-
1
-
-
0000557447
-
Adenoviridae: The viruses and their replication
-
Fields BN, Knipe DM, Howley PM, eds. Philadelphia: Lippincott-Raven Publishers
-
Shenk T. Adenoviridae: the viruses and their replication. In: Fields BN, Knipe DM, Howley PM, eds. Fields Virology. Philadelphia: Lippincott-Raven Publishers, 1996: 2111-2148.
-
(1996)
Fields Virology
, pp. 2111-2148
-
-
Shenk, T.1
-
2
-
-
0031052263
-
Isolation of a common receptor for Coxsackie B viruses and adenoviruses 2 and 5
-
Bergelson JM, Cunningham JA, Droguett G et al. Isolation of a common receptor for Coxsackie B viruses and adenoviruses 2 and 5. Science 1997: 275: 1320-1323.
-
(1997)
Science
, vol.275
, pp. 1320-1323
-
-
Bergelson, J.M.1
Cunningham, J.A.2
Droguett, G.3
-
3
-
-
0030994260
-
Adenovirus type 5 fiber knob binds to MHC class I alpha2 domain at the surface of human epithelial and B lymphoblastoid cells
-
Hong SS, Karayan L, Tournier J, Curiel DT, Boulanger PA. Adenovirus type 5 fiber knob binds to MHC class I alpha2 domain at the surface of human epithelial and B lymphoblastoid cells. Embo J 1997: 16: 2294-2306.
-
(1997)
Embo J
, vol.16
, pp. 2294-2306
-
-
Hong, S.S.1
Karayan, L.2
Tournier, J.3
Curiel, D.T.4
Boulanger, P.A.5
-
4
-
-
0027166647
-
Integrins alpha v beta 3 and alpha v beta 5 promote adenovirus internalization but not virus attachment
-
Wickham TJ, Mathias P, Cheresh DA, Nemerow GR. Integrins alpha v beta 3 and alpha v beta 5 promote adenovirus internalization but not virus attachment. Cell 1993: 73: 309-319.
-
(1993)
Cell
, vol.73
, pp. 309-319
-
-
Wickham, T.J.1
Mathias, P.2
Cheresh, D.A.3
Nemerow, G.R.4
-
5
-
-
0029794681
-
Targeted adenovirus gene transfer to endothelial and smooth muscle cells by using bispecific antibodies
-
Wickham TJ, Segal DM, Roelvink PW et al. Targeted adenovirus gene transfer to endothelial and smooth muscle cells by using bispecific antibodies. J Virol 1996: 70: 6831-6838.
-
(1996)
J Virol
, vol.70
, pp. 6831-6838
-
-
Wickham, T.J.1
Segal, D.M.2
Roelvink, P.W.3
-
6
-
-
0029794845
-
Gradient of RGD-dependent entry of adenoviral vector in nasal and intrapulmonary epithelia: Implications for gene therapy of cystic fibrosis
-
Goldman M, Su Q, Wilson JM. Gradient of RGD-dependent entry of adenoviral vector in nasal and intrapulmonary epithelia: implications for gene therapy of cystic fibrosis. Gene Ther 1996: 3: 811-818.
-
(1996)
Gene Ther
, vol.3
, pp. 811-818
-
-
Goldman, M.1
Su, Q.2
Wilson, J.M.3
-
7
-
-
0026949598
-
The importance of being acidic: The role of acidification in intracellular membrane traffic
-
Mellman I. The importance of being acidic: the role of acidification in intracellular membrane traffic. J Exp Biol 1992: 172: 39-45.
-
(1992)
J Exp Biol
, vol.172
, pp. 39-45
-
-
Mellman, I.1
-
8
-
-
0032502017
-
Fluorescent virions: Dynamic tracking of the pathway of adenoviral gene transfer vectors in living cells
-
Leopold PL, Ferris B, Grinberg I, Worgall S, Hackett NR, Crystal RG. Fluorescent virions: dynamic tracking of the pathway of adenoviral gene transfer vectors in living cells. Hum Gene Ther 1998: 9: 367-378.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 367-378
-
-
Leopold, P.L.1
Ferris, B.2
Grinberg, I.3
Worgall, S.4
Hackett, N.R.5
Crystal, R.G.6
-
9
-
-
0027496645
-
Stepwise dismantling of adenovirus 2 during entry into cells
-
Greber UF, Willetts M, Webster P, Helenius A. Stepwise dismantling of adenovirus 2 during entry into cells. Cell 1993: 75: 477-486.
