-
1
-
-
0028169809
-
Neural-targeted gene therapy for rodent and primate herniparkinsonism
-
Anton R, Kordower JH, Maidment NT, et al. Neural-targeted gene therapy for rodent and primate herniparkinsonism. Exp Neurol 1994; 127: 207-218.
-
(1994)
Exp Neurol
, vol.127
, pp. 207-218
-
-
Anton, R.1
Kordower, J.H.2
Maidment, N.T.3
-
2
-
-
0029093070
-
Upregulation of class I major histocompatibility complex antigens by interferon gamma is necessary for T-cell-mediated elimination of recombinant adenovirus-infected hepatocytes in vivo
-
Yang Y, Xiang Z, Ertl HC, et al. Upregulation of class I major histocompatibility complex antigens by interferon gamma is necessary for T-cell-mediated elimination of recombinant adenovirus-infected hepatocytes in vivo. Proc Natl Acad Sci U S A 1995; 92: 7257-7261.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 7257-7261
-
-
Yang, Y.1
Xiang, Z.2
Ertl, H.C.3
-
3
-
-
0028937785
-
Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses
-
Yang Y, Li Q, Ertl HC, et al. Cellular and humoral immune responses to viral antigens create barriers to lung-directed gene therapy with recombinant adenoviruses. J Virol 1995; 69: 2004-2015.
-
(1995)
J Virol
, vol.69
, pp. 2004-2015
-
-
Yang, Y.1
Li, Q.2
Ertl, H.C.3
-
4
-
-
0028246338
-
Ablation of E2A in recombinant adenoviruses improves transgene
-
Engelhardt JF, Ye X, Doranz B, et al. Ablation of E2A in recombinant adenoviruses improves transgene. Proc Natl Acad Sci U S A 1994; 91: 6196-6200.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 6196-6200
-
-
Engelhardt, J.F.1
Ye, X.2
Doranz, B.3
-
5
-
-
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, Schwarz EM, Gu D, 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 U S A 1995; 92: 1401-1415.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 1401-1415
-
-
Dai, Y.1
Schwarz, E.M.2
Gu, D.3
-
6
-
-
0028032357
-
Stable delivery of physiologic levels of recombinant erythropoietin to the systemic circulation by intramuscular injection of replication-defective adenovirus
-
Tripathy SK, Goldwasser E, Lu M-M, et al. Stable delivery of physiologic levels of recombinant erythropoietin to the systemic circulation by intramuscular injection of replication-defective adenovirus. Proc Natl Acad Sci U S A 1994; 91: 11557-11561.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 11557-11561
-
-
Tripathy, S.K.1
Goldwasser, E.2
Lu, M.-M.3
-
7
-
-
0029936764
-
Immune responses to transgene-encoded proteins limit the stability of gene expression after injection of replication-defective adenovirus vectors
-
Tripathy SK, Black HB, Goldwasser E, et al. 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.K.1
Black, H.B.2
Goldwasser, E.3
-
8
-
-
0030910842
-
Adenovirus vector-infected cells can escape adenovirus antigen-specific cytotoxic T-lymphocyte killing in vivo
-
Wadsworth SC, Zhou H, Smith AE, et al. Adenovirus vector-infected cells can escape adenovirus antigen-specific cytotoxic T-lymphocyte killing in vivo. J Virol 1997; 71: 5189-5196.
-
(1997)
J Virol
, vol.71
, pp. 5189-5196
-
-
Wadsworth, S.C.1
Zhou, H.2
Smith, A.E.3
-
9
-
-
0030669598
-
Long-term erythropoietin expression in rodents and non-human primates following intramuscular injection of a replication-defective adenoviral vector
-
Svensson EC, Black HB, Dogger DL, et al. Long-term erythropoietin expression in rodents and non-human primates following intramuscular injection of a replication-defective adenoviral vector. Hum Gene Ther 1997; 8: 1797-1806.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 1797-1806
-
-
Svensson, E.C.1
Black, H.B.2
Dogger, D.L.3
-
10
-
-
0029834562
-
Evaluation of promoter strength for hepatic gene expression in vivo following adenovirus-mediated gene transfer
-
Guo ZS, Wang LH, Eisensmith RC, et al. Evaluation of promoter strength for hepatic gene expression in vivo following adenovirus-mediated gene transfer. Gene Ther 1996; 3: 802-810.
