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  Ca2+ homeostasis and endoplasmic reticulum (ER) stress: An integrated view of calcium signaling.

Krebs, J., Agellon, L. B., & Michalak, M. (2015). Ca2+ homeostasis and endoplasmic reticulum (ER) stress: An integrated view of calcium signaling. Biochemical and Biophysical Research Communications, 460(1), 114-121. doi:10.1016/j.bbrc.2015.02.004.

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Item Permalink: http://hdl.handle.net/11858/00-001M-0000-0027-828E-2 Version Permalink: http://hdl.handle.net/11858/00-001M-0000-0027-CEFC-D
Genre: Journal Article

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2161128.pdf (Publisher version), 614KB
 
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 Creators:
Krebs, J.1, Author              
Agellon, L. B., Author
Michalak, M., Author
Affiliations:
1Department of NMR Based Structural Biology, MPI for biophysical chemistry, Max Planck Society, ou_578567              

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Free keywords: Ca2+ homeostasis; ER stress; Ca2+-binding proteins; Calcium transport; Membrane contact sites; Unfolded protein response (UPR); MicroRNAs
 Abstract: Cellular Ca2+ homeostasis is maintained through the integrated and coordinated function of Ca2+ transport molecules, Ca2+ buffers and sensors. These molecules are associated with the plasma membrane and different cellular compartments, such as the cytoplasm, nucleus, mitochondria, and cellular reticular network, including the endoplasmic reticulum (ER) to control free and bound Ca2+ levels in all parts of the cell. Loss of nutrients/energy leads to the loss of cellular homeostasis and disruption of Ca2+ signaling in both the reticular network and cytoplasmic compartments. As an integral part of cellular physiology and pathology, this leads to activation of ER stress coping responses, such as the unfolded protein response (UPR), and mobilization of pathways to regain ER homeostasis.

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Language(s): eng - English
 Dates: 2015-05-182015-04-24
 Publication Status: Published in print
 Pages: -
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 Table of Contents: -
 Rev. Method: Peer
 Identifiers: DOI: 10.1016/j.bbrc.2015.02.004
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Title: Biochemical and Biophysical Research Communications
Source Genre: Journal
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Pages: - Volume / Issue: 460 (1) Sequence Number: - Start / End Page: 114 - 121 Identifier: -