-
(1993)
Cell
, vol.75
, pp. 477-486
-
-
Greber, U.F.1
Willetts, M.2
Webster, P.3
Helenius, A.4
-
10
-
-
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
-
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
-
-
0026591331
-
Expression of heterologous sequences in adenoviral vectors
-
Berkner KL. Expression of heterologous sequences in adenoviral vectors. Curr Top Microbiol Immunol 1992: 158: 39-66.
-
(1992)
Curr Top Microbiol Immunol
, vol.158
, pp. 39-66
-
-
Berkner, K.L.1
-
13
-
-
0028857655
-
The use of adenoviral vectors for gene therapy and gene transfer in vivo
-
Bramson JL, Graham FL, Gauldie J. The use of adenoviral vectors for gene therapy and gene transfer in vivo. Curr Opin Biotechnol 1995: 6: 590-595.
-
(1995)
Curr Opin Biotechnol
, vol.6
, pp. 590-595
-
-
Bramson, J.L.1
Graham, F.L.2
Gauldie, J.3
-
14
-
-
0030623809
-
Human adenovirus vectors for gene transfer into mammalian cells
-
Hitt MM, Addison CL, Graham FL. Human adenovirus vectors for gene transfer into mammalian cells. Adv Pharmacol 1997: 40: 137-206.
-
(1997)
Adv Pharmacol
, vol.40
, pp. 137-206
-
-
Hitt, M.M.1
Addison, C.L.2
Graham, F.L.3
-
15
-
-
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
-
16
-
-
0030824640
-
Immune responses to reporter proteins and high viral dose limit duration of expression with adenoviral vectors: Comparison, of E2a wild type and E2a deleted vectors
-
Morral N, O'Neal W, Zhou H, Langston C, Beaudet A. Immune responses to reporter proteins and high viral dose limit duration of expression with adenoviral vectors: comparison, of E2a wild type and E2a deleted vectors. Hm Gene Ther 1997: 8: 1275-1286.
-
(1997)
Hm Gene Ther
, vol.8
, pp. 1275-1286
-
-
Morral, N.1
O'Neal, W.2
Zhou, H.3
Langston, C.4
Beaudet, A.5
-
17
-
-
0028328261
-
Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy
-
Yang Y, Nunes FA, Berencsi K, Furth EE, Gonczol E, Wilson JM. 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
Nunes, F.A.2
Berencsi, K.3
Furth, E.E.4
Gonczol, E.5
Wilson, J.M.6
-
18
-
-
0032530110
-
Cellular immune response to adenoviral vector infected cells does not require de novo viral gene expression: Implications for gene therapy
-
Kafri T, Morgan D, Krahl T, Sarvetnick N, Sherman L, Verma I. Cellular immune response to adenoviral vector infected cells does not require de novo viral gene expression: implications for gene therapy. Proc Natl Acad Sci USA 1998: 95: 11377-11382.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 11377-11382
-
-
Kafri, T.1
Morgan, D.2
Krahl, T.3
Sarvetnick, N.4
Sherman, L.5
Verma, I.6
-
19
-
-
0029743163
-
Cyclophosphamide diminishes inflammation and prolongs transgene expression following delivery of adenoviral vectors to mouse liver and lung
-
Jooss K, Yang Y, Wilson JM. Cyclophosphamide diminishes inflammation and prolongs transgene expression following delivery of adenoviral vectors to mouse liver and lung. Hum Gene Ther 1996: 7: 1555-1566.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 1555-1566
-
-
Jooss, K.1
Yang, Y.2
Wilson, J.M.3
-
20
-
-
0029741231
-
Transient immuno-suppression by FK506 permits a sustained high-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscles of adult dystrophic (mdx) mice
-
Lochmuller H, Petrof BJ, Pari G et al. Transient immuno-suppression by FK506 permits a sustained high-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscles of adult dystrophic (mdx) mice. Gene Ther 1996: 3: 706-716.
-
(1996)
Gene Ther
, vol.3
, pp. 706-716
-
-
Lochmuller, H.1
Petrof, B.J.2
Pari, G.3
-
21
-
-
0028807696
-
FK506 immunosuppression to control the immune reactions triggered by first-generation adenovirus-mediated gene transfer
-
Vilquin JT, Guerette B, Kinoshita I et al. FK506 immunosuppression to control the immune reactions triggered by first-generation adenovirus-mediated gene transfer. Hum Gene Ther 1995: 6: 1391-1401.
