Works matching IS 09697128 AND DT 2015 AND VI 22 AND IP 6

Results: 9

Shedding of clinical-grade lentiviral vectors is not detected in a gene therapy setting.

Published in:

Gene Therapy, 2015, v. 22, n. 6, p. 496, doi. 10.1038/gt.2015.10

By:

Cesani, M;
Plati, T;
Lorioli, L;
Benedicenti, F;
Redaelli, D;
Dionisio, F;
Biasco, L;
Montini, E;
Naldini, L;
Biffi, A

Publication type:

Article

A new method to monitor antigen-specific CD8<sup>+</sup> T cells, avoiding additional target cells and the restriction to human leukocyte antigen haplotype.

Published in:

Gene Therapy, 2015, v. 22, n. 6, p. 516, doi. 10.1038/gt.2015.15

By:

Prommersberger, S;
Höfflin, S;
Schuler-Thurner, B;
Schuler, G;
Schaft, N;
Dörrie, J

Publication type:

Article

Mesenchymal stromal cells overexpressing vascular endothelial growth factor in ovine myocardial infarction.

Published in:

Gene Therapy, 2015, v. 22, n. 6, p. 449, doi. 10.1038/gt.2015.28

By:

Locatelli, P;
Olea, F D;
Hnatiuk, A;
De Lorenzi, A;
Cerdá, M;
Giménez, C S;
Sepúlveda, D;
Laguens, R;
Crottogini, A

Publication type:

Article

The role of transduced bone marrow cells overexpressing BMP-2 in healing critical-sized defects in a mouse femur.

Published in:

Gene Therapy, 2015, v. 22, n. 6, p. 467, doi. 10.1038/gt.2015.14

By:

Pensak, M;
Hong, S;
Dukas, A;
Tinsley, B;
Drissi, H;
Tang, A;
Cote, M;
Sugiyama, O;
Lichtler, A;
Rowe, D;
Lieberman, J R

Publication type:

Article

Ameliorating pathogenesis by removing an exon containing a missense mutation: a potential exon-skipping therapy for laminopathies.

Published in:

Gene Therapy, 2015, v. 22, n. 6, p. 503, doi. 10.1038/gt.2015.8

By:

Scharner, J;
Figeac, N;
Ellis, J A;
Zammit, P S

Publication type:

Article

Lister strain vaccinia virus with thymidine kinase gene deletion is a tractable platform for development of a new generation of oncolytic virus.

Published in:

Gene Therapy, 2015, v. 22, n. 6, p. 476, doi. 10.1038/gt.2015.13

By:

Hughes, J;
Wang, P;
Alusi, G;
Shi, H;
Chu, Y;
Wang, J;
Bhakta, V;
McNeish, I;
McCart, A;
Lemoine, N R;
Wang, Y

Publication type:

Article

Expression of an engineered soluble coxsackievirus and adenovirus receptor by a dimeric AAV9 vector inhibits adenovirus infection in mice.

Published in:

Gene Therapy, 2015, v. 22, n. 6, p. 458, doi. 10.1038/gt.2015.19

By:

Röger, C;
Pozzuto, T;
Klopfleisch, R;
Kurreck, J;
Pinkert, S;
Fechner, H

Publication type:

Article

Intra-articular delivery of anti-Hif-2α siRNA by chondrocyte-homing nanoparticles to prevent cartilage degeneration in arthritic mice.

Published in:

Gene Therapy, 2015, v. 22, n. 6, p. 439, doi. 10.1038/gt.2015.16

By:

Pi, Y;
Zhang, X;
Shao, Z;
Zhao, F;
Hu, X;
Ao, Y

Publication type:

Article

The impact of HIV-1 genetic diversity on the efficacy of a combinatorial RNAi-based gene therapy.

Published in:

Gene Therapy, 2015, v. 22, n. 6, p. 485, doi. 10.1038/gt.2015.11

By:

Herrera-Carrillo, E;
Berkhout, B

Publication type:

Article