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Lentiviral Delivery of Proteins for Genome Engineering

Current gene therapy, 2016-01, Vol.16 (3), p.194

2016

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Delivering genes with human immunodeficiency virus-derived vehicles: still state-of-the-art after 25 years

Journal of biomedical science, 2022-10, Vol.29 (1), p.1-79, Article 79

2022

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Induction of Atherosclerosis in Mice and Hamsters Without Germline Genetic Engineering

Circulation research, 2014-05, Vol.114 (11), p.1684-1689

2014

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Lack of immunological DNA sensing in hepatocytes facilitates hepatitis B virus infection

Hepatology (Baltimore, Md.), 2016-09, Vol.64 (3), p.746-759

2016

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Lentiviral vectors for cutaneous RNA managing

Experimental dermatology, 2012-03, Vol.21 (3), p.162-170

2012

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Targeted Knockout of the Vegfa Gene in the Retina by Subretinal Injection of RNP Complexes Containing Cas9 Protein and Modified sgRNAs

Molecular therapy, 2021-01, Vol.29 (1), p.191-207

2021

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Targeted genome editing by lentiviral protein transduction of zinc-finger and TAL-effector nucleases

eLife, 2014-04, Vol.3, p.e01911-e01911

2014

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Prime editing in hematopoietic stem cells-From ex vivo to in vivo CRISPR-based treatment of blood disorders

Frontiers in genome editing, 2023-03, Vol.5, p.1148650-1148650

2023

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Dominant-negative SERPING1 variants cause intracellular retention of C1 inhibitor in hereditary angioedema

The Journal of clinical investigation, 2019-01, Vol.129 (1), p.388-405

2019

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Sustained transgene expression from sleeping beauty DNA transposons containing a core fragment of the HNRPA2B1-CBX3 ubiquitous chromatin opening element (UCOE)

BMC biotechnology, 2019-11, Vol.19 (1), p.75-75, Article 75

2019

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DNA transposon-based gene vehicles - scenes from an evolutionary drive

Journal of biomedical science, 2013-12, Vol.20 (1), p.92-92, Article 92

2013

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Overexpression of microRNA-155 increases IL-21 mediated STAT3 signaling and IL-21 production in systemic lupus erythematosus

Arthritis research & therapy, 2015-06, Vol.17 (1), p.154-154, Article 154

2015

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Suppression of Choroidal Neovascularization by AAV-Based Dual-Acting Antiangiogenic Gene Therapy

Molecular therapy. Nucleic acids, 2019-06, Vol.16, p.38-50

2019

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In Vivo Knockout of the Vegfa Gene by Lentiviral Delivery of CRISPR/Cas9 in Mouse Retinal Pigment Epithelium Cells

Molecular therapy. Nucleic acids, 2017-12, Vol.9 (C), p.89-99

2017

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Identification of BLNK and BTK as mediators of rituximab‐induced programmed cell death by CRISPR screens in GCB‐subtype diffuse large B‐cell lymphoma

Molecular oncology, 2020-09, Vol.14 (9), p.1978-1997

2020

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Potent microRNA suppression by RNA Pol II-transcribed 'Tough Decoy' inhibitors

RNA (Cambridge), 2013-02, Vol.19 (2), p.280-293

2013

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CRISPR-Cas9-directed gene tagging using a single integrase-defective lentiviral vector carrying a transposase-based Cas9 off switch

Molecular therapy. Nucleic acids, 2022-09, Vol.29, p.563-576

2022

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piggyPrime: High-Efficacy Prime Editing in Human Cells Using piggyBac-Based DNA Transposition

Frontiers in genome editing, 2021-11, Vol.3, p.786893-786893

2021

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Single-Cell Monitoring of Activated Innate Immune Signaling by a d2eGFP-Based Reporter Mimicking Time-Restricted Activation of IFNB1 Expression

Frontiers in cellular and infection microbiology, 2022-01, Vol.11, p.784762-784762

2022

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DNA transposition by protein transduction of the piggyBac transposase from lentiviral Gag precursors