-
(1995)
Hum Gene Ther
, vol.6
, pp. 1391-1401
-
-
Vilquin, J.T.1
Guerette, B.2
Kinoshita, I.3
-
22
-
-
0029875608
-
Use of transient CD4 lymphocyte depletion to prolong transgene expression of E1-deleted adenoviral vectors
-
Kolls JK, Lei D, Odom G et al. Use of transient CD4 lymphocyte depletion to prolong transgene expression of E1-deleted adenoviral vectors. Hum Gene Ther 1996: 7: 489-497.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 489-497
-
-
Kolls, J.K.1
Lei, D.2
Odom, G.3
-
23
-
-
0030943732
-
Macrophage depletion increases the safety, efficacy and persistence of adenovirus-mediated gene transfer in vivo
-
Kuzmin AI, Finegold MJ, Eisensmith RC. Macrophage depletion increases the safety, efficacy and persistence of adenovirus-mediated gene transfer in vivo. Gene Ther 1997: 4: 309-316.
-
(1997)
Gene Ther
, vol.4
, pp. 309-316
-
-
Kuzmin, A.I.1
Finegold, M.J.2
Eisensmith, R.C.3
-
24
-
-
0029877620
-
Anti-T cell receptor monoclonal antibody prolongs transgene expression following adenovirus-mediated in vivo gene transfer to mouse synovium
-
Sawchuk SJ, Boivin GP, Duwel LE 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
Boivin, G.P.2
Duwel, L.E.3
-
25
-
-
0031060294
-
Enhancement of in vivo adenovirus-mediated gene transfer and expression by prior depletion of tissue macrophages in the target organ
-
Wolff G, Worgall S, van RN, Song WR, Harvey BG, Crystal RG. 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
Worgall, S.2
Van, R.N.3
Song, W.R.4
Harvey, B.G.5
Crystal, R.G.6
-
26
-
-
0029944988
-
Transient immune blockade prevents formation of neutralizing antibody to recombinant adenovirus and allows repeated gene transfer to mouse liver
-
Yang Y, Greenough K, Wilson JM. Transient immune blockade prevents formation of neutralizing antibody to recombinant adenovirus and allows repeated gene transfer to mouse liver. Gene Ther 1996: 3: 412-420.
-
(1996)
Gene Ther
, vol.3
, pp. 412-420
-
-
Yang, Y.1
Greenough, K.2
Wilson, J.M.3
-
27
-
-
0029790327
-
Prevention of immune reactions triggered by first-generation adenoviral vectors by monoclonal antibodies and CTLA4Ig
-
Guerette B, Vilquin JT, Gingras M, Gravel C, Wood KJ, Tremblay JP. Prevention of immune reactions triggered by first-generation adenoviral vectors by monoclonal antibodies and CTLA4Ig. Hum Gene Ther 1996: 7: 1455-1463.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 1455-1463
-
-
Guerette, B.1
Vilquin, J.T.2
Gingras, M.3
Gravel, C.4
Wood, K.J.5
Tremblay, J.P.6
-
28
-
-
0031883333
-
Blunting of immune responses to adenoviral vectors in mouse liver and lung with CTLA4Ig
-
Jooss K, Turka LA, Wilson JM. Blunting of immune responses to adenoviral vectors in mouse liver and lung with CTLA4Ig. Gene Ther 1998: 5: 309-319.
-
(1998)
Gene Ther
, vol.5
, pp. 309-319
-
-
Jooss, K.1
Turka, L.A.2
Wilson, J.M.3
-
29
-
-
0030847771
-
Constitutive expression of murine CTLA4Ig from a recombinant adenovirus vector results in prolonged transgene expression
-
Schowalter DB, Meuse L, Wilson CB, Linsley PS, Kay MA. Constitutive expression of murine CTLA4Ig from a recombinant adenovirus vector results in prolonged transgene expression. Gene Ther 1997: 4: 853-860.
-
(1997)
Gene Ther
, vol.4
, pp. 853-860
-
-
Schowalter, D.B.1
Meuse, L.2
Wilson, C.B.3
Linsley, P.S.4
Kay, M.A.5
-
30
-
-
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, Embree LJ, Schowalter D 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
Embree, L.J.2
Schowalter, D.3
-
31
-
-
0029968305
-
Circumventing the immune response to adenovirus-mediated gene therapy
-
Kass-Eisler A, Leinwand L, Gall J, Bloom B, Falck-Pedersen E. Circumventing the immune response to adenovirus-mediated gene therapy. Gene Ther 1996: 3: 154-162.
-
(1996)
Gene Ther
, vol.3
, pp. 154-162
-
-
Kass-Eisler, A.1
Leinwand, L.2
Gall, J.3
Bloom, B.4
Falck-Pedersen, E.5
-
32
-
-
0029955391
-
Neonatal cotton rats do not exhibit destructive immune responses to adenoviral vectors
-
Zepeda M, Wilson JM. Neonatal cotton rats do not exhibit destructive immune responses to adenoviral vectors. Gene Ther 1996: 3: 973-979.
