N. Licata

发表

MicroRNA signatures predict dysregulated vitamin D receptor and calcium pathways status in limb girdle muscle dystrophies (LGMD) 2A/2B

C. Angelini, C. Rodolico, A. Toscano, 2016, Cell biochemistry and function.

A Phase 1/2 Study of Flavocoxid, an Oral NF-κB Inhibitor, in Duchenne Muscular Dystrophy

A. Bitto, F. Squadrito, S. Messina, 2021, Brain sciences.

Effect of exercise on telomere length and telomere proteins expression in mdx mice

S. Messina, A. De Luca, G. Vita, 2020, Molecular and Cellular Biochemistry.

Skeletal phenotype of mandibuloacral dysplasia associated with mutations in ZMPSTE24.

G. Novelli, T. Cundy, M. D'Apice, 2010, Bone.

Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita

S. Portaro, C. Rodolico, A. Toscano, 2015, NeuroMolecular Medicine.

Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?

A. di Masi, A. Antoccia, G. Novelli, 2015, BMC Medical Genetics.

Dysregulation of the Fas/FasL system in mononuclear cells recovered from peritoneal fluid of women with endometriosis.

E. Sturlese, R. De Dominici, F. M. Salmeri, 2011, Journal of reproductive immunology.

Modulation of neuronal nitric oxide synthase and apoptosis by the isoflavone genistein in Mdx mice.

A. Bitto, N. Irrera, L. Minutoli, 2015, BioFactors.

Clinical, Molecular, and Functional Characterization of CLCN1 Mutations in Three Families with Recessive Myotonia Congenita

S. Portaro, C. Rodolico, A. Toscano, 2015, NeuroMolecular Medicine.

Modulation of neuronal nitric oxide synthase and apoptosis by the isoflavone genistein in Mdx mice.

A. Bitto, N. Irrera, L. Minutoli, 2015, BioFactors.