-
1
-
-
0036019191
-
Tetracycline-inducible interleukin-10 gene transfer mediated by an adeno-associated virus: Application to experimental arthritis
-
Apparailly F, Millet V, Noel D, Jacquet C, Sany J, Jorgensen C (2002) Tetracycline-inducible interleukin-10 gene transfer mediated by an adeno-associated virus: application to experimental arthritis. Hum Gene Ther 13:1179-1188
-
(2002)
Hum Gene Ther
, vol.13
, pp. 1179-1188
-
-
Apparailly, F.1
Millet, V.2
Noel, D.3
Jacquet, C.4
Sany, J.5
Jorgensen, C.6
-
2
-
-
0036328505
-
Constitutive and regulated expression of processed insulin following in vivo hepatic gene transfer
-
Auricchio A,GaoGP,YuQC, Raper S, RiveraVM,ClacksonT,WilsonJM (2002a) Constitutive and regulated expression of processed insulin following in vivo hepatic gene transfer. Gene Ther 9:963-971
-
(2002)
Gene Ther
, vol.9
, pp. 963-971
-
-
Auricchio, A.1
Gao, G.P.2
Yu, Q.C.3
Raper, S.4
Rivera, V.M.5
Clackson, T.6
Wilson, J.M.7
-
3
-
-
0036664935
-
Pharmacological regulation of protein expression fromadenoassociated viral vectors in the eye
-
Auricchio A, Rivera VM, Clackson T, O'Connor EE, Maguire AM, Tolentino MJ, Bennett J,Wilson JM (2002b) Pharmacological regulation of protein expression fromadenoassociated viral vectors in the eye. Mol Ther 6:238-242
-
(2002)
Mol Ther
, vol.6
, pp. 238-242
-
-
Auricchio, A.1
Rivera, V.M.2
Clackson, T.3
O'connor, E.E.4
Maguire, A.M.5
Tolentino, M.J.6
Bennett, J.7
Wilson, J.M.8
-
4
-
-
11244328982
-
RNAinterference and the use of small interfering RNA to study gene function in mammalian systems
-
Bantounas I, Phylactou LA,Uney JB (2004) RNAinterference and the use of small interfering RNA to study gene function in mammalian systems. J Mol Endocrinol 33:545-557
-
(2004)
J Mol Endocrinol
, vol.33
, pp. 545-557
-
-
Bantounas, I.1
Phylactou, L.A.2
Uney, J.B.3
-
5
-
-
9244230548
-
The enhancer domain of the human cytomegalovirusmajor immediate-early promoter determines cell type-specific expression in transgenic mice
-
Baskar JF, Smith PP, Nilaver G, Jupp RA, Hoffmann S, Peffer NJ, Tenney DJ, Colberg-Poley AM, Ghazal P, Nelson JA (1996) The enhancer domain of the human cytomegalovirusmajor immediate-early promoter determines cell type-specific expression in transgenic mice. J Virol 70:3207-3214
-
(1996)
J Virol
, vol.70
, pp. 3207-3214
-
-
Baskar, J.F.1
Smith, P.P.2
Nilaver, G.3
Jupp, R.A.4
Hoffmann, S.5
Peffer, N.J.6
Tenney, D.J.7
Colberg-Poley, A.M.8
Ghazal, P.9
Nelson, J.A.10
-
6
-
-
0032170592
-
Control of erythropoietin delivery by doxycycline in mice after intramuscular injection of adeno-associated vector
-
Bohl D, Salvetti A, Moullier P, Heard JM (1998) Control of erythropoietin delivery by doxycycline in mice after intramuscular injection of adeno-associated vector. Blood 92:1512-1517
-
(1998)
Blood
, vol.92
, pp. 1512-1517
-
-
Bohl, D.1
Salvetti, A.2
Moullier, P.3
Heard, J.M.4
-
7
-
-
0037790709
-
Immune responses to replication-defective HSV-1 type vectorswithin the CNS: Implications for gene therapy
-
Bowers WJ, Olschowka JA, Federoff HJ (2003) Immune responses to replication-defective HSV-1 type vectorswithin the CNS: implications for gene therapy. Gene Ther 10:941-945
-
(2003)
Gene Ther
, vol.10
, pp. 941-945
-
-
Bowers, W.J.1
Olschowka, J.A.2
Federoff, H.J.3
-
9
-
-
0027228422
-
Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: Concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells
-
Burns JC, Friedmann T, DrieverW, Burrascano M, Yee JK (1993) Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells. Proc Natl Acad Sci U S A 90:8033-8037
-
(1993)
Proc Natl Acad Sci U S A
, vol.90
, pp. 8033-8037
-
-
Burns, J.C.1
Friedmann, T.2
Driever, W.3
Burrascano, M.4
Yee, J.K.5
-
10
-
-
0034572459
-
Several log increase in therapeutic transgene delivery by distinct adeno-associated viral serotype vectors
-
Chao H, Liu Y, Rabinowitz J, Li C, Samulski RJ, Walsh CE (2000) Several log increase in therapeutic transgene delivery by distinct adeno-associated viral serotype vectors. Mol Ther 2:619-623
-
(2000)
Mol Ther
, vol.2
, pp. 619-623
-
-
Chao, H.1
Liu, Y.2
Rabinowitz, J.3
Li, C.4
Samulski, R.J.5
Walsh, C.E.6
-
11
-
-
0042941765
-
Down-regulation of CXCR4 by inducible small interfering RNA inhibits breast cancer cell invasion in vitro
-
Chen Y, Stamatoyannopoulos G, Song CZ (2003) Down-regulation of CXCR4 by inducible small interfering RNA inhibits breast cancer cell invasion in vitro. Cancer Res 63:4801-4804
-
(2003)
Cancer Res
, vol.63
, pp. 4801-4804
-
-
Chen, Y.1
Stamatoyannopoulos, G.2
Song, C.Z.3
-
12
-
-
1642525149
-
Optimal design of a single recombinant adeno-associated virus derived from serotypes 1 and 2 to achieve more tightly regulated transgene expression from nonhuman primate muscle
-
Chenuaud P, Larcher T, Rabinowitz JE, Provost N, Joussemet B, Bujard H, Samulski RJ, Favre D, Moullier P (2004) Optimal design of a single recombinant adeno-associated virus derived from serotypes 1 and 2 to achieve more tightly regulated transgene expression from nonhuman primate muscle. Mol Ther 9:410-418
-
(2004)
Mol Ther
, vol.9
