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Variable phenotypes of knockin mice carrying the M712T Gne mutation.
Sela I, Yakovlev L, Becker Cohen M, Elbaz M, Yanay N, Ben Shlomo U, Yotvat H, Fellig Y, Argov Z, Mitrani-Rosenbaum S. Sela I, et al. Among authors: becker cohen m. Neuromolecular Med. 2013 Mar;15(1):180-91. doi: 10.1007/s12017-012-8209-7. Epub 2012 Dec 13. Neuromolecular Med. 2013. PMID: 23238814
Mitochondrial processes are impaired in hereditary inclusion body myopathy.
Eisenberg I, Novershtern N, Itzhaki Z, Becker-Cohen M, Sadeh M, Willems PH, Friedman N, Koopman WJ, Mitrani-Rosenbaum S. Eisenberg I, et al. Among authors: becker cohen m. Hum Mol Genet. 2008 Dec 1;17(23):3663-74. doi: 10.1093/hmg/ddn261. Epub 2008 Aug 23. Hum Mol Genet. 2008. PMID: 18723858
GNE is involved in the early development of skeletal and cardiac muscle.
Milman Krentsis I, Sela I, Eiges R, Blanchard V, Berger M, Becker Cohen M, Mitrani-Rosenbaum S. Milman Krentsis I, et al. Among authors: becker cohen m. PLoS One. 2011;6(6):e21389. doi: 10.1371/journal.pone.0021389. Epub 2011 Jun 24. PLoS One. 2011. PMID: 21731727 Free PMC article.
Variable myopathic presentation in a single family with novel skeletal RYR1 mutation.
Attali R, Aharoni S, Treves S, Rokach O, Becker Cohen M, Fellig Y, Straussberg R, Dor T, Daana M, Mitrani-Rosenbaum S, Nevo Y. Attali R, et al. Among authors: becker cohen m. PLoS One. 2013 Jul 24;8(7):e69296. doi: 10.1371/journal.pone.0069296. Print 2013. PLoS One. 2013. PMID: 23894444 Free PMC article.
Survival-apoptosis associated signaling in GNE myopathy-cultured myoblasts.
Harazi A, Chaouat M, Shlomai Z, Levitzki R, Becker-Cohen M, Sadeh M, Dabby R, Ben-Bassat H, Mitrani-Rosenbaum S. Harazi A, et al. Among authors: becker cohen m. J Recept Signal Transduct Res. 2015;35(4):249-57. doi: 10.3109/10799893.2014.956755. Epub 2014 Dec 16. J Recept Signal Transduct Res. 2015. PMID: 25510413
34 results