#fragilexsyndrome search results
A new study implicates a deficiency of the ribosome quality control factor ASCC3 in #FragileXSyndrome and shows that using #CRISPR to activate the factor can treat cognitive and social deficits in a young mouse model. @StanfordPath scim.ag/3KRv4SF
#FragileXSyndrome is one of the most common causes of inherited intellectual disability. Discover how CDC and partners use data to support children and adolescents with fragile X syndrome, and their families: bit.ly/3PKKVTo #ThisIsFragileX
Today is World Fragile X Syndrome Day! What is it? A genetic disorder causing intellectual disabilities, behavioral and learning challenges, and various developmental characteristics. Let’s spread awareness and support understanding! #FragileXSyndrome #GeneticDisorders
Fragile X syndrome is a genetic condition that causes a range of developmental problems including learning disabilities and cognitive impairment. Usually, males are more severely affected by this disorder than females. #fragilexsyndrome
For people with developmental delays, keeping cues and explanations to a minimum helps reduce transition and processing time. For cleans today I told Owen he had 15 reps total—and I let him split up sets/reps himself. #fragilexsyndrome
Ohhhh this kid….. a hard fought battle during Esso minor hockey week…. Sadly a loss by shootout. Ty’s heard is broken. By my heart is so full…. To see so much emotion and passion from this kid. Grateful for hockey. Passion wins and beats #fragilexsyndrome
Follow along this July to learn more about #FragileX. #FragileXSyndrome is one of the most common causes of inherited intellectual disability.
Chadwick et al. utilized computational methods to identify two drugs to treat #fragileXsyndrome, with combined treatment reversing cognitive and behavioural deficits. @healx shorturl.at/gmyBW
Harmony Biosciences released top-line data results from their Phase 3 RECONNECT trial. While it's not the news we hoped for—the trial did not meet its endpoint—we appreciate the work Harmony and Zynerba did on this important potential treatment for #fragilexsyndrome.
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
July is #FragileXSyndromeAwarenessMonth. #FragileXSyndrome is a genetic disorder that affects a person’s development, particularly behaviour and ability to learn.
Recently awarded CAVALIERE O.M.R.I. - Knight of the Order of Merit of the Italian Republic. Grateful to all my mentors, students and colleagues for contributing to my academic journey. Honored by President Mattarella for my work on #FragileXSyndrome and #Autism. Thank you all!
Magdalena Dziembowska's research on local translation of synaptic proteins in fragile X syndrome is mind-blogging. Exciting news for potential new therapeutic approaches and a deeper understanding of the brain's inner workings. #neuroscience #fragileXsyndrome #brainresearch
CarolinaEast Medical Center is joining over 400 locations worldwide that are going teal on July 22 for #WorldFragileXDay, showing our support for individuals with #FragileXsyndrome. FXS is the most common inherited cause of autism and intellectual disabilities worldwide. 💚💙
Participating in a clinical trial? Check out this list of Dos and Don’ts from the @NFXFoundation #FragileXSyndrome #FXS fragilex.org/blog/dos-and-d…
#FragileXsyndrome (FXS) is a leading inherited cause of #autism, with no FDA-approved treatments. Spinogenix is working to change that—our therapy, SPG601, just received FDA Fast Track Designation, bringing hope to families. Learn more | spinogenix.com/july-is-fragil…. @TheArcUS
Alongside Shionogi, we’re spotlighting caregivers this #FragileXAwarenessMonth, as they have unique experiences. Jessie, mother of 5 with #FragileXSyndrome, shares her experience and what she hopes the future of care looks like. #FragileXawareness #FragileX
FXS may be complex, but research is paving the way for a brighter future! Discover the latest advancements in Fragile X Syndrome research here: studies.science37.com/the-future-of-… #FXSresearch #FragileXSyndrome
Fragile X syndrome (FXS) and autism are not the same, though there are similarities. Some individuals with Fragile X syndrome also have an autism diagnosis. Resource: hubs.ly/Q01WP68b0 #fragilex #fragilexsyndrome #nonprofit #fragilexawareness
A new study implicates a deficiency of the ribosome quality control factor ASCC3 in #FragileXSyndrome and shows that using #CRISPR to activate the factor can treat cognitive and social deficits in a young mouse model. @StanfordPath scim.ag/3KRv4SF
Today, Wednesday, Oct 8, from 4 to 5 pm, join our last @daanutsav "Everyone Can doodle and draw" session, where there are no rules, no pressure, just creativity, and the joy of letting your pen wander with young Varun Naren, living with #FragileXSyndrome. #joyofgiving #doodling
Harmony Biosciences released top-line data results from their Phase 3 RECONNECT trial. While it's not the news we hoped for—the trial did not meet its endpoint—we appreciate the work Harmony and Zynerba did on this important potential treatment for #fragilexsyndrome.
