about
iPSC-Derived neural stem cells act via kinase inhibition to exert neuroprotective effects in spinal muscular atrophy with respiratory distress type 1Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches.Direct reprogramming of human astrocytes into neural stem cells and neurons.Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis model.Research advances in gene therapy approaches for the treatment of amyotrophic lateral sclerosis.Generation of skeletal muscle cells from embryonic and induced pluripotent stem cells as an in vitro model and for therapy of muscular dystrophies.Mitochondrial fusion proteins and human diseases.Cellular therapy to target neuroinflammation in amyotrophic lateral sclerosis.MFN2-related neuropathies: Clinical features, molecular pathogenesis and therapeutic perspectives.Selective mitochondrial depletion, apoptosis resistance, and increased mitophagy in human Charcot-Marie-Tooth 2A motor neurons.Effect of Combined Systemic and Local Morpholino Treatment on the Spinal Muscular Atrophy Δ7 Mouse Model Phenotype
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description
hulumtuese
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Federica Rizzo
@ast
Federica Rizzo
@en
Federica Rizzo
@es
Federica Rizzo
@nl
Federica Rizzo
@sl
type
label
Federica Rizzo
@ast
Federica Rizzo
@en
Federica Rizzo
@es
Federica Rizzo
@nl
Federica Rizzo
@sl
prefLabel
Federica Rizzo
@ast
Federica Rizzo
@en
Federica Rizzo
@es
Federica Rizzo
@nl
Federica Rizzo
@sl
P1053
J-2303-2018
P106
P21
P31
P3829
P496
0000-0002-7677-0330