-
1
-
-
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
-
2
-
-
0030477690
-
Efficient gene transfer by a human immunodeficiency virus type 1 (HIV-1)-derived vector utilizing a stable HIV packaging cell line
-
Corbeau P, Kraus G, Wong-Staal F. Efficient gene transfer by a human immunodeficiency virus type 1 (HIV-1)-derived vector utilizing a stable HIV packaging cell line. Proc Natl Acad Sci U S A. 1996;93:14070-14075.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 14070-14075
-
-
Corbeau, P.1
Kraus, G.2
Wong-Staal, F.3
-
3
-
-
0030716959
-
Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors
-
Kafri T, Blomer U, Peterson DA, Gage FH, Verma IM. Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors. Nat Genet. 1997;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
-
4
-
-
0031743608
-
Self-inactivating lentivirus vector for safe efficient in vivo gene delivery
-
Zufferey R, Dull T, Mendal RJ, et al. Self-inactivating lentivirus vector for safe efficient in vivo gene delivery. J Virol. 1998;72:9873-9880.
-
(1998)
J Virol
, vol.72
, pp. 9873-9880
-
-
Zufferey, R.1
Dull, T.2
Mendal, R.J.3
-
6
-
-
1842411367
-
Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector
-
Blomer U, Naldini L, Kafri T, Trono D, Verma IM, Gage FH. Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector. J Virol. 1997;71:6641-6649.
-
(1997)
J Virol
, vol.71
, pp. 6641-6649
-
-
Blomer, U.1
Naldini, L.2
Kafri, T.3
Trono, D.4
Verma, I.M.5
Gage, F.H.6
-
7
-
-
13044309472
-
Stable transduction of quiescent CD34(+)CD38(-) human hematopoietic cells by HIV-1-based lentiviral vectors
-
Case SS, Price MA, Jordan CT, et al. Stable transduction of quiescent CD34(+)CD38(-) human hematopoietic cells by HIV-1-based lentiviral vectors. Proc Natl Acad Sci U S A. 1999;96:2988-2993.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 2988-2993
-
-
Case, S.S.1
Price, M.A.2
Jordan, C.T.3
-
8
-
-
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 FH, Trono D, Verma IM. 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;93:11382-11388.
-
(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
-
-
0034688261
-
Lentiviral and Murine retroviral transduction of T-cells for expression of human CD40 ligand
-
Barry SC, Seppen J, Ramesh N, et al. Lentiviral and Murine retroviral transduction of T-cells for expression of human CD40 ligand. Hum Gene Ther. 2000;11:323-332.
-
(2000)
Hum Gene Ther
, vol.11
, pp. 323-332
-
-
Barry, S.C.1
Seppen, J.2
Ramesh, N.3
-
11
-
-
0033865631
-
Apical gene transfer into quiescent human and canine polarized intestinal epithelial cells by lentiviral vectors
-
Seppen J, Barry SC, Klingspoor JH, et al. Apical gene transfer into quiescent human and canine polarized intestinal epithelial cells by lentiviral vectors. J Virol. 2000;74:7642-7645.
-
(2000)
J Virol
, vol.74
, pp. 7642-7645
-
-
Seppen, J.1
Barry, S.C.2
Klingspoor, J.H.3
-
12
-
-
0028095020
-
A general method for the generation of high-titer, pantropic retroviral vectors: Highly efficient infection of primary hepatocytes
-
Yee J-K, Miyanohara A, LaPorte P, Bouic K, Burns JC, Friedmann T. A general method for the generation of high-titer, pantropic retroviral vectors: highly efficient infection of primary hepatocytes. Proc Natl Acad Sci U S A. 1994;91:9564-9568.
