Characteristics of Lentiviral Vectors Harboring the Proximal Promoter of the vav Proto-oncogene: A Weak and Efficient Promoter for Gene Therapy-Reference-Cited by-同舟云学术

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Characteristics of Lentiviral Vectors Harboring the Proximal Promoter of the vav Proto-oncogene: A Weak and Efficient Promoter for Gene Therapy

Published:2007-08 Issue:8 Volume:15 Page:1487-1494
ISSN:1525-0016
Container-title:Molecular Therapy
language:en
Short-container-title:Molecular Therapy

Author:

Almarza Elena,Río Paula,Meza Nestor W,Aldea Montserrat,Agirre Xabier,Guenechea Guillermo,Segovia José C,Bueren Juan A

Publisher

Elsevier BV

Subject

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

Reference38 articles.

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

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

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

4. Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI 1, PRDM16 or SETBP1;Ott;Nat Med,2006

5. Murine leukemia induced by retroviral gene marking;Li;Science,2002

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1. Non‐industrial production of therapeutic lentiviral vectors: How to provide vectors to academic CAR‐T;Biotechnology and Bioengineering;2024-07-04

2. New transgenic mouse models enabling pan-hematopoietic or selective hematopoietic stem cell depletion in vivo;Scientific Reports;2022-02-24

3. TALEN mediated gene editing in a mouse model of Fanconi anemia;Scientific Reports;2020-04-24

4. Therapeutic gene editing in hematopoietic progenitor cells from a mouse model of Fanconi anemia;2018-07-05

5. A reproducible method for the isolation and expansion of ovine mesenchymal stromal cells from bone marrow for use in regenerative medicine preclinical studies;Journal of Tissue Engineering and Regenerative Medicine;2016-11-18

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