-
-
0036232384
-
Replication and packaging of helper-dependent adenoviral vectors
-
Sato M, Suzuki S, Kubo S, Mitani K. Replication and packaging of helper-dependent adenoviral vectors. Gene Therapy 2002; 9: 472-476.
-
(2002)
Gene Therapy
, vol.9
, pp. 472-476
-
-
Sato, M.1
Suzuki, S.2
Kubo, S.3
Mitani, K.4
-
20
-
-
1442339189
-
Long-term in vivo transduction of neurons throughout the rat cns using novel helper- dependent cav-2 vectors
-
Soudais C, Skander N, Kremer EJ. Long-term in vivo transduction of neurons throughout the rat CNS using novel helper- dependent CAV-2 vectors. FASEB J 2004; 18: 391-393.
-
(2004)
FASEB J
, vol.18
, pp. 391-393
-
-
Soudais, C.1
Skander, N.2
Kremer, E.J.3
-
21
-
-
0030462599
-
A helper-dependent adenovirus vector system: Removal of helper virus by cre-mediated excision of the viral packaging signal
-
Parks RJ et al. A helper-dependent adenovirus vector system: removal of helper virus by Cre-mediated excision of the viral packaging signal. Proc Natl Acad Sci USA 1996; 93: 13565-13570.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 13565-13570
-
-
Parks, R.J.1
-
22
-
-
0034888424
-
Self-excising retroviral vectors encoding the cre recombinase overcome cre-mediated cellular toxicity
-
Silver DP, Livingston DM. Self-excising retroviral vectors encoding the Cre recombinase overcome Cre-mediated cellular toxicity. Mol Cell 2001; 8: 233-243.
-
(2001)
Mol Cell
, vol.8
, pp. 233-243
-
-
Silver, D.P.1
Livingston, D.M.2
-
23
-
-
27544514437
-
Adenovirus inhibition of cellular protein synthesis and the specific translation of late viral mrna
-
Zang Y, Schneider R. Adenovirus inhibition of cellular protein synthesis and the specific translation of late viral mRNA. Semin Virol 1993; 4: 233-243.
-
(1993)
Semin Virol
, vol.4
, pp. 233-243
-
-
Zang, Y.1
Schneider, R.2
-
24
-
-
4644240778
-
Helper-dependent adenoviral vectors for gene therapy
-
Templeton NS, Marcel Dekker Inc: New York
-
Ng PG, Graham FL. Helper-dependent adenoviral vectors for gene therapy. In: Templeton NS (ed). Gene and Cell Therapy. Marcel Dekker Inc: New York, 2004 pp 53-70.
-
(2004)
Gene and Cell Therapy
, pp. 53-70
-
-
Ng, P.G.1
Graham, F.L.2
-
25
-
-
0024286701
-
Autoregulation of 2 micron circle gene expression provides a model for maintenance of stable plasmid copy levels
-
Som T, Armstrong KA, Volkert FC, Broach JR. Autoregulation of 2 micron circle gene expression provides a model for maintenance of stable plasmid copy levels. Cell 1988; 52: 27-37.
-
(1988)
Cell
, vol.52
, pp. 27-37
-
-
Som, T.1
Armstrong, K.A.2
Volkert, F.C.3
Broach, J.R.4
-
26
-
-
0034981674
-
Development of a flp/frt system for generating helper-dependent adenoviral vectors
-
Ng P et al. Development of a FLP/frt system for generating helper-dependent adenoviral vectors. Mol Ther 2001; 3: 809-815.
-
(2001)
Mol Ther
, vol.3
, pp. 809-815
-
-
Ng, P.1
-
28
-
-
1842424937
-
Development of a size-restricted pix-deleted helper virus for amplification of helper-dependent adenovirus vectors
-
Sargent KL et al. Development of a size-restricted pIX-deleted helper virus for amplification of helper-dependent adenovirus vectors. Gene Therapy 2004; 11: 504-511.
-
(2004)
Gene Therapy
, vol.11
, pp. 504-511
-
-
Sargent, K.L.1
-
29
-
-
0038782552
-
An hsv amplicon- based helper system for helper-dependent adenoviral vectors
-
Kubo S, Saeki Y, Chiocca EA, Mitani K. An HSV amplicon- based helper system for helper-dependent adenoviral vectors. Biochem Biophys Res Commun 2003; 307: 826-830.
-
(2003)
Biochem Biophys Res Commun
, vol.307
, pp. 826-830
-
-
Kubo, S.1
Saeki, Y.2
Chiocca, E.A.3
Mitani, K.4
-
30
-
-
0034973111
-
A novel system for the production of fully deleted adenovirus vectors that does not require helper adenovirus
-
Cheshenko N, Krougliak N, Eisensmith RC, Krougliak VA. A novel system for the production of fully deleted adenovirus vectors that does not require helper adenovirus. Gene Therapy 2001; 8: 846-854.
-
(2001)
Gene Therapy
, vol.8
, pp. 846-854
-
-
Cheshenko, N.1
Krougliak, N.2
Eisensmith, R.C.3
Krougliak, V.A.4
-
31
-
-
0023122268
-
Growth of 293 cells in suspension culture
-
Graham FL. Growth of 293 cells in suspension culture. J Gen Virol 1987; 68 (Pt 3): 937-940.
-
(1987)
J Gen Virol
, vol.68
, pp. 937-940
-
-
Graham, F.L.1
-
32
-
-
0037429005
-
Optimization of the generation and propagation of gutless adenoviral vectors
-
Sakhuja K et al. Optimization of the generation and propagation of gutless adenoviral vectors. Hum Gene Ther 2003; 14: 243-254.
