-
1
-
-
0035135747
-
Viral vectors for gene therapy: The art of turning infectious agents into vehicles of therapeutics
-
Kay MA, Glorioso JC, Naldini L. Viral vectors for gene therapy: the art of turning infectious agents into vehicles of therapeutics. Nat Med 2001; 7: 33-40.
-
(2001)
Nat Med
, vol.7
, pp. 33-40
-
-
Kay, M.A.1
Glorioso, J.C.2
Naldini, L.3
-
2
-
-
0033974016
-
Latest developments in gene transfer technology: Achievements, perspectives, and controversies over therapeutic applications
-
Romano G, Micheli P, Pacilio C, Giordano A. Latest developments in gene transfer technology: achievements, perspectives, and controversies over therapeutic applications. Stem Cells 2000; 18: 19-39.
-
(2000)
Stem Cells
, vol.18
, pp. 19-39
-
-
Romano, G.1
Micheli, P.2
Pacilio, C.3
Giordano, A.4
-
3
-
-
3042603743
-
Vectors derived from the human immunodeficiency virus, hiv-1
-
Barker E, Planelles V. Vectors derived from the human immunodeficiency virus, hiv-1. Front Biosci 2003; 8: D491-510.
-
(2003)
Front Biosci
, vol.8
-
-
Barker, E.1
Planelles, V.2
-
4
-
-
0029996147
-
In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector
-
Naldini L, Blomer U, Gallay P, Ory D, Mulligan R, Gage F, Verma IM, Trono D. In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 1996; 272: 263-7.
-
(1996)
Science
, vol.272
, pp. 263-267
-
-
Naldini, L.1
Blomer, U.2
Gallay, P.3
Ory, D.4
Mulligan, R.5
Gage, F.6
Verma, I.M.7
Trono, D.8
-
5
-
-
0034672356
-
The human immunodeficiency virus type-1 central flap is a crucial determinat for lentiviral vector nuclear import and gene transduction of human hematopoietic stem cells
-
Sirven A, Pflumio F, Zennou V, Titeux M, Vainchenker W, Coulombel L, Dubart-Kupperschmitt A, Charmeau P. The human immunodeficiency virus type-1 central flap is a crucial determinat for lentiviral vector nuclear import and gene transduction of human hematopoietic stem cells. Blood 2000; 96: 4103-10.
-
(2000)
Blood
, vol.96
, pp. 4103-4110
-
-
Sirven, A.1
Pflumio, F.2
Zennou, V.3
Titeux, M.4
Vainchenker, W.5
Coulombel, L.6
Dubart-Kupperschmitt, A.7
Charmeau, P.8
-
6
-
-
0034040751
-
Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences
-
Follenzi A, Ailles LE, Bakovic S, Geuna M, Naldini L. Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences. Nat Genet 2000; 25: 217-22.
-
(2000)
Nat Genet
, vol.25
, pp. 217-222
-
-
Follenzi, A.1
Ailles, L.E.2
Bakovic, S.3
Geuna, M.4
Naldini, L.5
-
7
-
-
0036846846
-
Lentivirus-mediated gene transfer into hematopoietic repopulating cells in baboons
-
Horn PA, Morris JC, Bukovsky AA, Andrews RG, Naldini L, Kurre P, Kiem H-P. Lentivirus-mediated gene transfer into hematopoietic repopulating cells in baboons. Gene Ther 2002; 9: 1464-71.
-
(2002)
Gene Ther
, vol.9
, pp. 1464-1471
-
-
Horn, P.A.1
Morris, J.C.2
Bukovsky, A.A.3
Andrews, R.G.4
Naldini, L.5
Kurre, P.6
Kiem, H.-P.7
-
8
-
-
0033755914
-
Lentivirus vector gene expression during ES cell-derived hematopoietic development in vitro
-
Hamaguci I, Woods N-B, Panagopoulos I, Andersson E, Mikkola H, Fahlman C, Zufferey R, Carlsson L, Trono D, Karlsson S. Lentivirus vector gene expression during ES cell-derived hematopoietic development in vitro. J Virol 2000; 74: 10778-84.
