@SEUR_responde tengo un envío programado para hoy, estoy en casa y recibo un mail diciendo que no lo entregan por ausencia. No han venido a entregar nada y dicen que es por mí ausencia??
📢 Researchers from @CIMA_unav have developed a novel combination of radiotherapy and immunotherapy that improves antitumor response in animal models of #breastcancer. Read the full story ⬇️ https://t.co/AcuH8k7AUw
We are hiring!!!
Thanks to the support of @WorldwideCancer we are hiring a lab assistant/technician to join the lab for an exciting project aiming to maximize immune cell recruitment into tumors. See offer below on how to apply.
🇫🇷Depuis 2007, @FondationLOreal s'engage avec l'@UNESCO et @AcadSciences pour accélérer les carrières des jeunes chercheuses. Les candidatures pour le Prix Jeunes Talents France 2025 L'Oréal-UNESCO sont ouvertes. Candidatez avant le 26 février 👉 https://t.co/AWJd4qnWwD #FWIS2025
🚨 Job Alert! Please RT 🙏
@ERC_Research-funded postdoc position in our team (up to 3 years) to explore dosage compensation during mouse development 🧬🐭 Join a dynamic, collaborative community @CbiToulouse!
👉 See how to apply here: https://t.co/h3u05G6wgs
📢 Tomorrow begins the RNA Symposium at Cima! International experts will discuss the latest advances in RNA-based therapies, genetic regulations and more. 🧬 Don't miss out, keep an eye on updates coming soon!
La fête de la Science 2024 #FDS2024 commence aujourd'hui.
F&S participe à de nombreuses actions à retrouver dans l'Agenda :
https://t.co/Hez9KQ3HCA
Ce soir 4 octobre : Nuit des chercheur·e·s à Toulouse.
5, 8 et 13 octobre : XXelles et Science Pluri'elles en région PACA
Sammy Basso @SammyBasso, one of the most remarkable people to share our world, passed away last night from complications associated with progeria, the ultra-rare ‘rapid aging’ genetic disease Sammy both suffered from and transcended.
Sammy realized that a base editing treatment that corrects the root cause of progeria and rescues animals with the disease would likely not be ready in time for him, but worked tirelessly every day to bring this potential treatment to other patients so they might have a better life.
Sammy made the most of every day, living with great purpose, intention, and joy that was inspiring, infectious, and reminded us of what’s truly important.
We miss him terribly. 😔
https://t.co/tdk0TOIi7N
https://t.co/iHDDU9gHfF
Esta compañía está usando mi nombre y foto sin mi autorización para propaganda engañosa. Nunca he contribuido a este estudio ni soy parasitóloga como dicen
https://t.co/dQsqdzmCQ7
📢 Exciting News! The @EU_Commission has granted Orphan Drug Designation (#ODD) to VTX-806, @Vivet_tx's gene therapy product for the treatment of cerebrotendinous xanthomatosis (#CTX), a rare #neurodegenerativedisease in patients. Link to 🗞️PR in comments below 👇
Finally got my hands on this book!
It explains social & gender inequalities observed in the field of Mathematics:
Why are women underrepresented in Math? How can we encourage them? How to feel less alone as a female student who loves Math?
@OlgaPa_Ro@cle_perronnet @ClaireMARC5
Gran discurso de la reina Letizia en el marco del día de las enfermedades raras. Los pacientes y sus familias necesitan apoyo. Los médicos tratantes y los investigadores necesitamos más inversión para avanzar en la búsqueda de un tratamiento efectivo para estas enfermedades.
El discurso de la reina Letizia pidiendo acceso en equidad a tratamientos de enfermedades raras: "Otro año más buscando que todos nos impliquemos y que las administraciones sigan con su compromiso con las demandas históricas de vuestro colectivo" https://t.co/eqZGlOIGrb
Hoy, último día de febrero, desde el Cima nos sumamos a las acciones de concienciación por el Día Mundial de las #EnfermedadesRaras.
Por este motivo, esta noche, nuestro edificio se iluminará con los colores del #RareDiseaseDay.
💚🩷💜💙
Today, on #29F Rare Disease Day, we join the global community to raise awareness and support those battling these conditions. Together, we can make a difference in research and treatment! @CIMA_unav#RareDiseaseDay#ShowYourStripes
February 29 is #RareDiseaseDay, the rarest day of the year!! Show your stripes for rare diseases awareness. There is still so much progress to be done to find an effective treatment for most of these diseases.
El 29 de febrero es el #DíaMundialEnfermedadesRaras. Aunque se llaman así porque son poco frecuentes, se estima que hay más de 7.000 y que afectan a más 300 millones de personas en el mundo. @ggasegui, del @CIMA_unav, nos acerca #En5Tuits a los avances para su tratamiento.
On the occasion of Rare Disease Day, an informative meeting between specialists and patients on polycystic kidney disease will take place next Thursday 29. 19.00, Cima main hall. Don't miss it!