H. Osman

A multicenter comparison of quantification methods for antisense oligonucleotide-induced DMD exon 51 skipping in Duchenne muscular dystrophy cell cultures

J. Goeman, F. Muntoni, N. Datson, 2018, PloS one.

Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients

E. Bertini, E. Mercuri, A. Yuryev, 2021, Frontiers in Physiology.

Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression.

M. Falzarano, H. Osman, A. Ferlini, 2017, Biochimica et biophysica acta. Gene regulatory mechanisms.

Urine-Derived Stem Cells Express 571 Neuromuscular Disorders Causing Genes, Making Them a Potential in vitro Model for Rare Genetic Diseases

S. Bicciato, M. Falzarano, H. Osman, 2021, Frontiers in Physiology.

Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype.

E. Mercuri, F. Crea, A. Amodeo, 2016, Human gene therapy.

Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy

G. Pesole, E. Bertini, K. Bushby, 2016, Journal of Cell Science.