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dc.contributor.authorSAMANO SALAZAR, CYNTHIA GABRIELA-
dc.contributor.authorBAN, JELENA-
dc.contributor.authorMUNITIC, IVANA-
dc.contributor.authorMLADINIC, MIRANDA-
dc.coverage.spatial<dc:creator id="info:eu-repo/dai/mx/cvu/164923">CYNTHIA GABRIELA SAMANO SALAZAR</dc:creator>-
dc.coverage.temporal<dc:subject>info:eu-repo/classification/cti/3</dc:subject>-
dc.date.accessioned2020-04-06T22:05:53Z-
dc.date.available2020-04-06T22:05:53Z-
dc.date.issued2019-
dc.identifier.citationCroatian Medical Journal, vol. 60, núm. 2, april, 2019en_US
dc.identifier.urihttp://ilitia.cua.uam.mx:8080/jspui/handle/123456789/313-
dc.description.abstractThe toolkit for repairing damaged neurons in amyotrophic lateral sclerosis (ALS) and spinal cord injury (SCI) is extremely limited. Here, we reviewed the in vitro and in vivo studies and clinical trials on nonneuronal cells in the neurodegenerative processes common to both these conditions. Special focus was directed to microglia and astrocytes, because their activation and proliferation, also known as neuroinflammation, is a key driver of neurodegeneration. Neuroinflammation is a multifaceted process that evolves during the disease course, and can be either beneficial or toxic to neurons. Given the fundamental regulatory functions of glia, pathogenic mechanisms in neuroinflammation represent promising therapeutic targets. We also discussed neuroprotective, immunosuppressive, and stem-cell based approaches applicable to both ALS and SCI.en_US
dc.description.sponsorshipCroatian Medical Journalen_US
dc.language.isoInglésen_US
dc.publisherCroatia : Medicinska nakladaen_US
dc.relation.haspart1332-8166-
dc.rightshttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6509626/pdf/CroatMedJ_60_0109.pdf-
dc.rightshttps://doi.org/10.3325/cmj.2019.60.109-
dc.subjectEsclerosis lateral amitróficaen_US
dc.subjectMédula espinal - Heridas y lesionesen_US
dc.subjectSitema nerviosoen_US
dc.titleGlia in amyotrophic lateral sclerosis and spinal cord injury : common therapeutic targetsen_US
dc.typeArtículoen_US
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