The SYBIL EU FP-7 project is sadly finishing, and we had a great final meeting here on home turf in Newcastle. SYBIL led to many exciting collaborations and papers and we hope to keep in touch with everyone and continue on the SYBIL projects and beyond. Watch this space..
Thank you all for amazing 5 years!
On Saturday the 28th of July we were presenting our bench to bedside research at the Great North Museum Hancock as part of the Great Exhibition of the North, an event celebrating innovation and excellence of science and technology in the North East. We chatted to approximately 100 people of all ages, presented out work and specimens and answered many interesting questions. Thank you all for visiting and making it a really enjoyable day!
If you missed us and would like to come see us another time, we’ll be present at Dame Allan’s Schools careers fair in October or keep an eye out for advertisements of our flagship Genetics Matters event, coming up end of February as part of the International Rare Disease Day!
MBE 2018 in Manchester was a great meeting, wiuth presentations from SYBIL and RUBICON scientists, and our own RUBICON satellite meeting. It’s great doing science with so many friends all over the globe!
IGM and ICM scientists involved in the MRC funded CIMA (Centre for Integrated research into Musculoskeletal Ageing) project have organised an informative public engagement afternoon on Wednesday the 20th of June 2018 to chat to the members of the public about joints in health and disease, joint diseases and the impact of diet and exercise on joints’ health. The attendance is FREE, full programme attached below:
The BeHEARD (Helping Empower and Accelerate Research Discoveries) Challenge is hosted annually by the Rare Genomics Institute and is open globally to researchers, foundations, or anyone whose research is constrained due to limited resources. It provides technology and financial grants for rare disease research. Families with a child afflicted with a rare disease have the opportunity to work with a network of academic researchers to develop research proposals tailored to advancing treatments for their child’s disease.
We just heard that our group won the technology prize in the 2017/18 competition. The prize is a vector constructed by Cyagen (worth $8,950) which will be used to generate a conditional knock-out mouse model that will greatly enhance our sudies of skeletal dysplasias. We are very grateful for this prize and we’re looking forward to the exciting project ahead!
Beth Gibson (our PhD student) is back from her RUBICON secondment in Hong Kong. Beth had a successful and productive secondment analysing the spinal phenotype of two mouse models of aggrecanopathies, and particiapted in several meetings and conferecnces including the Little People of Hong Kong society. We would like to thank Danny and his lab for hosting Beth and look forward to future collaboration.
We had a great time, hope you enjoyed it too!
Our International Rare Disease Day event is back!
Save the date and come see us on Saturday the 24th February for a fun afternoon filled with science and cake 🙂
To book your FREE place, click here
Congratulations to Dr Ella Dennis, our first Newcastle PhD. Well done! 🙂
On the 31st of October 2017 we are organising a research showcase in collaboration with Findacure. Members of the public, patient organisations, clinical researchers and scientists all wellcome, please see below for details.
