Intrathymic delivery a new route for adenoviral-associated vector gene therapy
Author:
Publisher
Elsevier BV
Subject
Immunology,Immunology and Allergy
Reference10 articles.
1. Treating Immunodeficiency through HSC gene therapy;Booth;Trends Mol Med,2016
2. Gene therapy for immunodeficiency due to adenosine deaminase deficiency;Aiuti;N Engl J Med,2009
3. Lentiviral haemopoietic stem/progenitor cell gene therapy for treatment of Wiskott-Aldrich syndrome: interim results of a non-randomised, open-label, phase 1/2 clinical study;Ferrua;Lancet Haematol,2019
4. Lentiviral gene therapy combined with low-dose busulfan in infants with SCID-X1;Mamcarz;N Engl J Med,2019
5. Intrathymic administration of hematopoietic progenitor cells enhances T cell reconstitution in ZAP-70 severe combined immunodeficiency;Adjali;Proc Natl Acad Sci U S A,2005
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