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Alexander Astrakhan

University of Washington

6

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244

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Ubiquitous high-level gene expression in hematopoietic lineages provides effective lentiviral gene therapy of murine Wiskott-Aldrich syndrome

2012 Blood
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Development of B-lineage Predominant Lentiviral Vectors for Use in Genetic Therapies for B Cell Disorders

2011 Molecular Therapy
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B cell–specific lentiviral gene therapy leads to sustained B-cell functional recovery in a murine model of X-linked agammaglobulinemia

2010 Blood
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Local increase in thymic stromal lymphopoietin induces systemic alterations in B cell development

2007 Nature Immunology
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341. Lentiviral Vector-Mediated Gene Therapy as Treatment for Wiskott-Aldrich Syndrome (WAS): Pre-Clinical Studies in Human Cell Lines and WASp -/- Mice

2005 Molecular Therapy
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