EpiGenRare - Rare Disease Research UK (@epigenrare) 's Twitter Profile
EpiGenRare - Rare Disease Research UK

@epigenrare

Official Rare Disease UK EpiGenRare account. Improving the lives of people with epigenetic rare conditions.

ID: 1795365773885517824

linkhttps://rd-research.org.uk/node/epigenrare/ calendar_today28-05-2024 08:05:50

10 Tweet

149 Followers

395 Following

Manchester Rare Conditions Centre (@mft_imrare) 's Twitter Profile Photo

We are excited to announce the dates & venue for the 20th Manchester Dysmorphology Conference! Date: Sun 16th – Wed 19th November 2025. Venue: Hilton Hotel,Deansgate, Manchester. Check our socials & website(mrcc.org.uk) for updates on the conference Dian Donnai Siddharth Banka

Siddharth Banka (@smbanka) 's Twitter Profile Photo

🚨Job alert 🚨 NW GMSA Generation Study Operational Manager Advert link 👉nhsjobs.com/job/UK/Manches… Find out more about the study👉generationstudy.co.uk and genomicsengland.co.uk/initiatives/ne… NWGMSA Manchester Rare Conditions Centre Genomics England

Nicky Whiffin (@nickywhiffin) 's Twitter Profile Photo

I wrote a blog post to break down the science behind RNU4-2 in a way that families could understand: rarediseasegenomics.org/blog/rnu4-2-th… Key lesson: truly lay writing is incredibly important, but also super hard (this took me a while!) If you have any RNU4-2 families, please do share!

Rare Disease Research UK (@rdrukhub) 's Twitter Profile Photo

📢Our 2nd Annual Conference is happening on 25th March 2025! Mark your calendars and join us in #Manchester 🔔Stay tuned for more updates! #RDRUKcon #RareDiseaseResearch #raredisease #Livingrare #hopeforrare

📢Our 2nd Annual Conference is happening on 25th March 2025! Mark your calendars and join us in #Manchester

🔔Stay tuned for more updates!

#RDRUKcon #RareDiseaseResearch #raredisease #Livingrare #hopeforrare
NIHR Manchester Biomedical Research Centre (@manchesterbrc) 's Twitter Profile Photo

👏 Congratulations to Dr Neil Roberts on being awarded a Medical Research Council grant to develop a new gene therapy for the rare bladder disease, urofacial syndrome. This follows his project funded by Manchester BRC's Next Generation Therapeutics Theme through Translation Manchester’s A2E scheme.

👏 Congratulations to Dr Neil Roberts on being awarded a <a href="/The_MRC/">Medical Research Council</a> grant to develop a new gene therapy for the rare bladder disease, urofacial syndrome.

This follows his project funded by Manchester BRC's Next Generation Therapeutics Theme through <a href="/Translation_Mcr/">Translation Manchester</a>’s A2E scheme.
Rare Disease Research UK (@rdrukhub) 's Twitter Profile Photo

🌟Would you like to share your views about clinical trials for rare conditions? Apply to join the focus group now! Application deadline: 13 October