Yesterday, Stichting Kind Beter welcomed the HOPE team to Mountain Design to reflect on the first year and a half of the project. Within HOPE, we are developing an innovative platform using brain organoids, enabling existing and new medicines to be tested on a large scale for FOXP1 syndrome and, ultimately, for other rare genetic […]
The International FOXP1 conference was held on June 19 and 20 in the Leonardo Hotel in Ijmuiden, organized by Stichting Kind Beter and the International FOXP1 Foundation. The event welcomed more than 200 attendees from around the globe, including 75 families, 30 researchers, 49 individuals with FOXP1 syndrome, and more than 30 siblings, for […]
On 1st of June 2021 we started a new research project on FOXP1 syndrome. To do most of the work in this project Elena Daoutsali came back to us, after she left when her PhD period was finished. Good to have her back! Forkhead-box protein P1 (FOXP1) is part of the forkhead-box family of transcription […]