-
1
-
-
0037189401
-
Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning
-
DOI 10.1126/science.1070104
-
Aiuti, A., Slavin, S., Aker, M., et al. (2002). Correction of ADA-SCID by stem cell gene therapy combined with non-myeloablative conditioning. Science 296, 2410-2413. (Pubitemid 34734219)
-
(2002)
Science
, vol.296
, Issue.5577
, pp. 2410-2413
-
-
Aiuti, A.1
Slavin, S.2
Aker, M.3
Ficara, F.4
Deola, S.5
Mortellaro, A.6
Morecki, S.7
Andolfi, G.8
Tabucchi, A.9
Carlucci, F.10
Marinello, E.11
Cattaneo, F.12
Vai, S.13
Servida, P.14
Miniero, R.15
Roncarolo, M.G.16
Bordignon, C.17
-
2
-
-
72449162211
-
Development of a scalable process for high-yield lentiviral vector production by transient transfection of HEK293 suspension cultures
-
Ansorge, S., Lanthier, S., Transfiguracion, J., et al. (2009). Development of a scalable process for high-yield lentiviral vector production by transient transfection of HEK293 suspension cultures. J. Gene Med. 11, 868-876.
-
(2009)
J. Gene Med.
, vol.11
, pp. 868-876
-
-
Ansorge, S.1
Lanthier, S.2
Transfiguracion, J.3
-
3
-
-
0242382679
-
Optimized lentiviral vector production and purification procedure prevents immune response after transduction of mouse brain
-
DOI 10.1038/sj.gt.3302094
-
Baekelandt, V., Eggermont, K., Michiels, M., et al. (2003). Optimized lentiviral vector production and purification procedure prevents immune response after transduction of mouse brain. Gene Ther. 10, 1933-1940. (Pubitemid 37337069)
-
(2003)
Gene Therapy
, vol.10
, Issue.23
, pp. 1933-1940
-
-
Baekelandt, V.1
Eggermont, K.2
Michiels, M.3
Nuttin, B.4
Debyser, Z.5
-
4
-
-
11144354757
-
Correction of metachromatic leukodystrophy in the mouse model by transplantation of genetically modified hematopoietic stem cells
-
DOI 10.1172/JCI200419205
-
Biffi, A., De Palma, M., Quattrini, A., et al. (2004). Correction of metachromatic leukodystrophy in the mouse model by transplantation of genetically modified hematopoietic stem cells. J. Clin. Invest. 113, 1118-1129. (Pubitemid 38544097)
-
(2004)
Journal of Clinical Investigation
, vol.113
, Issue.8
, pp. 1118-1129
-
-
Biffi, A.1
De Palma, M.2
Quattrini, A.3
Del Carro, U.4
Amadio, S.5
Visigalli, I.6
Sessa, M.7
Fasano, S.8
Brambilla, R.9
Marchesini, S.10
Bordignon, C.11
Naldini, L.12
-
5
-
-
0027228422
-
Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: Concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells
-
Burns, J.C., Friedmann, T., Driever, W., et al. (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. (Pubitemid 23260849)
-
(1993)
Proceedings of the National Academy of Sciences of the United States of America
, vol.90
, Issue.17
, pp. 8033-8037
-
-
Burns, J.C.1
Friedmann, T.2
Driever, W.3
Burrascano, M.4
Yee, J.-K.5
-
6
-
-
70449427834
-
Hematopoietic stem cell gene therapy with a lentiviral vector in X-linked adrenoleukodystrophy
-
Cartier, N., Hacein-Bey-Abina, S., Bartholomae, C.C., et al. (2009). Hematopoietic stem cell gene therapy with a lentiviral vector in X-linked adrenoleukodystrophy. Science 326, 818-823.