-
(2000)
J Virol
, vol.74
, pp. 10778-10784
-
-
Hamaguci, I.1
Woods, N.-B.2
Panagopoulos, I.3
Andersson, E.4
Mikkola, H.5
Fahlman, C.6
Zufferey, R.7
Carlsson, L.8
Trono, D.9
Karlsson, S.10
-
9
-
-
0034670033
-
Lentivirus-based vectors transduce mouse hematopoietic stem cells with similar efficiency to Moloney leukemia virus-based vectors
-
Barrette S, Douglas JL, Seidel NE, Bodine DM. Lentivirus-based vectors transduce mouse hematopoietic stem cells with similar efficiency to Moloney leukemia virus-based vectors. Blood 2000; 96: 3385-91.
-
(2000)
Blood
, vol.96
, pp. 3385-3391
-
-
Barrette, S.1
Douglas, J.L.2
Seidel, N.E.3
Bodine, D.M.4
-
10
-
-
0034669932
-
High-level transgene expression in human hematopoietic progenitors and differentiated blood lineages after transduction with improved lentiviral vectors
-
Salmon P, Kinlder V, Ducrey O, Chapuis B, Zubler RH, Trono D. High-level transgene expression in human hematopoietic progenitors and differentiated blood lineages after transduction with improved lentiviral vectors. Blood 2000; 96: 3392-8.
-
(2000)
Blood
, vol.96
, pp. 3392-3398
-
-
Salmon, P.1
Kinlder, V.2
Ducrey, O.3
Chapuis, B.4
Zubler, R.H.5
Trono, D.6
-
11
-
-
0035118978
-
Stable transduction with lentiviral vectors and amplification of immature hematopoietic progenitors from cord blood of preterm human fetuses
-
Luther-Wyrsch A, Costello E, Thali M, Buetti E, Nissen C, Surbek D, Holzgreve W, Gratwohl A, Tichelli A, Wodnar-Filipowicz. Stable transduction with lentiviral vectors and amplification of immature hematopoietic progenitors from cord blood of preterm human fetuses. Hum Gene Ther 2001; 12: 377-89.
-
(2001)
Hum Gene Ther
, vol.12
, pp. 377-389
-
-
Luther-Wyrsch, A.1
Costello, E.2
Thali, M.3
Buetti, E.4
Nissen, C.5
Surbek, D.6
Holzgreve, W.7
Gratwohl, A.8
Tichelli, A.9
Wodnar-Filipowicz10
-
12
-
-
0034721690
-
Neurodegeneration prevented by lentiviral vector delivery of GDNF in primate models of Parkinson's disease
-
Kordower JH, Emborg ME, Bloch J, Ma SY, Chu Y, Leventhal L, McBride J, Chen EY, Palfi S, Roitberg BZ, Brown WD, Holden JE, Pyzalski R, Taylor MD, Carvey P, Ling Z, Trono D, Hantraye P, Deglon N, Aebischer P. Neurodegeneration prevented by lentiviral vector delivery of GDNF in primate models of Parkinson's disease. Science 2000; 290: 767-73.
-
(2000)
Science
, vol.290
, pp. 767-773
-
-
Kordower, J.H.1
Emborg, M.E.2
Bloch, J.3
Ma, S.Y.4
Chu, Y.5
Leventhal, L.6
McBride, J.7
Chen, E.Y.8
Palfi, S.9
Roitberg, B.Z.10
Brown, W.D.11
Holden, J.E.12
Pyzalski, R.13
Taylor, M.D.14
Carvey, P.15
Ling, Z.16
Trono, D.17
Hantraye, P.18
Deglon, N.19
Aebischer, P.20
more..
-
13
-
-
0035099437
-
In vivo gene therapy of metachromatic leukodystrophy by lentiviral vector: Corrections of neuropathology and protection against impairments in affected mice
-
Consiglio A, Quattrini A, Martino S, Bensadoun JC, Dolcetta D, Trojani A, Benaglia G, Marchesini S, Cestari V, Oliverio A, Bordignon C, Naldini L. In vivo gene therapy of metachromatic leukodystrophy by lentiviral vector: corrections of neuropathology and protection against impairments in affected mice. Nat Med 2001; 7: 310-6.
-
(2001)
Nat Med
, vol.7
, pp. 310-316
-
-
Consiglio, A.1
Quattrini, A.2
Martino, S.3
Bensadoun, J.C.4
Dolcetta, D.5
Trojani, A.6
Benaglia, G.7
Marchesini, S.8
Cestari, V.9
Oliverio, A.10
Bordignon, C.11
Naldini, L.12
-
14
-
-
0036247444
-
Characterization of lentiviral vector-mediated gene transfer in adult mouse broin
-
Baekelandt V, Claeys A, Eggermont K, Lauwers E, De Strooper B, Nuttin B, Debyser Z. Characterization of lentiviral vector-mediated gene transfer in adult mouse broin. Hum Gene Ther 2002; 13: 841-53.
