C. Pellegrini

发表

Melanocytes: a new potential tool to study and monitoring Duchenne muscular dystrophy

N. Maraldi, L. Cocco, C. Pellegrini, 2012 .

Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis

A. Ferlini, N. Maraldi, M. Paulsson, 2012, Matrix biology : journal of the International Society for Matrix Biology.

Autophagy activation in COL6 myopathic patients by a low-protein-diet pilot trial

D. Cocchi, N. Maraldi, M. Sandri, 2016, Autophagy.

Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies

A. Ferlini, M. Paulsson, P. Sabatelli, 2014, Biochimica et biophysica acta.

Critical Evaluation of the Use of Cell Cultures for Inclusion in Clinical Trials of Patients Affected by Collagen VI Myopathies

P. Bonaldo, P. Bernardi, A. Angelin, 2011, Journal of cellular physiology.

Melanocytes from Patients Affected by Ullrich Congenital Muscular Dystrophy and Bethlem Myopathy have Dysfunctional Mitochondria That Can be Rescued with Cyclophilin Inhibitors

N. Maraldi, N. Zini, P. Bernardi, 2014, Front. Aging Neurosci..

Antisense-induced messenger depletion corrects a COL6A2 dominant mutation in Ullrich myopathy.

A. Ferlini, E. Pegoraro, P. Bonaldo, 2012, Human gene therapy.

All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype

M. Murdocca, C. Capanni, G. Lattanzi, 2015, Oncotarget.

Melanocytes—A Novel Tool to Study Mitochondrial Dysfunction in Duchenne Muscular Dystrophy

A. Ferlini, N. Maraldi, P. Bernardi, 2012, Journal of cellular physiology.

Effect of Mechanical Strain on the Collagen VI Pericellular Matrix in Anterior Cruciate Ligament Fibroblasts

F. Traina, N. Maraldi, P. Sabatelli, 2014, Journal of cellular physiology.

Altered adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browning

P. Iozzo, C. Capanni, L. Zanotti, 2019, Experimental & Molecular Medicine.

New therapeutic approaches to HGPS based on progerin inhibition

C. Pellegrini, 2015, Orphanet Journal of Rare Diseases.

Cytoskeletal and extracellular matrix alterations in limb girdle muscular dystrophy 2I muscle fibers.

P. Sabatelli, L. Merlini, C. Faldini, 2012, Neurology India.