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Gene and Cell Therapy for Muscular Dystrophies: Are We Getting There?
Galli F, Bragg L, Meggiolaro L, Rossi M, Caffarini M, Naz N, Santoleri S, Cossu G. Galli F, et al. Among authors: cossu g. Hum Gene Ther. 2018 Oct;29(10):1098-1105. doi: 10.1089/hum.2018.151. Hum Gene Ther. 2018. PMID: 30132372 Free PMC article. Review.
Reversible immortalisation enables genetic correction of human muscle progenitors and engineering of next-generation human artificial chromosomes for Duchenne muscular dystrophy.
Benedetti S, Uno N, Hoshiya H, Ragazzi M, Ferrari G, Kazuki Y, Moyle LA, Tonlorenzi R, Lombardo A, Chaouch S, Mouly V, Moore M, Popplewell L, Kazuki K, Katoh M, Naldini L, Dickson G, Messina G, Oshimura M, Cossu G, Tedesco FS. Benedetti S, et al. Among authors: cossu g. EMBO Mol Med. 2018 Feb;10(2):254-275. doi: 10.15252/emmm.201607284. EMBO Mol Med. 2018. PMID: 29242210 Free PMC article.
632 results