Servier to Acquire KER-0193 from Kaerus Bioscience Ltd. for ~$450M #servier #kaerusbioscience #fragilexsyndrome #bkchannelmodulator #pii #ker0193 #pharma pharmashots.com/27870/servier-…
pharmashots.com
Servier to Acquire KER-0193 from Kaerus Bioscience for ~$450M
Shots:Servier has entered into a definitive agreement with Kaerus Bioscience to acquire KER-0193, a potential treatment for Fragile X syndrome (FXS)As per the deal, Kaerus will receive a total of...
Govind Namdev on doing Fragile, 'I always feel a sense of social responsibility' yespunjab.com/?p=148458 #GovindNamdev #FragileShortFilm #FragileXSyndrome #SocialCauseCinema #RajneeshDuggall #MentalHealthAwareness #HereditaryDisorders #IndianShortFilms #AwarenessThroughCinema…
Govind Namdev on doing Fragile, 'I always feel a sense of social responsibility' yespunjab.com/?p=148458 #GovindNamdev #FragileShortFilm #FragileXSyndrome #SocialCauseCinema #RajneeshDuggall #MentalHealthAwareness #HereditaryDisorders #IndianShortFilms #AwarenessThroughCinema…
Unlocking hope for #FragileXSyndrome through promising research advancements! Learn more in our blog about the latest breakthroughs shaping a brighter future. studies.science37.com/the-future-of-…
New factsheets about #Fragilexsyndrome (full mutations) and Fragile X premutations are available now! These will help health professionals discuss Fragile X characteristics, testing and family implications with their patients. genetics.edu.au/SitePages/Frag… @FragileXAus @TheRACP @RACGP
Caregivers of individuals with Fragile X Syndrome face emotional exhaustion, mental fatigue, and physical stress—yet their experiences often go unheard. psychologs.com/caregiver-burn… #FragileXSyndrome #CaregiverBurnout #HiddenStruggles #NeurodivergentCare #ParentingChallenges
Hey educators! 👋 Join us July 27th for a FREE session on supporting preschoolers with Fragile X Syndrome. Let's make a difference together! 💡 Link in comments #SpecialNeedsSupport #FragileXSyndrome #TeacherTraining #EveryChildMatters #profgeedee
Our Fragile X caregiver stories created with Shionogi continue with Diane, mom to eight, four of whom live with #FragileXSyndrome. Diane shares what she loves most about her “beautiful chaos” and the ways their family creates happiness. #FragileX #FragileXawareness
Tonight, Spark is lighting up magenta to recognize the advancements made in Fragile X syndrome research! 💖 @FragileXCanada #fragilexsyndrome
Sharad Malhotra graced the red carpet screening of the film on Fragile X Syndrome #SharadMalhotra #RedCarpetElegance #FragileXSyndrome #CinemaWithCause #sbbxtra #saasbahuaurbetiyaan
CarolinaEast Medical Center is joining over 400 locations worldwide that are going teal on July 22 for #WorldFragileXDay, showing our support for individuals with #FragileXsyndrome. FXS is the most common inherited cause of autism and intellectual disabilities worldwide. 💚💙
Today is World Fragile X Day. Fragile X syndrome (FXS) is the most common form of inherited developmental disability worldwide. There is no cure for FXS, but an early diagnosis with a genetic blood test can still help. #WorldFragileXDay #FragileXSyndrome storymd.com/journal/4m8gyb…
Fragile X Syndrome: Small Gene, Big Impact! Read more in our blog! theknowhow.ae/fragile-x-awar… Contact our global experts for trusted advice.. theknowhow.ae #Fragile-X-AwarenessDay #FragileXSyndrome #FMR1 #SpecialNeedsAwareness #independent_second_opinion #medical #TKH
We’re proud to feature Kara, an FXS mom and member of our board of directors, in the next inspirational caregiver video, developed with Shionogi. 👉Hear how self-advocacy has defined their family. hubs.ly/Q03x98yq0 #FragileX #FragileXsyndrome #FragileXawareness
Alongside Shionogi, we’re spotlighting caregivers this #FragileXAwarenessMonth, as they have unique experiences. Jessie, mother of 5 with #FragileXSyndrome, shares her experience and what she hopes the future of care looks like. #FragileXawareness #FragileX
psychologs.com/fragile-x-synd… #FragileX #FragileXSyndrome #FXS #NeurodevelopmentalDisorders #GeneticAwareness #AutismAndFragileX