-
(2009)
Science
, vol.326
, pp. 818-823
-
-
Cartier, N.1
Hacein-Bey-Abina, S.2
Bartholomae, C.C.3
-
7
-
-
77956928344
-
Transfusion independence and HMGA2 activation after gene therapy of human b-thalassaemia
-
Cavazzana-Calvo, M., Payen, E., Negre, O., et al. (2010). Transfusion independence and HMGA2 activation after gene therapy of human b-thalassaemia. Nature 467, 318-322.
-
(2010)
Nature
, vol.467
, pp. 318-322
-
-
Cavazzana-Calvo, M.1
Payen, E.2
Negre, O.3
-
8
-
-
20144389599
-
A lentiviral vector encoding the human Wiskott-Aldrich syndrome protein corrects immune and cytoskeletal defects in WASP knockout mice
-
DOI 10.1038/sj.gt.3302440
-
Charrier, S., Stockholm, D., Seye, K., et al. (2005). A lentiviral vector encoding the human Wiskott-Aldrich syndrome protein corrects immune and cytoskeletal defects in WASP knockout mice. Gene Ther. 12, 597-606. (Pubitemid 40468107)
-
(2005)
Gene Therapy
, vol.12
, Issue.7
, pp. 597-606
-
-
Charrier, S.1
Stockholm, D.2
Seye, K.3
Opolon, P.4
Taveau, M.5
Gross, D.-A.6
Bucher-Laurent, S.7
Delenda, C.8
Vainchenker, W.9
Danos, O.10
Galy, A.11
-
9
-
-
33847178027
-
Lentiviral vectors targeting WASp expression to hematopoietic cells, efficiently transduce and correct cells from WAS patients
-
Charrier, S., Dupre, L., Scaramuzza, S., et al. (2007). Lentiviral vectors targeting WASp expression to hematopoietic cells, efficiently transduce and correct cells from WAS patients. Gene Ther. 14, 415-428.
-
(2007)
Gene Ther.
, vol.14
, pp. 415-428
-
-
Charrier, S.1
Dupre, L.2
Scaramuzza, S.3
-
10
-
-
68049104312
-
Quantitative proteomic analysis of lentiviral vectors using 2-DE
-
Denard, J., Rundwasser, S., Laroudie, N., et al. (2009). Quantitative proteomic analysis of lentiviral vectors using 2-DE. Proteomics 9, 3666-3676.
-
(2009)
Proteomics
, vol.9
, pp. 3666-3676
-
-
Denard, J.1
Rundwasser, S.2
Laroudie, N.3
-
11
-
-
35648966566
-
Optimized protocol for the large scale production of HIV pseudovirions by transient transfection of HEK293T cells with linear fully deacylated polyethylenimine
-
DOI 10.1016/j.jviromet.2007.07.011, PII S0166093407002662
-
Devitt, G., Thomas, M., Klibanov, A.M., et al. (2007). Optimized protocol for the large scale production of HIV pseudovirions by transient transfection of HEK293T cells with linear fully deacylated polyethylenimine. J. Virol. Methods 146, 298-304. (Pubitemid 350030948)
-
(2007)
Journal of Virological Methods
, vol.146
, Issue.1-2
, pp. 298-304
-
-
Devitt, G.1
Thomas, M.2
Klibanov, A.M.3
Pfeiffer, T.4
Bosch, V.5
-
12
-
-
77955608799
-
\+ cells in patients undergoing transplantation for AIDS-related lym-phoma
-
\+ cells in patients undergoing transplantation for AIDS-related lym-phoma. Sci. Transl. Med. 2, 36ra43.
-
(2010)
Sci. Transl. Med.