-
(2002)
Hum Gene Ther
, vol.13
, pp. 841-853
-
-
Baekelandt, V.1
Claeys, A.2
Eggermont, K.3
Lauwers, E.4
De Strooper, B.5
Nuttin, B.6
Debyser, Z.7
-
15
-
-
0035013429
-
The HIV-1 DNA flap stimulates HIV vector-mediated cell transduction in the brain
-
Zennou V, Serguera C, Sarkis C, Colin P, Perret E, Mallet J, Charneau P. The HIV-1 DNA flap stimulates HIV vector-mediated cell transduction in the brain. Nat Biotechnol 2001; 19: 446-50.
-
(2001)
Nat Biotechnol
, vol.19
, pp. 446-450
-
-
Zennou, V.1
Serguera, C.2
Sarkis, C.3
Colin, P.4
Perret, E.5
Mallet, J.6
Charneau, P.7
-
16
-
-
0037108187
-
Gene therapy of Fanconi anemia: Preclinical efficacy using lentiviral vectors
-
Galimi F, Noll M, Kanazawa Y, Lax T, Chen C, Grompe M, Verma IM. Gene therapy of Fanconi anemia: preclinical efficacy using lentiviral vectors. Blood 2002; 100: 2732-6.
-
(2002)
Blood
, vol.100
, pp. 2732-2736
-
-
Galimi, F.1
Noll, M.2
Kanazawa, Y.3
Lax, T.4
Chen, C.5
Grompe, M.6
Verma, I.M.7
-
17
-
-
0036529821
-
Efficient gene transfer into human primary blood lymphocytes by surface-engineered lentiviral vectors that disply a T cell-activating polypeptide
-
Maurice M, Verhoeyen E, Salmon P, Trono D, Russell SJ, Cosset F-L. Efficient gene transfer into human primary blood lymphocytes by surface-engineered lentiviral vectors that disply a T cell-activating polypeptide. Blood 2002; 99: 2342-50.
-
(2002)
Blood
, vol.99
, pp. 2342-2350
-
-
Maurice, M.1
Verhoeyen, E.2
Salmon, P.3
Trono, D.4
Russell, S.J.5
Cosset, F.-L.6
-
18
-
-
0036898193
-
Restoration of type VII collagen expression and function in dystrophic epidermolysis bullosa
-
Chen M, Kasahara N, Keene DR, Chan L, Hoeffler WK, Finlay D, Barkova M, Cannon PM, Mazurek C, Woodley DT. Restoration of type VII collagen expression and function in dystrophic epidermolysis bullosa. Nat Genet 2002; 32: 670-5.
-
(2002)
Nat Genet
, vol.32
, pp. 670-675
-
-
Chen, M.1
Kasahara, N.2
Keene, D.R.3
Chan, L.4
Hoeffler, W.K.5
Finlay, D.6
Barkova, M.7
Cannon, P.M.8
Mazurek, C.9
Woodley, D.T.10
-
19
-
-
0035105820
-
Filovirus-pseudotyped lentiviral vector can efficiently and stably transduce airway epithelia in vivo
-
Kobinger GP, Weiner DJ, Yu QC, Wilson JM. Filovirus-pseudotyped lentiviral vector can efficiently and stably transduce airway epithelia in vivo. Nat Biotechnol 2001; 19: 225-30.
-
(2001)
Nat Biotechnol
, vol.19
, pp. 225-230
-
-
Kobinger, G.P.1
Weiner, D.J.2
Yu, Q.C.3
Wilson, J.M.4
-
20
-
-
0343628721
-
Therapeutic haemoglobin synthesis in β-tholassaemic mice expressing lentivirus-encoded human β-globin
-
May C, Rivella S, Callegari J, Heller G, Gaensler KM, Luzzatto L, Sadelain M. Therapeutic haemoglobin synthesis in β-tholassaemic mice expressing lentivirus-encoded human β-globin. Nature 2000; 406: 82-6.
