Ben Davies
Dr, Transgenic Core Head
Genetically modified models represent one of the most powerful methods of functional gene analysis in vivo. Furthermore, the ability to introduce specific mutations into the genome enables models of human disease to be generated, facilitating insights into the pathophysiology of disease and providing a model with which therapeutic strategies and diagnostic tools can be optimized.
Our group provides groups within Oxford University access to transgenic technologies both on a fee-for-service type arrangement and on a collaborative basis. Technologies offered include embryo microinjection, embryonic stem cell transfection, Knock-out/-in construct design and in vivo shRNA mediated gene Knock-down. In addition, embryo rederivation and cryoconservation services are offered to facilitate the management, transfer and security of genetically modified strains.
The research activity of the group is focused on the development of novel methodologies for the generation of genetically modified models. The aims being to improve the reliability of the technology and to reduce the animal cost of research involving genetically modified models.
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| Fluorescent 1 and 2 cell embryos |
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| A single ES cell colony expressing Green Fluorescent Protein growing on a fibroblast feeder layer |
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| Microinjection of embryonic stem cells into a blastocyst |
Recent publications
The Structured RNA-binding Domains and Condensation Capacity of FUS Shape its RNA-binding Landscape and Function
Preprint
Jutzi D. et al, (2026)
Humanized Kcnv2 E151X Mouse Captures Hallmarks of KCNV2-Associated Retinal Dystrophy
Preprint
Xhaferri N. et al, (2026)
n improved vitrification protocol for the fast and safe storage of mouse oocytes
Journal article
Hodgson T. et al, (2025), Biology of Reproduction, 113, 1355 - 1363
The ERCC6L2-MRI-KU complex coordinates NHEJ at staggered DNA double-strand breaks
Preprint
Reichl PI. et al, (2025)
Optimizing approaches for targeted integration of transgenic cassettes by integrase-mediated cassette exchange in mouse and human stem cells.
Journal article
Rath P. et al, (2025), Stem cells (Dayton, Ohio), 43