-
(1996)
Gene Ther
, vol.3
, pp. 973-979
-
-
Zepeda, M.1
Wilson, J.M.2
-
33
-
-
0031888263
-
In vitro and in vitro and in vivo biology of recombinant adenovirus vectors with E1, E1/ E2A, or E1/E4 deleted
-
Lusky M, Christ M, Rittner K et al. In vitro and In vitro and in vivo biology of recombinant adenovirus vectors with E1, E1/ E2A, or E1/E4 deleted. J Virol 1998: 72: 2022-2032.
-
(1998)
J Virol
, vol.72
, pp. 2022-2032
-
-
Lusky, M.1
Christ, M.2
Rittner, K.3
-
34
-
-
0029670374
-
Lack of persistence of E1-recombinant adenoviral vectors containing a temperature-sensitive E2A mutation in immunocompetent mice and hemophilia B dogs
-
Fang B, Wang H, Gordon G et al. Lack of persistence of E1-recombinant adenoviral vectors containing a temperature-sensitive E2A mutation in immunocompetent mice and hemophilia B dogs. Gene Ther 1996: 3: 217-222.
-
(1996)
Gene Ther
, vol.3
, pp. 217-222
-
-
Fang, B.1
Wang, H.2
Gordon, G.3
-
35
-
-
0033529902
-
Systemic correction of the muscle disorder glycogen storage disease type II after hepatic targeting of a modified adenovirus vector encoding human acid-alpha-glucosidase
-
Amalfitano A, McVie-Wylie AJ, Hu H et al. Systemic correction of the muscle disorder glycogen storage disease type II after hepatic targeting of a modified adenovirus vector encoding human acid-alpha-glucosidase. Proc Natl Acad Sci USA 1999: 96: 8861-8866.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 8861-8866
-
-
Amalfitano, A.1
McVie-Wylie, A.J.2
Hu, H.3
-
36
-
-
0033540652
-
Persistence of an [E1-, polymerase-] adenovirus vector despite transduction of a neoantigen into immune-competent mice
-
Hu H, Serra D, Amalfitano A. Persistence of an [E1-, polymerase-] adenovirus vector despite transduction of a neoantigen into immune-competent mice. Hum Gene Ther 1999: 10: 355-364.
-
(1999)
Hum Gene Ther
, vol.10
, pp. 355-364
-
-
Hu, H.1
Serra, D.2
Amalfitano, A.3
-
37
-
-
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
-
38
-
-
0029966514
-
Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis
-
Fisher KJ, Choi H, Burda J, Chen SJ, Wilson JM. Recombinant adenovirus deleted of all viral genes for gene therapy of cystic fibrosis. Virology 1996: 217: 11-22.
-
(1996)
Virology
, vol.217
, pp. 11-22
-
-
Fisher, K.J.1
Choi, H.2
Burda, J.3
Chen, S.J.4
Wilson, J.M.5
-
39
-
-
0029962474
-
In vivo expression of full-length human dystrophin from adenoviral vectors deleted of all viral genes
-
Haecker SE, Stedman HH, Balice-Gordon RJ et al. In vivo expression of full-length human dystrophin from adenoviral vectors deleted of all viral genes. Hum Gene Ther 1996: 7: 1907-1914.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 1907-1914
-
-
Haecker, S.E.1
Stedman, H.H.2
Balice-Gordon, R.J.3
-
40
-
-
0030016358
-
Encapsidated adenovirus minichromosomes allow delivery and expression of a 14 kb dystrophin cDNA to muscle cells
-
Kumar-Singh R, Chamberlain JS. Encapsidated adenovirus minichromosomes allow delivery and expression of a 14 kb dystrophin cDNA to muscle cells. Hum Mol Genet 1996: 5: 913-921.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 913-921
-
-
Kumar-Singh, R.1
Chamberlain, J.S.2
-
41
-
-
0029943155
-
A new adenoviral vector: Replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and beta-galactosidase
-
Kochanek S, Clemens PR, Mitani K, Chen HH, Chan S, Caskey CT. A new adenoviral vector: replacement of all viral coding sequences with 28 kb of DNA independently expressing both full-length dystrophin and beta-galactosidase. Proc Natl Acad Sci USA 1996: 93: 5731-5736.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 5731-5736
-
-
Kochanek, S.1
Clemens, P.R.2
Mitani, K.3
Chen, H.H.4
Chan, S.5
Caskey, C.T.6
-
42
-
-
0025265591
-
Adenovirus type 5 packaging domain is composed of a repeated element that is functionally redundant
-
Grable M, Hearing P. Adenovirus type 5 packaging domain is composed of a repeated element that is functionally redundant. J Virol 1990: 64: 2047-2056.
