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

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! https://t.co/TNuFRwL5II

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

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. https://t.co/JaIJLbaEdC #RDTC #LifeArc2030

NATA is proud to support #RareDiseaseDay 2023, working with @EpilepsyRUK, @ActionforAT and @PCDresearch to translate research into benefits for patients with #raredisease. https://t.co/pZ9OhBRTVr #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 📝

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: pcdresearch@outlook.com. 5/6

The additional upside to this project is that it has the added potential for the post-doc to perform in-vivo validation using an inducible mouse model in the second year. 4/6

In recognition of the breath of application represented in this project, it is our mission to be goal-focussed rather than pathway-driven. We hope this will spur novel ideas across multiple fields under a common purpose. 3/6

The scope of this project will be to investigate the delivery/optimisation of nucleic acid therapeutics such as mRNA and anti-sense, with the aim of functional restoration of ciliary function. 2/6

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: https://t.co/GqN1uGCseF

Ever wondered what your donations are used for? This is a quick insight into what your donations can do! 👇 #PCD #PCDresearch

We attended the @beatpcd conference this weekend and it was fantastic to hear from all of the researchers, patients and support groups from around the world. We gave a quick intro to our charity, please get in touch if you have any questions! #PCD #BEATPCD #PCDresearch

Watch our latest video to find out about what causes PCD 👇 If you would like to donate, please use this link: https://t.co/GqN1uGCseF Please also share our charity with your own network, raising awareness helps us access new resources! #PCD #PCDresearch

You can help raise money for PCD Research by donating online #JustGiving https://t.co/8DCraq8IQp #londonlandmarkshalfmarathon #llhm2023 #pcdresearch

Many of you will have noticed a new charity recently, called @PCDresearch . We're excited to work alongside each other to improve the lives of people with #PCD. A quick guide to what each of us do! PCD Support UK: https://t.co/zwRX1Fy0IW PCD Research: https://t.co/jiHei5bjza

My friend Ian Brooks is fundraising for PCD Research. Check out their @JustGiving page and please donate if you can. Thank you! #JustGiving