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Safety and immunogenicity of the rVSV∆G-ZEBOV-GP Ebola virus vaccine candidate in healthy adults: a phase 1b randomised, multicentre, double-blind, placebo-controlled, dose-response study

The Lancet infectious diseases, 2017-08, Vol.17 (8), p.854-866

2017

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T Lymphocyte-Directed Gene Therapy for ADA$^-$ SCID: Initial Trial Results After 4 Years

Science (American Association for the Advancement of Science), 1995-10, Vol.270 (5235), p.475-480

1995

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Adenoviral vectors capable of replication improve the efficacy of HSVtk/GCV suicide gene therapy of cancer

Gene therapy, 1999, Vol.6 (1), p.57-62

1999

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The bystander effect in the HSVtk/ganciclovir system and its relationship to gap junctional communication

Gene therapy, 1998-12, Vol.5 (12), p.1705-1711

1998

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Restoration of adrenal steroidogenesis by adenovirus-mediated transfer of human cytochrome P450 21-hydroxylase into the adrenal gland of 21-hydroxylase-deficient mice

Gene therapy, 1999-11, Vol.6 (11), p.1898-1903

1999

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Trans-complementing adenoviral vectors for oncolytic therapy of malignant melanoma

The journal of gene medicine, 2004-06, Vol.6 (6), p.652-662

2004

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Characterization of the antitumor immune response generated by treatment of murine tumors with recombinant adenoviruses expressing HSVtk, IL-2, IL-6 or B7-1

Gene therapy, 1997-12, Vol.4 (12), p.1322-1329

1997

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Adeno-retroviral chimeric viruses as in vivo transducing agents

Gene therapy, 1999-03, Vol.6 (3), p.454-459

1999

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Evaluating metabolic syndrome in a medical physiology laboratory

Advances in physiology education, 2004-12, Vol.28 (4), p.195-198

2004

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AV.TK-mediated killing of subcutaneous tumors in situ results in effective immunization against established secondary intracranial tumor deposits

Gene therapy, 2001-09, Vol.8 (17), p.1315-1322

2001

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Modified human immunodeficiency virus-based lentiviral vectors display decreased sensitivity to trans-dominant Rev

Human gene therapy, 2000-04, Vol.11 (6), p.895-908

2000

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The release of inflammatory cytokines from human peripheral blood mononuclear cells in vitro following exposure to adenovirus variants and capsid

Human gene therapy, 2002-01, Vol.13 (1), p.129-141

2002

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A phase I study of intralesional administration of an adenovirus vector expressing the HSV-1 thymidine kinase gene (AdV.RSV-TK) in combination with escalating doses of ganciclovir in patients with cutaneous metastatic malignant melanoma

Human gene therapy, 2000-02, Vol.11 (3), p.487-503

2000

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A Novel Approach Using Transcomplementing Adenoviral Vectors for Gene Therapy of Adrenocortical Cancer

Hormone and metabolic research, 2002-06, Vol.34 (6), p.279-287

2002

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Anti-tumor immunity generated by tumor cells engineered to express B7-1 via retroviral or adenoviral gene transfer

Cancer letters, 1999-01, Vol.135 (1), p.1-10

1999

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Enhancement of the herpes simplex virus thymidine kinase/ganciclovir bystander effect and its antitumor efficacy in vivo by pharmacologic manipulation of gap junctions

Human gene therapy, 1998-11, Vol.9 (16), p.2385-2391

1998

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Adenoviral Vectors Can Impair Adrenocortical Steroidogenesis: Clinical Implications for Natural Infections and Gene Therapy

Proceedings of the National Academy of Sciences - PNAS, 2002-05, Vol.99 (11), p.7484-7489

2002

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Retrovirus mediated gene transfer as therapy for adenosine deaminase (ADA) deficiency

Leukemia, 1995-10, Vol.9, p.S70-S70

1995

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Generation of a conditionally neo(r)-containing retroviral producer cell line: effects of neo(r) on retroviral titer and transgene expression

Gene therapy, 1998-05, Vol.5 (5), p.684-691

1998

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CD8+ T-cell mediated anti-tumor responses cross-reacting against 9L and RT2 rat glioma cell lines

Cellular immunology, 2003-10, Vol.225 (2), p.113-121

2003

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Adeno-retroviral chimeric viruses as in vivo transducing agents

Gene therapy, 1999-03, Vol.6 (3), p.454-459

1999

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Efficient directional cloning of recombinant adenovirus vectors using DNA-protein complex

Nucleic acids research, 1998-04, Vol.26 (8), p.1947-1950

1998

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Strategies for gene therapy

Pathologie biologie (Paris), 1993-10, Vol.41 (8), p.672-676

1993

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Gut epithelial cells as targets for gene therapy of hemophilia

Human gene therapy, 1997-08, Vol.8 (12), p.1481-1490

1997

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Safety and immunogenicity of the rVSV∆G-ZEBOV-GP Ebola virus vaccine candidate in healthy adults: a phase 1b randomised, multicentre, double-blind, placebo-controlled, dose-response study

T Lymphocyte-Directed Gene Therapy for ADA$^-$ SCID: Initial Trial Results After 4 Years

Adenoviral vectors capable of replication improve the efficacy of HSVtk/GCV suicide gene therapy of cancer

The bystander effect in the HSVtk/ganciclovir system and its relationship to gap junctional communication

Restoration of adrenal steroidogenesis by adenovirus-mediated transfer of human cytochrome P450 21-hydroxylase into the adrenal gland of 21-hydroxylase-deficient mice

Trans-complementing adenoviral vectors for oncolytic therapy of malignant melanoma

Characterization of the antitumor immune response generated by treatment of murine tumors with recombinant adenoviruses expressing HSVtk, IL-2, IL-6 or B7-1

A Recombinant Vesicular Stomatitis Virus Ebola Vaccine

Adeno-retroviral chimeric viruses as in vivo transducing agents

Evaluating metabolic syndrome in a medical physiology laboratory

AV.TK-mediated killing of subcutaneous tumors in situ results in effective immunization against established secondary intracranial tumor deposits

Modified human immunodeficiency virus-based lentiviral vectors display decreased sensitivity to trans-dominant Rev

The release of inflammatory cytokines from human peripheral blood mononuclear cells in vitro following exposure to adenovirus variants and capsid

A phase I study of intralesional administration of an adenovirus vector expressing the HSV-1 thymidine kinase gene (AdV.RSV-TK) in combination with escalating doses of ganciclovir in patients with cutaneous metastatic malignant melanoma

A Novel Approach Using Transcomplementing Adenoviral Vectors for Gene Therapy of Adrenocortical Cancer

Anti-tumor immunity generated by tumor cells engineered to express B7-1 via retroviral or adenoviral gene transfer

Enhancement of the herpes simplex virus thymidine kinase/ganciclovir bystander effect and its antitumor efficacy in vivo by pharmacologic manipulation of gap junctions

Adenoviral Vectors Can Impair Adrenocortical Steroidogenesis: Clinical Implications for Natural Infections and Gene Therapy

Retrovirus mediated gene transfer as therapy for adenosine deaminase (ADA) deficiency

Generation of a conditionally neo(r)-containing retroviral producer cell line: effects of neo(r) on retroviral titer and transgene expression

CD8+ T-cell mediated anti-tumor responses cross-reacting against 9L and RT2 rat glioma cell lines

Adeno-retroviral chimeric viruses as in vivo transducing agents

Efficient directional cloning of recombinant adenovirus vectors using DNA-protein complex

Strategies for gene therapy

Gut epithelial cells as targets for gene therapy of hemophilia

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