-
1
-
-
0003024233
-
The adenoviruses
-
Ginsberg HS, ed. New York: Plenum Press
-
1 Strauss SE. The adenoviruses. Ginsberg HS, ed. The adenoviruses. New York: Plenum Press, 1984:451-96.
-
(1984)
The Adenoviruses
, pp. 451-496
-
-
Strauss, S.E.1
-
2
-
-
0026558496
-
In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium
-
2 Rosenfeld MA, Yoshimura K, Trapnell BC, et al. In vivo transfer of the human cystic fibrosis transmembrane conductance regulator gene to the airway epithelium. Cell 1992;68:143-55.
-
(1992)
Cell
, vol.68
, pp. 143-155
-
-
Rosenfeld, M.A.1
Yoshimura, K.2
Trapnell, B.C.3
-
3
-
-
0027377523
-
Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis
-
3 Zabner J, Couture LA, Gregory RJ, et al. Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis. Cell 1993;75:207-16.
-
(1993)
Cell
, vol.75
, pp. 207-216
-
-
Zabner, J.1
Couture, L.A.2
Gregory, R.J.3
-
4
-
-
0028168641
-
Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis
-
4 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
-
5
-
-
0025487393
-
Evaluation of the transfer and expression in mice of an enzyme-encoding gene using a human adenovirus vector
-
5 Stratford-Perricaudet LD, Levrero M, Chasse JF, et al. Evaluation of the transfer and expression in mice of an enzyme-encoding gene using a human adenovirus vector. Hum Gene Ther 1990;1:241-56.
-
(1990)
Hum Gene Ther
, vol.1
, pp. 241-256
-
-
Stratford-Perricaudet, L.D.1
Levrero, M.2
Chasse, J.F.3
-
6
-
-
0026906987
-
Adenovirus-mediated in vivo gene transfer and expression in normal rat liver
-
6 Jaffe H, Danel C, Longenecker G, et al. Adenovirus-mediated in vivo gene transfer and expression in normal rat liver. Nat Genet 1992;1:372-8.
-
(1992)
Nat Genet
, vol.1
, pp. 372-378
-
-
Jaffe, H.1
Danel, C.2
Longenecker, G.3
-
7
-
-
0028274169
-
In vivo hepatic gene therapy: Complete albeit transient correction of factor IX deficiency in hemophilia B dogs
-
7 Kay MA, Landen CN, Rothenberg SR, et al. In vivo hepatic gene therapy: complete albeit transient correction of factor IX deficiency in hemophilia B dogs. Proc Natl Acad Sci USA 1994;91:2353-7.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 2353-2357
-
-
Kay, M.A.1
Landen, C.N.2
Rothenberg, S.R.3
-
8
-
-
0027258140
-
Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery
-
8 Ishibashi S, Brown MS, Goldstein JL, et al. Hypercholesterolemia in low density lipoprotein receptor knockout mice and its reversal by adenovirus-mediated gene delivery. J Clin Invest 1993;92:883-93.
-
(1993)
J Clin Invest
, vol.92
, pp. 883-893
-
-
Ishibashi, S.1
Brown, M.S.2
Goldstein, J.L.3
-
9
-
-
0028234357
-
In vivo correction of low density lipoprotein receptor deficiency in the Watanabe Heritable hyperlipidemic rabbit with recombinant adenoviruses
-
9 Kozarsky KF, McKinley DR, Austin LL, et al. In vivo correction of low density lipoprotein receptor deficiency in the Watanabe Heritable hyperlipidemic rabbit with recombinant adenoviruses. J Biol Chem 1994;269:13695-702.
-
(1994)
J Biol Chem
, vol.269
, pp. 13695-13702
-
-
Kozarsky, K.F.1
McKinley, D.R.2
Austin, L.L.3
-
10
-
-
0023339694
-
An albumin enhancer located 10 kb upstream functions along with its promoter to direct efficient, liver-specific expression in transgenic mice
-
10 Pinkert CA, Ornitz DM, Brinster RL, et al. An albumin enhancer located 10 kb upstream functions along with its promoter to direct efficient, liver-specific expression in transgenic mice. Gene Dev 1987;1:268-76.
