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Preclinical characterization of antagomiR-218 as a potential treatment for myotonic dystrophy.
Cerro-Herreros E, González-Martínez I, Moreno N, Espinosa-Espinosa J, Fernández-Costa JM, Colom-Rodrigo A, Overby SJ, Seoane-Miraz D, Poyatos-García J, Vilchez JJ, López de Munain A, Varela MA, Wood MJ, Pérez-Alonso M, Llamusí B, Artero R. Cerro-Herreros E, et al. Among authors: fernandez costa jm. Mol Ther Nucleic Acids. 2021 Jul 29;26:174-191. doi: 10.1016/j.omtn.2021.07.017. eCollection 2021 Dec 3. Mol Ther Nucleic Acids. 2021. PMID: 34513303 Free PMC article.
Myotonic dystrophy: candidate small molecule therapeutics.
Konieczny P, Selma-Soriano E, Rapisarda AS, Fernandez-Costa JM, Perez-Alonso M, Artero R. Konieczny P, et al. Drug Discov Today. 2017 Nov;22(11):1740-1748. doi: 10.1016/j.drudis.2017.07.011. Epub 2017 Aug 2. Drug Discov Today. 2017. PMID: 28780071 Free article. Review.
Expanded CTG repeats trigger miRNA alterations in Drosophila that are conserved in myotonic dystrophy type 1 patients.
Fernandez-Costa JM, Garcia-Lopez A, Zuñiga S, Fernandez-Pedrosa V, Felipo-Benavent A, Mata M, Jaka O, Aiastui A, Hernandez-Torres F, Aguado B, Perez-Alonso M, Vilchez JJ, Lopez de Munain A, Artero RD. Fernandez-Costa JM, et al. Hum Mol Genet. 2013 Feb 15;22(4):704-16. doi: 10.1093/hmg/dds478. Epub 2012 Nov 8. Hum Mol Genet. 2013. PMID: 23139243
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