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Autoimmunity against a defective ribosomal insulin gene product in type 1 diabetes

Nature medicine, 2017-04, Vol.23 (4), p.501-507

2017

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Integrating gene delivery and gene-editing technologies by adenoviral vector transfer of optimized CRISPR-Cas9 components

Gene therapy, 2020-05, Vol.27 (5), p.209-225

2020

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Characterization of a replicating expanded tropism oncolytic reovirus carrying the adenovirus E4orf4 gene

Gene therapy, 2018-08, Vol.25 (5), p.331-344

2018

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Lentiviral Vectors Efficiently Transduce Quiescent Mature 3T3-L1 Adipocytes

Molecular therapy, 2004-02, Vol.9 (2), p.209-217

2004

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Genetically Engineered Human Islets Protected From CD8-mediated Autoimmune Destruction In Vivo

Molecular therapy, 2013-08, Vol.21 (8), p.1592-1601

2013

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The stability of envelope-pseudotyped lentiviral vectors

Gene therapy, 2021-02, Vol.28 (1-2), p.89-104

2021

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A primer to gene therapy: Progress, prospects, and problems

Journal of inherited metabolic disease, 2021-01, Vol.44 (1), p.54-71

2021

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Induction of Robust Type I Interferon Levels by Oncolytic Reovirus Requires Both Viral Replication and Interferon-α/β Receptor Signaling

Human gene therapy, 2021-10, Vol.32 (19-20), p.1171-1185

2021

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Nonhuman Primate Adenoviruses of the Human Adenovirus B Species Are Potent and Broadly Acting Oncolytic Vector Candidates

Human gene therapy, 2022-03, Vol.33 (5-6), p.275-289

2022

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Gastrointestinal cancer-associated fibroblasts expressing Junctional Adhesion Molecule-A are amenable to infection by oncolytic reovirus

Cancer gene therapy, 2022-12, Vol.29 (12), p.1918-1929

2022

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Arming oncolytic reovirus with GM-CSF gene to enhance immunity

Cancer gene therapy, 2019-09, Vol.26 (9-10), p.268-281

2019

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Antibody-mediated delivery of viral epitopes to redirect EBV-specific CD8+ T-cell immunity towards cancer cells

Cancer gene therapy, 2024-01, Vol.31 (1), p.58-68

2024

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Reovirus mutant jin-3 exhibits lytic and immune-stimulatory effects in preclinical human prostate cancer models

Cancer gene therapy, 2022-06, Vol.29 (6), p.793-802

2022

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Modification of mammalian reoviruses for use as oncolytic agents

Expert opinion on biological therapy, 2009-12, Vol.9 (12), p.1509-1520

2009

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Cell replacement therapies: is it time to reprogram?

Human gene therapy, 2014-10, Vol.25 (10), p.866-874

2014

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Changing faces in virology: the dutch shift from oncogenic to oncolytic viruses

Human gene therapy, 2014-10, Vol.25 (10), p.875-884

2014

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Optimization of short-term transgene expression by sodium butyrate and ubiquitous chromatin opening elements (UCOEs)

The journal of gene medicine, 2007-08, Vol.9 (8), p.639-648

2007

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Off-label prescription of genetically modified organism medicines in europe: emerging conflicts of interest?

Human gene therapy, 2014-10, Vol.25 (10), p.893-896

2014

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Optimizing reporter constructs for in vivo bioluminescence imaging of interferon-γ stimulated mesenchymal stromal cells

Experimental hematology, 2014-09, Vol.42 (9), p.793-803.e1

2014

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Gene therapy in The Netherlands: highlights from the Low Countries

The journal of gene medicine, 2007-10, Vol.9 (10), p.895-903

2007

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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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Gene therapy and cement injection for restabilization of loosened hip prostheses

Human gene therapy, 2008-01, Vol.19 (1), p.83-96

2008

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Development of an inducible suicide gene system based on human caspase 8

Cancer gene therapy, 2005-07, Vol.12 (7), p.627-639

2005

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Gene therapy for the treatment of hip prosthesis loosening: adverse events in a phase 1 clinical study

Human gene therapy, 2008-10, Vol.19 (10), p.1029-1038

2008

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Autoimmunity against a defective ribosomal insulin gene product in type 1 diabetes

Integrating gene delivery and gene-editing technologies by adenoviral vector transfer of optimized CRISPR-Cas9 components

Characterization of a replicating expanded tropism oncolytic reovirus carrying the adenovirus E4orf4 gene

Lentiviral Vectors Efficiently Transduce Quiescent Mature 3T3-L1 Adipocytes

Genetically Engineered Human Islets Protected From CD8-mediated Autoimmune Destruction In Vivo

The stability of envelope-pseudotyped lentiviral vectors

A primer to gene therapy: Progress, prospects, and problems

Induction of Robust Type I Interferon Levels by Oncolytic Reovirus Requires Both Viral Replication and Interferon-α/β Receptor Signaling

Nonhuman Primate Adenoviruses of the Human Adenovirus B Species Are Potent and Broadly Acting Oncolytic Vector Candidates

Gastrointestinal cancer-associated fibroblasts expressing Junctional Adhesion Molecule-A are amenable to infection by oncolytic reovirus

Arming oncolytic reovirus with GM-CSF gene to enhance immunity

Antibody-mediated delivery of viral epitopes to redirect EBV-specific CD8+ T-cell immunity towards cancer cells

Reovirus mutant jin-3 exhibits lytic and immune-stimulatory effects in preclinical human prostate cancer models

Modification of mammalian reoviruses for use as oncolytic agents

Cell replacement therapies: is it time to reprogram?

Changing faces in virology: the dutch shift from oncogenic to oncolytic viruses

Optimization of short-term transgene expression by sodium butyrate and ubiquitous chromatin opening elements (UCOEs)

Off-label prescription of genetically modified organism medicines in europe: emerging conflicts of interest?

Optimizing reporter constructs for in vivo bioluminescence imaging of interferon-γ stimulated mesenchymal stromal cells

Gene therapy in The Netherlands: highlights from the Low Countries

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

Adenovirus-derived vectors for prostate cancer gene therapy

Gene therapy and cement injection for restabilization of loosened hip prostheses

Development of an inducible suicide gene system based on human caspase 8

Gene therapy for the treatment of hip prosthesis loosening: adverse events in a phase 1 clinical study

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