-
1
-
-
0035182556
-
In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector: Efficient long-term transduction of corneal endothelium and retinal pigment epithelium
-
Bainbridge, J. W., et al. (2001). In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector: Efficient long-term transduction of corneal endothelium and retinal pigment epithelium. Gene Ther. 8: 1665-1668.
-
(2001)
Gene Ther.
, vol.8
, pp. 1665-1668
-
-
Bainbridge, J.W.1
-
2
-
-
0033779574
-
Multiple blocks to human immunodeficiency virus type 1 replication in rodent cells
-
Bieniasz, P. D., and Cullen, B. R. (2000). Multiple blocks to human immunodeficiency virus type 1 replication in rodent cells. J. Virol. 74: 9868-9877.
-
(2000)
J. Virol.
, vol.74
, pp. 9868-9877
-
-
Bieniasz, P.D.1
Cullen, B.R.2
-
3
-
-
0028372046
-
The ratio of defective HIV-1 particles to replication-competent infectious virions
-
Bourinbaiar, A. S. (1994). The ratio of defective HIV-1 particles to replication-competent infectious virions. Acta Virol. 38: 59-61.
-
(1994)
Acta Virol.
, vol.38
, pp. 59-61
-
-
Bourinbaiar, A.S.1
-
4
-
-
0343851161
-
Development of lentiviral vectors for gene therapy for human diseases
-
Buchschacher, G. L., and Wong-Staal, F. (2000). Development of lentiviral vectors for gene therapy for human diseases. Blood 95: 2499-2504.
-
(2000)
Blood
, vol.95
, pp. 2499-2504
-
-
Buchschacher, G.L.1
Wong-Staal, F.2
-
5
-
-
0027376309
-
A nuclear localization signal within HIV-1 matrix protein that governs infection of non-dividing cells
-
Bukrinsky, M. I., et al. (1993). A nuclear localization signal within HIV-1 matrix protein that governs infection of non-dividing cells. Nature 365: 666-669.
-
(1993)
Nature
, vol.365
, pp. 666-669
-
-
Bukrinsky, M.I.1
-
6
-
-
0033831002
-
Lentiviral vector transduction of hematopoietic stem cells that mediate long-term reconstitution of lethally irradiated mice
-
Chen, W., et al. (2000). Lentiviral vector transduction of hematopoietic stem cells that mediate long-term reconstitution of lethally irradiated mice. Stem Cells 18: 352-359.
-
(2000)
Stem Cells
, vol.18
, pp. 352-359
-
-
Chen, W.1
-
7
-
-
0031897966
-
A replication-competent retrovirus arising from a split-function packaging cell line was generated by recombination events between the vector, one of the packaging constructs, and endogenous retroviral sequences
-
Chong, H., Starkey, W., and Vile, R. G. (1998). A replication-competent retrovirus arising from a split-function packaging cell line was generated by recombination events between the vector, one of the packaging constructs, and endogenous retroviral sequences. J. Virol. 72: 2663-2670.
-
(1998)
J. Virol.
, vol.72
, pp. 2663-2670
-
-
Chong, H.1
Starkey, W.2
Vile, R.G.3
-
8
-
-
0029737735
-
Replication-competent retrovirus produced by a 'split-function' third generation amphotropic packaging cell line
-
Chong, H., and Vile, R. G. (1996). Replication-competent retrovirus produced by a 'split-function' third generation amphotropic packaging cell line. Gene Ther. 3: 624-629.
-
(1996)
Gene Ther.
, vol.3
, pp. 624-629
-
-
Chong, H.1
Vile, R.G.2
-
9
-
-
0034006180
-
Efficient gene transfer and expression of biologically active glial cell line-derived neurotrophic factor in rat motoneurons transduced with lentiviral vectors
-
Cisterni, C., Henderson, C. E., Aebischer, P., Pettmann, B., and Deglon, N. (2000). Efficient gene transfer and expression of biologically active glial cell line-derived neurotrophic factor in rat motoneurons transduced with lentiviral vectors. J. Neurochem. 74: 1820-1828.
-
(2000)
J. Neurochem.
, vol.74
, pp. 1820-1828
-
-
Cisterni, C.1
Henderson, C.E.2
Aebischer, P.3
Pettmann, B.4
Deglon, N.5
-
10
-
-
0035839061
-
Building a small-animal model for AIDS, block by block
-
Cohen, J. (2001). Building a small-animal model for AIDS, block by block. Science 293: 1034-1036.
-
(2001)
Science
, vol.293
, pp. 1034-1036
-
-
Cohen, J.1
-
11
-
-
0031710033
-
A third-generation lentivirus vector with a conditional packaging system
-
Dull, T., et al. (1998). A third-generation lentivirus vector with a conditional packaging system. J. Virol. 72: 8463-8471.