-
(2003)
Hum Gene Ther
, vol.14
, pp. 243-254
-
-
Sakhuja, K.1
-
33
-
-
4544344036
-
Immune responses against adenoviral vectors and their transgene products: A review of strategies for evasion
-
Schagen FH, Ossevoort M, Toes RE, Hoeben RC. Immune responses against adenoviral vectors and their transgene products: a review of strategies for evasion. Crit Rev Oncol Hematol 2004; 50: 51-70.
-
(2004)
Crit Rev Oncol Hematol
, vol.50
, pp. 51-70
-
-
Schagen, F.H.1
Ossevoort, M.2
Toes, R.E.3
Hoeben, R.C.4
-
34
-
-
0031034030
-
Innate immune mechanisms dominate elimination of adenoviral vectors following in vivo administration
-
Worgall S, Wolff G, Falck-Pedersen E, Crystal RG. Innate immune mechanisms dominate elimination of adenoviral vectors following in vivo administration. Hum Gene Ther 1997; 8: 37-44.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 37-44
-
-
Worgall, S.1
Wolff, G.2
Falck-Pedersen, E.3
Crystal, R.G.4
-
35
-
-
0038069517
-
The role of capsid-endothelial interactions in the innate immune response to adenovirus vectors
-
Liu Q et al. The role of capsid-endothelial interactions in the innate immune response to adenovirus vectors. Hum Gene Ther 2003; 14: 627-643.
-
(2003)
Hum Gene Ther
, vol.14
, pp. 627-643
-
-
Liu, Q.1
-
36
-
-
17844393413
-
Activation of innate immunity in nonhuman primates following intraportal administration of adenoviral vectors
-
Schnell MA et al. Activation of innate immunity in nonhuman primates following intraportal administration of adenoviral vectors. Mol Ther 2001; 3: 708-722.
-
(2001)
Mol Ther
, vol.3
, pp. 708-722
-
-
Schnell, M.A.1
-
37
-
-
0033865751
-
Immune response to recombinant adenovirus in humans: Capsid components from viral input are targets for vector-specific cytotoxic t lymphocytes
-
Molinier-Frenkel V et al. Immune response to recombinant adenovirus in humans: capsid components from viral input are targets for vector-specific cytotoxic T lymphocytes. J Virol 2000; 74: 7678-7682.
-
(2000)
J Virol
, vol.74
, pp. 7678-7682
-
-
Molinier-Frenkel, V.1
-
38
-
-
0028179006
-
Lymphocyte responses and cytokines
-
Paul WE, Seder RA. Lymphocyte responses and cytokines. Cell 1994; 76: 241-251.
-
(1994)
Cell
, vol.76
, pp. 241-251
-
-
Paul, W.E.1
Seder, R.A.2
-
39
-
-
0030943732
-
Macrophage depletion increases the safety, efficacy and persistence of adenovirusmediated gene transfer in
-
Kuzmin AI, Finegold MJ, Eisensmith RC. Macrophage depletion increases the safety, efficacy and persistence of adenovirusmediated gene transfer in vivo. Gene Therapy 1997; 4: 309-316.
-
(1997)
Vivo. Gene Therapy
, vol.4
, pp. 309-316
-
-
Kuzmin, A.I.1
Finegold, M.J.2
Eisensmith, R.C.3
-
40
-
-
0031060294
-
Enhancement of in vivo adenovirus-mediated gene transfer and expression by prior depletion of tissue macrophages in the target organ
-
Wolff G et al. Enhancement of in vivo adenovirus-mediated gene transfer and expression by prior depletion of tissue macrophages in the target organ. J Virol 1997; 71: 624-629.
-
(1997)
J Virol
, vol.71
, pp. 624-629
-
-
Wolff, G.1
-
41
-
-
0028934815
-
Cellular and humoral immune responses to adenoviral vectors containing factor ix gene: Tolerization of factor ix and vector antigens allows for long-term expression
-
Dai Y et al. Cellular and humoral immune responses to adenoviral vectors containing factor IX gene: tolerization of factor IX and vector antigens allows for long-term expression. Proc Natl Acad Sci USA 1995; 92: 1401-1405.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 1401-1405
-
-
Dai, Y.1
-
42
-
-
0029154012
-
Gene therapy for hemophilia b: Host immunosuppression prolongs the therapeutic effect of adenovirus-mediated factor ix expression
-
Fang B et al. Gene therapy for hemophilia B: host immunosuppression prolongs the therapeutic effect of adenovirus-mediated factor IX expression. Hum Gene Ther 1995; 6: 1039-1044.
-
(1995)
Hum Gene Ther
, vol.6
, pp. 1039-1044
-
-
Fang, B.1
-
43
-
-
0030749713
-
Transient immunosuppression with deoxyspergualin improves longevity of transgene expression and ability to readminister adenoviral vector to the mouse lung
-
Kaplan JM, Smith AE. Transient immunosuppression with deoxyspergualin improves longevity of transgene expression and ability to readminister adenoviral vector to the mouse lung. Hum Gene Ther 1997; 8: 1095-1104.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 1095-1104
-
-
Kaplan, J.M.1
Smith, A.E.2
-
44
-
-
0034056004
-
Immunomodulation with fk506 around the time of intravenous re-administration of an adenoviral vector facilitates gene transfer into primed rat liver
-
Kuriyama S et al. Immunomodulation with FK506 around the time of intravenous re-administration of an adenoviral vector facilitates gene transfer into primed rat liver. Int J Cancer 2000; 85: 839-844.
