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Multidisciplinary study of a new ClC-1 mutation causing myotonia congenita: a paradigm to understand and treat ion channelopathies.
Imbrici P, Altamura C, Camerino GM, Mangiatordi GF, Conte E, Maggi L, Brugnoni R, Musaraj K, Caloiero R, Alberga D, Marsano RM, Ricci G, Siciliano G, Nicolotti O, Mora M, Bernasconi P, Desaphy JF, Mantegazza R, Camerino DC. Imbrici P, et al. Among authors: marsano rm. FASEB J. 2016 Oct;30(10):3285-3295. doi: 10.1096/fj.201500079R. Epub 2016 Jun 20. FASEB J. 2016. PMID: 27324117 Free PMC article.
Functional Characterization of Two Novel Mutations in SCN5A Associated with Brugada Syndrome Identified in Italian Patients.
Balla C, Conte E, Selvatici R, Marsano RM, Gerbino A, Farnè M, Blunck R, Vitali F, Armaroli A, Brieda A, Liantonio A, De Luca A, Ferlini A, Rapezzi C, Bertini M, Gualandi F, Imbrici P. Balla C, et al. Among authors: marsano rm. Int J Mol Sci. 2021 Jun 17;22(12):6513. doi: 10.3390/ijms22126513. Int J Mol Sci. 2021. PMID: 34204499 Free PMC article.
Structural and Comparative Analyses of Insects Suggest the Presence of an Ultra-Conserved Regulatory Element of the Genes Encoding Vacuolar-Type ATPase Subunits and Assembly Factors.
Lovero D, Porcelli D, Giordano L, Lo Giudice C, Picardi E, Pesole G, Pignataro E, Palazzo A, Marsano RM. Lovero D, et al. Among authors: marsano rm. Biology (Basel). 2023 Aug 13;12(8):1127. doi: 10.3390/biology12081127. Biology (Basel). 2023. PMID: 37627011 Free PMC article.
Functional characterization of the Bari1 transposition system.
Palazzo A, Marconi S, Specchia V, Bozzetti MP, Ivics Z, Caizzi R, Marsano RM. Palazzo A, et al. Among authors: marsano rm. PLoS One. 2013 Nov 14;8(11):e79385. doi: 10.1371/journal.pone.0079385. eCollection 2013. PLoS One. 2013. PMID: 24244492 Free PMC article.
46 results