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Lentiviruses as gene transfer agents for delivery to non-dividing cells

Current opinion in biotechnology, 1998-10, Vol.9 (5), p.457-463

Naldini, Luigi

1998

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Therapeutic benefit of lentiviral-mediated neonatal intracerebral gene therapy in a mouse model of globoid cell leukodystrophy

Human molecular genetics, 2014-06, Vol.23 (12), p.3250-3268

2014

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Genomic instability in induced stem cells

Cell death and differentiation, 2011-05, Vol.18 (5), p.745-753

2011

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Ectopic FOXP3 Expression Preserves Primitive Features Of Human Hematopoietic Stem Cells While Impairing Functional T Cell Differentiation

Scientific reports, 2017-11, Vol.7 (1), p.15820-10, Article 15820

2017

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Cardiomyocytes Induce Endothelial Cells to Trans-Differentiate into Cardiac Muscle: Implications for Myocardium Regeneration

Proceedings of the National Academy of Sciences - PNAS, 2001-09, Vol.98 (19), p.10733-10738

2001

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Post-natal cardiomyocytes can generate iPS cells with an enhanced capacity toward cardiomyogenic re-differentation

Cell death and differentiation, 2012-07, Vol.19 (7), p.1162-1174

2012

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Shedding of clinical-grade lentiviral vectors is not detected in a gene therapy setting

Gene therapy, 2015-06, Vol.22 (6), p.496-502

2015

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

Human gene therapy, 2002-01, Vol.13 (2), p.243-260

2002

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Efficient Transfer, Integration, and Sustained Long-Term Expression of the Transgene in Adult Rat Brains Injected with a Lentiviral Vector

Proceedings of the National Academy of Sciences - PNAS, 1996-10, Vol.93 (21), p.11382-11388

1996

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P1359: USING GENE‐MODIFIED AUTOLOGOUS STEM CELLS PROGENY TO REEDUCATE THE TUMOR IMMUNE MICROENVIRONMENT OF SOLID TUMORS (TEM‐GBM STUDY)

HemaSphere, 2022-06, Vol.6 (Suppl), p.1244-1245

2022

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Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector

Journal of Virology, 1997-09, Vol.71 (9), p.6641-6649

1997

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PO-040 Development of a tunable form of interferon alpha for in vivo cancer gene therapy

ESMO open, 2018-07, Vol.3 (Suppl 2), p.A242-A243

2018

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S106: LONG‐TERM FOLLOW‐UP OF BETA‐THALASSEMIA PATIENTS TREATED WITH HEMATOPOIETIC STEM CELL GENE THERAPY

HemaSphere, 2022-01, Vol.6 (Suppl), p.3-3

2022

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Safety of arylsulfatase A overexpression for gene therapy of metachromatic leukodystrophy

Human gene therapy, 2007-09, Vol.18 (9), p.821

2007

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Reversible immortalization allows human artificial chromosome-mediated gene correction of human dystrophic muscle progenitor cells

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S252-S252

2015

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Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome

Science (American Association for the Advancement of Science), 2013-08, Vol.341 (6148), p.865-865

2013

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Hepatocyte Growth Factor Is a Regulator of Monocyte-Macrophage Function

The Journal of immunology (1950), 2001-01, Vol.166 (2), p.1241-1247

2001

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BM-derived cells that foster tumor growth and their manipulation

European journal of cancer supplements, 2008, Vol.6 (9), p.67-67

Naldini, L

2008

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Update on safety and efficacy of lentiviral hematopoietic stem cell gene therapy (HSC-GT) for metachromatic leukodystrophy (MLD)

European journal of paediatric neurology, 2017-06, Vol.21, p.e20-e20

2017

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Extracellular proteolytic cleavage by urokinase is required for activation of hepatocyte growth factor/scatter factor

The EMBO journal, 1992-12, Vol.11 (13), p.4825-4833

1992

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RON is a heterodimeric tyrosine kinase receptor activated by the HGF homologue MSP

The EMBO journal, 1994-08, Vol.13 (15), p.3524-3532

1994

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A new-generation stable inducible packaging cell line for lentiviral vectors

Human gene therapy, 2001-05, Vol.12 (8), p.981-997

2001

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Scatter factor and hepatocyte growth factor are indistinguishable ligands for the MET receptor

The EMBO journal, 1991-10, Vol.10 (10), p.2867-2878

1991

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HIV-1-derived lentiviral vectors

Current topics in microbiology and immunology, 2002, Vol.261, p.31

2002

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Molecular evidence of inefficient transduction of proliferating human B lymphocytes by VSV-pseudotyped HIV-1-derived lentivectors

Virology (New York, N.Y.), 2004-08, Vol.325 (2), p.413-424

2004

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Lentiviruses as gene transfer agents for delivery to non-dividing cells

Therapeutic benefit of lentiviral-mediated neonatal intracerebral gene therapy in a mouse model of globoid cell leukodystrophy

Genomic instability in induced stem cells

Ectopic FOXP3 Expression Preserves Primitive Features Of Human Hematopoietic Stem Cells While Impairing Functional T Cell Differentiation

Cardiomyocytes Induce Endothelial Cells to Trans-Differentiate into Cardiac Muscle: Implications for Myocardium Regeneration

Post-natal cardiomyocytes can generate iPS cells with an enhanced capacity toward cardiomyogenic re-differentation

Shedding of clinical-grade lentiviral vectors is not detected in a gene therapy setting

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

Efficient Transfer, Integration, and Sustained Long-Term Expression of the Transgene in Adult Rat Brains Injected with a Lentiviral Vector

P1359: USING GENE‐MODIFIED AUTOLOGOUS STEM CELLS PROGENY TO REEDUCATE THE TUMOR IMMUNE MICROENVIRONMENT OF SOLID TUMORS (TEM‐GBM STUDY)

Highly efficient and sustained gene transfer in adult neurons with a lentivirus vector

PO-040 Development of a tunable form of interferon alpha for in vivo cancer gene therapy

S106: LONG‐TERM FOLLOW‐UP OF BETA‐THALASSEMIA PATIENTS TREATED WITH HEMATOPOIETIC STEM CELL GENE THERAPY

Safety of arylsulfatase A overexpression for gene therapy of metachromatic leukodystrophy

Reversible immortalization allows human artificial chromosome-mediated gene correction of human dystrophic muscle progenitor cells

Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome

Hepatocyte Growth Factor Is a Regulator of Monocyte-Macrophage Function

BM-derived cells that foster tumor growth and their manipulation

Update on safety and efficacy of lentiviral hematopoietic stem cell gene therapy (HSC-GT) for metachromatic leukodystrophy (MLD)

Extracellular proteolytic cleavage by urokinase is required for activation of hepatocyte growth factor/scatter factor

RON is a heterodimeric tyrosine kinase receptor activated by the HGF homologue MSP

A new-generation stable inducible packaging cell line for lentiviral vectors

Scatter factor and hepatocyte growth factor are indistinguishable ligands for the MET receptor

HIV-1-derived lentiviral vectors

Molecular evidence of inefficient transduction of proliferating human B lymphocytes by VSV-pseudotyped HIV-1-derived lentivectors

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