-
(1987)
Gene Dev
, vol.1
, pp. 268-276
-
-
Pinkert, C.A.1
Ornitz, D.M.2
Brinster, R.L.3
-
11
-
-
0026336989
-
A potential approach for gene therapy targeting hepatoma using a liver-specific promoter on a retroviral vector
-
11 Kuriyama S, Yoshikawa M, Ishizaka S, et al. A potential approach for gene therapy targeting hepatoma using a liver-specific promoter on a retroviral vector. Cell Struct Funct 1991;16:503-10.
-
(1991)
Cell Struct Funct
, vol.16
, pp. 503-510
-
-
Kuriyama, S.1
Yoshikawa, M.2
Ishizaka, S.3
-
12
-
-
0028875936
-
Transfer of genes to humans: Early lessons and obstacles to success
-
12 Crystal RG. Transfer of genes to humans: early lessons and obstacles to success. Science 1995;270:404-10.
-
(1995)
Science
, vol.270
, pp. 404-410
-
-
Crystal, R.G.1
-
13
-
-
0030855887
-
Liver-directed gene transfer in non-human primates
-
13 Sullivan DE, Dash S, Du H, et al. Liver-directed gene transfer in non-human primates. Hum Gene Ther 1997;8:1195-206.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 1195-1206
-
-
Sullivan, D.E.1
Dash, S.2
Du, H.3
-
14
-
-
0027968048
-
Adoptive immunotherapy with murine tumor-specific T lymphocytes engineered to secrete interleukin 2
-
14 Nakamura Y, Wakimoto H, Abe J, et al. Adoptive immunotherapy with murine tumor-specific T lymphocytes engineered to secrete interleukin 2. Cancer Res 1994;54:5757-60.
-
(1994)
Cancer Res
, vol.54
, pp. 5757-5760
-
-
Nakamura, Y.1
Wakimoto, H.2
Abe, J.3
-
15
-
-
0025884056
-
Efficient selection for high-expression transfectants with a novel eukaryotic vector
-
15 Niwa H, Yamamura K, Miyazaki J, et al. Efficient selection for high-expression transfectants with a novel eukaryotic vector. Gene 1991;108:193-200.
-
(1991)
Gene
, vol.108
, pp. 193-200
-
-
Niwa, H.1
Yamamura, K.2
Miyazaki, J.3
-
16
-
-
0030070724
-
Efficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome
-
16 Miyake S, Makimura M, Kanegae Y, et al. Efficient generation of recombinant adenoviruses using adenovirus DNA-terminal protein complex and a cosmid bearing the full-length virus genome. Proc Natl Acad Sci USA 1996;93: 1320-4.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 1320-1324
-
-
Miyake, S.1
Makimura, M.2
Kanegae, Y.3
-
17
-
-
0002025785
-
Manipulation of adenovirus vectors
-
Murray EJ, ed. Clifton: Humana Press
-
17 Graham FL, Prevec L. Manipulation of adenovirus vectors. In: Murray EJ, ed. Methods in molecular biology. Clifton: Humana Press, 1991:109-28.
-
(1991)
Methods in Molecular Biology
, pp. 109-128
-
-
Graham, F.L.1
Prevec, L.2
-
18
-
-
0016180377
-
Galactosamine hepatitis: Key role of the nucleotide deficiency period in the pathogenesis of cell injury and cell death
-
18 Decker K, Keppler D. Galactosamine hepatitis: key role of the nucleotide deficiency period in the pathogenesis of cell injury and cell death. Rev Physiol Biochem Pharmacol 1974; 71:77-105.
