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Selection of Gene Expression Profile of Alzheimer’s Disease by cDNA Microarray
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DOI   10.11656/j.issn.1672-1519.2004.06.05
Key Words   AD;SAM;gene expression profile;cDNA microarray
Author NameAffiliation
FAN Xiao-nong The First Affiliated Hospital to Tianjin University of TCM, Tianjin 300193, China 
WEN Ting-yi The First Affiliated Hospital to Tianjin University of TCM, Tianjin 300193, China 
DU Yuan-hao The First Affiliated Hospital to Tianjin University of TCM, Tianjin 300193, China 
韩景献 The First Affiliated Hospital to Tianjin University of TCM, Tianjin 300193, China 
李平 The First Affiliated Hospital to Tianjin University of TCM, Tianjin 300193, China 
王舒 The First Affiliated Hospital to Tianjin University of TCM, Tianjin 300193, China 
刘庆忠 The First Affiliated Hospital to Tianjin University of TCM, Tianjin 300193, China 
石学敏 The First Affiliated Hospital to Tianjin University of TCM, Tianjin 300193, China 
Abstract
    [Objective] To select the abnormal expression genes of Alzheimer’s Disease (AD) in Senescence Accelerated Mouse (SAM) and discuss their role in the pathogenesis of AD.[Methods] Using 15400 mouse cDNA microarray the abnormal expression genes in AD were screened.[Results] Two hundred and forty two genes related to dementia were selected, 234 genes related to senile were selected. One hundred and ten genes were selected in both groups considered to be related to both senile and dementia. Most the selected genes were down-regulated,the number of them were almost two-fold than that of up-regulated. The gene function of 22 in 110 were known. The down-regulated genes were mostly related to the pathological functions in releasing of synaptic vesicle, signal transduction, cell skeleton, energy metabolism, etc. On the other hand, the up-regulated genes were mainly involved in the pathologic functions of cell cycle, ion channel, protein synthesis, inflammatory reaction, and so on.[Conclusion]"Gene expression profile of AD" may find some rules in many clues in researches of AD and provide some evidences to reduce the blindness in the late study.

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