Jonathan D. Lea

A novel high mobility group box 1 neutralizing chimeric antibody attenuates drug‐induced liver injury and postinjury inflammation in mice

K. Tracey, Huan Yang, J. Stéen, 2016, Hepatology.

Evaluation of plasma microRNA-122, high-mobility group box 1 and keratin-18 concentrations to stratify acute gallstone disease: a pilot observational cohort study in an emergency general surgery unit

J. Dear, D. Mole, D. Antoine, 2018, BMJ Open.

Biomarker evaluation of plasma microRNA-122, high-mobility group box-1 and keratin-18 in acute gallstone disease

J. Dear, D. Mole, D. Antoine, 2017, bioRxiv.

Redox-Dependent HMGB1 Isoforms as Pivotal Co-Ordinators of Drug-Induced Liver Injury: Mechanistic Biomarkers and Therapeutic Targets.

D. Antoine, J. Clarke, Jonathan D. Lea, 2016, Antioxidants & redox signaling.

Circulating levels of miR-122 increase post-mortem, particularly following lethal dosing with pentobarbital sodium: implications for pre-clinical liver injury studies.

A. Kipar, B. K. Park, C. Goldring, 2017, Toxicology research.

Mutations in MexB that affect the efflux of antibiotics with cytoplasmic targets.

H. Venter, Jonathan D. Lea, Thelma Ohene-Agyei, 2012, FEMS microbiology letters.