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题材史视阈下古代小说谱系化的三种样态刍议 被引量:1
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作者 李春光 《湖北师范大学学报(哲学社会科学版)》 2023年第1期45-53,共9页
在宗法制度的观照下,在谱录形式的话语中,古代小说的谱系化建构问题自有其理论依据与书写程式。谱系之书,从时间上序说族群的来龙去脉、从价值上旌扬族群的丰功伟绩,无疑给古代小说题材选择与创作中的谱系化倾向提供了范本。在题材史视... 在宗法制度的观照下,在谱录形式的话语中,古代小说的谱系化建构问题自有其理论依据与书写程式。谱系之书,从时间上序说族群的来龙去脉、从价值上旌扬族群的丰功伟绩,无疑给古代小说题材选择与创作中的谱系化倾向提供了范本。在题材史视阈下,历史小说创作出现了史谱化的倾向、家将小说创作出现了族谱化倾向、神魔小说创作出现了神谱化倾向。这三种谱系化的创作样态,自然也就构成了一道颇具民族性的文化景观。 展开更多
关键词 神谱化 题材史
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A novel linear microprobe array for the fabrication of neural microelectrodes 被引量:3
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作者 ZHAO Shan Shan PEI Wei Hua +7 位作者 ZHAO Hui WANG Yi Jun CHEN San Yuan CHEN Yuan Fang ZHANG He GUO Dong Mei GUI Qiang CHEN Hong Da 《Science China(Technological Sciences)》 SCIE EI CAS CSCD 2015年第2期346-351,共6页
A novel linear microprobe array(LMPA)has been developed by a conventional microfabrication method from silicon.The LMPA leverages the properties of conventional microwire with additional features of naturally formed r... A novel linear microprobe array(LMPA)has been developed by a conventional microfabrication method from silicon.The LMPA leverages the properties of conventional microwire with additional features of naturally formed regular spacing.With the help of periodic microprobe arrays and double-side V-grooves fabricated in advance between each pair of the two microprobes’rear ends,the number of microprobe units for assembly in one array can be flexibly chosen by cleavage fracture from the LMPA.The fabrication method was demonstrated and the prototype device was assessed by electrochemical impedance spectroscopy(EIS)and in vivo test.The SNR of the spikes recorded was 6. 展开更多
关键词 LMPA regular spacing cleavage fracture V-groove
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The complex genetics in autism spectrum disorders 被引量:11
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作者 HUA Rui WEI MengPing ZHANG Chen 《Science China(Life Sciences)》 SCIE CAS CSCD 2015年第10期933-945,共13页
Autism spectrum disorders(ASD) are a pervasive neurodevelopmental disease characterized by deficits in social interaction and nonverbal communication, as well as restricted interests and stereotypical behavior. Geneti... Autism spectrum disorders(ASD) are a pervasive neurodevelopmental disease characterized by deficits in social interaction and nonverbal communication, as well as restricted interests and stereotypical behavior. Genetic changes/heritability is one of the major contributing factors, and hundreds to thousands of causative and susceptible genes, copy number variants(CNVs), linkage regions, and micro RNAs have been associated with ASD which clearly indicates that ASD is a complex genetic disorder. Here, we will briefly summarize some of the high-confidence genetic changes in ASD and their possible roles in their pathogenesis. 展开更多
关键词 autism spectrum disorders GENETICS causative genes copy number variants
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