Suppression of Clonal Dominance in Cultured Human Lymphoid Cells by Addition of the cHS4 Insulator to a Lentiviral Vector-Reference-Cited by-同舟云学术

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Suppression of Clonal Dominance in Cultured Human Lymphoid Cells by Addition of the cHS4 Insulator to a Lentiviral Vector

Published:2007-04 Issue:4 Volume:15 Page:801-809
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Evans-Galea Marguerite V,Wielgosz Matthew M,Hanawa Hideki,Srivastava Deo Kumar,Nienhuis Arthur W

Publisher

Elsevier BV

Subject

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

Reference43 articles.

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

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

3. Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gamma-retroviral vector;Gaspar;Lancet,2004

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

5. Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1;Ott;Nat Med,2006

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2. Sustained transgene expression from sleeping beauty DNA transposons containing a core fragment of the HNRPA2B1-CBX3 ubiquitous chromatin opening element (UCOE);BMC Biotechnology;2019-11-09

3. Efficacy and safety of a clinically relevant foamy vector design in human hematopoietic repopulating cells;The Journal of Gene Medicine;2018-07

4. Viral Vectors: The Road to Reducing Genotoxicity;Toxicological Sciences;2016-11-01

5. Emerging cellular and gene therapies for congenital anemias;American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2016-10-28

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