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The Transcriptional and Functional Properties of Mouse Epiblast Stem Cells Resemble the Anterior Primitive Streak

Cell stem cell, 2014-01, Vol.14 (1), p.107-120

2014

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Identification of liver-specific enhancer-promoter activity in the 3' untranslated region of the wild-type AAV2 genome

Nature genetics, 2017-08, Vol.49 (8), p.1267-1273

2017

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Altered Hippocampal and Striatal Expression of Endothelial Markers and VIP/PACAP Neuropeptides in a Mouse Model of Systemic Lupus Erythematosus

International journal of molecular sciences, 2023-07, Vol.24 (13), p.11118

2023

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Performance of Cardiotropic rAAV Vectors Is Dependent on Production Method

Viruses, 2022-07, Vol.14 (8), p.1623

2022

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Adeno-associated Virus-mediated Rescue of Neonatal Lethality in Argininosuccinate Synthetase-deficient Mice

Molecular therapy, 2013-10, Vol.21 (10), p.1823-1831

2013

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Efficient in vivo editing of OTC-deficient patient-derived primary human hepatocytes

JHEP reports, 2020-02, Vol.2 (1), p.100065-100065, Article 100065

2020

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Use of a Hybrid Adeno-Associated Viral Vector Transposon System to Deliver the Insulin Gene to Diabetic NOD Mice

Cells (Basel, Switzerland), 2020-10, Vol.9 (10), p.2227

2020

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A User's Guide to the Inverted Terminal Repeats of Adeno-Associated Virus

Human gene therapy. Part B. Methods, 2019-12, Vol.30 (6), p.206

2019

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Adeno-associated virus vectors: immunobiology and potential use for immune modulation

Current gene therapy, 2012-08, Vol.12 (4), p.333

2012

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Structural and functional characterization of capsid binding by anti-AAV9 monoclonal antibodies from infants after SMA gene therapy

Molecular therapy, 2023-07, Vol.31 (7), p.1979-1993

2023

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Gain-of-function factor H-related 5 protein impairs glomerular complement regulation resulting in kidney damage

Proceedings of the National Academy of Sciences - PNAS, 2021-03, Vol.118 (13), p.1

2021

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Adeno-Associated Virus Vector Gene Delivery Elevates Factor I Levels and Downregulates the Complement Alternative Pathway In Vivo

Human gene therapy, 2021-11, Vol.32 (21-22), p.1370

2021

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1778-P: Delivery of the Insulin Gene Using an Integrating Adeno-Associated Viral Vector (AAV) to Diabetic NOD Mice

Diabetes (New York, N.Y.), 2019-06, Vol.68 (Supplement_1)

2019

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AAV-mediated gene delivery of the calreticulin anti-angiogenic domain inhibits ocular neovascularization

Angiogenesis (London), 2018-02, Vol.21 (1), p.95-109

2018

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Exploiting the unique regenerative capacity of the liver to underpin cell and gene therapy strategies for genetic and acquired liver disease

The international journal of biochemistry & cell biology, 2014-11, Vol.56, p.141-152

2014

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Direct recognition of hepatocyte-expressed MHC class I alloantigens is required for tolerance induction

JCI insight, 2018-08, Vol.3 (15)

2018

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Liver-directed gene expression using recombinant AAV 2/8 vectors--a tolerogenic strategy for gene delivery?

Discovery medicine, 2010-06, Vol.9 (49), p.519-527

2010

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Human induced pluripotent stem cells derived under feeder-free conditions display unique cell cycle and DNA replication gene profiles

Stem cells and development, 2011-04, Vol.21 (2), p.206

2011

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Antigen fusion with C3d3 augments or inhibits humoral immunity to AAV genetic vaccines in a transgene‐dependent manner

Immunology and cell biology, 2010-02, Vol.88 (2), p.228-232

2010

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AAV vectors encoding malarial antigens stimulate antigen-specific immunity but do not protect from parasite infection

