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Quantitative proteome analysis of LAP1-deficient human fibroblasts: A pilot approach for predicting the signaling pathways deregulated in LAP1-associated diseases.
Pereira CD, Espadas G, Martins F, Bertrand AT, Servais L, Sabidó E, Chevalier P, da Cruz E Silva OAB, Rebelo S. Pereira CD, et al. Among authors: bertrand at. Biochem Biophys Rep. 2024 Jun 26;39:101757. doi: 10.1016/j.bbrep.2024.101757. eCollection 2024 Sep. Biochem Biophys Rep. 2024. PMID: 39035020 Free PMC article.
Recent insights in striated muscle laminopathies.
Leconte M, Bonne G, Bertrand AT. Leconte M, et al. Among authors: bertrand at. Curr Opin Neurol. 2024 Oct 1;37(5):509-514. doi: 10.1097/WCO.0000000000001297. Epub 2024 Jul 11. Curr Opin Neurol. 2024. PMID: 38989655 Review.
Preclinical Advances of Therapies for Laminopathies.
Benarroch L, Cohen E, Atalaia A, Ben Yaou R, Bonne G, Bertrand AT. Benarroch L, et al. Among authors: bertrand at. J Clin Med. 2021 Oct 21;10(21):4834. doi: 10.3390/jcm10214834. J Clin Med. 2021. PMID: 34768351 Free PMC article. Review.
Consequences of Lmna Exon 4 Mutations in Myoblast Function.
Gómez-Domínguez D, Epifano C, Miguel F, Castaño AG, Vilaplana-Martí B, Martín A, Amarilla-Quintana S, Bertrand AT, Bonne G, Ramón-Azcón J, Rodríguez-Milla MA, Pérez de Castro I. Gómez-Domínguez D, et al. Among authors: bertrand at. Cells. 2020 May 21;9(5):1286. doi: 10.3390/cells9051286. Cells. 2020. PMID: 32455813 Free PMC article.
A Muscle Hybrid Promoter as a Novel Tool for Gene Therapy.
Piekarowicz K, Bertrand AT, Azibani F, Beuvin M, Julien L, Machowska M, Bonne G, Rzepecki R. Piekarowicz K, et al. Among authors: bertrand at. Mol Ther Methods Clin Dev. 2019 Sep 12;15:157-169. doi: 10.1016/j.omtm.2019.09.001. eCollection 2019 Dec 13. Mol Ther Methods Clin Dev. 2019. PMID: 31660418 Free PMC article.
The Pathogenesis and Therapies of Striated Muscle Laminopathies.
Brull A, Morales Rodriguez B, Bonne G, Muchir A, Bertrand AT. Brull A, et al. Among authors: bertrand at. Front Physiol. 2018 Oct 30;9:1533. doi: 10.3389/fphys.2018.01533. eCollection 2018. Front Physiol. 2018. PMID: 30425656 Free PMC article. Review.
Gene Therapy via Trans-Splicing for LMNA-Related Congenital Muscular Dystrophy.
Azibani F, Brull A, Arandel L, Beuvin M, Nelson I, Jollet A, Ziat E, Prudhon B, Benkhelifa-Ziyyat S, Bitoun M, Lorain S, Bonne G, Bertrand AT. Azibani F, et al. Among authors: bertrand at. Mol Ther Nucleic Acids. 2018 Mar 2;10:376-386. doi: 10.1016/j.omtn.2017.12.012. Epub 2017 Dec 30. Mol Ther Nucleic Acids. 2018. PMID: 29499949 Free PMC article.
31 results