-
(2000)
Int J Cancer
, vol.85
, pp. 839-844
-
-
Kuriyama, S.1
-
45
-
-
0032505771
-
Nonspecific inflammation inhibits adenovirus-mediated pulmonary gene transfer and expression independent of specific acquired immune responses
-
Otake K, Ennist DL, Harrod K, Trapnell BC. Nonspecific inflammation inhibits adenovirus-mediated pulmonary gene transfer and expression independent of specific acquired immune responses. Hum Gene Ther 1998; 9: 2207-2222.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 2207-2222
-
-
Otake, K.1
Ennist, D.L.2
Harrod, K.3
Trapnell, B.C.4
-
46
-
-
0033544951
-
A phase i study of adenovirus-mediated transfer of the human cystic fibrosis transmembrane conductance regulator gene to a lung segment of individuals with cystic fibrosis
-
Zuckerman JB et al. A phase I study of adenovirus-mediated transfer of the human cystic fibrosis transmembrane conductance regulator gene to a lung segment of individuals with cystic fibrosis. Hum Gene Ther 1999; 10: 2973-2985.
-
(1999)
Hum Gene Ther
, vol.10
, pp. 2973-2985
-
-
Zuckerman, J.B.1
-
47
-
-
0030005390
-
Stabilization of transgene expression by incorporation of e3 region genes into an adenoviral factor ix vector and by transient anti-cd4 treatment of the host
-
Poller W et al. Stabilization of transgene expression by incorporation of E3 region genes into an adenoviral factor IX vector and by transient anti-CD4 treatment of the host. Gene Therapy 1996; 3: 521-530.
-
(1996)
Gene Therapy
, vol.3
, pp. 521-530
-
-
Poller, W.1
-
48
-
-
0029877620
-
Anti-t cell receptor monoclonal antibody prolongs transgene expression following adenovirus-mediated in vivo gene transfer to mouse synovium
-
Sawchuk SJ et al. Anti-T cell receptor monoclonal antibody prolongs transgene expression following adenovirus-mediated in vivo gene transfer to mouse synovium. Hum Gene Ther 1996; 7: 499-506.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 499-506
-
-
Sawchuk, S.J.1
-
49
-
-
0029113869
-
Long-term hepatic adenovirus-mediated gene expression in mice following ctla4ig administration
-
Kay MA et al. Long-term hepatic adenovirus-mediated gene expression in mice following CTLA4Ig administration. Nat Genet 1995; 11: 191-197.
-
(1995)
Nat Genet
, vol.11
, pp. 191-197
-
-
Kay, M.A.1
-
50
-
-
0030984335
-
Transient immunomodulation with anti-cd40 ligand antibody and ctla4ig enhances persistence and secondary adenovirus-mediated gene transfer into mouse liver
-
Kay MA et al. Transient immunomodulation with anti-CD40 ligand antibody and CTLA4Ig enhances persistence and secondary adenovirus-mediated gene transfer into mouse liver. Proc Natl Acad Sci USA 1997; 94: 4686-4691.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 4686-4691
-
-
Kay, M.A.1
-
51
-
-
0031942297
-
Effects of macrophage depletion and anti-cd40 ligand on transgene expression and redosing with recombinant adenovirus
-
Stein CS, Pemberton JL, van Rooijen N, Davidson BL. Effects of macrophage depletion and anti-CD40 ligand on transgene expression and redosing with recombinant adenovirus. Gene Therapy 1998; 5: 431-439.
-
(1998)
Gene Therapy
, vol.5
, pp. 431-439
-
-
Stein, C.S.1
Pemberton, J.L.2
Van Rooijen, N.3
Davidson, B.L.4
-
52
-
-
0031849666
-
Transient inhibition of cd28 and cd40 ligand interactions prolongs adenovirus-mediated transgene expression in the lung and facilitates expression after secondary vector administration
-
Wilson CB et al. Transient inhibition of CD28 and CD40 ligand interactions prolongs adenovirus-mediated transgene expression in the lung and facilitates expression after secondary vector administration. J Virol 1998; 72: 7542-7550.
-
(1998)
J Virol
, vol.72
, pp. 7542-7550
-
-
Wilson, C.B.1
-
53
-
-
0030908652
-
Long-lasting adenovirus transgene expression in mice through neonatal intrathymic tolerance induction without the use of immunosuppression
-
DeMatteo RP et al. Long-lasting adenovirus transgene expression in mice through neonatal intrathymic tolerance induction without the use of immunosuppression. J Virol 1997; 71: 5330-5335.
-
(1997)
J Virol
, vol.71
, pp. 5330-5335
-
-
DeMatteo, R.P.1
-
54
-
-
17344370857
-
Oral tolerization to adenoviral proteins permits repeated adenovirus-mediated gene therapy in rats with pre-existing immunity to adenoviruses
-
Ilan Y et al. Oral tolerization to adenoviral proteins permits repeated adenovirus-mediated gene therapy in rats with pre-existing immunity to adenoviruses. Hepatology 1998; 27: 1368-1376.
