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Immunohistochemical study on the distribution of phosphorylated extracellular signal-regulated kinase (ERK) in the central nervous system of SOD1(G93A) transgenic mice

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dc.contributor.authorChung, YH-
dc.contributor.authorJoo, KM-
dc.contributor.authorLim, HC-
dc.contributor.authorCho, MH-
dc.contributor.authorKim, D-
dc.contributor.authorLee, WB-
dc.contributor.authorCha, CI-
dc.date.available2019-05-30T07:37:37Z-
dc.date.issued2005-07-
dc.identifier.issn0006-8993-
dc.identifier.issn1872-6240-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/24564-
dc.description.abstractIn the present study, we performed immunohistochemical studies to investigate the changes of phosphorylated extracellular signal-regulated kinases (PERK) in the central nervous system of SOD1(G93A) transgenic mice. In symptomatic transgenic mice, pERK-immunoreactive astrocytes were detected in the spinal cord, brainstem, central gray and cerebellar nuclei. In contrast to symptomatic mice, no pERK-immunoreactive astrocytes were observed in any brain region of wtSOD1 and presymptomatic mice, and the number and intensity of stained neurons were not different at the age of 8 weeks and 13 weeks. Interestingly, region-specific alterations in pERK immunoreactivity were observed in the hippocampal region and cerebellum. These results provide the first evidence that pERK-immunoreactive astrocytes were found in the CNS of SOD1(G93A) transgenic mice after clinical symptoms, showing a possible consequence of the pathological process of ALS. This study has also demonstrated that pERK increases in the hippocampus and cerebellum, suggesting a role of pERK in an abnormality of cognitive and/or motor function in ALS, respectively. However, the mechanisms underlying the increased immunoreactivity for pERK and the functional implications require elucidation. (C) 2005 Elsevier B.V All rights reserved.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherELSEVIER SCIENCE BV-
dc.titleImmunohistochemical study on the distribution of phosphorylated extracellular signal-regulated kinase (ERK) in the central nervous system of SOD1(G93A) transgenic mice-
dc.typeArticle-
dc.identifier.doi10.1016/j.brainres.2005.05.060-
dc.identifier.bibliographicCitationBRAIN RESEARCH, v.1050, no.1-2, pp 203 - 209-
dc.description.isOpenAccessN-
dc.identifier.wosid000231127200026-
dc.identifier.scopusid2-s2.0-21544444452-
dc.citation.endPage209-
dc.citation.number1-2-
dc.citation.startPage203-
dc.citation.titleBRAIN RESEARCH-
dc.citation.volume1050-
dc.type.docTypeArticle-
dc.publisher.location네델란드-
dc.subject.keywordAuthoramyotrophic lateral sclerosis (ALS)-
dc.subject.keywordAuthorextracellular signal-regulated kinases (ERK)-
dc.subject.keywordAuthorSOD1(G93A) mutant transgenic mice-
dc.subject.keywordAuthorastrocyte-
dc.subject.keywordPlusAMYOTROPHIC-LATERAL-SCLEROSIS-
dc.subject.keywordPlusCU/ZN SOD MUTATION-
dc.subject.keywordPlusSUPEROXIDE-DISMUTASE MUTATION-
dc.subject.keywordPlusACTIVATED PROTEIN-KINASE-
dc.subject.keywordPlusEVENT-RELATED POTENTIALS-
dc.subject.keywordPlusNITRIC-OXIDE SYNTHASE-
dc.subject.keywordPlusEXPRESS-
dc.subject.keywordPlusBRAIN-
dc.subject.keywordPlusDEGENERATION-
dc.subject.keywordPlusDISEASE-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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