Naldini L - Search Results

1

Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome.

Aiuti A, Biasco L, Scaramuzza S, Ferrua F, Cicalese MP, Baricordi C, Dionisio F, Calabria A, Giannelli S, Castiello MC, Bosticardo M, Evangelio C, Assanelli A, Casiraghi M, Di Nunzio S, Callegaro L, Benati C, Rizzardi P, Pellin D, Di Serio C, Schmidt M, Von Kalle C, Gardner J, Mehta N, Neduva V, Dow DJ, Galy A, Miniero R, Finocchi A, Metin A, Banerjee PP, Orange JS, Galimberti S, Valsecchi MG, Biffi A, Montini E, Villa A, Ciceri F, Roncarolo MG, Naldini L. Aiuti A, et al. Among authors: naldini l. Science. 2013 Aug 23;341(6148):1233151. doi: 10.1126/science.1233151. Epub 2013 Jul 11. Science. 2013. PMID: 23845947 Free PMC article. Clinical Trial.

2

In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector.

Naldini L, Blömer U, Gallay P, Ory D, Mulligan R, Gage FH, Verma IM, Trono D. Naldini L, et al. Science. 1996 Apr 12;272(5259):263-7. doi: 10.1126/science.272.5259.263. Science. 1996. PMID: 8602510

3

Lentiviral vectors.

Naldini L, Verma IM. Naldini L, et al. Adv Virus Res. 2000;55:599-609. doi: 10.1016/s0065-3527(00)55020-9. Adv Virus Res. 2000. PMID: 11050959 Review. No abstract available.

4

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

5

Efficient gene delivery and targeted expression to hepatocytes in vivo by improved lentiviral vectors.

Follenzi A, Sabatino G, Lombardo A, Boccaccio C, Naldini L. Follenzi A, et al. Among authors: naldini l. Hum Gene Ther. 2002 Jan 20;13(2):243-60. doi: 10.1089/10430340252769770. Hum Gene Ther. 2002. PMID: 11812281

6

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.

7

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.

8

Targeting lentiviral vector expression to hepatocytes limits transgene-specific immune response and establishes long-term expression of human antihemophilic factor IX in mice.

Follenzi A, Battaglia M, Lombardo A, Annoni A, Roncarolo MG, Naldini L. Follenzi A, et al. Among authors: naldini l. Blood. 2004 May 15;103(10):3700-9. doi: 10.1182/blood-2003-09-3217. Epub 2003 Dec 30. Blood. 2004. PMID: 14701690 Free article.

9

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.

10

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.

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