Stereocilia News and Research

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Stereocilia are apical modifications of the cell, which are distinct from microvilli and cilia.
Study documents and visualizes hearing loss-associated genes in the inner ear

Study documents and visualizes hearing loss-associated genes in the inner ear

Scientists identify new genes associated with familial Meniere's disease

Scientists identify new genes associated with familial Meniere's disease

New findings challenge the decades-old working mechanism of the hearing organ

New findings challenge the decades-old working mechanism of the hearing organ

UMSOM researchers determine role of protein in development of hearing hair cells

UMSOM researchers determine role of protein in development of hearing hair cells

Study reveals key insight into the development of hair bundles

Study reveals key insight into the development of hair bundles

Hearing partially restored in deaf lab mice using novel therapy

Hearing partially restored in deaf lab mice using novel therapy

IUPUI cell biologist receives $1.9 million grant to tackle age-related hearing loss

IUPUI cell biologist receives $1.9 million grant to tackle age-related hearing loss

Study sheds light on how key protein allows hearing to work

Study sheds light on how key protein allows hearing to work

Inner ear gene therapy holds promise for treating patients with hearing loss and dizziness

Inner ear gene therapy holds promise for treating patients with hearing loss and dizziness

TSRI study shows how mutations in Tmie gene can cause deafness from birth

TSRI study shows how mutations in Tmie gene can cause deafness from birth

Researchers explore hair cells of inner ear to reverse hearing loss

Researchers explore hair cells of inner ear to reverse hearing loss

IRCM researchers identify new proteins crucial for hearing

IRCM researchers identify new proteins crucial for hearing

Stereocilia not only move sideways but also change in length: Study

Stereocilia not only move sideways but also change in length: Study

CIB2 gene responsible for progression and severity of Usher syndrome

CIB2 gene responsible for progression and severity of Usher syndrome

CIB2 genetic mutation responsible for deafness associated with Usher syndrome type 1

CIB2 genetic mutation responsible for deafness associated with Usher syndrome type 1

Unknown 'root' extension in hair cells of the inner ear

Unknown 'root' extension in hair cells of the inner ear

Study reveals specific functional deficit in inner ear mechanotransduction channels

Study reveals specific functional deficit in inner ear mechanotransduction channels

Gene-therapy trial to restore hearing in deaf mice

Gene-therapy trial to restore hearing in deaf mice

New role for harmonin protein in Usher syndrome

New role for harmonin protein in Usher syndrome

SMPX gene mutation causes hereditary hearing impairment

SMPX gene mutation causes hereditary hearing impairment