Nucleic acids research, 2014-02, Vol.42 (4), p.e28

2014

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Time-Restricted PiggyBac DNA Transposition by Transposase Protein Delivery Using Lentivirus-Derived Nanoparticles

Molecular therapy. Nucleic acids, 2018-06, Vol.11 (C), p.253-262

2018

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Anti-Apoptotic Effects of Lentiviral Vector Transduction Promote Increased Rituximab Tolerance in Cancerous B-Cells

PloS one, 2016-04, Vol.11 (4), p.e0153069

2016

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Improved Lentiviral Gene Delivery to Mouse Liver by Hydrodynamic Vector Injection through Tail Vein

Molecular therapy. Nucleic acids, 2018-09, Vol.12, p.672-683

2018

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Development of transgenic cloned pig models of skin inflammation by DNA transposon-directed ectopic expression of human β1 and α2 integrin

PloS one, 2012-05, Vol.7 (5), p.e36658-e36658

2012

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Postintegrative Gene Silencing within the Sleeping Beauty Transposition System

Molecular and Cellular Biology, 2007-12, Vol.27 (24), p.8824-8833

2007

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Biotechnology & Applied Microbiology
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Gene Expression
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Gene Therapy
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Genetic Vectors - Genetics
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Genetic Vectors
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Lentiviral Delivery of Proteins for Genome Engineering

Delivering genes with human immunodeficiency virus-derived vehicles: still state-of-the-art after 25 years

Induction of Atherosclerosis in Mice and Hamsters Without Germline Genetic Engineering

Lack of immunological DNA sensing in hepatocytes facilitates hepatitis B virus infection

Lentiviral vectors for cutaneous RNA managing

Targeted Knockout of the Vegfa Gene in the Retina by Subretinal Injection of RNP Complexes Containing Cas9 Protein and Modified sgRNAs

Targeted genome editing by lentiviral protein transduction of zinc-finger and TAL-effector nucleases

Prime editing in hematopoietic stem cells-From ex vivo to in vivo CRISPR-based treatment of blood disorders

Dominant-negative SERPING1 variants cause intracellular retention of C1 inhibitor in hereditary angioedema

Sustained transgene expression from sleeping beauty DNA transposons containing a core fragment of the HNRPA2B1-CBX3 ubiquitous chromatin opening element (UCOE)

DNA transposon-based gene vehicles - scenes from an evolutionary drive

Overexpression of microRNA-155 increases IL-21 mediated STAT3 signaling and IL-21 production in systemic lupus erythematosus

Suppression of Choroidal Neovascularization by AAV-Based Dual-Acting Antiangiogenic Gene Therapy

In Vivo Knockout of the Vegfa Gene by Lentiviral Delivery of CRISPR/Cas9 in Mouse Retinal Pigment Epithelium Cells

Identification of BLNK and BTK as mediators of rituximab‐induced programmed cell death by CRISPR screens in GCB‐subtype diffuse large B‐cell lymphoma

Potent microRNA suppression by RNA Pol II-transcribed 'Tough Decoy' inhibitors

CRISPR-Cas9-directed gene tagging using a single integrase-defective lentiviral vector carrying a transposase-based Cas9 off switch

piggyPrime: High-Efficacy Prime Editing in Human Cells Using piggyBac-Based DNA Transposition

Single-Cell Monitoring of Activated Innate Immune Signaling by a d2eGFP-Based Reporter Mimicking Time-Restricted Activation of IFNB1 Expression

DNA transposition by protein transduction of the piggyBac transposase from lentiviral Gag precursors

Time-Restricted PiggyBac DNA Transposition by Transposase Protein Delivery Using Lentivirus-Derived Nanoparticles

Anti-Apoptotic Effects of Lentiviral Vector Transduction Promote Increased Rituximab Tolerance in Cancerous B-Cells

Improved Lentiviral Gene Delivery to Mouse Liver by Hydrodynamic Vector Injection through Tail Vein

Development of transgenic cloned pig models of skin inflammation by DNA transposon-directed ectopic expression of human β1 and α2 integrin

Postintegrative Gene Silencing within the Sleeping Beauty Transposition System

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