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Authors = Yukihiro Hasegawa

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Open AccessReview Endoplasmic Reticulum (ER) Stress and Endocrine Disorders
Int. J. Mol. Sci. 2017, 18(2), 382; doi:10.3390/ijms18020382
Received: 22 December 2016 / Revised: 24 January 2017 / Accepted: 3 February 2017 / Published: 11 February 2017
Cited by 1 | Viewed by 884 | PDF Full-text (923 KB) | HTML Full-text | XML Full-text
Abstract
The endoplasmic reticulum (ER) is the organelle where secretory and membrane proteins are synthesized and folded. Unfolded proteins that are retained within the ER can cause ER stress. Eukaryotic cells have a defense system called the “unfolded protein response” (UPR), which protects cells
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The endoplasmic reticulum (ER) is the organelle where secretory and membrane proteins are synthesized and folded. Unfolded proteins that are retained within the ER can cause ER stress. Eukaryotic cells have a defense system called the “unfolded protein response” (UPR), which protects cells from ER stress. Cells undergo apoptosis when ER stress exceeds the capacity of the UPR, which has been revealed to cause human diseases. Although neurodegenerative diseases are well-known ER stress-related diseases, it has been discovered that endocrine diseases are also related to ER stress. In this review, we focus on ER stress-related human endocrine disorders. In addition to diabetes mellitus, which is well characterized, several relatively rare genetic disorders such as familial neurohypophyseal diabetes insipidus (FNDI), Wolfram syndrome, and isolated growth hormone deficiency type II (IGHD2) are discussed in this article. Full article
(This article belongs to the Special Issue Modulators of Endoplasmic Reticulum Stress 2016)
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