Cargando…
The X‐linked juvenile retinoschisis protein retinoschisin is a novel regulator of mitogen‐activated protein kinase signalling and apoptosis in the retina
X‐linked juvenile retinoschisis (XLRS) is a hereditary retinal dystrophy in young males, caused by mutations in the RS1 gene. The function of the encoded protein, termed retinoschisin, and the molecular mechanisms underlying XLRS pathogenesis are still unresolved, although a direct interaction partn...
Autores principales: | Plössl, Karolina, Weber, Bernhard H.F., Friedrich, Ulrike |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5345684/ https://www.ncbi.nlm.nih.gov/pubmed/27995734 http://dx.doi.org/10.1111/jcmm.13019 |
Ejemplares similares
-
Retinoschisin is linked to retinal Na/K-ATPase signaling and localization
por: Plössl, Karolina, et al.
Publicado: (2017) -
Retinoschisin and Cardiac Glycoside Crosstalk at the Retinal Na/K-ATPase
por: Schmid, Verena, et al.
Publicado: (2020) -
Identification of the retinoschisin-binding site on the retinal Na/K-ATPase
por: Plössl, Karolina, et al.
Publicado: (2019) -
Retinoschisin and novel Na/K-ATPase interaction partners Kv2.1 and Kv8.2 define a growing protein complex at the inner segments of mammalian photoreceptors
por: Schmid, Verena, et al.
Publicado: (2022) -
Structural analysis of X-linked retinoschisis mutations reveals distinct classes which differentially effect retinoschisin function
por: Ramsay, Ewan P., et al.
Publicado: (2016)