-
(1994)
Proc Natl Acad Sci U S A
, vol.91
, pp. 9564-9568
-
-
Yee, J.-K.1
Miyanohara, A.2
LaPorte, P.3
Bouic, K.4
Burns, J.C.5
Friedmann, T.6
-
13
-
-
0030586693
-
Use of cis- and trans-acting regulatory sequences to improve expression of human immunodeficiency virus vectors in human lymphocytes
-
Parolin C, Taddeo B, Palu G, Sodroski J. Use of cis- and trans-acting regulatory sequences to improve expression of human immunodeficiency virus vectors in human lymphocytes. Virology. 1996;222:415-422.
-
(1996)
Virology
, vol.222
, pp. 415-422
-
-
Parolin, C.1
Taddeo, B.2
Palu, G.3
Sodroski, J.4
-
14
-
-
0032520144
-
Infectivity enhancement by HIV-1 nef is dependent on the pathway of virus entry: Implications for HIV-based gene transfer systems
-
Luo T, Douglas JL, Livingston RL, Garcia JV. Infectivity enhancement by HIV-1 nef is dependent on the pathway of virus entry: implications for HIV-based gene transfer systems. Virology. 1998;241:224-233.
-
(1998)
Virology
, vol.241
, pp. 224-233
-
-
Luo, T.1
Douglas, J.L.2
Livingston, R.L.3
Garcia, J.V.4
-
15
-
-
0027049472
-
The molecular mechanism of erythropoietin action
-
Koury MJ, Bondurant MC. The molecular mechanism of erythropoietin action. Eur J Biochem. 1992;210:649-663.
-
(1992)
Eur J Biochem
, vol.210
, pp. 649-663
-
-
Koury, M.J.1
Bondurant, M.C.2
-
16
-
-
0034254356
-
Erythropoietin, iron, and erythropoiesis
-
Goodnough LT, Skikne B, Brugnara C. Erythropoietin, iron, and erythropoiesis. Blood. 2000;96:823-833.
-
(2000)
Blood
, vol.96
, pp. 823-833
-
-
Goodnough, L.T.1
Skikne, B.2
Brugnara, C.3
-
17
-
-
0032147041
-
Stomach implant for long term erythropoietin expression in rats
-
Lejnieks DV, Ramesh N, Lau S, Osborne WRA. Stomach implant for long term erythropoietin expression in rats. Blood. 1998;92:888-893.
-
(1998)
Blood
, vol.92
, pp. 888-893
-
-
Lejnieks, D.V.1
Ramesh, N.2
Lau, S.3
Osborne, W.R.A.4
-
18
-
-
0031686754
-
High-titer human immunodeficiency virus type 1-based vector systems for gene delivery into nondividing cells
-
Mochizuki H, Schwartz JP, Tanaka K, Brady RO, Reiser J. High-titer human immunodeficiency virus type 1-based vector systems for gene delivery into nondividing cells. J Virol. 1998;72:8873-8883.
-
(1998)
J Virol
, vol.72
, pp. 8873-8883
-
-
Mochizuki, H.1
Schwartz, J.P.2
Tanaka, K.3
Brady, R.O.4
Reiser, J.5
-
19
-
-
0030467991
-
Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles
-
Reiser J, Harmison G, Kluepfel-Stahl S, Brady RO, Karlsson S, Schubert M. Transduction of nondividing cells using pseudotyped defective high-titer HIV type 1 particles. Proc Natl Acad Sci U S A. 1996;93:15266-15271.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, pp. 15266-15271
-
-
Reiser, J.1
Harmison, G.2
Kluepfel-Stahl, S.3
Brady, R.O.4
Karlsson, S.5
Schubert, M.6
-
20
-
-
0029118346
-
Gene therapy for long-term expression of erythropoietin in rats
-
Osborne WRA, Ramesh N, Lau S, Clowes MM, Dale DC, Clowes AW. Gene therapy for long-term expression of erythropoietin in rats. Proc Natl Acad Sci U S A. 1995;92:8055-8058.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 8055-8058
-
-
Osborne, W.R.A.1
Ramesh, N.2
Lau, S.3
Clowes, M.M.4
Dale, D.C.5
Clowes, A.W.6
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