2011-2014 - Postdoctoral researcher (University of Copenhagen)
2014-2017 - Postdoctoral researcher (University of Oxford)
After completing my doctoral research in Durham, I joined the group of Niels Mailand in the Center for Protein Research, University Copenhagen. After three years, I returned to the UK to work with Ivan Ahel in the Sir William Dunn School of Pathology, with the support of a Marie Skłodowska-Curie Fellowship and a Nicholas Kurti Junior Research Fellowship, Brasenose College, University of Oxford.
During my postdoctoral research I focussed on investigating how post-translational modifications (PTMs) regulate and impact DNA repair in mammalian cells.
Now, with the support of a CRUK Career Development Fellowship, I will investigate how PTM signalling controls replication-coupled DNA repair.
2012-2013 - Masters/Part III student (University of Cambridge)
2013-2017 - PhD student (Imperial College London/MRC LMS)
2017-2018 - Postdoctoral researcher (Helmholtz Zentrum München)
Ben carried out his Bachelor and Masters studies in Natural Sciences at the University of Cambridge, with his Part III project concerning the function of a ubiquitin-like modifier (Urm1) in Archaea. He moved to the MRC London Institute of Medical Sciences in 2013 to start his doctoral research with Till Bartke before moving to Munich with Till for a short Post-doc in the Institute of Functional Epigenetics (IFE) at the Helmholtz Zentrum München. During his PhD/Post-doc with Till, Ben was involved in investigating how modifications on histones and DNA are written and read by chromatin reader proteins, with particular attention on how UHRF1 ubiquitylates histone H3 in its role for maintaining DNA methylation after replication.
Now, Ben is will investigate the biochemical activity and function of proteins involved in the PTM-signalling associated with replication-coupled DNA repair.
As well as her Biochemistry undergraduate practical classes, Phoebe carried out a summer project at UCL and was keen to pursue cell biology methodologies in the lab.
During the 18-week Part II project, Phoebe is working on aspects of how mammalian cells use single-stranded DNA as a platform for protein signalling.