0c0dd9bcacfc15bba1edba258a63bac4 pmc_35151370.pdf 17d3480e4838545359aa75f9c422354f574208b1 pmc_35151370.pdf d082d1d2d86e7fbe5d900cbbb9d29fa538d9e52172f9c477302316abe9665b01 pmc_35151370.pdf Title: A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics Subject: Acta Neuropathologica Communications, https://doi.org/10.1186/s40478-022-01314-x Keywords: FUS (fused in sarcoma),Frontotemporal dementia (FTD),NCDN (neurochondrin),Norbin,Genetic variant,De novo mutation,FTLD-FET,Neurodegeneration,mGluR1/5,Cytoplasmic granules Author: Gaël Nicolas Creator: Springer Producer: Acrobat Distiller 10.1.8 (Windows); modified using iText® 5.3.5 ©2000-2012 1T3XT BVBA (SPRINGER SBM; licensed version) CreationDate: Fri Feb 11 07:29:07 2022 CET ModDate: Sat Feb 12 13:55:03 2022 CET Tagged: no UserProperties: no Suspects: no Form: AcroForm JavaScript: no Pages: 18 Encrypted: no Page size: 595.276 x 790.866 pts 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Type 1C WinAnsi yes yes no 904 0 Jhove (Rel. 1.22.1, 2019-04-17) Date: 2022-05-10 02:27:30 CEST RepresentationInformation: pmc_35151370.pdf ReportingModule: PDF-hul, Rel. 1.12.1 (2019-04-17) LastModified: 2022-02-27 18:46:15 CET Size: 2103298 Format: PDF Version: 1.6 Status: Well-Formed and valid SignatureMatches: PDF-hul MIMEtype: application/pdf PDFMetadata: Objects: 1424 FreeObjects: 1 IncrementalUpdates: 0 DocumentCatalog: ViewerPreferences: HideToolbar: false HideMenubar: false HideWindowUI: false FitWindow: false CenterWindow: false DisplayDocTitle: false NonFullScreenPageMode: UseNone Direction: L2R ViewArea: CropBox ViewClip: CropBox PrintArea: CropBox PageClip: CropBox PageLayout: SinglePage PageMode: UseOutlines Language: EN Outlines: Item: Title: A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics Children: Item: Title: Abstract Item: Title: Introduction Item: Title: Materials and methods Children: Item: Title: Source of materials Item: Title: Neuropathological examination and immunohistochemistry Item: Title: Protein extraction and western blotting from brain Item: Title: Exome sequencing and genetic analyses Item: Title: Replication analysis Item: Title: Primary neuron culture Item: Title: Cell culture Item: Title: Lentivirus production and infection Item: Title: Immunofluorescence staining of neurons Item: Title: Confocal microscopy image acquisition Item: Title: Quantitative image analysis Item: Title: Western blotting and subcellular fractionation Item: Title: Quantitative RT-PCR Item: Title: Statistical analyses Item: Title: Results Children: Item: Title: Identification of a de novo variant in the NCDN gene in a FTLD-FET patient Item: Title: NCDN haploinsufficiency affects FUS expression and localization in neurons Item: Title: FUS loss-of-function affects NCDN expression in neurons Item: Title: Discussion Item: Title: Conclusions Item: Title: Acknowledgements Item: Title: References Info: Title: A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics Author: Gaël Nicolas Subject: Acta Neuropathologica Communications, https://doi.org/10.1186/s40478-022-01314-x Keywords: FUS (fused in sarcoma),Frontotemporal dementia (FTD),NCDN (neurochondrin),Norbin,Genetic variant,De novo mutation,FTLD-FET,Neurodegeneration,mGluR1/5,Cytoplasmic granules Creator: Springer Producer: Acrobat Distiller 10.1.8 (Windows); modified using iText® 5.3.5 ©2000-2012 1T3XT BVBA (SPRINGER SBM; licensed version) CreationDate: Fri Feb 11 07:59:07 CET 2022 ModDate: Sat Feb 12 13:55:03 CET 2022 ID: 0x6f2cd86a9fb344e30cc0ddc72cba9a83, 0x4bfc72083324150a8e36e101adf64285 Filters: FilterPipeline: FlateDecode FilterPipeline: DCTDecode Images: Image: NisoImageMetadata: FormatName: image/png ImageWidth: 39 ImageHeight: 39 BitsPerSample: 8 BitsPerSampleUnit: integer 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Communications, https://doi.org/10.1186/s40478-022-01314-x FUS (fused in sarcoma) Frontotemporal dementia (FTD) NCDN (neurochondrin) Norbin Genetic variant De novo mutation FTLD-FET Neurodegeneration mGluR1/5 Cytoplasmic granules A postzygotic de novo NCDN mutation identified in a sporadic FTLD patient results in neurochondrin haploinsufficiency and altered FUS granule dynamics Gaël Nicolas Myriam Sévigny François Lecoquierre Florent Marguet Andréanne Deschênes Maria Carment del Pelaez Sébastien Feuillette Anaïs Audebrand Magalie Lecourtois Stéphane Rousseau Anne-Claire Richard Kévin Cassinari Vincent Deramecourt Charles Duyckaerts Anne Boland Jean-François Deleuze Vincent Meyer Jordi Clarimon Echavarria Ellen Gelpi Haruhiko Akiyama Masato Hasegawa Ito Kawakami Tsz H. Wong Jeroen G. J. Van Rooij John C. Van Swieten Dominique Campion Paul A. Dutchak David Wallon Flavie Lavoie-Cardinal Annie Laquerrière Anne Rovelet-Lecrux Chantelle F. Sephton 10.1186/s40478-022-01314-x 2010-04-23 true springer.com springerlink.com https://doi.org/10.1186/s40478-022-01314-x 10.1186/s40478-022-01314-x 2051-5960 journal Acta Neuropathologica Communications The Author(s) 2010-04-23 true 10.1186/s40478-022-01314-x noindex springer.com springerlink.com VoR uuid:9476edfb-919a-47f0-b053-8d8f29f74b67 uuid:206da7f5-bd70-4296-93f1-d3d3b9dbeebf default 1 converted uuid:0ce1968e-1c4e-4080-bae1-775f896e0fa1 converted to PDF/A-2b pdfToolbox 2022-02-11T12:00:23+05:30 converted uuid:21101083-8c2f-42ab-8a12-e95f461a6e30 converted to PDF/A-2b pdfToolbox 2022-02-11T12:01:04+05:30 2 B Gaël Nicolas http://orcid.org/0000-0001-9391-7800 Anne Rovelet-Lecrux http://orcid.org/0000-0003-4454-3659 Chantelle F. 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