, pp. 410-418
-
-
Chenuaud, P.1
Larcher, T.2
Rabinowitz, J.E.3
Provost, N.4
Joussemet, B.5
Bujard, H.6
Samulski, R.J.7
Favre, D.8
Moullier, P.9
-
13
-
-
0033541640
-
Highly purified recombinant adenoassociatedvirus vectors are biologically active and free of detectable helper andwild-type viruses
-
Clark KR, Liu X, McGrath JP, Johnson PR (1999) Highly purified recombinant adenoassociatedvirus vectors are biologically active and free of detectable helper andwild-type viruses. Hum Gene Ther 10:1031-1039
-
(1999)
Hum Gene Ther
, vol.10
, pp. 1031-1039
-
-
Clark, K.R.1
Liu, X.2
McGrath, J.P.3
Johnson, P.R.4
-
14
-
-
11844285667
-
Viral delivery of recombinant short hairpin RNAs
-
Davidson BL,Harper SQ (2005) Viral delivery of recombinant short hairpin RNAs.Methods Enzymol 392:145-173
-
(2005)
Methods Enzymol
, vol.392
, pp. 145-173
-
-
Davidson, B.L.1
Harper, S.Q.2
-
15
-
-
0034724209
-
Recombinant adeno-associated virus type 2, 4, and 5 vectors: Transduction of variant cell types and regions in the mammalian central nervous system
-
Davidson BL, Stein CS, Heth JA, Martins I, Kotin RM, Derksen TA, Zabner J, Ghodsi A, Chiorini JA (2000) Recombinant adeno-associated virus type 2, 4, and 5 vectors: transduction of variant cell types and regions in the mammalian central nervous system. Proc Natl Acad Sci U S A 97:3428-3432
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 3428-3432
-
-
Davidson, B.L.1
Stein, C.S.2
Heth, J.A.3
Martins, I.4
Kotin, R.M.5
Derksen, T.A.6
Zabner, J.7
Ghodsi, A.8
Chiorini, J.A.9
-
16
-
-
0142105497
-
Identification of PDGFR as a receptor for AAV-5 transduction
-
Di Pasquale G, Davidson BL, Stein CS, Martins I, Scudiero D, Monks A, Chiorini JA (2003) Identification of PDGFR as a receptor for AAV-5 transduction. Nat Med 9:1306-1312
-
(2003)
Nat Med
, vol.9
, pp. 1306-1312
-
-
Di Pasquale, G.1
Davidson, B.L.2
Stein, C.S.3
Martins, I.4
Scudiero, D.5
Monks, A.6
Chiorini, J.A.7
-
17
-
-
19944429120
-
Lentivirus-based genetic manipulations of cortical neurons and their optical and electrophysiological monitoring in vivo
-
DittgenT,Nimmerjahn A,Komai S, LicznerskiP,Waters J,MargrieTW,Helmchen F,DenkW, Brecht M, Osten P (2004) Lentivirus-based genetic manipulations of cortical neurons and their optical and electrophysiological monitoring in vivo. Proc Natl Acad Sci U S A 101:18206-18211
-
(2004)
Proc Natl Acad Sci U S A
, vol.101
, pp. 18206-18211
-
-
Dittgen, T.1
Nimmerjahn, A.2
Komai, S.3
Licznerski, P.4
Waters, J.5
Margrie, T.W.6
Helmchen, F.7
Denk, W.8
Brecht, M.9
Osten, P.10
-
18
-
-
0031710033
-
A thirdgeneration lentivirus vector with a conditional packaging system
-
Dull T, Zufferey R, Kelly M, Mandel RJ, Nguyen M, Trono D, Naldini L (1998) A thirdgeneration lentivirus vector with a conditional packaging system. J Virol 72:8463-8471
-
(1998)
J Virol
, vol.72
, pp. 8463-8471
-
-
Dull, T.1
Zufferey, R.2
Kelly, M.3
Mandel, R.J.4
Nguyen, M.5
Trono, D.6
Naldini, L.7
-
19
-
-
0035666134
-
Insulators coupled to a minimal bidirectional tet cassette for tight regulation of rAAV-mediated gene transfer in the mammalian brain
-
Fitzsimons HL, McKenzie JM, During MJ (2001) Insulators coupled to a minimal bidirectional tet cassette for tight regulation of rAAV-mediated gene transfer in the mammalian brain. Gene Ther 8:1675-1681
-
(2001)
Gene Ther
, vol.8
, pp. 1675-1681
-
-
Fitzsimons, H.L.1
McKenzie, J.M.2
During, M.J.3
-
20
-
-
0030867223
-
Tetracycline-responsive gene expression in mouse brain after amplicon-mediated gene transfer
-
Fotaki ME, Pink JR, Mous J (1997) Tetracycline-responsive gene expression in mouse brain after amplicon-mediated gene transfer. Gene Ther 4:901-908
-
(1997)
Gene Ther
, vol.4
, pp. 901-908
-
-
Fotaki, M.E.1
Pink, J.R.2
Mous, J.3
-
22
-
-
0033767759
-
Streptogramin-based gene regulation systems for mammalian cells
-
Fussenegger M, Morris RP, Fux C, Rimann M, von Stockar B, Thompson CJ, Bailey JE (2000) Streptogramin-based gene regulation systems for mammalian cells. Nat Biotechnol 18:1203-1208
-
(2000)
Nat Biotechnol
, vol.18
, pp. 1203-1208
-
-
Fussenegger, M.1
Morris, R.P.2
Fux, C.3
Rimann, M.4
Von Stockar, B.5
Thompson, C.J.6
Bailey, J.E.7
-
23
-
-
2342646914
-
Gene therapy platform for bone regeneration using an exogenously regulated, AAV-2-based gene expression system
-
Gafni Y, Pelled G, Zilberman Y, Turgeman G, Apparailly F, Yotvat H, Galun E, Gazit Z, Jorgensen C, Gazit D (2004) Gene therapy platform for bone regeneration using an exogenously regulated, AAV-2-based gene expression system. Mol Ther 9:587-595
-
(2004)
Mol Ther
, vol.9
, pp. 587-595
-
-
Gafni, Y.1
Pelled, G.2
Zilberman, Y.3
Turgeman, G.4
Apparailly, F.5
Yotvat, H.6
Galun, E.7
Gazit, Z.8
Jorgensen, C.9
Gazit, D.10
-
24
-
-
0345708273
-
CD46 is a cellular receptor for group B adenoviruses
-
Gaggar A, Shayakhmetov DM, Lieber A (2003) CD46 is a cellular receptor for group B adenoviruses. Nat Med 9:1408-1412
-
(2003)
Nat Med
, vol.9
, pp. 1408-1412
-
-
Gaggar, A.1
Shayakhmetov, D.M.2
Lieber, A.3
-
25
-
-
0037015049
-
Novel adeno-associated viruses fromrhesusmonkeysasvectors forhumangene therapy
