-
1
-
-
0031916435
-
Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity
-
G. Schiedner et al., Genomic DNA transfer with a high-capacity adenovirus vector results in improved in vivo gene expression and decreased toxicity Nat. Genet. 18 1998 180-183
-
(1998)
Nat. Genet.
, vol.18
, pp. 180-183
-
-
Schiedner, G.1
-
2
-
-
0036592086
-
A new adenoviral helper-dependent vector results in long-term therapeutic levels of human coagulation factor IX at low doses in vivo
-
A. Ehrhardt and M.A. Kay A new adenoviral helper-dependent vector results in long-term therapeutic levels of human coagulation factor IX at low doses in vivo Blood 99 2002 3923-3930
-
(2002)
Blood
, vol.99
, pp. 3923-3930
-
-
Ehrhardt, A.1
Kay, M.A.2
-
3
-
-
0030997346
-
Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors
-
R.O. Snyder et al., Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors Nat. Genet. 16 1997 270-276
-
(1997)
Nat. Genet.
, vol.16
, pp. 270-276
-
-
Snyder, R.O.1
-
4
-
-
0034254320
-
Therapeutic levels of human factor VIII and IX using HIV-1-based lentiviral vectors in mouse liver
-
F. Park K. Ohashi and M.A. Kay Therapeutic levels of human factor VIII and IX using HIV-1-based lentiviral vectors in mouse liver Blood 96 2000 1173-1176
-
(2000)
Blood
, vol.96
, pp. 1173-1176
-
-
Park, F.1
Ohashi, K.2
Kay, M.A.3
-
5
-
-
0034103009
-
Somatic integration and long-term transgene expression in normal and haemophilic mice using a DNA transposon system
-
S.R. Yant et al., Somatic integration and long-term transgene expression in normal and haemophilic mice using a DNA transposon system Nat. Genet. 25 2000 35-41
-
(2000)
Nat. Genet.
, vol.25
, pp. 35-41
-
-
Yant, S.R.1
-
6
-
-
0036842502
-
Site-specific genomic integration produces therapeutic factor IX levels in mice
-
E.C. Olivares et al., Site-specific genomic integration produces therapeutic factor IX levels in mice Nat. Biotechnol. 20 2002 1124-1128
-
(2002)
Nat. Biotechnol.
, vol.20
, pp. 1124-1128
-
-
Olivares, E.C.1
-
7
-
-
17444372024
-
Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors
-
R.O. Snyder et al., Correction of hemophilia B in canine and murine models using recombinant adeno-associated viral vectors Nat. Med. 5 1999 64-70
-
(1999)
Nat. Med.
, vol.5
, pp. 64-70
-
-
Snyder, R.O.1
-
8
-
-
0030716959
-
Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors
-
T. Kafri et al., Sustained expression of genes delivered directly into liver and muscle by lentiviral vectors Nat. Genet. 17 1997 314-317
-
(1997)
Nat. Genet.
, vol.17
, pp. 314-317
-
-
Kafri, T.1
-
9
-
-
0032506791
-
High doses of a helper-dependent adenoviral vector yield supraphysiological levels of alpha1-antitrypsin with negligible toxicity
-
N. Morral et al., High doses of a helper-dependent adenoviral vector yield supraphysiological levels of alpha1-antitrypsin with negligible toxicity Hum. Gene Ther. 9 1998 2709-2716
-
(1998)
Hum. Gene Ther.
, vol.9
, pp. 2709-2716
-
-
Morral, N.1
-
10
-
-
10744220531
-
Intravenous administration of an AAV-2 vector for the expression of factor IX in mice and a dog model of hemophilia B
-
T.C. Harding et al., Intravenous administration of an AAV-2 vector for the expression of factor IX in mice and a dog model of hemophilia B Gene Ther. 11 2004 204-213
-
(2004)
Gene Ther.
, vol.11
, pp. 204-213
-
-
Harding, T.C.1
-
11
-
-
0037089331
-
Sustained phenotypic correction of hemophilia B dogs with a factor IX null mutation by liver-directed gene therapy
-
J.D. Mount et al., Sustained phenotypic correction of hemophilia B dogs with a factor IX null mutation by liver-directed gene therapy Blood 99 2002 2670-2676
-
(2002)
Blood
, vol.99
, pp. 2670-2676
-
-
Mount, J.D.1
-
12
-
-
17444387438
-
Long-term correction of canine hemophilia B by gene transfer of blood coagulation factor IX mediated by adeno-associated viral vector
-
R.W. Herzog et al., Long-term correction of canine hemophilia B by gene transfer of blood coagulation factor IX mediated by adeno-associated viral vector Nat. Med. 5 1999 56-63
-
(1999)
Nat. Med.
