MORBIDONI, VALERIA

MORBIDONI, VALERIA  

Università di Padova  

Mostra records
Risultati 1 - 17 di 17 (tempo di esecuzione: 0.02 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Collagen VI regulates satellite cell self-renewal and muscle regeneration 2013 URCIUOLO, ANNAMORBIDONI, VALERIAMOLON, SIBILLAGRUMATI, PAOLOBLAAUW, BERTBONALDO, PAOLO + NATURE COMMUNICATIONS - -
Cyclosporin A promotes in vivo myogenic response in collagen VI-deficient myopathic mice 2014 GATTAZZO, FRANCESCAMOLON, SIBILLAMORBIDONI, VALERIABRAGHETTA, PAOLABLAAUW, BERTURCIUOLO, ANNABONALDO, PAOLO FRONTIERS IN AGING NEUROSCIENCE - -
Cyclosporin A Promotes in vivo Myogenic Response in Collagen VI-Deficient Myopathic Mice. 2014 MOLON, SIBILLAMORBIDONI, VALERIABRAGHETTA, PAOLABLAAUW, BERTURCIUOLO, ANNABONALDO, PAOLO + FRONTIERS IN AGING NEUROSCIENCE - -
The chaperone co-inducer BGP-15 alleviates ventilation-induced diaphragm dysfunction 2016 MORBIDONI, VALERIASALVIATI, LEONARDO + SCIENCE TRANSLATIONAL MEDICINE - -
Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet 2016 BORGIA, DORIANAPELLEGRINI, MATTEOURCIUOLO, ANNAMOLON, SIBILLAMORBIDONI, VALERIAMARABITA, MANUELAROMANELLO, VANINABLAAUW, BERTBONALDO, PAOLOSambataro, FabioSORARU', GIANNIVERGANI, LODOVICASANDRI, MARCOPENNUTO, MARIA + ACTA NEUROPATHOLOGICA - -
Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet 2016 Rocchi, AnnaUrciuolo, AnnaMorbidoni, ValeriaROMANELLO, VANINABLAAUW, BERTBONALDO, PAOLOSORARU', GIANNISANDRI, MARCO + ACTA NEUROPATHOLOGICA - -
The COQ2 genotype predicts the severity of Coenzyme Q10 deficiency 2016 MORBIDONI, VALERIASILIC-BENUSSI, MICOLDOIMO, MARACIMINALE, VINCENZOCASSINA, MATTEOBASSO, GIUSEPPESALVIATI, LEONARDOTREVISSON, EVA + HUMAN MOLECULAR GENETICS - -
Age-Associated Loss of OPA1 in Muscle Impacts Muscle Mass, Metabolic Homeostasis, Systemic Inflammation, and Epithelial Senescence 2017 TEZZE, CATERINAROMANELLO, VANINADESBATS, MARIA ANDREAFADINI, GIAN PAOLOALBIERO, MATTIAFAVARO, GIULIACICILIOT, STEFANOSORIANO GARCIA - CUERVA, MARIA EUGENIAMORBIDONI, VALERIACERQUA, CRISTINABLAAUW, BERTZAMPIERI, SANDRASALVIATI, LEONARDOSCORRANO, LUCASANDRI, MARCO + CELL METABOLISM - -
Alport syndrome: impact of digenic inheritance in patients management. 2017 TREVISSON, EVAMORBIDONI, VALERIA + CLINICAL GENETICS - -
COX16 is required for assembly of cytochrome c oxidase in human cells and is involved in copper delivery to COX2 2018 Cerqua, CristinaMorbidoni, ValeriaDesbats, Maria AndreaDoimo, MaraFrasson, ChiaraBALDOIN, MARIA CRISTINASartori, GeppoBasso, GiuseppeSalviati, LeonardoTrevisson, Eva + BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS - -
Parent-of-origin effect of hypomorphic pathogenic variants and somatic mosaicism impact on phenotypic expression of retinoblastoma 2018 Trevisson, EvaMorbidoni, Valeria + EUROPEAN JOURNAL OF HUMAN GENETICS - -
The Arg1038Gly missense variant in the NF1 gene causes a mild phenotype without neurofibromas 2019 Trevisson, EvaMorbidoni, ValeriaForzan, MonicaFUMINI, VALENTINAParrozzani, RaffaeleCassina, MatteoMidena, EdoardoSalviati, LeonardoClementi, Maurizio + MOLECULAR GENETICS & GENOMIC MEDICINE - -
Vanillic Acid Restores Coenzyme Q Biosynthesis and ATP Production in Human Cells Lacking COQ6 2019 Trevisson E.Canton M.Morbidoni V.Baschiera E.Desbats M. A.Salviati L. + OXIDATIVE MEDICINE AND CELLULAR LONGEVITY - -
DRP1-mediated mitochondrial shape controls calcium homeostasis and muscle mass 2019 Giulia FavaroVanina RomanelloTatiana VaranitaMaria Andrea DesbatsValeria MorbidoniCaterina TezzeMattia AlbieroMarta CanatoGaia GherardiDiego De StefaniCristina MammucariBert BlaauwLuca ScorranoLeonardo SalviatiMarco Sandri + NATURE COMMUNICATIONS - -
Usefulness and limitations of comprehensive characterization of mRNA splicing profiles in the definition of the clinical relevance of BRCA1/2 variants of uncertain significance 2019 Morbidoni, ValeriaTrevisson, Eva + CANCERS - -
Biallelic mutations in the TOGARAM1 gene cause a novel primary ciliopathy 2020 Morbidoni V.Cassina M.Salviati L.Trevisson E. + JOURNAL OF MEDICAL GENETICS - -
Hybrid minigene assay: An efficient tool to characterize mrna splicing profiles of nf1 variants 2021 Morbidoni V.Baschiera E.Fumini V.Desbats M. A.Cassina M.Salviati L.Trevisson E. + CANCERS - -