CBE, DBE, F.MedSci., FRS
Dr Lee's Professor of Anatomy
Kay Davies was an undergraduate at Somerville College and a Junior Research Fellow at Wolfson College, Oxford. She was elected as Dr Lee’s Professor of Anatomy at the University of Oxford in 1998. Professor Kay Davies was Head of Department from 2008 to 2011.
Her research interests lie in the molecular analysis of human genetic disease, particularly the genetic basis of neuromuscular and neurological disorders. She first became interested in muscular dystrophy more than 20 years ago and many of her research group are dedicated to finding effective treatments for Duchenne muscular dystrophy (DMD) and spinal muscular atrophy.
In 1999, she set up the MRC Functional Genomics Unit aimed at exploiting genome information for the analysis of the function of genes in the nervous system. In 2000, she co-founded the Oxford Centre of Gene Function with Professors Ashcroft (Physiology) and Donnelly (Statistics) to bring together genetics, physiology and bioinformatics in a new multidisciplinary building which was completed in 2003. She is co-director of this initiative. She is currently co-director of the MDUK Oxford Neuromuscular Centre.
She has an active interest in the ethical implications of her research and in the public understanding of science. She is a founding fellow of the Academy of Medical Sciences and was elected a Fellow of the Royal Society in 2003.
Publisher Correction: Therapies for rare diseases: therapeutic modalities, progress and challenges ahead.
Tambuyzer E. et al, (2020), Nat Rev Drug Discov
Chemical Proteomics and Phenotypic Profiling Identifies the Aryl Hydrocarbon Receptor as a Molecular Target of the Utrophin Modulator Ezutromid.
Wilkinson IVL. et al, (2019), Angew Chem Int Ed Engl
Surrogate gene therapy for muscular dystrophy.
Davies KE. and Chamberlain JS., (2019), Nat Med
Regenerative biomarkers for Duchenne muscular dystrophy
Guiraud S. and Davies KE., (2019), Neural Regeneration Research, 14, 1317 - 1320
Limitations to adaptive homeostasis in an hyperoxia-induced model of accelerated ageing.
Pomatto LCD. et al, (2019), Redox Biol, 24