-
1
-
-
0037189401
-
Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning
-
Aiuti A, Slavin S, Aker M, et al. Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning. Science 2002; 296: 2410-2413.
-
(2002)
Science
, vol.296
, pp. 2410-2413
-
-
Aiuti, A.1
Slavin, S.2
Aker, M.3
-
3
-
-
0028807727
-
T lymphocyte-directed gene therapy for ADA-SCID: Initial trial results after 4 years
-
Blaese RM, Culver KW, Miller AD, et al. T lymphocyte-directed gene therapy for ADA-SCID: initial trial results after 4 years. Science 2002; 270: 475-480.
-
(2002)
Science
, vol.270
, pp. 475-480
-
-
Blaese, R.M.1
Culver, K.W.2
Miller, A.D.3
-
4
-
-
0142084745
-
LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1
-
Hacein-Bey-Abina S, Von Kalle C, Schmidt M, et al. LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1. Science 2003; 302: 415-419.
-
(2003)
Science
, vol.302
, pp. 415-419
-
-
Hacein-Bey-Abina, S.1
Von Kalle, C.2
Schmidt, M.3
-
5
-
-
0036632178
-
RNA 3′ readthrough of oncoretrovirus and lentivirus: Implications for safety and efficacy
-
Zaiss A-K, Son S, Chang L-J. RNA 3′ readthrough of oncoretrovirus and lentivirus: implications for safety and efficacy. J Virol 2002; 76: 7209-7219.
-
(2002)
J. Virol.
, vol.76
, pp. 7209-7219
-
-
Zaiss, A.-K.1
Son, S.2
Chang, L.-J.3
-
6
-
-
0030913366
-
Quantification of latent tissue reservoirs and total body viral load in HfV-1 infection
-
Chun TW, Carruth L, Finzi D, et al. Quantification of latent tissue reservoirs and total body viral load in HfV-1 infection. Nature 1997; 387: 183-188.
-
(1997)
Nature
, vol.387
, pp. 183-188
-
-
Chun, T.W.1
Carruth, L.2
Finzi, D.3
-
7
-
-
0026503596
-
Acquired immunodeficiency syndrome-associated T-cell lymphoma: Evidence for human immunodeficiency virus type 1-associated T-cell transformation
-
Herndier BG, Shiramizu BT, Jewett NE, Aldape KD, Reyes GR, McGrath MS. Acquired immunodeficiency syndrome-associated T-cell lymphoma: evidence for human immunodeficiency virus type 1-associated T-cell transformation. Blood 1992; 79: 1768-1774.
-
(1992)
Blood
, vol.79
, pp. 1768-1774
-
-
Herndier, B.G.1
Shiramizu, B.T.2
Jewett, N.E.3
Aldape, K.D.4
Reyes, G.R.5
McGrath, M.S.6
-
8
-
-
0032849062
-
Search for the mechanism of genetic variation in the pro gene of human immunodeficiency virus
-
Rouzine IM, Coffin JM. Search for the mechanism of genetic variation in the pro gene of human immunodeficiency virus. J Virol 1999; 73: 8167-8178.
-
(1999)
J. Virol.
, vol.73
, pp. 8167-8178
-
-
Rouzine, I.M.1
Coffin, J.M.2
-
9
-
-
0029993858
-
Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector
-
(1996)
-
Naldini L, Blomer U, Gage FH, Trono D, Verma IM. (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 U S A 1996; 93: 11 382-11 388.
-
(1996)
Proc. Natl. Acad. Sci. U S A
, vol.93
, pp. 11382-11388
-
-
Naldini, L.1
Blomer, U.2
Gage, F.H.3
Trono, D.4
Verma, I.M.5
-
10
-
-
0036682975
-
Lentiviral vectors containing the human immunodeficiency virus type-1 central polypurine tract can efficiently transduce nondividing hepatocytes and antigen-presenting cells in vivo
-
VandenDriessche T, Thorrez L, Naldini L, et al. Lentiviral vectors containing the human immunodeficiency virus type-1 central polypurine tract can efficiently transduce nondividing hepatocytes and antigen-presenting cells in vivo. Blood 2002; 100: 813-822.
-
(2002)
Blood
, vol.100
, pp. 813-822
-
-
VandenDriessche, T.1
Thorrez, L.2
Naldini, L.3
-
11
-
-
0034672356
-
The human immunodeficiency virus type-1 central DNA flap is a crucial determinant for lentiviral nuclear import and gene transduction of human hematopoetic cells
-
Sirven AL, Pflumio F, Zennou V, et al. The human immunodeficiency virus type-1 central DNA flap is a crucial determinant for lentiviral nuclear import and gene transduction of human hematopoetic cells. Blood 2000; 96: 4103-4110.