-
(1998)
J. Virol.
, vol.72
, pp. 8463-8471
-
-
Dull, T.1
-
12
-
-
0034987307
-
Gene transfer into neurons from hippocampal slices: Comparison of recombinant Semliki Forest virus, adenovirus, adeno-associated virus, lentivirus, and measles virus
-
Ehrengruber, M. U., Hennou, S., Bueler, H., Naim, H. Y., Deglon, N., and Lundstrom, K. (2001). Gene transfer into neurons from hippocampal slices: Comparison of recombinant Semliki Forest virus, adenovirus, adeno-associated virus, lentivirus, and measles virus. Mol. Cell. Neurosci. 17: 855-871.
-
(2001)
Mol. Cell. Neurosci.
, vol.17
, pp. 855-871
-
-
Ehrengruber, M.U.1
Hennou, S.2
Bueler, H.3
Naim, H.Y.4
Deglon, N.5
Lundstrom, K.6
-
13
-
-
0035167956
-
Adeno-associated virus and lentivirus vectors mediate efficient and sustained transduction of cultured mouse and human dorsal root ganglia sensory neurons
-
Fleming, J., Ginn, S. L., Weinberger, R. P., Trahair, T. N., Smythe, J. A., and Alexander, I. E. (2001). Adeno-associated virus and lentivirus vectors mediate efficient and sustained transduction of cultured mouse and human dorsal root ganglia sensory neurons. Hum. Gene Ther. 12: 77-86.
-
(2001)
Hum. Gene Ther.
, vol.12
, pp. 77-86
-
-
Fleming, J.1
Ginn, S.L.2
Weinberger, R.P.3
Trahair, T.N.4
Smythe, J.A.5
Alexander, I.E.6
-
14
-
-
0034040751
-
Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences
-
Follenzi, A., Ailles, L. E., Bakovic, S., Geuna, M., and Naldini, L. (2000). Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences. Nat. Genet. 25: 217-222.
-
(2000)
Nat. Genet.
, vol.25
, pp. 217-222
-
-
Follenzi, A.1
Ailles, L.E.2
Bakovic, S.3
Geuna, M.4
Naldini, L.5
-
15
-
-
0030200513
-
Improved detection of replication-competent retrovirus
-
Forestell, S. P., Dando, J. S., Bohnlein, E., and Rigg, R. J. (1996). Improved detection of replication-competent retrovirus. J. Virol. Methods 60: 171-178.
-
(1996)
J. Virol. Methods
, vol.60
, pp. 171-178
-
-
Forestell, S.P.1
Dando, J.S.2
Bohnlein, E.3
Rigg, R.J.4
-
16
-
-
0032509090
-
Human immunodeficiency virus type 1 vpr protein transactivation function: Mechanism and identification of domains involved
-
Forget, J., Yao, X. J., Mercier, J., and Cohen, E. A. (1998). Human immunodeficiency virus type 1 vpr protein transactivation function: Mechanism and identification of domains involved. J. Mol. Biol. 284: 915-923.
-
(1998)
J. Mol. Biol.
, vol.284
, pp. 915-923
-
-
Forget, J.1
Yao, X.J.2
Mercier, J.3
Cohen, E.A.4
-
17
-
-
0035680947
-
Helper plasmids for production of HIV-1-derived vectors
-
Fuller, M., and Anson, D. S. (2001). Helper plasmids for production of HIV-1-derived vectors. Hum. Gene Ther. 12: 2081-2093.
-
(2001)
Hum. Gene Ther.
, vol.12
, pp. 2081-2093
-
-
Fuller, M.1
Anson, D.S.2
-
18
-
-
0032983917
-
Stable and efficient gene transfer into the mutant retinal pigment epithelial cells of the Mitf(vit) mouse using a lentiviral vector
-
Galileo, D. S., Hunter, K., and Smith, S. B. (1999). Stable and efficient gene transfer into the mutant retinal pigment epithelial cells of the Mitf(vit) mouse using a lentiviral vector. Curr. Eye Res. 18: 135-142.
-
(1999)
Curr. Eye Res.
, vol.18
, pp. 135-142
-
-
Galileo, D.S.1
Hunter, K.2
Smith, S.B.3
-
19
-
-
0030845528
-
Recombinant retroviruses pseudotyped with the vesicular stomatitis virus G glycoprotein mediate both stable gene transfer and pseudotransduction in human peripheral blood lymphocytes
-
Gallardo, H. F., Tan, C., Ory, D., and Sadelain, M. (1997). Recombinant retroviruses pseudotyped with the vesicular stomatitis virus G glycoprotein mediate both stable gene transfer and pseudotransduction in human peripheral blood lymphocytes. Blood 90: 952-957.
-
(1997)
Blood
, vol.90
, pp. 952-957
-
-
Gallardo, H.F.1
Tan, C.2
Ory, D.3
Sadelain, M.4
-
20
-
-
0034606640
-
Characterization of recombination events leading to the production of an ecotropic replication-competent retrovirus in a GP+envAM12-derived producer cell line
-
Garrett, E., Miller, A. R., Goldman, J. M., Apperley, J. F., and Melo, J. V. (2000). Characterization of recombination events leading to the production of an ecotropic replication-competent retrovirus in a GP+envAM12-derived producer cell line. Virology 266: 170-179.
