Unlocking the power of #AI for Angelman Syndrome research! Dive into curated transcripts, summaries, and meet our AI research assistant. Making science accessible, one step at a time. #AngelmanSyndrome#AIforGood https://t.co/QHnuAxJTLv
We have opened a shop on our website and are now running a #giveaway promotion where a winner will get 2 items from the shop for free! Please join here: https://t.co/YSjoqv9ST7
And the Production Support Engineer Award goes to... Carys Hughes from @SkyGroup ! Congratulations, Carys! 👏👏👏 It’s great to see you being recognised for your dynamic & innovative approach to your work & in inspiring others. Sponsored by @Blackmagic_News#RiseAwards21
FAST UK are delighted to offer a corporate partnership to your organisation. Brave, bold and ESG-focussed companies who want to change the world - we need you! Check out our new corporate fundraising pack and join the upcoming webinar: https://t.co/B1FvwiuiT2
Watch this video to learn about #AngelmanSyndrome, and discover how FAST UK works towards the cure and what you and your organisation can do to make this disease a story of the past. #CureAngelmanNow https://t.co/E5iKRBUsKZ
I'm a part time football fan, but this season is a particularly special one.
I’m ridiculously proud to see the Prem' go out in #HDR on #Sky. It’s a milestone that we have been working towards since before I joined the team in 2016, and the result of lots of people's hard work.
Literally hundreds of brilliant individuals from production, origination, platforms, creative, customer, operations, marketing, propositions, product and more have got us to this successful launch of live #HDR on #SkyQ. A sincere thanks to every single person. It’s awesome!
📌 Part 3️⃣: GTX-102 Phase 1/2 Clinical Trial
📽️ YouTube recording is available, follow the link!
🎓Prof Laurent Servais shares valuable information about trials and the upcoming GTX-102 trial in the UK
#CureAngelmanNow#ClinicalTrial#Research
https://t.co/EE5pqh6g5F
A few days ago my little daughter Emily was diagnosed with a very rare and currently incurable genetic disorder called Angelman Syndrome. Please read our story and consider making a donation towards the research that is going to find a treatment. https://t.co/AxSCTwzHI6