-
1
-
-
0029257496
-
The cryptic life style of adeno-associated virus
-
Berns KI, Linden RM. The cryptic life style of adeno-associated virus. Bioessays 1995; 17: 237-245.
-
(1995)
Bioessays
, vol.17
, pp. 237-245
-
-
Berns, K.I.1
Linden, R.M.2
-
2
-
-
0023731951
-
Adeno-associated virus: A vector system for efficient introduction and integration of DNA into a variety of mammalian cell types
-
Lebkowski JS, McNally MM, Okarma TB, Lerch LB. Adeno-associated virus: a vector system for efficient introduction and integration of DNA into a variety of mammalian cell types. Mol Cell Biol 1988; 8: 3988-3996.
-
(1988)
Mol Cell Biol
, vol.8
, pp. 3988-3996
-
-
Lebkowski, J.S.1
McNally, M.M.2
Okarma, T.B.3
Lerch, L.B.4
-
3
-
-
0028593971
-
Parvovirus-based vectors for human gene therapy
-
Srivastava A. Parvovirus-based vectors for human gene therapy. Blood Cells 1994; 20: 531-536.
-
(1994)
Blood Cells
, vol.20
, pp. 531-536
-
-
Srivastava, A.1
-
4
-
-
0021257303
-
Genetics of adeno-associated virus: Isolation and preliminary characterization of adeno-associated type 2 mutants
-
Hermonat PL et al. Genetics of adeno-associated virus: isolation and preliminary characterization of adeno-associated type 2 mutants. J Virol 1984; 51: 329-339.
-
(1984)
J Virol
, vol.51
, pp. 329-339
-
-
Hermonat, P.L.1
-
5
-
-
0021228018
-
Genetic analysis of adeno-associated virus: Properties of deletion mutants constructed in vitro and evidence for an adeno-associated virus replication function
-
Tratschin JD, Miller IL, Carter BJ. Genetic analysis of adeno-associated virus: properties of deletion mutants constructed in vitro and evidence for an adeno-associated virus replication function. J Virol 1984; 51: 611-619.
-
(1984)
J Virol
, vol.51
, pp. 611-619
-
-
Tratschin, J.D.1
Miller, I.L.2
Carter, B.J.3
-
6
-
-
0023216839
-
A recombinant plasmid from which an infectious adeno-associated virus genome can be excised in vitro and its use to study viral replication
-
Samulski RJ, Chang LS, Shenk T. A recombinant plasmid from which an infectious adeno-associated virus genome can be excised in vitro and its use to study viral replication. J Virol 1987; 61: 3096-3101.
-
(1987)
J Virol
, vol.61
, pp. 3096-3101
-
-
Samulski, R.J.1
Chang, L.S.2
Shenk, T.3
-
7
-
-
0024311525
-
Helper-free stocks of recombinant adeno-associated viruses, normal integration does not require viral gene expression
-
Samulski RJ, Chang LS, Shenk T. Helper-free stocks of recombinant adeno-associated viruses, normal integration does not require viral gene expression. J Virol 1989; 63: 3822-3828.
-
(1989)
J Virol
, vol.63
, pp. 3822-3828
-
-
Samulski, R.J.1
Chang, L.S.2
Shenk, T.3
-
8
-
-
0027992020
-
Recombinant adeno-associated virus-mediated gene transfer into hematopoietic progenitor cells
-
Goodman S et al. Recombinant adeno-associated virus-mediated gene transfer into hematopoietic progenitor cells. Blood 1994; 84: 1492-1500.
-
(1994)
Blood
, vol.84
, pp. 1492-1500
-
-
Goodman, S.1
-
9
-
-
0027985201
-
Recombinant adeno-associated virus (rAAV)-mediated expression of a human gamma-globin gene in human progenitor-derived erythroid cells
-
Miller JL et al. Recombinant adeno-associated virus (rAAV)-mediated expression of a human gamma-globin gene in human progenitor-derived erythroid cells. Proc Natl Acad Ssi USA 1994; 91: 10183-10187.
-
(1994)
Proc Natl Acad Ssi USA
, vol.91
, pp. 10183-10187
-
-
Miller, J.L.1
-
10
-
-
0028179244
-
Suppression of human alpha-globin gene expression mediated by the recombinant adeno-associated virus 2-based antisense vectors
-
Ponnazhagan S, Nallan M, Srivastava A. Suppression of human alpha-globin gene expression mediated by the recombinant adeno-associated virus 2-based antisense vectors. J Exp Med 1994; 179: 733-738.
