Cargando…
New Tmc1 Deafness Mutations Impact Mechanotransduction in Auditory Hair Cells
Transmembrane channel-like protein isoform 1 (TMC1) is a major component of the mechano-electrical transducer (MET) channel in cochlear hair cells and is subject to numerous mutations causing deafness. We report a new dominant human deafness mutation, TMC1 p.T422K, and have characterized the homolog...
Autores principales: | Beurg, Maryline, Schimmenti, Lisa A., Koleilat, Alaa, Amr, Sami S., Oza, Andrea, Barlow, Amanda J., Ballesteros, Angela, Fettiplace, Robert |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Society for Neuroscience
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8152607/ https://www.ncbi.nlm.nih.gov/pubmed/33824189 http://dx.doi.org/10.1523/JNEUROSCI.2537-20.2021 |
Ejemplares similares
-
The conductance and organization of the TMC1-containing mechanotransducer channel complex in auditory hair cells
por: Fettiplace, Robert, et al.
Publicado: (2022) -
A Tmc1 mutation reduces calcium permeability and expression of mechanoelectrical transduction channels in cochlear hair cells
por: Beurg, Maryline, et al.
Publicado: (2019) -
The effects of Tmc1 Beethoven mutation on mechanotransducer channel function in cochlear hair cells
por: Beurg, Maryline, et al.
Publicado: (2015) -
CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells
por: Giese, Arnaud P. J., et al.
Publicado: (2017) -
The contribution of TMC1 to adaptation of mechanoelectrical transduction channels in cochlear outer hair cells
por: Goldring, Adam C., et al.
Publicado: (2019)