PCDresearch @PCDresearch
Funding life saving research for Primary Ciliary Dyskinesia - donate today and help us find a cure! pcdresearch.org London, England Joined January 2022-
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Together with @NATA_MRC_UK we will fund a £250k 2yr grant to develop #mRNA therapy for PCD. #geneticdiseases #mRNAtreatments #GettingCiliaMoving #primaryciliarydyskinesia #geneticTherapies #ciliopathies #pcdawarenessmonth
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PCDresearch retweeted
Excited to be at the Rare Diseases Industry Accelerator Day « getting cilia moving » organized by @PCDresearch in London today. Amazing line up of speakers. It will be a great day! pcdresearch.org/gettingciliamo…
PCDresearch retweeted
That's a wrap on this year's @beatpcd @ErnLung meeting! Thank you @mgoutaki @Shoemelia for your efforts and growing this motivated community 😊👏 See you tomorrow at #ERSCongress
@mrjamesob hi heard you have been discussing about teenagers and smart phones, social media and fake news. We are holding a charity event with Alex Mahon CEO @Channel4 discussing this very topic with Hattie Brett (editor of @GraziaUK. pcdresearch.org/pcdevents/
@mrjamesob thanks so much for the shout out about our @PCDresearch event with Alex Mahon and Hattie Brent ❤️
@lifearc1 Such an inspirational initiative that will have amazing impact for the rare disease community. As Founder and Chair of @PCDresearch I was honoured to speak at this event about #primaryciliarydyskinesia and the challenges of rare disease.
PCDresearch retweeted
Last night we hosted the official launch of our #RareDiseaseTranslational Challenge. We'd like to say a huge thank you to those who attended the reception and thank our speakers for delivering inspiring talks throughout the evening. lifearc.org/strategy/rare-… #RDTC #LifeArc2030
@Prof_Marciniak @lifearc1 Thank you. Wonderful to hear about the potential for impact in #raredisease through @lifearc1 funding.
@NATAhub_org @EpilepsyRUK @ActionforAT Excited to be collaborating with @NATAhub_org to investigate mRNA therapy for #primaryciliarydyskinesia
PCDresearch retweeted
NATA is proud to support #rarediseaseDay 2023, working with @EpilepsyRUK, @ActionforAT and @PCDresearch to translate research into benefits for patients with #raredisease. rarediseaseday.org #NucleicAcidTherapies #oligotherapeutics
Today is #RareDiseaseDay! We are proud to participate in this campaign to raise awareness of rare diseases. The ultimate aim is to reach equity in social opportunity, healthcare and access to diagnosis for all people with a rare disease. This all starts with raised awareness!
There is still time to submit an application for this exciting project! We are looking forward to reading the applications 📝
Together with the MRC funded Nucleic Acid Therapy Accelerator (NATA) we are delighted to inform you that we will fund a two-year post-doctoral fellowship (£200,000) to start Q3 2023. Please read on for more details! 1/6
To be eligible, any overseas supervisors will need to partner with a supervisor based in the UK. The deadline for submissions is the 28th February, 2023. We look forward to reading your exciting proposals! 6/6
We are now looking for specific project proposals from people who would like to be a supervisor. If you would like to submit a proposal, please contact me (Dr. Harriet Holme) at: [email protected]. 5/6
Together with the MRC funded Nucleic Acid Therapy Accelerator (NATA) we are delighted to inform you that we will fund a two-year post-doctoral fellowship (£200,000) to start Q3 2023. Please read on for more details! 1/6
If you would like to donate, use this link: checkout.justgiving.com/c/3234524
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