Altered gene expression in slc4a11(−/−) mouse cornea highlights SLC4A11 roles

SLC4A11 is a H(+)/NH(3)/water transport protein, of corneal endothelial cells. SLC4A11 mutations cause congenital hereditary endothelial dystrophy and some cases of Fuchs endothelial corneal dystrophy. To probe SLC4A11’s roles, we compared gene expression in RNA from corneas of 17-week-old slc4a11(−...

Descripción completa

Detalles Bibliográficos
Autores principales: Alvarez, Bernardo V., Piché, Marilyse, Aizouki, Carolin, Rahman, Fariha, Derry, Jonathan M. J., Brunette, Isabelle, Casey, Joseph R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536660/
https://www.ncbi.nlm.nih.gov/pubmed/34686736
http://dx.doi.org/10.1038/s41598-021-98921-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8536660/
https://www.ncbi.nlm.nih.gov/pubmed/34686736
http://dx.doi.org/10.1038/s41598-021-98921-w

Ejemplares similares