<p>All 14 mutations were tested for their ability to make gap junctions in transiently transfected HeLa cells. Eight mutations (K188R, F191L, V198M, S199F, G200R, I203K, L205P, T208P) caused mis-trafficking, typically with intracellular aggregation. WT human Cx26 is shown at the top left for comparison, with an arrow pointing to a gap junction. The arrowhead in the F191L image points to a cell-cell apposition area with aggregate fluorescence.</p
<p>(A) Gap junction formation by the transfected Cx26 variants. Each panel contains two co-transfect...
Connexins are membrane proteins that assemble into gap-junction channels and are responsible for dir...
Connexins are membrane proteins that assemble into gap-junction channels and are responsible for dir...
<div><p>Human Connexin26 gene mutations cause hearing loss. These hereditary mutations are the leadi...
Three point mutations of the connexin26 (GJB2) gene associated with hereditary deafness were studied...
Three point mutations of the connexin26 (GJB2) gene associated with hereditary deafness were studied...
Mutations in the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26), are the major ...
In a study of 530 individuals with non-syndromic, sensorineural hearing loss, we identified 18 mutat...
In a study of 530 individuals with non-syndromic, sensorineural hearing loss, we identified 18 mutat...
Mutations in the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26), are the major ...
Mutations in the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26), are the major ...
Background: Gap junctions facilitate exchange of small molecules between adjacent cells, serving a c...
Background: Gap junctions facilitate exchange of small molecules between adjacent cells, serving a c...
Mutations in the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26), are the major ...
AbstractConnexin26 is a ubiquitous gap junction protein that serves critical homeostatic functions. ...
<p>(A) Gap junction formation by the transfected Cx26 variants. Each panel contains two co-transfect...
Connexins are membrane proteins that assemble into gap-junction channels and are responsible for dir...
Connexins are membrane proteins that assemble into gap-junction channels and are responsible for dir...
<div><p>Human Connexin26 gene mutations cause hearing loss. These hereditary mutations are the leadi...
Three point mutations of the connexin26 (GJB2) gene associated with hereditary deafness were studied...
Three point mutations of the connexin26 (GJB2) gene associated with hereditary deafness were studied...
Mutations in the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26), are the major ...
In a study of 530 individuals with non-syndromic, sensorineural hearing loss, we identified 18 mutat...
In a study of 530 individuals with non-syndromic, sensorineural hearing loss, we identified 18 mutat...
Mutations in the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26), are the major ...
Mutations in the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26), are the major ...
Background: Gap junctions facilitate exchange of small molecules between adjacent cells, serving a c...
Background: Gap junctions facilitate exchange of small molecules between adjacent cells, serving a c...
Mutations in the GJB2 gene, which encodes the gap junction protein connexin26 (Cx26), are the major ...
AbstractConnexin26 is a ubiquitous gap junction protein that serves critical homeostatic functions. ...
<p>(A) Gap junction formation by the transfected Cx26 variants. Each panel contains two co-transfect...
Connexins are membrane proteins that assemble into gap-junction channels and are responsible for dir...
Connexins are membrane proteins that assemble into gap-junction channels and are responsible for dir...