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Olig家族与中枢神经系统疾病 被引量:1

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摘要 2000年首次被人们发现的Olig基因是编码碱性-螺旋-环-螺旋(basic helix-loop-helix,bHLH)转录因子的一个亚家族,它参与了运动神经元、少突胶质细胞和星形胶质细胞的分化,在中枢神经系统(CNS)髓鞘形成和脱髓鞘疾病中发挥重要作用。在不同类别的胶质瘤中,Olig基因表达不同。此外,Olig基因还与脑缺血损伤密切相关。
出处 《中华神经科杂志》 CAS CSCD 北大核心 2008年第1期58-60,共3页 Chinese Journal of Neurology
基金 国家自然科学基金资助项目(30570626)
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参考文献24

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同被引文献16

  • 1Bronchain O J, Pollet N, Ymlahi-Ouazzani Q, et al. The olig family: phylogenetic analysis and early gene expression in Xenopus tropicalis. Dev Genes Evol,2007 ,217 :485-497.
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  • 4Xin M, Yue T, Ma Z, et al. Myelinogenesis and axonal recognition by oligodendrocytes in brain are uncoupled in Oligl-null mice. J Neurosci, 2005, 25:1354 -1365.
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  • 10Lu QR, Yuk D, Alberta JA, et al. Sonic hedgehog--regulated oligodendrocyte lineage genes encoding bHLH proteins in the mammalian central nervous system. Neuron,2000,25:317-329.

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