Top Tweets for #FoxP2
The latest work from Technische Universität Dresden and @Uni_of_Kufa by Dr. Ali Al-Fatlawi and his team is now featured in FBS!
Full article👉: https://t.co/BGE2xvcUnA
💡 What hidden genetic interactions drive #DevelopmentalLanguageDisorders?
#Genomics #Neurodevelopment #FOXP2
Els humans moderns presentem una versió del gen #FOXP2 amb dues mutacions que no es troben en els ximpanzés, i que semblen estar relacionades amb la capacitat de parla. Experiments amb animals, com ratolins modificats genèticament amb la versió humana del FOXP2, (VI-VIII)
Però la parla no depèn només de l’anatomia; també hi juga un paper fonamental la genètica. En aquest sentit, el gen #FOXP2 està implicat en el desenvolupament de les àrees del cervell relacionades amb el control motor necessari per a la parla i el llenguatge. (V-VIII)
🤖💬 Tens curiositat sobre com el gen FOXP2 està revolucionant l'enginyeria de prompting avançat?
💡 Parla amb el nostre My GPT aquí: https://t.co/SZgnhqSjYp
🌐 Llegeix l'article complet aquí: https://t.co/QlSvfMLHvz
#FOXP2 #IA #EnginyeriaDePrompting #innovacion
🧬 Què tenen en comú el gen FOXP2 i la IA avançada? Descobreix com aquest gen, clau en el desenvolupament del llenguatge, està inspirant noves tècniques en l’enginyeria de prompts per models de llenguatge.
#FOXP2 #Neurociència #EnginyeriaDePrompts
🔗 https://t.co/QlSvfMLHvz
Excellent work by
@LabNowakowski and collaborators, using thalamocortical #organoids to model in vitro the 22q11.2 microdeletion associated with neuropsychiatric disorders, uncovering a role for #FOXP2 🧫🧬🧠 @CellStemCell
https://t.co/SU7sFteUiF
New review of #genetic causes of childhood #apraxia of speech #CAS out! Since #FOXP2 in 2001, a further 36 genes have been linked to CAS, concluding 1/3 have a genetic cause for their severe speech disorder. @drdavidamor @ingridscheffer Morgan & Hildebrand https://t.co/HFfkpREsMB
Looking forward to Rare Disease Day on 29th Feb and supporting #showyourstripes. Will you?
My daughter has a rare genetic condition #FOXP2 a symptom of which is Childhood Apraxia of Speech #CAS
Did you know there are approx 10,000 rare conditions.
1:17 people are affected.
📰New #FactSheet on #FOXP2-related speech language disorder created w/ families now available on our website!⬇️
https://t.co/qN3HG97cwN
🗣️We are also recruiting for a FOXP2-SLD #speech & #language study.
📩Email [email protected] for info or see the flyer below ⬇️
Performance Partidos Políticos nas Redes Sociais
https://t.co/UpQg76719E
#foxp2 #partidos #politica @CostaJoao1 @ruidavid @namaraujo @_CDSPP @CDUPCPPEV @partidochega @BlocoDeEsquerda @LiberalPT @LivrePT @Partido_PAN @pcp_pt @PNR @psocialista @ppdpsd
Very interesting new work from the group of @alaurenoconnell @LOB_SU, looking at motor communication in amphibians, pointing to “generalizable function of #FoxP2 in social-motor coordination across terrestrial vertebrates”.
https://t.co/6Ox5AtYSfu
Mutations of a gene called Foxp2 have been linked to a speech disorder called apraxia that makes it difficult to produce sequences of sound. A new study sheds light on how this gene controls the ability to produce speech. @mcgovernmit
Read more: https://t.co/xAfXNLybbf
Calling all #SLPeeps & #SLT2B - interested in knowing what it is like to be a family living with FOXP2 and verbal dyspraxia?
Then check out this @M4RareDiseases' podcast with @pamslater26 🔽.
#FOXP2 #VerbalDyspraxia #CAS #DVD #GeneticCondition #RareDisease
We're number 8 in the @_feedspot 25 Best UK Disease Podcasts! Wahoo! For this week's podcast, Melissa speaks with Pam Slater, a devoted rare parent and verbal dyspraxia advocate who has a daughter with FOXP2 > https://t.co/dNZMbJTi32
Listened to the podcast @pamslater26 you were amazing.
Such powerful experience, thank you for all you do.
Really hope #slt #peadeatricdrs listen 🙏
#verbaldyspraxia #CAS #FOXP2 #SLT2b
We're number 8 in the @_feedspot 25 Best UK Disease Podcasts! Wahoo! For this week's podcast, Melissa speaks with Pam Slater, a devoted rare parent and verbal dyspraxia advocate who has a daughter with FOXP2 > https://t.co/dNZMbJTi32
@GeneticAll_UK @CSDRNetwork @DYSPRAXIAFDTN @SpeechAndLangUK @RCSLTpolicy @PeterDJust
Please do watch this fantastic video from @M4RareDiseases
This perfectly explains the journey with a rare disease, which is also our journey.
#FOXP2 #CAS #Verbaldyspraxia
#raredisease
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