Regulation of shelterin proteins TERF2IP and TRF2 by H3K4me3-p65 axis drives hyperglycemia dependent endothelial senescence

dc.contributor.authorMajumder, Syamantak
dc.contributor.authorChowdhury, Shibasish
dc.contributor.authorDey, Smita
dc.date.accessioned2024-08-22T10:37:15Z
dc.date.available2024-08-22T10:37:15Z
dc.date.issued2023-05
dc.description.abstractEndothelial senescence has been linked to several cardiovascular diseases. Dysregulation of proteins of the shelterin complex including TRF2 and TERF2IP causes senescence as it hampers DNA repair and cell proliferation. However, whether exposure to hyperglycemia interplays with proteins of the shelterin complex thus further dictates the senescent phenotype of endothelial cells (EC) remain to be explored.en_US
dc.identifier.uriURL
dc.identifier.urihttps://www.biorxiv.org/content/10.1101/2023.05.12.540614v2
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15359
dc.language.isoenen_US
dc.subjectBiologyen_US
dc.subjectTERF2IPen_US
dc.titleRegulation of shelterin proteins TERF2IP and TRF2 by H3K4me3-p65 axis drives hyperglycemia dependent endothelial senescenceen_US
dc.typePlan or blueprinten_US

Files

License bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
1.71 KB
Format:
Item-specific license agreed upon to submission
Description: