4.2 Article

HSP22 and its Role in Human Neurological Disease

期刊

CURRENT NEUROVASCULAR RESEARCH
卷 8, 期 4, 页码 323-333

出版社

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/156720211798121034

关键词

HSP22; chaperone activity; protein-kinase; apoptosis; interaction; neurological disease

资金

  1. National Undergraduate Scientific Project [YD10143]
  2. Central South University

向作者/读者索取更多资源

HSP22 (heat shock protein 22), belonging to the superfamily of small heat shock proteins, which has a molecular mass of 21.6KD and is able to exist in the form of monomer, has multiple functions including molecular chaperones, apoptosis and anti-apoptosis, lifespan extension, antioxidation and so on. In recent years, studies show that HSP22 plays a crucial role in many neurological diseases, such as hereditary nerve endings disease, Alzheimer disease and Charco-Marie-Tooth. This review explores the progress in HSP22 and its involvement in human neurological disease.

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