Wolfram syndrome 1 gene ( WFS1 ) product localizes to secretory granules and determines granule acidification in pancreatic -cells

By Hatanaka Masayuki   Tanabe Katsuya   Yanai Akie   Ohta Yasuharu   Kondo Manabu   Akiyama Masaru   Shinoda Koh   Oka Yoshitomo   Tanizawa Yukio  

Human Molecular Genetics, Vol. 20, Iss. 7, 2011-04 ,pp. : 1274-1284

Oxford University Press

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Wolfram syndrome: structural and functional analyses of mutant and wild-type wolframin, the WFS1 gene product

By Hofmann S.  

Human Molecular Genetics, Vol. 12, Iss. 16, 2003-08 ,pp. : 2003-2012

Oxford University Press

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Mutations in the Wolfram syndrome 1 gene ( WFS1 ) are a common cause of low frequency sensorineural hearing loss

By Kurnool P.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2501-2508

Oxford University Press

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Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

By Griffin A.  

Human Molecular Genetics, Vol. 10, Iss. 22, 2001-10 ,pp. : 2509-2514

Oxford University Press

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WFS1-deficiency increases endoplasmic reticulum stress, impairs cell cycle progression and triggers the apoptotic pathway specifically in pancreatic -cells

By Yamada Takahiro   Ishihara Hisamitsu   Tamura Akira   Takahashi Rui   Yamaguchi Suguru   Takei Daisuke   Tokita Ai   Satake Chihiro   Tashiro Fumi   Katagiri Hideki   Aburatani Hiroyuki   Miyazaki Jun-ichi   Oka Yoshitomo  

Human Molecular Genetics, Vol. 15, Iss. 10, 2006-05 ,pp. : 1600-1609

Oxford University Press

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