-
(2000)
Virology
, vol.266
, pp. 170-179
-
-
Garrett, E.1
Miller, A.R.2
Goldman, J.M.3
Apperley, J.F.4
Melo, J.V.5
-
21
-
-
0032982140
-
Requirements for efficient production and transduction of human immunodeficiency virus type 1-based vectors
-
Gasmi, M., Glynn, J., Jin, M. J., Jolly, D. J., Yee, J. K., and Chen, S. T. (1999). Requirements for efficient production and transduction of human immunodeficiency virus type 1-based vectors. J. Virol. 73: 1828-1834.
-
(1999)
J. Virol.
, vol.73
, pp. 1828-1834
-
-
Gasmi, M.1
Glynn, J.2
Jin, M.J.3
Jolly, D.J.4
Yee, J.K.5
Chen, S.T.6
-
22
-
-
0003124066
-
HIV-1 Vpr increases viral expression by manipulation of the cell cycle: A mechanism for selection of Vpr in vivo
-
Goh, W. C., et al. (1998). HIV-1 Vpr increases viral expression by manipulation of the cell cycle: A mechanism for selection of Vpr in vivo. Nat Med. 4: 65-71.
-
(1998)
Nat. Med.
, vol.4
, pp. 65-71
-
-
Goh, W.C.1
-
23
-
-
0032889273
-
Diminished production of human immunodeficiency virus type 1 in astrocytes results from inefficient translation of gag, env, and net mRNAs despite efficient expression of Tat and Rev
-
Gorry, P. R., et al. (1999). Diminished production of human immunodeficiency virus type 1 in astrocytes results from inefficient translation of gag, env, and net mRNAs despite efficient expression of Tat and Rev. J. Virol. 73: 352-361.
-
(1999)
J. Virol.
, vol.73
, pp. 352-361
-
-
Gorry, P.R.1
-
24
-
-
0032466415
-
Interactions of a vesicular stomatitis virus G protein fragment with phosphatidylserine: NMR and fluorescence studies
-
1415
-
Hall, M. P., Burson, K. K., and Huestis, W. H. (1998). Interactions of a vesicular stomatitis virus G protein fragment with phosphatidylserine: NMR and fluorescence studies. Biochim. Biophys. Acta 1415: 101-113.
-
(1998)
Biochim. Biophys. Acta
, pp. 101-113
-
-
Hall, M.P.1
Burson, K.K.2
Huestis, W.H.3
-
25
-
-
0028853961
-
Human immunodeficiency virus type 1 viral protein R (Vpr) arrests cells in the G2 phase of the cell cycle by inhibiting p34cdc2 activity
-
He, J., Choe, S., Walker, R., Di Marzio, P., Morgan, D. O., and Landau, N. R. (1995). Human immunodeficiency virus type 1 viral protein R (Vpr) arrests cells in the G2 phase of the cell cycle by inhibiting p34cdc2 activity. J. Virol. 69: 6705-6711.
-
(1995)
J. Virol.
, vol.69
, pp. 6705-6711
-
-
He, J.1
Choe, S.2
Walker, R.3
Di Marzio, P.4
Morgan, D.O.5
Landau, N.R.6
-
26
-
-
0035261902
-
Kinetic analyses of stability of simple and complex retroviral vectors
-
Higashikawa, F., and Chang, L. (2001). Kinetic analyses of stability of simple and complex retroviral vectors. Virology 280: 124-131.
-
(2001)
Virology
, vol.280
, pp. 124-131
-
-
Higashikawa, F.1
Chang, L.2
-
27
-
-
0033994340
-
Subcellular redistribution of Pit-2 P(i) transporter/amphotropic leukemia virus (A-MuLV) receptor in A-MuLV-infected NIH 3T3 fibroblasts: Involvement in superinfection interference
-
Jobbagy, Z., Garfield, S., Baptiste, L., Eiden, M. V., and Anderson, W. B. (2000). Subcellular redistribution of Pit-2 P(i) transporter/amphotropic leukemia virus (A-MuLV) receptor in A-MuLV-infected NIH 3T3 fibroblasts: Involvement in superinfection interference. J. Virol. 74: 2847-2854.
-
(2000)
J. Virol.
, vol.74
, pp. 2847-2854
-
-
Jobbagy, Z.1
Garfield, S.2
Baptiste, L.3
Eiden, M.V.4
Anderson, W.B.5
-
28
-
-
0029165291
-
The human immunodeficiency virus type 1 vpr gene arrests infected T cells in the G2 + M phase of the cell cycle
-
Jowett, J. B., Planelles, V., Poon, B., Shah, N. P., Chen, M. L., and Chen, I. S. (1995). The human immunodeficiency virus type 1 vpr gene arrests infected T cells in the G2 + M phase of the cell cycle. J. Virol. 69: 6304-6313.
