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Double-stranded RNA innate immune response activation from long-term adeno-associated virus vector transduction

JCI insight, 2018-06, Vol.3 (12)

2018

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Therapeutic Applications of Adeno-Associated Virus (AAV) Gene Transfer of HLA-G in the Eye

International journal of molecular sciences, 2022-03, Vol.23 (7), p.3465

2022

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Inhibition of experimental autoimmune uveitis by intravitreal AAV-Equine-IL10 gene therapy

PloS one, 2022-08, Vol.17 (8), p.e0270972-e0270972

2022

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Brute-Force Hyperpolarization for NMR and MRI

Journal of the American Chemical Society, 2015-07, Vol.137 (26), p.8428-8434

2015

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Adeno-Associated Virus Mediated Gene Therapy for Corneal Diseases

Pharmaceutics, 2020-08, Vol.12 (8), p.767

2020

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Oversized AAV Transductifon Is Mediated via a DNA-PKcs-independent, Rad51C-dependent Repair Pathway

Molecular therapy, 2013-12, Vol.21 (12), p.2205-2216

2013

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Harnessing the Natural Biology of Adeno-Associated Virus to Enhance the Efficacy of Cancer Gene Therapy

Viruses, 2021-06, Vol.13 (7), p.1205

2021

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Adeno-associated Virus as a Mammalian DNA Vector

Microbiology spectrum, 2015-08, Vol.3 (4)

2015

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Single Amino Acid Modification of Adeno-Associated Virus Capsid Changes Transduction and Humoral Immune Profiles

Journal of Virology, 2012-08, Vol.86 (15), p.7752-7759

2012

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Adeno-Associated Virus Vector Mediated Delivery of the HBV Genome Induces Chronic Hepatitis B Virus Infection and Liver Fibrosis in Mice

PloS one, 2015-06, Vol.10 (6), p.e0130052-e0130052

2015

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AAV Vectorization of DSB-mediated Gene Editing Technologies

Current gene therapy, 2016-01, Vol.16 (3), p.207-219

2016

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Viral single-strand DNA induces p53-dependent apoptosis in human embryonic stem cells

PloS one, 2011-11, Vol.6 (11), p.e27520-e27520

2011

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Proteasome Inhibitors Enhance Gene Delivery by AAV Virus Vectors Expressing Large Genomes in Hemophilia Mouse and Dog Models: A Strategy for Broad Clinical Application

Molecular therapy, 2010-11, Vol.18 (11), p.1907-1916

2010

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Promyelocytic Leukemia Protein Is a Cell-Intrinsic Factor Inhibiting Parvovirus DNA Replication

Journal of Virology, 2014-01, Vol.88 (2), p.925-936

2014

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AAV-mediated expression of HLA-G for the prevention of experimental ocular graft vs. host disease

Molecular therapy. Methods & clinical development, 2023-06, Vol.29, p.227-235

2023

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Ocular Tolerability and Immune Response to Corneal Intrastromal AAV-IDUA Gene Therapy in New Zealand White Rabbits

Molecular therapy. Methods & clinical development, 2020-09, Vol.18, p.24-32

2020

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A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequence

Molecular therapy. Methods & clinical development, 2015-01, Vol.2, p.15009-15009, Article 15009

2015

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Adeno-Associated Virus Serotype-Specific Inverted Terminal Repeat Sequence Role in Vector Transgene Expression

Human gene therapy, 2020-02, Vol.31 (3-4), p.151-162

2020

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Adeno-Associated Virus Vector Mobilization, Risk Versus Reality

Human gene therapy, 2020-10, Vol.31 (19-20), p.1054-1067

2020

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A chimeric anti-vascularization immunomodulator prevents high-risk corneal transplantation rejection via ex vivo gene therapy

Molecular therapy, 2024-11, Vol.32 (11), p.4006-4020

2024

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Integration of a CD19 CAR into the TCR Alpha Chain Locus Streamlines Production of Allogeneic Gene-Edited CAR T Cells

Molecular therapy, 2017-04, Vol.25 (4), p.949-961

2017

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Adeno-Associated Virus Vectors and Stem Cells: Friends or Foes?

Human gene therapy, 2017-06, Vol.28 (6), p.450-463

2017

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Serotype survey of AAV gene delivery via subconjunctival injection in mice

Gene therapy, 2018-09, Vol.25 (6), p.402-414

2018

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survey of ex vivo/in vitro transduction efficiency of mammalian primary cells and cell lines with Nine natural adeno-associated virus (AAV1-9) and one engineered adeno-associated virus serotype

Virology journal, 2013-03, Vol.10 (1), p.74-74, Article 74

2013

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Structure-Based Designed Nano-Dysferlin Significantly Improves Dysferlinopathy in BLA/J Mice

Molecular therapy, 2017-09, Vol.25 (9), p.2150-2162

2017

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Double-stranded RNA innate immune response activation from long-term adeno-associated virus vector transduction

Therapeutic Applications of Adeno-Associated Virus (AAV) Gene Transfer of HLA-G in the Eye

Inhibition of experimental autoimmune uveitis by intravitreal AAV-Equine-IL10 gene therapy

Brute-Force Hyperpolarization for NMR and MRI

Adeno-Associated Virus Mediated Gene Therapy for Corneal Diseases

Oversized AAV Transductifon Is Mediated via a DNA-PKcs-independent, Rad51C-dependent Repair Pathway

Harnessing the Natural Biology of Adeno-Associated Virus to Enhance the Efficacy of Cancer Gene Therapy

Adeno-associated Virus as a Mammalian DNA Vector

Single Amino Acid Modification of Adeno-Associated Virus Capsid Changes Transduction and Humoral Immune Profiles

Adeno-Associated Virus Vector Mediated Delivery of the HBV Genome Induces Chronic Hepatitis B Virus Infection and Liver Fibrosis in Mice

AAV Vectorization of DSB-mediated Gene Editing Technologies

Viral single-strand DNA induces p53-dependent apoptosis in human embryonic stem cells

Proteasome Inhibitors Enhance Gene Delivery by AAV Virus Vectors Expressing Large Genomes in Hemophilia Mouse and Dog Models: A Strategy for Broad Clinical Application

Promyelocytic Leukemia Protein Is a Cell-Intrinsic Factor Inhibiting Parvovirus DNA Replication

AAV-mediated expression of HLA-G for the prevention of experimental ocular graft vs. host disease

Ocular Tolerability and Immune Response to Corneal Intrastromal AAV-IDUA Gene Therapy in New Zealand White Rabbits

A comparison of AAV strategies distinguishes overlapping vectors for efficient systemic delivery of the 6.2 kb Dysferlin coding sequence

Adeno-Associated Virus Serotype-Specific Inverted Terminal Repeat Sequence Role in Vector Transgene Expression

Adeno-Associated Virus Vector Mobilization, Risk Versus Reality

A chimeric anti-vascularization immunomodulator prevents high-risk corneal transplantation rejection via ex vivo gene therapy

Integration of a CD19 CAR into the TCR Alpha Chain Locus Streamlines Production of Allogeneic Gene-Edited CAR T Cells

Adeno-Associated Virus Vectors and Stem Cells: Friends or Foes?

Serotype survey of AAV gene delivery via subconjunctival injection in mice

survey of ex vivo/in vitro transduction efficiency of mammalian primary cells and cell lines with Nine natural adeno-associated virus (AAV1-9) and one engineered adeno-associated virus serotype

Structure-Based Designed Nano-Dysferlin Significantly Improves Dysferlinopathy in BLA/J Mice

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