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There were detestably close synapses between homologous chromosomes during thellateprophase and early metaphase in mitosis of somatic cells.

发现在其有丝分裂的晚前期、中期阶段,咯对同源染色体都在进行联会。

Thress homologous chromosomes of trisomics associated as a trivalent or a bivalent and a univalent or three univalent during diakinesis and metaphase 1 ;Laggard chromosome and univalent separated in advance at anaphase I ,leading to distribution of 10-1-10,9-12,11-11,10-2-10,10-12,10-10,9-1-11 besides 10-ll;And there was distribution of 11-11-10-10, 10-10-10-12, 10-10-10-11, 10-11-11-11, 11-11-10-9, 10-10-10-10, 9-12-10-10, 9-9-11-11, 11-10-10-9, 12-10-9-11, 11-9-9-13, 10-10-10-9 at anaphase II ;n l microspore frequency were different of four trisomics.

三体在终变期和中期Ⅰ,3个同源染色体联会成三价体,或2个联会成二价体和1个单价体,或3个都为单价体;后期Ⅰ出现落后染色体或单价体提前分离,导致除10-11式分离外,还有10-1-10,9-12,11-11,10-2-10,10-12,10-10,9-1-11等不均衡分离方式;后期Ⅱ有11-11-10-10,10-10-10-12,10-10-10-11,10-11-11-11,11-11-10-9,10-10-10-10,9-12-10-10,9-9-11-11,11-10-10-9,12-10-9-11,11-9-9-13,10-10-10-9等分离方式;4个三体中的n 1小孢子频率不同。

This study provides genetic evidence that SUN1-telomere interaction is essential for telomere dynamic movement and is required for efficient homologous chromosome pairing/synapsis during mammalian gametogenesis.

我们的研究首次从遗传学上证明了SUN1蛋白和端粒的相互作用对于端粒在动物生殖细胞减数分裂中的动态变化,高效的同源染色体配对、联会以及哺乳动物的配子发生是必不可少的。

They are often morphologically distinct from A chromosomes, being smallerand more highly heterochromatic in most cases. B chromosomes do not pair with Achromosomes, and they are inherited in a non-Mendelian way, exhibiting meiotic andmitotic instability and nondisjunction. However, B chromosome DNA is quiteidentical to the corresponding sequence on the A chromosome complement. So far afew B chromosome specific DNA sequence have been identified. Specific DNAsequences on B chromosome have been the attractive research area on Bchromosomes.

现已在千余种植物和近三百种动物中被发现。B染色体与物种中正常染色体不同:独立于整倍体基因组之外,减数分裂时不与A染色体发生联会和配对,细胞分裂后期不分离,非孟德尔遗传,富含异染色质,不含对宿主主要性状有影响的基因等。B染色体DNA的分子组成既与A染色体极为相似,具有A染色体DNA分子组成的一般特征:富含重复序列和转座成分,染色体三大功能组件DNA高度同源;又与之相区别,含有B染色体特异的DNA序列,这些DNA序列可以为探讨B染色体的起源和进化提供有价值的信息。

Pairing of homologous chromosomes commences at one or several points on the chromosome and is clearly seen during PACHYTENE of meiosis I.

同源染色体两两成对平行靠拢,这一现象也称联会,联会发生在染色体的一点或多点上,可以在减数第一次分裂的粗线期观察到。

In this article, the specific genes of meiosis and pathways are described in these events in Saccharomyces cerevisiae.

本文简述了现已阐明的酿酒酵母减数分裂的重要事件如同源染色体配对、联会、基因重组、染色体分裂和特异性基因。

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。

However, the protein factors mediating meiotic telomeres attachment to the nuclear envelope and the requirement of this attachment for homologues pairing and synapsis have not been determined in animals.

然而,在动物中至今未能找到介导端粒和核膜附着的蛋白因子,端粒的核膜附着对于动物同源染色体的配对和联会的重要性亦未得到证实。

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。

The failure of homologous chromosomes to pair during meiosis.

不联会在减数分裂期间同源染色体不联会成对。

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