-
(1990)
J Virol
, vol.64
, pp. 2047-2056
-
-
Grable, M.1
Hearing, P.2
-
43
-
-
0029857641
-
In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes
-
Clemens PR, Kochanek S, Sunada Y et al. In vivo muscle gene transfer of full-length dystrophin with an adenoviral vector that lacks all viral genes. Gene Ther 1996: 3: 965-972.
-
(1996)
Gene Ther
, vol.3
, pp. 965-972
-
-
Clemens, P.R.1
Kochanek, S.2
Sunada, Y.3
-
44
-
-
0031049699
-
Persistence in muscle of an adenoviral vector that lacks all viral genes
-
Chen HH, Mack LM, Kelly R, Ontell M, Kochanek S, Clemens PR. 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
Mack, L.M.2
Kelly, R.3
Ontell, M.4
Kochanek, S.5
Clemens, P.R.6
-
45
-
-
0033540620
-
DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscle
-
Chen HH, Mack LM, Choi SY, Ontell M, Kochanek S, Clemens PR. 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.H.1
Mack, L.M.2
Choi, S.Y.3
Ontell, M.4
Kochanek, S.5
Clemens, P.R.6
-
46
-
-
0028842611
-
Interferon-gamma inhibits transgene expression driven by SV40 or CMV promoters but augments expression driven by the mammalian MHC I promoter
-
Harms JS, Splitter GA. Interferon-gamma inhibits transgene expression driven by SV40 or CMV promoters but augments expression driven by the mammalian MHC I promoter. Hum Gene Ther 1995: 6: 1291-1297.
-
(1995)
Hum Gene Ther
, vol.6
, pp. 1291-1297
-
-
Harms, J.S.1
Splitter, G.A.2
-
47
-
-
6844257545
-
Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles
-
Floyd SS Jr, Clemens PR, Ontell MR et al. Ex vivo gene transfer using adenovirus-mediated full-length dystrophin delivery to dystrophic muscles. Gene Ther 1998: 5: 19-30.
-
(1998)
Gene Ther
, vol.5
, pp. 19-30
-
-
Floyd S.S., Jr.1
Clemens, P.R.2
Ontell, M.R.3
-
48
-
-
0031055468
-
Construction of adenovirus vectors through cre-lox recombination
-
Hardy S, Kitamura M, Harris-Stansil T, Dai Y, Phipps ML. Construction of adenovirus vectors through Cre-lox recombination. J Virol 1997: 71: 1842-1849.
-
(1997)
J Virol
, vol.71
, pp. 1842-1849
-
-
Hardy, S.1
Kitamura, M.2
Harris-Stansil, T.3
Dai, Y.4
Phipps, M.L.5
-
49
-
-
0029861452
-
Recombinant adenoviruses with large deletions generated by cre-mediated excision exhibit different biological properties compared with first-generation vectors in vitro and in vivo
-
Lieber A, He CY, Kirillova I, Kay MA. Recombinant adenoviruses with large deletions generated by Cre-mediated excision exhibit different biological properties compared with first-generation vectors in vitro and in vivo. J Virol 1996: 70: 8944-8960.
-
(1996)
J Virol
, vol.70
, pp. 8944-8960
-
-
Lieber, A.1
He, C.Y.2
Kirillova, I.3
Kay, M.A.4
-
50
-
-
0030462599
-
A helper-dependent adenovirus vector system: Removal of helper virus by cre-mediated excision of the viral packaging signal
-
Parks RJ, Chen L, Anton M, Sankar U, Rudnicki MA, Graham FL. 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
Chen, L.2
Anton, M.3
Sankar, U.4
Rudnicki, Ma.5
Graham, F.L.6
-
51
-
-
0030765997
-
Persistence of recombinant adenovirus in vivo is not dependent on vector DNA replication
-
Nelson JE, Kay MA. Persistence of recombinant adenovirus in vivo is not dependent on vector DNA replication. J Virol 1997: 71: 8902-8907.
-
(1997)
J Virol
, vol.71
, pp. 8902-8907
-
-
Nelson, J.E.1
Kay, M.A.2
-
52
-
-
0030426525
-
Production and characterization of human 293 cell lines expressing the site-specific recombinase cre
-
Chen L, Anton M, Graham FL. Production and characterization of human 293 cell lines expressing the site-specific recombinase Cre. Somat Cell Mol Genet 1996: 22: 477-488.
