Genetics

Researcher builds new model to examine Usher syndrome

Usher syndrome, a rare inherited genetic disease, is a leading cause of combined deafness and blindness with type 2A (USH2A) being the most common form. USH2A, caused by mutations in the USH2A gene, can include hearing loss ...

Genetics

3D map reveals DNA organization within human retina cells

National Eye Institute researchers mapped the organization of human retinal cell chromatin, the fibers that package 3 billion nucleotide-long DNA molecules into compact structures that fit into chromosomes within each cell's ...

Neuroscience

Protein tenascin-C important in retinal blood flow disorders

Many eye diseases are associated with a restricted blood supply, known as ischaemia, which can lead to blindness. The role of the protein tenascin-C, an extracellular matrix component, in retinal ischaemia was investigated ...

Genetics

Gene therapy targets inner retina to combat blindness

Gene therapy to the inner retina prevented blindness in a mouse model of the neuro-degenerative disorder CLN3 Batten disease. Adeno-associated viral (AAV)-mediated expression of the human CLN3 gene led to significant survival ...

Neuroscience

After blindness, the adult brain can learn to see again

More than 40 million people worldwide are blind, and many of them reach this condition after many years of slow and progressive retinal degeneration. The development of sophisticated prostheses or new light-responsive elements, ...

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