-
(1996)
Gene Ther
, vol.3
, pp. 802-810
-
-
Guo, Z.S.1
Wang, L.H.2
Eisensmith, R.C.3
-
11
-
-
0029898279
-
Adenovirus-mediated generation of cAMP-stimulated Cl- transport in cystic fibrosis airway epithelia in vitro: Effect of promoter and administration method
-
Zabner J, Wadsworth SC, Smith AE, et al. Adenovirus-mediated generation of cAMP-stimulated Cl- transport in cystic fibrosis airway epithelia in vitro: effect of promoter and administration method. Gene Ther 1996; 3: 458-465.
-
(1996)
Gene Ther
, vol.3
, pp. 458-465
-
-
Zabner, J.1
Wadsworth, S.C.2
Smith, A.E.3
-
12
-
-
0026486612
-
Gene therapy via primary myoblasts: Long-term expression of factor IX protein following transplantation in vivo
-
Dai Y, Roman M, Naviaux RK, et al. Gene therapy via primary myoblasts: long-term expression of factor IX protein following transplantation in vivo. Proc Natl Acad Sci U S A 1992; 89: 10892-10895.
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 10892-10895
-
-
Dai, Y.1
Roman, M.2
Naviaux, R.K.3
-
13
-
-
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
-
14
-
-
0030880893
-
Expression of gp19K increases the persistence of transgene expression from an adenovirus vector in the mouse lung and liver
-
Bruder JT, Jie T, McVey DL, et al. Expression of gp19K increases the persistence of transgene expression from an adenovirus vector in the mouse lung and liver. J Virol 1997; 71: 7623-7628.
-
(1997)
J Virol
, vol.71
, pp. 7623-7628
-
-
Bruder, J.T.1
Jie, T.2
McVey, D.L.3
-
15
-
-
0033541522
-
-
Muruve DA ' Barnes MJ, Stillman IE, et al. Adenoviral gene therapy leads to rapid induction of multiple chemokines and acute neutrophil-dependent hepatic injury in vivo. Hum Gene Ther 1999; 10: 965-976.
-
Muruve DA ' Barnes MJ, Stillman IE, et al. Adenoviral gene therapy leads to rapid induction of multiple chemokines and acute neutrophil-dependent hepatic injury in vivo. Hum Gene Ther 1999; 10: 965-976.
-
-
-
-
16
-
-
0037790710
-
Molecular basis of the inflammatory response to adenovirus vectors
-
Liu Q, Muruve DA. Molecular basis of the inflammatory response to adenovirus vectors. Gene Ther 2003; 10: 935-940.
-
(2003)
Gene Ther
, vol.10
, pp. 935-940
-
-
Liu, Q.1
Muruve, D.A.2
-
17
-
-
1942533432
-
Adenovirus-induced maturation of dendritic cells through a PI3 kinase-mediated TNF-alpha induction pathway
-
Philpott NJ, Nociari M, Elkon KB, et al. Adenovirus-induced maturation of dendritic cells through a PI3 kinase-mediated TNF-alpha induction pathway. Proc Natl Acad Sci U S A 2004; 101: 6200-6205.
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 6200-6205
-
-
Philpott, N.J.1
Nociari, M.2
Elkon, K.B.3
-
18
-
-
0033868530
-
Stimulatory and inhibitory action of cytokines on the regulation of hCMV-IE promoter activity in human endothelial cells
-
Ritter T, Brandt C, Prosch S, et al. Stimulatory and inhibitory action of cytokines on the regulation of hCMV-IE promoter activity in human endothelial cells. Cytokine 2000; 12: 1163-1170.
-
(2000)
Cytokine
, vol.12
, pp. 1163-1170
-
-
Ritter, T.1
Brandt, C.2
Prosch, S.3
-
19
-
-
0031581174
-
Promoter attenuation in gene therapy: Interferon-gamma and tumor necrosis factor-alpha inhibit transgene expression
-
Qin L, Ding Y, Pahud DR, et al. Promoter attenuation in gene therapy: interferon-gamma and tumor necrosis factor-alpha inhibit transgene expression. Hum Gene Ther 1997; 8: 2019-2029.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 2019-2029
-
-
Qin, L.1
Ding, Y.2
Pahud, D.R.3
-
20
-
-
0017710978
-
Characteristics of a human cell line transformed by DNA from human adenovirus type 5
-
Graham FL, Smiley J, Russell WC, et al. Characteristics of a human cell line transformed by DNA from human adenovirus type 5. J Gen Virol 1977; 36: 59-77.
