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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Detalles Bibliográficos
Autores principales: Lucariello, Angela, Perna, Angelica, Sellitto, Carmine, Baldi, Alfonso, Iannaccone, Alessandro, Cobellis, Luigi, De Luca, Antonio, De Falco, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920918/
https://www.ncbi.nlm.nih.gov/pubmed/24588001
http://dx.doi.org/10.1155/2014/985478

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3920918/
https://www.ncbi.nlm.nih.gov/pubmed/24588001
http://dx.doi.org/10.1155/2014/985478

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