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Replication-Deficient Human Adenovirus Type 35 Vectors for Gene Transfer and Vaccination: Efficient Human Cell Infection and Bypass of Preexisting Adenovirus Immunity

Journal of Virology, 2003-08, Vol.77 (15), p.8263-8271

2003

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New helper cells and matched early region 1-deleted adenovirus vectors prevent generation of replication-competent adenoviruses

Human gene therapy, 1998-09, Vol.9 (13), p.1909-1917

1998

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High-Level Expression of Recombinant IgG in the Human Cell Line PER.C6

Biotechnology progress, 2003, Vol.19 (1), p.163-168

2003

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Molecular cytogenetic characterization by combined COBRA-FISH and fiber-FISH: application to PER.C6 cells

BioTechniques, 2004-08, Vol.37 (2), p.188, 190, 192 passim-194

2004

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Highly Efficient Transduction of Human Monocyte-Derived Dendritic Cells with Subgroup B Fiber-Modified Adenovirus Vectors Enhances Transgene-Encoded Antigen Presentation to Cytotoxic T Cells

The Journal of immunology (1950), 2001-04, Vol.166 (8), p.5236-5244

2001

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Treatment of malignant gliomas with a replicating adenoviral vector expressing herpes simplex virus-thymidine kinase

Cancer research (Chicago, Ill.), 2001-12, Vol.61 (24), p.8743-8750

2001

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A single short stretch of homology between adenoviral vector and packaging cell line can give rise to cytopathic effect-inducing, helper-dependent E1-positive particles

Human gene therapy, 2002-05, Vol.13 (8), p.909-920

2002

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Molecular cytogenetic characterization by combined COBRA-FISH and fiber-FISH: application to PER.C6

BioTechniques, 2004-08, Vol.37 (2), p.188-194

2004

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Feasibility of adenovirus-mediated nonsurgical synovectomy in collagen-induced arthritis-affected rhesus monkeys

Human gene therapy, 1999-05, Vol.10 (7), p.1139-1149

1999

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Lung Gene Therapy: In Vivo Adenovirus-Mediated Gene Transfer to Rhesus Monkey Airway Epithelium

Human gene therapy, 1994-01, Vol.5 (1), p.3-10

1994

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Characterization of the gene encoding human peroxisomal 3-oxoacyl-CoA thiolase (ACAA). No large DNA rearrangement in a thiolase-deficient patient

Biochimica et biophysica acta, 1991-08, Vol.1090 (1), p.43-51

1991

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Isolated limb perfusion for local gene delivery: efficient and targeted adenovirus-mediated gene transfer into soft tissue sarcomas

Annals of surgery, 2000-12, Vol.232 (6), p.814-821

2000

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In vivo adenovirus-mediated transfer of human CFTR cDNA to rhesus monkey airway epithelium: efficacy, toxicity and safety

Gene therapy, 1994-11, Vol.1 (6), p.385

1994

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Preclinical testing of recombinant adenoviral herpes simplex virus-thymidine kinase gene therapy for central nervous system malignancies

Neurosurgery, 1997-08, Vol.41 (2), p.442-452

1997

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Trans-complementation of E1-deleted adenovirus: a new vector to reduce the possibility of codissemination of wild-type and recombinant adenoviruses

Human gene therapy, 1995-06, Vol.6 (6), p.711-721

1995

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Aerosol-mediated delivery of recombinant adenovirus to the airways of nonhuman primates

Human gene therapy, 1995-12, Vol.6 (12), p.1587-1593

1995

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In vitro and in vivo gene transfer to pulmonary cells mediated by cationic liposomes

Biochimica et biophysica acta, 1996-04, Vol.1306 (1), p.55-62

1996

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Treatment of leptomeningeal metastases in a rat model using a recombinant adenovirus containing the HSV-tk gene

Journal of neurosurgery, 1996-10, Vol.85 (4), p.648-654

1996

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Cloning, biological characterization and high-level expression of rat Interleukin-3 using recombinant adenovirus: description of a new splicing variant

