Meet a researcher: Hassina Zeriri
It’s not very often that we come across a researcher working on a project inspired by their own lived experience of a sight loss condition.
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It’s not very often that we come across a researcher working on a project inspired by their own lived experience of a sight loss condition.
Researchers in the Netherlands are developing a “retina-on-a-chip” that mimics the key layers of the human retina, offering a powerful new way to study inherited retinal diseases (IRDs) and test potential treatments using human cells.
Researchers from Ghent University have published a study that has the potential to transform inherited retinal disease (IRD) treatment development.
Retina UK is delighted to announce that it has awarded three new research grants worth more than £870,000.
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Inherited progressive sight loss is caused by a range of rare genetic conditions. We specialise in those which affect the retina.
Retina UK is delighted that the Scottish Medicines Consortium (SMC) has accepted the gene therapy Luxturna (voretigene neparvovec) for ongoing use by the NHS in Scotland.
We regularly make applications for grants to fund our information and support projects and have recently been successful in securing £12,000 from The National Lottery Community Fund.
Biotechnology company ProQR has announced encouraging results from its phase 1/2 clinical trial of an innovative treatment for sight loss caused by faults in a specific section of the USH2A gene.