Characterization of the Human Artemis Promoter by Heterologous Gene Expression In Vitro and In Vivo-Reference-Cited by-同舟云学术

Characterization of the Human Artemis Promoter by Heterologous Gene Expression In Vitro and In Vivo

Published:2011-10 Issue:10 Volume:30 Page:751-761
ISSN:1044-5498
Container-title:DNA and Cell Biology
language:en
Short-container-title:DNA and Cell Biology

Author:

Multhaup Megan M.¹,Gurram Sweta¹,Podetz-Pedersen Kelly M.¹,Karlen Andrea D.¹,Swanson Debra L.¹,Somia Nikunj V.¹,Hackett Perry B.¹,Cowan Morton J.²,McIvor R. Scott¹

Affiliation:

1. Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota.

2. Department of Pediatrics, University of California, San Francisco, California.

Publisher

Mary Ann Liebert Inc

Subject

Cell Biology,Genetics,Molecular Biology,General Medicine

Link

http://www.liebertpub.com/doi/pdf/10.1089/dna.2011.1244

Reference29 articles.

1. Construction and Use of Retroviral Vectors Encoding the Toxic Gene Barnase

2. Gene Therapy for Immunodeficiency Due to Adenosine Deaminase Deficiency

3. The Cellular Amount of the Common γ-Chain Influences Spontaneous or Induced Cell Proliferation

4. Stable and Functional Lymphoid Reconstitution in Artemis-deficient Mice Following Lentiviral Artemis Gene Transfer Into Hematopoietic Stem Cells

5. ARTEMIS Nuclease Facilitates Apoptotic Chromatin Cleavage

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1. Lentiviral Gene Therapy for Artemis-Deficient SCID;New England Journal of Medicine;2022-12-22

2. Determining T and B Cell development by TREC/KREC analysis in primary immunodeficiency patients and healthy controls;Scandinavian Journal of Immunology;2022-01-03

3. Biosafety Studies of a Clinically Applicable Lentiviral Vector for the Gene Therapy of Artemis-SCID;Molecular Therapy - Methods & Clinical Development;2019-12

4. Lentivirus Mediated Correction of Artemis-Deficient Severe Combined Immunodeficiency;Human Gene Therapy;2017-01

5. Role of Transgene Regulation in Ex Vivo Lentiviral Correction of Artemis Deficiency;Human Gene Therapy;2015-04