-
(2000)
Blood
, vol.96
, pp. 4103-4110
-
-
Sirven, A.L.1
Pflumio, F.2
Zennou, V.3
-
12
-
-
0024443873
-
HIV-1 Gag mutants can dominantly interfere with the replication of the wild-type virus
-
Trono D, Feinberg MB, Baltimore D. HIV-1 Gag mutants can dominantly interfere with the replication of the wild-type virus. Cell 1989; 59: 113-120.
-
(1989)
Cell
, vol.59
, pp. 113-120
-
-
Trono, D.1
Feinberg, M.B.2
Baltimore, D.3
-
13
-
-
0029996147
-
In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector
-
Naldini L, Blomer U, Gallay P, et al. In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 1996; 272: 263-267.
-
(1996)
Science
, vol.272
, pp. 263-267
-
-
Naldini, L.1
Blomer, U.2
Gallay, P.3
-
14
-
-
0036199631
-
Transcriptional targeting of lentiviral vectors by long terminal repeat enhancer replacement
-
Lotti F, Menguzzato E, Rossi C, et al. Transcriptional targeting of lentiviral vectors by long terminal repeat enhancer replacement. J Virol 2002; 76: 3996-4007.
-
(2002)
J. Virol.
, vol.76
, pp. 3996-4007
-
-
Lotti, F.1
Menguzzato, E.2
Rossi, C.3
-
16
-
-
0034988922
-
Generation of a stable cell line producing high-titer self-inactivating lentiviral vectors
-
Xu K, Ma H, McCown TJ, Verma IM, Kafri T. Generation of a stable cell line producing high-titer self-inactivating lentiviral vectors. Mol Ther 2001; 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
-
17
-
-
0035949704
-
Delivery of the cre recombinase by a self-deleting lentiviral vector: Efficient gene targeting in vivo
-
Pfeifer A, Brandon EP, Kootstra N, Gage FH, Verma IM. Delivery of the cre recombinase by a self-deleting lentiviral vector: efficient gene targeting in vivo. Proc Natl Acad Sci U S A 2001; 98: 11450-11455.
-
(2001)
Proc. Natl. Acad. Sci. U S A
, vol.98
, pp. 11450-11455
-
-
Pfeifer, A.1
Brandon, E.P.2
Kootstra, N.3
Gage, F.H.4
Verma, I.M.5
-
18
-
-
0034646513
-
HIV-1 genome nuclear import is mediated by a central DNA flap
-
Zennou V, Petit C, Guetard D, Nerhbass U, Montagnier L, Charneau P. HIV-1 genome nuclear import is mediated by a central DNA flap. Cell 2001; 101: 173-185.
-
(2001)
Cell
, vol.101
, pp. 173-185
-
-
Zennou, V.1
Petit, C.2
Guetard, D.3
Nerhbass, U.4
Montagnier, L.5
Charneau, P.6
-
19
-
-
0026051132
-
Gene transfer into human lymphocytes by a defective human immunodeficiency virus type 1 vector
-
Poznansky M, Lever A, Bergeron L, Haseltine W, Sodroski J. Gene transfer into human lymphocytes by a defective human immunodeficiency virus type 1 vector. J Virol 1991; 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
-
20
-
-
0029764099
-
A conditionally replicating HIV-1 vector interferes with wild type HIV-1 replication and spread
-
Dropulic B, Hermanokova M, Pitha PM. A conditionally replicating HIV-1 vector interferes with wild type HIV-1 replication and spread. Proc Natl Acad Sci U S A 1996; 93: 11103-11108.
-
(1996)
Proc. Natl. Acad. Sci. U S A
, vol.93
, pp. 11103-11108
-
-
Dropulic, B.1
Hermanokova, M.2
Pitha, P.M.3
-
21
-
-
0036290645
-
Lentiviral transduction of human T-lymphocytes with a RANTES intrakine inhibits human immunodeficiency virus type 1 infection
-
Schroers R, Davis CM, Wagner H-J, Chen S-Y. Lentiviral transduction of human T-lymphocytes with a RANTES intrakine inhibits human immunodeficiency virus type 1 infection. Gene Ther 2002; 9 889-897.