-
(1977)
J Gen Virol
, vol.36
, pp. 59-77
-
-
Graham, F.L.1
Smiley, J.2
Russell, W.C.3
-
21
-
-
0018592110
-
Physical mapping of a large-plaque mutation of adenovirus type 2
-
Chinnadurai G, Chinnadurai S, Brusca J. Physical mapping of a large-plaque mutation of adenovirus type 2. J Virol 1979; 32: 623-628.
-
(1979)
J Virol
, vol.32
, pp. 623-628
-
-
Chinnadurai, G.1
Chinnadurai, S.2
Brusca, J.3
-
22
-
-
0028915634
-
The route of administration is a major determinant of the transduction efficiency of rat tissues by adenoviral recombinants
-
Huard J, Lochmuller H, Acsadi G, et al. The route of administration is a major determinant of the transduction efficiency of rat tissues by adenoviral recombinants. Gene Ther 1995; 2: 107-115.
-
(1995)
Gene Ther
, vol.2
, pp. 107-115
-
-
Huard, J.1
Lochmuller, H.2
Acsadi, G.3
-
23
-
-
0028484704
-
MHC class I-restricted cytotoxic T lymphocytes to viral antigens destroy hepatocytes in mice infected with E1-deleted recombinant adenoviruses
-
Yang Y, Ertl HC, Wilson JM. MHC class I-restricted cytotoxic T lymphocytes to viral antigens destroy hepatocytes in mice infected with E1-deleted recombinant adenoviruses. Immunity 1994; 1: 433-442.
-
(1994)
Immunity
, vol.1
, pp. 433-442
-
-
Yang, Y.1
Ertl, H.C.2
Wilson, J.M.3
-
24
-
-
0029028989
-
Clearance of adenovirus-infected hepatocytes by MHC class I-restricted CD4+ CTLs in vivo
-
Yang Y, Wilson JM. Clearance of adenovirus-infected hepatocytes by MHC class I-restricted CD4+ CTLs in vivo. J Immunol 1995; 155: 2564-2570.
-
(1995)
J Immunol
, vol.155
, pp. 2564-2570
-
-
Yang, Y.1
Wilson, J.M.2
-
25
-
-
9244220682
-
Immune responses to viral antigens versus transgene product in the elimination of recombinant adenovirus-infected hepatocytes in vivo
-
Yang Y, Jooss KU, Su Q, et al. Immune responses to viral antigens versus transgene product in the elimination of recombinant adenovirus-infected hepatocytes in vivo. Gene Ther 1996; 3: 137-144.
-
(1996)
Gene Ther
, vol.3
, pp. 137-144
-
-
Yang, Y.1
Jooss, K.U.2
Su, Q.3
-
26
-
-
0034022384
-
Effective repeat administration with adenovirus vectors to the muscle
-
Chen P, Kovesdi I, Bruder JT. Effective repeat administration with adenovirus vectors to the muscle. Gene Ther 2000; 7: 587-595.
-
(2000)
Gene Ther
, vol.7
, pp. 587-595
-
-
Chen, P.1
Kovesdi, I.2
Bruder, J.T.3
-
27
-
-
1842477415
-
Increased revascularization efficacy after administration of an adenovirus encoding VEGF(121)
-
Perrin LA, June JE, Rosebury W, et al. Increased revascularization efficacy after administration of an adenovirus encoding VEGF(121). Gene Ther 2004; 11: 512-521.
