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Inclusion of an IgG1-Fc spacer abrogates efficacy of CD19 CAR T cells in a xenograft mouse model.
Published in:
Gene Therapy, 2015, v. 22, n. 5, p. 391, doi. 10.1038/gt.2015.4
By:
- Almåsbak, H;
- Walseng, E;
- Kristian, A;
- Myhre, M R;
- Suso, E M;
- Munthe, L A;
- Andersen, J T;
- Wang, M Y;
- Kvalheim, G;
- Gaudernack, G;
- Kyte, J A
Publication type:
Article
Therapeutic effect of prenatal alkalization and PTC124 in Na+/HCO3− cotransporter 1 p.W516* knock-in mice.
Published in:
Gene Therapy, 2015, v. 22, n. 5, p. 374, doi. 10.1038/gt.2015.7
By:
- Fang, Y-W;
- Yang, S-S;
- Chau, T;
- Nakamura, M;
- Yamazaki, O;
- Seki, G;
- Yamada, H;
- Hsu, H-M;
- Cheng, C-J;
- Lin, S-H
Publication type:
Article
Localizing the RPGR protein along the cilium: a new method to determine efficacies to treat RPGR mutations.
Published in:
Gene Therapy, 2015, v. 22, n. 5, p. 413, doi. 10.1038/gt.2014.128
By:
- Da Costa, R;
- Glaus, E;
- Tiwari, A;
- Kloeckener-Gruissem, B;
- Berger, W;
- Neidhardt, J
Publication type:
Article
β-Cell-targeted blockage of PD1 and CTLA4 pathways prevents development of autoimmune diabetes and acute allogeneic islets rejection.
Published in:
Gene Therapy, 2015, v. 22, n. 5, p. 430, doi. 10.1038/gt.2015.18
By:
- El Khatib, M M;
- Sakuma, T;
- Tonne, J M;
- Mohamed, M S;
- Holditch, S J;
- Lu, B;
- Kudva, Y C;
- Ikeda, Y
Publication type:
Article
Safety and angiogenic effects of systemic gene delivery of a modified erythropoietin.
Published in:
Gene Therapy, 2015, v. 22, n. 5, p. 365, doi. 10.1038/gt.2015.12
By:
- de Lucas Cerrillo, A M;
- Bond, W S;
- Rex, T S
Publication type:
Article
Tolerance of activated pathogenic CD4+ T cells by transcriptional targeting of dendritic cells.
Published in:
Gene Therapy, 2015, v. 22, n. 5, p. 382, doi. 10.1038/gt.2015.6
By:
- de Andrade Pereira, B;
- Ackermann, M;
- Chaudhary, S;
- Vogel, R;
- Vogt, B;
- Dresch, C;
- Fraefel, C
Publication type:
Article
Harnessing the clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated Cas9 system to disrupt the hepatitis B virus.
Published in:
Gene Therapy, 2015, v. 22, n. 5, p. 404, doi. 10.1038/gt.2015.2
By:
- Zhen, S;
- Hua, L;
- Liu, Y-H;
- Gao, L-C;
- Fu, J;
- Wan, D-Y;
- Dong, L-H;
- Song, H-F;
- Gao, X
Publication type:
Article
Preferable sites and orientations of transgene inserted in the adenovirus vector genome: The E3 site may be unfavorable for transgene position.
Published in:
Gene Therapy, 2015, v. 22, n. 5, p. 421, doi. 10.1038/gt.2014.124
By:
- Suzuki, M;
- Kondo, S;
- Pei, Z;
- Maekawa, A;
- Saito, I;
- Kanegae, Y
Publication type:
Article
Chimeric rabies SADB19-VSVg-pseudotyped lentiviral vectors mediate long-range retrograde transduction from the mouse spinal cord.
Published in:
Gene Therapy, 2015, v. 22, n. 5, p. 357, doi. 10.1038/gt.2015.3
By:
- Schoderboeck, L;
- Riad, S;
- Bokor, A M;
- Wicky, H E;
- Strauss, M;
- Bostina, M;
- Oswald, M J;
- Empson, R M;
- Hughes, S M
Publication type:
Article

Found: 9

Inclusion of an IgG1-Fc spacer abrogates efficacy of CD19 CAR T cells in a xenograft mouse model.

Therapeutic effect of prenatal alkalization and PTC124 in Na<sup>+</sup>/HCO<sub>3</sub><sup>−</sup> cotransporter 1 p.W516* knock-in mice.

Localizing the RPGR protein along the cilium: a new method to determine efficacies to treat RPGR mutations.

β-Cell-targeted blockage of PD1 and CTLA4 pathways prevents development of autoimmune diabetes and acute allogeneic islets rejection.

Safety and angiogenic effects of systemic gene delivery of a modified erythropoietin.

Tolerance of activated pathogenic CD4+ T cells by transcriptional targeting of dendritic cells.

Harnessing the clustered regularly interspaced short palindromic repeat (CRISPR)/CRISPR-associated Cas9 system to disrupt the hepatitis B virus.

Preferable sites and orientations of transgene inserted in the adenovirus vector genome: The E3 site may be unfavorable for transgene position.

Chimeric rabies SADB19-VSVg-pseudotyped lentiviral vectors mediate long-range retrograde transduction from the mouse spinal cord.