BIANCHINI, ELISA

BIANCHINI, ELISA  

Dipartimento di Scienze Biomediche - DSB  

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Risultati 1 - 18 di 18 (tempo di esecuzione: 0.042 secondi).
Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
Different expression of sphingosine 1-phosphate receptor 1 in skeletal muscle in relation to gender, age and use. 2011 GERMINARIO, ELENABLAAUW, BERTBIANCHINI, ELISASANDONA', DORIANNADANIELI, DANIELA + JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY - Abstracts presented at the 39th European Muscle Conference
ERAD of defective type 1 membrane protein α-sarcoglycan. 2011 BIANCHINI, ELISASANDONA', DORIANNA + - - -
Extracellular ATP signaling during differentiation of C2C12 skeletal muscle cells: role in proliferation 2011 MARTINELLO, TIZIANAPAGANIN, MADDALENATARRICONE, ELENABIANCHINI, ELISASANDONA', DORIANNA + MOLECULAR AND CELLULAR BIOCHEMISTRY - -
ERAD plays a critical role in three severe muscle diseases. 2012 BIANCHINI, ELISADOROTEA, TIZIANOVALLE, GIORGIAVOLPE, POMPEOMASCARELLO, FRANCESCOSACCHETTO, ROBERTASANDONA', DORIANNA + - - Protein Quality Control and Ubiquitin Systems in Health and Disease
Adaptation of Mouse Skeletal Muscle to Long-Term Microgravity in the MDS Mission 2012 SANDONA', DORIANNABIANCHINI, ELISACICILIOT, STEFANODANIELI, DANIELAGERMINARIO, ELENAPICARD, ANNE ALEIDA + PLOS ONE - -
V247M alpha-sarcoglycan mutant: uncovering the ERAD pathway of a type I membrane protein 2012 Bianchini, Elisa - - -
PHARMACOLOGICAL RESCUE OF MISFOLDED PROTEINS: INNOVATIVE APPROACHES FOR THE CURE OF MUSCULAR DISEASES 2013 BIANCHINI, ELISAGOMIERO, CHIARADOROTEA, TIZIANOVALLE, GIORGIAMASCARELLO, FRANCESCOVOLPE, POMPEOSACCHETTO, ROBERTASANDONA', DORIANNA + - - Telethon
Inhibition of Ubiquitin Proteasome System Rescues the Defective Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA1) Protein Causing Chianina Cattle Pseudomyotonia. 2014 BIANCHINI, ELISACALI', TITOOTTOLINI, DENISBRINI, MARISAMASCARELLO, FRANCESCOSANDONA', DORIANNASACCHETTO, ROBERTA + THE JOURNAL OF BIOLOGICAL CHEMISTRY - -
Unveiling the degradative route of the V247M α-sarcoglycan mutant responsible for LGMD-2D. 2014 BIANCHINI, ELISAFANIN, MARINASANDONA', DORIANNA + HUMAN MOLECULAR GENETICS - -
Targeting the ER Quality Control as a novel therapeutic approach for sarcoglycanopathy 2015 Dorianna SandonàElisa BianchiniRoberta Sacchetto + - - Calreticulin Workshop 2015
CFTR correctors for the treatment of type 2D Limb Girdle Muscular Dystrophy 2016 Marcello CarottiElisa BianchiniChiara FecchioRoberta SacchettoDorianna Sandonà + - - Convegno Monotematico SIF: Rare Diseases and Orphan Drugs: from genes to personalized medicine
Rescue of folding-defective alpha-sarcoglycan mutants by means of protein folding correctors 2016 Chiara FecchioMarcello CarottiElisa BianchiniChiara GomieroRoberta SacchettoDorianna Sandonà - - ICINMD abstract book
Novel therapeutic perspectives for sarcoglycanopathy by assisting protein folding 2016 Dorianna SandonàRoberta SacchettoElisa BianchiniMarcello CarottiChiara Gomiero + - - International CONGRESS ON RESEARCH OF RARE and orphan DISEASES RE(ACT)® congress 2016
Novel therapeutic perspectives for sarcoglycanopathy: rescue of folding-defective mutants by means of protein folding correctors 2017 Dorianna SandonàRoberta SacchettoElisa BianchiniMarcello CarottiChiara FecchioChiara Gomiero - - 3rd IRDiRC Conference
Small molecules to rescue folding-defective sarcoglycans: in vivo assessment of novel therapeutic strategies 2017 Dorianna SandonàRoberta SacchettoElisa BianchiniMarcello CarottiChiara FecchioChiara Gomiero + - - Atti XIX Convention telethon
A CFTR Corrector For The Teatment Of Genetic Disorders Affecting Striated Muscle 2018 Sandonà DoriannaSacchetto RobertaBianchini ElisaVolpe PompeoMascarello Francesco + - - -
Sarcoglycanopathies, therapeutic approaches based on small molecules 2018 Dorianna SandonàChiara FecchioMarcello CarottiMichela SoardiElisa BianchiniRoberta Sacchetto - - 13th Meeting of the Mediterranean Society of Myology in connection with the 2nd Congress of the Turkish Neuromuscular Society
Repairing folding-defective α-sarcoglycan mutants by CFTR correctors, a potential therapy for Limb Girdle Muscular Dystrophy 2D 2018 Carotti, MarcelloSOARDI, MICHELABianchini, ElisaGomiero, ChiaraFecchio, ChiaraSacchetto, RobertaSandonà, Dorianna + HUMAN MOLECULAR GENETICS - -