, vol.5
, pp. 56-63
-
-
Herzog, R.W.1
-
13
-
-
0037429043
-
Optimization of cis-acting elements for gene expression from nonviral vectors in vivo
-
A. Ehrhardt et al., Optimization of cis-acting elements for gene expression from nonviral vectors in vivo Hum. Gene Ther. 14 2003 215-225
-
(2003)
Hum. Gene Ther.
, vol.14
, pp. 215-225
-
-
Ehrhardt, A.1
-
14
-
-
0034202522
-
Inclusion of the hepatic locus control region, an intron, and untranslated region increases and stabilizes hepatic factor IX gene expression in vivo but not in vitro
-
C.H. Miao et al., Inclusion of the hepatic locus control region, an intron, and untranslated region increases and stabilizes hepatic factor IX gene expression in vivo but not in vitro Mol. Ther. 1 2000 522-532
-
(2000)
Mol. Ther.
, vol.1
, pp. 522-532
-
-
Miao, C.H.1
-
15
-
-
0034960344
-
Extrachromosomal recombinant adeno-associated virus vector genomes are primarily responsible for stable liver transduction in vivo
-
H. Nakai et al., Extrachromosomal recombinant adeno-associated virus vector genomes are primarily responsible for stable liver transduction in vivo J. Virol. 75 2001 6969-6976
-
(2001)
J. Virol.
, vol.75
, pp. 6969-6976
-
-
Nakai, H.1
-
16
-
-
0034993252
-
Linear DNAs concatemerize in vivo and result in sustained transgene expression in mouse liver
-
Z.Y. Chen et al., Linear DNAs concatemerize in vivo and result in sustained transgene expression in mouse liver Mol. Ther. 3 2001 403-410
-
(2001)
Mol. Ther.
, vol.3
, pp. 403-410
-
-
Chen, Z.Y.1
-
17
-
-
0030662074
-
Molecular reconstruction of Sleeping Beauty, a Tc1-like transposon from fish, and its transposition in human cells
-
Z. Ivics et al., Molecular reconstruction of Sleeping Beauty, a Tc1-like transposon from fish, and its transposition in human cells Cell 91 1997 501-510
-
(1997)
Cell
, vol.91
, pp. 501-510
-
-
Ivics, Z.1
-
18
-
-
0037072818
-
Involvement of a bifunctional, paired-like DNA-binding domain and a transpositional enhancer in Sleeping Beauty transposition
-
Z. Izsvak et al., Involvement of a bifunctional, paired-like DNA-binding domain and a transpositional enhancer in Sleeping Beauty transposition J. Biol. Chem. 277 2002 34581-34588
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 34581-34588
-
-
Izsvak, Z.1
-
19
-
-
0141744705
-
Gene insertion and long-term expression in lung mediated by the Sleeping Beauty transposon system
-
L.R. Belur et al., Gene insertion and long-term expression in lung mediated by the Sleeping Beauty transposon system Mol. Ther. 8 2003 501-507
-
(2003)
Mol. Ther.
, vol.8
, pp. 501-507
-
-
Belur, L.R.1
-
20
-
-
0037587235
-
Sustainable correction of junctional epidermolysis bullosa via transposon-mediated nonviral gene transfer
-
S. Ortiz-Urda et al., Sustainable correction of junctional epidermolysis bullosa via transposon-mediated nonviral gene transfer Gene Ther. 10 2003 1099-1104
-
(2003)
Gene Ther.
, vol.10
, pp. 1099-1104
-
-
Ortiz-Urda, S.1
-
21
-
-
13144261694
-
Chromosomal transposition of a Tc1/mariner-like element in mouse embryonic stem cells
-
G. Luo et al., Chromosomal transposition of a Tc1/mariner-like element in mouse embryonic stem cells Proc. Natl. Acad. Sci. USA 95 1998 10769-10773
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 10769-10773
-
-
Luo, G.1
-
22
-
-
0036404918
-
Common physical properties of DNA affecting target site selection of sleeping beauty and other Tc1/mariner transposable elements
-
T.J. Vigdal et al., Common physical properties of DNA affecting target site selection of sleeping beauty and other Tc1/mariner transposable elements J. Mol. Biol. 323 2002 441-452
-
(2002)
J. Mol. Biol.
, vol.323
, pp. 441-452
-
-
Vigdal, T.J.1
-
23
-
-
0038054338
-
AAV serotype 2 vectors preferentially integrate into active genes in mice
-
H. Nakai et al., AAV serotype 2 vectors preferentially integrate into active genes in mice Nat. Genet. 34 2003 297-302
-
(2003)
Nat. Genet.