-
(2000)
Nature
, vol.406
, pp. 82-86
-
-
May, C.1
Rivella, S.2
Callegari, J.3
Heller, G.4
Gaensler, K.M.5
Luzzatto, L.6
Sadelain, M.7
-
21
-
-
0036137639
-
Production of human clotting Factor IX without toxicity in mice after vascular delivery of a lentiviral vector
-
Tsui LV, Kelly M, Zayek N, Rojas V, Ho K, Ge Y, Moskalenko M, Mondesire J, Davis J, Roey MV, Dull T, McArthur JG. Production of human clotting Factor IX without toxicity in mice after vascular delivery of a lentiviral vector. Nat Biotechnol 2002; 20: 53-7.
-
(2002)
Nat Biotechnol
, vol.20
, pp. 53-57
-
-
Tsui, L.V.1
Kelly, M.2
Zayek, N.3
Rojas, V.4
Ho, K.5
Ge, Y.6
Moskalenko, M.7
Mondesire, J.8
Davis, J.9
Roey, M.V.10
Dull, T.11
McArthur, J.G.12
-
22
-
-
0033780546
-
Cotransduction of nondividing cells using lentiviral vectors
-
Frimpong K, Spector SA. Cotransduction of nondividing cells using lentiviral vectors. Gene Ther 2000; 7: 1562-9.
-
(2000)
Gene Ther
, vol.7
, pp. 1562-1569
-
-
Frimpong, K.1
Spector, S.A.2
-
23
-
-
0034804819
-
Prostate-specific targeting using PSA promoter-based lentiviral vectors
-
Yu D, Chen D, Chiu C, Razmazma B, Chow YH, Pang S. Prostate-specific targeting using PSA promoter-based lentiviral vectors. Cancer Gene Ther 2001; 8: 628-35.
-
(2001)
Cancer Gene Ther
, vol.8
, pp. 628-635
-
-
Yu, D.1
Chen, D.2
Chiu, C.3
Razmazma, B.4
Chow, Y.H.5
Pang, S.6
-
24
-
-
0035190393
-
Development of lentiviral vectors for antiangiogenic gene delivery
-
Shichinoche T, Bochner BH, Mizutani K, Nishida M, Hegerich-Gilliam S, Naldini L, Kasohara N. Development of lentiviral vectors for antiangiogenic gene delivery. Cancer Gene Ther 2001; 8: 879-89.
-
(2001)
Cancer Gene Ther
, vol.8
, pp. 879-889
-
-
Shichinoche, T.1
Bochner, B.H.2
Mizutani, K.3
Nishida, M.4
Hegerich-Gilliam, S.5
Naldini, L.6
Kasohara, N.7
-
25
-
-
0036207552
-
Lentiviral gene transduction of kidney
-
Gusella GL, Federova E, Hanss B, Marras D, Klotman ME, Klotman PE. Lentiviral gene transduction of kidney. Hum Gene Ther 2002; 13: 407-14.
-
(2002)
Hum Gene Ther
, vol.13
, pp. 407-414
-
-
Gusella, G.L.1
Federova, E.2
Hanss, B.3
Marras, D.4
Klotman, M.E.5
Klotman, P.E.6
-
27
-
-
0035797863
-
Magnetic resonance imaging permits in vivo monitoring of catheter-based vascular gene delivery
-
Yang X, Atalar E, Li D, Serfaty JM, Wang D, Kumar A, Cheng L. Magnetic resonance imaging permits in vivo monitoring of catheter-based vascular gene delivery. Circulation 2001; 104: 1588-90.
-
(2001)
Circulation
, vol.104
, pp. 1588-1590
-
-
Yang, X.1
Atalar, E.2
Li, D.3
Serfaty, J.M.4
Wang, D.5
Kumar, A.6
Cheng, L.7
-
28
-
-
0035572944
-
Sustainable systemic delivery via a single injection of lentivirus into human skin tissue
-
Baek SC, Lin Q, Robbins PB, Fan H, Khavari PA. Sustainable systemic delivery via a single injection of lentivirus into human skin tissue. Hum Gene Ther 2001; 12: 1551-8.
-
(2001)
Hum Gene Ther
, vol.12
, pp. 1551-1558
-
-
Baek, S.C.1
Lin, Q.2
Robbins, P.B.3
Fan, H.4
Khavari, P.A.5
-
29
-
-
0034759534
-
Lentiviral vectors approach the clinic but fall back: National Institutes of Health Recombinant DNA Advisory Committee review of a first clinical protocol for use of a lentiviral vector
-
Podsakoff GM. Lentiviral vectors approach the clinic but fall back: National Institutes of Health Recombinant DNA Advisory Committee review of a first clinical protocol for use of a lentiviral vector. Mol Ther 2001; 4: 282-3.