-
(1974)
Rev Physiol Biochem Pharmacol
, vol.71
, pp. 77-105
-
-
Decker, K.1
Keppler, D.2
-
19
-
-
0000352873
-
Galactosamine-induced sensitization to the lethal effects of endotoxin
-
19 Galanos C, Freudenberg MA, Rertter W. Galactosamine-induced sensitization to the lethal effects of endotoxin. Proc Natl Acad Sci USA 1979;76:5939-43.
-
(1979)
Proc Natl Acad Sci USA
, vol.76
, pp. 5939-5943
-
-
Galanos, C.1
Freudenberg, M.A.2
Rertter, W.3
-
20
-
-
0022004113
-
D-Galactosamine hepatotoxicity is associated with endotoxin sensitivity and mediated by lymphoreticular cells in mice
-
20 Chojkier M, Fierer J. D-Galactosamine hepatotoxicity is associated with endotoxin sensitivity and mediated by lymphoreticular cells in mice. Gastroenterology 1985;88:115-21.
-
(1985)
Gastroenterology
, vol.88
, pp. 115-121
-
-
Chojkier, M.1
Fierer, J.2
-
21
-
-
0030749713
-
Transient immunosuppression with deoxyspergualin improves longevity of transgene expression and ability to readminister adenoviral vector to the mouse lung
-
21 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;8:1095-104.
-
(1997)
Hum Gene Ther
, vol.8
, pp. 1095-1104
-
-
Kaplan, J.M.1
Smith, A.E.2
-
22
-
-
0034056004
-
Immunomodulation with FK506 around the time of intravenous readministration of an adenoviral vector facilitates gene transfer into primed rat liver
-
22 Kuriyama S, Tominaga K, Mitoro A, et al. Immunomodulation with FK506 around the time of intravenous readministration of an adenoviral vector facilitates gene transfer into primed rat liver. Int J Cancer 2000;85:839-44.
-
(2000)
Int J Cancer
, vol.85
, pp. 839-844
-
-
Kuriyama, S.1
Tominaga, K.2
Mitoro, A.3
-
23
-
-
0029944988
-
Transient immune blockade prevents formation of neutralizing antibody to recombinant adenovirus and allows repeated gene transfer to mouse liver
-
23 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;3:412-20.
-
(1996)
Gene Ther
, vol.3
, pp. 412-420
-
-
Yang, Y.1
Greenough, K.2
Wilson, J.M.3
-
24
-
-
15144349956
-
Inhibitory effects of human sera on adenovirus-mediated gene transfer into rat liver
-
24 Kuriyama S, Tominaga K, Kikukawa M, et al. Inhibitory effects of human sera on adenovirus-mediated gene transfer into rat liver. Anticancer Res 1998;18:2345-52.
-
(1998)
Anticancer Res
, vol.18
, pp. 2345-2352
-
-
Kuriyama, S.1
Tominaga, K.2
Kikukawa, M.3
-
25
-
-
6544263753
-
Transient cyclophosphamide treatment before intraportal readministration of an adenoviral vector can induce re-expression of the original gene construct in rat liver
-
25 Kuriyama S, Tominaga K, Kikukawa M, et al. Transient cyclophosphamide treatment before intraportal readministration of an adenoviral vector can induce re-expression of the original gene construct in rat liver. Gene Ther 1999;6:749-57.
-
(1999)
Gene Ther
, vol.6
, pp. 749-757
-
-
Kuriyama, S.1
Tominaga, K.2
Kikukawa, M.3
-
26
-
-
0027760829
-
Gene therapy for the treatment of hepatoma by retroviral-mediated gene transfer of the herpes simplex virus thymidine kinase
-
26 Kuriyama S, Yoshikawa M, Tominaga K, et al. Gene therapy for the treatment of hepatoma by retroviral-mediated gene transfer of the herpes simplex virus thymidine kinase. Int Hepatol Commun 1993;1:253-9.
