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民族时间、家族时间及民族史书写范式反思——从畲、瑶家族文本研究出发 被引量:4
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作者 刘婷玉 《厦门大学学报(哲学社会科学版)》 CSSCI 北大核心 2012年第4期40-47,共8页
清末民初是我国民族史学奠基的时期,由于进化论的传入及内外交患的特殊历史环境,其时的民族史书写受到民族国家构建的影响,因其"线性史观"的痕迹而受到质疑。近年来学界对于畲族、瑶族家族文书的收集、整理,为反思这一民族史... 清末民初是我国民族史学奠基的时期,由于进化论的传入及内外交患的特殊历史环境,其时的民族史书写受到民族国家构建的影响,因其"线性史观"的痕迹而受到质疑。近年来学界对于畲族、瑶族家族文书的收集、整理,为反思这一民族史书写范式提供了新的文献基础。畲族家族文书的修撰集中在明清时期,在文本结构上保存了盘瓠传说等鲜明的民族特色。将这部分家族文书与瑶族文书相比对,可以发现二者相类似的叙述传说的"民族时间";将其与讲述具体迁徙过程的"家族时间"相剥离,可以提供一个视角,供我们反思"历史的"、"现在的"二分法的局限,并进一步思考由"民族时间"、"家族时间"的维度重建民族史书写范式的可能。 展开更多
关键词 畲族 瑶族 家族文书 民族时间 家族时间
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时间家族绘画疗法的操作及效果
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作者 陶新华 傅鹃花 《江苏教育》 2019年第48期43-44,共2页
艺术治疗的魅力在于有能力打破来访者在生活中长期积累下的言语防御,使无意识得以展现。
关键词 艺术治疗 时间家族绘画疗法 叙事疗法
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Maximal sequence length of exact match between members from a gene family during early evolution
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作者 温晓 郭兴益 樊龙江 《Journal of Zhejiang University-Science B(Biomedicine & Biotechnology)》 SCIE EI CAS CSCD 2005年第6期470-476,共7页
Mutation (substitution, deletion, insertion, etc.) in nucleotide acid causes the maximal sequence lengths of exact match (MALE) between paralogous members from a duplicate event to become shorter during evolution. In ... Mutation (substitution, deletion, insertion, etc.) in nucleotide acid causes the maximal sequence lengths of exact match (MALE) between paralogous members from a duplicate event to become shorter during evolution. In this work, MALE changes between members of 26 gene families from four representative species (Arabidopsis thaliana, Oryza sativa, Mus mus- culus and Homo sapiens) were investigated. Comparative study of paralogous’ MALE and amino acid substitution rate (dA<0.5) indicated that a close relationship existed between them. The results suggested that MALE could be a sound evolutionary scale for the divergent time for paralogous genes during their early evolution. A reference table between MALE and divergent time for the four species was set up, which would be useful widely, for large-scale genome alignment and comparison. As an example, de- tection of large-scale duplication events of rice genome based on the table was illustrated. 展开更多
关键词 Maximal length of exact match (MALE) Divergent time Gene family Minimal length of exact match (MILE) Genome alignment
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Temporal and Tissue-Specific Expression of Tomato 14-3-3 Gene Family in Response to Phosphorus Deficiency 被引量:1
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作者 XU Wei-Feng SHI Wei-Ming YAN Feng 《Pedosphere》 SCIE CAS CSCD 2012年第6期735-745,共11页
Plants adapt to phosphorus (P) deficiency through a complex of biological processes and many genes are involved. Tomato (Solanum lycopersicum L. 'Hezuo906') plants were selected to grown hydroponically to study ... Plants adapt to phosphorus (P) deficiency through a complex of biological processes and many genes are involved. Tomato (Solanum lycopersicum L. 'Hezuo906') plants were selected to grown hydroponically to study the temporal and spatial gene expression patterns of the 14-3-3 gene family and their roles in response to P deficiency in tomato plants. Using real-time reverse-transcriptase polymerase chain reaction (RT-PCR), we investigated the expression profiles in different tissues (root, stem and leaf) at short-term and long-term P-deficient stress phases. Results revealed that i) four members of 14-3-3 gene family (TFT1, TFT4, TFT6 and TFTT) were involved in the adaptation of tomato plants to P deficiency, ii) TFT7 responded quickly to P deficiency in the root, while TFT6 responded slowly to P deficiency in the leaf, iii) expression response of TFT4 to P-deficient stress was widely distributed in different tissues (root, stem and leaf) while TFT8 only displayed stem-specific expression, and iv) temporal and tissues-specific expression patterns to P deficiency suggested that isoform specificity existed in tomato 14-3-3 gene family. We propose that TFT7 (one member of e-like group in tomato 14-3-3 family) is the early responsive gene and may play a role in the adaptation of tomato plants to shortterm P deficiency, while TFT6 (one member of non-e group in tomato 14-3-3 family) is the later responsive gene and may play a role in the adaptation of tomato plants to long-term P deficiency. 展开更多
关键词 isoform specificity mRNA P starvation primer pairs real-time RT-PCR
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