Thomas Agnew
Oxford, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 13 publications
Biallelic ADPRHL2 mutations in complex neuropathy affect ADP ribosylation and DNA damage response.
Journal: Life science alliance
Published: February 16, 2021
Behavioural Characterisation of Macrod1 and Macrod2 Knockout Mice.
Journal: Cells
Published: January 06, 2021
Serine-linked PARP1 auto-modification controls PARP inhibitor response.
Journal: Nature communications
Published: September 21, 2020
Unrestrained poly-ADP-ribosylation provides insights into chromatin regulation and human disease.
Journal: Molecular cell
Published: August 04, 2020
A genetic modifier suggests that endurance exercise exacerbates Huntington's disease.
Journal: Human molecular genetics
Published: January 14, 2018
Validating the RedMIT/GFP-LC3 Mouse Model by Studying Mitophagy in Autosomal Dominant Optic Atrophy Due to the OPA1Q285STOP Mutation.
Journal: Frontiers in cell and developmental biology
Published: November 14, 2017
MacroD1 Is a Promiscuous ADP-Ribosyl Hydrolase Localized to Mitochondria.
Journal: Frontiers in microbiology
Published: October 11, 2017
Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical Practice.
Journal: Journal of clinical medicine
Published: June 19, 2017
Novel gene function revealed by mouse mutagenesis screens for models of age-related disease.
Journal: Nature communications
Published: February 29, 2016
Last Updated: 09/26/2026