-
(2001)
Mol Ther
, vol.4
, pp. 282-283
-
-
Podsakoff, G.M.1
-
30
-
-
0035661288
-
Lentivirus in the clinic. To the editor
-
Dropulic B. Lentivirus in the clinic. To the editor. Mol Ther 2001; 4: 511-2.
-
(2001)
Mol Ther
, vol.4
, pp. 511-512
-
-
Dropulic, B.1
-
31
-
-
0034724857
-
Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease
-
Cavazzana-Calvo M, Hacein-Bey S, de Saint Basile G, Gross F, Yvon E, Nusbaum P, Selz F, Hue C, Certain S, Casanova JL, Bousso P, Deist FL, Fischer A. Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease. Science 2000; 288: 669-72.
-
(2000)
Science
, vol.288
, pp. 669-672
-
-
Cavazzana-Calvo, M.1
Hacein-Bey, S.2
De Saint Basile, G.3
Gross, F.4
Yvon, E.5
Nusbaum, P.6
Selz, F.7
Hue, C.8
Certain, S.9
Casanova, J.L.10
Bousso, P.11
Deist, F.L.12
Fischer, A.13
-
32
-
-
0034049809
-
Gene therapy for human SCID: Dreams become reality
-
Buckley RH. Gene therapy for human SCID: dreams become reality. Nat Med 2000; 6: 623-4.
-
(2000)
Nat Med
, vol.6
, pp. 623-624
-
-
Buckley, R.H.1
-
33
-
-
0037020112
-
Gene therapy a suspect in leukemia-like disease
-
Marshall E. Gene therapy a suspect in leukemia-like disease. Science 2002; 298: 34-5.
-
(2002)
Science
, vol.298
, pp. 34-35
-
-
Marshall, E.1
-
34
-
-
0037136924
-
Gene therapy for SCID-a complication after remarkable progress
-
Buckley RH. Gene therapy for SCID-a complication after remarkable progress. Lancet 2002; 360: 1185-6.
-
(2002)
Lancet
, vol.360
, pp. 1185-1186
-
-
Buckley, R.H.1
-
35
-
-
0037461732
-
Second cancer case halts gene-therapy trials
-
Check E. Second cancer case halts gene-therapy trials. Nature 2003; 421: 305.
-
(2003)
Nature
, vol.421
, pp. 305
-
-
Check, E.1
-
36
-
-
0141728485
-
Gene transfer in experimental medicine
-
in press
-
Romano, G. Gene transfer in experimental medicine. Drug News Perspect (in press).
-
Drug News Perspect
-
-
Romano, G.1
-
37
-
-
0037448343
-
Risks and benefits of gene therapy
-
Noguchi P. Risks and benefits of gene therapy. N Engl J Med 2003; 348: 193-4.
-
(2003)
N Engl J Med
, vol.348
, pp. 193-194
-
-
Noguchi, P.1
-
38
-
-
0033118161
-
The effect of chromosomal translocations in acute leukemias: The LMO2 paradigm in transcription and development
-
Rabbitts TH, Bucher K, Chung G, Grutz G, Warren A, Yamada Y. The effect of chromosomal translocations in acute leukemias: the LMO2 paradigm in transcription and development. Cancer Res 1999; 59: Suppl: 1794s-8s.
-
(1999)
Cancer Res
, vol.59
, Issue.SUPPL.
-
-
Rabbitts, T.H.1
Bucher, K.2
Chung, G.3
Grutz, G.4
Warren, A.5
Yamada, Y.6
-
39
-
-
0036893743
-
Risks ond benefits of gene therapy for immunodeficiency: A reality check
-
Lemoine NR. Risks ond benefits of gene therapy for immunodeficiency: a reality check. Gene Ther 2002; 9: 1561-2.
-
(2002)
Gene Ther
, vol.9
, pp. 1561-1562
-
-
Lemoine, N.R.1
-
40
-
-
0034646513
-
HIV-1 genome nuclear impart is mediated by a central DNA flap
-
Zennou V, Petit C, Guetard D, Nerhbass U, Montognier L, Charneau P. HIV-1 genome nuclear impart is mediated by a central DNA flap. Cell 2000; 101: 173-85.
