Works matching IS 09697128 AND DT 2009 AND VI 16 AND IP 1

Results: 21

Novel anti-VEGF chimeric molecules delivered by AAV vectors for inhibition of retinal neovascularization.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 10, doi. 10.1038/gt.2008.115

By:

Pechan, P.;
Rubin, H.;
Lukason, M.;
Ardinger, J.;
DuFresne, E.;
Hauswirth, W. W.;
Wadsworth, S. C.;
Scaria, A.

Publication type:

Article

PET imaging of thymidine kinase gene expression in the liver of non-human primates following systemic delivery of an adenoviral vector.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 136, doi. 10.1038/gt.2008.122

By:

Fontanellas, A.;
Hervas-Stubbs, S.;
Sampedro, A.;
Collantes, M.;
Azpilicueta, A.;
Mauleón, I.;
Pañeda, A.;
Quincoces, G.;
Prieto, J.;
Melero, I.;
Peñuelas, I.

Publication type:

Article

Prevention of interferon-stimulated gene expression using microRNA-designed hairpins.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 142, doi. 10.1038/gt.2008.123

By:

Bauer, M.;
Kinkl, N.;
Meixner, A.;
Kremmer, E.;
Riemenschneider, M.;
Förstl, H.;
Gasser, T.;
Ueffing, M.

Publication type:

Article

Evaluation of safety and efficacy of RNAi against HIV-1 in the human immune system (Rag-2-/-γc-/-) mouse model.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 148, doi. 10.1038/gt.2008.124

By:

ter Brake, O.;
Legrand, N.;
von Eije, K. J.;
Centlivre, M.;
Spits, H.;
Weijer, K.;
Blom, B.;
Berkhout, B.

Publication type:

Article

An efficient transfection method for mouse embryonic stem cells.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 154, doi. 10.1038/gt.2008.125

By:

Ko, B. S.;
Chang, T. C.;
Shyue, S. K.;
Chen, Y. C.;
Liou, J. Y.

Publication type:

Article

Redox proteins thioredoxin 1 and thioredoxin 2 support retinal ganglion cell survival in experimental glaucoma.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 17, doi. 10.1038/gt.2008.126

By:

Munemasa, Y.;
Ahn, J. H.;
Kwong, J. M. K.;
Caprioli, J.;
Piri, N.

Publication type:

Article

SIVMAC Vpx improves the transduction of dendritic cells with nonintegrative HIV-1-derived vectors.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 159, doi. 10.1038/gt.2008.128

By:

Berger, G.;
Goujon, C.;
Darlix, J.-L.;
Cimarelli, A.

Publication type:

Article

Herpes simplex virus vector-mediated delivery of neurturin rescues erectile dysfunction of cavernous nerve injury.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 26, doi. 10.1038/gt.2008.132

By:

Kato, R.;
Wolfe, D.;
Coyle, C. H.;
Wechuck, J. B.;
Tyagi, P.;
Tsukamoto, T.;
Nelson, J. B.;
Glorioso, J. C.;
Chancellor, M. B.;
Yoshimura, N.

Publication type:

Article

Transplantation of BMSCs expressing hPDGF-A/hBD2 promotes wound healing in rats with combined radiation-wound injury.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 34, doi. 10.1038/gt.2008.133

By:

Hao, L.;
Wang, J.;
Zou, Z.;
Yan, G.;
Dong, S.;
Deng, J.;
Ran, X.;
Feng, Y.;
Luo, C.;
Wang, Y.;
Cheng, T.

Publication type:

Article

A small regulatory element from chromosome 19 enhances liver-specific gene expression.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 43, doi. 10.1038/gt.2008.134

By:

Li, C.;
Hirsch, M.;
Carter, P.;
Asokan, A.;
Zhou, X.;
Wu, Z.;
Samulski, R. J.

Publication type:

Article

Gene delivery into ischemic myocardium by double-targeted lipoplexes with anti-myosin antibody and TAT peptide.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 52, doi. 10.1038/gt.2008.135

By:

Ko, Y. T.;
Hartner, W. C.;
Kale, A.;
Torchilin, V. P.

Publication type:

Article

Enhancing transduction of the liver by adeno-associated viral vectors.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 60, doi. 10.1038/gt.2008.137

By:

Nathwani, A. C.;
Cochrane, M.;
McIntosh, J.;
Ng, C. Y. C.;
Zhou, J.;
Gray, J. T.;
Davidoff, A. M.

Publication type:

Article

Doxycycline-controlled splicing modulation by regulated antisense U7 snRNA expression cassettes.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 70, doi. 10.1038/gt.2008.138

By:

Marquis, J.;
Kämpfer, S. S.;
Angehrn, L.;
Schümperli, D.

Publication type:

Article

Microvascular free tissue transfer for gene delivery: in vivo evaluation of different routes of plasmid and adenoviral delivery.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 78, doi. 10.1038/gt.2008.140

By:

Agrawal, V. K.;
Copeland, K. M.;
Barbachano, Y.;
Rahim, A.;
Seth, R.;
White, C. L.;
Hingorani, M.;
Nutting, C. M.;
Kelly, M.;
Harris, P.;
Pandha, H.;
Melcher, A. A.;
Vile, R. G.;
Porter, C.;
Harrington, K. J.

