Cargando…
A mouse model of cone photoreceptor function loss (cpfl9) with degeneration due to a mutation in Gucy2e
During routine screening of mouse strains and stocks by the Eye Mutant Resource at The Jackson Laboratory for genetic mouse models of human ocular disorders, we identified cpfl9, a mouse model with cone photoreceptor function loss. The mice exhibited an early-onset phenotype that was easily recogniz...
Autores principales: | Naggert, Anna S. E. N., Collin, Gayle B., Wang, Jieping, Krebs, Mark P., Chang, Bo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9868315/ https://www.ncbi.nlm.nih.gov/pubmed/36698779 http://dx.doi.org/10.3389/fnmol.2022.1080136 |
Ejemplares similares
-
Mouse Models of Inherited Retinal Degeneration with Photoreceptor Cell Loss
por: Collin, Gayle B., et al.
Publicado: (2020) -
Diminished Cone Sensitivity in cpfl3 Mice Is Caused by Defective Transducin Signaling
por: Chen, Natalie S., et al.
Publicado: (2020) -
Photoreceptor Guanylate Cyclase (GUCY2D) Mutations Cause Retinal Dystrophies by Severe Malfunction of Ca(2+)-Dependent Cyclic GMP Synthesis
por: Wimberg, Hanna, et al.
Publicado: (2018) -
Adaptation memory in photoreceptors: different mechanisms in rods and cones
por: Nikolaeva, Darya A., et al.
Publicado: (2023) -
Development and Degeneration of Cone Bipolar Cells Are Independent of Cone Photoreceptors in a Mouse Model of Retinitis Pigmentosa
por: Chen, Miao, et al.
Publicado: (2012)