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Melanocytes from Patients Affected by Ullrich Congenital Muscular Dystrophy and Bethlem Myopathy have Dysfunctional Mitochondria That Can be Rescued with Cyclophilin Inhibitors.Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathiesExpression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis.Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathiesAll-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype.Melanocytes--a novel tool to study mitochondrial dysfunction in Duchenne muscular dystrophy.Joint sparing treatments in early ankle osteoarthritis: current procedures and future perspectivesAntisense-induced messenger depletion corrects a COL6A2 dominant mutation in Ullrich myopathyCytoskeletal and extracellular matrix alterations in limb girdle muscular dystrophy 2I muscle fibers.Effect of mechanical strain on the collagen VI pericellular matrix in anterior cruciate ligament fibroblasts.
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description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Camilla Pellegrini
@ast
Camilla Pellegrini
@en
Camilla Pellegrini
@es
Camilla Pellegrini
@nl
type
label
Camilla Pellegrini
@ast
Camilla Pellegrini
@en
Camilla Pellegrini
@es
Camilla Pellegrini
@nl
prefLabel
Camilla Pellegrini
@ast
Camilla Pellegrini
@en
Camilla Pellegrini
@es
Camilla Pellegrini
@nl
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54895675700
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0000-0003-2636-477X