-
(1998)
Hepatology
, vol.27
, pp. 1368-1376
-
-
Ilan, Y.1
-
55
-
-
0029983685
-
Sero-switch' adenovirus-mediated in vivo gene transfer: Circumvention of anti-adenovirus humoral immune defenses against repeat adenovirus vector administration by changing the adenovirus serotype
-
Mastrangeli A et al. 'Sero-switch' adenovirus-mediated in vivo gene transfer: circumvention of anti-adenovirus humoral immune defenses against repeat adenovirus vector administration by changing the adenovirus serotype. Hum Gene Ther 1996; 7: 79-87.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 79-87
-
-
Mastrangeli, A.1
-
56
-
-
13044304200
-
Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons
-
Morral N et al. Administration of helper-dependent adenoviral vectors and sequential delivery of different vector serotype for long-term liver-directed gene transfer in baboons. Proc Natl Acad Sci USA 1999; 96: 12816-12821.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 12816-12821
-
-
Morral, N.1
-
57
-
-
0037310512
-
A simian replication-defective adenoviral recombinant vaccine to hiv-1 gag
-
Fitzgerald JC et al. A simian replication-defective adenoviral recombinant vaccine to HIV-1 gag. J Immunol 2003; 170: 1416-1422.
-
(2003)
J Immunol
, vol.170
, pp. 1416-1422
-
-
Fitzgerald, J.C.1
-
58
-
-
0033989650
-
Canine adenovirus vectors: An alternative for adenovirus-mediated gene transfer
-
Kremer EJ, Boutin S, Chillon M, Danos O. Canine adenovirus vectors: an alternative for adenovirus-mediated gene transfer. J Virol 2000; 74: 505-512.
-
(2000)
J Virol
, vol.74
, pp. 505-512
-
-
Kremer, E.J.1
Boutin, S.2
Chillon, M.3
Danos, O.4
-
59
-
-
0031856891
-
Adenovirus complexed with polyethylene glycol and cationic lipid is shielded from neutralizing antibodies in vitro
-
Chillon M, Lee JH, Fasbender A, Welsh MJ. Adenovirus complexed with polyethylene glycol and cationic lipid is shielded from neutralizing antibodies in vitro. Gene Therapy 1998; 5: 995-1002.
-
(1998)
Gene Therapy
, vol.5
, pp. 995-1002
-
-
Chillon, M.1
Lee, J.H.2
Fasbender, A.3
Welsh, M.J.4
-
60
-
-
0035033758
-
Stealth' adenoviruses blunt cell-mediated and humoral immune responses against the virus and allow for significant gene expression upon readministration in the lung
-
Croyle MA, Chirmule N, Zhang Y, Wilson JM. 'Stealth' adenoviruses blunt cell-mediated and humoral immune responses against the virus and allow for significant gene expression upon readministration in the lung. J Virol 2001; 75: 4792-4801.
-
(2001)
J Virol
, vol.75
, pp. 4792-4801
-
-
Croyle, M.A.1
Chirmule, N.2
Zhang, Y.3
Wilson, J.M.4
-
61
-
-
0036412085
-
Pegylation of e1-deleted adenovirus vectors allows significant gene expression on readministration to liver
-
Croyle MA, Chirmule N, Zhang Y, Wilson JM. PEGylation of E1-deleted adenovirus vectors allows significant gene expression on readministration to liver. Hum Gene Ther 2002; 13: 1887-1900.
-
(2002)
Hum Gene Ther
, vol.13
, pp. 1887-1900
-
-
Croyle, M.A.1
Chirmule, N.2
Zhang, Y.3
Wilson, J.M.4
-
62
-
-
0029153297
-
Immunosuppression by fk506 markedly prolongs expression of adenovirus-delivered transgene in skeletal muscles of adult dystrophic [mdx] mice
-
Lochmuller H et al. Immunosuppression by FK506 markedly prolongs expression of adenovirus-delivered transgene in skeletal muscles of adult dystrophic [mdx] mice. Biochem Biophys Res Commun 1995; 213: 569-574.
-
(1995)
Biochem Biophys Res Commun
, vol.213
, pp. 569-574
-
-
Lochmuller, H.1
-
63
-
-
0028807696
-
Fk506 immunosuppression to control the immune reactions triggered by first-generation adenovirusmediated gene transfer
-
Vilquin JT et al. FK506 immunosuppression to control the immune reactions triggered by first-generation adenovirusmediated gene transfer. Hum Gene Ther 1995; 6: 1391-1401.
-
(1995)
Hum Gene Ther
, vol.6
, pp. 1391-1401
-
-
Vilquin, J.T.1
-
64
-
-
0033540620
-
Dna from both high-capacity and firstgeneration adenoviral vectors remains intact in skeletal muscle
-
Chen HH et al. DNA from both high-capacity and firstgeneration 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.H.1
-
65
-
-
0034630303
-
Prolonged expression and effective readministration of erythropoietin delivered with a fully deleted adenoviral vector
-
Maione D et al. Prolonged expression and effective readministration of erythropoietin delivered with a fully deleted adenoviral vector. Hum Gene Ther 2000; 11: 859-868.
-
(2000)
Hum Gene Ther
, vol.11
, pp. 859-868
-
-
Maione, D.1
-
66
-
-
13144283616
-
An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene
-
Morsy MA 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 USA 1998; 95: 7866-7871.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 7866-7871
-
-
Morsy, M.A.1
-
67
-
-
0034152718
-
Toxicity associated with repeated administration of first-generation adenovirus vectors does not occur with a helper-dependent vector
-
O'Neal WK et al. Toxicity associated with repeated administration of first-generation adenovirus vectors does not occur with a helper-dependent vector. Mol Med 2000; 6: 179-195.
-
(2000)
Mol Med
, vol.6
, pp. 179-195
-
-
O'Neal, W.K.1
-
68
-
-
0031916435
-
Genomic dna transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity
-
Schiedner G et al. Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity Nat Genet 1998; 18: 180-183.