-
GaoGP,AlviraMR,Wang L, CalcedoR, Johnston J,Wilson JM (2002) Novel adeno-associated viruses fromrhesusmonkeysasvectors forhumangene therapy.ProcNatlAcadSciUSA 99:11854-11859
-
(2002)
ProcNatlAcadSciUSA
, vol.99
, pp. 11854-11859
-
-
Gao, G.P.1
Alvira, M.R.2
Wang, L.3
Calcedo, R.4
Johnston, J.5
Wilson, J.M.6
-
26
-
-
0023784651
-
A defective HSV-1 vector expresses Escherichia coli betagalactosidase in cultured peripheral neurons
-
Geller AI, Breakefield XO (1988) A defective HSV-1 vector expresses Escherichia coli betagalactosidase in cultured peripheral neurons. Science 241:1667-1669
-
(1988)
Science
, vol.241
, pp. 1667-1669
-
-
Geller, A.I.1
Breakefield, X.O.2
-
27
-
-
0038344798
-
Prolonged dystrophin expression and functional correction of mdx mouse muscle following gene transfer with a helper-dependent (gutted) adenovirus-encoding murine dystrophin
-
Gilbert R, Dudley RW, Liu AB, Petrof BJ, Nalbantoglu J, Karpati G (2003) Prolonged dystrophin expression and functional correction of mdx mouse muscle following gene transfer with a helper-dependent (gutted) adenovirus-encoding murine dystrophin. Hum Mol Genet 12:1287-1299
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1287-1299
-
-
Gilbert, R.1
Dudley, R.W.2
Liu, A.B.3
Petrof, B.J.4
Nalbantoglu, J.5
Karpati, G.6
-
28
-
-
0032889563
-
Herpes simplex virus type 1 vector-mediated expression of nerve growth factor protects dorsal root ganglion neurons from peroxide toxicity
-
Goins WF, Lee KA, Cavalcoli JD, O'Malley ME, DeKosky ST, Fink DJ, Glorioso JC (1999) Herpes simplex virus type 1 vector-mediated expression of nerve growth factor protects dorsal root ganglion neurons from peroxide toxicity. J Virol 73:519-532
-
(1999)
J Virol
, vol.73
, pp. 519-532
-
-
Goins, W.F.1
Lee, K.A.2
Cavalcoli, J.D.3
O'malley, M.E.4
Dekosky, S.T.5
Fink, D.J.6
Glorioso, J.C.7
-
29
-
-
0026720075
-
Tight control of gene expression in mammalian cells by tetracycline-responsive promoters
-
Gossen M, Bujard H (1992) Tight control of gene expression in mammalian cells by tetracycline-responsive promoters. Proc Natl Acad Sci U S A 89:5547-5551
-
(1992)
Proc Natl Acad Sci U S A
, vol.89
, pp. 5547-5551
-
-
Gossen, M.1
Bujard, H.2
-
30
-
-
0029022369
-
Transcriptional activation by tetracyclines in mammalian cells
-
Gossen M, Freundlieb S, Bender G, Muller G, Hillen W, Bujard H (1995) Transcriptional activation by tetracyclines in mammalian cells. Science 268:1766-1769
-
(1995)
Science
, vol.268
, pp. 1766-1769
-
-
Gossen, M.1
Freundlieb, S.2
Bender, G.3
Muller, G.4
Hillen, W.5
Bujard, H.6
-
31
-
-
1542369977
-
From virus evolution to vector revolution: Use of naturally occurring serotypes of adeno-associated virus (AAV) as novel vectors for human gene therapy
-
Grimm D, Kay MA (2003) From virus evolution to vector revolution: use of naturally occurring serotypes of adeno-associated virus (AAV) as novel vectors for human gene therapy. Curr Gene Ther 3:281-304
-
(2003)
Curr Gene Ther
, vol.3
, pp. 281-304
-
-
Grimm, D.1
Kay, M.A.2
-
32
-
-
0032506752
-
Novel tools for production and purification of recombinant adeno-associated virus vectors
-
Grimm D, Kern A, Rittner K, Kleinschmidt JA (1998) Novel tools for production and purification of recombinant adeno-associated virus vectors. Hum Gene Ther 9:2745-2760
-
(1998)
Hum Gene Ther
, vol.9
, pp. 2745-2760
-
-
Grimm, D.1
Kern, A.2
Rittner, K.3
Kleinschmidt, J.A.4
-
33
-
-
0038150506
-
Helper virus-free, optically controllable, and two-plasmid-based production of adeno-associated virus vectors of serotypes 1 to 6
-
Grimm D, Kay MA, Kleinschmidt JA (2003) Helper virus-free, optically controllable, and two-plasmid-based production of adeno-associated virus vectors of serotypes 1 to 6. Mol Ther 7:839-850
-
(2003)
Mol Ther
, vol.7
, pp. 839-850
-
-
Grimm, D.1
Kay, M.A.2
Kleinschmidt, J.A.3
-
34
-
-
0032415073
-
Inducible long-term gene expression in brain with adeno-associated virus gene transfer
-
Haberman RP, McCown TJ, Samulski RJ (1998) Inducible long-term gene expression in brain with adeno-associated virus gene transfer. Gene Ther 5:1604-1611
-
(1998)
Gene Ther
, vol.5
, pp. 1604-1611
-
-
Haberman, R.P.1
McCown, T.J.2
Samulski, R.J.3
-
35
-
-
0034992340
-
Adeno-associated virus type 6 (AAV6) vectors mediate efficient transduction of airway epithelial cells inmouse lungs compared to that of AAV2 vectors
-
Halbert CL, Allen JM, Miller AD (2001) Adeno-associated virus type 6 (AAV6) vectors mediate efficient transduction of airway epithelial cells inmouse lungs compared to that of AAV2 vectors. J Virol 75:6615-6624
-
(2001)
J Virol
, vol.75
, pp. 6615-6624
-
-
Halbert, C.L.1
Allen, J.M.2
Miller, A.D.3
-
36
-
-
0037368410
-
Generation and characterization of chimeric recombinant AAV vectors
-
Hauck B, Chen L, XiaoW (2003) Generation and characterization of chimeric recombinant AAV vectors. Mol Ther 7:419-425
-
(2003)
Mol Ther
, vol.7
, pp. 419-425
-
-
Hauck, B.1
Chen, L.2
Xiao, W.3
-
37
-
-
4143079319
-
Adenovirus vector-mediated doxycycline-inducible RNA interference
-
