#fragilex search results
Spotlight on 🌟 Shelby Dauterman🌟 Meet Shelby, one of our 2025 RJH Summer Scholars! Her project explores neurovascular coupling in Fragile X syndrome to help inform new treatment strategies. 🎥 Watch her presentation here: hubs.ly/Q03NLx320 #FragileX #StudentResearch
Spotlight on 🌟 Tanvi Kamra 🌟 Meet Tanvi, one of our 2025 RJH Summer Scholars! Her project explores postmortem brain data to better understand Fragile X-associated conditions. 🎥Watch her presentation here: hubs.ly/Q03NKVdD0 #FragileX #StudentResearch #FragileXResearch
Our experience of a disabled young person leaving education is that there might be social care funding but it's impossible to recruit PAs. Parents/carers left picking up the pieces. #autism #FragileX
Good piece on @BBCPoliticsWest about National Star College students & the challenges they face for funding when they leave education. It’s an amazing place in the North Cotswolds which I’ve supported enthusiastically.
Spotlight on 🌟 Susana Lopez-Ignacio 🌟 Meet Susana, one of our 2025 RJH Summer Scholars! Her summer project explores how X-chromosome inactivation affects FXTAS. 🎥 Watch her 15-minute presentation here: hubs.ly/Q03NtvT30 #FragileX #StudentResearch #FragileXResearch
What about people unable to work due to disability or caring? Do we count? #autism #FragileX #epilepsy
National renewal means more homes, more jobs, and more money back in working people’s pockets. But to get there, we need to take on the blockers. We are cutting red tape to get Britain building.
👀 on CONNECTA Therapeutics! This biotech company is taking a fresh approach to #FragileX research! Their lead medicine aims to boost the brain’s ability to form & strengthen connections. Read more about CONNECTA & what's next for their research: hubs.ly/Q03MZz1-0
Today it's International #FragileX day so here's a thread I wrote a while ago about how it affects our family.
Today is European Fragile X Syndrome awareness day. #FragileX is a chromosomal abnormality and is the most common form of inherited learning disability. It's called Fragile X as the end of the chromosome looks like it's about to drop off.
#LegacyContent: Strategic Implementation of #FragileX Carrier Screening in China: A Focused Pilot Study. Free in the #OpenArchive: jmdjournal.org/article/S1525-…
Hearing you’ve just chatted to our lads @stuandmattmcd ……we (mum and dad) are in Tenerife so a couple of their pals have taken them #fragilex #learningdisabilities #excitement
And people ask M and I why we are terrified what will happen to our kids when we die. #FragileX #autism
- Man with Down’s admitted with a broken hip, easily fixed with surgery. - Mistakenly marked down as 'nil by mouth' for NINE DAYS. - Due to disability can’t explain he’s hungry. - Literally starves to death on the ward. Nobody notices him slowly dying. itv.com/news/2025-10-0…
Tell you who else deserve a fair deal - unpaid carers. £83.30 per week for often 24/7 care. #autism #FragileX #epilepsy
Care workers deserve fair pay, but funding it through council tax hikes won’t solve the crisis. The government must deliver a long term plan for social care. @alisonebennett
ZYN002 misses pivotal Fragile X trial — What does the setback mean for Harmony’s pipeline and stock outlook? business-news-today.com/zyn002-misses-… #HarmonyBiosciences #HRMY #FragileX #Biotech #RareDisease #Cannabidiol #StockMarket #ClinicalTrials #Investing #Pharma
Honoring a quiet hero. 🏆 Kent Satterfield — lifelong #CHS football supporter, volunteer, & friend to many — deserves a statue at CHS stadium. Let’s make it happen. Sign & share the petition 👉 change.org/p/install-a-st… #FragileX #Community #Legacy
She'd have to have taken a full bottle. I seriously question this video. Source or it didn't happen. I took Tylenol sparingly while pregnant, those children fine. Not saying there couldn't be adverse effects. Still, it can't account for all ASD kids. I do have a Fraggle #FragileX
On Hols in UAE with our 29 year old #fragilex son. He has traveled all over the world and always accepted as the beatiful mild mannered boy he is. Unfortunately the disdain he recieves here from All rissians is disgusting. Snapped today
#FragileX click images everything now is manipulated, a scam and a lie for security espiecally from big earshimsrlf and thr bushes watch his facial movements when he gives speeches involuntary movements they can't control when they lie giving generalised statrments
Unravel the mysteries of your DNA 🧬 Learn about rare genetic disorders like #FragileX syndrome and how tiny gene mutations can have a big impact. Discover more in our blog! #genetics #DNA #rarediseases studies.science37.com/the-role-of-ge…
studies.science37.com
The Role of Genetics in Rare Diseases: Understanding Conditions Like Fragile X Syndrome - Science...
Your DNA contains thousands of genes that direct how your body functions. Each gene contains instructions for making proteins essential for different processes—like building cells, transmitting...
