<p>(A-F) Immunofluorescence staining for CAV2 in the organ of Corti around apical part of cochlea in 3-week-old Cx26<sup>f/f</sup>P0Cre mice with <i>GJB2</i>-associated deafness and in littermate controls. Whole-mount cochleae were fixed and immunolabeled with anti-CAV2 (red). Nuclei were counterstained with DAPI (blue). In contrast to the controls, notable accumulation of CAV2 was observed at the organ of Corti in Cx26<sup>f/f</sup>P0Cre cochlea<b>e</b>. (G) shows the mean percentage of cells with accumulated CAV2 in control and Cx26<sup>f/f</sup>P0Cre cochleae. There was a statistically significant difference between the control and Cx26<sup>f/f</sup>P0Cre mice. Values represent the mean ± SE (n = 5 mice). ***P = 3.72 × 10<sup>−5</sup>, S...
Early cochlear development is marked by an exuberant outgrowth of neurites that innervate multiple t...
Ca(2+) acts as a fundamental signal transduction element in inner ear, delivering information about ...
<p>The circling mouse serves as a hearing loss model. It has spontaneous <i>tmie</i> gene mutations ...
<p>Cryosections of the organ of Corti around apical part of cochlea were immunolabeled with anti-CAV...
<p>Mice were infected with MCMV or mock infected as controls as described in Materials and Methods. ...
, which encodes connexin 26 (Cx26), a cochlear gap junction protein, represent a major cause of pre-...
<p>Accumulation of CAV2 was observed in OHCs around apical part of cochlea and colocalized with pres...
<p>(A) Neurons within the rodent auditory cortex can be excitatory or inhibitory. To express ChR2 in...
<p><b>(A)</b> Mononuclear cell infiltrate in the cochlea of infected mice. H&E staining of cochlea d...
<p>(A) C3 (green) and C5aR (red) deposition in the middle ear mucosa at 24 h post Spn infection. Nuc...
<p>Cochlear tissue isolated from infected and uninfected, control mice on PNd8 with number of mice i...
Mutations in the GJB2 gene [which encodes connexin 26 (Cx26)] are the most common causes of heredita...
Several studies have shown that type IV fibrocytes, located in the spiral ligament, degenerate first...
This experiment analyzes synaptic differences in the central auditory pathway between normal hearing...
Early cochlear development is marked by an exuberant outgrowth of neurites that innervate multiple t...
Early cochlear development is marked by an exuberant outgrowth of neurites that innervate multiple t...
Ca(2+) acts as a fundamental signal transduction element in inner ear, delivering information about ...
<p>The circling mouse serves as a hearing loss model. It has spontaneous <i>tmie</i> gene mutations ...
<p>Cryosections of the organ of Corti around apical part of cochlea were immunolabeled with anti-CAV...
<p>Mice were infected with MCMV or mock infected as controls as described in Materials and Methods. ...
, which encodes connexin 26 (Cx26), a cochlear gap junction protein, represent a major cause of pre-...
<p>Accumulation of CAV2 was observed in OHCs around apical part of cochlea and colocalized with pres...
<p>(A) Neurons within the rodent auditory cortex can be excitatory or inhibitory. To express ChR2 in...
<p><b>(A)</b> Mononuclear cell infiltrate in the cochlea of infected mice. H&E staining of cochlea d...
<p>(A) C3 (green) and C5aR (red) deposition in the middle ear mucosa at 24 h post Spn infection. Nuc...
<p>Cochlear tissue isolated from infected and uninfected, control mice on PNd8 with number of mice i...
Mutations in the GJB2 gene [which encodes connexin 26 (Cx26)] are the most common causes of heredita...
Several studies have shown that type IV fibrocytes, located in the spiral ligament, degenerate first...
This experiment analyzes synaptic differences in the central auditory pathway between normal hearing...
Early cochlear development is marked by an exuberant outgrowth of neurites that innervate multiple t...
Early cochlear development is marked by an exuberant outgrowth of neurites that innervate multiple t...
Ca(2+) acts as a fundamental signal transduction element in inner ear, delivering information about ...
<p>The circling mouse serves as a hearing loss model. It has spontaneous <i>tmie</i> gene mutations ...