-
(1996)
Somat Cell Mol Genet
, vol.22
, pp. 477-488
-
-
Chen, L.1
Anton, M.2
Graham, F.L.3
-
53
-
-
0032816327
-
Improved production of gutted adenovirus in cells expressing adenovirus preterminal protein and DNA polymerase
-
Hartigan-O'Connor D, Amalfitano A, Chamberlain JS. Improved production of gutted adenovirus in cells expressing adenovirus preterminal protein and DNA polymerase. J Virol 1999: 73: 7835-7841.
-
(1999)
J Virol
, vol.73
, pp. 7835-7841
-
-
Hartigan-O'Connor, D.1
Amalfitano, A.2
Chamberlain, J.S.3
-
54
-
-
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
-
55
-
-
0032850174
-
Effects of stuffer DNA on transgene expression from helper-dependent adenovirus vectors
-
Parks RJ, Bramson JL, Wan Y, Addison CL, Graham FL. Effects of stuffer DNA on transgene expression from helper-dependent adenovirus vectors. J Virol 1999: 73: 8027-8034.
-
(1999)
J Virol
, vol.73
, pp. 8027-8034
-
-
Parks, R.J.1
Bramson, J.L.2
Wan, Y.3
Addison, C.L.4
Graham, F.L.5
-
56
-
-
0031916435
-
Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity
-
Schiedner G, Morral N, Parks RJ 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
Morral, N.2
Parks, R.J.3
-
57
-
-
0033587482
-
Use of a liver-specific promoter reduces immune response to the transgene in adenoviral vectors
-
Pastore L, Morral N, Zhou H 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
Morral, N.2
Zhou, H.3
-
58
-
-
0032506791
-
High doses of a helper-dependent adenoviral vector yield supraphysiological levels of alpha 1-antitrypsin with negligible toxicity
-
Morral N, Parks RJ, Zhou H et al. High doses of a helper-dependent adenoviral vector yield supraphysiological levels of alpha 1-antitrypsin with negligible toxicity. Hum Gene Ther 1998: 9: 2709-2716.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 2709-2716
-
-
Morral, N.1
Parks, R.J.2
Zhou, H.3
-
59
-
-
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, O'Neal W, Rice K 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
O'Neal, W.2
Rice, K.3
-
60
-
-
13144283616
-
An adenoviral vector deleted for all viral coding sequences results in enhanced safety and extended expression of a leptin transgene
-
Morsy MA, 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 USA 1998: 95: 7866-7871.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 7866-7871
-
-
Morsy, M.A.1
Gu, M.2
Motzel, S.3
-
61
-
-
0030809684
-
Complementation of helper-dependent adenoviral vectors: Size effects and titer fluctuations
-
Alemany R, Dai Y, Lou YC 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
Dai, Y.2
Lou, Y.C.3
-
62
-
-
12944317288
-
Sustained high-level expression of full-length human factor VIII and restoration of clotting activity in hemophilic mice using a minimal adenovirus vector
-
Balague C, Zhou J, Dai Y et al. Sustained high-level expression of full-length human factor VIII and restoration of clotting activity in hemophilic mice using a minimal adenovirus vector. Blood 2000: 95: 820-828.
-
(2000)
Blood
, vol.95
, pp. 820-828
-
-
Balague, C.1
Zhou, J.2
Dai, Y.3
-
63
-
-
0030023343
-
Systematic analysis of repeated gene delivery into animal lungs with a recombinant adenovirus vector
-
Dong JY, Wang D, Van GF, Pascual DW, Frizzell RA. Systematic analysis of repeated gene delivery into animal lungs with a recombinant adenovirus vector. Hum Gene Ther 1996: 7: 319-331.
-
(1996)
Hum Gene Ther
, vol.7
, pp. 319-331
-
-
Dong, J.Y.1
Wang, D.2
Van, G.F.3
Pascual, D.W.4
Frizzell, R.A.5
-
64
-
-
0029873225
-
Biological response of nonhuman primates to long-term repeated lung exposure to Ad2/CFTR-2
-
St George J, Pennington SE, Kaplan JM et al. Biological response of nonhuman primates to long-term repeated lung exposure to Ad2/CFTR-2. Gene Ther 1996: 3: 103-116.