-
(1995)
J. Virol.
, vol.69
, pp. 6304-6313
-
-
Jowett, J.B.1
Planelles, V.2
Poon, B.3
Shah, N.P.4
Chen, M.L.5
Chen, I.S.6
-
29
-
-
0030716959
-
Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors
-
Kafri, T., Blomer, U., Peterson, D. A., Gage, F. H., and Verma, I. M. (1997). Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors. Nat. Genet. 17: 314-317.
-
(1997)
Nat. Genet.
, vol.17
, pp. 314-317
-
-
Kafri, T.1
Blomer, U.2
Peterson, D.A.3
Gage, F.H.4
Verma, I.M.5
-
30
-
-
0032889454
-
A packaging cell line for lentivirus vectors
-
Kafri, T., Van Praag, H., Ouyang, L., Gage, F. H., and Verma, I. M. (1999). A packaging cell line for lentivirus vectors. J. Virol. 73: 576-584.
-
(1999)
J. Virol.
, vol.73
, pp. 576-584
-
-
Kafri, T.1
Van Praag, H.2
Ouyang, L.3
Gage, F.H.4
Verma, I.M.5
-
31
-
-
0031985685
-
Minimal requirement for a lentivirus vector based on human immunodeficiency virus type 1
-
Kim, V. N., Mitrophanous, K., Kingsman, S. M., and Kingsman, A. J. (1998). Minimal requirement for a lentivirus vector based on human immunodeficiency virus type 1. J. Virol. 72: 811-816.
-
(1998)
J. Virol.
, vol.72
, pp. 811-816
-
-
Kim, V.N.1
Mitrophanous, K.2
Kingsman, S.M.3
Kingsman, A.J.4
-
32
-
-
0342699700
-
A Rev-independent human immunodeficiency virus type 1 (HIV-1)-based vector that exploits a codon-optimized HIV-1 gag-pol gene
-
Kotsopoulou, E., Kim, V. N., Kingsman, A. J., Kingsman, S. M., and Mitrophanous, K. A. (2000). A Rev-independent human immunodeficiency virus type 1 (HIV-1)-based vector that exploits a codon-optimized HIV-1 gag-pol gene. J. Virol. 74: 4839-4852.
-
(2000)
J. Virol.
, vol.74
, pp. 4839-4852
-
-
Kotsopoulou, E.1
Kim, V.N.2
Kingsman, A.J.3
Kingsman, S.M.4
Mitrophanous, K.A.5
-
33
-
-
0026623010
-
Packaging system for rapid production of murine leukemia virus vectors with variable tropism
-
Landau, N. R., and Littman, D. R. (1992). Packaging system for rapid production of murine leukemia virus vectors with variable tropism. J. Virol. 66: 5110-5113.
-
(1992)
J. Virol.
, vol.66
, pp. 5110-5113
-
-
Landau, N.R.1
Littman, D.R.2
-
34
-
-
0026654682
-
Human immunodeficiency virus infection of cells arrested in the cell cycle
-
Lewis, P., Hensel, M., and Emerman, M. (1992). Human immunodeficiency virus infection of cells arrested in the cell cycle. EMBO J. 11: 3053-3058.
-
(1992)
EMBO J.
, vol.11
, pp. 3053-3058
-
-
Lewis, P.1
Hensel, M.2
Emerman, M.3
-
35
-
-
0028055281
-
Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus
-
Lewis, P. F., and Emerman, M. (1994). Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus. J. Virol. 68: 510-516.
-
(1994)
J. Virol.
, vol.68
, pp. 510-516
-
-
Lewis, P.F.1
Emerman, M.2
-
36
-
-
0029062573
-
Induction of apoptosis in uninfected lymphocytes by HIV-1 Tat protein
-
Li, C. J., Friedman, D. J., Wang, C., Metelev, V., and Pardee, A. B. (1995). Induction of apoptosis in uninfected lymphocytes by HIV-1 Tat protein. Science 268: 429-431.
-
(1995)
Science
, vol.268
, pp. 429-431
-
-
Li, C.J.1
Friedman, D.J.2
Wang, C.3
Metelev, V.4
Pardee, A.B.5
-
37
-
-
0029931982
-
Pseudotransduction of hepatocytes by using concentrated pseudotyped vesicular stomatitis virus G glycoprotein (VSV-G)-Moloney murine leukemia virus-derived retrovirus vectors: Comparison of VSV-G and amphotropic vectors for hepatic gene transfer
-
Liu, M. L., Winther, B. L., and Kay, M. A. (1996). Pseudotransduction of hepatocytes by using concentrated pseudotyped vesicular stomatitis virus G glycoprotein (VSV-G)-Moloney murine leukemia virus-derived retrovirus vectors: Comparison of VSV-G and amphotropic vectors for hepatic gene transfer. J. Virol. 70: 2497-2502.
