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논문 기본 정보

자료유형
학술저널
저자정보
Lee Mi-Suk (Department of Biochemistry, Hallym University College of Medicine) Heo Jee-In (Department of Biochemistry, Hallym University College of Medicine) Kim Jae-Bong (Department of Biochemistry, Hallym University College of Medicine) Park Jae-Bong (Department of Biochemistry, Hallym University College of Medicine) Lee Jae-Yang (Department of Biochemistry, Hallym University College of Medicine) Han Jeong-A. (Department of Biochemistry and Molecular Biology, Kangwon National University College of Medicine) Kim Jong-Il (Department of Biochemistry, Hallym University College of Medicine)
저널정보
한국유전체학회 Genomics & informatics Genomics & informatics 제4권 제1호
발행연도
2006.1
수록면
23 - 32 (10page)

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In order to investigate the molecular basis of the aging process in brain, we have employed high-density oligonucleotide microarrays providing data on 10,108 gene clusters to define transcriptional patterns in three brain regions, cerebral cortex, cerebellum, and hippocampus. Comparison of the expression patterns between young (6-week-old) and aged (17-month-old) C57BL/6 male micerevealed that about ten percent (1098) of the genes showed a significant change in the expression level in at least one of the three tissues. Among them, 23 genes were upregulated and 62 genes were downregulated in all three tissues of the old mice. The number of genes upregulated exclusively in hippocampus (337) was much larger compared to other tissues. Gene ontology-based analysis showed the genes related with signal transduction or molecular transports are more likely to be upregulated than downregulated in the aging process of hippocampus. These data may provide some useful means for elucidating the molecular aspect of aging in hippocampus and other regions in brain.

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