-
1
-
-
24944585648
-
Gene therapy for hemophilia: An imperative to succeed
-
Hough C, Lillicrap D. Gene therapy for hemophilia: an imperative to succeed. J Thromb Haemost. 2005;3:1195-1205.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 1195-1205
-
-
Hough, C.1
Lillicrap, D.2
-
2
-
-
13244256883
-
Gene therapy for hemophilia? Yes
-
Negrier C. Gene therapy for hemophilia? Yes. J Thromb Haemost. 2004;2:1234-1235.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 1234-1235
-
-
Negrier, C.1
-
3
-
-
33646121524
-
Cellular and genetic therapies for haemophilia
-
Lillicrap D, VandenDriessche T, High K. Cellular and genetic therapies for haemophilia. Haemophilia. 2006;12(suppl 3):36-41.
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 3
, pp. 36-41
-
-
Lillicrap, D.1
VandenDriessche, T.2
High, K.3
-
4
-
-
33746733616
-
Gene therapy for hemophilia
-
Ponder KP. Gene therapy for hemophilia. Curr Opin Hematol. 2006;13:301-307.
-
(2006)
Curr Opin Hematol
, vol.13
, pp. 301-307
-
-
Ponder, K.P.1
-
5
-
-
0034050904
-
Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector
-
Kay MA, Manno CS, Ragni MV, et al. Evidence for gene transfer and expression of factor IX in haemophilia B patients treated with an AAV vector. Nat Genet. 2000;24:257-261.
-
(2000)
Nat Genet
, vol.24
, pp. 257-261
-
-
Kay, M.A.1
Manno, C.S.2
Ragni, M.V.3
-
6
-
-
33644820684
-
Successful transduction of liver in hemophilia by AAV-factor IX and limitations imposed by the host immune response
-
Manno CS, Pierce GF, Arruda VR, et al. Successful transduction of liver in hemophilia by AAV-factor IX and limitations imposed by the host immune response. Nat Med. 2006;12:342-347.
-
(2006)
Nat Med
, vol.12
, pp. 342-347
-
-
Manno, C.S.1
Pierce, G.F.2
Arruda, V.R.3
-
7
-
-
28244481870
-
Gene transfer for hemophilia: Can therapeutic efficacy in large animals be safely translated to patients?
-
High K. Gene transfer for hemophilia: can therapeutic efficacy in large animals be safely translated to patients? J Thromb Haemost. 2005;3:1682-1691.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 1682-1691
-
-
High, K.1
-
8
-
-
22244459917
-
Gene therapy: Twenty-first century medicine
-
Verma IM, Weitzman MD. Gene therapy: twenty-first century medicine. Annu Rev Biochem. 2005;74:711-738.
-
(2005)
Annu Rev Biochem
, vol.74
, pp. 711-738
-
-
Verma, I.M.1
Weitzman, M.D.2
-
9
-
-
0036171327
-
Efficient gene delivery and targeted expression to hepatocytes in vivo by improved lentiviral vectors
-
Follenzi A, Sabatino G, Lombardo A, Boccaccio C, Naldini L. Efficient gene delivery and targeted expression to hepatocytes in vivo by improved lentiviral vectors. Hum Gene Ther. 2002;13:243-260.
-
(2002)
Hum Gene Ther
, vol.13
, pp. 243-260
-
-
Follenzi, A.1
Sabatino, G.2
Lombardo, A.3
Boccaccio, C.4
Naldini, L.5
-
10
-
-
0034278156
-
Lentiviral vectors: Excellent tools for experimental gene transfer and promising candidates for gene therapy
-
Vigna E, Naldini L. Lentiviral vectors: excellent tools for experimental gene transfer and promising candidates for gene therapy. J Gene Med. 2000;2:308-316.
-
(2000)
J Gene Med
, vol.2
, pp. 308-316
-
-
Vigna, E.1
Naldini, L.2
-
11
-
-
2342561729
-
Targeting lentiviral vector expression to hepatocytes limits transgene-specific immune response and establishes long-term expression of human antihemophilic factor IX in mice
-
Follenzi A, Battaglia M, Lombardo A, Annoni A, Roncarolo MG, Naldini L. Targeting lentiviral vector expression to hepatocytes limits transgene-specific immune response and establishes long-term expression of human antihemophilic factor IX in mice. Blood. 2004;103:3700-3709.
