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List of shared articles
Times cited
CRISPR Therapeutics for Duchenne Muscular Dystrophy.
Esra Erkut, Toshifumi Yokota. Int J Mol Sci 2022
Esra Erkut, Toshifumi Yokota. Int J Mol Sci 2022
CRISPR-Cas9 Gene Therapy for Duchenne Muscular Dystrophy.
Cedric Happi Mbakam, Gabriel Lamothe, Guillaume Tremblay, Jacques P Tremblay. Neurotherapeutics 2022
Cedric Happi Mbakam, Gabriel Lamothe, Guillaume Tremblay, Jacques P Tremblay. Neurotherapeutics 2022
Restoration of dystrophin expression and correction of Duchenne muscular dystrophy by genome editing.
Tejal Aslesh, Esra Erkut, Toshifumi Yokota. Expert Opin Biol Ther 2021
Tejal Aslesh, Esra Erkut, Toshifumi Yokota. Expert Opin Biol Ther 2021
Molecular correction of Duchenne muscular dystrophy by splice modulation and gene editing.
Britt Hanson, Matthew J A Wood, Thomas C Roberts. RNA Biol 2021
Britt Hanson, Matthew J A Wood, Thomas C Roberts. RNA Biol 2021
Therapeutic Approaches for Duchenne Muscular Dystrophy: Old and New.
Samuel J Mackenzie, Stefan Nicolau, Anne M Connolly, Jerry R Mendell. Semin Pediatr Neurol 2021
Samuel J Mackenzie, Stefan Nicolau, Anne M Connolly, Jerry R Mendell. Semin Pediatr Neurol 2021
Supramolecular Nanosubstrate-Mediated Delivery for CRISPR/Cas9 Gene Disruption and Deletion.
Qian Ban, Peng Yang, Shih-Jie Chou, Li Qiao, Haidong Xia, Jingjing Xue, Fang Wang, Xiaobin Xu, Na Sun, Ryan Y Zhang,[...]. Small 2021
Qian Ban, Peng Yang, Shih-Jie Chou, Li Qiao, Haidong Xia, Jingjing Xue, Fang Wang, Xiaobin Xu, Na Sun, Ryan Y Zhang,[...]. Small 2021
Gene editing and modulation for Duchenne muscular dystrophy.
Anthony A Stephenson, Kevin M Flanigan. Prog Mol Biol Transl Sci 2021
Anthony A Stephenson, Kevin M Flanigan. Prog Mol Biol Transl Sci 2021