Modulation of Wolframin Expression in Human Placenta during Pregnancy: Comparison among Physiological and Pathological States

The WFS1 gene, encoding a transmembrane glycoprotein of the endoplasmic reticulum called wolframin, is mutated in Wolfram syndrome, an autosomal recessive disorder defined by the association of diabetes mellitus, optic atrophy, and further organ abnormalities. Disruption of the WFS1 gene in mice cau...

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Main Authors: Lucariello, Angela, Perna, Angelica, Sellitto, Carmine, Baldi, Alfonso, Iannaccone, Alessandro, Cobellis, Luigi, De Luca, Antonio, De Falco, Maria
Formato: Artigo
Idioma:Inglês
Publicado: Hindawi Publishing Corporation 2014
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Research Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3920918/
https://ncbi.nlm.nih.gov/pubmed/24588001
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2014/985478
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