-
(2004)
Blood
, vol.103
, pp. 3700-3709
-
-
Follenzi, A.1
Battaglia, M.2
Lombardo, A.3
Annoni, A.4
Roncarolo, M.G.5
Naldini, L.6
-
12
-
-
16244394824
-
Lentiviral vector retargeting to P-glycoprotein on metastatic melanoma through intravenous injection
-
Morizono K, Xie Y, Ringpis GE, et al. Lentiviral vector retargeting to P-glycoprotein on metastatic melanoma through intravenous injection. Nat Med. 2005;11:346-352.
-
(2005)
Nat Med
, vol.11
, pp. 346-352
-
-
Morizono, K.1
Xie, Y.2
Ringpis, G.E.3
-
13
-
-
0036665573
-
Biodistribution and toxicity studies of VSVG-pseudotyped lentiviral vector after intravenous administration in mice with the observation of in vivo transduction of bone marrow
-
Pan D, Gunther R, Duan W, et al. Biodistribution and toxicity studies of VSVG-pseudotyped lentiviral vector after intravenous administration in mice with the observation of in vivo transduction of bone marrow. Mol Ther. 2002;6:19-29.
-
(2002)
Mol Ther
, vol.6
, pp. 19-29
-
-
Pan, D.1
Gunther, R.2
Duan, W.3
-
14
-
-
33845531899
-
Efficacy and safety of adeno-associated viral vectors based on serotype 8 and 9 vs. lentiviral vectors for hemophilia B gene therapy
-
Vandendriessche T, Thorrez L, Acosta-Sanchez A, et al. Efficacy and safety of adeno-associated viral vectors based on serotype 8 and 9 vs. lentiviral vectors for hemophilia B gene therapy. J Thromb Haemost. 2007;5:16-24.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 16-24
-
-
Vandendriessche, T.1
Thorrez, L.2
Acosta-Sanchez, A.3
-
15
-
-
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
-
16
-
-
0036797102
-
HIV incidence in the United States, 1978-1999
-
Vu MQ, Steketee RW, Valleroy L, Weinstock H, Karon J, Janssen R. HIV incidence in the United States, 1978-1999. J Acquir Immune Defic Syndr. 2002;31:188-201.
-
(2002)
J Acquir Immune Defic Syndr
, vol.31
, pp. 188-201
-
-
Vu, M.Q.1
Steketee, R.W.2
Valleroy, L.3
Weinstock, H.4
Karon, J.5
Janssen, R.6
-
17
-
-
34248566925
-
Immune response after neonatal transfer of a human factor IX-expressing retroviral vector in dogs, cats, and mice
-
Xu L, Mei M, Haskins ME, et al. Immune response after neonatal transfer of a human factor IX-expressing retroviral vector in dogs, cats, and mice. Thromb Res. 2007;120:269-280.
-
(2007)
Thromb Res
, vol.120
, pp. 269-280
-
-
Xu, L.1
Mei, M.2
Haskins, M.E.3
-
18
-
-
0037853196
-
Efficient production of human FVIII in hemophilic mice using lentiviral vectors
-
Kootstra NA, Matsumura R, Verma IM. Efficient production of human FVIII in hemophilic mice using lentiviral vectors. Mol Ther. 2003;7:623-631.
-
(2003)
Mol Ther
, vol.7
, pp. 623-631
-
-
Kootstra, N.A.1
Matsumura, R.2
Verma, I.M.3
-
19
-
-
0034254320
-
Therapeutic levels of human factor VIII and IX using HIV-1-based lentiviral vectors in mouse liver
-
Park F, Ohashi K, Kay MA. Therapeutic levels of human factor VIII and IX using HIV-1-based lentiviral vectors in mouse liver. Blood. 2000;96:1173-1176.