Join us and Shionogi in celebrating caregivers, including Rene, this #FragileXAwarenessMonth. Together with parents like Rene, we’re working to increase understanding about living with #FragileXSyndrome. #FragileXawareness #FragileX
A new study implicates a deficiency of the ribosome quality control factor ASCC3 in #FragileXSyndrome and shows that using #CRISPR to activate the factor can treat cognitive and social deficits in a young mouse model. @StanfordPath scim.ag/3KRv4SF
#FragileXSyndrome is one of the most common causes of inherited intellectual disability. Discover how CDC and partners use data to support children and adolescents with fragile X syndrome, and their families: bit.ly/3PKKVTo #ThisIsFragileX
Chadwick et al. utilized computational methods to identify two drugs to treat #fragileXsyndrome, with combined treatment reversing cognitive and behavioural deficits. @healx shorturl.at/gmyBW
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
Today, Wednesday, Oct 8, from 4 to 5 pm, join our last @daanutsav "Everyone Can doodle and draw" session, where there are no rules, no pressure, just creativity, and the joy of letting your pen wander with young Varun Naren, living with #FragileXSyndrome. #joyofgiving #doodling
Ikigai Goa is commemorating World Fragile X Day by lighting up teal! Come and join us in celebrating the power of collaboration to create positive change.✨ Dm us to know more! #fragilexsyndrome #fragilexindia #worldfragilexday #lightup #fragilex2023 #fragilexmonth
Thank you @TajMahalMumbai for always supporting and raising awareness for #FragileXSyndrome. Yesterday, Taj Mahal Tower illuminated in a stunning shade of teal to shine a light on Fragile X Syndrome and raise awareness on #WorldFragileXDay! #FragileXAwareness #TajMahalTower
Thank you, Apollo Children's Hospital Chennai, for illuminating hope and raising #awareness about #FragileXSyndrome, a genetic condition affecting countless lives - together, we can make a positive impact on those living with Fragile X Syndrome.💙 #WorldFragileXDay
CarolinaEast Medical Center is joining over 400 locations worldwide that are going teal on July 22 for #WorldFragileXDay, showing our support for individuals with #FragileXsyndrome. FXS is the most common inherited cause of autism and intellectual disabilities worldwide. 💚💙
Follow along this July to learn more about #FragileX. #FragileXSyndrome is one of the most common causes of inherited intellectual disability.
Fragile X syndrome (FXS) and autism are not the same, though there are similarities. Some individuals with Fragile X syndrome also have an autism diagnosis. Resource: hubs.ly/Q01WP68b0 #fragilex #fragilexsyndrome #nonprofit #fragilexawareness
Atal Setu Bridge in Goa Stands for Fragile X Syndrome. As the bridge lights up in teal, it symbolizes the commitment to spread awareness, foster a supportive environment, and promote inclusion. #fragilexsyndrome #fragilexawareness #worldfragilexday
🧠 Drs. Dionne, Sabatié, and Laurent at @USherbrooke provides an overview of how 3D brain organoids have been used to investigate various neurodevelopmental disorders, including #FragileXSyndrome and Rett syndrome, and elucidate their pathophysiology. bit.ly/3AXoWDx
Fragile X is an “X-linked” condition, which means the FMR1 gene is on the X chromosome. Both males and females can have Fragile X syndrome or the Fragile X premutation. Resource: hubs.ly/Q01WNlCR0 #fragilex #fragilexsyndrome #fragilexawareness
Participating in a clinical trial? Check out this list of Dos and Don’ts from the @NFXFoundation #FragileXSyndrome #FXS fragilex.org/blog/dos-and-d…
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
Today is World Fragile X Syndrome Day! What is it? A genetic disorder causing intellectual disabilities, behavioral and learning challenges, and various developmental characteristics. Let’s spread awareness and support understanding! #FragileXSyndrome #GeneticDisorders
For people with developmental delays, keeping cues and explanations to a minimum helps reduce transition and processing time. For cleans today I told Owen he had 15 reps total—and I let him split up sets/reps himself. #fragilexsyndrome
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