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Two distinct skeletal muscle microRNA signatures revealing the complex mechanism of sporadic ALS.
Acta Neurol Belg. 2022 Dec;122(6):1499-1509. doi: 10.1007/s13760-021-01743-w. Epub 2021 Jul 9.
Acta Neurol Belg. 2022.
PMID: 34241798
The Common miRNA Signatures Associated with Mitochondrial Dysfunction in Different Muscular Dystrophies.
Aksu-Menges E, Akkaya-Ulum YZ, Dayangac-Erden D, Balci-Peynircioglu B, Yuzbasioglu A, Topaloglu H, Talim B, Balci-Hayta B.
Aksu-Menges E, et al.
Am J Pathol. 2020 Oct;190(10):2136-2145. doi: 10.1016/j.ajpath.2020.06.011. Epub 2020 Jul 7.
Am J Pathol. 2020.
PMID: 32650001
Free article.
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Reduced mitochondrial fission and impaired energy metabolism in human primary skeletal muscle cells of Megaconial Congenital Muscular Dystrophy.
Aksu-Menges E, Eylem CC, Nemutlu E, Gizer M, Korkusuz P, Topaloglu H, Talim B, Balci-Hayta B.
Aksu-Menges E, et al.
Sci Rep. 2021 Sep 13;11(1):18161. doi: 10.1038/s41598-021-97294-4.
Sci Rep. 2021.
PMID: 34518586
Free PMC article.
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Microtubule-associated protein 1B dysregulates microtubule dynamics and neuronal mitochondrial transport in spinal muscular atrophy.
Bora G, Hensel N, Rademacher S, Koyunoğlu D, Sunguroğlu M, Aksu-Mengeş E, Balcı-Hayta B, Claus P, Erdem-Yurter H.
Bora G, et al. Among authors: aksu menges e.
Hum Mol Genet. 2021 Feb 25;29(24):3935-3944. doi: 10.1093/hmg/ddaa275.
Hum Mol Genet. 2021.
PMID: 33410474
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