-
1
-
-
0026512501
-
Autologous transplantation of canine long-term marrow culture cells genetically marked by retroviral vectors
-
Carter RF, Abrams-Ogg AC, Dick JE et al. Autologous transplantation of canine long-term marrow culture cells genetically marked by retroviral vectors. Blood 1992;79:356-364.
-
(1992)
Blood
, vol.79
, pp. 356-364
-
-
Carter, R.F.1
Abrams-Ogg, A.C.2
Dick, J.E.3
-
2
-
-
16144365969
-
Identification of primitive human hematopoietic cells capable of repopulating NOD/SCID mouse bone marrow: Implications for gene therapy
-
Larochelle A, Vormoor J, Hanenberg H et al. Identification of primitive human hematopoietic cells capable of repopulating NOD/SCID mouse bone marrow: implications for gene therapy. Nat Med 1996;2:1329-1337.
-
(1996)
Nat Med
, vol.2
, pp. 1329-1337
-
-
Larochelle, A.1
Vormoor, J.2
Hanenberg, H.3
-
3
-
-
0029055941
-
Analysis of optimal conditions for retroviral-mediated transduction of primitive human hematopoietic cells
-
Nolta JA, Smogorzewska EM, Kohn DB. Analysis of optimal conditions for retroviral-mediated transduction of primitive human hematopoietic cells. Blood 1995;86:101-110.
-
(1995)
Blood
, vol.86
, pp. 101-110
-
-
Nolta, J.A.1
Smogorzewska, E.M.2
Kohn, D.B.3
-
4
-
-
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 1995;270:475-480.
-
(1995)
Science
, vol.270
, pp. 475-480
-
-
Blaese, R.M.1
Culver, K.W.2
Miller, A.D.3
-
5
-
-
0028789792
-
Gene therapy in peripheral blood lymphocytes and bone marrow for ADA-immunodeficient patients
-
Bordignon C, Notarangelo LD, Nobili N et al. Gene therapy in peripheral blood lymphocytes and bone marrow for ADA-immunodeficient patients. Science 1995;270:470-475.
-
(1995)
Science
, vol.270
, pp. 470-475
-
-
Bordignon, C.1
Notarangelo, L.D.2
Nobili, N.3
-
6
-
-
0028822228
-
Systemic gene therapy: Biodistribution and long-term expression of a transgene in mice
-
Thierry AR, Lunardi-Iskandar Y, Bryant JL et al. Systemic gene therapy: biodistribution and long-term expression of a transgene in mice. Proc Natl Acad Sci USA 1995;92:9742-9746.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 9742-9746
-
-
Thierry, A.R.1
Lunardi-Iskandar, Y.2
Bryant, J.L.3
-
7
-
-
0031058475
-
Recombinant adeno-associated virus mediates a high level of gene transfer but less efficient integration in the K562 human hematopoietic cell line
-
Malik P, McQuiston SA, Yu X-J et al. Recombinant adeno-associated virus mediates a high level of gene transfer but less efficient integration in the K562 human hematopoietic cell line. J Virol 1997;71:1776-1783.
-
(1997)
J Virol
, vol.71
, pp. 1776-1783
-
-
Malik, P.1
McQuiston, S.A.2
Yu, X.-J.3
-
8
-
-
0028170362
-
Prospects for the use of adeno-associated virus as a vector for human gene therapy
-
Kotin RM. Prospects for the use of adeno-associated virus as a vector for human gene therapy. Hum Gene Ther 1994;5:793-801.
-
(1994)
Hum Gene Ther
, vol.5
, pp. 793-801
-
-
Kotin, R.M.1
-
9
-
-
0028403237
-
Viral vector systems for gene therapy
-
Jolly D. Viral vector systems for gene therapy. Cancer Gen Ther 1994;1:51-64.
-
(1994)
Cancer Gen Ther
, vol.1
, pp. 51-64
-
-
Jolly, D.1
-
10
-
-
0028273185
-
Retrovirus-mediated gene transduction into canine peripheral blood repopulating cells
-
Kiem HP, Darovsky B, von Kalle C et al. Retrovirus-mediated gene transduction into canine peripheral blood repopulating cells. Blood 1994;83:1467-1473.