-
(1993)
Int Hepatol Commun
, vol.1
, pp. 253-259
-
-
Kuriyama, S.1
Yoshikawa, M.2
Tominaga, K.3
-
27
-
-
0028823770
-
Bystander effect caused by suicide gene expression indicates the feasibility of gene therapy for hepatocellular carcinoma
-
27 Kuriyama S, Nakatani T, Masui K, et al. Bystander effect caused by suicide gene expression indicates the feasibility of gene therapy for hepatocellular carcinoma. Hepatology 1995;22:1838-46.
-
(1995)
Hepatology
, vol.22
, pp. 1838-1846
-
-
Kuriyama, S.1
Nakatani, T.2
Masui, K.3
-
28
-
-
0029908175
-
Evaluation of pro-drugs ability to induce effective ablation of cells transduced with viral thymidine kinase gene
-
28 Kuriyama S, Nakatani T, Masui K, et al. Evaluation of pro-drugs ability to induce effective ablation of cells transduced with viral thymidine kinase gene. Anticancer Res 1996;16: 2623-8.
-
(1996)
Anticancer Res
, vol.16
, pp. 2623-2628
-
-
Kuriyama, S.1
Nakatani, T.2
Masui, K.3
-
29
-
-
17344382938
-
Tissue-specific expression of HSV-tk gene can induce efficient antitumor effect and protective immunity to wild-type hepatocellular carcinoma
-
29 Kuriyama S, Sakamoto T, Masui K, et al. Tissue-specific expression of HSV-tk gene can induce efficient antitumor effect and protective immunity to wild-type hepatocellular carcinoma. Int J Cancer 1997;71:470-5.
-
(1997)
Int J Cancer
, vol.71
, pp. 470-475
-
-
Kuriyama, S.1
Sakamoto, T.2
Masui, K.3
-
30
-
-
0032937083
-
Complete cure of established murine hepatocellular carcinoma is achievable by repeated injections of retroviruses carrying the herpes simplex virus thymidine kinase gene
-
30 Kuriyama S, Masui K, Kikukawa M, et al. Complete cure of established murine hepatocellular carcinoma is achievable by repeated injections of retroviruses carrying the herpes simplex virus thymidine kinase gene. Gene Ther 1999;6: 525-33.
-
(1999)
Gene Ther
, vol.6
, pp. 525-533
-
-
Kuriyama, S.1
Masui, K.2
Kikukawa, M.3
-
31
-
-
0032930673
-
Cytosine deaminase/5-fluorocytosine gene therapy can induce efficient anti-tumor effects and protective immunity in immunocompetent mice but not in athymic nude mice
-
31 Kuriyama S, Kikukawa M, Masui K, et al. Cytosine deaminase/5-fluorocytosine gene therapy can induce efficient anti-tumor effects and protective immunity in immunocompetent mice but not in athymic nude mice. Int J Cancer 1999;81:592-7.
-
(1999)
Int J Cancer
, vol.81
, pp. 592-597
-
-
Kuriyama, S.1
Kikukawa, M.2
Masui, K.3
-
32
-
-
0032848688
-
Cancer gene therapy with HSV-tk/GCV system depends on T-cell-mediated immune responses and causes apoptotic death of tumor cells in vivo
-
32 Kuriyama S, Kikukawa M, Masui K, et al. Cancer gene therapy with HSV-tk/GCV system depends on T-cell-mediated immune responses and causes apoptotic death of tumor cells in vivo. Int J Cancer 1999;83:374-80.
-
(1999)
Int J Cancer
, vol.83
, pp. 374-380
-
-
Kuriyama, S.1
Kikukawa, M.2
Masui, K.3
-
33
-
-
0032717286
-
Comparison of gene therapy with the herpes simplex virus thymidine kinase gene and the bacterial cytosine deaminase gene for the treatment of hepatocellular carcinoma
-
33 Kuriyama S, Mitoro A, Yamazaki M, et al. Comparison of gene therapy with the herpes simplex virus thymidine kinase gene and the bacterial cytosine deaminase gene for the treatment of hepatocellular carcinoma. Scand J Gastroenterol 1999;34:1033-41.