Hosono T, Mizuguchi H, Katayama K, Xu ZL, Sakurai F, Ishii-Watabe A, Kawabata K, Yamaguchi T, Nakagawa S, Mayumi T, Hayakawa T (2004) Adenovirus vector-mediated doxycycline-inducible RNA interference. Hum Gene Ther 15:813-819
-
(2004)
Hum Gene Ther
, vol.15
, pp. 813-819
-
-
Hosono, T.1
Mizuguchi, H.2
Katayama, K.3
Xu, Z.L.4
Sakurai, F.5
Ishii-Watabe, A.6
Kawabata, K.7
Yamaguchi, T.8
Nakagawa, S.9
Mayumi, T.10
Hayakawa, T.11
-
38
-
-
3242745238
-
Tight regulation from a single tet-off rAAV vector as demonstrated by flow cytometry and quantitative, real-time PCR
-
Jiang L, Rampalli S, George D, Press C, Bremer EG, O'Gorman MR, Bohn MC (2004) Tight regulation from a single tet-off rAAV vector as demonstrated by flow cytometry and quantitative, real-time PCR. Gene Ther 11:1057-1067
-
(2004)
Gene Ther
, vol.11
, pp. 1057-1067
-
-
Jiang, L.1
Rampalli, S.2
George, D.3
Press, C.4
Bremer, E.G.5
O'gorman, M.R.6
Bohn, M.C.7
-
40
-
-
0035818555
-
Lifetime correction of genetic deficiency in mice with a single injection of helper-dependent adenoviral vector
-
Kim IH, Jozkowicz A, Piedra PA, Oka K, Chan L (2001) Lifetime correction of genetic deficiency in mice with a single injection of helper-dependent adenoviral vector. Proc Natl Acad Sci U S A 98:13282-13287
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, pp. 13282-13287
-
-
Kim, I.H.1
Jozkowicz, A.2
Piedra, P.A.3
Oka, K.4
Chan, L.5
-
41
-
-
0036468677
-
Germline transmission and tissuespecific expression of transgenes delivered by lentiviral vectors
-
Lois C, Hong EJ, Pease S, Brown EJ, Baltimore D (2002) Germline transmission and tissuespecific expression of transgenes delivered by lentiviral vectors. Science 295:868-872
-
(2002)
Science
, vol.295
, pp. 868-872
-
-
Lois, C.1
Hong, E.J.2
Pease, S.3
Brown, E.J.4
Baltimore, D.5
-
42
-
-
28644442724
-
Comparison of single regulated lentiviral vectors with rtTA expression driven by an autoregulatory loop or a constitutive promoter
-
Markusic D, Oude-Elferink R, Das AT, Berkhout B, Seppen J (2005) Comparison of single regulated lentiviral vectors with rtTA expression driven by an autoregulatory loop or a constitutive promoter. Nucleic Acids Res 33:e63
-
(2005)
Nucleic Acids Res
, vol.33
-
-
Markusic, D.1
Oude-Elferink, R.2
Das, A.T.3
Berkhout, B.4
Seppen, J.5
-
43
-
-
0036430302
-
Gene delivery to the eye using adeno-associated viral vectors
-
Martin KR, Klein RL, Quigley HA (2002) Gene delivery to the eye using adeno-associated viral vectors. Methods 28:267-275
-
(2002)
Methods
, vol.28
, pp. 267-275
-
-
Martin, K.R.1
Klein, R.L.2
Quigley, H.A.3
-
44
-
-
0042662862
-
Establishment of conditional vectors for hairpin siRNA knockdowns
-
Matsukura S, Jones PA, Takai D (2003) Establishment of conditional vectors for hairpin siRNA knockdowns. Nucleic Acids Res 31:e77
-
(2003)
Nucleic Acids Res
, vol.31
-
-
Matsukura, S.1
Jones, P.A.2
Takai, D.3
-
45
-
-
0031875874
-
Adeno-associated virus vectors can be efficiently produced without helper virus
-
Matsushita T, Elliger S, Elliger C, Podsakoff G, Villarreal L, Kurtzman GJ, Iwaki Y, Colosi P (1998) Adeno-associated virus vectors can be efficiently produced without helper virus. Gene Ther 5:938-945
-
(1998)
Gene Ther
, vol.5
, pp. 938-945
-
-
Matsushita, T.1
Elliger, S.2
Elliger, C.3
Podsakoff, G.4
Villarreal, L.5
Kurtzman, G.J.6
Iwaki, Y.7
Colosi, P.8
-
46
-
-
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 (2001) Rabies virus glycoprotein pseudotyping of lentiviral vectors enables retrograde axonal transport and access to the nervous system after peripheral delivery.HumMolGenet 10:2109-2121
-
(2001)
HumMolGenet
, 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
-
47
-
-
0346777307
-
Adeno-associated virus terminal repeat (TR) mutant generates self-complementary vectors to overcome the rate-limiting step to transduction in vivo
-
McCarty DM, FuH,Monahan PE, Toulson CE, Naik P, Samulski RJ (2003) Adeno-associated virus terminal repeat (TR) mutant generates self-complementary vectors to overcome the rate-limiting step to transduction in vivo. Gene Ther 10:2112-2118
-
(2003)
Gene Ther
, vol.10
, pp. 2112-2118
-
-
McCarty, D.M.1
Fu, H.2
Monahan, P.E.3
Toulson, C.E.4
Naik, P.5
Samulski, R.J.6
-
48
-
-
10944269753
-
Integration of adeno-associated virus (AAV) and recombinant AAV vectors
-
McCarty DM, Young SMJr, Samulski RJ (2004) Integration of adeno-associated virus (AAV) and recombinant AAV vectors. Annu Rev Genet 38:819-845
-
(2004)
Annu Rev Genet
, vol.38
, pp. 819-845
-
-
McCarty, D.M.1
Young Jr., S.M.2
Samulski, R.J.3
-
49
-
-
9244257887
-
Biology of adenovirus and its use as a vector for gene therapy
-
McConnell MJ, Imperiale MJ (2004) Biology of adenovirus and its use as a vector for gene therapy. Hum Gene Ther 15:1022-1033
-
(2004)
Hum Gene Ther
, vol.15
, pp. 1022-1033
-
-
McConnell, M.J.1
Imperiale, M.J.2
-
50
-
-
4644223259
-
Mechanisms of gene silencing by double-stranded RNA
-
Meister G, Tuschl T (2004) Mechanisms of gene silencing by double-stranded RNA. Nature 431:343-349
-
(2004)
Nature
, vol.431
, pp. 343-349
-
-
Meister, G.1
Tuschl, T.2
-
51
-
-
