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Surface-Engineered Viral Vectors for Selective and Cell Type-Specific Gene Delivery

Trends in biotechnology (Regular ed.), 2015-12, Vol.33 (12), p.777-790

2015

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Virotherapy Research in Germany: From Engineering to Translation

Human gene therapy, 2017-10, Vol.28 (10), p.800

2017

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Chimäre Antigenrezeptoren (CARs) in der Onkologie: eine Übersicht zu klinischer Anwendung und neuen Entwicklungen

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2020, Vol.63 (11), p.1331-1340

2020

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Displaying Tetra‐Membrane Spanning Claudins on Enveloped Virus‐Like Particles for Cancer Immunotherapy

Biotechnology journal, 2018-03, Vol.13 (3), p.e1700345-n/a

2018

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Lentiviral vectors targeted to MHC II are effective in immunization

Human gene therapy, 2011-10, Vol.22 (10), p.1249

2011

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Ligand Coupling to the AAV Capsid for Cell-Specific Gene Transfer

Methods in molecular biology (Clifton, N.J.), 2019, Vol.1950, p.35

2019

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A new age of precision gene therapy

The Lancet (British edition), 2024-02, Vol.403 (10426), p.568-582

2024

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Viral gene transfer of APPsα rescues synaptic failure in an Alzheimer’s disease mouse model

Acta neuropathologica, 2016-02, Vol.131 (2), p.247-266

2016

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Genetic in vivo engineering of human T lymphocytes in mouse models

Nature protocols, 2021-07, Vol.16 (7), p.3210-3240

2021

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A single amino acid substitution in the measles virus F2 protein reciprocally modulates membrane fusion activity in pathogenic and oncolytic strains

Virus research, 2014-02, Vol.180, p.43-48

2014

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Covalent coupling of high-affinity ligands to the surface of viral vector particles by protein trans-splicing mediates cell type-specific gene transfer

Biomaterials, 2017-11, Vol.144, p.84-94

2017

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AAV vectors displaying bispecific DARPins enable dual-control targeted gene delivery

Biomaterials, 2023-12, Vol.303, p.122399-122399, Article 122399

2023

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Specific gene transfer to neurons, endothelial cells and hematopoietic progenitors with lentiviral vectors

Nature methods, 2010-11, Vol.7 (11), p.929

2010

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Designed Ankyrin Repeat Protein (DARPin) to target chimeric antigen receptor (CAR)-redirected T cells towards CD4+ T cells to reduce the latent HIV+ cell reservoir

Medical microbiology and immunology, 2020-12, Vol.209 (6), p.681-691

2020

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CD105 is a surface marker for receptor-targeted gene transfer into human long-term repopulating hematopoietic stem cells

Stem cells and development, 2015-03, Vol.24 (6), p.714

2015

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Lentiviral vectors with measles virus glycoproteins – dream team for gene transfer?

Trends in biotechnology (Regular ed.), 2009-05, Vol.27 (5), p.259-265

2009

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The European hospital exemption clause-new option for gene therapy?

Human gene therapy, 2012-01, Vol.23 (1), p.7

2012

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CD30 Receptor-Targeted Lentiviral Vectors for Human Induced Pluripotent Stem Cell-Specific Gene Modification

Stem cells and development, 2016-05, Vol.25 (9), p.729

2016

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In vitro incorporation of a cell-binding protein to a lentiviral vector using an engineered split intein enables targeted delivery of genetic cargo

Biotechnology and bioengineering, 2015-12, Vol.112 (12), p.2611-2617

2015

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Chimeric antigen receptors in oncology: clinical applications and new developments

Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz, 2020-11, Vol.63 (11), p.1331-1340

2020

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Is it going to be SIN?: a European Society of Gene Therapy commentary. Phasing-out the clinical use of non self-inactivating murine leukemia virus vectors: initiative on hold

The journal of gene medicine, 2006-10, Vol.8 (10), p.1274-1276

2006

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Retroviral display and high throughput screening

Combinatorial chemistry & high throughput screening, 2008-02, Vol.11 (2), p.99

2008

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Intrahepatic application of suicide gene-armed measles virotherapeutics: a safety study in transgenic mice and rhesus macaques

Human gene therapy. Clinical development, 2013-03, Vol.24 (1), p.11

2013

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Is it going to be SIN?

The journal of gene medicine, 2006-10, Vol.8 (10), p.1274-1276

2006

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Selection of functional human antibodies from retroviral display libraries

Nucleic acids research, 2005-01, Vol.33 (4), p.e35

2005

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Surface-Engineered Viral Vectors for Selective and Cell Type-Specific Gene Delivery

Virotherapy Research in Germany: From Engineering to Translation

Chimäre Antigenrezeptoren (CARs) in der Onkologie: eine Übersicht zu klinischer Anwendung und neuen Entwicklungen

Displaying Tetra‐Membrane Spanning Claudins on Enveloped Virus‐Like Particles for Cancer Immunotherapy

Lentiviral vectors targeted to MHC II are effective in immunization

Ligand Coupling to the AAV Capsid for Cell-Specific Gene Transfer

A new age of precision gene therapy

Viral gene transfer of APPsα rescues synaptic failure in an Alzheimer’s disease mouse model

Genetic in vivo engineering of human T lymphocytes in mouse models

A single amino acid substitution in the measles virus F2 protein reciprocally modulates membrane fusion activity in pathogenic and oncolytic strains

Covalent coupling of high-affinity ligands to the surface of viral vector particles by protein trans-splicing mediates cell type-specific gene transfer

AAV vectors displaying bispecific DARPins enable dual-control targeted gene delivery

Specific gene transfer to neurons, endothelial cells and hematopoietic progenitors with lentiviral vectors

Designed Ankyrin Repeat Protein (DARPin) to target chimeric antigen receptor (CAR)-redirected T cells towards CD4+ T cells to reduce the latent HIV+ cell reservoir

CD105 is a surface marker for receptor-targeted gene transfer into human long-term repopulating hematopoietic stem cells

Lentiviral vectors with measles virus glycoproteins – dream team for gene transfer?

The European hospital exemption clause-new option for gene therapy?

CD30 Receptor-Targeted Lentiviral Vectors for Human Induced Pluripotent Stem Cell-Specific Gene Modification

In vitro incorporation of a cell-binding protein to a lentiviral vector using an engineered split intein enables targeted delivery of genetic cargo

Chimeric antigen receptors in oncology: clinical applications and new developments

Is it going to be SIN?: a European Society of Gene Therapy commentary. Phasing-out the clinical use of non self-inactivating murine leukemia virus vectors: initiative on hold

Retroviral display and high throughput screening

Intrahepatic application of suicide gene-armed measles virotherapeutics: a safety study in transgenic mice and rhesus macaques

Is it going to be SIN?

Selection of functional human antibodies from retroviral display libraries

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