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Efficient generation of recombinant adenovirus vectors by homologous recombination in Escherichia coli

Journal of Virology, 1996-07, Vol.70 (7), p.4805-4810

1996

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The human cell line PER.C6 provides a new manufacturing system for the production of influenza vaccines

Vaccine, 2001-03, Vol.19 (17), p.2716-2721

2001

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Exploiting the Natural Diversity in Adenovirus Tropism for Therapy and Prevention of Disease

Journal of Virology, 2002-05, Vol.76 (9), p.4612-4620

2002

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In Vitro and In Vivo Biology of Recombinant Adenovirus Vectors with E1, E1/E2A, or E1/E4 Deleted

Journal of Virology, 1998-03, Vol.72 (3), p.2022-2032

1998

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Immune Response to Recombinant Adenovirus in Humans: Capsid Components from Viral Input Are Targets for Vector-Specific Cytotoxic T Lymphocytes

Journal of Virology, 2000-08, Vol.74 (16), p.7678-7682

2000

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1181 VLS-732: A NEW ANTI-HCV COMPOUND ACTING AS AN NS5B POLYMERASE CONFORMATIONAL MODULATOR

Journal of hepatology, 2012-04, Vol.56, p.S467-S468

2012

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Development of Minimal Lentivirus Vectors Derived from Simian Immunodeficiency Virus (SIVmac251) and Their Use for Gene Transfer into Human Dendritic Cells

Journal of Virology, 2000-09, Vol.74 (18), p.8307-8315

2000

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Characterization of novel safe lentiviral vectors derived from simian immunodeficiency virus (SIVmac251) that efficiently transduce mature human dendritic cells

Gene therapy, 2000-10, Vol.7 (19), p.1613-1623

2000

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Fiberless Recombinant Adenoviruses: Virus Maturation and Infectivity in the Absence of Fiber

Journal of Virology, 1999-02, Vol.73 (2), p.907-919

1999

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Adenovirus-mediated gene transfer : influence of transgene, mouse strain and type of immune response on persistence of transgene expression

Gene therapy, 1997-05, Vol.4 (5), p.473-482

1997

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1216 HIGHLY POTENT HCV NS5B INHIBITOR WITH ORIGINAL MECHANISM OF ACTION IDENTIFIED WITH THE 3D-SCREEN TECHNOLOGY

Journal of hepatology, 2011-03, Vol.54, p.S480-S480

2011

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Influence of adenoviral fiber mutations on viral encapsidation, infectivity and in vivo tropism

Gene therapy, 2001, Vol.8 (1), p.49-57

2001

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Programmed Cell Death and AIDS: Significance of T-Cell Apoptosis in Pathogenic and Nonpathogenic Primate Lentiviral Infections

Proceedings of the National Academy of Sciences - PNAS, 1994-09, Vol.91 (20), p.9431-9435

1994

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Regulation of Adenovirus-Mediated Transgene Expression by the Viral E4 Gene Products: Requirement for E4 ORF3

Journal of Virology, 1999-10, Vol.73 (10), p.8308-8319

1999

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Thérapie génique des hémophilies : Potentialités thérapeutiques et limitations technologiques

Transfusion clinique et biologique (Paris), 1997, Vol.4 (3), p.251-261

1997

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Inhibition in vitro et in vivo de la réplication du VIH1 par transfert rétroviral des gènes d'interféron α, β ou γ : Application à la thérapie génique du sida

Annales de biologie clinique (Paris), 1998-03, Vol.56 (2), p.167-173

1998

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Thérapie génique de maladies humaines héréditaires et acquises

Annales d'endocrinologie, 1995, Vol.56 (6), p.571-574

1995

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A new cellular model of response to estrogens: a bioluminescent test to characterize (anti) estrogen molecules

BioTechniques, 1990-10, Vol.9 (4), p.450

1990

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Gene therapy of spontaneous canine melanoma and feline fibrosarcoma by intratumoral administration of histoincompatible cells expressing human interleukin-2

Gene therapy, 1996-12, Vol.3 (12), p.1104

1996

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Molecular determinants of adenovirus serotype 5 fibre binding to its cellular receptor CAR

