Cell-specific and efficient expression in mouse and human B cells by a novel hybrid immunoglobulin promoter in a lentiviral vector-Reference-Cited by-同舟云学术

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Cell-specific and efficient expression in mouse and human B cells by a novel hybrid immunoglobulin promoter in a lentiviral vector

Published:2007-09-13 Issue:23 Volume:14 Page:1623-1631
ISSN:0969-7128
Container-title:Gene Therapy
language:en
Short-container-title:Gene Ther

Author:

Laurie K L,Blundell M P,Baxendale H E,Howe S J,Sinclair J,Qasim W,Brunsberg U,Thrasher A J,Holmdahl R,Gustafsson K

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Molecular Medicine

Link

http://www.nature.com/articles/3303021.pdf

Reference37 articles.

1. Cunningham-Rundles C, Ponda PP . Molecular defects in T- and B-cell primary immunodeficiency diseases. Nat Rev Immunol 2005; 5: 880–892.

2. Gaspar HB, Howe S, Thrasher AJ . Gene therapy progress and prospects: gene therapy for severe combined immunodeficiency. Gene Therapy 2003; 10: 1999–2004.

3. Larsen SR, Rasko JE . Lymphoproliferative disorders: prospects for gene therapy. Pathology 2005; 37: 523–533.

4. Melo ME, El Amine M, Tonnetti L, Fleischman L, Scott DW . Gene therapeutic approaches to induction and maintenance of tolerance. Int Rev Immunol 2001; 20: 627–645.

5. Wong W, Wood KJ . Transplantation tolerance by donor MHC gene transfer. Curr Gene Ther 2004; 4: 329–336.

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