, vol.2
-
-
Digiusto, D.L.1
Krishnan, A.2
Li, L.3
-
13
-
-
0031710033
-
A third-generation lentivirus vector with a conditional packaging system
-
Dull, T., Zufferey, R., Kelly, M., et al. (1998). A third-generation lentivirus vector with a conditional packaging system. J. Virol. 72, 8463-8471. (Pubitemid 28471781)
-
(1998)
Journal of Virology
, vol.72
, Issue.11
, 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
-
14
-
-
33645458063
-
Efficacy of gene therapy for Wiskott-Aldrich syndrome using a WAS promoter/cDNA-containing lentiviral vector and nonlethal irradiation
-
Dupre, L., Marangoni, F., Scaramuzza, S., et al. (2006). Efficacy of gene therapy for Wiskott-Aldrich syndrome using a WAS promoter/cDNA-containing lentiviral vector and nonlethal irradiation. Hum. Gene Ther. 17, 303-313.
-
(2006)
Hum. Gene Ther.
, vol.17
, pp. 303-313
-
-
Dupre, L.1
Marangoni, F.2
Scaramuzza, S.3
-
15
-
-
0041854294
-
Development of a sensitive assay for detection of replication-competent recombinant lentivirus in large-scale HIV-based vector preparations
-
DOI 10.1016/S1525-0016(03)00167-9
-
Escarpe, P., Zayek, N., Chin, P., et al. (2003). Development of a sensitive assay for detection of replication-competent recom-binant lentivirus in large-scale HIV-based vector preparations. Mol. Ther. 8, 332-341. (Pubitemid 37062843)
-
(2003)
Molecular Therapy
, vol.8
, Issue.2
, pp. 332-341
-
-
Escarpe, P.1
Zayek, N.2
Chin, P.3
Borellini, F.4
Zufferey, R.5
Veres, G.6
Kiermer, V.7
-
16
-
-
0034914353
-
A new-generation stable inducible packaging cell line for lentiviral vectors
-
DOI 10.1089/104303401750195935
-
Farson, D., Witt, R., McGuinness, R., et al. (2001). A new-generation stable inducible packaging cell line for lentiviral vectors. Hum. Gene Ther. 12, 981-997. (Pubitemid 32681861)
-
(2001)
Human Gene Therapy
, vol.12
, Issue.8
, pp. 981-997
-
-
Farson, D.1
Witt, R.2
McGuinness, R.3
Dull, T.4
Kelly, M.5
Song, J.6
Radeke, R.7
Bukovsky, A.8
Consiglio, A.9
Naldini, L.10
-
17
-
-
0035988776
-
HIV-based vectors: Preparation and use
-
Follenzi, A., and Naldini, L. (2002). HIV-based vectors: Preparation and use. Methods Mol. Med. 69, 259-274.
-
(2002)
Methods Mol. Med.
, vol.69
, pp. 259-274
-
-
Follenzi, A.1
Naldini, L.2
-
18
-
-
38949185099
-
Development of lentiviral gene therapy for Wiskott Aldrich syndrome
-
DOI 10.1517/14712598.8.2.181
-
Galy, A., Roncarolo, M.G., and Thrasher, A.J. (2008). Development of lentiviral gene therapy for Wiskott-Aldrich syndrome. Expert Opin. Biol. Ther. 8, 181-190. (Pubitemid 351233711)
-
(2008)
Expert Opinion on Biological Therapy
, vol.8
, Issue.2
, pp. 181-190
-
-
Galy, A.1
Roncarolo, M.-G.2
Thrasher, A.J.3
-
19
-
-
27644457706
-
Upscaling of lentiviral vector production by tangential flow filtration
-
DOI 10.1002/jgm.778
-
Geraerts, M., Michiels, M., Baekelandt, V., et al. (2005). Upscaling of lentiviral vector production by tangential flow filtration. J. Gene Med. 7, 1299-1310. (Pubitemid 41555436)
-
(2005)
Journal of Gene Medicine
, vol.7
, Issue.10
, pp. 1299-1310
-
-
Geraerts, M.1
Micheils, M.2
Baekelandt, V.3
Debyser, Z.4
Gijsbers, R.5
-
20
-
-
0017710978
-
Characteristics of a human cell line transformed by DNA from human adenovirus type 5
-
Graham, F.L., Smiley, J., Russell, W.C., et al. (1977). Characteristics of a human cell line transformed by DNA from human adenovirus type 5. J. Gen. Virol. 36, 59-74.
