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 ...

Medical research

Ganglion cells created in mice in bid to fix diseased eyes

While fish, reptiles and even some birds can regenerate damaged brain, eye and spinal cord cells, mammals cannot. For the first time, non-neuronal cells have been induced to mimic specific ganglion cells in the eyes of mice.

Genetics

Researchers develop gene therapy for rare ciliopathy

Researchers from the National Eye Institute (NEI) have developed a gene therapy that rescues cilia defects in retinal cells affected by a type of Leber congenital amaurosis (LCA), a disease that causes blindness in early ...

Psychology & Psychiatry

Trauma of diagnosis stays with eye disease patients

The way in which a patient is told they have serious eye disease can impact their psychological health and ability to cope with their condition in the long-term, according to new research published in the open-access journal ...

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