0032757387
-
Stable gene transfer to the nervous system using a non-primate lentiviral vector
-
Mitrophanous K, Yoon S, Rohll J, Patil D, Wilkes F, Kim V, Kingsman S, Kingsman A, Mazarakis N (1999) Stable gene transfer to the nervous system using a non-primate lentiviral vector. Gene Ther 6:1808-1818
-
(1999)
Gene Ther
, vol.6
, pp. 1808-1818
-
-
Mitrophanous, K.1
Yoon, S.2
Rohll, J.3
Patil, D.4
Wilkes, F.5
Kim, V.6
Kingsman, S.7
Kingsman, A.8
Mazarakis, N.9
-
52
-
-
0042319070
-
Development and application of siRNA expression vector
-
Miyagishi M, Taira K (2002) Development and application of siRNA expression vector. Nucleic Acids Res Suppl:113-114
-
(2002)
Nucleic Acids Res Suppl
, pp. 113-114
-
-
Miyagishi, M.1
Taira, K.2
-
53
-
-
0031666744
-
Development of a selfinactivating lentivirus vector
-
Miyoshi H, Blomer U, Takahashi M, Gage FH, Verma IM (1998) Development of a selfinactivating 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
-
54
-
-
9244253215
-
Targeted adenovirus vectors
-
Mizuguchi H, Hayakawa T (2004) Targeted adenovirus vectors. Hum Gene Ther 15:1034-1044
-
(2004)
Hum Gene Ther
, vol.15
, pp. 1034-1044
-
-
Mizuguchi, H.1
Hayakawa, T.2
-
55
-
-
11144248909
-
The innate immune response to adenovirus vectors
-
Muruve DA (2004) The innate immune response to adenovirus vectors. Hum Gene Ther 15:1157-1166
-
(2004)
Hum Gene Ther
, vol.15
, pp. 1157-1166
-
-
Muruve, D.A.1
-
56
-
-
0034033447
-
Increasing the size of rAAV-mediated expression cassettes in vivo by intermolecular joining of two complementary vectors
-
Nakai H, Storm TA, Kay MA (2000) Increasing the size of rAAV-mediated expression cassettes in vivo by intermolecular joining of two complementary vectors. Nat Biotechnol 18:527-532
-
(2000)
Nat Biotechnol
, vol.18
, pp. 527-532
-
-
Nakai, H.1
Storm, T.A.2
Kay, M.A.3
-
57
-
-
0029996147
-
Vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector
-
Naldini L, Blomer U, Gallay P, Ory D, Mulligan R, Gage FH, Verma IM, Trono D (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
Blomer, U.2
Gallay, P.3
Ory, D.4
Mulligan, R.5
Gage, F.H.6
Verma, I.M.7
Trono, D.8
-
58
-
-
0034052609
-
Control of the functional activity of an antisense RNA by a tetracycline-responsive derivative of the human U6 snRNA promoter
-
Ohkawa J, Taira K (2000) Control of the functional activity of an antisense RNA by a tetracycline-responsive derivative of the human U6 snRNA promoter. HumGene Ther 11:577-585
-
(2000)
HumGene Ther
, vol.11
, pp. 577-585
-
-
Ohkawa, J.1
Taira, K.2
-
59
-
-
4644311995
-
Toolbox for retrovectorologists
-
Pages JC, Bru T (2004) Toolbox for retrovectorologists. J Gene Med 6 [Suppl 1]: S67-S82
-
(2004)
J Gene Med
, vol.6
, Issue.SUPPL. 1
-
-
Pages, J.C.1
Bru, T.2
-
60
-
-
0346872991
-
Improved systemfor helper-dependent adenoviral vector production
-
PalmerD, Ng P (2003) Improved systemfor helper-dependent adenoviral vector production. Mol Ther 8:846-852
-
(2003)
Mol Ther
, vol.8
, pp. 846-852
-
-
Palmer, D.1
Ng, P.2
-
61
-
-
13844251902
-
Helper-dependent adenoviral vectors for gene therapy
-
Palmer DJ, Ng P (2005) Helper-dependent adenoviral vectors for gene therapy. Hum Gene Ther 16:1-16
-
(2005)
Hum Gene Ther
, vol.16
, pp. 1-16
-
-
Palmer, D.J.1
Ng, P.2
-
62
-
-
0036431481
-
Recombinant adeno-associated virus vector design and gene expression in the mammalian brain
-
Paterna JC, Büeler H (2002) Recombinant adeno-associated virus vector design and gene expression in the mammalian brain. Methods 28:208-218
-
(2002)
Methods
, vol.28
, pp. 208-218
-
-
Paterna, J.C.1
Büeler, H.2
-
63
-
-
10344245101
-
Lentiviral transgenesis
-
Pfeifer A (2004) Lentiviral transgenesis. Transgenic Res 13:513-522
-
(2004)
Transgenic Res
, vol.13
, pp. 513-522
-
-
Pfeifer, A.1
-
64
-
-
0142185264
-
Non-primate lentiviral vectors
-
Poeschla EM (2003) Non-primate lentiviral vectors. Curr Opin Mol Ther 5:529-540
-
(2003)
Curr Opin Mol Ther
, vol.5
, pp. 529-540
-
-
Poeschla, E.M.1
-
65
-
-
0031953134
-
Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors
-
Poeschla EM,Wong-Staal F, Looney DJ (1998) Efficient transduction of nondividing human cells by feline immunodeficiency virus lentiviral vectors. Nat Med 4:354-357
-
(1998)
Nat Med
, vol.4
, pp. 354-357
-
-
Poeschla, E.M.1
Wong-Staal, F.2
Looney, D.J.3
-
67
-
-
0034700090
-
Delivery of a stringent dimerizer-regulated gene expression system in a single retroviral vector
-
PollockR, IssnerR,Zoller K,Natesan S, RiveraVM,ClacksonT (2000) Delivery of a stringent dimerizer-regulated gene expression system in a single retroviral vector. Proc Natl Acad Sci U S A 97:13221-13226
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 13221-13226
-
-
Pollock, R.1
Issner, R.2
Zoller, K.3
Natesan, S.4
Rivera, V.M.5
Clackson, T.6
-
68
-
-
0036140216
-
Crosspackaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity
-
Rabinowitz JE, Rolling F, Li C, Conrath H, Xiao W, Xiao X, Samulski RJ (2002) Crosspackaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity. J Virol 76:791-801
-
(2002)
J Virol
, vol.76
, pp. 791-801
-
-
Rabinowitz, J.E.1