-
(2000)
Cell
, vol.101
, pp. 173-185
-
-
Zennou, V.1
Petit, C.2
Guetard, D.3
Nerhbass, U.4
Montognier, L.5
Charneau, P.6
-
41
-
-
0034124547
-
HIV nuclear impart: What's the flap?
-
Stevenson M. HIV nuclear impart: What's the flap? Nat Med 2000; 6: 626-8.
-
(2000)
Nat Med
, vol.6
, pp. 626-628
-
-
Stevenson, M.1
-
42
-
-
0346132122
-
Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cells
-
Yu SF, von Ruden T, Kantoff PW, Garber C, Seiberg M, Ruther U, Anderson WF, Wagner EF, Gilboa E. Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cells. Proc Natl Acad Sci USA 1986; 83: 3194-8.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 3194-3198
-
-
Yu, S.F.1
Von Ruden, T.2
Kantoff, P.W.3
Garber, C.4
Seiberg, M.5
Ruther, U.6
Anderson, W.F.7
Wagner, E.F.8
Gilboa, E.9
-
43
-
-
0035915983
-
Gene transfer systems derived from Visna virus: Analysis of virus production and infectivity
-
Berkowitz RD, Ilves H, Plavec I, Veres G. Gene transfer systems derived from Visna virus: analysis of virus production and infectivity. Virology 2001; 279: 116-29.
-
(2001)
Virology
, vol.279
, pp. 116-129
-
-
Berkowitz, R.D.1
Ilves, H.2
Plavec, I.3
Veres, G.4
-
44
-
-
0036147521
-
Comparison of gene transfer efficiency and gene expression levels achieved with equine infectious anemia virus- and human immunodeficiency virus type 1-derived lentivirus vectors
-
O'Rourke JP, Newbound GC, Kohn DB, Olsen JC, Bunnell BA. Comparison of gene transfer efficiency and gene expression levels achieved with equine infectious anemia virus- and human immunodeficiency virus type 1-derived lentivirus vectors. J Virol 2002; 76: 1510-5.
-
(2002)
J Virol
, vol.76
, pp. 1510-1515
-
-
O'Rourke, J.P.1
Newbound, G.C.2
Kohn, D.B.3
Olsen, J.C.4
Bunnell, B.A.5
-
45
-
-
0033029635
-
Minimum requirement for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors
-
Johnston JC, Gasmi M, Lim LE, Elder JH, Yee JK, Jolly DJ, Campbell KP, Davidson BL, Sauter SL. Minimum requirement for efficient transduction of dividing and nondividing cells by feline immunodeficiency virus vectors. J Virol 1999; 73: 4991-5000.
-
(1999)
J Virol
, vol.73
, pp. 4991-5000
-
-
Johnston, J.C.1
Gasmi, M.2
Lim, L.E.3
Elder, J.H.4
Yee, J.K.5
Jolly, D.J.6
Campbell, K.P.7
Davidson, B.L.8
Sauter, S.L.9
-
46
-
-
0033404760
-
Bad for cats, good for humans? Modified immunodeficiency virus for gene delivery
-
Crystal RG. Bad for cats, good for humans? Modified immunodeficiency virus for gene delivery. J Clin Invest 1999; 104: 1491-3.
-
(1999)
J Clin Invest
, vol.104
, pp. 1491-1493
-
-
Crystal, R.G.1
-
47
-
-
0036374935
-
Development of second and third generation bovine immunodeficiency virus based gene transfer systems
-
Matukanis M, Li M, Molina RP, Paszkiet B, Kaleko M, Luo T. Development of second and third generation bovine immunodeficiency virus based gene transfer systems. Hum Gene Ther 2002; 13: 1293-303.
-
(2002)
Hum Gene Ther
, vol.13
, pp. 1293-1303
-
-
Matukanis, M.1
Li, M.2
Molina, R.P.3
Paszkiet, B.4
Kaleko, M.5
Luo, T.6
-
48
-
-
0033428995
-
Feline immunodeficiency virus vectors persistently transduce nondividing airway epithelia and correct the cystic fibrosis defect
-
Wang G, Slepushkin V, Zabner J, Keshaviee S, Johnston JC, Sauter SL, Jolly DJ, Dubensky TW, Davidson BL, McCray PB. Feline immunodeficiency virus vectors persistently transduce nondividing airway epithelia and correct the cystic fibrosis defect. J Clin Invest 1999; 104: R55-62.
