24 results on '"Rinchetti, Paola"'
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2. Depletion of Mettl3 in cholinergic neurons causes adult-onset neuromuscular degeneration
3. Depletion of Mettl3 in cholinergic neurons causes adult-onset neuromuscular degeneration
4. Sumoylation regulates the assembly and activity of the SMN complex
5. Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy
6. Systematic elucidation of neuron-astrocyte interaction in models of amyotrophic lateral sclerosis using multi-modal integrated bioinformatics workflow
7. Brain Calcifications: Genetic, Molecular, and Clinical Aspects
8. MicroRNA Metabolism and Dysregulation in Amyotrophic Lateral Sclerosis
9. SMN post-translational modifications in spinal muscular atrophy
10. The SMN Complex at the Crossroad between RNA Metabolism and Neurodegeneration
11. Is spinal muscular atrophy a disease of the motor neurons only: pathogenesis and therapeutic implications?
12. Clinical and molecular features and therapeutic perspectives of spinal muscular atrophy with respiratory distress type 1
13. Retromer dysfunction in amyotrophic lateral sclerosis.
14. Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectives
15. DEVELOPMENT OF 3D IN VITRO MODEL TO STUDY MOLECULAR MECHANISMS OF SPINAL MUSCULAR ATROPHY
16. SETX (senataxin), the helicase mutated in AOA2 and ALS4, functions in autophagy regulation
17. SETX (senataxin), the helicase mutated in AOA2 and ALS4, functions in autophagy regulation.
18. Depletion of Mettl3in cholinergic neurons causes adult-onset neuromuscular degeneration
19. MicroRNA Metabolism and Dysregulation in Amyotrophic Lateral Sclerosis
20. Is spinal muscular atrophy a disease of the motor neurons only: pathogenesis and therapeutic implications?
21. AAV9-mediated gene therapy in a SMARD1 mouse model (PL1.003)
22. Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model
23. The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: A systematic review
24. iPSC-Derived Neural Stem Cells Ameliorate The Phenotype Of Spinal Muscular Atrophy with Respiratory Distress Type 1 (SMARD1) (S56.007)
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