-
(1996)
J. Virol.
, vol.70
, pp. 2497-2502
-
-
Liu, M.L.1
Winther, B.L.2
Kay, M.A.3
-
38
-
-
0030824787
-
Nuclear import, virion incorporation, and cell cycle arrest/differentiation are mediated by distinct functional domains of human immunodeficiency virus type 1 Vpr
-
Mahalingam, S., Ayyavoo, V., Patel, M., Kieber-Emmons, T., and Weiner, D. B. (1997). Nuclear import, virion incorporation, and cell cycle arrest/differentiation are mediated by distinct functional domains of human immunodeficiency virus type 1 Vpr. J. Virol. 71: 6339-6347.
-
(1997)
J. Virol.
, vol.71
, pp. 6339-6347
-
-
Mahalingam, S.1
Ayyavoo, V.2
Patel, M.3
Kieber-Emmons, T.4
Weiner, D.B.5
-
39
-
-
0029846223
-
High frequency of defective nef alleles in a long-term survivor with nonprogressive human immunodeficiency virus type 1 infection
-
Mariani, R., Kirchhoff, F., Greenough, T. C., Sullivan, J. L., Desrosiers, R. C., and Skowronski, J. (1996). High frequency of defective nef alleles in a long-term survivor with nonprogressive human immunodeficiency virus type 1 infection. J. Virol. 70: 7752-7764.
-
(1996)
J. Virol.
, vol.70
, pp. 7752-7764
-
-
Mariani, R.1
Kirchhoff, F.2
Greenough, T.C.3
Sullivan, J.L.4
Desrosiers, R.C.5
Skowronski, J.6
-
40
-
-
0034068397
-
A block to human immunodeficiency virus type 1 assembly in murine cells
-
Mariani, R., Rutter, G., Harris, M. E., Hope, T. J., Krausslich, H. G., and Landau, N. R. (2000). A block to human immunodeficiency virus type 1 assembly in murine cells. J. Virol. 74: 3859-3870.
-
(2000)
J. Virol.
, vol.74
, pp. 3859-3870
-
-
Mariani, R.1
Rutter, G.2
Harris, M.E.3
Hope, T.J.4
Krausslich, H.G.5
Landau, N.R.6
-
41
-
-
0029919588
-
Partial reconstitution of a replication-competent retrovirus in helper cells with partial overlaps between vector and helper cell genomes
-
Martinez, I., and Dornburg, R. (1996). Partial reconstitution of a replication-competent retrovirus in helper cells with partial overlaps between vector and helper cell genomes. Hum. Gene Ther. 7: 705-712.
-
(1996)
Hum. Gene Ther.
, vol.7
, pp. 705-712
-
-
Martinez, I.1
Dornburg, R.2
-
42
-
-
0031666744
-
Development of a self-inactivating lentivirus vector
-
Miyoshi, H., Blomer, U., Takahashi, M., Gage, F. H., and Verma, I. M. (1998). Development of a self-inactivating lentivirus vector. J. Virol. 72: 8150-8157.
-
(1998)
J. Virol.
, vol.72
, pp. 8150-8157
-
-
Miyoshi, H.1
Blomer, U.2
Takahashi, M.3
Gage, F.H.4
Verma, I.M.5
-
43
-
-
0030931963
-
Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector
-
Miyoshi, H., Takahashi, M., Gage, F. H., and Verma, I. M. (1997). Stable and efficient gene transfer into the retina using an HIV-based lentiviral vector. Proc. Natl. Acad. Sci. USA 94: 10319-10323.
-
(1997)
Proc. Natl. Acad. Sci. USA
, vol.94
, pp. 10319-10323
-
-
Miyoshi, H.1
Takahashi, M.2
Gage, F.H.3
Verma, I.M.4
-
44
-
-
0029993858
-
Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector
-
Naldini, L., Blomer, U., Gage, F. H., Trono, D., and Verma, I. M. (1996). Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector. Proc. Natl. Acad. Sci. USA 93: 11382-11388.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 11382-11388
-
-
Naldini, L.1
Blomer, U.2
Gage, F.H.3
Trono, D.4
Verma, I.M.5
-
45
-
-
0029996147
-
In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector
-
Naldini, L., et al. (1996). In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 272: 263-267.
-
(1996)
Science
, vol.272
, pp. 263-267
-
-
Naldini, L.1
-
46
-
-
0029862497
-
A stable human-derived packaging cell line for production of high titer retrovirus/vesicular stomatitis virus G pseudotypes
-
Ory, D. S., Neugeboren, B. A., and Mulligan, R. C. (1996). A stable human-derived packaging cell line for production of high titer retrovirus/vesicular stomatitis virus G pseudotypes. Proc. Natl. Acad. Sci, USA 93: 11400-11406.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 11400-11406
-
-
Ory, D.S.1
Neugeboren, B.A.2
Mulligan, R.C.3
-
47
-
-
0028043213
-
Characterization of a replication-competent retrovirus resulting from recombination of packaging and vector sequences
-
Otto, E., et al. (1994). Characterization of a replication-competent retrovirus resulting from recombination of packaging and vector sequences. Hum. Gene Ther. 5: 567-575.