-
(1977)
J. Gen. Virol.
, vol.36
, pp. 59-74
-
-
Graham, F.L.1
Smiley, J.2
Russell, W.C.3
-
22
-
-
0037129435
-
Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy
-
DOI 10.1056/NEJMoa012616
-
Hacein-Bey-Abina, S., Le Deist, F., Carlier, F., et al. (2002). Sustained correction of X-linked severe combined immunode-ficiencyby ex vivo gene therapy. N. Engl. J.Med. 346, 1185-1193. (Pubitemid 34984579)
-
(2002)
New England Journal of Medicine
, vol.346
, Issue.16
, pp. 1185-1193
-
-
Hacein-Bey-Abina, S.1
Le Deist, F.2
Carlier, F.3
Bouneaud, C.4
Hue, C.5
De Villartay, J.-P.6
Thrasher, A.J.7
Wulffraat, N.8
Sorensen, R.9
Dupuis-Girod, S.10
Fischer, A.11
Graham Davies, E.12
Kuis, W.13
Leiva, L.14
Cavazzana-Calvo, M.15
-
23
-
-
0038333587
-
Continuous high-titer HIV-1 vector production
-
DOI 10.1038/nbt815
-
Ikeda, Y., Takeuchi, Y., Martin, F., et al. (2003). Continuous high-titer HIV-1 vector production. Nat. Biotechnol. 21, 569-572. (Pubitemid 36532025)
-
(2003)
Nature Biotechnology
, vol.21
, Issue.5
, pp. 569-572
-
-
Ikeda, Y.1
Takeuchi, Y.2
Martin, F.3
Cosset, F.-L.4
Mitrophanous, K.5
Collins, M.6
-
24
-
-
0034244658
-
A stable system for the high-titer production of multiply attenuated lentiviral vectors
-
Klages, N., Zufferey, R., and Trono, D. (2000). A stable system for the high-titer production of multiply attenuated lentiviral vectors. Mol. Ther. 2, 170-176.
-
(2000)
Mol. Ther.
, vol.2
, pp. 170-176
-
-
Klages, N.1
Zufferey, R.2
Trono, D.3
-
25
-
-
61849181323
-
Simplified lentivirus vector production in protein-free media using polyethylenimine-mediated transfection
-
Kuroda, H., Kutner, R.H., Bazan, N.G., et al. (2009). Simplified lentivirus vector production in protein-free media using polyethylenimine- mediated transfection. J. Virol. Methods 157, 113-121.
-
(2009)
J. Virol. Methods
, vol.157
, pp. 113-121
-
-
Kuroda, H.1
Kutner, R.H.2
Bazan, N.G.3
-
26
-
-
64749107970
-
Production, concentration and titration of pseudotyped HIV-1-based len-tiviral vectors
-
Kutner, R.H., Zhang, X.Y., and Reiser, J. (2009). Production, concentration and titration of pseudotyped HIV-1-based len-tiviral vectors. Nat. Protoc. 4, 495-505.
-
(2009)
Nat. Protoc.