-
(1998)
Nat Genet
, vol.18
, pp. 180-183
-
-
Schiedner, G.1
-
69
-
-
0037108592
-
Helper-dependent adenoviral vectors efficiently express transgenes in human dendritic cells but still stimulate antiviral immune responses
-
Roth MD et al. Helper-dependent adenoviral vectors efficiently express transgenes in human dendritic cells but still stimulate antiviral immune responses. J Immunol 2002; 169: 4651-4656.
-
(2002)
J Immunol
, vol.169
, pp. 4651-4656
-
-
Roth, M.D.1
-
70
-
-
2442638935
-
Helper-dependent adenovirus vectors elicit intact innate but attenuated adaptive host immune responses in vivo
-
Muruve DA et al. Helper-dependent adenovirus vectors elicit intact innate but attenuated adaptive host immune responses in vivo. J Virol 2004; 78: 5966-5972.
-
(2004)
J Virol
, vol.78
, pp. 5966-5972
-
-
Muruve, D.A.1
-
71
-
-
0038446697
-
Humoral immune response in mice against a circulating antigen induced by adenoviral transfer is strictly dependent on expression in antigen-presenting cells
-
De Geest BR, Van Linthout SA, Collen D. Humoral immune response in mice against a circulating antigen induced by adenoviral transfer is strictly dependent on expression in antigen-presenting cells. Blood 2003; 101: 2551-2556.
-
(2003)
Blood
, vol.101
, pp. 2551-2556
-
-
De Geest, B.R.1
Van Linthout, S.A.2
Collen, D.3
-
72
-
-
2342551048
-
Factors influencing therapeutic efficacy and the host immune response to helper-dependent adenoviral gene therapy in hemophilia a mice
-
Brown BD et al. Factors influencing therapeutic efficacy and the host immune response to helper-dependent adenoviral gene therapy in hemophilia A mice. J Thromb Haemost 2004; 2: 111-118.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 111-118
-
-
Brown, B.D.1
-
73
-
-
4644353743
-
Car chasing: Canine adenovirus vectors-all bite and no bark?
-
Kremer EJ. CAR chasing: canine adenovirus vectors-all bite and no bark? J Gene Med 2004; 6 (Suppl 1): S139-S151.
-
(2004)
J Gene Med
, vol.6
, pp. S139-S151
-
-
Kremer, E.J.1
-
74
-
-
0034691208
-
Peripheral infection with adenovirus causes unexpected long-term brain inflammation in animals injected intracranially with first-generation, but not with high-capacity, adenovirus vectors: Toward realistic long-term neurological gene therapy for chronic diseases
-
Thomas CE et al. Peripheral infection with adenovirus causes unexpected long-term brain inflammation in animals injected intracranially with first-generation, but not with high-capacity, adenovirus vectors: toward realistic long-term neurological gene therapy for chronic diseases. Proc Natl Acad Sci USA 2000; 97: 7482-7487.
-
(2000)
Proc Natl Acad Sci USA
, vol.97
, pp. 7482-7487
-
-
Thomas, C.E.1
-
75
-
-
0034926344
-
Pre-existing antiadenoviral immunity is not a barrier to efficient and stable transduction of the brain, mediated by novel high-capacity adenovirus vectors
-
Thomas CE et al. Pre-existing antiadenoviral immunity is not a barrier to efficient and stable transduction of the brain, mediated by novel high-capacity adenovirus vectors. Hum Gene Ther 2001; 12: 839-846.
-
(2001)
Hum Gene Ther
, vol.12
, pp. 839-846
-
-
Thomas, C.E.1
-
76
-
-
0742307422
-
Acute toxicity after high-dose systemic injection of helper-dependent adenoviral vectors into nonhuman primates
-
Brunetti-Pierri N et al. Acute toxicity after high-dose systemic injection of helper-dependent adenoviral vectors into nonhuman primates. Hum Gene Ther 2004; 15: 35-46.
-
(2004)
Hum Gene Ther
, vol.15
, pp. 35-46
-
-
Brunetti-Pierri, N.1
-
77
-
-
16344373567
-
Pegylated helper-dependent adenoviral vectors: Highly efficient vectors with an enhanced safety profile
-
Croyle MA et al. PEGylated helper-dependent adenoviral vectors: highly efficient vectors with an enhanced safety profile. Gene Therapy 2005; 12: 579-587.
-
(2005)
Gene Therapy
, vol.12
, pp. 579-587
-
-
Croyle, M.A.1
-
78
-
-
10944247251
-
Evaluation of polyethylene glycol modification of first-generation and helper-dependent adenoviral vectors to reduce innate immune responses
-
Mok H, Palmer DJ, Ng P, Barry MA. Evaluation of polyethylene glycol modification of first-generation and helper-dependent adenoviral vectors to reduce innate immune responses. Mol Ther 2005; 11: 66-79.
-
(2005)
Mol Ther
, vol.11
, pp. 66-79
-
-
Mok, H.1
Palmer, D.J.2
Ng, P.3
Barry, M.A.4
-
79
-
-
8844261139
-
Vaccination with helper-dependent adenovirus enhances the generation of transgene-specific ctl
-
Harui A et al. Vaccination with helper-dependent adenovirus enhances the generation of transgene-specific CTL. Gene Therapy 2004; 11: 1617-1626.
