So excited to have been a part of this important paper! “The integrated stress response contributes to tRNA synthetase–associated peripheral neuropathy” @jacksonlab @ScienceMagazine https://t.co/WOHXsWbIQN
When your summer student did a great job and wants a #NMJ themed Tres Leches you make a NMJ themed Tres Leches with twizzler axons and chocolate covered pretzel synapses #SSP24
My advice to grad students starting this fall:
Year 1: thug it out
Year 2: trust the process
Year 3: lay low and find yourself
Year 4: you do you
Year 5-6: prove the haters wrong
“Mice with CMT2D treated with our compound led to improvements in all measured outcomes,” says Timothy Hines, Ph.D., (@ScienceSquatch) from The Jackson Laboratory (@jacksonlab) during his CMT2D research update.
#CMTASTAR
This month we are sharing with you our plans for Rare disease day, a chance to request a Rare Bear to your child, C-Path mito taskforce and registry update, and more!
Please find the newsletter here: https://t.co/lcf8Uw47EQ
#leighsyndrome#mitochondrialdisease
🎉 🎉Our paper, "Single-nucleoid architecture reveals heterogeneous packaging of mitochondrial DNA," is now published! https://t.co/EWg8FtAWrF @NatureSMB
See the tweets below ⬇️ for a summary. Congratulations to the whole team! @rsisaac@mtcicero26@stergachislab 🎉🎉
Most common first concerns are balance or coordination issues, developmental delays in motor development, and lower muscle tone - observed in at least 60% of participants.
Please join the registry here: https://t.co/TSmOuM7aba
#curemito#leighsyndrome#mitochondrialdisese#mito
We'll be sharing the pictures drawn by the mito kids, their friends and siblings for the Color for Mito contest! Please like and share to support the kids! This pictures is by Freya, who is 9 and her sister Harriet (4) battles Mito.
#leighsyndrome#mitochondrialdisease#mito
It’s Sept 1st, which launches the month-long effort to raise awareness of #CMT. At #CMTRF, we consider September as CMT Action Month – because in order to cure CMT, we need more than awareness, we need ACTION: https://t.co/hC8ApfUlzQ
#cmtawareness#cmtactionmonth#CMTaction
Have you registered for Empower and Inspire: 2nd Annual Leigh Syndrome Symposium? Dr. Steven Gray will deliver a keynote talk about gene therapy for neurological disorders. Please register at: https://t.co/xzcJhyBazY
#leighsyndrome#mitochondrialdisease#mito
Patient families often say that the moment they got a diagnosis or other difficult news has stayed with them forever - they remember every word, every detail of that conversation.
Find more information at: https://t.co/x4LqdLSgTw
#leighsyndrome#mitochondrialdisese#mito
Thank you @RBurgessLab for the invitation to talk about our research. Had a great time talking to faculty and trainees- @Samia_Pratt, @ChelsyFinch and Jonathan. @AcadiaNPS is always beautiful- happy to have finally visited @jacksonlab as well!
Uma Arora, a @TuftsGSBS/@jacksonlab Ph.D. graduate ('23) who worked in the @Dumont_Lab, shares lessons learned and future plans in a recent spotlight profile. Uma is now a postdoctoral fellow in the Sankaran lab (@bloodgenes) at the @broadinstitute. 👏 https://t.co/Mne6X1uhUW
If you are a clinician, genetic counselor, or other medical professional who have treated patients with Leigh syndrome and are knowledgeable about it, please enter your information in the form below.
#curemito#leighsyndrome#mitochondrialdisese#mito
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