"La síndrome de Rett és una malaltia molt devastadora"
Coincidint amb el Dia Mundial de les Malalties Rares conversem amb la doctora Sònia Guil de @CarrerasIJC, que juntament amb el seu equip ha identificat la molècula que controla la patogènesi de la síndrome.@bdncom#Badalona
📻 🔬@BadalonaMati de @bdncom commemora el Dia de les Malalties Minoritàries amb una entrevista a la investigadora Sònia Guil (@GroupGuil) sobre els seus últims avenços en la investigació del Síndrome de Rett 🧬👶
¿Vols saber més? 👉 https://t.co/BYywbxVeIP
📺🔬 La notícia del @GroupGuil sobre els últims avenços en la #SindromedeRett a @rtvenoticias
La investigació és el primer pas cap a la cura 💪
Si vols saber-ne més, t'ho expliquem aquí 👉 https://t.co/DVaEzyCX6R
💜🌍 Today is Rare Disease Day! 🌍💜
Together, we stand with the 300 million people worldwide living with rare diseases. In uniting on this day we can raise awareness, advocate for change, and promote a more equitable future! ⚖️
Learn more: https://t.co/AUKfGZJLJB
🧬👶 #RettSyndrome is a rare genetic disease affecting 1 in 10,000 newborn girls
💙 On the #RareDiseaseDay, we focus on the latest work by @GroupGuil, devoted to study this syndrome with the aim to find new therapeutical approaches.🔬💪
What's new on their research? 🧵👇
Different languages, one mission: curing leukemia 💪
🔬🌍 At the IJC, researchers from all over the world come together through science. On #InternationalMotherTongueDay, we are committed to collaborative, inclusive and multicultural research 🫂
💙 Together we are unstoppable!
❕🔬 A step closer to understanding #RettSyndrome!
📢 New research by @GroupGuil@con_edi shows that MeCP2 loss disrupts the long non-coding RNA NEAT1, impairing cellular maintenance. 🧬 These findings open doors to potential new therapies. 🙌
Read more 👉 https://t.co/OLcohNV6SK
🙌 Hey PhD!
📢 @NuclearDn aims to train 16 Doctoral Candidates 👨🔬 in the emerging field of metabolic regulation of genome function and cell identity 🧬🧫
Take a look 👀 https://t.co/wpDbATJ6pV
📅 Apply until 17th March
🔬 @MarcusBuschbeck
🇪🇺 @MSCActions @EU_Commission
📌Our latest study on #RettSyndrome is out on @NAR_Open! Huge congratulations to the team for their hard work and dedication. https://t.co/T4xzWiahHC in this study we show how autophagy is affected by the lack of the #ncRNA NEAT1🧵
Our study highlights NEAT1 as a key downstream mediator of MECP2, linking it to protein metabolism, autophagy, & neuronal maturation. ⬇️Don't miss it! ⬇️https://t.co/T4xzWiahHC
💫🔬 Research saves lives
Today, on #WorldCancerDay ❤️🩹, we honor the brave individuals fighting against this disease and all the dedicated researchers working tirelessly to making cancer a curable disease.
We will remain unstoppable until we find a cure! 💪
🎉New Doctor in the House! 🎉
A huge congratulations to Deepthi on successfully defending her PhD thesis on the fascinating role of RPSAP52 in cancer and the therapeutic potential of GapMERS. 🧬💪Wishing you all the best in your next adventure! 🌟#PhDDefense#CancerResearch#STEM
@waltzing_piglet 🗨️Sònia Guil, @GroupGuil: "Reconocer el trabajo de estos investigadores es poner de relieve lo esencial de la investigación básica (incluyendo organismos modelos no humanos), lo cual muchas veces es poco valorado por las decisiones en política científica"
https://t.co/dDBiicDdr4