Cargando…
A Claudin-9–Based Ion Permeability Barrier Is Essential for Hearing
Hereditary hearing loss is one of the most common birth defects, yet the majority of genes required for audition is thought to remain unidentified. Ethylnitrosourea (ENU)–mutagenesis has been a valuable approach for generating new animal models of deafness and discovering previously unrecognized gen...
Autores principales: | Nakano, Yoko, Kim, Sung H., Kim, Hyoung-Mi, Sanneman, Joel D., Zhang, Yuzhou, Smith, Richard J. H., Marcus, Daniel C., Wangemann, Philine, Nessler, Randy A., Bánfi, Botond |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2720454/ https://www.ncbi.nlm.nih.gov/pubmed/19696885 http://dx.doi.org/10.1371/journal.pgen.1000610 |
Ejemplares similares
-
Claudin expression during early postnatal development of the murine cochlea
por: Kudo, Takayuki, et al.
Publicado: (2018) -
Slc26a7 Chloride Channel Activity and Localization in Mouse Reissner’s Membrane Epithelium
por: Kim, Kyunghee X., et al.
Publicado: (2014) -
SLC26A4 Targeted to the Endolymphatic Sac Rescues Hearing and Balance in Slc26a4 Mutant Mice
por: Li, Xiangming, et al.
Publicado: (2013) -
Failure of Fluid Absorption in the Endolymphatic Sac Initiates Cochlear Enlargement that Leads to Deafness in Mice Lacking Pendrin Expression
por: Kim, Hyoung-Mi, et al.
Publicado: (2010) -
Epithelial Cell Stretching and Luminal Acidification Lead to a Retarded Development of Stria Vascularis and Deafness in Mice Lacking Pendrin
por: Kim, Hyoung-Mi, et al.
Publicado: (2011)