Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/7003
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dc.contributor.authorMarin, Marijaen_US
dc.contributor.authorGolić, Igoren_US
dc.contributor.authorMarkelić, Milicaen_US
dc.contributor.authorStančić, Anaen_US
dc.contributor.authorOtašević, Vesnaen_US
dc.contributor.authorJanković, Aleksandraen_US
dc.contributor.authorKorać, Batoen_US
dc.contributor.authorKorać, Aleksandraen_US
dc.date.accessioned2024-01-09T08:13:08Z-
dc.date.available2024-01-09T08:13:08Z-
dc.date.issued2017-07-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/7003-
dc.descriptionBerlin, Germany, 21-23 June, 2017en_US
dc.description.abstractDuchenne-Becker muscular dystrophy (DBMD) might be caused by a widespread genetic defect in surface membranes, which could be expressed in membranes not pathologically involved in DBMD. This hypothesis was supported by a substantial amount of evidence of abnormalities in erythrocytes from patients with DBMD. Catalases are well studied enzymes that play critical roles in protecting cells against the toxic effects of hydrogen peroxide. In previous years a lot of papers on oxidative status in DBMD are mostly confirmed increased activity of enzymes involved in the elimination of reactive oxygen species in order to protect the cells from damage, including superoxide dismutase, catalase and glutathione peroxidase. Immunohistochemistry and immunogold labeling were used to study erythrocytes from patients with Duchenne-Becker muscular dystrophy and from age-matched normal boys. There were significant differences in the catalase localization of erythrocytes from Duchenne patients when compared to controls. Hence, the internal catalase localization in the erythrocyte is atypical in DBMD, supporting the concept that a membrane and cytoskeletal defect involving multiple tissues is present in this disorder.en_US
dc.language.isoenen_US
dc.publisherSociety for Free Radical Research-Europeen_US
dc.relationMinistry of Education, Science and Technological Development, Republic of Serbia, Grant no. 173055en_US
dc.relation.ispartofFree Radical Biology and Medicine Journalen_US
dc.subjectDuchenne-Becker muscular dystrophyen_US
dc.subjectErythrocytesen_US
dc.subjectCatalaseen_US
dc.titleCatalase localization in Duchenne-Becker patients’ erythrocytesen_US
dc.typeConference Paperen_US
dc.relation.conferenceOCC World Congress and Annual SFRR-E Conference 2017 Metabolic Stress and Redox Regulationen_US
dc.identifier.doi10.1016/j.freeradbiomed.2017.04.326-
dc.description.rankM34en_US
dc.description.startpageP241en_US
dc.description.volume108en_US
dc.description.issueSupplement 1en_US
dc.relation.grantno173055en_US
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeConference Paper-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of Cell and Tissue Biology-
crisitem.author.deptChair of Cell and Tissue Biology-
crisitem.author.deptChair of Cell and Tissue Biology-
crisitem.author.orcid0000-0001-5944-5053-
crisitem.author.orcid0000-0002-5444-7735-
crisitem.author.orcid0000-0001-5272-579X-
crisitem.author.orcid0000-0002-3044-9963-
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