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BOOK YOUR FREE PLACE TODAY

10 June 2019

Are you a researcher with an interest in

the RET gene?

Do you treat patients with diseases that involve the RET gene?

It's time to put our heads together as a collective to explore and exploit potential synergies in research

Join us on Monday 10th June at the Francis Crick Institute in London

ABOUT THE EVENT

The RET Research Collaborative Network presents its inaugural meeting.  Exchange ideas and collaborate to facilitate innovation in research and clinical care.  RET gene mutations are responsible for a range of rare diseases including multiple endocrine neoplasia II, famillial and sporadic medullary thyroid cancer and phaeochromocytomas, Hirschsprung's disease, congenital kidney and urinary tract abnormalities and intellectual disabilities.

PROGRAMME

The programme will consist of a series of 'lightening' talks by expert speakers within the following themes:

  • An Introduction to RET and MEN2

  • RET and Hirschsprung's Disease

  • Diverse Roles of RET

  • Targeting RET in Oncology

There will be plenty of networking opportunities throughout the day.

Click here to view the full programme

SUPPORTED BY
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