| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5893956 | International Journal of Developmental Neuroscience | 2013 | 9 Pages | 
Abstract
												⺠Spontaneous remyelination in MS fails with disease progression. ⺠Remyelination decline is multifactorial. ⺠Cell therapy may rely on NPCs transplantation or stimulation of local OPCs. ⺠Oligodendrogenesis may be a key target in cell therapy for MS. ⺠Ex vivo models of demyelination constitute an important tool toward MS cell therapy.
											Keywords
												inducible pluripotent stem cellsTRSPLPIPSCsNGFEAECNPcuprizoneCNS repairCPZMAGPDGFRαNSCsEmbryonic neural stem cellseGFPSVZMSCsMBPNPCsOPCsProteolipid proteinRemyelinationexperimental autoimmune encephalomyelitisTriiodothyronineCNSDIVdays in vitroCell therapyMesenchymal stem cellsNeural precursor cellsNeural stem cellsOligodendrocyte precursor cellscentral nervous systemperipheral nervous systemdentate gyrusnerve growth factorsubventricular zoneMultiple sclerosisMyelin basic proteinPNSMyelin-associated glycoproteinPlatelet-derived growth factor receptor alphaoligodendrocytes
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											Authors
												Sofia Grade, Liliana Bernardino, João O. Malva, 
											