Naldini L - Search Results

1

Correction of metachromatic leukodystrophy in the mouse model by transplantation of genetically modified hematopoietic stem cells.

Biffi A, De Palma M, Quattrini A, Del Carro U, Amadio S, Visigalli I, Sessa M, Fasano S, Brambilla R, Marchesini S, Bordignon C, Naldini L. Biffi A, et al. Among authors: naldini l. J Clin Invest. 2004 Apr;113(8):1118-29. doi: 10.1172/JCI19205. J Clin Invest. 2004. PMID: 15085191 Free PMC article.

2

In vivo gene therapy of metachromatic leukodystrophy by lentiviral vectors: correction of neuropathology and protection against learning impairments in affected mice.

Consiglio A, Quattrini A, Martino S, Bensadoun JC, Dolcetta D, Trojani A, Benaglia G, Marchesini S, Cestari V, Oliverio A, Bordignon C, Naldini L. Consiglio A, et al. Among authors: naldini l. Nat Med. 2001 Mar;7(3):310-6. doi: 10.1038/85454. Nat Med. 2001. PMID: 11231629

3

Transduction of a gene expression cassette using advanced generation lentiviral vectors.

De Palma M, Naldini L. De Palma M, et al. Among authors: naldini l. Methods Enzymol. 2002;346:514-29. doi: 10.1016/s0076-6879(02)46074-0. Methods Enzymol. 2002. PMID: 11883088 No abstract available.

4

Transcriptional targeting of lentiviral vectors by long terminal repeat enhancer replacement.

Lotti F, Menguzzato E, Rossi C, Naldini L, Ailles L, Mavilio F, Ferrari G. Lotti F, et al. Among authors: naldini l. J Virol. 2002 Apr;76(8):3996-4007. doi: 10.1128/jvi.76.8.3996-4007.2002. J Virol. 2002. PMID: 11907239 Free PMC article.

5

Molecular evidence of lentiviral vector-mediated gene transfer into human self-renewing, multi-potent, long-term NOD/SCID repopulating hematopoietic cells.

Ailles L, Schmidt M, Santoni de Sio FR, Glimm H, Cavalieri S, Bruno S, Piacibello W, Von Kalle C, Naldini L. Ailles L, et al. Among authors: naldini l. Mol Ther. 2002 Nov;6(5):615-26. Mol Ther. 2002. PMID: 12409260 Free article.

6

Human T lymphocytes transduced by lentiviral vectors in the absence of TCR activation maintain an intact immune competence.

Cavalieri S, Cazzaniga S, Geuna M, Magnani Z, Bordignon C, Naldini L, Bonini C. Cavalieri S, et al. Among authors: naldini l. Blood. 2003 Jul 15;102(2):497-505. doi: 10.1182/blood-2003-01-0297. Epub 2003 Mar 20. Blood. 2003. PMID: 12649146 Free article.

7

Targeting exogenous genes to tumor angiogenesis by transplantation of genetically modified hematopoietic stem cells.

De Palma M, Venneri MA, Roca C, Naldini L. De Palma M, et al. Among authors: naldini l. Nat Med. 2003 Jun;9(6):789-95. doi: 10.1038/nm871. Epub 2003 May 12. Nat Med. 2003. PMID: 12740570

8

In vivo targeting of tumor endothelial cells by systemic delivery of lentiviral vectors.

De Palma M, Venneri MA, Naldini L. De Palma M, et al. Among authors: naldini l. Hum Gene Ther. 2003 Aug 10;14(12):1193-206. doi: 10.1089/104303403322168028. Hum Gene Ther. 2003. PMID: 12908970

9

Robust in vivo gene transfer into adult mammalian neural stem cells by lentiviral vectors.

Consiglio A, Gritti A, Dolcetta D, Follenzi A, Bordignon C, Gage FH, Vescovi AL, Naldini L. Consiglio A, et al. Among authors: naldini l. Proc Natl Acad Sci U S A. 2004 Oct 12;101(41):14835-40. doi: 10.1073/pnas.0404180101. Epub 2004 Oct 4. Proc Natl Acad Sci U S A. 2004. PMID: 15466696 Free PMC article.

10

Lentiviral vector-mediated gene transfer in T cells from Wiskott-Aldrich syndrome patients leads to functional correction.

Dupré L, Trifari S, Follenzi A, Marangoni F, Lain de Lera T, Bernad A, Martino S, Tsuchiya S, Bordignon C, Naldini L, Aiuti A, Roncarolo MG. Dupré L, et al. Among authors: naldini l. Mol Ther. 2004 Nov;10(5):903-15. doi: 10.1016/j.ymthe.2004.08.008. Mol Ther. 2004. PMID: 15509508 Free article.

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