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Translational Mini‐Review Series on Immunodeficiency: Molecular defects in common variable immunodeficiency

Clinical and experimental immunology, 2007-09, Vol.149 (3), p.401-409

2007

Volltextzugriff (PDF)

Validation of a mutated PRE sequence allowing high and sustained transgene expression while abrogating WHV-X protein synthesis: application to the gene therapy of WAS

Gene therapy, 2009-05, Vol.16 (5), p.605-619

2009

Volltextzugriff (PDF)

Lentiviral vectors targeting WASp expression to hematopoietic cells, efficiently transduce and correct cells from WAS patients

Gene therapy, 2007-03, Vol.14 (5), p.415-428

2007

Volltextzugriff (PDF)

Scale-up and manufacturing of clinical-grade self-inactivating γ-retroviral vectors by transient transfection

Gene therapy, 2012-03, Vol.19 (3), p.246-254

2012

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Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors

Gene therapy, 2009-04, Vol.16 (4), p.509-520

2009

Volltextzugriff (PDF)

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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Long-term preservation of retinal function in the RCS rat model of retinitis pigmentosa following lentivirus-mediated gene therapy

Gene therapy, 2005-04, Vol.12 (8), p.694-701

2005

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Neonatal dendritic cells are intrinsically biased against Th‐1 immune responses

Clinical and experimental immunology, 2002-04, Vol.128 (1), p.118-123

2002

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Critical Variables affecting clinical-grade production of the self-inactivating gamma-retroviral vector for the treatment of X-linked severe combined immunodeficiency

Gene therapy, 2012-08, Vol.19 (8), p.872-876

2012

Volltextzugriff (PDF)

Chronic granulomatous disease

Clinical and experimental immunology, 2000-10, Vol.122 (1), p.1-9

2000

Volltextzugriff (PDF)

Lentiviral transduction of the murine lung provides efficient pseudotype and developmental stage-dependent cell-specific transgene expression

Gene therapy, 2008-08, Vol.15 (16), p.1167-1175

2008

Volltextzugriff (PDF)

Genetic Variants Associated With Neutrophil Function in Aggressive Periodontitis and Healthy Controls

Journal of periodontology (1970), 2010-04, Vol.81 (4), p.527-534

2010

Volltextzugriff (PDF)

In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium

Gene therapy, 2001-11, Vol.8 (21), p.1665-1668

2001

Volltextzugriff (PDF)

Lentiviral vectors transcriptionally targeted to hematopoietic cells by WASP gene proximal promoter sequences

Gene therapy, 2005-04, Vol.12 (8), p.715-723

2005

Volltextzugriff (PDF)

Correction of SCID-X1 using an enhancerless Vav promoter

Human gene therapy, 2011-03, Vol.22 (3), p.263

2011

Volltextzugriff (PDF)

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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The Wiskott-Aldrich syndrome

Journal of Allergy and Clinical Immunology, 2006-04, Vol.117 (4), p.725-738

2006

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Current progress on gene therapy for primary immunodeficiencies

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

2013

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Dendritic Cells: The Bare Bones of Immunity

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

2004

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

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

2003

Volltextzugriff (PDF)

Gene therapy for the Wiskott–Aldrich syndrome

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

2011

Volltextzugriff (PDF)

The Wiskott–Aldrich syndrome

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

2000

Volltextzugriff (PDF)

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Translational Mini‐Review Series on Immunodeficiency: Molecular defects in common variable immunodeficiency

Validation of a mutated PRE sequence allowing high and sustained transgene expression while abrogating WHV-X protein synthesis: application to the gene therapy of WAS

Lentiviral vectors targeting WASp expression to hematopoietic cells, efficiently transduce and correct cells from WAS patients

Scale-up and manufacturing of clinical-grade self-inactivating γ-retroviral vectors by transient transfection

Efficient gene delivery to the adult and fetal CNS using pseudotyped non-integrating lentiviral vectors

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

Long-term preservation of retinal function in the RCS rat model of retinitis pigmentosa following lentivirus-mediated gene therapy

Neonatal dendritic cells are intrinsically biased against Th‐1 immune responses

Critical Variables affecting clinical-grade production of the self-inactivating gamma-retroviral vector for the treatment of X-linked severe combined immunodeficiency

Chronic granulomatous disease

Lentiviral transduction of the murine lung provides efficient pseudotype and developmental stage-dependent cell-specific transgene expression

Genetic Variants Associated With Neutrophil Function in Aggressive Periodontitis and Healthy Controls

In vivo gene transfer to the mouse eye using an HIV-based lentiviral vector; efficient long-term transduction of corneal endothelium and retinal pigment epithelium

Lentiviral vectors transcriptionally targeted to hematopoietic cells by WASP gene proximal promoter sequences

Correction of SCID-X1 using an enhancerless Vav promoter

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

The Wiskott-Aldrich syndrome

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

Current progress on gene therapy for primary immunodeficiencies

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

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