-
(1996)
Gene Ther
, vol.3
, pp. 103-116
-
-
St George, J.1
Pennington, S.E.2
Kaplan, J.M.3
-
65
-
-
0029968303
-
Humoral and cellular immune responses of nonhuman primates to long-term repeated lung exposure to Ad2/CFTR-2
-
Kaplan JM, St George J, Pennington SE et al. Humoral and cellular immune responses of nonhuman primates to long-term repeated lung exposure to Ad2/CFTR-2. Gene Ther 1996: 3: 117-127.
-
(1996)
Gene Ther
, vol.3
, pp. 117-127
-
-
Kaplan, J.M.1
St George, J.2
Pennington, S.E.3
-
66
-
-
0032827780
-
Use of helper-dependent adenoviral vectors of alternative serotypes permits repeat vector administration
-
Parks RJ, Evelegh CM, Graham FL. Use of helper-dependent adenoviral vectors of alternative serotypes permits repeat vector administration. Gene Ther 1999: 6: 1565-1573.
-
(1999)
Gene Ther
, vol.6
, pp. 1565-1573
-
-
Parks, R.J.1
Evelegh, C.M.2
Graham, F.L.3
-
67
-
-
16944367354
-
Circumvention of anti-adenovirus neutralizing immunity by administration of an adenoviral vector of an alternate serotype
-
Mack CA, Song WR, Carpenter H 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
Song, W.R.2
Carpenter, H.3
-
68
-
-
0030768124
-
Increased in vitro and in vivo gene transfer by adenovirus vectors containing chimeric fiber proteins
-
Wickham TJ, Tzeng E, Shears LL 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.J.1
Tzeng, E.2
Shears, L.L.3
-
69
-
-
0033582216
-
Adenovirus-mediated regulable target gene expression in vivo
-
Burcin MM, Schiedner G, Kochanek S, Tsai SY, O'Malley BW. 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
Schiedner, G.2
Kochanek, S.3
Tsai, S.Y.4
O'Malley, B.W.5
-
70
-
-
0033057474
-
Site-specific integration mediated by a hybrid adenovirus/adeno-associated virus vector
-
Recchia A, Parks RJ, Lamartina S et al. Site-specific integration mediated by a hybrid adenovirus/adeno-associated virus vector. Proc Natl Acad Sci USA 1999: 96: 2615-2620.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 2615-2620
-
-
Recchia, A.1
Parks, R.J.2
Lamartina, S.3
-
71
-
-
17444372024
-
Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors
-
Snyder RO, Miao C, Meuse L et al. Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors. Nat Med 1999: 5: 64-70.
-
(1999)
Nat Med
, vol.5
, pp. 64-70
-
-
Snyder, R.O.1
Miao, C.2
Meuse, L.3
-
72
-
-
12644271889
-
Phase I study of a recombinant adenovirus-mediated gene transfer in lung cancer patients
-
Tursz T, Cesne AL, Baldeyrou P et al. Phase I study of a recombinant adenovirus-mediated gene transfer in lung cancer patients. J Natl Cancer Inst 1996: 88: 1857-1863.
-
(1996)
J Natl Cancer Inst
, vol.88
, pp. 1857-1863
-
-
Tursz, T.1
Cesne, A.L.2
Baldeyrou, P.3
-
73
-
-
16944367069
-
A phase I study of adenovirus mediated gene transfer of interleukin 2 cDNA into metastatic breast cancer or melanoma
-
Stewart AK, Lassam NJ, Graham FL et al. A phase I study of adenovirus mediated gene transfer of interleukin 2 cDNA into metastatic breast cancer or melanoma. Hum Gene Ther 1997: 8: 1403-1414.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 1403-1414
-
-
Stewart, A.K.1
Lassam, N.J.2
Graham, F.L.3
-
74
-
-
17344365479
-
A phase 1 study of adenovirus-mediated wild-type p53 gene transfer in patients with advanced non-small cell lung cancer
-
Schuler M, Rochlitz C, Horowitz JA et al. A phase 1 study of adenovirus-mediated wild-type p53 gene transfer in patients with advanced non-small cell lung cancer. Hum Gene Ther 1998: 9: 2075-2082.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 2075-2082
-
-
Schuler, M.1
Rochlitz, C.2
Horowitz, J.A.3
-
75
-
-
0031828108
-
Gene therapy for non-small cell lung cancer: A preliminary report of a phase 1 trial of adenoviral p53 gene replacement
-
Roth JA, Swisher SG, Merritt JA et al. Gene therapy for non-small cell lung cancer: a preliminary report of a phase 1 trial of adenoviral p53 gene replacement. Semin Oncol 1998: 25: 33-37.