-
(2000)
Blood
, vol.96
, pp. 1173-1176
-
-
Park, F.1
Ohashi, K.2
Kay, M.A.3
-
20
-
-
0034960875
-
In vivo treatment of hemophilia A and mucopolysaccharidosis type VII using nonprimate lentiviral vectors
-
Stein CS, Kang Y, Sauter SL, et al. In vivo treatment of hemophilia A and mucopolysaccharidosis type VII using nonprimate lentiviral vectors. Mol Ther. 2001;3:850-856.
-
(2001)
Mol Ther
, vol.3
, pp. 850-856
-
-
Stein, C.S.1
Kang, Y.2
Sauter, S.L.3
-
21
-
-
0036137639
-
Production of human clotting factor IX without toxicity in mice after vascular delivery of a lentiviral vector
-
Tsui LV, Kelly M, Zayek N, et al. Production of human clotting factor IX without toxicity in mice after vascular delivery of a lentiviral vector. Nat Biotechnol. 2002;20:53-57.
-
(2002)
Nat Biotechnol
, vol.20
, pp. 53-57
-
-
Tsui, L.V.1
Kelly, M.2
Zayek, N.3
-
22
-
-
29944432812
-
Permanent partial phenotypic correction and tolerance in a mouse model of hemophilia B by stem cell gene delivery of human factor IX
-
Bigger BW, Siapati EK, Mistry A, et al. Permanent partial phenotypic correction and tolerance in a mouse model of hemophilia B by stem cell gene delivery of human factor IX. Gene Ther. 2006;13:117-126.
-
(2006)
Gene Ther
, vol.13
, pp. 117-126
-
-
Bigger, B.W.1
Siapati, E.K.2
Mistry, A.3
-
23
-
-
33747076039
-
Stem cell-derived erythroid cells mediate long-term systemic protein delivery
-
Chang AH, Stephan MT, Sadelain M. Stem cell-derived erythroid cells mediate long-term systemic protein delivery. Nat Biotechnol. 2006;24:1017-1021.
-
(2006)
Nat Biotechnol
, vol.24
, pp. 1017-1021
-
-
Chang, A.H.1
Stephan, M.T.2
Sadelain, M.3
-
24
-
-
2342551048
-
Factors influencing therapeutic efficacy and the host immune response to helper-dependent adenoviral gene therapy in hemophilia A mice
-
Brown BD, Shi CX, Rawle FE, et al. Factors influencing therapeutic efficacy and the host immune response to helper-dependent adenoviral gene therapy in hemophilia A mice. J Thromb Haemost. 2004;2:111-118.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 111-118
-
-
Brown, B.D.1
Shi, C.X.2
Rawle, F.E.3
-
25
-
-
0037988905
-
Induction of immune tolerance to coagulation factor IX antigen by in vivo hepatic gene transfer
-
Mingozzi F, Liu YL, Dobrzynski E, et al. Induction of immune tolerance to coagulation factor IX antigen by in vivo hepatic gene transfer. J Clin Invest. 2003;111:1347-1356.
-
(2003)
J Clin Invest
, vol.111
, pp. 1347-1356
-
-
Mingozzi, F.1
Liu, Y.L.2
Dobrzynski, E.3
-
26
-
-
33947583453
-
In vivo administration of lentiviral vectors triggers a type I interferon response that restricts hepatocyte gene transfer and promotes vector clearance
-
Brown BD, Sitia G, Annoni A, et al. In vivo administration of lentiviral vectors triggers a type I interferon response that restricts hepatocyte gene transfer and promotes vector clearance. Blood. 2007;109:2797-2805.
-
(2007)
Blood
, vol.109
, pp. 2797-2805
-
-
Brown, B.D.1
Sitia, G.2
Annoni, A.3
-
27
-
-
33846081072
-
Tubulovesicular structures within vesicular stomatitis virus G protein-pseudotyped lentiviral vector preparations carry DNA and stimulate antiviral responses via toll-like receptor 9
-
Pichlmair A, Diebold SS, Gschmeissner S, et al. Tubulovesicular structures within vesicular stomatitis virus G protein-pseudotyped lentiviral vector preparations carry DNA and stimulate antiviral responses via toll-like receptor 9. J Virol. 2007;81:539-547.
