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chromatid相关的网络例句

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与 chromatid 相关的网络例句 [注:此内容来源于网络,仅供参考]

In evl-14 mutant animals, synaptonemal complexes were detectable at the pachytene arrest, but more than the usual six DAPI-staining positive structures were seen in diakinesis, suggesting that EVL-14/PDS-5 is important for the maintenance of sister chromatid cohesion in the late prophase.

这一结果提示EVL-14/PDS-5对于在减数分裂的晚前期维持姐妹染色单体粘连是十分重要的。

Genes important for male gametogenesis involved in highly con-served landmark events such as meiotic recombination, formation of the synaptonemal complex, sister chromatid cohesion, spermiogenesis during postmeiotic stages, and checkpoints and factors required for the meiotic cell cycle .

精子发生中的重要基因与一系列精子发生过程中阶段性的细胞事件密切相关,例如减数分裂重组、联会丝复合物的形成、姊妹染色体的结合、减数分裂后精子的变态以及减数分裂周期中的关键点和必需因子等。

Institute of Genetics,Fudan University,ShanghaiThe C-banding and BrdUrd-Hoechst-Giemsa replication pattern in somatic chromosomes in Bufo bufo gargarizans and sister chromatid differential staining technique of the somatic cells in Amphibia are presented in this article.

本文报道了中华大蟾蜍的C带和BrdUrd-Hoechst-Giemsa复制带,并以中华大蟾蜍为代表确立了两栖类体细胞的姐妹染色单体差别染色方法。

The dynamic behaviou r of chromatid core formation suggests that this structure represents a real str cutural component existing in metaphase chromosomes and that it may play certain important role in the maintenance,stabilization and condensation of chromos omes.

染色体形成的动态行为,一方面暗示了这种结构在染色体集缩和维持中期染色体的形态方面起某种重要作用;另一方面说明了轴是染色体中存在的一种真实结构。

From 400 metaphases of the control group, 4 abnormal cells were found, with 1% chromatid-type aberration ratio.

对照兔在400个中期分裂相中见4个,单体畸变率为1%。

Meantime, 12 abnormal cells in 800 metaphases of the control group were found, with 1.5% chromatid-type aberration ratio.

实验兔在800个中期分裂相中见12个,单体畸变率为1.5%。

YR-cohesion chromosome model will give a better answer to the questions such as exchange,centromere,holocentromere,synaptonemal complex,polytene chromosome,puff,lampbrush chromosome,chromosome banding,non-segregation of sister chromatid,pollentube pathway and biological evolution.

YR-染色体模型能自然、合理地解释所有遗传现象,如交换、着丝粒、全身着丝粒或弥散型着丝粒染色体、同源染色体联会及联会复合体的中央区、多线染色体与膨突、灯刷染色体、染色体分带、姊妹染色体由前期到中期不分开、花粉管会导入外源遗传物质、高等生命是怎样从原始生物进化而来的等等。

Aluminum-induced Ultraweak Luminescence Changes and Sister-Chromatid Exchanges in Root Tip Cells of Barley. Plant Science, 2005, 167:1391-1399 Maojun Xu, Jufang Dong, Muyuan Zhu.

发现铝毒通过ROS 诱导SCE 发生的关系,建立了新的铝毒检测指标;(3)研究了细胞凋亡与植物耐铝毒型, BC,代谢产物表达的关系。

The markers usually used in the molecular epidemiologic study includes internal dose marker, Ames test, DNA adducts, and cytogenetic markers, e.g. chromosome abeeration, sister chromatid exchange and micronucleus.

本文讨论目前常用的生物侦测方法,包括内在剂量测定,致癌物—DNA结合物的生物有效剂量测定及生物效应的测定。

The results demonstrated that the dup(p21) and the del(p11) were of paternal origin and i was of maternal origin. The dup(p21) arose from an unequal sister chromatid exchange. The del(p11) occurred through X chromosom e breakage and deletion machanism.

结果表明,dup(p21)和del(p11)起源于父方,而i起源于母方。dup(p21)是由X染色体姊妹染色单体不均等的互换所引起的,del(p 11)是由于X染色体断裂后丢失所致,i的发生是由于卵母细胞X染色体着丝粒错分裂。

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Do you know, i need you to come back

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