-
(1994)
Hum. Gene Ther.
, vol.5
, pp. 567-575
-
-
Otto, E.1
-
48
-
-
0034254320
-
Therapeutic levels of human factor VIII and IX using HIV-1 -based lentiviral vectors in mouse liver
-
Park, F., Ohashi, K., and Kay, M. A. (2000). Therapeutic levels of human factor VIII and IX using HIV-1 -based lentiviral vectors in mouse liver. Blood 96: 1173-1176.
-
(2000)
Blood
, vol.96
, pp. 1173-1176
-
-
Park, F.1
Ohashi, K.2
Kay, M.A.3
-
49
-
-
0034989411
-
Transduction of liver cells by lentiviral vectors: Analysis in living animals by fluorescence imaging
-
Pfeifer, A., et al. (2001). Transduction of liver cells by lentiviral vectors: Analysis in living animals by fluorescence imaging. Mol. Ther. 3: 319-322.
-
(2001)
Mol. Ther.
, vol.3
, pp. 319-322
-
-
Pfeifer, A.1
-
50
-
-
0029859406
-
Development of HIV vectors for anti-HIV gene therapy
-
Poeschla, E., Corbeau, P., and Wong-Staal, F. (1996). Development of HIV vectors for anti-HIV gene therapy. Proc. Natl. Acad. Sci. USA 93: 11395-11399.
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 11395-11399
-
-
Poeschla, E.1
Corbeau, P.2
Wong-Staal, F.3
-
51
-
-
0026051132
-
Gene transfer into human lymphocytes by a defective human immunodeficiency virus type 1 vector
-
Poznansky, M., Lever, A., Bergeron, L., Haseltine, W., and Sodroski, J. (1991). Gene transfer into human lymphocytes by a defective human immunodeficiency virus type 1 vector. J. Virol. 65: 532-536.
-
(1991)
J. Virol.
, vol.65
, pp. 532-536
-
-
Poznansky, M.1
Lever, A.2
Bergeron, L.3
Haseltine, W.4
Sodroski, J.5
-
52
-
-
0030030403
-
The nef gene from a long-term HIV type 1 nonprogressor
-
Premkumar, D. R., et al. (1996). The nef gene from a long-term HIV type 1 nonprogressor. AIDS Res. Hum. Retroviruses 12: 337-345.
-
(1996)
AIDS Res. Hum. Retroviruses
, vol.12
, pp. 337-345
-
-
Premkumar, D.R.1
-
53
-
-
0028958856
-
Recombinant retroviral vector interferes with the detection of amphotropic replication competent retrovirus in standard culture assays
-
Printz, M., Reynolds, J., Mento, S. J., Jolly, D., Kowal, K., and Sajjadi, N. (1995). Recombinant retroviral vector interferes with the detection of amphotropic replication competent retrovirus in standard culture assays. Gene Ther. 2: 143-150.
-
(1995)
Gene Ther.
, vol.2
, pp. 143-150
-
-
Printz, M.1
Reynolds, J.2
Mento, S.J.3
Jolly, D.4
Kowal, K.5
Sajjadi, N.6
-
54
-
-
0029004014
-
HIV type 1 Tat protein induces apoptosis and death in Jurkat cells
-
Purvis, S. F., Jacobberger, J. W., Sramkoski, R. M., Patki, A. H., and Lederman, M. M. (1995). HIV type 1 Tat protein induces apoptosis and death in Jurkat cells. AIDS Res. Hum. Retroviruses 11: 443-450.
-
(1995)
AIDS Res. Hum. Retroviruses
, vol.11
, pp. 443-450
-
-
Purvis, S.F.1
Jacobberger, J.W.2
Sramkoski, R.M.3
Patki, A.H.4
Lederman, M.M.5
-
55
-
-
0032487336
-
Infection of human fetal cardiac myocytes by a human immunodeficiency virus-1-derived vector
-
Rebolledo, M. A., Krogstad, P., Chen, F., Shannon, K. M., and Klitzner, T. S. (1998). Infection of human fetal cardiac myocytes by a human immunodeficiency virus-1-derived vector. Circ. Res. 83: 738-742.
-
(1998)
Circ. Res.
, vol.83
, pp. 738-742
-
-
Rebolledo, M.A.1
Krogstad, P.2
Chen, F.3
Shannon, K.M.4
Klitzner, T.S.5
-
56
-
-
0028929878
-
Helper virus-free transfer of human immunodeficiency virus type 1 vectors
-
Richardson, J. H., Kaye, J. F., Child, L. A., and Lever, A. M. (1995). Helper virus-free transfer of human immunodeficiency virus type 1 vectors. J. Gen. Virol. 76: 691-696.
-
(1995)
J. Gen. Virol.
, vol.76
, pp. 691-696
-
-
Richardson, J.H.1
Kaye, J.F.2
Child, L.A.3
Lever, A.M.4
-
57
-
-
0027158091
-
Integration of murine leukemia virus DNA depends on mitosis
-
Roe, T., Reynolds, T. C., Yu, G., and Brown, P. O. (1993). Integration of murine leukemia virus DNA depends on mitosis. EMBO J. 12: 2099-2108.
