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Antibody-epitope conjugates deliver immunogenic T-cell epitopes more efficiently when close to cell surfaces

mAbs, 2024, Vol.16 (1), p.2329321-2329321

2024

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Correction of murine Rag1 deficiency by self-inactivating lentiviral vector-mediated gene transfer

Leukemia, 2011-09, Vol.25 (9), p.1471-1483

2011

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Developing a potentially immunologically inert tetracycline-regulatable viral vector for gene therapy in the peripheral nerve

Gene therapy, 2014-06, Vol.21 (6), p.549-557

2014

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The chicken chorioallantoic membrane tumor assay as model for qualitative testing of oncolytic adenoviruses

Cancer gene therapy, 2012-01, Vol.19 (1), p.58-68

2012

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How not to be seen: immune-evasion strategies in gene therapy

Gene therapy, 2008-02, Vol.15 (4), p.239-246

2008

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A transductionally retargeted adenoviral vector for virotherapy of Her2/neu-expressing prostate cancer

Human gene therapy, 2012-01, Vol.23 (1), p.70-82

2012

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A strategy for genetic modification of the spike-encoding segment of human reovirus T3D for reovirus targeting

Gene therapy, 2008-12, Vol.15 (24), p.1567-1578

2008

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Efficient incorporation of a functional hyper-stable single-chain antibody fragment protein-IX fusion in the adenovirus capsid

Gene therapy, 2007-04, Vol.14 (8), p.664-670

2007

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Characterization of an immune-evading doxycycline-inducible lentiviral vector for gene therapy in the spinal cord

Experimental neurology, 2022-09, Vol.355, p.114120-114120, Article 114120

2022

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A cathepsin-cleavage site between the adenovirus capsid protein IX and a tumor-targeting ligand improves targeted transduction

Gene therapy, 2012-09, Vol.19 (9), p.899-906

2012

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Toll-like receptor triggering augments activation of human mast cells by anti-citrullinated protein antibodies

Annals of the rheumatic diseases, 2015-10, Vol.74 (10), p.1915-1923

2015

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Comprehensive sequence analysis of the E1A proteins of human and simian adenoviruses

Virology (New York, N.Y.), 2004-11, Vol.329 (2), p.477-492

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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Herpesvirus microRNAs for use in gene therapy immune-evasion strategies

Gene therapy, 2017-07, Vol.24 (7), p.385-391

2017

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Adenovirus targeting to HLA-A1 MAGE-A1-positive tumor cells by fusing a single-chain T-cell receptor with minor capsid protein IX

Gene therapy, 2008-07, Vol.15 (13), p.978-989

2008

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Replicating reoviruses with a transgene replacing the codons for the head domain of the viral spike

Gene therapy, 2015-03, Vol.22 (3), p.267-279

2015

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Human adenovirus type 35 vector for gene therapy of brain cancer: improved transduction and bypass of pre-existing anti-vector immunity in cancer patients

Cancer gene therapy, 2007-02, Vol.14 (2), p.211-219

2007

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Transient infection of freshly isolated human colorectal tumor cells by reovirus T3D intermediate subviral particles

Cancer gene therapy, 2008-05, Vol.15 (5), p.284-292

2008

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Severe hepatic dysfunction after adenovirus-mediated transfer of the herpes simplex virus thymidine kinase gene and ganciclovir administration

Gene therapy, 1998-04, Vol.5 (4), p.451-458

1998

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Mammalian orthoreovirus T3D infects U-118 MG cell spheroids independent of junction adhesion molecule-A

Gene therapy, 2014-06, Vol.21 (6), p.609-617

2014

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Polycistronic lentivirus induced pluripotent stem cells from skin biopsies after long term storage, blood outgrowth endothelial cells and cells from milk teeth

Differentiation (London), 2013-02, Vol.85 (3), p.101-109

2013

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Heterogeneous reovirus susceptibility in human glioblastoma stem-like cell cultures

Cancer gene therapy, 2013-09, Vol.20 (9), p.507-513

2013

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Creation of immune 'stealth' genes for gene therapy through fusion with the Gly-Ala repeat of EBNA-1

Gene therapy, 2003-11, Vol.10 (24), p.2020-2028

2003

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Recombinant adenoviral vectors have adjuvant activity and stimulate T cell responses against tumor cells

Gene therapy, 2000-08, Vol.7 (16), p.1410-1416

2000

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A comparative study between catalase gene therapy and the cardioprotector monohydroxyethylrutoside (MonoHER) in protecting against doxorubicin-induced cardiotoxicity in vitro

British journal of cancer, 2003-12, Vol.89 (11), p.2140-2146

2003

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Antibody-epitope conjugates deliver immunogenic T-cell epitopes more efficiently when close to cell surfaces

Correction of murine Rag1 deficiency by self-inactivating lentiviral vector-mediated gene transfer

Developing a potentially immunologically inert tetracycline-regulatable viral vector for gene therapy in the peripheral nerve

The chicken chorioallantoic membrane tumor assay as model for qualitative testing of oncolytic adenoviruses

How not to be seen: immune-evasion strategies in gene therapy

A transductionally retargeted adenoviral vector for virotherapy of Her2/neu-expressing prostate cancer

A strategy for genetic modification of the spike-encoding segment of human reovirus T3D for reovirus targeting

Efficient incorporation of a functional hyper-stable single-chain antibody fragment protein-IX fusion in the adenovirus capsid

Characterization of an immune-evading doxycycline-inducible lentiviral vector for gene therapy in the spinal cord

A cathepsin-cleavage site between the adenovirus capsid protein IX and a tumor-targeting ligand improves targeted transduction

Toll-like receptor triggering augments activation of human mast cells by anti-citrullinated protein antibodies

Comprehensive sequence analysis of the E1A proteins of human and simian adenoviruses

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

Herpesvirus microRNAs for use in gene therapy immune-evasion strategies

Adenovirus targeting to HLA-A1 MAGE-A1-positive tumor cells by fusing a single-chain T-cell receptor with minor capsid protein IX

Replicating reoviruses with a transgene replacing the codons for the head domain of the viral spike

Human adenovirus type 35 vector for gene therapy of brain cancer: improved transduction and bypass of pre-existing anti-vector immunity in cancer patients

Transient infection of freshly isolated human colorectal tumor cells by reovirus T3D intermediate subviral particles

Severe hepatic dysfunction after adenovirus-mediated transfer of the herpes simplex virus thymidine kinase gene and ganciclovir administration

Mammalian orthoreovirus T3D infects U-118 MG cell spheroids independent of junction adhesion molecule-A

Polycistronic lentivirus induced pluripotent stem cells from skin biopsies after long term storage, blood outgrowth endothelial cells and cells from milk teeth

Heterogeneous reovirus susceptibility in human glioblastoma stem-like cell cultures

Creation of immune 'stealth' genes for gene therapy through fusion with the Gly-Ala repeat of EBNA-1

Recombinant adenoviral vectors have adjuvant activity and stimulate T cell responses against tumor cells

A comparative study between catalase gene therapy and the cardioprotector monohydroxyethylrutoside (MonoHER) in protecting against doxorubicin-induced cardiotoxicity in vitro

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