Where? Belgium, The Netherlands, Germany, Italy, France, Spain and Czech Republic. Who? Talented PhD candidates who are passionate about vision research and eager to explore interdisciplinary and intersectoral PhD opportunities.

More info on: progret.eu @Euraxess @UGent Radboudumc Universität Tübingen Tigem Telethon INM_Montpellier Centro Andaluz de Biología del Desarrollo Charles University Evotec Elfride De Baere Frauke Coppieters Rob Collin Susanne Roosing Pietro De Angeli Sandro Banfi Lab Vision_INM Juan Tena Juan R. Martinez-Morales

Vision_INM supports #RareDiseaseDay Working daily for and alongside patients affected with rare inherited retinal disorders

Reminder for prospective PhD candidates, applications for our Marie Skłodowska-Curie Doctoral Network (2024-2027) named ProgRET closes Friday 15th March. All information on the program and application process can be found here: progret.eu/apply.html @Euroaxess #IRD #Retina

We are hosting the 4th International #Choroideremia Research Symposium on 17th May and CHM patient information day on 18th May 2024. All patients welcome to attend. Please contact [email protected] for further information. CHM @CureCHM #IRDs #Retina

Correction to contact address: [email protected]

Dual CRALBP isoforms unveiled: iPSC-derived retinal modelling and AAV2/5-RLBP1 gene transfer raise considerations for effective therapy biorxiv.org/cgi/content/sh… #biorxiv_molbio

We are happy to report that our latest article concerning #RLBP1, #IRDs and #gene therapy is available on BioRxiv. A collaboration with the Université de Lausanne and NIH.

Very much impressed by the professionalism, enthusiasm, knowledge and warm interactions of CureCHM Big thank you Viki Vision_INM and INM_Montpellier colleagiues for the invitation, congrats on this top scientific and patient meeting 👌

USH2A variants causing retinitis pigmentosa or Usher syndrome provoke differential retinal phenotypes in disease-specific organoids hubs.li/Q02vx0Cr0 Human Genetics and Genomics Advances paper hand-picked by our editors Vision_INM INM_Montpellier ASHG

Absolutely thrilled that our article on #USH2A retinal #organoids published in Human Genetics and Genomics Advances was hand-picked by the editors of Cell Press

Nous recrutons un(e) IE pour travailler sur l’édition génomique des iPSC. Pour plus de détails et afin de candidater, consulter : umontpellier.nous-recrutons.fr/poste/q0npkp4p…

Just finished a fantastic ISER meeting here in Buenos Aires, Argentina. Presented our work on #USH2A- and #RLBP1-associated IRDs. Heard a lot of exciting science. Congratulations to the organisers.

I am thrilled to announce that our latest article concerning #RLBP1, associated #IRD models, and #AAV-mediated gene replacement therapy is available online in Molecular Therapy. A big thank you to everyone involved. kwnsfk27.r.eu-west-1.awstrack.me/L0/https:%2F%2…

I am proud to announce that we made the cover of the December issue of Molecular Therapy with an image of CRALBP expression in a human #retinal #organoid accompanying our published paper on #RLBP1. Congratulations H. Boukhaddaoiu for imaging and N. Erkilic for differentiation.

The new year has just begun and we already have novel RNU breakthroughs to share, this time in the eye genetics field: De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa medrxiv.org/content/10.110…