Gene, 1998-04, Vol.211 (1), p.151-158

1998

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Experimental adenoviral “suicide” gene therapy for CNS malignancies

Clinical neurology and neurosurgery, 1997-07, Vol.99, p.S6-S6

1997

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Isolated limb perfusion for local gene delivery : Efficient and targeted adenovirus-mediated gene transfer into soft tissue sarcomas. Discussion

Annals of surgery, 2000, Vol.232 (6), p.814-821

2000

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Pseudotyping of Adenoviral Vectors

Vector Targeting for Therapeutic Gene Delivery, 2002, p.87-121

2002

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Infection efficiency of type 5 adenoviral vectors in synovial tissue can be enhanced with a type 16 fiber

Arthritis and rheumatism, 2001-03, Vol.44 (3), p.570-577

2001

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PER.C6® Cells for the Manufacture of Biopharmaceutical Proteins

Modern Biopharmaceuticals, 2005, p.779-807

2005

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The influence of synovial fluid on adenovirus‐mediated gene transfer to the synovial tissue

Arthritis and rheumatism, 2001-01, Vol.44 (1), p.48-52

2001

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Replication-Deficient Human Adenovirus Type 35 Vectors for Gene Transfer and Vaccination: Efficient Human Cell Infection and Bypass of Preexisting Adenovirus Immunity

New helper cells and matched early region 1-deleted adenovirus vectors prevent generation of replication-competent adenoviruses

High-Level Expression of Recombinant IgG in the Human Cell Line PER.C6

Molecular cytogenetic characterization by combined COBRA-FISH and fiber-FISH: application to PER.C6 cells

Highly Efficient Transduction of Human Monocyte-Derived Dendritic Cells with Subgroup B Fiber-Modified Adenovirus Vectors Enhances Transgene-Encoded Antigen Presentation to Cytotoxic T Cells

Treatment of malignant gliomas with a replicating adenoviral vector expressing herpes simplex virus-thymidine kinase

A single short stretch of homology between adenoviral vector and packaging cell line can give rise to cytopathic effect-inducing, helper-dependent E1-positive particles

Molecular cytogenetic characterization by combined COBRA-FISH and fiber-FISH: application to PER.C6

Feasibility of adenovirus-mediated nonsurgical synovectomy in collagen-induced arthritis-affected rhesus monkeys

Lung Gene Therapy: In Vivo Adenovirus-Mediated Gene Transfer to Rhesus Monkey Airway Epithelium

Characterization of the gene encoding human peroxisomal 3-oxoacyl-CoA thiolase (ACAA). No large DNA rearrangement in a thiolase-deficient patient

Isolated limb perfusion for local gene delivery: efficient and targeted adenovirus-mediated gene transfer into soft tissue sarcomas

In vivo adenovirus-mediated transfer of human CFTR cDNA to rhesus monkey airway epithelium: efficacy, toxicity and safety

Preclinical testing of recombinant adenoviral herpes simplex virus-thymidine kinase gene therapy for central nervous system malignancies

Trans-complementation of E1-deleted adenovirus: a new vector to reduce the possibility of codissemination of wild-type and recombinant adenoviruses

Aerosol-mediated delivery of recombinant adenovirus to the airways of nonhuman primates

In vitro and in vivo gene transfer to pulmonary cells mediated by cationic liposomes

Treatment of leptomeningeal metastases in a rat model using a recombinant adenovirus containing the HSV-tk gene

Cloning, biological characterization and high-level expression of rat Interleukin-3 using recombinant adenovirus: description of a new splicing variant

Experimental adenoviral “suicide” gene therapy for CNS malignancies

Isolated limb perfusion for local gene delivery : Efficient and targeted adenovirus-mediated gene transfer into soft tissue sarcomas. Discussion

Pseudotyping of Adenoviral Vectors

Infection efficiency of type 5 adenoviral vectors in synovial tissue can be enhanced with a type 16 fiber

PER.C6® Cells for the Manufacture of Biopharmaceutical Proteins

The influence of synovial fluid on adenovirus‐mediated gene transfer to the synovial tissue

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