NIZZARDO, MONICA

NIZZARDO, MONICA  

Dipartimento di Fisiopatologia Medico-Chirurgica e dei Trapianti  

Risultati 1 - 13 di 13 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autore(i) Tipo File Abstract
CSF transplantation of a specific iPSC-derived neural stem cell subpopulation ameliorates the disease phenotype in a mouse model of spinal muscular atrophy with respiratory distress type 1 1-nov-2019 Nizzardo, MonicaBucchia, MonicaRamirez, AgneseBresolin, NereoComi, Giacomo PietroCorti, Stefania + Article (author) -
Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1) 1-gen-2020 M. NizzardoA. GovoniM. TaianaN. BresolinG. P. ComiS. Corti + Article (author) -
Downregulation of glutamic acid decarboxylase in Drosophila TDP- 43-null brains provokes paralysis by affecting the organization of the neuromuscular synapses 1-gen-2018 M. NizzardoF. Rizzo + Article (author) -
Effect of combined systemic and local morpholino treatment on the spinal muscular atrophy δ7 mouse model phenotype 1-gen-2014 M. NizzardoC. SimoneS. SalaniF. RizzoN. BresolinG.P. ComiS. Corti + Article (author) -
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model 1-gen-2015 M. NizzardoC. SimoneF. RizzoS. SalaniP. RinchettiR. Del BoS. DamettiN. BresolinG. ComiS. Corti + Conference Object -
Genetic correction of spinal muscular atrophy-induced pluripotent stem cells and motoneurons as a disease model and cell source for transplantation 1-gen-2012 G. RiboldiM. NizzardoM. NardiniC. SimoneM. FalconeD. RonchiS. SalaniF. MagriF. RizzoA. GovoniI. FaravelliN. BresolinG.P. ComiS. Corti + Article (author) -
Genome-wide RNA-seq and proteomic analysis of motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease, partially rescued by riboflavin 1-apr-2017 F. RizzoA. RamirezS. SalaniA. BordoniF. FortunatoN. BresolinG.P. ComiM. NizzardoS. Corti + Article (author) -
The mitochondrial disulfide relay system protein GFER is mutated in autosomal recessive myopathy with congenital cataract and COX deficiency. 1-giu-2009 A. Di FonzoD. RonchiE. FassoneC. LampertiS. CortiA. BordoniF. FortunatoM. NizzardoS. SalaniN. BresolinG.P. Comi. + Conference Object -
Molecular analysis of SMARD1 patient-derived cells demonstrates that nonsense-mediated mRNA decay is impaired 27-gen-2022 Taiana, MichelaGovoni, AlessandraSalani, SabrinaGalli, NoemiSaladini, MatteoBersani, MargheritaDel Bo, RobertoSansone, ValeriaBresolin, NereoComi, GiacomoCorti, StefaniaNizzardo, Monica + Article (author) -
Molecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA) 1-gen-2014 G. RiboldiM. NizzardoC. SimoneI. FaravelliN. BresolinG.P. ComiS. Corti + Article (author) -
Motoneuron Transplantation Rescues the Phenotype of SMARD1 (Spinal Muscular Atrophy with Respiratory Distress Type 1) 23-set-2009 S. CortiM. NizzardoM. NardiniS. SalaniR. Del BoD. PapadimitriouF. LocatelliN. BresolinG.P. Comi + Article (author) -
Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches 1-gen-2015 M. NizzardoC. SimoneS. DamettiS. SalaniG. UlziS. PagliaraniF. RizzoE. FrattiniN. BresolinG. ComiS. Corti + Article (author) -
Therapeutic applications of the cell-penetrating HIV-1 Tat peptide 1-gen-2015 M. NizzardoA. RamirezS. Corti + Article (author) -