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Immortalized human myotonic dystrophy type 1 muscle cell lines to address patient heterogeneity.
Núñez-Manchón J, Capó J, Martínez-Piñeiro A, Juanola E, Pesovic J, Mosqueira-Martín L, González-Imaz K, Maestre-Mora P, Odria R, Cerro-Herreros E, Naldaiz-Gastesi N, López de Munain A, Artero R, Savic-Pavicevic D, Vallejo-Illarramendi A, Mamchaoui K, Bigot A, Mouly V, Suelves M, Nogales-Gadea G. Núñez-Manchón J, et al. Among authors: mamchaoui k. iScience. 2024 May 7;27(6):109930. doi: 10.1016/j.isci.2024.109930. eCollection 2024 Jun 21. iScience. 2024. PMID: 38832025 Free PMC article.
Cellular senescence in human myoblasts is overcome by human telomerase reverse transcriptase and cyclin-dependent kinase 4: consequences in aging muscle and therapeutic strategies for muscular dystrophies.
Zhu CH, Mouly V, Cooper RN, Mamchaoui K, Bigot A, Shay JW, Di Santo JP, Butler-Browne GS, Wright WE. Zhu CH, et al. Among authors: mamchaoui k. Aging Cell. 2007 Aug;6(4):515-23. doi: 10.1111/j.1474-9726.2007.00306.x. Epub 2007 Jun 8. Aging Cell. 2007. PMID: 17559502 Free article.
Immortalized skin fibroblasts expressing conditional MyoD as a renewable and reliable source of converted human muscle cells to assess therapeutic strategies for muscular dystrophies: validation of an exon-skipping approach to restore dystrophin in Duchenne muscular dystrophy cells.
Chaouch S, Mouly V, Goyenvalle A, Vulin A, Mamchaoui K, Negroni E, Di Santo J, Butler-Browne G, Torrente Y, Garcia L, Furling D. Chaouch S, et al. Among authors: mamchaoui k. Hum Gene Ther. 2009 Jul;20(7):784-90. doi: 10.1089/hum.2008.163. Hum Gene Ther. 2009. PMID: 19358679
93 results