Latest Stereocilia Stories
Discovery May Point to Way to Restore Hearing Loss Caused by Sound, Age Charlottesville, VA (PRWEB) May 20, 2014 The ability to discern pitch – to
Young Researcher Invited to Present Findings at the American Junior Academy of Science’s Annual Meeting in Chicago.
A team of NIH-supported researchers is the first to show, in mice, an unexpected two-step process that happens during the growth and regeneration of inner ear tip links.
An important new study from The Scripps Research Institute (TSRI) has has identified a molecule that plays a critical role in the conversion of sound waves to brain signals.
The workings of the inner ear have been long thought to be well documented and understood.
A team of researchers has reportedly discovered a new genetic mutation that leads to deafness and hearing loss associated with a relatively rare condition.
The hair cells of the inner ear have a previously unknown "root" extension that may allow them to communicate with nerve cells and the brain to regulate sensitivity to sound vibrations and head position.
From tracking activities within bacteria to creating images of molecules that make up human hair, several experiments have already demonstrated the unique abilities of the revolutionary imaging technique called multi-isotope imaging mass spectometry, or MIMS, developed by researchers at Brigham and Women's Hospital (BWH).
Mutated genes in the sensory hair cells of the inner ear prevent sound waves from being converted into electrical signals- a fundamental first step in hearing. Restoring electrical signals in the sensory cells of deaf mice by introducing new genes allowed the mice to hear.
Researchers have found long-sought genes in the sensory hair cells of the inner ear that, when mutated, prevent sound waves from being converted to electric signals – a fundamental first step in hearing.
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