On 28th November OxTalks will move to the new Halo platform and will become 'Oxford Events' (full details are available on the Staff Gateway).
There will be an OxTalks freeze beginning on Friday 14th November. This means you will need to publish any of your known events to OxTalks by then as there will be no facility to publish or edit events in that fortnight. During the freeze, all events will be migrated to the new Oxford Events site. It will still be possible to view events on OxTalks during this time.
If you have any questions, please contact halo@digital.ox.ac.uk
In humans, fetal survival depends on proper patterning and morphogenesis of the embryo and its accompanying placenta. Abnormal morphogenesis in the embryo underlies developmental abnormalities such as DiGeorge syndrome and Mandibulofacial dysostosis with microcephaly (MFDM), and results in increased morbidity and mortality. We use the mouse model to study the genetic and cellular basis of morphogenesis during the embryonic period; furthermore, the availability of next generation sequencing has enabled the rapid identification of genes associated with developmental abnormalities. The goals of my research program are (1) to use forward genetics to identify the genes responsible for malformations in human and mouse during pregnancy; (2) to use reverse genetics in the mouse model to characterize the cellular pathways regulated by genes implicated in developmental syndromes.
