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Prohormone convertase 2 activity is increased in the hippocampus of Wfs1 knockout mice

Background: Mutations in WFS1 gene cause Wolfram syndrome, which is a rare autosomal recessive disorder, characterized by diabetes insipidus, diabetes mellitus, optic nerve atrophy, and deafness. The WFS1 gene product wolframin is located in the endoplasmic reticulum. Mice lacking this gene exhibit...

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Detalhes bibliográficos
Publicado no:Front Mol Neurosci
Main Authors: Tein, Karin, Kasvandik, Sergo, Kõks, Sulev, Vasar, Eero, Terasmaa, Anton
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2015
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4548212/
https://ncbi.nlm.nih.gov/pubmed/26379490
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnmol.2015.00045
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