, vol.4
, pp. 495-505
-
-
Kutner, R.H.1
Zhang, X.Y.2
Reiser, J.3
-
27
-
-
0344305491
-
Correction of a mouse model of sickle cell disease: Lentiviral/ antisickling β-globin gene transduction of unmobilized, purified hematopoietic stem cells
-
DOI 10.1182/blood-2003-04-1251
-
Levasseur, D.N., Ryan, T.M., Pawlik, K.M., et al. (2003). Correction of a mouse model of sickle cell disease: lentiviral/ anti-sickling b-globin gene transduction of unmobilized, purified hematopoietic stem cells. Blood 102, 4312-4319. (Pubitemid 37494089)
-
(2003)
Blood
, vol.102
, Issue.13
, pp. 4312-4319
-
-
Levasseur, D.N.1
Ryan, T.M.2
Pawlik, K.M.3
Townes, T.M.4
-
28
-
-
33751251058
-
Gene transfer in humans using a conditionally replicating lentiviral vector
-
DOI 10.1073/pnas.0608138103
-
Levine, B.L., Humeau, L.M., Boyer, J., et al. (2006). Gene transfer in humans using a conditionally replicating lentiviral vector. Proc. Natl. Acad. Sci. U.S.A. 103, 17372-17377. (Pubitemid 44788976)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.46
, pp. 17372-17377
-
-
Levine, B.L.1
Humeau, L.M.2
Boyer, J.3
MacGregor, R.-R.4
Rebello, T.5
Lu, X.6
Binder, G.K.7
Slepushkin, V.8
Lemiale, F.9
Mascola, J.R.10
Bushman, F.D.11
Dropulic, B.12
June, C.H.13
-
29
-
-
20844445774
-
Safe two-plasmid production for the first clinical lentivirus vector that achieves >99% transduction in primary cells using a one-step protocol
-
DOI 10.1002/jgm.593
-
Lu, X., Humeau, L., Slepushkin, V., et al. (2004). Safe two-plasmid production for the first clinical lentivirus vector that achieves >99% transduction in primary cells using a one-step protocol. J. Gene Med. 6, 963-973. (Pubitemid 40228111)
-
(2004)
Journal of Gene Medicine
, vol.6
, Issue.9
, pp. 963-973
-
-
Lu, X.1
Humeau, L.2
Slepushkin, V.3
Binder, G.4
Yu, Q.5
Slepushkina, T.6
Chen, Z.7
Merling, R.8
Davis, B.9
Chang, Y.-N.10
Dropulic, B.11
-
30
-
-
70349501369
-
Diverse ge-nomic integration of a lentiviral vector developed for the treatment of Wiskott-Aldrich syndrome
-
Mantovani, J., Charrier, S., Eckenberg, R., et al. (2009). Diverse ge-nomic integration of a lentiviral vector developed for the treatment of Wiskott-Aldrich syndrome. J. Gene Med. 11, 645-654.
-
(2009)
J. Gene Med.
, vol.11
, pp. 645-654
-
-
Mantovani, J.1
Charrier, S.2
Eckenberg, R.3
-
31
-
-
67349217158
-
Evidence for long-term efficacy and safety of gene therapy for Wiskott-Al-drich syndrome in preclinical models
-
Marangoni, F., Bosticardo, M., Charrier, S., et al. (2009). Evidence for long-term efficacy and safety of gene therapy for Wiskott-Al-drich syndrome in preclinical models. Mol. Ther. 17, 1073-1082.
-
(2009)
Mol. Ther.
, vol.17
, pp. 1073-1082
-
-
Marangoni, F.1
Bosticardo, M.2
Charrier, S.3
-
32
-
-
28444441522
-
Detailed design and comparative analysis of protocols for optimized production of high-performance HIV-1-derived lentiviral particles
-
DOI 10.1016/j.ymben.2005.06.006, PII S1096717605000546
-
Mitta, B., Rimann, M., and Fussenegger, M. (2005). Detailed design and comparative analysis of protocols for optimized production of high-performance HIV-1-derived lentiviral particles. Metab. Eng. 7, 426-436. (Pubitemid 41790471)
-
(2005)
Metabolic Engineering
, vol.7
, Issue.5-6
, pp. 426-436
-
-
Mitta, B.1
Rimann, M.2
Fussenegger, M.3
-
33
-
-
0031666744
-
Development of a self-inactivating lentivirus vector
-
Miyoshi, H., Blomer, U., Takahashi, M., et al. (1998). Development of a self-inactivating lentivirus vector. J. Virol. 72, 8150-8157.
