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dc.creatorBajić, Vladan
dc.creatorPotparević, Biljana
dc.creatorŽivković, Lada
dc.creatorIsenović, Esma
dc.creatorArendt, Thomas
dc.date.accessioned2019-09-02T11:47:47Z
dc.date.available2019-09-02T11:47:47Z
dc.date.issued2015
dc.identifier.issn0149-7634
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/2430
dc.description.abstractNeurons are postmitotic cells that are in permanent cell cycle arrest. However, components of the cell cycle machinery that are expressed in Alzheimer's disease (AD) neurons are showing features of a cycling cell and those attributed to a postmitotic cell as well. Furthermore, the unique physiological operations taking place in neurons, ascribed to "core cell cycle regulators" are also key regulators in cell division. Functions of these cell cycle regulators include neuronal migration, axonal elongation, axon pruning, dendrite morphogenesis and synaptic maturation and plasticity. In this review, we focus on cohesion and cohesion related proteins in reference to their neuronal functions and how impaired centromere/cohesion dynamics may connect cell cycle dysfunction to aneuploidy in AD.en
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/173034/RS//
dc.rightsrestrictedAccess
dc.sourceNeuroscience and Biobehavioral Reviews
dc.subjectAlzheimer's disease (AD)en
dc.subjectAneuploidyen
dc.subjectGenomic mosaicismen
dc.subjectCell cycleen
dc.subjectCohesionen
dc.titleCohesion and the aneuploid phenotype in Alzheimer's disease: A tale of genome instabilityen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractБајић, Владан; Aрендт, Тхомас; Исеновић, Есма; Потпаревић, Биљана; Живковић, Лада;
dc.citation.volume55
dc.citation.spage365
dc.citation.epage374
dc.citation.other55: 365-374
dc.citation.rankaM21
dc.identifier.wos000358271000025
dc.identifier.doi10.1016/j.neubiorev.2015.05.010
dc.identifier.pmid26003528
dc.identifier.scopus2-s2.0-84930622205
dc.type.versionpublishedVersion


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