-
(2004)
Gene Therapy
, vol.11
, pp. 1617-1626
-
-
Harui, A.1
-
80
-
-
0031049699
-
Persistence in muscle of an adenoviral vector that lacks all viral genes
-
Chen HH et al. Persistence in muscle of an adenoviral vector that lacks all viral genes. Proc Natl Acad Sci USA 1997; 94: 1645-1650.
-
(1997)
Proc Natl Acad Sci USA
, vol.94
, pp. 1645-1650
-
-
Chen, H.H.1
-
81
-
-
0035515281
-
Potential of adenoviral p53 gene therapy and irradiation for the treatment of malignant gliomas
-
Kim IA et al. Potential of adenoviral p53 gene therapy and irradiation for the treatment of malignant gliomas. Int J Oncol 2001; 19: 1041-1047.
-
(2001)
Int J Oncol
, vol.19
, pp. 1041-1047
-
-
Kim, I.A.1
-
82
-
-
0032506791
-
High doses of a helper-dependent adenoviral vector yield supraphysiological levels of alpha1-antitrypsin with negligible toxicity
-
Morral N et al. High doses of a helper-dependent adenoviral vector yield supraphysiological levels of alpha1-antitrypsin with negligible toxicity. Hum Gene Ther 1998; 9: 2709-2716.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 2709-2716
-
-
Morral, N.1
-
83
-
-
0141593513
-
A gene-deleted adenoviral vector results in phenotypic correction of canine hemophilia b without liver toxicity or thrombocytopenia
-
Ehrhardt A et al. A gene-deleted adenoviral vector results in phenotypic correction of canine hemophilia B without liver toxicity or thrombocytopenia. Blood 2003; 102: 2403-2411.
-
(2003)
Blood
, vol.102
, pp. 2403-2411
-
-
Ehrhardt, A.1
-
84
-
-
0036154968
-
Sustained human factor viii expression in hemophilia a mice following systemic delivery of a gutless adenoviral vector
-
Reddy PS et al. Sustained human factor VIII expression in hemophilia A mice following systemic delivery of a gutless adenoviral vector. Mol Ther 2002; 5: 63-73.
-
(2002)
Mol Ther
, vol.5
, pp. 63-73
-
-
Reddy, P.S.1
-
85
-
-
0037566365
-
Long-term stable expression of human apolipoprotein a-i mediated by helper-dependent adenovirus gene transfer inhibits atherosclerosis progression and remodels atherosclerotic plaques in a mouse model of familial hypercholesterolemia
-
Belalcazar LM et al. Long-term stable expression of human apolipoprotein A-I mediated by helper-dependent adenovirus gene transfer inhibits atherosclerosis progression and remodels atherosclerotic plaques in a mouse model of familial hypercholesterolemia. Circulation 2003; 107: 2726-2732.
-
(2003)
Circulation
, vol.107
, pp. 2726-2732
-
-
Belalcazar, L.M.1
-
86
-
-
0035814955
-
Long-term stable correction of low-density lipoprotein receptor-deficient mice with a helper-dependent adenoviral vector expressing the very low-density lipoprotein receptor
-
Oka K et al. Long-term stable correction of low-density lipoprotein receptor-deficient mice with a helper-dependent adenoviral vector expressing the very low-density lipoprotein receptor. Circulation 2001; 103: 1274-1281.
-
(2001)
Circulation
, vol.103
, pp. 1274-1281
-
-
Oka, K.1
-
87
-
-
1242338802
-
Helper-dependent adenoviral vector-mediated long-term expression of human apolipoprotein a-i reduces atherosclerosis in apo e-deficient mice
-
Pastore L et al. Helper-dependent adenoviral vector-mediated long-term expression of human apolipoprotein A-I reduces atherosclerosis in apo E-deficient mice. Gene 2004; 327: 153-160.
-
(2004)
Gene
, vol.327
, pp. 153-160
-
-
Pastore, L.1
-
88
-
-
4444333453
-
Long-term correction of ornithine transcarbamy- lase deficiency by wpre-mediated overexpression using a helper-dependent adenovirus
-
Mian A et al. Long-term correction of ornithine transcarbamy- lase deficiency by WPRE-mediated overexpression using a helper-dependent adenovirus. Mol Ther 2004; 10: 492-499.
-
(2004)
Mol Ther
, vol.10
, pp. 492-499
-
-
Mian, A.1
-
89
-
-
0038413922
-
Neurod-betacellulin gene therapy induces islet neogenesis in the liver and reverses diabetes in mice
-
Kojima H et al. NeuroD-betacellulin gene therapy induces islet neogenesis in the liver and reverses diabetes in mice. Nat Med 2003; 9: 596-603.
-
(2003)
Nat Med
, vol.9
, pp. 596-603
-
-
Kojima, H.1
-
90
-
-
0033997907
-
Liver-specific alpha 2 interferon gene expression results in protection from induced hepatitis
-
Aurisicchio L et al. Liver-specific alpha 2 interferon gene expression results in protection from induced hepatitis. J Virol 2000; 74: 4816-4823.
-
(2000)
J Virol
, vol.74
, pp. 4816-4823
-
-
Aurisicchio, L.1
-
91
-
-
4444289122
-
Helper-dependent adenoviral vector-mediated delivery of woodchuck-specific genes for alpha interferon (Ifn- alpha) and ifn-gamma: Ifn-alpha but not ifn-gamma reduces woodchuck hepatitis virus replication in chronic infection
-
Fiedler M et al. Helper-dependent adenoviral vector-mediated delivery of woodchuck-specific genes for alpha interferon (IFN- alpha) and IFN-gamma: IFN-alpha but not IFN-gamma reduces woodchuck hepatitis virus replication in chronic infection in vivo. J Virol 2004; 78: 10111-10121.
