Compensation for chronic oxidative stress in ALADIN null mice

Mutations in the AAAS gene coding for the nuclear pore complex protein ALADIN lead to the autosomal recessive disorder triple A syndrome. Triple A patients present with a characteristic phenotype including alacrima, achalasia and adrenal insufficiency. Patient fibroblasts show increased levels of ox...

Descripción completa

Detalles Bibliográficos
Autores principales: Jühlen, Ramona, Peitzsch, Mirko, Gärtner, Sebastian, Landgraf, Dana, Eisenhofer, Graeme, Huebner, Angela, Koehler, Katrin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2018
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829508/
https://www.ncbi.nlm.nih.gov/pubmed/29362278
http://dx.doi.org/10.1242/bio.030742

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5829508/
https://www.ncbi.nlm.nih.gov/pubmed/29362278
http://dx.doi.org/10.1242/bio.030742

Ejemplares similares