-
(2004)
Gene Ther
, vol.11
, pp. 512-521
-
-
Perrin, L.A.1
June, J.E.2
Rosebury, W.3
-
28
-
-
0028328261
-
Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy
-
Yang Y, Nunes FA, Berencsi K, et al. Cellular immunity to viral antigens limits E1-deleted adenoviruses for gene therapy. Proc Natl Acad Sci U S A 1994; 91: 4407-4411.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 4407-4411
-
-
Yang, Y.1
Nunes, F.A.2
Berencsi, K.3
-
29
-
-
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
-
30
-
-
0033982331
-
Sustained expression of human apolipoprotein A-I after adenoviral gene transfer in C57BL/6 mice: Role of apolipoprotein A-I promoter, apolipoprotein A-I introns, and human apolipoprotein E enhancer
-
De Geest B, Van Linthout S, Lox M, et al. Sustained expression of human apolipoprotein A-I after adenoviral gene transfer in C57BL/6 mice: role of apolipoprotein A-I promoter, apolipoprotein A-I introns, and human apolipoprotein E enhancer. Hum Gene Ther 2000; 11: 101-112.
-
(2000)
Hum Gene Ther
, vol.11
, pp. 101-112
-
-
De Geest, B.1
Van Linthout, S.2
Lox, M.3
-
31
-
-
0034218590
-
Analysis of muscle creatine kinase regulatory elements in recombinant adenoviral vectors
-
Hauser MA, Robinson A, Hartigan-O'Connor D, et al. Analysis of muscle creatine kinase regulatory elements in recombinant adenoviral vectors. Mol Ther 2000; 2: 16-25.
-
(2000)
Mol Ther
, vol.2
, pp. 16-25
-
-
Hauser, M.A.1
Robinson, A.2
Hartigan-O'Connor, D.3
-
32
-
-
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, et al. 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
-
33
-
-
0033540620
-
DNA from both high-capacity and first-generation adenoviral vectors remains intact in skeletal muscle
-
Chen HH, Mack LM, Choi SY, 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.H.1
Mack, L.M.2
Choi, S.Y.3
-
34
-
-
0029079981
-
A retroviral vector containing a muscle-specific enhancer drives gene expression only in differentiated muscle fibers
-
Ferrari G, Salvatori G, Rossi C, et al. A retroviral vector containing a muscle-specific enhancer drives gene expression only in differentiated muscle fibers. Hum Gene Ther 1995; 6: 733-742.
-
(1995)
Hum Gene Ther
, vol.6
, pp. 733-742
-
-
Ferrari, G.1
Salvatori, G.2
Rossi, C.3
-
35
-
-
0034991473
-
TNFalpha and IFNgamma induced by innate anti-adenoviral immune responses inhibit adenovirus-mediated transgene expression
-
Sung RS, Qin L, Bromberg JS. TNFalpha and IFNgamma induced by innate anti-adenoviral immune responses inhibit adenovirus-mediated transgene expression. Mol Ther 2001; 3: 757-767.
-
(2001)
Mol Ther
, vol.3
, pp. 757-767
-
-
Sung, R.S.1
Qin, L.2
Bromberg, J.S.3
-
36
-
-
8244264752
-
Efficient muscle-specific transgene expression after adenovirus-mediated gene transfer in mice using a 1.35 kb muscle creatine kinase promoter/ enhancer
-
Larochelle N, Lochmuller H, Zhao J, et al. Efficient muscle-specific transgene expression after adenovirus-mediated gene transfer in mice using a 1.35 kb muscle creatine kinase promoter/ enhancer. Gene Ther 1997; 4: 465-472.
-
(1997)
Gene Ther
, vol.4
, pp. 465-472
-
-
Larochelle, N.1
Lochmuller, H.2
Zhao, J.3
-
37
-
-
0024320433
-
Muscle creatine kinase sequence elements regulating skeletal and cardiac muscle expression in transgenic mice
-
Johnson JE, Wold BJ, Hauschka SD. Muscle creatine kinase sequence elements regulating skeletal and cardiac muscle expression in transgenic mice. Mol Cell Biol 1989; 9: 3393-3399.
-
(1989)
Mol Cell Biol
, vol.9
, pp. 3393-3399
-
-
Johnson, J.E.1
Wold, B.J.2
Hauschka, S.D.3
-
38
-
-
0032077904
-
Implications of maturation for viral gene delivery to skeletal muscle
-
van Deutekom JCT, Floyd SS, Booth DK, et al. Implications of maturation for viral gene delivery to skeletal muscle. Neuromuscul Disord 1998; 8: 135-148.
-
(1998)
Neuromuscul Disord
, vol.8
, pp. 135-148
-
-
van Deutekom, J.C.T.1
Floyd, S.S.2
Booth, D.K.3
|