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Permanent partial phenotypic correction and tolerance in a mouse model of hemophilia B by stem cell gene delivery of human factor IX

Gene therapy, 2006-01, Vol.13 (2), p.117-126

2006

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Wiskott-Aldrich syndrome protein is necessary for efficient IgG-mediated phagocytosis

Blood, 2000-05, Vol.95 (9), p.2943-2946

2000

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Immunotherapy for neuroblastoma using syngeneic fibroblasts transfected with IL-2 and IL-12

British journal of cancer, 2007-07, Vol.97 (2), p.210-217

2007

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Current progress on gene therapy for primary immunodeficiencies

Gene therapy, 2013-10, Vol.20 (10), p.963-969

2013

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Enhanced human cell engraftment in mice deficient in RAG2 and the common cytokine receptor γ chain

British journal of haematology, 1998-11, Vol.103 (2), p.335-342

1998

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Cutting Edge: The Wiskott-Aldrich Syndrome Protein Is Required for Efficient Phagocytosis of Apoptotic Cells

The Journal of immunology (1950), 2001-04, Vol.166 (8), p.4831-4834

2001

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Dendritic Cells: The Bare Bones of Immunity

Current biology, 2004-11, Vol.14 (22), p.R965-R967

2004

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Cell-specific and efficient expression in mouse and human B cells by a novel hybrid immunoglobulin promoter in a lentiviral vector

Gene therapy, 2007-12, Vol.14 (23), p.1623-1631

2007

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Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retina

Gene therapy, 2003-08, Vol.10 (16), p.1336-1344

2003

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Gene therapy for the Wiskott-Aldrich syndrome

Current opinion in allergy and clinical immunology, 2011-12, Vol.11 (6), p.545-550

2011

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The Wiskott–Aldrich syndrome

Clinical and experimental immunology, 2000-04, Vol.120 (1), p.2-9

2000

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Hypoxia-regulated transgene expression in experimental retinal and choroidal neovascularization

Gene therapy, 2003-06, Vol.10 (12), p.1049-1054

2003

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Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy

The New England journal of medicine, 2002-04, Vol.346 (16), p.1185-1193

2002

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Reconstitution of neutrophil NADPH oxidase activity in the cell-free system by four components: p67-phox, p47-phox, p21rac1, and cytochrome b-245

The Journal of biological chemistry, 1992-08, Vol.267 (24), p.16767-16770

1992

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Gene therapy progress and prospects: gene therapy for severe combined immunodeficiency

Gene therapy, 2003-11, Vol.10 (24), p.1999-2004

2003

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Gene Transfer into the Mouse Retina Mediated by an Adeno-Associated Viral Vector

Human molecular genetics, 1996-05, Vol.5 (5), p.591-594

1996

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Molecular Evidence of Genome Editing in a Mouse Model of Immunodeficiency

Scientific reports, 2018-05, Vol.8 (1), p.8214-13, Article 8214

2018

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Progress and Prospects: Gene Therapy Clinical Trials (Part 1)

Gene therapy, 2007-10, Vol.14 (20), p.1439-1447

2007

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T cell transduction and suicide with an enhanced mutant thymidine kinase

Gene therapy, 2002-06, Vol.9 (12), p.824-827

2002

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Configuration of human dendritic cell cytoskeleton by Rho GTPases, the WAS protein, and differentiation

Blood, 2001-08, Vol.98 (4), p.1142-1149

2001

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Kinetics of transgene expression in mouse retina following sub-retinal injection of recombinant adeno-associated virus

Vision research (Oxford), 2002-02, Vol.42 (4), p.541-549

2002

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T cell suicide gene therapy to aid haematopoietic stem cell transplantation

Current gene therapy, 2005-02, Vol.5 (1), p.121-132

2005

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Chorioretinal lesions in patients and carriers of chronic granulomatous disease

The Journal of pediatrics, 1999-06, Vol.134 (6), p.780-783

1999

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WASP and WIP regulate podosomes in migrating leukocytes

Journal of microscopy (Oxford), 2008-09, Vol.231 (3), p.494-505

2008

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Inhibition of retinal neovascularisation by gene transfer of soluble VEGF receptor sFlt-1

Gene therapy, 2002-03, Vol.9 (5), p.320-326

2002

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Permanent partial phenotypic correction and tolerance in a mouse model of hemophilia B by stem cell gene delivery of human factor IX

Wiskott-Aldrich syndrome protein is necessary for efficient IgG-mediated phagocytosis

Immunotherapy for neuroblastoma using syngeneic fibroblasts transfected with IL-2 and IL-12

Current progress on gene therapy for primary immunodeficiencies

Enhanced human cell engraftment in mice deficient in RAG2 and the common cytokine receptor γ chain

Cutting Edge: The Wiskott-Aldrich Syndrome Protein Is Required for Efficient Phagocytosis of Apoptotic Cells

Dendritic Cells: The Bare Bones of Immunity

Cell-specific and efficient expression in mouse and human B cells by a novel hybrid immunoglobulin promoter in a lentiviral vector

Stable rAAV-mediated transduction of rod and cone photoreceptors in the canine retina

Gene therapy for the Wiskott-Aldrich syndrome

The Wiskott–Aldrich syndrome

Hypoxia-regulated transgene expression in experimental retinal and choroidal neovascularization

Sustained Correction of X-Linked Severe Combined Immunodeficiency by ex Vivo Gene Therapy

Reconstitution of neutrophil NADPH oxidase activity in the cell-free system by four components: p67-phox, p47-phox, p21rac1, and cytochrome b-245

Gene therapy progress and prospects: gene therapy for severe combined immunodeficiency

Gene Transfer into the Mouse Retina Mediated by an Adeno-Associated Viral Vector

Molecular Evidence of Genome Editing in a Mouse Model of Immunodeficiency

Progress and Prospects: Gene Therapy Clinical Trials (Part 1)

T cell transduction and suicide with an enhanced mutant thymidine kinase

Configuration of human dendritic cell cytoskeleton by Rho GTPases, the WAS protein, and differentiation

Kinetics of transgene expression in mouse retina following sub-retinal injection of recombinant adeno-associated virus

T cell suicide gene therapy to aid haematopoietic stem cell transplantation

Chorioretinal lesions in patients and carriers of chronic granulomatous disease

WASP and WIP regulate podosomes in migrating leukocytes

Inhibition of retinal neovascularisation by gene transfer of soluble VEGF receptor sFlt-1

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