-
(2002)
Gene Ther.
, vol.9
, pp. 889-897
-
-
Schroers, R.1
Davis, C.M.2
Wagner, H.-J.3
Chen, S.-Y.4
-
22
-
-
0036294019
-
Enhanced inhibition of human immunodeficiency virus type 1 replication by novel lentiviral vectors expressing human immunodeficiency virus type 1 envelope antisense RNA
-
Mautino MR, Morgan RA. Enhanced inhibition of human immunodeficiency virus type 1 replication by novel lentiviral vectors expressing human immunodeficiency virus type 1 envelope antisense RNA. Hum Gene Ther 2002; 13: 1027-1037.
-
(2002)
Hum. Gene Ther.
, vol.13
, pp. 1027-1037
-
-
Mautino, M.R.1
Morgan, R.A.2
-
23
-
-
6844248803
-
A virus model for examining the intracellular efficiency of a ribozyme targeted to HrV-1
-
Dropulic B, Jeang K-T. A virus model for examining the intracellular efficiency of a ribozyme targeted to HrV-1. Methods Enzymol 1993; 5: 43-49.
-
(1993)
Methods Enzymol.
, vol.5
, pp. 43-49
-
-
Dropulic, B.1
Jeang, K.-T.2
-
24
-
-
13644261398
-
-
Available
-
Available: http://www.fda.gov/ohrms/dockets/ac/01/briefing/3794b3.htm.
-
-
-
-
25
-
-
0035513970
-
Clinical protocol. A phase I open-label clinical trial of the safety and tolerability of single escalating doses of autologous CD4 T cells transduced with VRX496 in HIV-positive subjects
-
MacGregor RR. Clinical protocol. A phase I open-label clinical trial of the safety and tolerability of single escalating doses of autologous CD4 T cells transduced with VRX496 in HIV-positive subjects. Hum Gene Ther 2001; 12: 2028-2029.
-
(2001)
Hum. Gene Ther.
, vol.12
, pp. 2028-2029
-
-
MacGregor, R.R.1
-
26
-
-
0022495870
-
Production of acquired immunodeficiency syndrome-associated retrovirus in human and nonhuman cells transfected with an infectious molecular clone
-
Adachi A, Gendelman HE, Koenig S, et al. Production of acquired immunodeficiency syndrome-associated retrovirus in human and nonhuman cells transfected with an infectious molecular clone. J Virol 1986; 59: 284-291.
-
(1986)
J. Virol.
, vol.59
, pp. 284-291
-
-
Adachi, A.1
Gendelman, H.E.2
Koenig, S.3
-
27
-
-
33846430437
-
Large-scale purification of a lentiviral vector by size exclusion chromatography or mustang Q ion exchange capsule
-
Sep/Oct
-
Slepushkin V, Chang N, Cohen R, et al. Large-scale purification of a lentiviral vector by size exclusion chromatography or mustang Q ion exchange capsule. Bioproc J 2003; Sep/Oct: 89-95.
-
(2003)
Bioproc. J.
, pp. 89-95
-
-
Slepushkin, V.1
Chang, N.2
Cohen, R.3
-
28
-
-
2642579534
-
QC release testing of an HIV-1 based lentiviral vector lot and transduced cellular product
-
Jul/Aug
-
Schonely K, Afable C, Slepushkin V, et al. QC release testing of an HIV-1 based lentiviral vector lot and transduced cellular product. Bioproc J 2003; Jul/Aug: 39-47.
-
(2003)
Bioproc. J.
, pp. 39-47
-
-
Schonely, K.1
Afable, C.2
Slepushkin, V.3
-
29
-
-
0038333587
-
Continuous high-titer HIV-1 vector production
-
Ikeda Y, Tekeuchi Y, Martin F, Cosset FL, Mitrophanous K, Collins M. Continuous high-titer HIV-1 vector production. Nat Biotechnol 2002; 21: 569-572.
-
(2002)
Nat. Biotechnol.
, vol.21
, pp. 569-572
-
-
Ikeda, Y.1
Tekeuchi, Y.2
Martin, F.3
Cosset, F.L.4
Mitrophanous, K.5
Collins, M.6
-
30
-
-
0024448572
-
Sequences required for self-catalysed cleavage of the satellite RNA of tobacco ringspot virus
-
Haseloff J, Gerlach WL. Sequences required for self-catalysed cleavage of the satellite RNA of tobacco ringspot virus. Gene 1989; 82: 43-52.