Servier acquires potential treatment for Fragile X syndrome, the most common genetic cause of autism spectrum disorder 👉 servier.com/en/newsroom/ac… #Servier #FragileX #Autism #RareDisease
@Servier in $450M #deal for @medicxi-funded phase II #fragileX program bioworld.com/articles/723920 #biopharma @KaerusBio
Katarzyna Tutak @tutakkasia with Anna Baud & Krzysztof Sobczak @UAM_IBMiB identified novel modifiers of #fragileX linked Repeat Associated Non-AUG #RAN translation associated with RPS25, RPS26 and chaperone TSR2. Just published in @eLife- congratulations! elifesciences.org/articles/98631
Spotlight on 🌟 Tanvi Kamra 🌟 Meet Tanvi, one of our 2025 RJH Summer Scholars! Her project explores postmortem brain data to better understand Fragile X-associated conditions. 🎥Watch her presentation here: hubs.ly/Q03NKVdD0 #FragileX #StudentResearch #FragileXResearch
Congratulations to Yuan-Chen Tsai, PhD, a postdoctoral research fellow in @AnatomyNeurobio at the #UCIMedSchool, for being awarded a @FRAXAresearch fellowship for her work on #FragileX syndrome and autism. bit.ly/3MHdSO7
SCC is illuminated teal tonight for World Fragile X Day. The @FRAXAresearch Research Foundation is raising awareness of Fragile X Syndrome and the progress in treating, and one day ultimately curing, this rare genetic condition. #FragileX #FragileXsyndrome #WorldFragileXDay
In a world of chaos, it's important to learn about each other and what makes us all different - to practice empathy and keep growing as a person. Thank you for giving me a platform to raise awareness about #FragileX and for helping me reach our goal on the FIRST DAY!
Congratulations to our chair @pengjinATL for being named @aaas Fellow (along with 9 others @EmoryUniversity) "distinguished contributions to the field of neurogenetics and neuroepigenetics" #fragileX news.emory.edu/stories/2024/0…
People with sensory overstimulation tend to find calmness and brain re-organization from pushing, pulling and carrying heavy objects. Owen and I worked through this calming series today bec he is VERY excited about vacation soon 😂#adaptivefitness #fragilex
The @hmar_research, @crgenomica, @I3ptT received €2.7 million from @CienciaGob to start the Phase IIA clinical trials of the drug #CTH120 aimed at the treatment of #fragileXsyndrome 👉imim.cat/news/610 #FragileX #SXF #RareDiseases #OrphanDrug #NextGenerationEU
No link between #FMR1 premutation status and ADHD or anxiety. #FragileX #prematureovarianinsufficiency #femalecarrier bit.ly/4khduUw
Investigació per la Síndrome X Fràgil Vols fer-te voluntari? Busquem voluntaris sans entre 18 i 55 anys per un assaig clínic a @hospitaldelmar @HMar_research Més informació👉 imim.es/estudis-clinic… 📩[email protected] #FXS #FragileX
Congratulations to MCB postdoc Vipendra Kumar, who was recently awarded a fellowship from @FRAXAresearch! Dr. Kumar and his PI, Dr. Nien-Pei Tsai (@TsaiNien) , are exploring possible therapeutics for #FragileX. #FXresearch
📢 We’re hiring a Health Technician! 🎯 Join a Phase IIa trial in Fragile X Syndrome 🔬 MARTrial Unit · PI: Dr. Ana M. Aldea 📌 MD degree + Clinical Trials experience required 🔗 researchmar.net/ofertes/en_det… #JobOffer #ClinicalResearch #FragileX #Pharmacology
Nova executed on key research & drug development milestones in 2022, setting the stage for a meaningful 2023. Our focus is on conducting the first-ever human study testing psilocybin therapy for #FragileX, the leading genetic cause of autism. bit.ly/3GkZyrf $NOVA $NMLSF
Congratulations to @EmoryGCTP student Emily Peery, one of four Randi J. Hagerman Summer Scholars studying #fragilex supported by @NFXFoundation working w/ @EmilyGAllen77
We thank everyone for the widespread use of #FragileX Premutation Associated Conditions (FXPAC) to describe issues affecting fragile x premutation carriers #grateful for support of researchers in using terminology which is positive, affirming & inclusive.bit.ly/41vnJfj
Great times at the Fragile X and Autism GRC with old and new friends. Exciting prospects ahead for science and patient care! 🌟 #FragileX #Autism @shcheglovitov
Medicare rebated genetic tests are now available to determine carrier status of #cysticfibrosis #spinalmuscularatrophy and #fragilex for anyone planning or in the early stages of pregnancy. Learn more about reproductive carrier screening here genetics.edu.au/SitePages/Repr… @ACRRM @RACGP
#FragileX syndrome is a genetic disorder that affects a person’s development, especially that person’s behavior and ability to learn. People with the syndrome may have no noticeable symptoms. Learn more: nichd.nih.gov/health/topics/… #FragileXAwarenessDay
Investigació per la #SíndromeXFràgil Vols fer-te voluntari? Busquem voluntaris sans entre 18 i 55 anys per un assaig clínic a @hospitaldelmar @HMar_research + INFO👉 imim.es/estudis-clinic… 📩👉[email protected] #FXS #FragileX
A family looks to understand fragile X syndrome and identify treatment targets to help their son and others like him: hubs.la/Q03jnT9j0 #RareDisease #FragileX
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