Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/90486
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dc.contributor.authorBoia, Raquel-
dc.contributor.authorRuzafa, Noelia-
dc.contributor.authorAires, Inês Dinis-
dc.contributor.authorPereiro, Xandra-
dc.contributor.authorAmbrósio, António Francisco-
dc.contributor.authorVecino, Elena-
dc.contributor.authorSantiago, Ana Raquel-
dc.date.accessioned2020-08-03T16:41:21Z-
dc.date.available2020-08-03T16:41:21Z-
dc.date.issued2020-03-25-
dc.identifier.issn1422-0067pt
dc.identifier.urihttps://hdl.handle.net/10316/90486-
dc.description.abstractThe retinal ganglion cells (RGCs) are the output cells of the retina into the brain. In mammals, these cells are not able to regenerate their axons after optic nerve injury, leaving the patients with optic neuropathies with permanent visual loss. An effective RGCs-directed therapy could provide a beneficial effect to prevent the progression of the disease. Axonal injury leads to the functional loss of RGCs and subsequently induces neuronal death, and axonal regeneration would be essential to restore the neuronal connectivity, and to reestablish the function of the visual system. The manipulation of several intrinsic and extrinsic factors has been proposed in order to stimulate axonal regeneration and functional repairing of axonal connections in the visual pathway. However, there is a missing point in the process since, until now, there is no therapeutic strategy directed to promote axonal regeneration of RGCs as a therapeutic approach for optic neuropathies.pt
dc.description.sponsorshipThis work was supported by Foundation for Science and Technology (FCT), Portugal (Fellowships PD/BD/114115/2015 and PD/BD/127821/2016, Grant PTDC/NEU-OSD/3123/2014 and Strategic Projects UID/NEU/04539/2013, UID/NEU/04539/2019, UIDP/04539/2020 and UIDB/04539/2020), FEDER-COMPETE POCI-01-0145-FEDER-016849, FCOMP-01-0124-FEDER-028417, POCI-01-0145-FEDER-007440) and Centro 2020 Regional Operational Programme (CENTRO-01-0145-FEDER-000008: BrainHealth 2020). Grupos UPV/EHU GIU18/50, PUE 2018-04 and ELKARTEK KK-2019/00086 to E.V.pt
dc.language.isoengpt
dc.publisherMDPIpt
dc.relationPortuguese Foundation for Science and Technologypt
dc.relationEuropean Union (EU)pt
dc.relationCentro 2020 Regional Operational Programmept
dc.relationGrupo UPV/EHUpt
dc.relationGrupo PUEpt
dc.relationGrupo ELKARTEKpt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt
dc.subjectretinal ganglion cellspt
dc.subjectneurodegenerationpt
dc.subjectaxonal regenerationpt
dc.subjectneuroprotectionpt
dc.subjectoptic neuropathiespt
dc.titleNeuroprotective Strategies for Retinal Ganglion Cell Degeneration: Current Status and Challenges Aheadpt
dc.typearticle-
degois.publication.firstPage2262pt
degois.publication.issue7pt
degois.publication.locationST ALBAN-ANLAGE 66, CH-4052 BASEL, SWITZERLANDpt
degois.publication.titleInternational Journal of Molecular Sciencespt
dc.relation.publisherversionijms-21-02262-v2.pdfpt
dc.peerreviewedyespt
dc.identifier.doi10.3390/ijms21072262pt
degois.publication.volume21pt
dc.date.embargo2020-03-25*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.openairetypearticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-0477-1641-
crisitem.author.orcid0000-0002-7541-7041-
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