Modeling Human Severe Combined Immunodeficiency and Correction by CRISPR/Cas9-Enhanced Gene Targeting-Reference-Cited by-同舟云学术

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Modeling Human Severe Combined Immunodeficiency and Correction by CRISPR/Cas9-Enhanced Gene Targeting

Published:2015-09 Issue:10 Volume:12 Page:1668-1677
ISSN:2211-1247
Container-title:Cell Reports
language:en
Short-container-title:Cell Reports

Author:

Chang Chia-Wei,Lai Yi-Shin,Westin Erik,Khodadadi-Jamayran Alireza,Pawlik Kevin M.,Lamb Lawrence S.,Goldman Frederick D.,Townes Tim M.

Publisher

Elsevier BV

Subject

General Biochemistry, Genetics and Molecular Biology

Reference56 articles.

1. Gene therapy for immunodeficiency due to adenosine deaminase deficiency;Aiuti;N. Engl. J. Med.,2009

2. Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy;Biffi;Science,2013

3. Polycistronic lentiviral vector for “hit and run” reprogramming of adult skin fibroblasts to induced pluripotent stem cells;Chang;Stem Cells,2009

4. Broad T-cell receptor repertoire in T-lymphocytes derived from human induced pluripotent stem cells;Chang;PLoS ONE,2014

5. Multiplex genome engineering using CRISPR/Cas systems;Cong;Science,2013

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2. Advances in applications of the CRISPR/Cas9 system for respiratory diseases;Progress in Molecular Biology and Translational Science;2024

3. Exosomes for CRISPR-Cas9 Delivery: The Cutting Edge in Genome Editing;Molecular Biotechnology;2023-11-27

4. CRISPR-Cas9 engineering of the RAG2 locus via complete coding sequence replacement for therapeutic applications;Nature Communications;2023-10-27

5. Recent Advances in CRISPR/Cas9 Delivery Approaches for Therapeutic Gene Editing of Stem Cells;Stem Cell Reviews and Reports;2023-09-18

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