-
(1993)
EMBO J.
, vol.12
, pp. 2099-2108
-
-
Roe, T.1
Reynolds, T.C.2
Yu, G.3
Brown, P.O.4
-
58
-
-
0032698781
-
A high-titer lentiviral production system mediates efficient transduction of differentiated cells including beating cardiac myocytes
-
Sakoda, T., Kasahara, N., Hamamori, Y., and Kedes, L. (1999). A high-titer lentiviral production system mediates efficient transduction of differentiated cells including beating cardiac myocytes. J. Mol. Cell. Cardiol. 31: 2037-2047.
-
(1999)
J. Mol. Cell. Cardiol.
, vol.31
, pp. 2037-2047
-
-
Sakoda, T.1
Kasahara, N.2
Hamamori, Y.3
Kedes, L.4
-
59
-
-
0031979771
-
Grossly defective nef gene sequences in a human immunodeficiency virus type 1-seropositive long-term nonprogressor
-
Salvi, R., Garbuglia, A. R., Di Caro, A., Pulciani, S., Montella, F., and Benedetto, A. (1998). Grossly defective nef gene sequences in a human immunodeficiency virus type 1-seropositive long-term nonprogressor. J. Virol. 72: 3646-3657.
-
(1998)
J. Virol.
, vol.72
, pp. 3646-3657
-
-
Salvi, R.1
Garbuglia, A.R.2
Di Caro, A.3
Pulciani, S.4
Montella, F.5
Benedetto, A.6
-
60
-
-
0020712445
-
Inhibition of VSV binding and infectivity by phosphatidylserine: Is phosphatidylserine a VSV-binding site?
-
Schlegel, R., Tralka, T. S., Willingham, M. C., and Pastan, I. (1983). Inhibition of VSV binding and infectivity by phosphatidylserine: Is phosphatidylserine a VSV-binding site? Cell 32: 639-646.
-
(1983)
Cell
, vol.32
, pp. 639-646
-
-
Schlegel, R.1
Tralka, T.S.2
Willingham, M.C.3
Pastan, I.4
-
61
-
-
0029794456
-
Broad host range of human T-cell leukemia virus type 1 demonstrated with an improved pseudotyping system
-
Sutton, R. E., and Littman, D. R. (1996). Broad host range of human T-cell leukemia virus type 1 demonstrated with an improved pseudotyping system. J. Virol. 70: 7322-7326.
-
(1996)
J. Virol.
, vol.70
, pp. 7322-7326
-
-
Sutton, R.E.1
Littman, D.R.2
-
62
-
-
0032956732
-
Transduction of human progenitor hematopoietic stem cells by human immunodeficiency virus type 1-based vectors is cell cycle dependent
-
Sutton, R. E., Reitsma, M. J., Uchida, N., and Brown, P. O. (1999). Transduction of human progenitor hematopoietic stem cells by human immunodeficiency virus type 1-based vectors is cell cycle dependent. J. Virol. 73: 3649-3660.
-
(1999)
J. Virol.
, vol.73
, pp. 3649-3660
-
-
Sutton, R.E.1
Reitsma, M.J.2
Uchida, N.3
Brown, P.O.4
-
63
-
-
0031747965
-
Human immunodeficiency virus type 1 vectors efficiently transduce human hematopoietic stem cells
-
Sutton, R. E., Wu, H. T., Rigg, R., Bohnlein, E., and Brown, P. O. (1998). Human immunodeficiency virus type 1 vectors efficiently transduce human hematopoietic stem cells. J. Virol. 72: 5781-5788.
-
(1998)
J. Virol.
, vol.72
, pp. 5781-5788
-
-
Sutton, R.E.1
Wu, H.T.2
Rigg, R.3
Bohnlein, E.4
Brown, P.O.5
-
64
-
-
0033972740
-
Lentiviral vectors: Turning a deadly foe into a therapeutic agent
-
Trono, D. (2000). Lentiviral vectors: Turning a deadly foe into a therapeutic agent. Gene Ther. 7: 20-23.
-
(2000)
Gene Ther.
, vol.7
, pp. 20-23
-
-
Trono, D.1
-
65
-
-
0032578385
-
HIV, but not murine leukemia virus, vectors mediate high efficiency gene transfer into freshly isolated G0/G1 human hematopoietic stem cells
-
Uchida, N., et al. (1998). HIV, but not murine leukemia virus, vectors mediate high efficiency gene transfer into freshly isolated G0/G1 human hematopoietic stem cells. Proc. Natl. Acad. Sci. USA 95: 11939-11944.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 11939-11944
-
-
Uchida, N.1
-
66
-
-
0035950597
-
HIV-1 Vpr transactivates LTR-directed expression through sequences present within - 278 to - 176 and increases virus replication in vitro
-
Vanitharani, R., et al. (2001). HIV-1 Vpr transactivates LTR-directed expression through sequences present within - 278 to - 176 and increases virus replication in vitro. Virology 289: 334-342.
