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Year Number of Results
2011 1
2012 1
2013 1
2014 2
2017 1
2018 2
2019 3
2021 0
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Page 1
Dysregulation of Circular RNAs in Myotonic Dystrophy Type 1.
Voellenkle C, Perfetti A, Carrara M, Fuschi P, Renna LV, Longo M, Sain SB, Cardani R, Valaperta R, Silvestri G, Legnini I, Bozzoni I, Furling D, Gaetano C, Falcone G, Meola G, Martelli F. Voellenkle C, et al. Among authors: renna lv. Int J Mol Sci. 2019 Apr 19;20(8):1938. doi: 10.3390/ijms20081938. Int J Mol Sci. 2019. PMID: 31010208 Free PMC article.
SCN4A as modifier gene in patients with myotonic dystrophy type 2.
Binda A, Renna LV, Bosè F, Brigonzi E, Botta A, Valaperta R, Fossati B, Rivolta I, Meola G, Cardani R. Binda A, et al. Among authors: renna lv. Sci Rep. 2018 Jul 23;8(1):11058. doi: 10.1038/s41598-018-29302-z. Sci Rep. 2018. PMID: 30038349 Free PMC article.
High-throughput analysis of the RNA-induced silencing complex in myotonic dystrophy type 1 patients identifies the dysregulation of miR-29c and its target ASB2.
Cappella M, Perfetti A, Cardinali B, Garcia-Manteiga JM, Carrara M, Provenzano C, Fuschi P, Cardani R, Renna LV, Meola G, Falcone G, Martelli F. Cappella M, et al. Among authors: renna lv. Cell Death Dis. 2018 Jun 28;9(7):729. doi: 10.1038/s41419-018-0769-5. Cell Death Dis. 2018. PMID: 29955039 Free PMC article.
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