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International Journal of Cardiology|July 22, 2016
Fo ATP synthase C subunit serum levels in patients with ST-segment Elevation Myocardial Infarction: Preliminary findingsGianluca Campo, Giampaolo Morciano, Rita Pavasini, et al.
Human Mutation|March 25, 2009
Identification and characterization of novel collagen VI non-canonical splicing mutations causing Ullrich congenital muscular dystrophyElena Martoni, Anna Urciuolo, Patrizia Sabatelli, et al.
Human Mutation|September 18, 2009
Exon skipping-mediated dystrophin reading frame restoration for small mutationsPietro Spitali, Paola Rimessi, Marina Fabris, et al.
Cell Reports|April 14, 2021
A naturally occurring mutation in ATP synthase subunit c is associated with increased damage following hypoxia/reoxygenation in STEMI patientsGiampaolo Morciano, Gaia Pedriali, Massimo Bonora, et al.
Frontiers in Genetics|July 13, 2019
C6orf10 Low-Frequency and Rare Variants in Italian Multiple Sclerosis PatientsNicole Ziliotto, Giovanna Marchetti, Chiara Scapoli, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|September 5, 2017
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expressionSamuele Gherardi, Matteo Bovolenta, Chiara Passarelli, et al.
Thrombosis and Haemostasis|November 7, 2014
An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosisGiovanna Marchetti, Domenico Girelli, Carlotta Zerbinati, et al.
BMC Genomics|December 2, 2008
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathiesMatteo Bovolenta, Marcella Neri, Sergio Fini, et al.
BMC Medical Genetics|August 17, 2012
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotypeSimona Brioschi, Francesca Gualandi, Chiara Scotton, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 26, 2009
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mousePaola Rimessi, Patrizia Sabatelli, Marina Fabris, et al.
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