-
(1998)
J. Virol.
, vol.72
, pp. 8150-8157
-
-
Miyoshi, H.1
Blomer, U.2
Takahashi, M.3
-
34
-
-
0029993858
-
Efficient transfer, integration, and sustained long-term expression of the transgene in adult rat brains injected with a lentiviral vector
-
DOI 10.1073/pnas.93.21.11382
-
Naldini, L., Blomer, U., Gage, F.H., et al. (1996). Efficient transfer, integration, and sustained long-term expression of the trans-gene in adult rat brains injected with a lentiviral vector. Proc. Natl. Acad. Sci. U.S.A. 93, 11382-11388. (Pubitemid 26347130)
-
(1996)
Proceedings of the National Academy of Sciences of the United States of America
, vol.93
, Issue.21
, pp. 11382-11388
-
-
Naldini, L.1
Blomer, U.2
Gage, F.H.3
Trono, D.4
Verma, I.M.5
-
35
-
-
21044453936
-
Generation of a packaging cell line for prolonged large-scale production of high-titer HIV-1-based lentiviral vector
-
DOI 10.1002/jgm.726
-
Ni, Y., Sun, S., Oparaocha, I., et al. (2005). Generation of a packaging cell line for prolonged large-scale production of high-titer HIV-1-based lentiviral vector. J. Gene Med. 7, 818-834. (Pubitemid 40872867)
-
(2005)
Journal of Gene Medicine
, vol.7
, Issue.6
, pp. 818-834
-
-
Ni, Y.1
Sun, S.2
Oparaocha, I.3
Humeau, L.4
Davis, B.5
Cohen, R.6
Binder, G.7
Chang, Y.-N.8
Slepushkin, V.9
Dropulic, B.10
-
36
-
-
33646061085
-
The Wiskott-Aldrich syndrome
-
DOI 10.1016/j.jaci.2006.02.005, PII S0091674906003162
-
Ochs, H.D., and Thrasher, A.J. (2006). The Wiskott-Aldrich syndrome. J. Allergy Clin. Immunol. 117, 725-738. (Pubitemid 44313817)
-
(2006)
Journal of Allergy and Clinical Immunology
, vol.117
, Issue.4
, pp. 725-738
-
-
Ochs, H.D.1
Thrasher, A.J.2
-
37
-
-
29244443951
-
Production scale-up and validation of packaging cell clearance of clinical-grade retroviral vector stocks produced in Cell Factories
-
DOI 10.1038/sj.gt.3302648, PII 3302648
-
Przybylowski, M., Hakakha, A., Stefanski, J., et al. (2006). Production scale-up and validation of packaging cell clearance of clinical-grade retroviral vector stocks produced in cell factories. Gene Ther. 13, 95-100. (Pubitemid 41823856)
-
(2006)
Gene Therapy
, vol.13
, Issue.1
, pp. 95-100
-
-
Przybylowski, M.1
Hakakha, A.2
Stefanski, J.3
Hodges, J.4
Sadelain, M.5
Riviere, I.6
-
38
-
-
0034083194
-
Production and concentration of pseudotyped HIV-1-based gene transfer vectors
-
Reiser, J. (2000). Production and concentration of pseudotyped HIV-1-based gene transfer vectors. Gene Ther. 7, 910-913. (Pubitemid 30386654)
-
(2000)
Gene Therapy
, vol.7
, Issue.11
, pp. 910-913
-
-
Reiser, J.1
-
39
-
-
60649103432
-
Clinical application of lentiviral vectors: Concepts and practice
-
Schambach, A., and Baum, C. (2008). Clinical application of lentiviral vectors: concepts and practice. Curr. Gene Ther. 8, 474-482.
-
(2008)
Curr. Gene Ther.
