Top Tweets for #Mef2c
Health : శస్త్రచికిత్స లేకుండానే.. గుండె కణాల పునరుత్పత్తి సాధ్యమేనా?
#HeartRegeneration #HeartAttack #MedicalBreakthrough #Ascl1 #Mef2c #ScarTissue #CellReprogramming #UNC #UNCMedicine
https://t.co/3aS7HcSb7c
Health : శస్త్రచికిత్స లేకుండానే.. గుండె కణాల పునరుత్పత్తి సాధ్యమేనా?
#HeartRegeneration #HeartAttack #MedicalBreakthrough #Ascl1 #Mef2c #ScarTissue #CellReprogramming #UNC #UNCMedicine #Cardiology #HeartRepair #NoSurgery #SelfRepair #InjectionTherapy #HeartHealth #ScienceNews #HealthNews #RegenerativeMedicine #HeartFailure #Research
https://t.co/4tzC7RL57N
Hoy 14 de mayo es el Día de Concienciación del Síndrome #MEF2C
Compartimos el vídeo de @AsociacionMEF2C para dar visibilidad a las personas que conviven con esta enfermedad y a sus familias #DiaConcienciacionMEF2C #MEF2CAwarenessDay #EnfermedadesRaras
https://t.co/zKSSxtUaYe
De uitslag...of ik het confronterend vond vroegen ze. Nee niet echt, het was precies wat ik van tevoren had gezegd. Tussen de 7 en 9 maanden max. We gaan zien hoe ver die kleine het gaat schoppen🩵 #mef2c
Goeiemorgen
Oudste was om 4.15 wakker en kwam bij mij liggen...niet meer geslapen🙈
Straks meekijken met ontwikkelingsonderzoek van de jongste, ben benieuwd🥹
Gelukkig mocht ik koffie pakken🥰
Fijne vrijdag🤗
Congratulations to our @WCMEnglanderIPM colleague Dr. M. Elizabeth Ross on her new $1.1 million grant from the Rare Birds Foundation to study a neurodevelopmental disorder called #MEF2C Haploinsufficiency syndrome (#MCHS).
https://t.co/73GcX9G0Fg
Carlos, padre de Elian, con autismo y síndrome #MEF2C: "Cuidar de una persona tan dependiente es agotador" #EnfermedadesRaras https://t.co/KbdIkD0rpR por @mercheborja en @20m #Capaces
💙 MEF2C Awareness Day – May 14th 💙
On May 14th, light a candle, wear blue, and put blue lights on display to show your support for the MEF2C community! Together, we can make a difference. 🧑🤝🧑 #MEF2CAwareness #MEF2C#MEF2CAwareness #MEF2C
🌟 It is Rare Disease Day 2025! 🌟
Today, we celebrate our beloved MEF2C warriors and raise awareness about MEF2C Haploinsufficiency.
Happy #RareDiseaseDay2025 💙
#MEF2C #Awareness #Support #Hope #MCHS #RareDiseaseDay2025 @muscmind @ChristophWCowan @RareRevolution
💛 The @S_Searchlight team attended the #MEF2C conference hosted by the US MEF2C Foundation. Here’s what we accomplished: Dr. @WendyKChung shared updates on #MEF2C participant data, we collected blood samples & answered research questions. Proud to support advocacy groups! 🤝
It is an honor to be part of this distinguished panel. I would like to thank the US MEF2C Foundation for the kind invitation.
@BostonChildrens @harvardmed
We are excited to share the result of a Nursery fundraiser event held to celebrate one of our little Mefties! They managed to raise £552! Wow! We are beyond grateful! #wegotthis #findacure #MEF2C #theskyisthelimit #meftiesrock #tinywarriors #raredisease @BarncliffeDaynursery
@Mef2cFoundation in partnership with @MedUnivSC is thrilled to announce the launch of Pathways To Hope For MEF2C Haploinsufficiency Syndrome, a multi-year program aimed at developing therapeutics .
https://t.co/JGogqtXagF
#MEF2C #Haploinsufficiency
#autism #AutismAwareness #Mef2c
New gene for autism discovered!
#https://www.nature.com/articles/s41593-023-01499-x
In our @hug_leipzig JC today @ahtingsi follwed up #ESHG2023 w/ an overview on 5' UTRs: constraint, uORFs, oORFs, #MEF2C, variant classification etc. Great JC + awesome work by @nickywhiffin 👌 👇
https://t.co/8RQ395i0eM
https://t.co/9srO98WRJt
https://t.co/AGLqdLNH0W
Our daughter was recently diagnosed with a rare genetic condition MEF2C. We are asking for support! Please share, donate (QR code in picture) or buy a shirt- link below! Continue the promising research @MedUnivSC #MEF2C #hope
Merch to support: https://t.co/8wpRNV79Ep
Beyond the brain: A link between hearing loss and an autism spectrum disorder
Learn More: https://t.co/IVumt2xXhR
@MedUnivSC @SfNJournals
#MUSC #ASD #glia #MEF2C #autism #meded #eMednews
Casi una veintena de asociaciones sin ánimo de lucro se presentarán en la Feria Solidaria de #Castellón #solidarea el 11 de diciembre.
En @canolopera queremos dar a conocer la ilusión y esperanza que ponen todas ellas en su trabajo altruista.
Os presentamos a la Asociación #MEF2C
Desde que se creó esta asociación el número de familias ha crecido. Son pequeños y pocos pero valientes. Cada día se superan en sus límites. Y su sonrisa vale millones.¿Nos ayudas a compartir?
#MEF2C #LoImposibleSoloCuestaMas
Very educational thread by @nickywhiffin explaining how de novo 5' non-coding variants can cause NDD. Love the clear slides! Variants can be found in exome data. #MEF2C gene prominent here, due to factors explained, but likely not alone. Another variant upstream of #STXBP1 💡👇
Super excited to share our new preprint!
Using exome sequencing data from ~10k patients with severe developmental disorders (DD) from the DDD project we decipher 3 distinct mechanisms through which ‘non-coding’ variants cause MEF2C loss-of-function https://t.co/KGK8X651Fh 1/10
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