-
(1994)
J Exp Med
, vol.179
, pp. 733-738
-
-
Ponnazhagan, S.1
Nallan, M.2
Srivastava, A.3
-
11
-
-
0040417435
-
Adeno-associated virus 2-mediated high efficiency gene transfer into immature and mature subsets of hematopoietic progenitor cells in human umbilical cord blood
-
Zhou SZ et al. Adeno-associated virus 2-mediated high efficiency gene transfer into immature and mature subsets of hematopoietic progenitor cells in human umbilical cord blood. J Exp Med 1994; 179: 1867-1875.
-
(1994)
J Exp Med
, vol.179
, pp. 1867-1875
-
-
Zhou, S.Z.1
-
12
-
-
0027055182
-
Dual-target inhibition of HTV-1 in vitro by means of an adeno-associated virus antisense vector
-
Chatterjee S, Johnson PR, Wong KKJr. Dual-target inhibition of HTV-1 in vitro by means of an adeno-associated virus antisense vector. Science 1992; 258: 1485-1488.
-
(1992)
Science
, vol.258
, pp. 1485-1488
-
-
Chatterjee, S.1
Johnson, P.R.2
Wong Jr., K.K.3
-
13
-
-
0026687233
-
- channels by protein kinase A corrected by insertion of CFTR
-
- channels by protein kinase A corrected by insertion of CFTR. Nature 1992; 358: 581-584.
-
(1992)
Nature
, vol.358
, pp. 581-584
-
-
Egan, M.1
-
14
-
-
0027484584
-
Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector
-
Flotte TR et al. Stable in vivo expression of the cystic fibrosis transmembrane conductance regulator with an adeno-associated virus vector. Proc Natl Acad Sci USA 1993; 90: 10613-10617
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 10613-10617
-
-
Flotte, T.R.1
-
15
-
-
0028169741
-
Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain
-
Kaplitt MG et al. Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brain. Nat Genet 1994; 8: 148-154.
-
(1994)
Nat Genet
, vol.8
, pp. 148-154
-
-
Kaplitt, M.G.1
-
16
-
-
0026772206
-
In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors
-
Culver KW et al. In vivo gene transfer with retroviral vector-producer cells for treatment of experimental brain tumors. Science 1992; 256: 1550-1552.
-
(1992)
Science
, vol.256
, pp. 1550-1552
-
-
Culver, K.W.1
-
17
-
-
0028038843
-
Gene therapy for the treatment of malignant brain tumors with in vivo tumor transduction with the herpes simplex thymidine kinase gene/ganciclovir system
-
Culver KW et al. Gene therapy for the treatment of malignant brain tumors with in vivo tumor transduction with the herpes simplex thymidine kinase gene/ganciclovir system. Hum Gene Ther 1994; 5: 343-379.
-
(1994)
Hum Gene Ther
, vol.5
, pp. 343-379
-
-
Culver, K.W.1
-
18
-
-
0027548077
-
Gene therapy for the treatment of brain tumors using intra-tumoral transduction with the thymidine kinase gene and intravenous ganciclovir
-
Oldfield EH et al. Gene therapy for the treatment of brain tumors using intra-tumoral transduction with the thymidine kinase gene and intravenous ganciclovir. Hum Gene Ther 1993; 4: 39-69
-
(1993)
Hum Gene Ther
, vol.4
, pp. 39-69
-
-
Oldfield, E.H.1
-
19
-
-
0027531548
-
In situ retroviral-mediated gene transfer for the treatment of brain tumors in rats
-
Ram Z et al. In situ retroviral-mediated gene transfer for the treatment of brain tumors in rats. Cancer Res 1993; 53: 83-88.
-
(1993)
Cancer Res
, vol.53
, pp. 83-88
-
-
Ram, Z.1
-
20
-
-
0028202066
-
Gene therapy for brain tumors, regression of experimental gliomas by adenovirus-mediated gene transfer in vivo
-
Chen SH et al. Gene therapy for brain tumors, regression of experimental gliomas by adenovirus-mediated gene transfer in vivo. Proc Natl Acad Sci USA 1994; 91: 3054-3057.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 3054-3057
-
-
Chen, S.H.1
-
21
-
-
0027973509
-
Adenovirus-mediated gene therapy of experimental gliomas
-
Perez-Cruet MJ et al. Adenovirus-mediated gene therapy of experimental gliomas. J Neurosci Res 1994; 39: 506-511.
-
(1994)
J Neurosci Res
, vol.39
, pp. 506-511
-
-
Perez-Cruet, M.J.1
-
22
-
-
0028328261
-
Cellular immunity to viral antigens limits El-deleted adenoviruses for gene therapy
-
Yang Y et al. Cellular immunity to viral antigens limits El-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
-
23
-
-
0027424439
-
UK scientists test liposome gene therapy technique
-
Dickson D. UK scientists test liposome gene therapy technique. Nature 1993; 365: 4.