Rolling, F.2
Li, C.3
Conrath, H.4
Xiao, W.5
Xiao, X.6
Samulski, R.J.7
-
69
-
-
0242609127
-
Early and reversible neuropathology induced by tetracycline-regulated lentiviral overexpression ofmutant huntingtin in rat striatum
-
Regulier E, Trottier Y, Perrin V, Aebischer P, Deglon N (2003) Early and reversible neuropathology induced by tetracycline-regulated lentiviral overexpression ofmutant huntingtin in rat striatum. Hum Mol Genet 12:2827-2836
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2827-2836
-
-
Regulier, E.1
Trottier, Y.2
Perrin, V.3
Aebischer, P.4
Deglon, N.5
-
70
-
-
9544226448
-
A humanized system for pharmacologic control of gene expression
-
Rivera VM, Clackson T, Natesan S, Pollock R, Amara JF, Keenan T, Magari SR, Phillips T, Courage NL, Cerasoli F Jr, Holt DA, Gilman M (1996) A humanized system for pharmacologic control of gene expression. Nat Med 2:1028-1032
-
(1996)
Nat Med
, vol.2
, pp. 1028-1032
-
-
Rivera, V.M.1
Clackson, T.2
Natesan, S.3
Pollock, R.4
Amara, J.F.5
Keenan, T.6
Magari, S.R.7
Phillips, T.8
Courage, N.L.9
Cerasoli Jr., F.10
Holt, D.A.11
Gilman, M.12
-
71
-
-
0033587741
-
Long-term regulated expression of growth hormone in mice after intramuscular gene transfer
-
Rivera VM,Ye X,Courage NL, Sachar J,Cerasoli F Jr,Wilson JM, GilmanM (1999) Long-term regulated expression of growth hormone in mice after intramuscular gene transfer. Proc Natl Acad Sci U S A 96:8657-8662
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 8657-8662
-
-
Rivera, V.M.1
Ye, X.2
Courage, N.L.3
Sachar, J.4
Cerasoli Jr., F.5
Wilson, J.M.6
Gilman, M.7
-
72
-
-
0032506707
-
Herpes simplex virus type 1 DNA amplified as bacterial artificial chromosome in Escherichia coli: Rescue of replication-competent virus progeny and packaging of amplicon vectors
-
Saeki Y, Ichikawa T, Saeki A, Chiocca EA, Tobler K, Ackermann M, Breakefield XO, Fraefel C (1998) Herpes simplex virus type 1 DNA amplified as bacterial artificial chromosome in Escherichia coli: rescue of replication-competent virus progeny and packaging of amplicon vectors. Hum Gene Ther 9:2787-2794
-
(1998)
Hum Gene Ther
, vol.9
, pp. 2787-2794
-
-
Saeki, Y.1
Ichikawa, T.2
Saeki, A.3
Chiocca, E.A.4
Tobler, K.5
Ackermann, M.6
Breakefield, X.O.7
Fraefel, C.8
-
73
-
-
0034991897
-
Improved helper virus-free packaging system for HSV amplicon vectors using an ICP27-deleted, oversized HSV-1 DNA in a bacterial artificial chromosome
-
Saeki Y, Fraefel C, Ichikawa T, Breakefield XO, Chiocca EA (2001) Improved helper virus-free packaging system for HSV amplicon vectors using an ICP27-deleted, oversized HSV-1 DNA in a bacterial artificial chromosome. Mol Ther 3:591-601
-
(2001)
Mol Ther
, vol.3
, pp. 591-601
-
-
Saeki, Y.1
Fraefel, C.2
Ichikawa, T.3
Breakefield, X.O.4
Chiocca, E.A.5
-
74
-
-
0036846578
-
Tight control of gene expression by a helper-dependent adenovirus vector carrying the rtTA2 (s)-M2 tetracycline transactivator and repressor system
-
Salucci V, Scarito A, Aurisicchio L, Lamartina S, Nicolaus G, Giampaoli S, Gonzalez-Paz O, Toniatti C, Bujard H, Hillen W, Ciliberto G, Palombo F (2002) Tight control of gene expression by a helper-dependent adenovirus vector carrying the rtTA2 (s)-M2 tetracycline transactivator and repressor system. Gene Ther 9:1415-1421
-
(2002)
Gene Ther
, vol.9
, pp. 1415-1421
-
-
Salucci, V.1
Scarito, A.2
Aurisicchio, L.3
Lamartina, S.4
Nicolaus, G.5
Giampaoli, S.6
Gonzalez-Paz, O.7
Toniatti, C.8
Bujard, H.9
Hillen, W.10
Ciliberto, G.11
Palombo, F.12
-
75
-
-
0031947861
-
Persistence and expression of the herpes simplex virus genome in the absence of immediate-early proteins
-
Samaniego LA, Neiderhiser L, DeLuca NA (1998) Persistence and expression of the herpes simplex virus genome in the absence of immediate-early proteins. J Virol 72:3307-3320
-
(1998)
J Virol
, vol.72
, pp. 3307-3320
-
-
Samaniego, L.A.1
Neiderhiser, L.2
Deluca, N.A.3
-
76
-
-
0031916435
-
GenomicDNAtransferwith a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity
-
Schiedner G,Morral N, Parks RJ,Wu Y, Koopmans SC, Langston C, Graham FL, Beaudet AL, Kochanek S (1998) GenomicDNAtransferwith a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity. Nat Genet 18:180-183
-
(1998)
Nat Genet
, vol.18
, pp. 180-183
-
-
Schiedner, G.1
Morral, N.2
Parks, R.J.3
Wu, Y.4
Koopmans, S.C.5
Langston, C.6
Graham, F.L.7
Beaudet, A.L.8
Kochanek, S.9
-
77
-
-
0346873921
-
Oncolytic viruses: Clinical applications as vectors for the treatment of malignant gliomas
-
Shah AC, Benos D, Gillespie GY, Markert JM (2003) Oncolytic viruses: clinical applications as vectors for the treatment of malignant gliomas. J Neurooncol 65:203-226
-
(2003)
J Neurooncol
, vol.65
, pp. 203-226
-
-
Shah, A.C.1
Benos, D.2
Gillespie, G.Y.3
Markert, J.M.4
-
78
-
-
12744255421
-
Promoters andserotypes: Targeting of adeno-associated virus vectors for gene transfer in the rat central nervous system in vitro and in vivo
-
ShevtsovaZ,Malik JM,MichelU, BahrM,Kugler S (2005) Promoters andserotypes: targeting of adeno-associated virus vectors for gene transfer in the rat central nervous system in vitro and in vivo. Exp Physiol 90:53-59
