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1061. Upstream Polyadenylation Enhancers in the U3 Region of Self-Inactivating Retroviral and Lentiviral Vectors Improve Titer and Gene Expression, and Prevent Transcriptional Read-Through

Molecular therapy, 2006-05, Vol.13 (S1), p.S407-S407

2006

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2 Retroviral vector development: reducing genotoxicity of integrated DNA and creating virus-like particles for transient cell modification

The CliniBook, 2012, p.100-111

2012

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457. Reverse Transcriptase Deficient Retroviral Vectors for Transient Cell Modification

Molecular therapy, 2006-05, Vol.13 (S1), p.S177-S177

2006

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An apparatus for in-vacuum loading of nanoparticles into an optical trap

Review of scientific instruments, 2022-11, Vol.93 (11)

2022

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Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery

Nucleic acids research, 2011-09, Vol.39 (16), p.7147-7160

2011

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Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery

Nucleic acids research, 2012-01, Vol.40 (2), p.939-939

2012

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Bromo- and Extraterminal Domain Chromatin Regulators Serve as Cofactors for Murine Leukemia Virus Integration

Journal of Virology, 2013-12, Vol.87 (23), p.12721-12736

2013

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The caspase-inhibitor Emricasan efficiently counteracts cisplatin- and neomycin-induced cytotoxicity in cochlear cells

Journal of molecular medicine (Berlin, Germany), 2024-09, Vol.102 (9), p.1163-1174

2024

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Cell and virus genetics at the roots of gene therapy, retrovirology, and hematopoietic stem cell biology: Wolfram Ostertag (1937-2010)

Human gene therapy, 2010-11, Vol.21 (11), p.1501-1503

2010

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Cellular Restriction of Retrovirus Particle-Mediated mRNA Transfer

Journal of Virology, 2008-03, Vol.82 (6), p.3069-3077

2008

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The CliniBook: Clinical gene transfer state of the art

Cohen-Haguenauer, Odile

1, 2012

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Correction for Gupta et al., “Bromo- and Extraterminal Domain Chromatin Regulators Serve as Cofactors for Murine Leukemia Virus Integration”

Journal of virology, 2024-04, Vol.98 (4)

2024

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Correction to: Potent and reversible lentiviral vector restriction in murine induced pluripotent stem cells

Retrovirology, 2017-10, Vol.14 (1), p.48-48, Article 48

2017

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CRISPR/Cas9 Genome Editing Using Gold‐Nanoparticle‐Mediated Laserporation

Advanced biosystems, 2018-11, Vol.2 (11), p.n/a

2018

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CRISPR/Cas9 Immunoengineering of Hoxb8-Immortalized Progenitor Cells for Revealing CCR7-Mediated Dendritic Cell Signaling and Migration Mechanisms in vivo

Frontiers in immunology, 2018-08, Vol.9, p.1949-1949

2018

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Design and Characterization of an “All-in-One” Lentiviral Vector System Combining Constitutive Anti-GD2 CAR Expression and Inducible Cytokines

Cancers, 2020-02, Vol.12 (2), p.375

2020

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Development of Novel Efficient SIN Vectors with Improved Safety Features for Wiskott–Aldrich Syndrome Stem Cell Based Gene Therapy

Molecular pharmaceutics, 2011-10, Vol.8 (5), p.1525-1537

2011

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Effect of Nateglinide on the Incidence of Diabetes and Cardiovascular Events

The New England journal of medicine, 2010-04, Vol.362 (16), p.1463-1476

2010

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Effect of Valsartan on the Incidence of Diabetes and Cardiovascular Events

The New England journal of medicine, 2010-04, Vol.362 (16), p.1477-1490

2010

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Efficient homing of T cells via afferent lymphatics requires mechanical arrest and integrin-supported chemokine guidance

Nature communications, 2020-02, Vol.11 (1), p.1114-1114, Article 1114

2020

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Eliminating HIV-1 Packaging Sequences from Lentiviral Vector Proviruses Enhances Safety and Expedites Gene Transfer for Gene Therapy

Molecular therapy, 2017-08, Vol.25 (8), p.1790-1804

2017

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Gammaretroviral vectors: biology, technology and application

Viruses, 2011-06, Vol.3 (6), p.677-713

2011

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Generation of an NFκB-Driven Alpharetroviral "All-in-One" Vector Construct as a Potent Tool for CAR NK Cell Therapy

Frontiers in immunology, 2021-11, Vol.12, p.751138-751138

2021

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1061. Upstream Polyadenylation Enhancers in the U3 Region of Self-Inactivating Retroviral and Lentiviral Vectors Improve Titer and Gene Expression, and Prevent Transcriptional Read-Through

2 Retroviral vector development: reducing genotoxicity of integrated DNA and creating virus-like particles for transient cell modification

457. Reverse Transcriptase Deficient Retroviral Vectors for Transient Cell Modification

An apparatus for in-vacuum loading of nanoparticles into an optical trap

Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery

Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery

Bromo- and Extraterminal Domain Chromatin Regulators Serve as Cofactors for Murine Leukemia Virus Integration

The caspase-inhibitor Emricasan efficiently counteracts cisplatin- and neomycin-induced cytotoxicity in cochlear cells

Cell and virus genetics at the roots of gene therapy, retrovirology, and hematopoietic stem cell biology: Wolfram Ostertag (1937-2010)

Cellular Restriction of Retrovirus Particle-Mediated mRNA Transfer

The CliniBook: Clinical gene transfer state of the art

Correction for Gupta et al., “Bromo- and Extraterminal Domain Chromatin Regulators Serve as Cofactors for Murine Leukemia Virus Integration”

Correction to: Potent and reversible lentiviral vector restriction in murine induced pluripotent stem cells

CRISPR/Cas9 Genome Editing Using Gold‐Nanoparticle‐Mediated Laserporation

CRISPR/Cas9 Immunoengineering of Hoxb8-Immortalized Progenitor Cells for Revealing CCR7-Mediated Dendritic Cell Signaling and Migration Mechanisms in vivo

Design and Characterization of an "All-in-One" Lentiviral Vector System Combining Constitutive Anti-G D2 CAR Expression and Inducible Cytokines

Design and Characterization of an “All-in-One” Lentiviral Vector System Combining Constitutive Anti-GD2 CAR Expression and Inducible Cytokines

Development of Novel Efficient SIN Vectors with Improved Safety Features for Wiskott–Aldrich Syndrome Stem Cell Based Gene Therapy

Early Psychosis Intervention-Spreading Evidence-based Treatment (EPI-SET): protocol for an effectiveness-implementation study of a structured model of care for psychosis in youth and emerging adults

Effect of Nateglinide on the Incidence of Diabetes and Cardiovascular Events

Effect of Valsartan on the Incidence of Diabetes and Cardiovascular Events

Efficient homing of T cells via afferent lymphatics requires mechanical arrest and integrin-supported chemokine guidance

Eliminating HIV-1 Packaging Sequences from Lentiviral Vector Proviruses Enhances Safety and Expedites Gene Transfer for Gene Therapy

Gammaretroviral vectors: biology, technology and application

Generation of an NFκB-Driven Alpharetroviral "All-in-One" Vector Construct as a Potent Tool for CAR NK Cell Therapy

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