-
(2007)
J Virol
, vol.81
, pp. 539-547
-
-
Pichlmair, A.1
Diebold, S.S.2
Gschmeissner, S.3
-
28
-
-
0037103167
-
Dangerous liaisons: The role of "danger" signals in the immune response to gene therapy
-
Brown BD, Lillicrap D. Dangerous liaisons: the role of "danger" signals in the immune response to gene therapy. Blood. 2002;100:1133-1140.
-
(2002)
Blood
, vol.100
, pp. 1133-1140
-
-
Brown, B.D.1
Lillicrap, D.2
-
29
-
-
0030758328
-
A factor IX-deficient mouse model for hemophilia B gene therapy
-
Wang L, Zoppe M, Hackeng TM, Griffin JH, Lee KF, Verma IM. A factor IX-deficient mouse model for hemophilia B gene therapy. Proc Natl Acad Sci U S A. 1997;94:11563-11566.
-
(1997)
Proc Natl Acad Sci U S A
, vol.94
, pp. 11563-11566
-
-
Wang, L.1
Zoppe, M.2
Hackeng, T.M.3
Griffin, J.H.4
Lee, K.F.5
Verma, I.M.6
-
30
-
-
0028925539
-
Quantification of antigen specific CD8+ T cells using an ELISPOT assay
-
Miyahira Y, Murata K, Rodriguez D, et al. Quantification of antigen specific CD8+ T cells using an ELISPOT assay. J Immunol Methods. 1995;181:45-54.
-
(1995)
J Immunol Methods
, vol.181
, pp. 45-54
-
-
Miyahira, Y.1
Murata, K.2
Rodriguez, D.3
-
31
-
-
33646564701
-
Endogenous microRNA regulation suppresses transgene expression in hematopoietic lineages and enables stable gene transfer
-
Brown BD, Venneri MA, Zingale A, Sergi LS, Naldini L. Endogenous microRNA regulation suppresses transgene expression in hematopoietic lineages and enables stable gene transfer. Nat Med. 2006;12:585-591.
-
(2006)
Nat Med
, vol.12
, pp. 585-591
-
-
Brown, B.D.1
Venneri, M.A.2
Zingale, A.3
Sergi, L.S.4
Naldini, L.5
-
32
-
-
29144470346
-
Real-time quantification of microRNAs by stem-loop RTPCR
-
Chen C, Ridzon DA, Broomer AJ, et al. Real-time quantification of microRNAs by stem-loop RTPCR. Nucleic Acids Res. 2005;33:e179.
-
(2005)
Nucleic Acids Res
, vol.33
-
-
Chen, C.1
Ridzon, D.A.2
Broomer, A.J.3
-
33
-
-
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. Efficient Tet-dependent expression of human factor IX in vivo by a new self-regulating lentiviral vector. Mol Ther. 2005;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
-
34
-
-
0038446697
-
Humoral immune response in mice against a circulating antigen induced by adenoviral transfer is strictly dependent on expression in antigen-presenting cells
-
De Geest BR, Van Linthout SA, Collen D. Humoral immune response in mice against a circulating antigen induced by adenoviral transfer is strictly dependent on expression in antigen-presenting cells. Blood. 2003;101:2551-2556.
-
(2003)
Blood
, vol.101
, pp. 2551-2556
-
-
De Geest, B.R.1
Van Linthout, S.A.2
Collen, D.3
-
35
-
-
15244351083
-
Coordinate dual-gene transgenesis by lentiviral vectors carrying synthetic bidirectional promoters
-
Amendola M, Venneri MA, Biffi A, Vigna E, Naldini L. Coordinate dual-gene transgenesis by lentiviral vectors carrying synthetic bidirectional promoters. Nat Biotechnol. 2005;23:108-116.
-
(2005)
Nat Biotechnol
, vol.23
, pp. 108-116
-
-
Amendola, M.1
Venneri, M.A.2
Biffi, A.3
Vigna, E.4
Naldini, L.5
-
36
-
-
0346727524
-
MicroRNAs modulate hematopoietic lineage differentiation
-
Chen CZ, Li L, Lodish HF, Bartel DP. MicroRNAs modulate hematopoietic lineage differentiation. Science. 2004;303:83-86.
