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A structure formed during homologous recombination after synapsis.

联会之后的同源重组过程中形成的结构。

Synapsis The association of homologous chromosomes during the prophase stage of meiosis that leads to the production of a haploid number of bivalents.

联会:能产生单倍二价体的减数分裂前期,同源染色体的联合现象。

Besides, terminal synapsis was observed to occur in the meiosis of spermatocytes based on the analysis of signal distribution of 5S rDNA on chromosomes obtained from testis.3. 18S rDNA and histone gene h3 were mapped to the chromosomes of C.

此外,通过对5S rDNA在精巢染色体上信号分布特征的观察,认为中国明对虾的同源染色体在第一次减数分裂中期可能发生了末端联会。3。

We identified a homologue of human osteoclast-stimulating factor from the rice field eel, a teleost with characteristic of naturally sex transformation from female, via intersex to male during its life.

我们从它的性腺中,克隆到人破骨细胞刺激因子Ostf(osteoclast-stimulating factor)的同源基因。

By screening a rice genomic library, we isolated a TB1-like gene-Oryza sativa Teosinte Branched (OsTB1) in rice. We also isolated the cDNA of OsTB1 by RT-PCR.

通过筛选水稻的基因组文库,得到了水稻中的一个TB1同源基因Oryza sativa Teosinte Branched1 (OsTB1)。

In conclusion, abnormal meiosis of PM-Cs is the cytogenetic causes for fertility reduction of tetraploid melon.

花粉母细胞减数分裂的异常是同源四倍体甜瓜育性低的细胞学原因。

A total of 42 positive differential fragments were obtained,of which 5 fragments had no homolog in the NCBI and EMBL.

在获得的42个阳性阶段特异性表达的基因中,有5个在NCBI和EMBL数据库中没有同源序列,登录EMBL,申请了登录号。

These ten genes correspond to six of the ten known subunits of TRAPP complex in yeast.

这10个基因的编码产物与酵母TRAPP蛋白复合体已知10个亚基中的6个分别同源。

Treacle and its homolog cousin, Nopp140, are nucleolar phosphoproteins involved in pre-rRNA transcription and processing.

Treacle以及它的同源蛋白Nopp140皆位於细胞核仁,参与在核醣体核醣核酸前趋物的生成和加工。

Methods The phage displayed antigens of paragonimus were used to examine the sera of patients with paragonimiasis,schistosomiasis,trichinosis and healthy people,and their sensitivity and specificity were acquired;The templates of the mimic antigen were purified to determine the sequence and the sequence homology was analyzed by Blast.

方法建立肺吸虫噬菌体模拟抗原的ELISA,对肺吸虫病人、日本血吸虫病人、旋毛虫病人及健康者血清进行检测,分析其敏感性和特异性;提纯噬菌体模拟肽的DNA模板进行序列测定,以Blast软件分析其序列同源性。

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