(Medical Xpress) -- Researchers have known since 1997 that mutations in the KCQN4 channel (a pathway that leads from the external environment to neurons) lead to progressive deafness and that the KCQN4 channel is only found ...
In collaboration with the universities of Miami, Columbia and San Francisco, scientists from the Institut Pasteur, Inserm, CNRS, Collège de France, Sorbonne University and the University of Clermont Auvergne have restored ...
Feb 20, 2019
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A new gene therapy approach can reverse hearing loss caused by a genetic defect in a mouse model of congenital deafness, according to a preclinical study published by Cell Press in the July 26 issue of the journal Neuron. ...
Jul 25, 2012
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Usher Syndrome type 1F is a rare but severe genetic disease that causes deafness, lack of balance, and progressive blindness.
Apr 26, 2023
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For many of us, a visit to the doctor's office can be wrought with anxiety. A persistent cough that won't go away or an ailment we hope is nothing serious can make GP visits emotionally difficult. Now imagine that you can't ...
Nov 29, 2019
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In experiments using mice, a team of UC San Francisco researchers has discovered a gene that plays an essential role in noise-induced deafness. Remarkably, by administering an experimental chemical—identified in a separate ...
Oct 19, 2018
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For scientists who study the genetics of hearing and deafness, finding the exact genetic machinery in the inner ear that responds to sound waves and converts them into electrical impulses, the language of the brain, has been ...
Dec 6, 2012
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A new study by University of Manchester audiologists has highlighted the difficulties people face with impacted ear wax.
Jan 27, 2023
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Fatigue, weight gain, chills, hair loss, anxiety, excessive perspiration—these symptoms are a few of the signs that the thyroid gland, which regulates the body's heart rate and plays a crucial role in its metabolism, has ...
Sep 22, 2014
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Researchers at the University of Cincinnati (UC) and Cincinnati Children's Hospital Medical Center have found a new genetic mutation responsible for deafness and hearing loss associated with Usher syndrome type 1.
Sep 30, 2012
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