Sensory hair bundles in the inner ear are composed of stereocilia that can be interconnected by a variety of different link types, including tip links, horizontal top connectors, shaft connectors, and ankle links. The ankle link antigen is an epitope specifically associated with ankle links and the calycal processes of photoreceptors in chicks. Mass spectrometry and immunoblotting were used to identify this antigen as the avian ortholog of the very large G-protein-coupled receptor VLGR1, the product of the Usher syndrome USH2C (Mass1) locus. Like ankle links, Vlgr1 is expressed transiently around the base of developing hair bundles in mice. Ankle links fail to form in the cochleae of mice carrying a targeted mutation in Vlgr1 (Vlgr1/del7TM)...
Cochlear inner and outer hair cells are the functional units of mammalian hearing. At their apex, sp...
Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at le...
Usher syndrome type III (USH3) characterized by progressive loss of vision and hearing is caused by ...
International audienceSeveral lines of evidence indicate that very large G-protein-coupled receptor ...
A screen for protein tyrosine phosphatases (PTPs) expressed in the chick inner ear yielded a high pr...
Sound and acceleration are detected by hair bundles, mechanosensory structures located at the apical...
A monoclonal antibody, mAb E40, that specifically recognizes hair cells and photoreceptors was deriv...
Immunocytochemical studies have shown that protocadherin-15 (PCDH15) and cadherin-23 (CDH23) are ass...
Usher syndrome is the leading cause of genetic deaf-blindness. Monoallelic mutations in PDZD7 increa...
<div><p>The molecular mechanisms underlying hair cell synaptic maturation are not well understood. C...
The molecular mechanisms underlying hair cell synaptic maturation are not well understood. Cadherin-...
AbstractCadherin 23 is required for normal development of the sensory hair bundle, and recent eviden...
Lipopolysaccharide-responsive beige-like anchor protein (LRBA) belongs to the enigmatic class of BEA...
peer reviewedLipopolysaccharide-responsive beige-like anchor protein (LRBA) belongs to the enigmatic...
Tasmanian devil (tde) mice are deaf and exhibit circling behaviour. Sensory hair cells of mutants sh...
Cochlear inner and outer hair cells are the functional units of mammalian hearing. At their apex, sp...
Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at le...
Usher syndrome type III (USH3) characterized by progressive loss of vision and hearing is caused by ...
International audienceSeveral lines of evidence indicate that very large G-protein-coupled receptor ...
A screen for protein tyrosine phosphatases (PTPs) expressed in the chick inner ear yielded a high pr...
Sound and acceleration are detected by hair bundles, mechanosensory structures located at the apical...
A monoclonal antibody, mAb E40, that specifically recognizes hair cells and photoreceptors was deriv...
Immunocytochemical studies have shown that protocadherin-15 (PCDH15) and cadherin-23 (CDH23) are ass...
Usher syndrome is the leading cause of genetic deaf-blindness. Monoallelic mutations in PDZD7 increa...
<div><p>The molecular mechanisms underlying hair cell synaptic maturation are not well understood. C...
The molecular mechanisms underlying hair cell synaptic maturation are not well understood. Cadherin-...
AbstractCadherin 23 is required for normal development of the sensory hair bundle, and recent eviden...
Lipopolysaccharide-responsive beige-like anchor protein (LRBA) belongs to the enigmatic class of BEA...
peer reviewedLipopolysaccharide-responsive beige-like anchor protein (LRBA) belongs to the enigmatic...
Tasmanian devil (tde) mice are deaf and exhibit circling behaviour. Sensory hair cells of mutants sh...
Cochlear inner and outer hair cells are the functional units of mammalian hearing. At their apex, sp...
Usher syndrome type II (USH2) is a genetically heterogeneous autosomal recessive disorder with at le...
Usher syndrome type III (USH3) characterized by progressive loss of vision and hearing is caused by ...