1、

Progress of MADS-box Gene Research in Plant

植物MADS-box基因研究进展

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2、

Cloning of Flower Development Associated MADS box Gene Fragments in Lilium

百合花发育相关MADS box基因的克隆

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3、

Isolation and Functional Analysis of a MADS Box Gene in Populus tomentosa

一个毛白杨MADS盒基因的克隆与功能分析

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4、

A regional localization of SRY box gene on bivalent chromosomes of Monopterus alba

二价染色体上黄鳝SRY盒基因的高分辨区域定位

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5、

Cloning of high mobility group box B1 gene and its relationship with development of neural tube

高迁移率族蛋白B1基因的克隆及其与神经管发育的相关关系

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6、

The encoding method and the method of realizing the parameters of genetic unit bounding box of part gene are given first.

首先给出了零件基因模型,并在此基础上给出了基于编码表示的体基因基因串,以及基于包围盒表示的基因单元参数的描述方法。

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7、

An A was replaced by a G in codon 38 upstream of the 5 ′ border outside the HMG box of the SRY gene, resulting in the replacement of the amino acid glutamate by glycine.

一个突变发生在SRY基因的5′端HMG盒外的核苷酸第113位腺嘌呤(A)被鸟嘌呤(G)取代,并导致谷氨酸被甘氨酸替换;

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8、

Regulatory elements W box, X box, Y box, CCAAT box and TATA-like box which were associated with the expression of structural gene were found in all the URR sequences.

这些序列中均存在与基因表达调控有关的W BOX、X box、Y BOX、CCAAT box以及类TATA Box调控元件,且遵循严格的空间顺序。

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9、

At the same time, the gene of AGAMOUS which is a MADS-box gene was identified.

同时还识别了一个控制花器官发育的MADS-box基因AGAMOUS。

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10、

The sequence includes typical TATA box and CAAT box. The expression of the Rubber Elongation Factor gene in the latex and in the leaf has been detected by Northern blot.

为证实该基因为乳管特异表达,我们通过Northern Blot对橡胶延伸因子基因在胶乳和叶片中的表达做分析。

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11、

Molecular Cloning and Expression of Flowering-related MADS-box Gene in Diospyros kaki

柿花发育相关的MADS-box基因克隆与表达

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12、

The Transcriptional Regulation Study on Human δ Globin Gene with CAAT Box C → T Point Mutation in Its Promoter

人δ珠蛋白基因启动子区CAAT盒C→T突变对其转录的影响

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13、

On the other hand the rib operon of the Bacillus subtilis was also modified: eliminating the rfn box, replacing the rib promoter by constructive bacteriophage promoter spol and taking the tetracycline resistance gene as a selectable marker etc.

另外我们对枯草芽孢杆菌中的核黄素操纵子做了进一步的优化和改造,主要包括:调控序列的去除、外源强启动子spol的加入、原启动子的去除以及四环素抗性基因的加入等。

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14、

GC-box is not a key cis-acting element in human insulin gene promoter

GC盒不是人胰岛素基因启动子中关键顺式作用元件

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