LRIT3 Differentially Affects Connectivity and Synaptic Transmission of Cones to ON- and OFF-Bipolar Cells

PURPOSE: Mutations in LRIT3 lead to complete congenital stationary night blindness (cCSNB). Using a cCSNB mouse model lacking Lrit3 (nob6), we recently have shown that LRIT3 has a role in the correct localization of TRPM1 (transient receptor potential melastatin 1) to the dendritic tips of ON-bipola...

Descripción completa

Detalles Bibliográficos
Autores principales: Neuillé, Marion, Cao, Yan, Caplette, Romain, Guerrero-Given, Debbie, Thomas, Connon, Kamasawa, Naomi, Sahel, José-Alain, Hamel, Christian P., Audo, Isabelle, Picaud, Serge, Martemyanov, Kirill A., Zeitz, Christina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Association for Research in Vision and Ophthalmology 2017
Materias:
Visual Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374884/
https://www.ncbi.nlm.nih.gov/pubmed/28334377
http://dx.doi.org/10.1167/iovs.16-20745

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5374884/
https://www.ncbi.nlm.nih.gov/pubmed/28334377
http://dx.doi.org/10.1167/iovs.16-20745

Ejemplares similares