Publication type:

Article

Lentiviral gene transfer to reduce atherosclerosis progression by long-term CC-chemokine inhibition.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 93, doi. 10.1038/gt.2008.141

By:

Bursill, C. A.;
McNeill, E.;
Wang, L.;
Hibbitt, O. C.;
Wade-Martins, R.;
Paterson, D. J.;
Greaves, D. R.;
Channon, K. M.

Publication type:

Article

Extended release of adenovirus from silica implants in vitro and in vivo.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 103, doi. 10.1038/gt.2008.142

By:

Kangasniemi, L.;
Koskinen, M.;
Jokinen, M.;
Toriseva, M.;
Ala-Aho, R.;
Kähäri, V.-M.;
Jalonen, H.;
Ylä-Herttuala, S.;
Moilanen, H.;
Stenman, U.-H.;
Diaconu, I.;
Kanerva, A.;
Pesonen, S.;
Hakkarainen, T.;
Hemminki, A.

Publication type:

Article

Transgene optimization significantly improves SIN vector titers, gp91phox expression and reconstitution of superoxide production in X-CGD cells.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 111, doi. 10.1038/gt.2008.143

By:

Moreno-Carranza, B;
Gentsch, M.;
Stein, S.;
Schambach, A.;
Santilli, G.;
Rudolf, E.;
Ryser, M. F.;
Haria, S.;
Thrasher, A. J.;
Baum, C.;
Brenner, S.;
Grez, M.

Publication type:

Article

Microwave irradiation enhances gene and oligonucleotide delivery and induces effective exon skipping in myoblasts.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 119, doi. 10.1038/gt.2008.144

By:

Doran, T. J.;
Lu, P. J.;
Vanier, G. S.;
Collins, M. J.;
Wu, B.;
Lu, Q. L.

Publication type:

Article

Polymeric gene delivery of ischemia-inducible VEGF significantly attenuates infarct size and apoptosis following myocardial infarct.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 127, doi. 10.1038/gt.2008.146

By:

Yockman, J. W.;
Choi, D.;
Whitten, M. G.;
Chang, C. W.;
Kastenmeier, A.;
Erickson, H.;
Albanil, A.;
Lee, M.;
Kim, S. W.;
Bull, D. A.

Publication type:

Article

Cystic fibrosis: Ferreting with fibroblasts for cystic fibrosis.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 1, doi. 10.1038/gt.2008.155

By:

Griesenbach, U.;
Alton, E. W. F. W.

Publication type:

Article

Progress & Prospects: Gene therapy in aging.

Published in:

Gene Therapy, 2009, v. 16, n. 1, p. 3, doi. 10.1038/gt.2008.166

By:

Rattan, S. I. S.;
Singh, R.

Publication type:

Article

Works matching IS 09697128 AND DT 2009 AND VI 16 AND IP 1

Novel anti-VEGF chimeric molecules delivered by AAV vectors for inhibition of retinal neovascularization.

PET imaging of thymidine kinase gene expression in the liver of non-human primates following systemic delivery of an adenoviral vector.

Prevention of interferon-stimulated gene expression using microRNA-designed hairpins.

Evaluation of safety and efficacy of RNAi against HIV-1 in the human immune system (Rag-2<sup>-/-</sup>γ<sub>c</sub><sup>-/-</sup>) mouse model.

An efficient transfection method for mouse embryonic stem cells.

Redox proteins thioredoxin 1 and thioredoxin 2 support retinal ganglion cell survival in experimental glaucoma.

SIV<sub>MAC</sub> Vpx improves the transduction of dendritic cells with nonintegrative HIV-1-derived vectors.

Herpes simplex virus vector-mediated delivery of neurturin rescues erectile dysfunction of cavernous nerve injury.

Transplantation of BMSCs expressing hPDGF-A/hBD2 promotes wound healing in rats with combined radiation-wound injury.

A small regulatory element from chromosome 19 enhances liver-specific gene expression.

Gene delivery into ischemic myocardium by double-targeted lipoplexes with anti-myosin antibody and TAT peptide.

Enhancing transduction of the liver by adeno-associated viral vectors.

Doxycycline-controlled splicing modulation by regulated antisense U7 snRNA expression cassettes.

Microvascular free tissue transfer for gene delivery: in vivo evaluation of different routes of plasmid and adenoviral delivery.

Lentiviral gene transfer to reduce atherosclerosis progression by long-term CC-chemokine inhibition.

Extended release of adenovirus from silica implants in vitro and in vivo.

Transgene optimization significantly improves SIN vector titers, gp91<sup>phox</sup> expression and reconstitution of superoxide production in X-CGD cells.

Microwave irradiation enhances gene and oligonucleotide delivery and induces effective exon skipping in myoblasts.

Polymeric gene delivery of ischemia-inducible VEGF significantly attenuates infarct size and apoptosis following myocardial infarct.

Cystic fibrosis: Ferreting with fibroblasts for cystic fibrosis.

Progress & Prospects: Gene therapy in aging.