Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-7291
Full metadata record
DC FieldValueLanguage
dc.contributor.authorHutten, Saskia-
dc.contributor.authorDormann, Dorothee-
dc.date.accessioned2022-07-04T08:39:08Z-
dc.date.available2022-07-04T08:39:08Z-
dc.date.issued2021-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7305-
dc.description.abstractAmyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) are fatal neurodegenerative disordes, whose underlying molecular mechanisms are only beginning to emerge. A common molecular hallmark of both diseases is the relocalization of nuclear RNA-binding proteins (RBP) into cytoplasmic aggregates. Defects in nuclear import and aberrant phase separation appear to underlie RBP mislocalization and aggregation and could potentially be targeted in future therapies.de_DE
dc.language.isogerde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc570 Biowissenschaftende_DE
dc.subject.ddc570 Life sciencesen_GB
dc.titleGestörter Kerntransport und Phasentrennung von RNA-Bindeproteinende_DE
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-7291-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 10 Biologiede
jgu.organisation.number7970-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleBiospektrumde
jgu.journal.volume27de
jgu.pages.start365de
jgu.pages.end367de
jgu.publisher.year2021-
jgu.publisher.nameSpektrumde
jgu.publisher.placeHeidelbergde
jgu.publisher.issn1868-6249de
jgu.organisation.placeMainz-
jgu.subject.ddccode570de
jgu.publisher.doi10.1007/s12268-021-1599-zde
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

Files in This Item:
  File Description SizeFormat
Thumbnail
gestörter_kerntransport_und_p-20220701135221168.pdf657.7 kBAdobe PDFView/Open