-
(2001)
Virology
, vol.289
, pp. 334-342
-
-
Vanitharani, R.1
-
67
-
-
0034694017
-
Rev-independent expression of synthetic gag-pol genes of human immunodeficiency virus type 1 and simian immunodeficiency virus: Implications for the safety of lentiviral vectors
-
Wagner, R., et al. (2000). Rev-independent expression of synthetic gag-pol genes of human immunodeficiency virus type 1 and simian immunodeficiency virus: Implications for the safety of lentiviral vectors. Hum. Gene Ther. 11: 2403-2413.
-
(2000)
Hum. Gene Ther.
, vol.11
, pp. 2403-2413
-
-
Wagner, R.1
-
68
-
-
0035731632
-
Lentiviral-mediated gene transfer into haematopoietic stem cells
-
Woods, N. B., Mikkola, H., Nilsson, E., Olsson, K., Trono, D., and Karlsson, S. (2001). Lentiviral-mediated gene transfer into haematopoietic stem cells. J. Intern. Med. 249: 339-343.
-
(2001)
J. Intern. Med.
, vol.249
, pp. 339-343
-
-
Woods, N.B.1
Mikkola, H.2
Nilsson, E.3
Olsson, K.4
Trono, D.5
Karlsson, S.6
-
69
-
-
0034218268
-
Development of a novel trans-lentiviral vector that affords predictable safety
-
Wu, X., et al. (2000). Development of a novel trans-lentiviral vector that affords predictable safety. Mol. Ther. 2: 47-55.
-
(2000)
Mol. Ther.
, vol.2
, pp. 47-55
-
-
Wu, X.1
-
70
-
-
0034988922
-
Generation of a stable cell line producing high-titer self-inactivating lentiviral vectors
-
Xu, K., Ma, H., Mccown, T. J., Verma, I. M., and Kafri, T. (2001). Generation of a stable cell line producing high-titer self-inactivating lentiviral vectors. Mol. Ther. 3: 97-104.
-
(2001)
Mol. Ther.
, vol.3
, pp. 97-104
-
-
Xu, K.1
Ma, H.2
McCown, T.J.3
Verma, I.M.4
Kafri, T.5
-
71
-
-
0022458049
-
Vesicular stomatitis virus binds and fuses with phospholipid domain in target cell membranes
-
Yamada, S., and Ohnishi, S. (1986). Vesicular stomatitis virus binds and fuses with phospholipid domain in target cell membranes. Biochemistry 25: 3703-3708.
-
(1986)
Biochemistry
, vol.25
, pp. 3703-3708
-
-
Yamada, S.1
Ohnishi, S.2
-
72
-
-
0034128313
-
Comparison of proviral accessory genes between long-term nonprogressors and progressors of human immunodeficiency virus type 1 infection
-
Yamada, T., and Iwamoto, A. (2000). Comparison of proviral accessory genes between long-term nonprogressors and progressors of human immunodeficiency virus type 1 infection. Arch. Virol. 145: 1021-1027.
-
(2000)
Arch. Virol.
, vol.145
, pp. 1021-1027
-
-
Yamada, T.1
Iwamoto, A.2
-
73
-
-
0031950195
-
Vpr stimulates viral expression and induces cell killing in human immunodeficiency virus type 1-infected dividing Jurkat T cells
-
Yao, X. J., et al. (1998). Vpr stimulates viral expression and induces cell killing in human immunodeficiency virus type 1-infected dividing Jurkat T cells. J. Virol. 72: 4686-4693.
-
(1998)
J. Virol.
, vol.72
, pp. 4686-4693
-
-
Yao, X.J.1
-
74
-
-
0034646513
-
HIV-1 genome nuclear import is mediated by a central DNA flap
-
Zennou, V., Petit, C., Guetard, D., Nerhbass, U., Montagnier, L., and Charneau, P. (2000). HIV-1 genome nuclear import is mediated by a central DNA flap. Cell 101: 173-185.
-
(2000)
Cell
, vol.101
, pp. 173-185
-
-
Zennou, V.1
Petit, C.2
Guetard, D.3
Nerhbass, U.4
Montagnier, L.5
Charneau, P.6
-
75
-
-
0031743608
-
Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery
-
Zufferey, R., et al. (1998). Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery. J. Virol. 72: 9873-9880.
-
(1998)
J. Virol.
, vol.72
, pp. 9873-9880
-
-
Zufferey, R.1
-
76
-
-
0030819379
-
Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo
-
Zufferey, R., Nagy, D., Mandel, R. J., Naldini, L., and Trono, D. (1997). Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo. Nat. Biotechnol. 15: 871-875.
-
(1997)
Nat. Biotechnol.
, vol.15
, pp. 871-875
-
-
Zufferey, R.1
Nagy, D.2
Mandel, R.J.3
Naldini, L.4
Trono, D.5
|