, vol.8
, pp. 474-482
-
-
Schambach, A.1
Baum, C.2
-
40
-
-
0036463583
-
Gene transfer into hematopoi-etic stem cells using lentiviral vectors
-
Scherr, M., and Eder, M. (2002). Gene transfer into hematopoi-etic stem cells using lentiviral vectors. Curr. Gene Ther. 2, 45-55.
-
(2002)
Curr. Gene Ther.
, vol.2
, pp. 45-55
-
-
Scherr, M.1
Eder, M.2
-
41
-
-
0036957811
-
Efficient gene transfer into the CNS by lentiviral vectors purified by anion exchange chromatography
-
DOI 10.1038/sj.gt.3301848
-
Scherr, M., Battmer, K., Eder, M., et al. (2002). Efficient gene transfer into the CNS by lentiviral vectors purified by anion exchange chromatography. Gene Ther. 9, 1708-1714. (Pubitemid 36104615)
-
(2002)
Gene Therapy
, vol.9
, Issue.24
, pp. 1708-1714
-
-
Scherr, M.1
Battmer, K.2
Eder, M.3
Schule, S.4
Hohenberg, H.5
Ganser, A.6
Grez, M.7
Blomer, U.8
-
42
-
-
2642579534
-
QC release testing of an HIV-1 based lentiviral vector lot and transduced cellular product
-
Schonely, K., Afable, C., Slepushkin, V., et al. (2003). QC release testing of an HIV-1 based lentiviral vector lot and transduced cellular product. Bioproc. J. 2, 39-47.
-
(2003)
Bioproc. J.
, vol.2
, pp. 39-47
-
-
Schonely, K.1
Afable, C.2
Slepushkin, V.3
-
43
-
-
33645888418
-
Downstream processing of oncoretroviral and lentiviral gene therapy vectors
-
Segura, M.M., Kamen, A., and Garnier, A. (2006). Downstream processing of oncoretroviral and lentiviral gene therapy vectors. Biotechnol. Adv. 24, 321-337.
-
(2006)
Biotechnol. Adv.
, vol.24
, pp. 321-337
-
-
Segura, M.M.1
Kamen, A.2
Garnier, A.3
-
44
-
-
35648981154
-
Production of lentiviral vectors by large-scale transient transfection of suspension cultures and affinity chromatography purification
-
DOI 10.1002/bit.21467
-
Segura, M.M., Garnier, A., Durocher, Y., et al. (2007). Production of lentiviral vectors by large-scale transient transfection of suspension cultures and affinity chromatography purification. Biotechnol. Bioeng. 98, 789-799. (Pubitemid 350032683)
-
(2007)
Biotechnology and Bioengineering
, vol.98
, Issue.4
, pp. 789-799
-
-
Segura, M.M.1
Garnier, A.2
Durocher, Y.3
Coelho, H.4
Kamen, A.5
-
45
-
-
0030892087
-
Development of antibodies to fetal calf serum with arthus-like reactions in human immunodeficiency virus-infected patients given syngeneic lymphocyte infusions
-
Selvaggi, T.A., Walker, R.E., and Fleisher, T.A. (1997). Development of antibodies to fetal calf serum with arthus-like reactions in human immunodeficiency virus-infected patients given syngeneic lymphocyte infusions. Blood 89, 776-779. (Pubitemid 27121269)
-
(1997)
Blood
, vol.89
, Issue.3
, pp. 776-779
-
-
Selvaggi, T.A.1
Walker, R.E.2
Fleisher, T.A.3
-
46
-
-
33846430437
-
Large-scale purification of a lentiviral vector by size exclusion chroma-tography or Mustang Q ion exchange capsule
-
Slepushkin, V., Chang, N., Cohen, R., et al. (2003). Large-scale purification of a lentiviral vector by size exclusion chroma-tography or Mustang Q ion exchange capsule. Bioproc. J. 2, 89-95.
-
(2003)
Bioproc. J.
