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

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dc.contributor.author Majumder, Syamantak
dc.contributor.author Chowdhury, Shibasish
dc.date.accessioned 2024-08-22T10:37:15Z
dc.date.available 2024-08-22T10:37:15Z
dc.date.issued 2023-05
dc.identifier.uri URL
dc.identifier.uri https://www.biorxiv.org/content/10.1101/2023.05.12.540614v2
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/15359
dc.description.abstract Endothelial 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.language.iso en en_US
dc.subject Biology en_US
dc.subject TERF2IP en_US
dc.title Regulation of shelterin proteins TERF2IP and TRF2 by H3K4me3-p65 axis drives hyperglycemia dependent endothelial senescence en_US
dc.type Plan or blueprint en_US


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