-
(1994)
Blood
, vol.83
, pp. 1467-1473
-
-
Kiem, H.P.1
Darovsky, B.2
Von Kalle, C.3
-
11
-
-
0026666055
-
Long-term expression of human adenosine deaminase in rhesus monkeys transplanted with retrovirus-infected bone-marrow cells
-
van Beusechem VW, Kukler A, Heidt PJ et al. Long-term expression of human adenosine deaminase in rhesus monkeys transplanted with retrovirus-infected bone-marrow cells. Proc Natl Acad Sci USA 1992;89:7640-7644.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 7640-7644
-
-
Van Beusechem, V.W.1
Kukler, A.2
Heidt, P.J.3
-
12
-
-
8944258557
-
+ cord blood cells is expressed by their T-cell progeny in the SCID-hu thymus
-
+ cord blood cells is expressed by their T-cell progeny in the SCID-hu thymus. Blood 1996;88:107-113.
-
(1996)
Blood
, vol.88
, pp. 107-113
-
-
Champseix, C.1
Marechal, V.2
Khazaal, I.3
-
13
-
-
0029068059
-
Retrovirally marked CD34-enriched peripheral blood and bone marrow cells contribute to long-term engraftment after autologous transplantation
-
Dunbar CE, Cottler Fox M, O'Shaughnessy JA et al. Retrovirally marked CD34-enriched peripheral blood and bone marrow cells contribute to long-term engraftment after autologous transplantation. Blood 1995;85:3048-3057.
-
(1995)
Blood
, vol.85
, pp. 3048-3057
-
-
Dunbar, C.E.1
Cottler Fox, M.2
O'Shaughnessy, J.A.3
-
14
-
-
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
-
15
-
-
0029857689
-
Targeting retrovirus entry
-
Cosset FL, Russel SJ. Targeting retrovirus entry. Gene Ther 1996;3:946-956.
-
(1996)
Gene Ther
, vol.3
, pp. 946-956
-
-
Cosset, F.L.1
Russel, S.J.2
-
16
-
-
0029872245
-
+ cells with a human immunodeficiency virus type-1 based retroviral vector pseudotyped with vesicular stomatitis virus envelope glycoprotein G
-
+ cells with a human immunodeficiency virus type-1 based retroviral vector pseudotyped with vesicular stomatitis virus envelope glycoprotein G. J Virol 1996;70:2581-2585.
-
(1996)
J Virol
, vol.70
, pp. 2581-2585
-
-
Akkina, R.K.1
Walton, R.M.2
Chen, M.L.3
-
17
-
-
0030271317
-
Strategies for targeted gene therapy
-
Harris JD, Lemoine NR. Strategies for targeted gene therapy. Trends Genet 1996;12:400-405.
-
(1996)
Trends Genet
, vol.12
, pp. 400-405
-
-
Harris, J.D.1
Lemoine, N.R.2
-
18
-
-
0028839609
-
High-titer packaging cells producing recombinant retroviruses resistant to human serum
-
Cosset FL, Takouchi Y, Battini JL et al. High-titer packaging cells producing recombinant retroviruses resistant to human serum. J Virol 1995;69:7430-7436.
-
(1995)
J Virol
, vol.69
, pp. 7430-7436
-
-
Cosset, F.L.1
Takouchi, Y.2
Battini, J.L.3
-
19
-
-
0029164582
-
Effects of retroviral vector design on expression of human adenosine deaminase in murine bone marrow transplant recipients engrafted with genetically modified cells
-
Riviere I, Brose K, Mulligan RC. Effects of retroviral vector design on expression of human adenosine deaminase in murine bone marrow transplant recipients engrafted with genetically modified cells. Proc Natl Acad Sci USA 1995;92:6733-6737.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 6733-6737
-
-
Riviere, I.1
Brose, K.2
Mulligan, R.C.3
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