Works matching IS 09697128 AND DT 2006 AND VI 13 AND IP 7

Results: 11

RNAi therapeutics: SNALPing siRNAs in vivo.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 583, doi. 10.1038/sj.gt.3302661
By:
- Rossi, J. J.
Publication type:
Article
Administration-route and gender-independent long-term therapeutic correction of phenylketonuria (PKU) in a mouse model by recombinant adeno-associated virus 8 pseudotyped vector-mediated gene transfer.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 587, doi. 10.1038/sj.gt.3302684
By:
- Ding, Z.;
- Georgiev, P.;
- Thöny, B.
Publication type:
Article
Nonviral gene delivery: Thinking of silica.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 585, doi. 10.1038/sj.gt.3302662
By:
- Luo, D.;
- Saltzman, W. M.
Publication type:
Article
Herpes simplex virus 1 recombinant virions exhibiting the amino terminal fragment of urokinase-type plasminogen activator can enter cells via the cognate receptor.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 621, doi. 10.1038/sj.gt.3302685
By:
- Kamiyama, H.;
- Zhou, G.;
- Roizman, B.
Publication type:
Article
Dentin matrix protein 1 induces cytodifferentiation of dental pulp stem cells into odontoblasts.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 611, doi. 10.1038/sj.gt.3302687
By:
- Almushayt, A.;
- Narayanan, K.;
- Zaki, A. E.;
- George, A.
Publication type:
Article
Inhibition of CD26 peptidase activity significantly improves engraftment of retrovirally transduced hematopoietic progenitors.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 652, doi. 10.1038/sj.gt.3302695
By:
- Tian, C.;
- Bagley, J.;
- Forman, D.;
- Iacomini, J.
Publication type:
Article
Induction of effective therapeutic antitumor immunity by direct in vivo administration of lentiviral vectors.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 630, doi. 10.1038/sj.gt.3302697
By:
- Dullaers, M.;
- van Meirvenne, S.;
- Heirman, C.;
- Straetman, L.;
- Bonehill, A.;
- Aerts, J. L.;
- Thielemans, K.;
- Breckpot, K.
Publication type:
Article
Human monocytes expressing a CEA-specific chimeric CD64 receptor specifically target CEA-expressing tumour cells in vitro and in vivo.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 602, doi. 10.1038/sj.gt.3302706
By:
- Biglari, A.;
- Southgate, T. D.;
- Fairbairn, L. J.;
- Gilham, D. E.
Publication type:
Article
Enhanced transduction of mouse salivary glands with AAV5-based vectors.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 594, doi. 10.1038/sj.gt.3302691
By:
- Katano, H.;
- Kok, M. R.;
- Cotrim, A. P.;
- Yamano, S.;
- Schmidt, M.;
- Afione, S.;
- Baum, B. J.;
- Chiorini, J. A.
Publication type:
Article
Woodchuck hepatitis virus post-transcriptional regulatory element deleted from X protein and promoter sequences enhances retroviral vector titer and expression.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 641, doi. 10.1038/sj.gt.3302698
By:
- Schambach, A.;
- Bohne, J.;
- Baum, C.;
- Hermann, F. G.;
- Egerer, L.;
- von Laer, D.;
- Giroglou, T.
Publication type:
Article
Genospheres: self-assembling nucleic acid-lipid nanoparticles suitable for targeted gene delivery.
Published in:
Gene Therapy, 2006, v. 13, n. 7, p. 646, doi. 10.1038/sj.gt.3302699
By:
- Hayes, M. E.;
- Drummond, D. C.;
- Kirpotin, D. B.;
- Zheng, W. W.;
- Noble, C. O.;
- Park, J. W.;
- Marks, J. D.;
- Benz, C. C.;
- Hong, K.
Publication type:
Article