-
(1999)
Scand J Gastroenterol
, vol.34
, pp. 1033-1041
-
-
Kuriyama, S.1
Mitoro, A.2
Yamazaki, M.3
-
34
-
-
0029957314
-
Construction of retroviral vectors to induce strong hepatoma cell-specific expression of cytokine genes
-
34 Cao G, Kuriyama S, Du P, et al. Construction of retroviral vectors to induce strong hepatoma cell-specific expression of cytokine genes. J Gastroenterol Hepatol 1996;11:1053-61.
-
(1996)
J Gastroenterol Hepatol
, vol.11
, pp. 1053-1061
-
-
Cao, G.1
Kuriyama, S.2
Du, P.3
-
35
-
-
0031052118
-
Complete regression of established murine hepatocellular carcinoma by in vivo tumor necrosis factor α gene transfer
-
35 Cao G, Kuriyama S, Du P, et al. Complete regression of established murine hepatocellular carcinoma by in vivo tumor necrosis factor α gene transfer. Gastroenterology 1997;112:501-10.
-
(1997)
Gastroenterology
, vol.112
, pp. 501-510
-
-
Cao, G.1
Kuriyama, S.2
Du, P.3
-
36
-
-
0034662319
-
A novel approach for inducing enhanced and selective transgene expression in hepatocellular carcinoma cells
-
36 Cao G, Kuriyama S, Tsujinoue H, et al. A novel approach for inducing enhanced and selective transgene expression in hepatocellular carcinoma cells. Int J Cancer 2000;87: 247-52.
-
(2000)
Int J Cancer
, vol.87
, pp. 247-252
-
-
Cao, G.1
Kuriyama, S.2
Tsujinoue, H.3
-
37
-
-
0031043426
-
In vivo gene therapy for α-fetoprotein-producing hepatocellular carcinoma by adenovirus-mediated transfer of cytosine deaminase gene
-
37 Kanai F, Lan KH, Shiratori Y, et al. In vivo gene therapy for α-fetoprotein-producing hepatocellular carcinoma by adenovirus-mediated transfer of cytosine deaminase gene. Cancer Res 1997;57:461-5.
-
(1997)
Cancer Res
, vol.57
, pp. 461-465
-
-
Kanai, F.1
Lan, K.H.2
Shiratori, Y.3
-
38
-
-
15844416306
-
Gene therapy for α-fetoprotein-producing human hepatoma cells by adenovirus-mediated transfer of the herpes simplex virus thymidine kinase gene
-
38 Kanai F, Shiratori Y, Yoshida Y, et al. Gene therapy for α-fetoprotein-producing human hepatoma cells by adenovirus-mediated transfer of the herpes simplex virus thymidine kinase gene. Hepatology 1996;23:1359-68.
-
(1996)
Hepatology
, vol.23
, pp. 1359-1368
-
-
Kanai, F.1
Shiratori, Y.2
Yoshida, Y.3
-
39
-
-
0028808656
-
Adenovirus-mediated gene therapy of hepatocellular carcinoma using cancer-specific gene expression
-
39 Kaneko S, Hallenbeck P, Kotani T, et al. Adenovirus-mediated gene therapy of hepatocellular carcinoma using cancer-specific gene expression. Cancer Res 1995;55:5283-7.
-
(1995)
Cancer Res
, vol.55
, pp. 5283-5287
-
-
Kaneko, S.1
Hallenbeck, P.2
Kotani, T.3
-
40
-
-
0027980863
-
Hepatocellular carcinoma in western Sydney: Aetiology, changes in incidence, and opportunities for better outcomes
-
40 Brotodihardjo AE, Tait N, Weltman MD, et al. Hepatocellular carcinoma in western Sydney: aetiology, changes in incidence, and opportunities for better outcomes. Med J Aust 1994;161:433-5.
