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Prion potentiation after life-long dormancy in mice devoid of PrP.
Brain Commun. 2021 Apr 28;3(2):fcab092. doi: 10.1093/braincomms/fcab092. eCollection 2021.
Brain Commun. 2021.
PMID: 33997785
Free PMC article.
Basal exon skipping and nonsense-associated altered splicing allows bypassing complete CEP290 loss-of-function in individuals with unusually mild retinal disease.
Barny I, Perrault I, Michel C, Soussan M, Goudin N, Rio M, Thomas S, Attié-Bitach T, Hamel C, Dollfus H, Kaplan J, Rozet JM, Gerard X.
Barny I, et al. Among authors: michel c.
Hum Mol Genet. 2018 Aug 1;27(15):2689-2702. doi: 10.1093/hmg/ddy179.
Hum Mol Genet. 2018.
PMID: 29771326
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AON-Mediated Exon Skipping to Bypass Protein Truncation in Retinal Dystrophies Due to the Recurrent CEP290 c.4723A > T Mutation. Fact or Fiction?
Barny I, Perrault I, Michel C, Goudin N, Defoort-Dhellemmes S, Ghazi I, Kaplan J, Rozet JM, Gerard X.
Barny I, et al. Among authors: michel c.
Genes (Basel). 2019 May 14;10(5):368. doi: 10.3390/genes10050368.
Genes (Basel). 2019.
PMID: 31091803
Free PMC article.
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