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 ...

Ophthalmology

How video goggles and a tiny implant could cure blindness

At 16, Lynda Johnson was ready to learn how to drive. Yes, she had a progressive eye disease, retinitis pigmentosa, which already had stolen her night vision. But throughout her childhood, the Millbrae, California, girl had ...

Ophthalmology

Researchers identify treatment target for blinding diseases

New research published in Cell Reports identifies a potential treatment target for blinding diseases such as retinitis pigmentosa and advanced dry age-related macular degeneration. In the study, researchers at Washington ...

Medical research

Stem cell-based screen identifies potential new treatments

Vision loss related to aging or inherited genetic disease, such as age-related macular degeneration and retinitis pigmentosa (RP), respectively, is estimated to impact 16 million people worldwide and is often caused by defects ...

Neuroscience

Visual pigment rhodopsin forms two-molecule complexes in vivo

The study of rhodopsin—the molecule that allows the eye to detect dim light—has a long and well-recognized history of more than 100 years. Nevertheless, there is still controversy about the structure in which the molecule ...

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