-
(2005)
Exp Physiol
, vol.90
, pp. 53-59
-
-
Shevtsova, Z.1
Malik, J.M.2
Michel, U.3
Bahr, M.4
Kugler, S.5
-
79
-
-
0020451027
-
The herpes simplex virus amplicon: A new eucaryotic defectivevirus cloning-amplifying vector
-
Spaete RR, FrenkelN (1982) The herpes simplex virus amplicon: a new eucaryotic defectivevirus cloning-amplifying vector. Cell 30:295-304
-
(1982)
Cell
, vol.30
, pp. 295-304
-
-
Spaete, R.R.1
Frenkel, N.2
-
80
-
-
0031870243
-
An enhanced packaging system for helper-dependent herpes simplex virus vectors
-
Stavropoulos TA, Strathdee CA (1998) An enhanced packaging system for helper-dependent herpes simplex virus vectors. J Virol 72:7137-7143
-
(1998)
J Virol
, vol.72
, pp. 7137-7143
-
-
Stavropoulos, T.A.1
Strathdee, C.A.2
-
81
-
-
0031906147
-
Membrane-associated heparan sulfate proteoglycan is a receptor for adeno-associated virus type 2 virions
-
Summerford C, Samulski RJ (1998) Membrane-associated heparan sulfate proteoglycan is a receptor for adeno-associated virus type 2 virions. J Virol 72:1438-1445
-
(1998)
J Virol
, vol.72
, pp. 1438-1445
-
-
Summerford, C.1
Samulski, R.J.2
-
82
-
-
0034121579
-
Overcoming adeno-associated virus vector size limitation through viral DNA heterodimerization
-
Sun L, Li J, Xiao X (2000) Overcoming adeno-associated virus vector size limitation through viral DNA heterodimerization. Nat Med 6:599-602
-
(2000)
Nat Med
, vol.6
, pp. 599-602
-
-
Sun, L.1
Li, J.2
Xiao, X.3
-
83
-
-
4344702714
-
RecombinantAAVmediated gene delivery to the central nervous system
-
TenenbaumL, ChtartoA, Lehtonen E,Velu T, Brotchi J, LevivierM (2004) RecombinantAAVmediated gene delivery to the central nervous system. J GeneMed 6 [Suppl 1]:S212-S222
-
(2004)
J GeneMed
, vol.6
, Issue.SUPPL. 1
-
-
Tenenbaum, L.1
Chtarto, A.2
Lehtonen, E.3
Velu, T.4
Brotchi, J.5
Levivier, M.6
-
84
-
-
0036245743
-
Expanding small RNA interference
-
Tuschl T (2002) Expanding small RNA interference. Nat Biotechnol 20:446-448
-
(2002)
Nat Biotechnol
, vol.20
, pp. 446-448
-
-
Tuschl, T.1
-
85
-
-
0035190644
-
Retroviral vectors for the transduction of autoregulated, bidirectional expression cassettes
-
Unsinger J, Kroger A, Hauser H, Wirth D (2001) Retroviral vectors for the transduction of autoregulated, bidirectional expression cassettes. Mol Ther 4:484-489
-
(2001)
Mol Ther
, vol.4
, pp. 484-489
-
-
Unsinger, J.1
Kroger, A.2
Hauser, H.3
Wirth, D.4
-
86
-
-
10744219596
-
Specific inhibition of gene expression using a stably integrated, inducible small-interfering-RNA vector
-
van deWetering M,Oving I,MuncanV, Pon FongMT, BrantjesH, van LeenenD,Holstege FC, Brummelkamp TR, Agami R, Clevers H (2003) Specific inhibition of gene expression using a stably integrated, inducible small-interfering-RNA vector. EMBO Rep 4:609-615
-
(2003)
EMBO Rep
, vol.4
, pp. 609-615
-
-
Van Dewetering, M.1
Oving, I.2
Muncan, V.3
Pon Fong, M.T.4
Brantjes, H.5
Van Leenen, D.6
Holstege, F.C.7
Brummelkamp, T.R.8
Agami, R.9
Clevers, H.10
-
87
-
-
0036193248
-
Robust and efficient regulation of transgene expression in vivo by improved tetracycline-dependent lentiviral vectors
-
Vigna E, Cavalieri S, Ailles L, Geuna M, Loew R, Bujard H, Naldini L (2002) Robust and efficient regulation of transgene expression in vivo by improved tetracycline-dependent lentiviral vectors. Mol Ther 5:252-261
-
(2002)
Mol Ther
, vol.5
, pp. 252-261
-
-
Vigna, E.1
Cavalieri, S.2
Ailles, L.3
Geuna, M.4
Loew, R.5
Bujard, H.6
Naldini, L.7
-
88
-
-
17644388429
-
Efficient Tet-dependent expression of human factor IX in vivo by a new self-regulating lentiviral vector
-
Vigna E, Amendola M, Benedicenti F, Simmons AD, Follenzi A, Naldini L (2005) Efficient Tet-dependent expression of human factor IX in vivo by a new self-regulating lentiviral vector. Mol Ther 11:763-775
-
(2005)
Mol Ther
, vol.11
, pp. 763-775
-
-
Vigna, E.1
Amendola, M.2
Benedicenti, F.3
Simmons, A.D.4
Follenzi, A.5
Naldini, L.6
-
89
-
-
0034756520
-
An infectious transfer and expression systemfor genomic DNA loci in human andmouse cells
-
Wade-Martins R, Smith ER, Tyminski E, Chiocca EA, Saeki Y (2001) An infectious transfer and expression systemfor genomic DNA loci in human andmouse cells. Nat Biotechnol 19:1067-1070
-
(2001)
Nat Biotechnol
, vol.19
, pp. 1067-1070
-
-
Wade-Martins, R.1
Smith, E.R.2
Tyminski, E.3
Chiocca, E.A.4
Saeki, Y.5
-
90
-
-
0038489121
-
Single HSV-amplicon vector mediates druginduced gene expression via dimerizer system
-
Wang S, Petravicz J, Breakefield XO (2003) Single HSV-amplicon vector mediates druginduced gene expression via dimerizer system. Mol Ther 7:790-800
-
(2003)
Mol Ther
, vol.7
, pp. 790-800
-
-
Wang, S.1
Petravicz, J.2
Breakefield, X.O.3
-
91
-
-
0348038748
-
Rapid and highly efficient transduction by double-stranded adeno-associated virus vectors in vitro and in vivo
-
Wang Z, Ma HI, Li J, Sun L, Zhang J, Xiao X (2003) Rapid and highly efficient transduction by double-stranded adeno-associated virus vectors in vitro and in vivo. Gene Ther 10:2105-2111
-
(2003)
Gene Ther
