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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

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Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy

Nature genetics, 2000-07, Vol.25 (3), p.306-310

2000

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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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T cell suicide gene therapy to aid haematopoietic stem cell transplantation

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

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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Improvement of neuronal visual responses in the superior colliculus in Prph2(Rd2/Rd2) mice following gene therapy

Molecular and cellular neuroscience, 2004-01, Vol.25 (1), p.103-110

2004

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High-titer recombinant adeno-associated virus production from replicating amplicons and herpes vectors deleted for glycoprotein H

Human gene therapy, 1999-10, Vol.10 (15), p.2527-2537

1999

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A defined window for efficient gene marking of severe combined immunodeficient-repopulating cells using a gibbon ape leukemia virus-pseudotyped retroviral vector

Human gene therapy, 2000, Vol.11 (1), p.91-100

2000

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Gene therapy for primary immunodeficiencies

Human gene therapy, 2012-07, Vol.23 (7), p.668

2012

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Lipid-mediated enhancement of transfection by a nonviral integrin-targeting vector

Human gene therapy, 1998-03, Vol.9 (4), p.575-585

1998

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Gene transfer to primary chronic granulomatous disease monocytes

The Lancet (British edition), 1995-07, Vol.346 (8967), p.92-93

1995

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Normal development of human fetal hematopoiesis between eight and seventeen weeks’ gestation

American journal of obstetrics and gynecology, 2000-10, Vol.183 (4), p.1029-1034

2000

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Use of nonintegrating lentiviral vectors for gene therapy

Human gene therapy, 2007-06, Vol.18 (6), p.483

2007

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Adeno-associated virus gene transfer to mouse retina

Human gene therapy, 1998-01, Vol.9 (1), p.81-86

1998

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The Wiskott-Aldrich syndrome: disordered actin dynamics in haematopoietic cells

Immunological reviews, 2000-12, Vol.178 (1), p.118-128

2000

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Wasp in immune-system organization and function

Nature reviews. Immunology, 2002-09, Vol.2 (9), p.635-646

Thrasher, Adrian J

2002

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Gene therapy for Fanconi anemia: one step closer to the clinic

Human gene therapy, 2012-02, Vol.23 (2), p.141

2012

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Non-Clinical Efficacy and Safety Studies on G1XCGD, a Lentiviral Vector for Ex Vivo Gene Therapy of X-Linked Chronic Granulomatous Disease

Human gene therapy. Clinical development, 2018-06, Vol.29 (2), p.69

2018

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Progress and prospects: advancements in retroviral vector design, generation, and application

Human gene therapy, 2011-10, Vol.22 (10), p.1171

2011

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Adeno-associated and Herpes Simplex Viruses as Vectors for Gene Transfer to the Corneal Endothelium

Cornea, 2000-05, Vol.19 (3), p.369-373

2000

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Lentiviral gene therapy against human immunodeficiency virus type 1, using a novel human TRIM21-cyclophilin A restriction factor

Human gene therapy, 2012-11, Vol.23 (11), p.1176

2012

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Gene therapy for primary immunodeficiency

Biochemical Society transactions, 1997-05, Vol.25 (2), p.537

1997

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Effective gene therapy with nonintegrating lentiviral vectors

Nature medicine, 2006-03, Vol.12 (3), p.348-353

2006

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Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

The Lancet (British edition), 2004-12, Vol.364 (9452), p.2181-2187

2004

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

Restoration of photoreceptor ultrastructure and function in retinal degeneration slow mice by gene therapy

Gene therapy for the Wiskott–Aldrich syndrome

T cell suicide gene therapy to aid haematopoietic stem cell transplantation

Chorioretinal lesions in patients and carriers of chronic granulomatous disease

Improvement of neuronal visual responses in the superior colliculus in Prph2(Rd2/Rd2) mice following gene therapy

High-titer recombinant adeno-associated virus production from replicating amplicons and herpes vectors deleted for glycoprotein H

A defined window for efficient gene marking of severe combined immunodeficient-repopulating cells using a gibbon ape leukemia virus-pseudotyped retroviral vector

Gene therapy for primary immunodeficiencies

Lipid-mediated enhancement of transfection by a nonviral integrin-targeting vector

Gene transfer to primary chronic granulomatous disease monocytes

Normal development of human fetal hematopoiesis between eight and seventeen weeks’ gestation

Use of nonintegrating lentiviral vectors for gene therapy

Adeno-associated virus gene transfer to mouse retina

The Wiskott-Aldrich syndrome: disordered actin dynamics in haematopoietic cells

Wasp in immune-system organization and function

Gene therapy for Fanconi anemia: one step closer to the clinic

Non-Clinical Efficacy and Safety Studies on G1XCGD, a Lentiviral Vector for Ex Vivo Gene Therapy of X-Linked Chronic Granulomatous Disease

Progress and prospects: advancements in retroviral vector design, generation, and application

Adeno-associated and Herpes Simplex Viruses as Vectors for Gene Transfer to the Corneal Endothelium

Lentiviral gene therapy against human immunodeficiency virus type 1, using a novel human TRIM21-cyclophilin A restriction factor

Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1 , PRDM16 or SETBP1

Gene therapy for primary immunodeficiency

Effective gene therapy with nonintegrating lentiviral vectors

Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

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