, vol.2
, pp. 89-95
-
-
Slepushkin, V.1
Chang, N.2
Cohen, R.3
-
47
-
-
67149117119
-
Efficient construction of producer cell lines for a SIN lentiviral vector for SCID-X1 gene therapy by concatemeric array transfection
-
Throm, R.E., Ouma, A.A., Zhou, S., et al. (2009). Efficient construction of producer cell lines for a SIN lentiviral vector for SCID-X1 gene therapy by concatemeric array transfection. Blood 113, 5104-5110.
-
(2009)
Blood
, vol.113
, pp. 5104-5110
-
-
Throm, R.E.1
Ouma, A.A.2
Zhou, S.3
-
48
-
-
0043269712
-
Size-exclusion chromatography purification of high-titer vesicular stomatitis virus G glycoprotein-pseudotyped retrovectors for cell and gene therapy applications
-
DOI 10.1089/104303403322167984
-
Transfiguracion, J., Jaalouk, D.E., Ghani, K., et al. (2003). Size-exclusion chromatography purification of high-titer vesicular stomatitis virus G glycoprotein-pseudotyped retrovectors for cell and gene therapy applications. Hum. Gene Ther. 14, 1139-1153. (Pubitemid 36930404)
-
(2003)
Human Gene Therapy
, vol.14
, Issue.12
, pp. 1139-1153
-
-
Transfiguracion, J.1
Jaalouk, D.E.2
Ghani, K.3
Galipeau, J.4
Kamen, A.5
-
49
-
-
0036376741
-
Immune response to fetal calf serum by two adenosine deaminase-deficient patients after T cell gene therapy
-
DOI 10.1089/10430340260201699
-
Tuschong, L., Soenen, S.L., Blaese, R.M., et al. (2002). Immune response to fetal calf serum by two adenosine deaminase-deficient patients after T cell gene therapy. Hum. Gene Ther. 13, 1605-1610. (Pubitemid 35034680)
-
(2002)
Human Gene Therapy
, vol.13
, Issue.13
, pp. 1605-1610
-
-
Tuschong, L.1
Soenen, S.L.2
Blaese, R.M.3
Candotti, F.4
Muul, L.M.5
-
50
-
-
67349202780
-
Validation of a mutated PRE sequence allowing high and sustained transgene expression while abrogating WHV-X protein synthesis: Application to the gene therapy of WAS
-
Zanta-Boussif, M.A., Charrier, S., Brice-Ouzet, A., et al. (2009). Validation of a mutated PRE sequence allowing high and sustained transgene expression while abrogating WHV-X protein synthesis: Application to the gene therapy of WAS. Gene Ther. 16, 605-619.
-
(2009)
Gene Ther.
, vol.16
, pp. 605-619
-
-
Zanta-Boussif, M.A.1
Charrier, S.2
Brice-Ouzet, A.3
-
51
-
-
0031743608
-
Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery
-
Zufferey, R., Dull, T., Mandel, R.J., et al. (1998). Self-inactivating lentivirus vector for safe and efficient in vivo gene delivery. J. Virol. 72, 9873-9880. (Pubitemid 28520853)
-
(1998)
Journal of Virology
, vol.72
, Issue.12
, 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
-
52
-
-
41149133413
-
Physiological promoters reduce the genotoxic risk of integrating gene vectors
-
DOI 10.1038/mt.2008.5, PII MT20085
-
Zychlinski, D., Schambach, A., Modlich, U., et al. (2008). Physiological promoters reduce the genotoxic risk of integrating gene vectors. Mol. Ther. 16, 718-725. (Pubitemid 351426173)
-
(2008)
Molecular Therapy
, vol.16
, Issue.4
, pp. 718-725
-
-
Zychlinski, D.1
Schambach, A.2
Modlich, U.3
Maetzig, T.4
Meyer, J.5
Grassman, E.6
Mishra, A.7
Baum, C.8
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