-
(2004)
Vivo. J Virol
, vol.78
, pp. 10111-10121
-
-
Fiedler, M.1
-
92
-
-
0033587482
-
Use of a liver-specific promoter reduces immune response to the transgene in adenoviral vectors
-
Pastore L et al. Use of a liver-specific promoter reduces immune response to the transgene in adenoviral vectors. Hum Gene Ther 1999; 10: 1773-1781.
-
(1999)
Hum Gene Ther
, vol.10
, pp. 1773-1781
-
-
Pastore, L.1
-
93
-
-
0029968305
-
Circumventing the immune response to adenovirus-mediated gene therapy
-
Kass-Eisler A et al. Circumventing the immune response to adenovirus-mediated gene therapy. Gene Therapy 1996; 3: 154-162.
-
(1996)
Gene Therapy
, vol.3
, pp. 154-162
-
-
Kass-Eisler, A.1
-
94
-
-
16944367354
-
Circumvention of anti-adenovirus neutralizing immunity by administration of an adenoviral vector of an alternate serotype
-
Mack CA et al. Circumvention of anti-adenovirus 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.A.1
-
95
-
-
0031903186
-
Circumvention of immunity to the adenovirus major coat protein hexon
-
Roy S, Shirley PS, McClelland A, Kaleko M. Circumvention of immunity to the adenovirus major coat protein hexon. J Virol 1998; 72: 6875-6879.
-
(1998)
J Virol
, vol.72
, pp. 6875-6879
-
-
Roy, S.1
Shirley, P.S.2
McClelland, A.3
Kaleko, M.4
-
97
-
-
0033582216
-
Adenovirus-mediated regulable target gene expression in vivo
-
Burcin MM et al. Adenovirus-mediated regulable target gene expression in vivo. Proc Natl Acad Sci USA 1999; 96: 355-360.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 355-360
-
-
Burcin, M.M.1
-
98
-
-
0036846578
-
Tight control of gene expression by a helper- dependent adenovirus vector carrying the rtta2(S)-m2 tetracycline transactivator and repressor system
-
Salucci V et al. Tight control of gene expression by a helper- dependent adenovirus vector carrying the rtTA2(s)-M2 tetracycline transactivator and repressor system. Gene Therapy 2002; 9: 1415-1421.
-
(2002)
Gene Therapy
, vol.9
, pp. 1415-1421
-
-
Salucci, V.1
-
99
-
-
0038697443
-
In vivo ligand-inducible regulation of gene expression in a gutless adenoviral vector system
-
Zerby D et al. In vivo ligand-inducible regulation of gene expression in a gutless adenoviral vector system. Hum Gene Ther 2003; 14: 749-761.
-
(2003)
Hum Gene Ther
, vol.14
, pp. 749-761
-
-
Zerby, D.1
-
100
-
-
0037790861
-
Episomal persistence of recombinant adenoviral vector genomes during the cell cycle in vivo
-
Ehrhardt A, Xu H, Kay MA. Episomal persistence of recombinant adenoviral vector genomes during the cell cycle in vivo. J Virol 2003; 77: 7689-7695.
-
(2003)
J Virol
, vol.77
, pp. 7689-7695
-
-
Ehrhardt, A.1
Xu, H.2
Kay, M.A.3
-
101
-
-
1142279547
-
Helper-dependent adenoviral vectors containing modified fiber for improved transduction of developing and mature muscle cells
-
Bramson JL et al. Helper-dependent adenoviral vectors containing modified fiber for improved transduction of developing and mature muscle cells. Hum Gene Ther 2004; 15: 179-188.
-
(2004)
Hum Gene Ther
, vol.15
, pp. 179-188
-
-
Bramson, J.L.1
-
102
-
-
0034803805
-
Targeting of high-capacity adenoviral vectors
-
Biermann V et al. Targeting of high-capacity adenoviral vectors. Hum Gene Ther 2001; 12: 1757-1769.
-
(2001)
Hum Gene Ther
, vol.12
, pp. 1757-1769
-
-
Biermann, V.1
-
104
-
-
1142273131
-
Sustained improvement of muscle function one year after full-length dystrophin gene transfer into mdx mice by a gutted helper-dependent adenoviral vector
-
Dudley RW et al. Sustained improvement of muscle function one year after full-length dystrophin gene transfer into mdx mice by a gutted helper-dependent adenoviral vector. Hum Gene Ther 2004; 15: 145-156.
-
(2004)
Hum Gene Ther
, vol.15
, pp. 145-156
-
-
Dudley, R.W.1
-
105
-
-
0038344798
-
Prolonged dystrophin expression and functional correction of mdx mouse muscle following gene transfer with a helper-dependent (Gutted) adenovirus-encoding murine dystrophin
-
Gilbert R et al. Prolonged dystrophin expression and functional correction of mdx mouse muscle following gene transfer with a helper-dependent (gutted) adenovirus-encoding murine dystrophin. Hum Mol Genet 2003; 12: 1287-1299.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1287-1299
-
-
Gilbert, R.1
-
106
-
-
11844269203
-
Comparison of high-capacity and first-generation adenoviral vector gene delivery to murine muscle in utero
-
Bilbao R et al. Comparison of high-capacity and first-generation adenoviral vector gene delivery to murine muscle in utero. Gene Therapy 2005; 12: 39-47.