-
(2004)
Science
, vol.303
, pp. 83-86
-
-
Chen, C.Z.1
Li, L.2
Lodish, H.F.3
Bartel, D.P.4
-
37
-
-
28344438648
-
A minicircuitry comprised of microRNA-223 and transcription factors NFI-A and C/EBPalpha regulates human granulopoiesis
-
Fazi F, Rosa A, Fatica A, et al. A minicircuitry comprised of microRNA-223 and transcription factors NFI-A and C/EBPalpha regulates human granulopoiesis. Cell. 2005;123:819-831.
-
(2005)
Cell
, vol.123
, pp. 819-831
-
-
Fazi, F.1
Rosa, A.2
Fatica, A.3
-
38
-
-
0034151775
-
Role of vector in activation of T cell subsets in immune responses against the secreted transgene product factor IX
-
Fields PA, Kowalczyk DW, Arruda VR, et al. Role of vector in activation of T cell subsets in immune responses against the secreted transgene product factor IX. Mol Ther. 2000;1:225-235.
-
(2000)
Mol Ther
, vol.1
, pp. 225-235
-
-
Fields, P.A.1
Kowalczyk, D.W.2
Arruda, V.R.3
-
39
-
-
0035282898
-
Factors influencing in vivo transduction by recombinant adeno-associated viral vectors expressing the human factor IX cDNA
-
Nathwani AC, Davidoff A, Hanawa H, Zhou JF, Vanin EF, Nienhuis AW. Factors influencing in vivo transduction by recombinant adeno-associated viral vectors expressing the human factor IX cDNA. Blood. 2001;97:1258-1265.
-
(2001)
Blood
, vol.97
, pp. 1258-1265
-
-
Nathwani, A.C.1
Davidoff, A.2
Hanawa, H.3
Zhou, J.F.4
Vanin, E.F.5
Nienhuis, A.W.6
-
40
-
-
33947721625
-
miR-181a is an intrinsic modulator of T cell sensitivity and selection
-
Li QJ, Chau J, Ebert PJ, et al. miR-181a is an intrinsic modulator of T cell sensitivity and selection. Cell. 2007;129:147-161.
-
(2007)
Cell
, vol.129
, pp. 147-161
-
-
Li, Q.J.1
Chau, J.2
Ebert, P.J.3
-
41
-
-
34247584465
-
Requirement of bic/microRNA-155 for normal immune function
-
Rodriguez A, Vigorito E, Clare S, et al. Requirement of bic/microRNA-155 for normal immune function. Science. 2007;316:608-611.
-
(2007)
Science
, vol.316
, pp. 608-611
-
-
Rodriguez, A.1
Vigorito, E.2
Clare, S.3
-
42
-
-
0032005213
-
Human factor IX corrects the bleeding diathesis of mice with hemophilia B
-
Kung SH, Hagstrom JN, Cass D, et al. Human factor IX corrects the bleeding diathesis of mice with hemophilia B. Blood. 1998;91:784-790.
-
(1998)
Blood
, vol.91
, pp. 784-790
-
-
Kung, S.H.1
Hagstrom, J.N.2
Cass, D.3
-
43
-
-
1942435249
-
Micromanagers of gene expression: The potentially widespread influence of metazoan microRNAs
-
Bartel DP, Chen CZ. Micromanagers of gene expression: the potentially widespread influence of metazoan microRNAs. Nat Rev Genet. 2004;5:396-400.
-
(2004)
Nat Rev Genet
, vol.5
, pp. 396-400
-
-
Bartel, D.P.1
Chen, C.Z.2
-
44
-
-
17144417748
-
Dendritic cells as therapeutic vaccines against cancer
-
Banchereau J, Palucka AK. Dendritic cells as therapeutic vaccines against cancer. Nat Rev Immunol. 2005;5:296-306.
-
(2005)
Nat Rev Immunol
, vol.5
, pp. 296-306
-
-
Banchereau, J.1
Palucka, A.K.2
-
45
-
-
0036715411
-
Immature, semi-mature and fully mature dendritic cells: Which signals induce tolerance or immunity?
