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Page 1
Laminopathies disrupt epigenomic developmental programs and cell fate.
Perovanovic J, Dell'Orso S, Gnochi VF, Jaiswal JK, Sartorelli V, Vigouroux C, Mamchaoui K, Mouly V, Bonne G, Hoffman EP. Perovanovic J, et al. Among authors: mamchaoui k. Sci Transl Med. 2016 Apr 20;8(335):335ra58. doi: 10.1126/scitranslmed.aad4991. Sci Transl Med. 2016. PMID: 27099177 Free PMC article.
The mitotic clock in skeletal muscle regeneration, disease and cell mediated gene therapy.
Mouly V, Aamiri A, Bigot A, Cooper RN, Di Donna S, Furling D, Gidaro T, Jacquemin V, Mamchaoui K, Negroni E, Périé S, Renault V, Silva-Barbosa SD, Butler-Browne GS. Mouly V, et al. Among authors: mamchaoui k. Acta Physiol Scand. 2005 May;184(1):3-15. doi: 10.1111/j.1365-201X.2005.01417.x. Acta Physiol Scand. 2005. PMID: 15847639 Review.
Myoblast transfer therapy: is there any light at the end of the tunnel?
Mouly V, Aamiri A, Périé S, Mamchaoui K, Barani A, Bigot A, Bouazza B, François V, Furling D, Jacquemin V, Negroni E, Riederer I, Vignaud A, St Guily JL, Butler-Browne GS. Mouly V, et al. Among authors: mamchaoui k. Acta Myol. 2005 Oct;24(2):128-33. Acta Myol. 2005. PMID: 16550930 Review.
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
Type B mandibuloacral dysplasia with congenital myopathy due to homozygous ZMPSTE24 missense mutation.
Ben Yaou R, Navarro C, Quijano-Roy S, Bertrand AT, Massart C, De Sandre-Giovannoli A, Cadiñanos J, Mamchaoui K, Butler-Browne G, Estournet B, Richard P, Barois A, Lévy N, Bonne G. Ben Yaou R, et al. Among authors: mamchaoui k. Eur J Hum Genet. 2011 Jun;19(6):647-54. doi: 10.1038/ejhg.2010.256. Epub 2011 Jan 26. Eur J Hum Genet. 2011. PMID: 21267004 Free PMC article.
Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders.
Mamchaoui K, Trollet C, Bigot A, Negroni E, Chaouch S, Wolff A, Kandalla PK, Marie S, Di Santo J, St Guily JL, Muntoni F, Kim J, Philippi S, Spuler S, Levy N, Blumen SC, Voit T, Wright WE, Aamiri A, Butler-Browne G, Mouly V. Mamchaoui K, et al. Skelet Muscle. 2011 Nov 1;1:34. doi: 10.1186/2044-5040-1-34. Skelet Muscle. 2011. PMID: 22040608 Free PMC article.
90 results