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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書誌詳細
主要な著者: Lucariello, Angela, Perna, Angelica, Sellitto, Carmine, Baldi, Alfonso, Iannaccone, Alessandro, Cobellis, Luigi, De Luca, Antonio, De Falco, Maria
フォーマット: Artigo
言語:Inglês
出版事項: Hindawi Publishing Corporation 2014
主題:
Research Article
オンライン･アクセス: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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