CORDIS Project
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This project investigates the role of the CRB1 gene in retinal diseases, focusing on its function in cell interactions that affect vision. Using genetic models, the research aims to develop gene therapy techniques to restore function and potentially cure conditions like retinitis pigmentosa.
Mutations in the Crumbs homologue 1 (CRB1) gene cause photoreceptor degeneration resulting in progressive retinitis pigmentosa (RP) or Leber congenital amaurosis (LCA), which both currently are untreatable blinding diseases. CRB1 is localized in Mueller glia cells at a subapical region (SAR) adjacent to adherens junctions between Mueller glia cells and photoreceptors.
Loss of CRB1 function results in loss of adhesion between Mueller glia cells and photoreceptors.
This ultimately results in the d…
KONINKLIJKE NEDERLANDSE AKADEMIE VAN WETENSCHAPPEN - KNAW
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Netherlands, AMSTERDAM
Type: Company (for-profit)
Activity type: Private for-profit entities (excluding Higher or Secondary Education Establishments)
Germany, Tuebingen
Type: University / higher education
Activity type: Higher or Secondary Education Establishments
SME: No
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