Efficient Gene Reframing Therapy for Recessive Dystrophic Epidermolysis Bullosa with CRISPR/Cas9
Author:
Funder
Japan Society for the Promotion of Science through a Grant-in-Aid for Young Scientists
Publisher
Elsevier BV
Subject
Cell Biology,Dermatology,Molecular Biology,Biochemistry
Reference51 articles.
1. Microhomology-based choice of Cas9 nuclease target sites;Bae;Nat Methods,2014
2. Easy quantitative assessment of genome editing by sequence trace decomposition;Brinkman;Nucleic Acids Res,2014
3. Gene editing for the efficient correction of a recurrent COL7A1 mutation in recessive dystrophic epidermolysis bullosa keratinocytes;Chamorro;Mol Ther Nucleic Acids,2016
4. Ultraviolet A irradiation upregulates type VII collagen expression in human dermal fibroblasts;Chen;J Invest Dermatol,1997
5. Type VII collagen: the anchoring fibril protein at fault in dystrophic epidermolysis bullosa;Chung;Dermatol Clin,2010
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1. Highly efficient CRISPR/Cas9‐mediated exon skipping for recessive dystrophic epidermolysis bullosa;Bioengineering & Translational Medicine;2024-01-17
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3. New advancements in CRISPR based gene therapy of Duchenne muscular dystrophy;Gene;2023-05
4. Cytosine Deaminase Base Editing to Restore COL7A1 in Dystrophic Epidermolysis Bullosa Human: Murine Skin Model;JID Innovations;2023-05
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