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...

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Detalles Bibliográficos
Autores principales: Plössl, Karolina, Weber, Bernhard H.F., Friedrich, Ulrike
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Original Articles
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

Internet

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

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