Gene Therapy of Storage Disorders by Retroviral and Lentiviral Vectors
Author:
Affiliation:
1. San Raffaele Telethon Institute for Gene Therapy and Vita Salute University, H. San Raffaele Scientific Institute, Milan 20132, Italy.
Publisher
Mary Ann Liebert Inc
Subject
Genetics,Molecular Biology,Molecular Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/hum.2005.16.1133
Reference101 articles.
1. Molecular Evidence of Lentiviral Vector-Mediated Gene Transfer into Human Self-Renewing, Multi-potent, Long-Term NOD/SCID Repopulating Hematopoietic Cells
2. Correction of ADA-SCID by Stem Cell Gene Therapy Combined with Nonmyeloablative Conditioning
3. Immune reconstitution in ADA-SCID after PBL gene therapy and discontinuation of enzyme replacement
4. Immune reconstitution without graft-versus-host disease after haemopoietic stem-cell transplantation: a phase 1/2 study
5. Human CD34+ cells differentiate into microglia and express recombinant therapeutic protein
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