-
(1999)
J Clin Invest
, vol.104
-
-
Wang, G.1
Slepushkin, V.2
Zabner, J.3
Keshaviee, S.4
Johnston, J.C.5
Sauter, S.L.6
Jolly, D.J.7
Dubensky, T.W.8
Davidson, B.L.9
McCray, P.B.10
-
49
-
-
18344368012
-
Functional correction of established central nervous system deficits in an animal model of lysosomal storage disease with feline immunodeficiency virs-based vectors
-
Brooks AI, Stein CS, Hughes SM, Heth J, McCray PM, Sauter SL, Johnston JC, Cory-Slechta DA, Federoff HJ, Davidson BL. Functional correction of established central nervous system deficits in an animal model of lysosomal storage disease with feline immunodeficiency virs-based vectors. Proc Natl Acad Sci USA 2002; 99: 6216-21.
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 6216-6221
-
-
Brooks, A.I.1
Stein, C.S.2
Hughes, S.M.3
Heth, J.4
McCray, P.M.5
Sauter, S.L.6
Johnston, J.C.7
Cory-Slechta, D.A.8
Federoff, H.J.9
Davidson, B.L.10
-
50
-
-
0036204263
-
Gene transfer to the nonhuman primate retina with recombinant feline immunodeficiency virus vectors
-
Lotery AJ, Derksen TA, Russell SR, Mullins RF, Sauter S, Affatigato LM, Stone EM, Davidson BL. Gene transfer to the nonhuman primate retina with recombinant feline immunodeficiency virus vectors. Hum Gene Ther 2002; 13: 689-96
-
(2002)
Hum Gene Ther
, vol.13
, pp. 689-696
-
-
Lotery, A.J.1
Derksen, T.A.2
Russell, S.R.3
Mullins, R.F.4
Sauter, S.5
Affatigato, L.M.6
Stone, E.M.7
Davidson, B.L.8
-
51
-
-
0034781791
-
Rabies virus glycoprotein pseudotyping of lentiviral vectors enables retrograde axonal transport and access to the nervous system after peripheral delivery
-
Mazarakis ND, Azzouz M, Rohll JB, Ellard FM, Wilkes FJ, Olsen AL, Carter EE, Barber RD, Baban DF, Kingsman SM, Kingsman AJ, O'Malley K, Mitrophanous KA. Rabies virus glycoprotein pseudotyping of lentiviral vectors enables retrograde axonal transport and access to the nervous system after peripheral delivery. Hum Mol Genet 2001; 10: 2109-21.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2109-2121
-
-
Mazarakis, N.D.1
Azzouz, M.2
Rohll, J.B.3
Ellard, F.M.4
Wilkes, F.J.5
Olsen, A.L.6
Carter, E.E.7
Barber, R.D.8
Baban, D.F.9
Kingsman, S.M.10
Kingsman, A.J.11
O'Malley, K.12
Mitrophanous, K.A.13
-
52
-
-
0036376655
-
Sustained transduction of ocular cells with a bovine immunodeficiency viral vector
-
Takahashi K, Luo T., Saishin Y, Saishin Y, Sung J, Hackett S, Brazzell RK, Kaleko M, Campochiaro PA. Sustained transduction of ocular cells with a bovine immunodeficiency viral vector. Hum Gene Ther 13: 1305-16.
-
Hum Gene Ther
, vol.13
, pp. 1305-1316
-
-
Takahashi, K.1
Luo, T.2
Saishin, Y.3
Saishin, Y.4
Sung, J.5
Hackett, S.6
Brazzell, R.K.7
Kaleko, M.8
Campochiaro, P.A.9
-
53
-
-
0033539613
-
An ancient family of human endogenous retroviruses encodes a functional homolog of the HIV-1 Rev protein
-
Yang J, Bogerd HP, Peng S, Wiegand H, Truant R, Cullen BR. An ancient family of human endogenous retroviruses encodes a functional homolog of the HIV-1 Rev protein. Proc Natl Acad Sci USA 1999; 96: 13404-8.
