News tagged with usher syndrome
Study finds new role for protein in hearing
University of Iowa scientists have discovered a new role for a protein that is mutated in Usher syndrome, one of the most common forms of deaf-blindness in humans. The findings, which were published Aug. 8 in Nature Neuroscience, may he ...
Medicine & Health / Neuroscience
Aug 15, 2011 |
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Treatment approach to human Usher syndrome: Small molecules ignore stop signals
Usher syndrome is the most common form of combined congenital deaf-blindness in humans and affects 1 in 6,000 of the population. It is a recessive inherited disease that is both clinically and genetically ...
Jul 01, 2011 |
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Latest advances in gene therapy for ocular disease are highlighted in Human Gene Therapy
Disorders of the eye are excellent targets for gene therapy because the ocular environment is readily accessible, relatively easy to monitor, and sequestered from the rest of the body. A series of articles ...
May 09, 2011 |
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Genetic modifier in Usher syndrome will lead to better diagnosis
Gothenburg, Sweden: Usher syndrome (USH), an inherited condition involving both hearing and vision loss, is not a simply recessively inherited disease, a scientist will tell the annual conference of the European Society ...
Jun 11, 2010 |
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Study offers clues to beating hearing loss
Researchers at the University of Leeds have made a significant step forward in understanding the causes of some forms of deafness.
Mar 04, 2009 |
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