Journal of general virology, 1999-06, Vol.80 (6), p.1519-1527

1999

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Inhibition of costimulation allows for repeated systemic administration of adenoviral vector in rhesus monkeys

Gene therapy, 2004-02, Vol.11 (3), p.241-252

2004

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Conditional repression of the E2 transcription unit in E1-E3-deleted adenovirus vectors is correlated with a strong reduction in viral DNA replication and late gene expression in vitro

Journal of Virology, 1997-04, Vol.71 (4), p.3307-3311

1997

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In vivo cancer gene therapy by adenovirus-mediated transfer of a bifunctional yeast cytosine deaminase/uracil phosphoribosyltransferase fusion gene

Cancer research (Chicago, Ill.), 2000-07, Vol.60 (14), p.3813-3822

2000

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Complementation cell lines for viral vectors to be used in gene therapy

Cytotechnology (Dordrecht), 1996-01, Vol.19 (1), p.43-54

MEHTALI, M

1996

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Radioisotopic imaging allows optimization of adenovirus lung deposition for cystic fibrosis gene therapy

Human gene therapy, 2001, Vol.12 (1), p.1-11

2001

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Efficient generation of recombinant adenovirus vectors by homologous recombination in Escherichia coli

The human cell line PER.C6 provides a new manufacturing system for the production of influenza vaccines

Exploiting the Natural Diversity in Adenovirus Tropism for Therapy and Prevention of Disease

In Vitro and In Vivo Biology of Recombinant Adenovirus Vectors with E1, E1/E2A, or E1/E4 Deleted

Immune Response to Recombinant Adenovirus in Humans: Capsid Components from Viral Input Are Targets for Vector-Specific Cytotoxic T Lymphocytes

1181 VLS-732: A NEW ANTI-HCV COMPOUND ACTING AS AN NS5B POLYMERASE CONFORMATIONAL MODULATOR

Development of Minimal Lentivirus Vectors Derived from Simian Immunodeficiency Virus (SIVmac251) and Their Use for Gene Transfer into Human Dendritic Cells

Characterization of novel safe lentiviral vectors derived from simian immunodeficiency virus (SIVmac251) that efficiently transduce mature human dendritic cells

Fiberless Recombinant Adenoviruses: Virus Maturation and Infectivity in the Absence of Fiber

Adenovirus-mediated gene transfer : influence of transgene, mouse strain and type of immune response on persistence of transgene expression

1216 HIGHLY POTENT HCV NS5B INHIBITOR WITH ORIGINAL MECHANISM OF ACTION IDENTIFIED WITH THE 3D-SCREEN TECHNOLOGY

Influence of adenoviral fiber mutations on viral encapsidation, infectivity and in vivo tropism

Programmed Cell Death and AIDS: Significance of T-Cell Apoptosis in Pathogenic and Nonpathogenic Primate Lentiviral Infections

Regulation of Adenovirus-Mediated Transgene Expression by the Viral E4 Gene Products: Requirement for E4 ORF3

Thérapie génique des hémophilies : Potentialités thérapeutiques et limitations technologiques

Inhibition in vitro et in vivo de la réplication du VIH1 par transfert rétroviral des gènes d'interféron α, β ou γ : Application à la thérapie génique du sida

Thérapie génique de maladies humaines héréditaires et acquises

A new cellular model of response to estrogens: a bioluminescent test to characterize (anti) estrogen molecules

Gene therapy of spontaneous canine melanoma and feline fibrosarcoma by intratumoral administration of histoincompatible cells expressing human interleukin-2

Molecular determinants of adenovirus serotype 5 fibre binding to its cellular receptor CAR

Inhibition of costimulation allows for repeated systemic administration of adenoviral vector in rhesus monkeys

Conditional repression of the E2 transcription unit in E1-E3-deleted adenovirus vectors is correlated with a strong reduction in viral DNA replication and late gene expression in vitro

In vivo cancer gene therapy by adenovirus-mediated transfer of a bifunctional yeast cytosine deaminase/uracil phosphoribosyltransferase fusion gene

Complementation cell lines for viral vectors to be used in gene therapy

Radioisotopic imaging allows optimization of adenovirus lung deposition for cystic fibrosis gene therapy

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