, vol.34
, pp. 297-302
-
-
Nakai, H.1
-
24
-
-
0037162715
-
HIV-1 integration in the human genome favors active genes and local hotspots
-
A.R. Schroder et al., HIV-1 integration in the human genome favors active genes and local hotspots Cell 110 2002 521-529
-
(2002)
Cell
, vol.110
, pp. 521-529
-
-
Schroder, A.R.1
-
25
-
-
0035008830
-
Site-specific genomic integration in mammalian cells mediated by phage φC31 integrase
-
B. Thyagarajan et al., Site-specific genomic integration in mammalian cells mediated by phage φC31 integrase Mol. Cell. Biol. 21 2001 3926-3934
-
(2001)
Mol. Cell. Biol.
, vol.21
, pp. 3926-3934
-
-
Thyagarajan, B.1
-
26
-
-
0036797451
-
Stable nonviral genetic correction of inherited human skin disease
-
S. Ortiz-Urda et al., Stable nonviral genetic correction of inherited human skin disease Nat. Med. 8 2002 1166-1170
-
(2002)
Nat. Med.
, vol.8
, pp. 1166-1170
-
-
Ortiz-Urda, S.1
-
27
-
-
1542397137
-
Phage integrases: Biology and applications
-
A.C. Groth and M.P. Calos Phage integrases: Biology and applications J. Mol. Biol. 335 2004 667-678
-
(2004)
J. Mol. Biol.
, vol.335
, pp. 667-678
-
-
Groth, A.C.1
Calos, M.P.2
-
28
-
-
0034705105
-
A phage integrase directs efficient site-specific integration in human cells
-
A.C. Groth et al., A phage integrase directs efficient site-specific integration in human cells Proc. Natl. Acad. Sci. USA 97 2000 5995-6000
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 5995-6000
-
-
Groth, A.C.1
-
29
-
-
0038618975
-
φC31 integrase-mediated nonviral genetic correction of junctional epidermolysis bullosa
-
S. Ortiz-Urda et al., φC31 integrase-mediated nonviral genetic correction of junctional epidermolysis bullosa Hum. Gene Ther. 14 2003 923-928
-
(2003)
Hum. Gene Ther.
, vol.14
, pp. 923-928
-
-
Ortiz-Urda, S.1
-
30
-
-
2642519089
-
Silencing of episomal transgene expression by plasmid bacterial DNA elements in vivo
-
Z.Y. Chen et al., Silencing of episomal transgene expression by plasmid bacterial DNA elements in vivo Gene Ther. 11 2004 856-864
-
(2004)
Gene Ther.
, vol.11
, pp. 856-864
-
-
Chen, Z.Y.1
-
31
-
-
0030773872
-
Adeno-associated virus vector integration junctions
-
E.A. Rutledge and D.W. Russell Adeno-associated virus vector integration junctions J. Virol. 71 1997 8429-8436
-
(1997)
J. Virol.
, vol.71
, pp. 8429-8436
-
-
Rutledge, E.A.1
Russell, D.W.2
-
32
-
-
0142213094
-
Helper-independent Sleeping Beauty transposon-transposase vectors for efficient nonviral gene delivery and persistent gene expression in vivo
-
J.G. Mikkelsen et al., Helper-independent Sleeping Beauty transposon-transposase vectors for efficient nonviral gene delivery and persistent gene expression in vivo Mol. Ther. 8 2003 654-665
-
(2003)
Mol. Ther.
, vol.8
, pp. 654-665
-
-
Mikkelsen, J.G.1
-
33
-
-
0032553652
-
Efficient construction of a recombinant adenovirus vector by an improved in vitro ligation method
-
H. Mizuguchi and M.A. Kay Efficient construction of a recombinant adenovirus vector by an improved in vitro ligation method Hum. Gene Ther. 9 1998 2577-2583
-
(1998)
Hum. Gene Ther.
, vol.9
, pp. 2577-2583
-
-
Mizuguchi, H.1
Kay, M.A.2
-
34
-
-
0033543098
-
A simple method for constructing E1- and E1/E4-deleted recombinant adenoviral vectors
-
H. Mizuguchi and M.A. Kay A simple method for constructing E1- and E1/ E4-deleted recombinant adenoviral vectors Hum. Gene Ther. 10 1999 2013-2017
-
(1999)
Hum. Gene Ther.
, vol.10
, pp. 2013-2017
-
-
Mizuguchi, H.1
Kay, M.A.2
-
35
-
-
0032510752
-
In vitro site-specific integration of bacteriophage DNA catalyzed by a recombinase of the resolvase/invertase family
-
H.M. Thorpe and M.C. Smith In vitro site-specific integration of bacteriophage DNA catalyzed by a recombinase of the resolvase/invertase family Proc. Natl. Acad. Sci. USA 95 1998 5505-5510
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 5505-5510
-
-
Thorpe, H.M.1
Smith, M.C.2
-
36
-
-
0032805251
-
Hydrodynamics-based transfection in animals by systemic administration of plasmid DNA
-
F. Liu Y. Song and D. Liu Hydrodynamics-based transfection in animals by systemic administration of plasmid DNA Gene Ther. 6 1999 1258-1266
-
(1999)
Gene Ther.
