Congratulations Taylor Lab Cambridge Clinical Mitochondrial Research Group & all! We're all very excited to see how you will address unmet need in #mitochondrial disease via this new LifeArc Centre 💚💜The Lily Foundation UCL_QS_CNMD Muscular Dystrophy UK Prof Michael Hanna Horvath Lab Jelle van den Ameele Newcastle University

Our Newcastle University #raredisease experts are proud to play a key role in the new LifeArc Translational Research Centres! We're coordinating a cross-disease trials acceleration platform & partnering in the #mitochondrial centre led from Cambridge University tinyurl.com/2x6je7sp

For more details, you can read the full press release here: t.ly/YcO-U

The MitoCAMB team really enjoyed playing even a small part in this art exhibition. Looking forward to seeing all the art up close and personal!

We're thrilled to announce our pivotal role in the creation of a new cutting-edge, multi-site centre for #mito chondrialdisease research in partnership @LifeArc1 & Muscular Dystrophy UK Read more: bit.ly/44eekdP
#mito #research #collaboration #raredisease #patients

We’re delighted to announce, thanks to our partnership with LifeArc and @4LilyFoundation, the establishment of a new research centre, giving hope to thousands of people living with rare mitochondrial diseases.

Read the full story: shorturl.at/akH67

Excited to join @LifeArc1 Centre for #Rare #Mito diseases! Looking forward to working with The Lily Foundation Muscular Dystrophy UK @Cam_Mito UCL_QS_CNMD @TaylorLabNCL to translate our discoveries into therapies for #Mito patients
Prof Michael Hanna Robert Pitceathly Horvath Lab Jelle van den Ameele MRC MBU

Super excited to be a part of this important LifeArc #mito programme going forward over the next 5 years Newcastle University NCL_RareDisease Gavin Hudson Laura Greaves Matthias Trost 🇪🇺 Sarah Pickett Stewart Lab, Mitophile David Stroud

It's been an inspiring start to #LATSS2024 , with talks from Stéphane Maikovsky, Patrick Chinnery, Dame Kate Bingham and Clare Terlouw and Lord James O'Shaughnessy leading us in.

We’re VERY pleased to be working with The Lily Foundation UCL_QS_CNMD Taylor Lab & Muscular Dystrophy UK on the LifeArc Centre for #Rare #Mito diseases! We hope this will have a huge impact on #raredisease research and #mito patients. Robert Pitceathly Prof Michael Hanna Horvath Lab Jelle van den Ameele

Rare disease research at Cambridge has received a major boost from charity @LifeArc1.

Our researchers such as Stefan Marciniak will play leading roles in the LifeArc Centres for Rare Mitochondrial Diseases and Rare Respiratory Diseases.

Cambridge Clinical Mitochondrial Research Group

cam.ac.uk/research/news/…

Very excited for the start of the @LifeArc Translational Science Summit in London today - fantastic speakers, fab venue and a new brand that really brings it all to life. Swing by the LifeArc stand for a catch-up and a golfing challenge! #LATSS

The countdown is on! Just 5 days until researchers, partners and industry experts from the world of translational science come together at the Translational Science Summit.

What's everyone most looking forward to?

Plan your day: translationalsciencesummit.org/agenda

Delighted to launch 'Science Without Anguish': what I’ve learned from years of handling the emotional ups and downs of research life. Perhaps parts of it will work for you?
This week: why I'm writing it, what topics I will cover and source material.
sciencewithoutanguish.com

LAST CHANCE - Booking closes FRIDAY for UK Neuromuscular Translational Research Conference! 17th and 18th April 2024 See the latest programme and register here bit.ly/3GOXhUY

📢Check out our latest paper - a pilot study - 7T MRI detects widespread brain iron deposition in #neuroferritinopathy Jelle van den Ameele Horvath Lab WBIC onlinelibrary.wiley.com/doi/10.1002/ac…

The fabulous NHS HSS for Rare Mitochondrial Disorders Oxford team are holding a Clinical Study day for any health professionals working with mitochondrial disease patients. More details on the attached poster. To register please complete this form: freeonlinesurveys.com/s/lMMwD63V

Check out BBC Look North's interview with Dr Catriona Crombie, Head of LifeArc's Rare Disease Translational Challenge – talking about the clinical trial we funded to treat neuroferritinopathy, an ultra-rare, incurable brain disease.

🎥 bbc.co.uk/iplayer/episod…

Sometimes science and history overlap in unexpected ways...

We're proud to contribute £750,000 to this project to help further research into possible treatments for neuroferritinopathy.

Learn more: lifearc.org/news/2024/life…

New hope for sisters trapped in their bodies bbc.in/3Tu0MpX