American society of gene therapy (ASGT) ad hoc subcommittee on retroviral-mediated gene transfer to hematopoietic stem cells-Reference-Cited by-同舟云学术

American society of gene therapy (ASGT) ad hoc subcommittee on retroviral-mediated gene transfer to hematopoietic stem cells

Published:2003-08 Issue:2 Volume:8 Page:180-187
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Kohn Donald B,Sadelain Michel,Dunbar Cynthia,Bodine David,Kiem Hans-Peter,Candotti Fabio,Tisdale John,Riviére Isabelle,Blau C.Anthony,Richard Robert E,Sorrentino Brian,Nolta Jan,Malech Harry,Brenner Malcolm,Cornetta Kenneth,Cavagnaro Joy,High Katherine,Glorioso Joseph

Publisher

Elsevier BV

Subject

Drug Discovery,Pharmacology,Genetics,Molecular Biology,Molecular Medicine

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3. Gene therapy of human severe combined immunodeficiency (SCID)-X1 disease;Cavazzana-Calvo;Science,2000

4. Sustained correction of X-linked severe combined immunodeficiency by ex vivo gene therapy;Hacein-Bey-Abina;N. Engl. J. Med.,2002

5. Correction of ADA-SCID by stem cell gene therapy combined with nonmyeloablative conditioning;Aiuti;Science,2002

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