-
(2005)
Gene Therapy
, vol.12
, pp. 39-47
-
-
Bilbao, R.1
-
107
-
-
0036790998
-
Functional correction of adult mdx mouse muscle using gutted adenoviral vectors expressing full-length dystrophin
-
DelloRusso C et al. Functional correction of adult mdx mouse muscle using gutted adenoviral vectors expressing full-length dystrophin. Proc Natl Acad Sci USA 2002; 99: 12979-12984.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 12979-12984
-
-
DelloRusso, C.1
-
108
-
-
0034244414
-
Prolonged transgene expression mediated by a helper-dependent adenoviral vector (Hdad) in the central nervous system
-
Zou L, Zhou H, Pastore L, Yang K. Prolonged transgene expression mediated by a helper-dependent adenoviral vector (hdAd) in the central nervous system. Mol Ther 2000; 2:105-113.
-
(2000)
Mol Ther
, vol.2
, pp. 105-113
-
-
Zou, L.1
Zhou, H.2
Pastore, L.3
Yang, K.4
-
109
-
-
0034986065
-
Acute direct adenoviral vector cytotoxicity and chronic, but not acute, inflammatory responses correlate with decreased vector-mediated transgene expression in the brain
-
Thomas CE et al. Acute direct adenoviral vector cytotoxicity and chronic, but not acute, inflammatory responses correlate with decreased vector-mediated transgene expression in the brain. Mol Ther 2001; 3: 36-46.
-
(2001)
Mol Ther
, vol.3
, pp. 36-46
-
-
Thomas, C.E.1
-
110
-
-
0036790941
-
Autologous transplantation of genetically modified iris pigment epithelial cells: A promising concept for the treatment of age-related macular degeneration and other disorders of the eye
-
Semkova I et al. Autologous transplantation of genetically modified iris pigment epithelial cells: a promising concept for the treatment of age-related macular degeneration and other disorders of the eye. Proc Natl Acad Sci USA 2002; 99: 13090-13095.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 13090-13095
-
-
Semkova, I.1
-
111
-
-
2342592123
-
Intraocular gutless adenoviral-vectored vegf stimulates anterior segment but not retinal neovascularization
-
Oshima Y et al. Intraocular gutless adenoviral-vectored VEGF stimulates anterior segment but not retinal neovascularization. J Cell Physiol 2004; 199: 399-411.
-
(2004)
J Cell Physiol
, vol.199
, pp. 399-411
-
-
Oshima, Y.1
-
112
-
-
3142680351
-
Helper-dependent adenovirus vectors devoid of all viral genes cause less myocardial inflammation compared with first-generation adenovirus vectors
-
Fleury S et al. Helper-dependent adenovirus vectors devoid of all viral genes cause less myocardial inflammation compared with first-generation adenovirus vectors. Basic Res Cardiol 2004; 99: 247-256.
-
(2004)
Basic Res Cardiol
, vol.99
, pp. 247-256
-
-
Fleury, S.1
-
113
-
-
1642444207
-
Early adenoviral gene expression mediates immunosuppression by transduced dendritic cell (Dc): Implications for immunotherapy using genetically modified dc
-
Tuettenberg A et al. Early adenoviral gene expression mediates immunosuppression by transduced dendritic cell (DC): implications for immunotherapy using genetically modified DC. J Immunol 2004; 172: 1524-1530.
-
(2004)
J Immunol
, vol.172
, pp. 1524-1530
-
-
Tuettenberg, A.1
-
114
-
-
4544329958
-
Improved vascular gene transfer with a helper-dependent adenoviral vector
-
Wen S, Graf S, Massey PG, Dichek DA. Improved vascular gene transfer with a helper-dependent adenoviral vector. Circulation 2004; 110: 1484-1491.
-
(2004)
Circulation
, vol.110
, pp. 1484-1491
-
-
Wen, S.1
Graf, S.2
Massey, P.G.3
Dichek, D.A.4
-
115
-
-
0347364650
-
Protection of cftr knockout mice from acute lung infection by a helper-dependent adenoviral vector expressing cftr in airway epithelia
-
Koehler DR et al. Protection of Cftr knockout mice from acute lung infection by a helper-dependent adenoviral vector expressing Cftr in airway epithelia. Proc Natl Acad Sci USA 2003; 100: 15364-15369.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 15364-15369
-
-
Koehler, D.R.1
-
116
-
-
13944271703
-
Transfer of the full-length dystrophin- coding sequence into muscle cells by a dual high-capacity hybrid viral vector with site-specific integration ability
-
Goncalves MA et al. Transfer of the full-length dystrophin- coding sequence into muscle cells by a dual high-capacity hybrid viral vector with site-specific integration ability. J Virol 2005; 79: 3146-3162.
-
(2005)
J Virol
, vol.79
, pp. 3146-3162
-
-
Goncalves, M.A.1
-
117
-
-
0036789403
-
Transposition from a gutless adeno-transposon vector stabilizes transgene expression in vivo
-
Yant SR et al. Transposition from a gutless adeno-transposon vector stabilizes transgene expression in vivo. Nat Biotechnol 2002; 20: 999-1005.
-
(2002)
Nat Biotechnol
, vol.20
, pp. 999-1005
-
-
Yant, S.R.1
-
118
-
-
0345734204
-
Long-term transgene expression in proliferating cells mediated by episomally maintained highcapacity adenovirus vectors
-
Kreppel F, Kochanek S. Long-term transgene expression in proliferating cells mediated by episomally maintained highcapacity adenovirus vectors. J Virol 2004; 78: 9-22.
-
(2004)
J Virol
, vol.78
, pp. 9-22
-
-
Kreppel, F.1
Kochanek, S.2
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