21730c0f69135def1171f5dbb7ac49df 2022_Gonz_lez_Berm_dez_et_al_Biogerontology.pdf 524826e5ea8c419e46ba2b7abb302f99ab2b741f 2022_Gonz_lez_Berm_dez_et_al_Biogerontology.pdf b1ae23f3711adc1e17621db3eda36cfbcc055594988dc56e2dd469e799c12c8a 2022_Gonz_lez_Berm_dez_et_al_Biogerontology.pdf Title: Role of H4K16 acetylation in 53BP1 recruitment to double-strand break sites in in vitro aged cells Subject: Biogerontology, https://doi.org/10.1007/s10522-022-09979-6 Keywords: H4K16 acetylation; 53BP1; In vitro aging; Double strand break repair; DNA damage Author: Lourdes González-Bermúdez Creator: Springer Producer: Acrobat Distiller 10.1.8 (Windows) CreationDate: Mon Jul 18 07:42:12 2022 CEST ModDate: Tue Aug 9 15:37:19 2022 CEST Tagged: no UserProperties: no Suspects: no Form: AcroForm JavaScript: no Pages: 16 Encrypted: no Page size: 547.087 x 737.008 pts Page rot: 0 File size: 4502084 bytes Optimized: yes PDF version: 1.6 name type encoding emb sub uni object ID ------------------------------------ ----------------- ---------------- --- --- --- --------- ZWSUQA+STIX-Regular Type 1C Custom yes yes yes 465 0 STIX-Bold Type 1C Custom yes no yes 466 0 TWYAIB+Wingdings-Regular Type 1C WinAnsi yes yes yes 480 0 STIX-Regular2 Type 1C WinAnsi yes no yes 488 0 Springnew-Regular Type 1C WinAnsi yes no yes 492 0 Springnew-Regular2 Type 1C WinAnsi yes no yes 247 0 IEULII+Code2000 CID TrueType Identity-H yes yes yes 261 0 YFQTYC+STIXMath-Regular Type 1C Custom yes yes yes 332 0 STIX-Italic Type 1C WinAnsi yes no yes 386 0 Jhove (Rel. 1.22.1, 2019-04-17) Date: 2023-02-04 02:35:59 CET RepresentationInformation: 2022_Gonz_lez_Berm_dez_et_al_Biogerontology.pdf ReportingModule: PDF-hul, Rel. 1.12.1 (2019-04-17) LastModified: 2023-02-03 10:30:08 CET Size: 4502084 Format: PDF Version: 1.6 Status: Well-Formed and valid SignatureMatches: PDF-hul MIMEtype: application/pdf Profile: Linearized PDF PDFMetadata: Objects: 560 FreeObjects: 1 IncrementalUpdates: 1 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: Role of H4K16 acetylation in 53BP1 recruitment to double-strand break sites in in vitro aged cells Children: Item: Title: Abstract Item: Title: Introduction Item: Title: Methods Children: Item: Title: Cell culture and treatments Item: Title: Cell cycle analysis by flow cytometry Item: Title: Fluorescent immunodetection Item: Title: Protein extraction and western blotting Item: Title: RNA collection and RT-qPCR Item: Title: Sh-RNA expressing plasmids Item: Title: Lentivirus generation and infection Item: Title: Statistical analysis Item: Title: Results Children: Item: Title: Deficient 53BP1 recruitment to DSBs during in vitro aging correlates with diminished H4K16 acetylation Item: Title: Differential H4K16 acetylation dynamics in early and late passage HDFs after DSBs induction Item: Title: Increased 53BP1 recruitment after DSB induction in aged HDFs depends on a specific H4K16 acetylation level Item: Title: MOF silencing alters 53BP1 recruitment to induced DSBs Item: Title: Discussion Item: Title: Conclusions Item: Title: Acknowledgements Item: Title: References Info: Title: Role of H4K16 acetylation in 53BP1 recruitment to double-strand break sites in in vitro aged cells Author: Lourdes González-Bermúdez Subject: Biogerontology, https://doi.org/10.1007/s10522-022-09979-6 Keywords: H4K16 acetylation; 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