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Cited by 254

The DOI matches its Crossref record; 119 of the 119 references it cites were found in a registry or an index.

Endoplasmic Reticulum Stress and Lipid Metabolism: Mechanisms and Therapeutic Potential

Open access
Basseri, Sana, Austin, Richard C.·2012·Biochemistry Research International

Abstract

The endoplasmic reticulum (ER) plays a crucial role in protein folding, assembly, and secretion. Disruption of ER homeostasis may lead to accumulation of misfolded or unfolded proteins in the ER lumen, a condition referred to as ER stress. In response to ER stress, a signal transduction pathway known as the unfolded protein response (UPR) is activated. UPR activation allows the cell to cope with an increased protein-folding demand on the ER. Recent studies have shown that ER stress/UPR activation plays a critical role in lipid metabolism and homeostasis. ER-stress-dependent dysregulation of lipid metabolism may lead to dyslipidemia, insulin resistance, cardiovascular disease, type 2 diabetes, and obesity. In this paper, we examine recent findings illustrating the important role ER stress/UPR signalling pathways play in regulation of lipid metabolism, and how they may lead to dysregulation of lipid homeostasis.

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Crossref · 10.1155/2012/841362

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Metadata

Authors
Basseri, S., & Austin, R. C.
Venue
Biochemistry Research International
Published
2012
Volume
2012
Pages
1-13
ISSN
  • 2090-2247 (ISSN-L)
  • 2090-2255
OpenAlex
W2010965956
Cited by
254
References
119
FWCI
3.95
Type
journal article
Language
en
Open access
gold

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CoChat. (2026). Citation check: Endoplasmic Reticulum Stress and Lipid Metabolism: Mechanisms and Therapeutic Potential. https://app.cochat.ai/papers/10.1155/2012/841362
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Basseri, S., & Austin, R. C. (2012). Endoplasmic Reticulum Stress and Lipid Metabolism: Mechanisms and Therapeutic Potential. Biochemistry Research International. https://doi.org/10.1155/2012/841362

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.