Eleanor Hendy

ORCID: 0009-0003-3808-9901
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About
Contact & Profiles
Research Areas
  • Telomeres, Telomerase, and Senescence
  • Epigenetics and DNA Methylation
  • Cytomegalovirus and herpesvirus research
  • Genomics and Chromatin Dynamics
  • CRISPR and Genetic Engineering
  • Immune cells in cancer
  • Autism Spectrum Disorder Research
  • Immune Cell Function and Interaction
  • Cancer-related gene regulation

University of Exeter
2024

Asthma UK
2018-2021

King's College London
2018-2021

Abstract GATA3 is as a lineage-specific transcription factor that drives the differentiation of CD4 + T helper 2 (Th2) cells, but also involved in variety processes such immune regulation, proliferation and maintenance other cell non-T lineages. Here we show mechanism utilised by cells to increase mitochondrial mass response DNA damage through actions AMPK. Activated AMPK increases expression PPARG coactivator 1 alpha ( PPARGC1A or PGC1α protein) at level translation, while enhances nuclear...

10.1038/s41467-021-23715-7 article EN cc-by Nature Communications 2021-06-07

Abstract Loss-of-function mutations in genes encoding lysine methyltransferases (KMTs) and demethylases (KDMs) responsible for regulating the trimethylation of histone 3 on 4 (H3K4me3) are associated with neurodevelopmental conditions, including autism spectrum disorder intellectual disability. To study specific role H3K4me3 demethylation, we investigated phenotypes mice without KDM5B demethylase activity. These exhibited autism-like behaviours increased brain size. levels expression were...

10.1101/2024.05.28.596232 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2024-05-29

Introductory paragraph GATA binding protein 3 (GATA3) has traditionally been regarded as a lineage-specific transcription factor that drives the differentiation of CD4 + T helper (Th) 2 cells. However, increasing evidence shows GATA3 is involved in myriad processes such immune regulation, proliferation and maintenance other cell non-T lineages. We show here previously unknown mechanism utilized by cells to increase mitochondrial mass response DNA damage through GATA3, AMP-activated kinase...

10.1101/727479 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2019-08-06
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