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CRISPR/Cas9 delivery with one single adenoviral vector devoid of all viral genes

Scientific reports, 2017-12, Vol.7 (1), p.17113-11, Article 17113

2017

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One-Vector System for Multiplexed CRISPR/Cas9 against Hepatitis B Virus cccDNA Utilizing High-Capacity Adenoviral Vectors

Molecular therapy. Nucleic acids, 2018-09, Vol.12, p.242-253

2018

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Viral Vector-Based Delivery of CRISPR/Cas9 and Donor DNA for Homology-Directed Repair in an In Vitro Model for Canine Hemophilia B

Molecular therapy. Nucleic acids, 2019-03, Vol.14, p.364-376

2019

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An Engineered Virus Library as a Resource for the Spectrum-wide Exploration of Virus and Vector Diversity

Cell reports (Cambridge), 2017-05, Vol.19 (8), p.1698-1709

2017

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Designer nuclease‐mediated gene correction via homology‐directed repair in an in vitro model of canine hemophilia B

The journal of gene medicine, 2018-05, Vol.20 (5), p.e3020-n/a

2018

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How to Support Start-Ups in Developing a Sustainable Business Model: The Case of an European Social Impact Accelerator

Sustainability, 2021-03, Vol.13 (6), p.3337

2021

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Efficient and safe correction of hemophilia A by lentiviral vector-transduced BOECs in an implantable device

Molecular therapy. Methods & clinical development, 2021-12, Vol.23, p.551-566

2021

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Regulatory-Compliant Validation of a Highly Sensitive qPCR for Biodistribution Assessment of Hemophilia A Patient Cells

Molecular therapy. Methods & clinical development, 2020-09, Vol.18, p.176-188

2020

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Evaluation and quantification of spectral information in tissue by confocal microscopy

Journal of biomedical optics, 2012-10, Vol.17 (10), p.106011-106011

2012

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Quantification of designer nuclease induced mutation rates: a direct comparison of different methods

Molecular therapy. Methods & clinical development, 2016-01, Vol.3 (C), p.16047-16047, Article 16047

2016

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Minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates

Lung India, 2012-10, Vol.29 (4), p.309-312

2012

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Progress and Problems with Viral Vectors for Delivery of Talens

Journal of molecular and genetic medicine, 2014, Vol.8 (1)

Bergmann, Thorsten

2014

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18. Delivery of CRISPR/Cas9 or TALENs Against Hepatitis B Virus cccDNA by High-Capacity Adenoviral Vectors

Molecular therapy, 2016-05, Vol.24, p.S9-S9

2016

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The Use of Interferon Gamma Release Assays in the Diagnosis of Active Tuberculosis

Tuberculosis Research and Treatment, 2012-01, Vol.2012 (2012), p.106-109

2012

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15. A Novel Fast Production Pipeline for High Capacity Adenoviral Vectors to Deliver All Components of CRISPR/Cas9 System for Somatic Gene Editing Using One Single Viral Vector with Multiple Guide RNAs

Molecular therapy, 2016-05, Vol.24, p.S8-S8

2016

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Gene therapeutic approaches to inhibit hepatitis B virus replication

World journal of hepatology, 2015-02, Vol.7 (2), p.150-164

2015

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103. Pas de Deux – A Single Inducible High-Capacity Adenoviral Vector for Delivery of a Functional TALEN Pair Directed Against Human Dystrophin for the Treatment of Duchenne Muscular Dystrophy (DMD)

Molecular therapy, 2015-05, Vol.23, p.S43-S43

2015

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573. Towards Gene Correction in a Large Animal Model: Gene Correction of Canine Coagulation Factor IX Deficiency Via Homologous Recombination Mediated By Designer Nucleases

Molecular therapy, 2015-05, Vol.23, p.S228-S228

2015

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669. Standard Free Droplet Digital PCR as a New Tool for More Precise and Reliable Quality Control of Gene Therapy Vectors

Molecular therapy, 2015-05, Vol.23, p.S266-S266

2015

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Cloning and Large-Scale Production of High-Capacity Adenoviral Vectors Based on the Human Adenovirus Type 5