, vol.6
, pp. 1258-1266
-
-
Liu, F.1
Song, Y.2
Liu, D.3
-
37
-
-
0033166561
-
High levels of foreign gene expression in hepatocytes after tail vein injections of naked plasmid DNA
-
G. Zhang V. Budker and J.A. Wolff High levels of foreign gene expression in hepatocytes after tail vein injections of naked plasmid DNA Hum. Gene Ther. 10 1999 1735-1737
-
(1999)
Hum. Gene Ther.
, vol.10
, pp. 1735-1737
-
-
Zhang, G.1
Budker, V.2
Wolff, J.A.3
-
38
-
-
0037790861
-
Episomal persistence of recombinant adenoviral vector genomes during the cell cycle in vivo
-
A. Ehrhardt H. Xu and M.A. Kay Episomal persistence of recombinant adenoviral vector genomes during the cell cycle in vivo J. Virol. 77 2003 7689-7695
-
(2003)
J. Virol.
, vol.77
, pp. 7689-7695
-
-
Ehrhardt, A.1
Xu, H.2
Kay, M.A.3
-
39
-
-
0003234944
-
A method for multiple portal vein infusions in mice: Quantitation of adenovirus-mediated hepatic gene transfer
-
M.J.T.F.D. Vrancken-Peeters et al., A method for multiple portal vein infusions in mice: Quantitation of adenovirus-mediated hepatic gene transfer BioTechniques 20 1996 278-285
-
(1996)
BioTechniques
, vol.20
, pp. 278-285
-
-
Vrancken-Peeters, M.J.T.F.D.1
-
40
-
-
0141593513
-
A gene-deleted adenoviral vector results in phenotypic correction of canine hemophilia B without liver toxicity or thrombocytopenia
-
A. Ehrhardt et al., A gene-deleted adenoviral vector results in phenotypic correction of canine hemophilia B without liver toxicity or thrombocytopenia Blood 102 2003 2403-2411
-
(2003)
Blood
, vol.102
, pp. 2403-2411
-
-
Ehrhardt, A.1
-
41
-
-
0042700227
-
Gene transfer into genomes of human cells by the Sleeping Beauty transposon system
-
A.M. Geurts et al., Gene transfer into genomes of human cells by the Sleeping Beauty transposon system Mol. Ther. 8 2003 108-117
-
(2003)
Mol. Ther.
, vol.8
, pp. 108-117
-
-
Geurts, A.M.1
-
42
-
-
0034950612
-
Long-term and therapeutic-level hepatic gene expression of human factor IX after naked plasmid transfer in vivo
-
C.H. Miao et al., Long-term and therapeutic-level hepatic gene expression of human factor IX after naked plasmid transfer in vivo Mol. Ther. 3 2001 947-957
-
(2001)
Mol. Ther.
, vol.3
, pp. 947-957
-
-
Miao, C.H.1
-
43
-
-
0036478954
-
Chromosomal effects of adeno-associated virus vector integration
-
D.G. Miller E.A. Rutledge and D.W. Russell Chromosomal effects of adeno-associated virus vector integration Nat. Genet. 30 2002 147-148
-
(2002)
Nat. Genet.
, vol.30
, pp. 147-148
-
-
Miller, D.G.1
Rutledge, E.A.2
Russell, D.W.3
-
44
-
-
0035989006
-
CpG-depleted plasmid DNA vectors with enhanced safety and long-term gene expression in vivo
-
N.S. Yew et al., CpG-depleted plasmid DNA vectors with enhanced safety and long-term gene expression in vivo Mol. Ther. 5 2002 731-738
-
(2002)
Mol. Ther.
, vol.5
, pp. 731-738
-
-
Yew, N.S.1
-
45
-
-
0041315884
-
Minicircle DNA vectors devoid of bacterial DNA result in persistent and high-level transgene expression in vivo
-
Z.Y. Chen et al., Minicircle DNA vectors devoid of bacterial DNA result in persistent and high-level transgene expression in vivo Mol. Ther. 8 2003 495-500
-
(2003)
Mol. Ther.
, vol.8
, pp. 495-500
-
-
Chen, Z.Y.1
-
46
-
-
4744374701
-
Mutational analysis of the N-terminal DNA-binding domain of Sleeping Beauty transposase: Critical residues for DNA binding and hyperactivity in mammalian cells
-
S.R. Yant et al., Mutational analysis of the N-terminal DNA-binding domain of Sleeping Beauty transposase: Critical residues for DNA binding and hyperactivity in mammalian cells Mol. Cell. Biol. 24 2004 9239-9247
-
(2004)
Mol. Cell. Biol.
, vol.24
, pp. 9239-9247
-
-
Yant, S.R.1
|