Rob Collin (Dept. of Human Genetics) and Carel Hoyng (Dept. of Ophthalmology), theme Sensory disorders, have received a prestigious award from the Translational Research Acceleration Program of the Foundation Fighting Blindness USA.
This program is dedicated to further translate innovative therapeutic proof-of-concept to patients with retinal disease. With this three-year award, Rob and Carel, together with their team of collaborators, aim to bring antisense oligonucleotide-based splicing modulation therapy for patients with Stargardt disease up to the phase of clinical testing.
Related news items
Surprisingly dominant cause underlying type I congenital defect of glycosylation
21 October 2021 Alex Garanto, Melissa Bärenfänger, Mirian Janssen, and Dirk Lefeber published a new study, identifying a surprisingly dominant genetic cause underlying type I congenital defect of glycosylation with neuromusculoskeletal phenotypes. read moreTreatment of brain diseases at risk if neuroscientists can no longer conduct their research
5 August 2021 In order to treat brain diseases such as depression, Alzheimer's or ADHD, more research into the brain is needed. read moreRetina-on-chip modeling and treating eye diseases in a dish
10 June 2021Alex Garanto, together with Anneke den Hollander and Andries van der Meer (UTwente) have received 1,17M€ to develop a retina-on-chip model to improve our understanding in eye diseases and to develop treatments against them.
read more