-
Lutz MB, Schuler G. Immature, semi-mature and fully mature dendritic cells: which signals induce tolerance or immunity? Trends Immunol. 2002;23:445-449.
-
(2002)
Trends Immunol
, vol.23
, pp. 445-449
-
-
Lutz, M.B.1
Schuler, G.2
-
46
-
-
0037270978
-
Hepatic T cells and liver tolerance
-
Crispe IN. Hepatic T cells and liver tolerance. Nat Rev Immunol. 2003;3:51-62.
-
(2003)
Nat Rev Immunol
, vol.3
, pp. 51-62
-
-
Crispe, I.N.1
-
47
-
-
33645240071
-
Prevention of cytotoxic T lymphocyte responses to factor IX-expressing hepatocytes by gene transfer-induced regulatory T cells
-
Dobrzynski E, Fitzgerald JC, Cao O, Mingozzi F, Wang L, Herzog RW. Prevention of cytotoxic T lymphocyte responses to factor IX-expressing hepatocytes by gene transfer-induced regulatory T cells. Proc Natl Acad Sci U S A. 2006;103:4592-4597.
-
(2006)
Proc Natl Acad Sci U S A
, vol.103
, pp. 4592-4597
-
-
Dobrzynski, E.1
Fitzgerald, J.C.2
Cao, O.3
Mingozzi, F.4
Wang, L.5
Herzog, R.W.6
-
48
-
-
13544253713
-
Complement regulatory proteins are incorporated into lentiviral vectors and protect particles against complement inactivation
-
Schauber-Plewa C, Simmons A, Tuerk MJ, Pacheco CD, Veres G. Complement regulatory proteins are incorporated into lentiviral vectors and protect particles against complement inactivation. Gene Ther. 2005;12:238-245.
-
(2005)
Gene Ther
, vol.12
, pp. 238-245
-
-
Schauber-Plewa, C.1
Simmons, A.2
Tuerk, M.J.3
Pacheco, C.D.4
Veres, G.5
-
49
-
-
23944484509
-
Persistent expression of factor VIII in vivo following nonprimate lentiviral gene transfer
-
Kang Y, Xie L, Tran DT, et al. Persistent expression of factor VIII in vivo following nonprimate lentiviral gene transfer. Blood. 2005;106:1552-1558.
-
(2005)
Blood
, vol.106
, pp. 1552-1558
-
-
Kang, Y.1
Xie, L.2
Tran, D.T.3
-
50
-
-
15244345941
-
The MET oncogene drives a genetic programme linking cancer to haemostasis
-
Boccaccio C, Sabatino G, Medico E, et al. The MET oncogene drives a genetic programme linking cancer to haemostasis. Nature. 2005;434:396-400.
-
(2005)
Nature
, vol.434
, pp. 396-400
-
-
Boccaccio, C.1
Sabatino, G.2
Medico, E.3
-
51
-
-
33644822908
-
Effective gene therapy with nonintegrating lentiviral vectors
-
Yanez-Munoz RJ, Balaggan KS, MacNeil A, et al. Effective gene therapy with nonintegrating lentiviral vectors. Nat Med. 2006;12:348-353.
-
(2006)
Nat Med
, vol.12
, pp. 348-353
-
-
Yanez-Munoz, R.J.1
Balaggan, K.S.2
MacNeil, A.3
-
52
-
-
33745108790
-
Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration
-
Montini E, Cesana D, Schmidt M, et al. Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration. Nat Biotechnol. 2006;24:687-696.
-
(2006)
Nat Biotechnol
, vol.24
, pp. 687-696
-
-
Montini, E.1
Cesana, D.2
Schmidt, M.3
-
53
-
-
0036819773
-
Update on hematopoietic stem cell gene transfer using non-human primate models
-
Hu J, Dunbar CE. Update on hematopoietic stem cell gene transfer using non-human primate models. Curr Opin Mol Ther. 2002;4:482-490.
-
(2002)
Curr Opin Mol Ther
, vol.4
, pp. 482-490
-
-
Hu, J.1
Dunbar, C.E.2
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