-
(1998)
Semin Oncol
, vol.25
, pp. 33-37
-
-
Roth, J.A.1
Swisher, S.G.2
Merritt, J.A.3
-
76
-
-
17344365922
-
Adenovirus-mediated herpes simplex virus thymidine kinase/ganciclovir gene therapy in patients with localized malignancy: Results of a phase I clinical trial in malignant mesothelioma
-
Sterman DH, Treat J, Litzky LA et al. Adenovirus-mediated herpes simplex virus thymidine kinase/ganciclovir gene therapy in patients with localized malignancy: results of a phase I clinical trial in malignant mesothelioma. Hum Gene Ther 1998: 9: 1083-1092.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 1083-1092
-
-
Sterman, D.H.1
Treat, J.2
Litzky, L.A.3
-
77
-
-
0033135221
-
In situ gene therapy for adenocarcinoma of the prostate: A phase I clinical trial
-
Herman JR, Adler HL, Aguilar-Cordova E et al. In situ gene therapy for adenocarcinoma of the prostate: a phase I clinical trial. Hum Gene Ther 1999: 10: 1239-1249.
-
(1999)
Hum Gene Ther
, vol.10
, pp. 1239-1249
-
-
Herman, J.R.1
Adler, H.L.2
Aguilar-Cordova, E.3
-
78
-
-
17344366044
-
Impact of preexisting and induced humoral and cellular immune responses in an adenovirus-based gene therapy phase I clinical trial for localized mesothelioma
-
Molnar-Kimber KL, Sterman DH, Chang M et al. Impact of preexisting and induced humoral and cellular immune responses in an adenovirus-based gene therapy phase I clinical trial for localized mesothelioma. Hum Gene Ther 1998: 9: 2121-2133.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 2121-2133
-
-
Molnar-Kimber, K.L.1
Sterman, D.H.2
Chang, M.3
-
79
-
-
0027377523
-
Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis
-
Zabner J, Couture LA, Gregory RJ, Graham SM, Smith AE, Welsh MJ. Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis. Cell 1993: 75: 207-216.
-
(1993)
Cell
, vol.75
, pp. 207-216
-
-
Zabner, J.1
Couture, L.A.2
Gregory, R.J.3
Graham, S.M.4
Smith, A.E.5
Welsh, M.J.6
-
80
-
-
16944367323
-
Aerosol administration of a recombinant adenovirus expressing CFTR to cystic fibrosis patients: A phase I clinical trial
-
Bellon G, Michel-Calemard L, Thouvenot D et al. Aerosol administration of a recombinant adenovirus expressing CFTR to cystic fibrosis patients: a phase I clinical trial. Hum Gene Ther 1997: 8: 15-25.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 15-25
-
-
Bellon, G.1
Michel-Calemard, L.2
Thouvenot, D.3
-
81
-
-
0028168641
-
Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis
-
Crystal RG, McElvaney NG, Rosenfeld MA et al. Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis. Nat Genet 1994: 8: 42-51.
-
(1994)
Nat Genet
, vol.8
, pp. 42-51
-
-
Crystal, R.G.1
McElvaney, N.G.2
Rosenfeld, M.A.3
-
82
-
-
0028113998
-
Gene therapy for cystic fibrosis using E1-deleted adenovirus: A phase I trial in the nasal cavity. The University of North Carolina at Chapel Hill
-
Boucher RC, Knowles MR, Johnson LG et al. Gene therapy for cystic fibrosis using E1-deleted adenovirus: a phase I trial in the nasal cavity. The University of North Carolina at Chapel Hill. Hum Gene Ther 1994: 5: 615-639.
-
(1994)
Hum Gene Ther
, vol.5
, pp. 615-639
-
-
Boucher, R.C.1
Knowles, M.R.2
Johnson, L.G.3
-
83
-
-
0033520056
-
Angiogenesis gene therapy: Phase I assessment of direct intramyocardial administration of an adenovirus vector expressing VEGFI21 cDNA to individuals with clinically significant severe coronary artery disease
-
Rosengart TK, Lee LY, Patel SR et al. Angiogenesis gene therapy: phase I assessment of direct intramyocardial administration of an adenovirus vector expressing VEGFI21 cDNA to individuals with clinically significant severe coronary artery disease. Circulation 1999: 100: 468-474.
-
(1999)
Circulation
, vol.100
, pp. 468-474
-
-
Rosengart, T.K.1
Lee, L.Y.2
Patel, S.R.3
-
84
-
-
0033579358
-
Gene therapy death prompts review of adenovirus vector
-
Marshall E. Gene therapy death prompts review of adenovirus vector. Science 1999: 286: 2244-2245.
-
(1999)
Science
, vol.286
, pp. 2244-2245
-
-
Marshall, E.1
|