-
(1989)
Gene
, vol.82
, pp. 43-52
-
-
Haseloff, J.1
Gerlach, W.L.2
-
31
-
-
3042735441
-
Efficient lentiviral vector-mediated control of HIV-1 replication in CD4 T lymphocytes from diverse HIV+ infected patients grouped according to CD4 count and viral load
-
in press
-
Humeau L, Binder G, Lu X, et al. Efficient lentiviral vector-mediated control of HIV-1 replication in CD4 T lymphocytes from diverse HIV+ infected patients grouped according to CD4 count and viral load. Mol Ther; in press.
-
Mol. Ther.
-
-
Humeau, L.1
Binder, G.2
Lu, X.3
-
32
-
-
3042731708
-
Antisense-mediated inhibition of HIV replication using an HIV-1-based vector results in severely attenuated mutants incapable of developing resistance
-
in press
-
Lu X, Yu Q, Binder G, et al. Antisense-mediated inhibition of HIV replication using an HIV-1-based vector results in severely attenuated mutants incapable of developing resistance. J Virol 2004; in press.
-
(2004)
J. Virol.
-
-
Lu, X.1
Yu, Q.2
Binder, G.3
-
33
-
-
0036425611
-
A human immunodeficiency virus type 1 pol gene-derived sequence (cPPT/CTS) increases the efficiency of transduction of human nondividing monocytes and T lymphocytes by lentiviral vectors
-
Manganini M, Serafini M, Barnbacioni F, et al. A human immunodeficiency virus type 1 pol gene-derived sequence (cPPT/CTS) increases the efficiency of transduction of human nondividing monocytes and T lymphocytes by lentiviral vectors. Hum Gene Ther 2002; 13 1793-1807.
-
(2002)
Hum. Gene Ther.
, vol.13
, pp. 1793-1807
-
-
Manganini, M.1
Serafini, M.2
Barnbacioni, F.3
-
34
-
-
0034120890
-
Gene transfer into stimulated and unstimulated T lymphocytes by HIV-1-derived lentiviral vectors
-
Costello E, Munoz M, Buetti E, Meylan PRA, Diggelmann H, Thali M. Gene transfer into stimulated and unstimulated T lymphocytes by HIV-1-derived lentiviral vectors. Gene Ther 2000; 7: 596-604.
-
(2000)
Gene Ther.
, vol.7
, pp. 596-604
-
-
Costello, E.1
Munoz, M.2
Buetti, E.3
Meylan, P.R.A.4
Diggelmann, H.5
Thali, M.6
-
35
-
-
0032477912
-
Enhanced T cell engraftment after retroviral delivery of an antiviral gene in HIV-infected individuals
-
Ranga U, Woffendin C, Verma S, et al. Enhanced T cell engraftment after retroviral delivery of an antiviral gene in HIV-infected individuals. Proc Natl Acad Sci U S A 1998; 95: 1201-1206.
-
(1998)
Proc. Natl. Acad. Sci. U S A
, vol.95
, pp. 1201-1206
-
-
Ranga, U.1
Woffendin, C.2
Verma, S.3
-
36
-
-
0034254611
-
+ T cells in human immunodeficiency virus-infected subjects
-
+ T cells in human immunodeficiency virus-infected subjects. Blood 2000; 96: 785-792.
-
(2000)
Blood
, vol.96
, pp. 785-792
-
-
Mitsuyasu, R.T.1
Anton, P.A.2
Deeks, S.G.3
-
37
-
-
0034040751
-
Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences
-
Follenzi A, Ailles LE, Bakovic S, Genua N, Naldini L. Gene transfer by lentiviral vectors is limited by nuclear translocation and rescued by HIV-1 pol sequences. Nat Genet 2000; 25: 217-222.
-
(2000)
Nat. Genet.
, vol.25
, pp. 217-222
-
-
Follenzi, A.1
Ailles, L.E.2
Bakovic, S.3
Genua, N.4
Naldini, L.5
-
38
-
-
0037481021
-
Human T lymphocytes transduced by lentiviral vectors in the absence of TCR-activation maintain an intact immune competence
-
Cavalieri S, Cazzaniga S, Geuna M, et al. Human T lymphocytes transduced by lentiviral vectors in the absence of TCR-activation maintain an intact immune competence. Blood 2003; 102: 497-505.
-
(2003)
Blood
, vol.102
, pp. 497-505
-
-
Cavalieri, S.1
Cazzaniga, S.2
Geuna, M.3
|