-
(1993)
Nature
, vol.365
, pp. 4
-
-
Dickson, D.1
-
24
-
-
0028001717
-
Bystander tumoricidal effect in the treatment of experimental brain tumors
-
Wu JK et al. Bystander tumoricidal effect in the treatment of experimental brain tumors. Neurosurgery 1994; 35: 1094-1102.
-
(1994)
Neurosurgery
, vol.35
, pp. 1094-1102
-
-
Wu, J.K.1
-
25
-
-
0027988463
-
Stereotactic delivery of a recombinant adenovirus into a C6 glioma cell line in a rat brain tumor model
-
Badie B, Hunt K, Economou JS, Black KL. Stereotactic delivery of a recombinant adenovirus into a C6 glioma cell line in a rat brain tumor model. Neurosurgery 1994; 35: 910-915.
-
(1994)
Neurosurgery
, vol.35
, pp. 910-915
-
-
Badie, B.1
Hunt, K.2
Economou, J.S.3
Black, K.L.4
-
26
-
-
0028071271
-
The effect of thymidine kinase transduction and ganciclovir therapy on tumor vasculature and growth of 9L gliomas in rats
-
Ram Z et al. The effect of thymidine kinase transduction and ganciclovir therapy on tumor vasculature and growth of 9L gliomas in rats. J Neurosurg 1994; 81: 256-260.
-
(1994)
J Neurosurg
, vol.81
, pp. 256-260
-
-
Ram, Z.1
-
27
-
-
0028323573
-
Development of antitumor immunity following thymidine kinase-mediated killing of experimental brain tumors
-
Barba D, Hardin J, Sadelain M, Gage FH. Development of antitumor immunity following thymidine kinase-mediated killing of experimental brain tumors. Proc Natl Acad Sci USA 1994; 91: 4348-4352.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 4348-4352
-
-
Barba, D.1
Hardin, J.2
Sadelain, M.3
Gage, F.H.4
-
28
-
-
0028218528
-
In vivo transfer of the human interleukin-2 gene: Negative tumoricidal results in experimental brain tumors
-
Ram Z et al. In vivo transfer of the human interleukin-2 gene: negative tumoricidal results in experimental brain tumors. J Neurosurg 1994; 80: 535-540.
-
(1994)
J Neurosurg
, vol.80
, pp. 535-540
-
-
Ram, Z.1
-
29
-
-
0025279872
-
Gene transfer by retrovirus vectors only occurs in cells that are actively replicating at the time of infection
-
Miller DG, Adam MA, Miller AD. Gene transfer by retrovirus vectors only occurs in cells that are actively replicating at the time of infection. Mol Cell Biol 1990; 10: 4239-4242.
-
(1990)
Mol Cell Biol
, vol.10
, pp. 4239-4242
-
-
Miller, D.G.1
Adam, M.A.2
Miller, A.D.3
-
30
-
-
12344249949
-
Amphotrophic murine leukemia retrovirus is not an acute pathogen for primates
-
Cornetta K et al. Amphotrophic murine leukemia retrovirus is not an acute pathogen for primates Hum Gene Ther 1990; 1: 15-30.
-
(1990)
Hum Gene Ther
, vol.1
, pp. 15-30
-
-
Cornetta, K.1
-
31
-
-
0010600516
-
AAV vectors can be efficiently produced without a helper virus
-
Colosi P, Elliger S, Elliger C, Kurtzman G. AAV vectors can be efficiently produced without a helper virus Blood 1995; 86 (Suppl. 1): 627a.
-
(1995)
Blood
, vol.86
, Issue.1 SUPPL.
-
-
Colosi, P.1
Elliger, S.2
Elliger, C.3
Kurtzman, G.4
-
32
-
-
0025997947
-
The encephalomyocarditis virus internal ribosome entry site allows efficient coexpression of two genes from a recombinant provirus in cultured cells and in embryos
-
Ghattas IK, Sanes JR, Majors JE. The encephalomyocarditis virus internal ribosome entry site allows efficient coexpression of two genes from a recombinant provirus in cultured cells and in embryos. Mol Cell Biol 1991; 11: 5848-5849.
-
(1991)
Mol Cell Biol
, vol.11
, pp. 5848-5849
-
-
Ghattas, I.K.1
Sanes, J.R.2
Majors, J.E.3
-
33
-
-
0026588638
-
Retroviral vectors containing putative internal ribosome entry sites: Development of a polycistronic gene transfer system and applications to human gene therapy
-
Morgan RA et al. Retroviral vectors containing putative internal ribosome entry sites: development of a polycistronic gene transfer system and applications to human gene therapy. Nucleic Acids Res 1992; 20: 1293-1299.
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 1293-1299
-
-
Morgan, R.A.1
|