-
(1999)
Proc Natl Acad Sci USA
, vol.96
, pp. 13404-13408
-
-
Yang, J.1
Bogerd, H.P.2
Peng, S.3
Wiegand, H.4
Truant, R.5
Cullen, B.R.6
-
54
-
-
0029938821
-
The viruses in all of us: Characteristics and biological significance of human endogenous retrovirus sequences
-
Lower R, Lower J, Kurth R. The viruses in all of us: characteristics and biological significance of human endogenous retrovirus sequences. Proc Natl Acad Sci USA 1996; 93: 5177-84.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 5177-5184
-
-
Lower, R.1
Lower, J.2
Kurth, R.3
-
55
-
-
0033819512
-
Mutational definition of functional domains within the Rev homolog encoded by human endogenous retrovirus K
-
Bogerd HP, Wiegand HL, Yang J, Cullen BR. Mutational definition of functional domains within the Rev homolog encoded by human endogenous retrovirus K. J Virol 2000; 74: 9353-61.
-
(2000)
J Virol
, vol.74
, pp. 9353-9361
-
-
Bogerd, H.P.1
Wiegand, H.L.2
Yang, J.3
Cullen, B.R.4
-
56
-
-
0031751113
-
Beneficial role of human endogenous retroviruses: Facts and hypothesis
-
Larsson E, Anderson G. Beneficial role of human endogenous retroviruses: facts and hypothesis. Scand J Immunol 1998; 48: 329-38.
-
(1998)
Scand J Immunol
, vol.48
, pp. 329-338
-
-
Larsson, E.1
Anderson, G.2
-
58
-
-
0030960338
-
Inactivation of the human immunodeficiency virus type 1 inhibitory elements allows Rev-independent expression of gag and Gag/protease and partcle formation
-
Schneider R, Campbell M, Nasioulas G, Felber BK, Pavlakis GN. Inactivation of the human immunodeficiency virus type 1 inhibitory elements allows Rev-independent expression of gag and Gag/protease and partcle formation. J Virol 1997; 71: 4892-903.
-
(1997)
J Virol
, vol.71
, pp. 4892-4903
-
-
Schneider, R.1
Campbell, M.2
Nasioulas, G.3
Felber, B.K.4
Pavlakis, G.N.5
-
59
-
-
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 VN, Kingsman AJ, Kingsman SM, Mitrophanous KA. A Rev-independent human immunodeficiency virus type 1 (HIV-1)-based vector that exploits a codon-optimized HIV-1 gag-pol gene. J Virol 2000; 74: 4839-52.
-
(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
-
60
-
-
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., Graf M, Bieler K, Wolf H, Grunwald T, Foley P, Uberla K, 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 2000; 11: 2403-13.
-
(2000)
Hum Gene Ther
, vol.11
, pp. 2403-2413
-
-
Wagner, R.1
Graf, M.2
Bieler, K.3
Wolf, H.4
Grunwald, T.5
Foley, P.6
Uberla, K.7
-
61
-
-
0032798121
-
Gene transfer technology in therapy: Current applications and future goals
-
Romano G, Pacilio C, Giordano A. Gene transfer technology in therapy: current applications and future goals. Stem Cells 1999; 17: 191-202.
-
(1999)
Stem Cells
, vol.17
, pp. 191-202
-
-
Romano, G.1
Pacilio, C.2
Giordano, A.3
-
62
-
-
0035970312
-
Packaging cell line DNA contamination of vector supernatants: Implication for laboratory and clinical research
-
Chen J, Reeves L, Sanburn N, Croop J, Williams DA, Cornetta K. Packaging cell line DNA contamination of vector supernatants: implication for laboratory and clinical research. Virology 2001; 282: 186-97.
-
(2001)
Virology
, vol.282
, pp. 186-197
-
-
Chen, J.1
Reeves, L.2
Sanburn, N.3
Croop, J.4
Williams, D.A.5
Cornetta, K.6
-
63
-
-
17344367454
-
Evaluating the potential of germ line transmission after intravenous administration of recombinant adenovirus in the C3H mouse
-
Ye X, Gao GP, Pabin C, Raper SE, Wilson JM. Evaluating the potential of germ line transmission after intravenous administration of recombinant adenovirus in the C3H mouse. Hum Gene Ther 1998; 9: 2135-42.
-
(1998)
Hum Gene Ther
, vol.9
, pp. 2135-2142
-
-
Ye, X.1
Gao, G.P.2
Pabin, C.3
Raper, S.E.4
Wilson, J.M.5
|