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Gene Augmentation of CHM Using Non-Viral Episomal Vectors in Models of Choroideremia

International journal of molecular sciences, 2023-10, Vol.24 (20), p.15225

2023

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Beta HPV38 oncoproteins act with a hit-and-run mechanism in ultraviolet radiation-induced skin carcinogenesis in mice

PLoS pathogens, 2018-01, Vol.14 (1), p.e1006783

2018

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Treatment of phenylketonuria using minicircle‐based naked‐DNA gene transfer to murine liver

Hepatology (Baltimore, Md.), 2014-09, Vol.60 (3), p.1035-1043

2014

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A nonviral, nonintegrating DNA nanovector platform for the safe, rapid, and persistent manufacture of recombinant T cells

Science advances, 2021-04, Vol.7 (16)

2021

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Perivascular tenascin C triggers sequential activation of macrophages and endothelial cells to generate a pro-metastatic vascular niche in the lungs

Nature cancer, 2022-04, Vol.3 (4), p.486-504

2022

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Folliculin Controls the Intracellular Survival and Trans-Epithelial Passage of Neisseria gonorrhoeae

Frontiers in cellular and infection microbiology, 2020-09, Vol.10, p.422-422

2020

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Novel Non-integrating DNA Nano-S/MAR Vectors Restore Gene Function in Isogenic Patient-Derived Pancreatic Tumor Models

Molecular therapy. Methods & clinical development, 2020-06, Vol.17, p.957-968

2020

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A Simple Nonviral Method to Generate Human Induced Pluripotent Stem Cells Using SMAR DNA Vectors

Genes, 2024-04, Vol.15 (5), p.575

2024

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pEPito: a significantly improved non-viral episomal expression vector for mammalian cells

BMC biotechnology, 2010-03, Vol.10 (1), p.20-20, Article 20

2010

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An episomal DNA vector platform for the persistent genetic modification of pluripotent stem cells and their differentiated progeny

Stem cell reports, 2022-01, Vol.17 (1), p.143-158

2022

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Sustained Expression from DNA Vectors

Advances in genetics, 2015, Vol.89, p.113-152

2015

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Genetic modification of cancer cells using non-viral, episomal S/MAR vectors for in vivo tumour modelling

PloS one, 2012-10, Vol.7 (10), p.e47920-e47920

2012

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Birt-Hogg-Dube syndrome is a novel ciliopathy

Human molecular genetics, 2013-11, Vol.22 (21), p.4383-4397

2013

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Development of an Orthotopic HPV16-Dependent Base of Tongue Tumor Model in MHC-Humanized Mice

Pathogens (Basel), 2023-01, Vol.12 (2), p.188

2023

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Safe and stable generation of induced pluripotent stem cells using doggybone DNA vectors

Molecular therapy. Methods & clinical development, 2021-12, Vol.23, p.348-358

2021

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Safety Profile of Stromal Hydration of Clear Corneal Incisions with Cefuroxime in the Mouse Model

Journal of ocular pharmacology and therapeutics, 2016-09, Vol.32 (7), p.469-475

2016

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Systemic gene transfer of polyethylenimine (PEI)–plasmid DNA complexes to neonatal mice

Journal of controlled release, 2011-03, Vol.150 (3), p.298-306

2011

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Development of S/MAR minicircles for enhanced and persistent transgene expression in the mouse liver

Journal of molecular medicine (Berlin, Germany), 2011-05, Vol.89 (5), p.515-529

2011

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Novel chimeric antigen receptors for the effective and safe treatment of NY‐BR‐1 positive breast cancer

Clinical and translational medicine, 2024-07, Vol.14 (7), p.e1776-n/a

2024

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Non-viral episomal modification of cells using S/MAR elements

Expert opinion on biological therapy, 2011-09, Vol.11 (9), p.1177-1191

2011

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Delivery of non-viral naked DNA vectors to liver in small weaned pigs by hydrodynamic retrograde intrabiliary injection

Molecular therapy. Methods & clinical development, 2022-03, Vol.24, p.268-279

2022

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Corneal gene delivery: chitosan oligomer as a carrier of CpG rich, CpG free or S/MAR plasmid DNA

The journal of gene medicine, 2012-02, Vol.14 (2), p.100-108

2012

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Delivery and long-term expression of a 135 kb LDLR genomic DNA locus in vivo by hydrodynamic tail vein injection

The journal of gene medicine, 2007-06, Vol.9 (6), p.488-497

2007

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Nuclear-targeted minicircle to enhance gene transfer with non-viral vectors in vitro and in vivo

The journal of gene medicine, 2006-06, Vol.8 (6), p.754-763

2006

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Minimal-length Synthetic shRNAs Formulated with Lipid Nanoparticles are Potent Inhibitors of Hepatitis C Virus IRES-linked Gene Expression in Mice

Molecular therapy. Nucleic acids, 2013, Vol.2 (9), p.e123-e123, Article e123

2013

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Gene Augmentation of CHM Using Non-Viral Episomal Vectors in Models of Choroideremia

Beta HPV38 oncoproteins act with a hit-and-run mechanism in ultraviolet radiation-induced skin carcinogenesis in mice

Treatment of phenylketonuria using minicircle‐based naked‐DNA gene transfer to murine liver

A nonviral, nonintegrating DNA nanovector platform for the safe, rapid, and persistent manufacture of recombinant T cells

Perivascular tenascin C triggers sequential activation of macrophages and endothelial cells to generate a pro-metastatic vascular niche in the lungs

Folliculin Controls the Intracellular Survival and Trans-Epithelial Passage of Neisseria gonorrhoeae

Novel Non-integrating DNA Nano-S/MAR Vectors Restore Gene Function in Isogenic Patient-Derived Pancreatic Tumor Models

A Simple Nonviral Method to Generate Human Induced Pluripotent Stem Cells Using SMAR DNA Vectors

pEPito: a significantly improved non-viral episomal expression vector for mammalian cells

An episomal DNA vector platform for the persistent genetic modification of pluripotent stem cells and their differentiated progeny

Sustained Expression from DNA Vectors

Genetic modification of cancer cells using non-viral, episomal S/MAR vectors for in vivo tumour modelling

Birt-Hogg-Dube syndrome is a novel ciliopathy

Development of an Orthotopic HPV16-Dependent Base of Tongue Tumor Model in MHC-Humanized Mice

Safe and stable generation of induced pluripotent stem cells using doggybone DNA vectors

Safety Profile of Stromal Hydration of Clear Corneal Incisions with Cefuroxime in the Mouse Model

Systemic gene transfer of polyethylenimine (PEI)–plasmid DNA complexes to neonatal mice

Development of S/MAR minicircles for enhanced and persistent transgene expression in the mouse liver

Novel chimeric antigen receptors for the effective and safe treatment of NY‐BR‐1 positive breast cancer

Non-viral episomal modification of cells using S/MAR elements

Delivery of non-viral naked DNA vectors to liver in small weaned pigs by hydrodynamic retrograde intrabiliary injection

Corneal gene delivery: chitosan oligomer as a carrier of CpG rich, CpG free or S/MAR plasmid DNA

Delivery and long-term expression of a 135 kb LDLR genomic DNA locus in vivo by hydrodynamic tail vein injection

Nuclear-targeted minicircle to enhance gene transfer with non-viral vectors in vitro and in vivo

Minimal-length Synthetic shRNAs Formulated with Lipid Nanoparticles are Potent Inhibitors of Hepatitis C Virus IRES-linked Gene Expression in Mice

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