Journal of visualized experiments, 2016-01 (107), p.e52894-e52894

2016

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Nucleocytoplasmic Distribution of the Arabidopsis Chromatin-Associated HMGB2/3 and HMGB4 Proteins

Plant physiology (Bethesda), 2010-12, Vol.154 (4), p.1831-1841

2010

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48. High-Throughput Cloning and Tagging of an Engineered Adenovirus-Library Empowers Vector Diversity for Broad Applications

Molecular therapy, 2015-05, Vol.23, p.S21-S21

2015

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14. Engineering and Characterization of a Cloned Adenoviral-Library to Explore Natural Virus Diversity

Molecular therapy, 2016-05, Vol.24, p.S7-S8

2016

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Gene therapeutic approaches to inhibit hepatitis B virusreplication

世界肝病学杂志：英文版（电子版）, 2015 (2), p.150-164

Maren Gebbing Thorsten Bergmann Eric Schulz Anja Ehrhardt

2015

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Cloning and Large-Scale Production of High-Capacity Adenoviral Vectors Based on the Human Adenovirus Type 5

Journal of visualized experiments, 2016-01 (107)

2016

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CRISPR/Cas9 delivery with one single adenoviral vector devoid of all viral genes

One-Vector System for Multiplexed CRISPR/Cas9 against Hepatitis B Virus cccDNA Utilizing High-Capacity Adenoviral Vectors

Viral Vector-Based Delivery of CRISPR/Cas9 and Donor DNA for Homology-Directed Repair in an In Vitro Model for Canine Hemophilia B

An Engineered Virus Library as a Resource for the Spectrum-wide Exploration of Virus and Vector Diversity

Designer nuclease‐mediated gene correction via homology‐directed repair in an in vitro model of canine hemophilia B

How to Support Start-Ups in Developing a Sustainable Business Model: The Case of an European Social Impact Accelerator

Efficient and safe correction of hemophilia A by lentiviral vector-transduced BOECs in an implantable device

Regulatory-Compliant Validation of a Highly Sensitive qPCR for Biodistribution Assessment of Hemophilia A Patient Cells

Evaluation and quantification of spectral information in tissue by confocal microscopy

Quantification of designer nuclease induced mutation rates: a direct comparison of different methods

Minimal inhibitory concentrations of first-line drugs of multidrug-resistant tuberculosis isolates

Progress and Problems with Viral Vectors for Delivery of Talens

18. Delivery of CRISPR/Cas9 or TALENs Against Hepatitis B Virus cccDNA by High-Capacity Adenoviral Vectors

The Use of Interferon Gamma Release Assays in the Diagnosis of Active Tuberculosis

15. A Novel Fast Production Pipeline for High Capacity Adenoviral Vectors to Deliver All Components of CRISPR/Cas9 System for Somatic Gene Editing Using One Single Viral Vector with Multiple Guide RNAs

Gene therapeutic approaches to inhibit hepatitis B virus replication

103. Pas de Deux – A Single Inducible High-Capacity Adenoviral Vector for Delivery of a Functional TALEN Pair Directed Against Human Dystrophin for the Treatment of Duchenne Muscular Dystrophy (DMD)

573. Towards Gene Correction in a Large Animal Model: Gene Correction of Canine Coagulation Factor IX Deficiency Via Homologous Recombination Mediated By Designer Nucleases

669. Standard Free Droplet Digital PCR as a New Tool for More Precise and Reliable Quality Control of Gene Therapy Vectors

Cloning and Large-Scale Production of High-Capacity Adenoviral Vectors Based on the Human Adenovirus Type 5

Nucleocytoplasmic Distribution of the Arabidopsis Chromatin-Associated HMGB2/3 and HMGB4 Proteins

48. High-Throughput Cloning and Tagging of an Engineered Adenovirus-Library Empowers Vector Diversity for Broad Applications

14. Engineering and Characterization of a Cloned Adenoviral-Library to Explore Natural Virus Diversity

Gene therapeutic approaches to inhibit hepatitis B virusreplication

Cloning and Large-Scale Production of High-Capacity Adenoviral Vectors Based on the Human Adenovirus Type 5

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