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Mostrati risultati da 1 a 12 di 12
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Beta-agonist stimulation ameliorates the phenotype of spinal and bulbar muscular atrophy mice and patient-derived myotubes 2017 MALENA, ADRIANAMAINO, ELEONORABORGIA, DORIANABLAAUW, BERTPLEBANI, MARIOVERGANI, LODOVICAPEGORARO, ELENASORARU', GIANNISAMBATARO, FABIO + SCIENTIFIC REPORTS - -
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients 2017 Borgia, DorianaMalena, AdrianaSpinazzi, MarcoAndrea Desbats, MariaSalviati, LeonardoMIOTTO, GIOVANNITosatto, LauraPegoraro, ElenaSorarù, GianniPennuto, MariaVergani, LodovicaMIOTTO GIOVANNI + HUMAN MOLECULAR GENETICS - -
Reliable and versatile immortal muscle cell models from healthy and myotonic dystrophy type 1 primary human myoblasts 2016 PANTIC, BORISBORGIA, DORIANAGIUNCO, SILVIAMALENA, ADRIANASALVATORI, SERGIODE ROSSI, ANITAPEGORARO, ELENAVERGANI, LODOVICA + EXPERIMENTAL CELL RESEARCH - -
Mitochondrial quality control: Cell-type-dependent responses to pathological mutant mitochondrial DNA. 2016 MALENA, ADRIANAPANTIC, BORISBORGIA, DORIANAPERISSINOTTO, EGLESANDRI, MARCOVERGANI, LODOVICA + AUTOPHAGY - -
MBNL142 and MBNL143 gene isoforms, overexpressed in DM1-patient muscle, encode for nuclear proteins interacting with Src family kinases 2013 MALENA, ADRIANATIBALDI, ELENALORO, EMANUELEPAGANO, MARIO ANGELO PRIMOPANTIC, BORISMARIN, ORIANOBRUNATI, ANNA MARIAVERGANI, LODOVICA + CELL DEATH & DISEASE - -
Normal myogenesis and increased apoptosis in myotonic dystrophy type-1 muscle cells. 2010 MALENA, ADRIANAANGELINI, CORRADOSANDRI, MARCOVERGANI, LODOVICA + CELL DEATH AND DIFFERENTIATION - -
INHIBITION OF MITOCHONDRIAL FISSION FAVOURS MUTANT OVER WILD-TYPE MITOCHONDRIAL DNA 2009 MALENA, ADRIANAVERGANI, LODOVICA + HUMAN MOLECULAR GENETICS - -
Mitochondrial DNA heteroplasmy in muscle cybrids harbouring A3243G Melas mutation 2008 Malena, Adriana - - -
Dominant optic atrophy caused by a novel OPA1 mutation: Disruption of the mitochondrial network with preserved bioenergetics. 2008 SPINAZZI, MARCOBORTOLOZZI, MARIOLORO, EMANUELEMALENA, ADRIANASCORRANO, LUCAANGELINI, CORRADOVERGANI, LODOVICA + BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS - -
A novel deletion in the GTPase domain of OPA1 causes defects in mitochondrial morphology and distribution, but not in function. 2008 SPINAZZI, MARCOBORTOLOZZI, MARIOLORO, EMANUELECASARIN, ALBERTOMALENA, ADRIANAANGELINI, CORRADOSCORRANO, LUCASALVIATI, LEONARDO + HUMAN MOLECULAR GENETICS - -
Functional and molecular responses to stress conditions in heteroplasmic MELAS (3243) RD cybrids. 2006 VERGANI, LODOVICAMALENA, ADRIANA + - - -
Functional and molecular responses to stress conditions in heteroplasmic MELAS 3243 RD cybrids. 2006 MALENA, ADRIANAVERGANI, LODOVICA + - - -
Mostrati risultati da 1 a 12 di 12
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