Vaccine, 2007-01, Vol.25 (6), p.1014-1022

2007

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Limiting γc expression differentially affects signaling via the interleukin (IL)-7 and IL-15 receptors

Blood, 2007-07, Vol.110 (1), p.91-98

2007

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Robust anti-tumor immunity and memory in Rag-1-deficient mice following adoptive transfer of cytokine-primed splenocytes and tumor CD80 expression

Cancer Immunology, Immunotherapy, 2007-12, Vol.56 (12), p.1955-1965

2007

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1103. Augmentation of Immunity Against AAV- Encoded Transgenes by Use of the Genetic Adjuvants C3d3 and CTLA4

Molecular therapy, 2006-05, Vol.13 (S1), p.S424-S424

2006

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Gene therapy in transplantation

Transplantation reviews (Philadelphia, Pa.), 2009-07, Vol.23 (3), p.159-170

2009

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HeLa cells cocultured with peripheral blood lymphocytes acquire an immuno‐inhibitory phenotype through up‐regulation of indoleamine 2,3‐dioxygenase activity

Immunology, 2002-04, Vol.105 (4), p.478-487

2002

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The Transcriptional and Functional Properties of Mouse Epiblast Stem Cells Resemble the Anterior Primitive Streak

Identification of liver-specific enhancer-promoter activity in the 3' untranslated region of the wild-type AAV2 genome

Altered Hippocampal and Striatal Expression of Endothelial Markers and VIP/PACAP Neuropeptides in a Mouse Model of Systemic Lupus Erythematosus

Performance of Cardiotropic rAAV Vectors Is Dependent on Production Method

Adeno-associated Virus-mediated Rescue of Neonatal Lethality in Argininosuccinate Synthetase-deficient Mice

Efficient in vivo editing of OTC-deficient patient-derived primary human hepatocytes

Use of a Hybrid Adeno-Associated Viral Vector Transposon System to Deliver the Insulin Gene to Diabetic NOD Mice

A User's Guide to the Inverted Terminal Repeats of Adeno-Associated Virus

Adeno-associated virus vectors: immunobiology and potential use for immune modulation

Structural and functional characterization of capsid binding by anti-AAV9 monoclonal antibodies from infants after SMA gene therapy

Gain-of-function factor H-related 5 protein impairs glomerular complement regulation resulting in kidney damage

Adeno-Associated Virus Vector Gene Delivery Elevates Factor I Levels and Downregulates the Complement Alternative Pathway In Vivo

1778-P: Delivery of the Insulin Gene Using an Integrating Adeno-Associated Viral Vector (AAV) to Diabetic NOD Mice

AAV-mediated gene delivery of the calreticulin anti-angiogenic domain inhibits ocular neovascularization

Exploiting the unique regenerative capacity of the liver to underpin cell and gene therapy strategies for genetic and acquired liver disease

Direct recognition of hepatocyte-expressed MHC class I alloantigens is required for tolerance induction

Liver-directed gene expression using recombinant AAV 2/8 vectors--a tolerogenic strategy for gene delivery?

Human induced pluripotent stem cells derived under feeder-free conditions display unique cell cycle and DNA replication gene profiles

Antigen fusion with C3d3 augments or inhibits humoral immunity to AAV genetic vaccines in a transgene‐dependent manner

AAV vectors encoding malarial antigens stimulate antigen-specific immunity but do not protect from parasite infection

Limiting γc expression differentially affects signaling via the interleukin (IL)-7 and IL-15 receptors

Robust anti-tumor immunity and memory in Rag-1-deficient mice following adoptive transfer of cytokine-primed splenocytes and tumor CD80 expression

1103. Augmentation of Immunity Against AAV- Encoded Transgenes by Use of the Genetic Adjuvants C3d3 and CTLA4

Gene therapy in transplantation

HeLa cells cocultured with peripheral blood lymphocytes acquire an immuno‐inhibitory phenotype through up‐regulation of indoleamine 2,3‐dioxygenase activity

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