-
(1994)
Med J Aust
, vol.161
, pp. 433-435
-
-
Brotodihardjo, A.E.1
Tait, N.2
Weltman, M.D.3
-
41
-
-
0031915983
-
Portal hemodynamics by duplex Doppler sonography in different grades of cirrhosis
-
41 Chawla Y, Santa N, Dhiman RK, et al. Portal hemodynamics by duplex Doppler sonography in different grades of cirrhosis. Dig Dis Sci 1998;43:354-7.
-
(1998)
Dig Dis Sci
, vol.43
, pp. 354-357
-
-
Chawla, Y.1
Santa, N.2
Dhiman, R.K.3
-
42
-
-
0007729835
-
Diagnosis of portal vein tumor thrombus by pulsed Doppler ultrasonography
-
42 Furuse J, Matsutani S, Yoshikawa M, et al. Diagnosis of portal vein tumor thrombus by pulsed Doppler ultrasonography. J Clin Ultrasound 1994;171:1097-104.
-
(1994)
J Clin Ultrasound
, vol.171
, pp. 1097-1104
-
-
Furuse, J.1
Matsutani, S.2
Yoshikawa, M.3
-
43
-
-
0030915005
-
Adenovirus-mediated gene transfer into human hepatocytes: Analysis of the biochemical functionality of transduced cells
-
43 Castell JV, Hernández D, Gómez-Foix AM, et al. Adenovirus-mediated gene transfer into human hepatocytes: analysis of the biochemical functionality of transduced cells. Gene Ther 1997;4:455-64.
-
(1997)
Gene Ther
, vol.4
, pp. 455-464
-
-
Castell, J.V.1
Hernández, D.2
Gómez-Foix, A.M.3
-
44
-
-
0032927656
-
Adenovirus-mediated gene expression in the septal cells of cirrhotic rat livers
-
44 Nakamura T, Akiyoshi H, Saito I, et al. Adenovirus-mediated gene expression in the septal cells of cirrhotic rat livers. J Hepatol 1999;30:101-6.
-
(1999)
J Hepatol
, vol.30
, pp. 101-106
-
-
Nakamura, T.1
Akiyoshi, H.2
Saito, I.3
-
45
-
-
0031975745
-
The murine CAR homolog is a receptor for coxsackie B viruses and adenoviruses
-
45 Bergelson JM, Krithivas A, Celi L, et al. The murine CAR homolog is a receptor for coxsackie B viruses and adenoviruses. J Virol 1998;72:415-19.
-
(1998)
J Virol
, vol.72
, pp. 415-419
-
-
Bergelson, J.M.1
Krithivas, A.2
Celi, L.3
-
46
-
-
0029584267
-
Differential short-term transduction efficiency of adult versus newborn mouse tissues by adenoviral recombinants
-
46 Huard J, Lochmuller H, Acsadi G, et al. Differential short-term transduction efficiency of adult versus newborn mouse tissues by adenoviral recombinants. Exp Mol Pathol 1995;62:131-43.
-
(1995)
Exp Mol Pathol
, vol.62
, pp. 131-143
-
-
Huard, J.1
Lochmuller, H.2
Acsadi, G.3
-
47
-
-
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
-
47 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 USA 1995;92: 1401-5.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 1401-1405
-
-
Dai, Y.1
Schwarz, E.M.2
Gu, D.3
-
48
-
-
0033541522
-
Adenoviral gene therapy leads to rapid induction of multiple chemokines and acute neutrophil-dependent hepatic injury in vivo
-
48 Muruve DA, Barnes MJ, Stillman IF, et al. Adenoviral gene therapy leads to rapid induction of multiple chemokines and acute neutrophil-dependent hepatic injury in vivo. Hum Gene Ther 1999;10:965-76. Gut 2000;47:571-574
-
(1999)
Hum Gene Ther
, vol.10
, pp. 965-976
-
-
Muruve, D.A.1
Barnes, M.J.2
Stillman, I.F.3
|