, vol.10
, pp. 2105-2111
-
-
Wang, Z.1
Ma, H.I.2
Li, J.3
Sun, L.4
Zhang, J.5
Xiao, X.6
-
92
-
-
19644378907
-
Adenoassociated virus serotype 8 efficiently delivers genes tomuscle and heart
-
Wang Z, Zhu T, Qiao C, Zhou L, Wang B, Zhang J, Chen C, Li J, Xiao X (2005) Adenoassociated virus serotype 8 efficiently delivers genes tomuscle and heart. Nat Biotechnol 23:321-328
-
(2005)
Nat Biotechnol
, vol.23
, pp. 321-328
-
-
Wang, Z.1
Zhu, T.2
Qiao, C.3
Zhou, L.4
Wang, B.5
Zhang, J.6
Chen, C.7
Li, J.8
Xiao, X.9
-
93
-
-
4644254892
-
Approaches for trigger-inducible viral transgene regulation in gene-based tissue engineering
-
WeberW, FusseneggerM (2004) Approaches for trigger-inducible viral transgene regulation in gene-based tissue engineering. Curr Opin Biotechnol 15:383-391
-
(2004)
Curr Opin Biotechnol
, vol.15
, pp. 383-391
-
-
Weber, W.1
Fussenegger, M.2
-
94
-
-
0043210428
-
Conditional suppression of cellular genes: Lentivirus vectormediated drug-inducible RNA interference
-
Wiznerowicz M, TronoD (2003) Conditional suppression of cellular genes: lentivirus vectormediated drug-inducible RNA interference. J Virol 77:8957-8961
-
(2003)
J Virol
, vol.77
, pp. 8957-8961
-
-
Wiznerowicz, M.1
Trono, D.2
-
95
-
-
11344252479
-
Harnessing HIV for therapy, basic research and biotechnology
-
Wiznerowicz M, Trono D (2005) Harnessing HIV for therapy, basic research and biotechnology. Trends Biotechnol 23:42-47
-
(2005)
Trends Biotechnol
, vol.23
, pp. 42-47
-
-
Wiznerowicz, M.1
Trono, D.2
-
96
-
-
2642642141
-
Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirus
-
Xiao X, Li J, Samulski RJ (1998) Production of high-titer recombinant adeno-associated virus vectors in the absence of helper adenovirus. J Virol 72:2224-2232
-
(1998)
J Virol
, vol.72
, pp. 2224-2232
-
-
Xiao, X.1
Li, J.2
Samulski, R.J.3
-
97
-
-
0034612248
-
Trans-splicing vectors expand the utility of adeno-associated virus for gene therapy
-
Yan Z, Zhang Y, Duan D, Engelhardt JF (2000) Trans-splicing vectors expand the utility of adeno-associated virus for gene therapy. Proc Natl Acad Sci U S A 97:6716-6721
-
(2000)
Proc Natl Acad Sci U S A
, vol.97
, pp. 6716-6721
-
-
Yan, Z.1
Zhang, Y.2
Duan, D.3
Engelhardt, J.F.4
-
98
-
-
0032949030
-
Regulated delivery of therapeutic proteins after in vivo somatic cell gene transfer
-
Ye X, RiveraVM,ZoltickP,Cerasoli F Jr, SchnellMA, Gao G,Hughes JV, Gilman M,WilsonJM (1999) Regulated delivery of therapeutic proteins after in vivo somatic cell gene transfer. Science 283:88-91
-
(1999)
Science
, vol.283
, pp. 88-91
-
-
Ye, X.1
Rivera, V.M.2
Zoltick, P.3
Cerasoli Jr., F.4
Schnell, M.A.5
Gao, G.6
Hughes, J.V.7
Gilman, M.8
Wilson, J.M.9
-
99
-
-
0028705684
-
Generation of high-titer pseudotyped retroviral vectors with very broad host range
-
Yee JK, Friedmann T, Burns JC (1994) Generation of high-titer pseudotyped retroviral vectors with very broad host range. Methods Cell Biol 43:99-112
-
(1994)
Methods Cell Biol
, vol.43
, pp. 99-112
-
-
Yee, J.K.1
Friedmann, T.2
Burns, J.C.3
-
100
-
-
0346132122
-
Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cells
-
Yu SF, von Ruden T, Kantoff PW, Garber C, SeibergM, RutherU,AndersonWF, Wagner EF, Gilboa E (1986) Self-inactivating retroviral vectors designed for transfer of whole genes into mammalian cells. Proc Natl Acad Sci U S A 83:3194-3198
-
(1986)
Proc Natl Acad Sci U S A
, 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
-
101
-
-
19644381507
-
Production of recombinant adeno-associated virus vectors
-
Zolotukhin S (2005) Production of recombinant adeno-associated virus vectors. Hum Gene Ther 16:551-557
-
(2005)
Hum Gene Ther
, vol.16
, pp. 551-557
-
-
Zolotukhin, S.1
-
102
-
-
0033022953
-
Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield
-
Zolotukhin S, Byrne BJ, Mason E, Zolotukhin I, Potter M, Chesnut K, Summerford C, Samulski RJ,MuzyczkaN (1999) Recombinant adeno-associated virus purification using novel methods improves infectious titer and yield. Gene Ther 6:973-985
-
(1999)
Gene Ther
, vol.6
, pp. 973-985
-
-
Zolotukhin, S.1
Byrne, B.J.2
Mason, E.3
Zolotukhin, I.4
Potter, M.5
Chesnut, K.6
Summerford, C.7
Samulski, R.J.8
Muzyczka, N.9
-
103
-
-
0035915813
-
Helper-dependent adenoviral vector-mediated gene transfer in aged rat brain
-
Zou L, Yuan X, Zhou H, Lu H, Yang K (2001) Helper-dependent adenoviral vector-mediated gene transfer in aged rat brain. Hum Gene Ther 12:181-191
-
(2001)
Hum Gene Ther
, vol.12
, pp. 181-191
-
-
Zou, L.1
Yuan, X.2
Zhou, H.3
Lu, H.4
Yang, K.5
-
104
-
-
0030819379
-
Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo
-
Zufferey R, Nagy D, Mandel RJ, Naldini L, 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
-
105
-
-
0031743608
-
Selfinactivating lentivirus vector for safe and efficient in vivo gene delivery
-
Zufferey R, Dull T, Mandel RJ, Bukovsky A, Quiroz D, Naldini L, Trono D (1998) Selfinactivating 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
Dull, T.2
Mandel, R.J.3
Bukovsky, A.4
Quiroz, D.5
Naldini, L.6
Trono, D.7
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