Functional assessment of SLC4A11, an integral membrane protein mutated in corneal dystrophies
SLC4A11, a member of the SLC4 family of bicarbonate transporters, is a widely expressed integral membrane protein, abundant in kidney and cornea. Mutations of SLC4A11 cause some cases of the blinding corneal dystrophies, congenital hereditary endothelial dystrophy, and Fuchs endothelial corneal dyst...
Guardado en:
| Autores principales: | Loganathan, Sampath K., Schneider, Hans Peter, Morgan, Patricio Eduardo, Deitmer, Joachim W., Casey, Joseph R. |
|---|---|
| Formato: | Articulo |
| Lenguaje: | Inglés |
| Publicado: |
2016
|
| Materias: | |
| Acceso en línea: | http://sedici.unlp.edu.ar/handle/10915/99458 https://ri.conicet.gov.ar/11336/54183 https://www.physiology.org/doi/10.1152/ajpcell.00078.2016 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5130586/ |
| Aporte de: |
Ejemplares similares
-
Actualización sobre factores de riesgo asociados a daño corneal post Cross-Linking
por: González Castellanos, Juan C., et al.
Publicado: (2020) -
Analysis of pupil and corneal wave aberration data supplied by the SN CT 1000 topography system
por: Comastri, S.A., et al. -
Analysis of pupil and corneal wave aberration data supplied by the SN CT 1000 topography system
por: Comastri, Silvia Ana Elba, et al.
Publicado: (2006) -
Desarrollo de un modelo de neovascularización corneal en conejos para evaluar el efecto terapéutico de una formulación antiangiogénica
por: Ángos, J, et al.
Publicado: (2024) -
Clinical and spirometric alterations in Duchenne muscular dystrophy
por: Andrada, L.E., et al.