Top Tweets for #Fmr1
Fragile X Syndrome: Small Gene, Big Impact!
Read more in our blog! https://t.co/nxkJMTmyeX
Contact our global experts for trusted advice.. https://t.co/bJug6ozuvx
#Fragile-X-AwarenessDay #FragileXSyndrome #FMR1 #SpecialNeedsAwareness #independent_second_opinion #medical #TKH
No link between #FMR1 premutation status and ADHD or anxiety. #FragileX #prematureovarianinsufficiency #femalecarrier https://t.co/RHBa5FpWYr
I'll be attending @IrishSocGen next week with @KaurKirren, visit our booth to find out more about our new @pacbio #PureTarget gene panel for 20 repeat expansion loci relevant to neurodegenerative disease
#FMR1 #C9orf72 #RFC1 #ataxia
https://t.co/4rj3lBVi1Q
New research unveils insights into the delicate balance of executive function.
Loss in this area may be an early sign of FXTAS, a neurodegenerative condition.
Know more: https://t.co/HuXaMBBsc2
Credit: @UCDavisHealth
#FXTAS #Parkinsons #NeuroResearch #FMR1 #meded #eMednews
🌈This review delves into the latest treatments and molecular interventions for #FXS and the role of #FMR1 gene mutations, permutations, and potential treatments to improve the lives of those affected...
📎https://t.co/iAKXVdMIdf
#FXSResearch
#Neurobiology
#HopeForFXS
Over 1/3 women with an FMR1 premutation have mental health impacts, and the association is highly related to socioeconomic and physical health factors #GIMOpen #FXPOI #FXTAS #FMR1 #premutation https://t.co/CV2VzJop7W
We are all carriers of gene mutations, many of which are silent, you may be a carrier of the FMR1 mutation but not show the effects of FXS. Genetic testing is the key to unlocking this knowledge! #Genetictesting #FMR1
Enjoying chatting with #FTD researchers and clinicians from around the world about #FMR1 related #FXTAS as a potentially important mimic/phenocopy of FTD (with gratitude to my patient and their family for letting us share their story!) #ISFTD2022 @PennFTDCenter
#FragileXSyndrome is one of the most widely known #genetic causes for intellectual disability. The gene responsible is #FMR1. Embrace genetics-informed #patient care with GeneDx testing: https://t.co/WAWAym497e. #WorldFragileXDay
(1/2) The silencing of the #FMR1 gene & consequent lack of FMRP protein is the major contribution to the pathophysiology of #FragileXSyndrome.
#FragileX #FXS #WorldFragileXDay #FragileXAwarenessDay #FXResearch #FragileXAwareness
(1/2) #FragileXSyndrome is the leading monogenic cause of #autism. With the discovery of the #FMR1 gene silencing as the cause of #FragileX, we've seen extensive investigations both in pathophysiological & clinical aspects.
#FXS #WorldFragileXDay #FragileXAwarenessDay #BioTech
Rethinking genetic disease https://t.co/M4FZ42KGrR #genetics #genomics #FMR1
Nice review! Relevance beyond just #FragileX: #Haploinsufficiency
“When doctors listen closely to their patients, w enough care, they are not just being kind. They are part of a process of discovery.”
The #NationalFragileXFoundation recently shared some exciting news: The #FMR1Gene has officially been renamed. #FMR1 now stands for #FragileX messenger ribonucleoprotein 1, removing the reference to terminology signifying intellectual #disability.
https://t.co/n0XmD2ofWv
Happy #DNADay2022 y’all to those who celebrate!
To commemorate today, I’m happy to report the #FMR1 gene has been renamed to Fragile X Messenger Ribonucleoprotein 1.
#FragileX #GeneChat
https://t.co/SfOdg11ndN
.@LouveauAntoine meningeal #lymphatics in #autismspectrum have ⬇️ drainage @ASNeurochem @clevelandclinic #fmr1 #fragilex #tightjunction #VEGFc #ASN2022
The #Fmr1 gene, which is mutated in #FragileX syndrome, is the focus of Dr. Ethan Greenblatt’s (@VanCityFlyGuy) work as an #EarlyCareer investigator at @UBCLifeSciences.
🪰 Learn more about his #Drosophila #oocyte model to study translational regulation: https://t.co/Y3hUWNjE67
"The Use of “#Retardation” in #FRAXA, #FMRP, #FMR1 and Other #Designations" from Herring et al.
#cellsmdpi #cellbiology #opinion @DrKirstenJ @jojohjhj
Full text: https://t.co/JeW3UhB4cs
Congratulations to Emmanuel Marquez-Legorreta and the lab for this beautiful study that looked at how a mutation in the #fmr1 gene affects larval zebrafish habituation to repeated visual looming stimuli!
Hope you enjoy this veteran of the preprint world, out today in @NatureComms. Our brain-wide cellular-resolution calcium imaging shows the #zebrafish visual escape network, how it changes during habituation, and how this process is slower in fmr1 mutants. https://t.co/KEbVvx3n4W
A team of @UCRiverside #SchoolofMedicine researchers, led by Iryna Ethell @Ethelliryna and Ph.D. student Maham Rais, have discovered that reactivation of the #Fmr1 gene could be a treatment for #FragileXsyndrome #autism
https://t.co/edWyrFBNMM
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