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Heat Shock Protein 70 in Alzheimer’s Disease
Rui-Chun Lu, Meng‐Shan Tan, Hao Wang, Anmu Xie, Jin‐Tai Yu, Lan Tan
BioMed Research International · 2014 · ▲ 102 citations
Abstract
Alzheimer's disease (AD) is the most common neurodegenerative disease that caused dementia which has no effective treatment. Growing evidence has demonstrated that AD is a "protein misfolding disorder" that exhibits common features of misfolded, aggregation-prone proteins and selective cell loss in the mature nervous system. Heat shock protein 70 (HSP70) attracts extensive attention worldwide, because it plays a crucial role in preventing protein misfolding and inhibiting aggregation and represents a class of proteins potentially involved in AD pathogenesis. Numerous studies have indicated that HSP70 could suppress the progression of AD with in vitro and in vivo experiments. Thus, targeting HSP70 and the related compounds might represent a promising strategy for the treatment of AD.
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- 10.1155/2014/435203
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- 2026-06-27 MST
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APA
Lu, R., Tan, M., Wang, H., Xie, A., Yu, J., & Tan, L. (2014). Heat Shock Protein 70 in Alzheimer’s Disease. <em>BioMed Research International</em>. https://doi.org/10.1155/2014/435203
Vancouver
Lu R, Tan M, Wang H, Xie A, Yu J, Tan L. Heat Shock Protein 70 in Alzheimer’s Disease. BioMed Research International. 2014. doi:10.1155/2014/435203.
BibTeX
@article{ruichun2014HeatSh,
title = {Heat Shock Protein 70 in Alzheimer’s Disease},
author = {Rui-Chun Lu and Meng‐Shan Tan and Hao Wang and Anmu Xie and Jin‐Tai Yu and Lan Tan},
journal = {BioMed Research International},
year = {2014},
doi = {10.1155/2014/435203},
}
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