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x chromosome相关的网络例句

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与 x chromosome 相关的网络例句 [注:此内容来源于网络,仅供参考]

The results showed that karyotypic type of Ya01-21was 2n=104=100m+4sm(4SAT), Chromosome length ratio of the longest and the shortest 4.25, the average arm-ratio 1.35, belonging to 2C type of chromosome. Molecule identified combine with chromosome studied indicated that Ya01-21 was a progenies of Erianthus arundinaceum. following the law of n+n; ITS identify showed that Ya01-21 is a progenies of Erianthus arundinaceum, the somatic chromosome karyotypic type of Ya01-36 was 2n=132=130m+2sm, Chromosome length ratio of the longest and the shortest 3.94, the average arm-ratio 1.27, belonging to 2B type of chromosome, combining the advance of characters the law of 2n+n can be resumed.

研究结果表明,崖城01-21的体细胞染色体核型公式为2n=104=100m+4sm(4SAT),最长与最短染色体的长度比为4.25,平均臂比1.35,染色体属2C型,分子鉴定结合细胞学研究认为其为斑茅的真实后代,其染色体遗传为n+n;崖城01-36经ITS签定为真实杂种,其体细胞染色体核型公式为2n=132=130m+2sm,最长与最短染色体的长度比为3.94,平均臂比1.27,染色体属2B型,结合其性状的进展,推断亲本向其传递染色体可能以2n+n的方式进行。

The number of the chromosomes in Henan large tail sheep is 2n=54, the karyotypes of male and female sheep are 54, XY and 54, XX, respectively. There are 26 pairs of autosomes and 1 pair of sex-chromosome. Among 26 pairs of autosomes, 3 pairs are metacentric chromosomes, 23 pairs are telocentric chromosomes. X chromosome is the biggest subtelocentric chromosome and Y chromosome is the smallest submetacentric chromosome.

河南大尾寒羊二倍体染色体数目为2n=54,公羊核型54,XY;母羊核型54,XX.27对染色体中包括26对常染色体和1对性染色体,常染色体中有3对为中着丝粒染色体,23对为端着丝粒染色体;性染色体中,X染色体为最大的端着丝粒染色体,Y染色体为最小的中着丝粒染色体。

Abnormal chromosome was detected in 17 fetuses. Among them, trisome 21, trisome 18, trisome 13, Turner syndrome, Klinefelter syndrome, short arm deletion of chromosome 18, and inverted chromosome 9 were detected in 8, 3, 1, 1, 1, and 2 fetuses, respectively. Abnormal chromosome was found in 5 out of 8 fetuses who received serum screening. Ultrasound showed abnormal chromosome in 11 fetuses.

共诊断17例胎儿染色体异常,其中21三体8例,18三体3例,13三体1例, 1 Turner综合征1例,Klinefelter综合征1例, 18染色体短臂微缺失1例,9号染色体臂间倒位2例(1例来源于母亲)。17例中有8例进行了唐氏儿血清学筛查,5例异常,11例超声检查胎儿有结构异常。

The single micronucleus and multi-micronucleus were observed at the interphase. The chromosome aberrational cells including chromosome fragment, lagging chromosome, chromosome bridge and circular chromosome were found during the mitosis. RAPD analysis of seedling genomic DNA variation in M 2 generation of three mutants showed their DNA sequences had changed. The result confirmed that the implantation of 7Li +3 ions could induce genetic mutation in wheat.

对幼苗根尖细胞学研究观察,获得单桥、双桥、桥断裂、落后染色体、三级、断片和微核等畸变类型;对已获得的小麦突变株,分别进行M2 代DNA分子的RAPD分析,结果发现DNA均发生变异,证明7Li+ 3 注入通过内靶核反应能够诱发小麦在分子水平上产生遗传变异。

CML is cytogenetically marked by the philadelphia chromosome, which originates from a reciprocal translocation between chromosome 9 and 22 and is molecularly marked a chimeric bcr-abl gene, resulting from juxta-positive of the abl proto-oncogene on chromosome 9 with the bcr gene, which is normally located on chromosome 22. The chimeric bcr-abl gene expression an 8. 5kb hybrid mRNA transcript giving rise to a 210-KD fusion protein (P210〓) with increased tyrosine kinase activity. P210〓 plays a key role in the pathogenesis of CML. The continuous cell line K562 was established from the pleural effusion of a 53-year-old female with CML in terminal blast crisis, and was a human erythroleukemia line, contained Ph chromosome.

绝大多数慢粒患者白血病细胞中具有Ph染色体,是由9号染色体长臂3区4带和22号染色体长臂1区1带相互易位形成,即t(9;22),使位于9q〓的c-abl原癌基因在第二外显子的5'端断裂并易位到22 q〓的M-bcr基因第2或第3外显子的3'端,形成异常的bcr-abl嵌合基因,该基因转导出异常的mRNA,编码并翻译出P210蛋白,该蛋白具有很强的酪氨酸激酶活性,使粒细胞发生恶性增殖。K562细胞属于慢粒急变、红白血病细胞株,具有Ph染色体。

In the BC〓F〓 and BC〓F〓 generation of Yannong15×Thinopyron intermedium hybrid, 4 octoploids which had chromosome number of 2n=56 and could form 28 bivalent at PMC MI, 14 disomic addition lines which had chromosome number of 2n=44 and could form 22 bivalent at PMC MI; three monosomic addition lines which had chromosome number 2n=43 and had the chromosome configuration of 21Ⅱ+1Ⅰ at PMC MI, 1 substitution line which had chromosome number 2n=42 and could form 21 bivalent at PMC MI were selected by observation of mitosis in root tip cell and meiosis in pollen mother cell.

在烟农15与中间偃麦草杂交的BC〓F〓和BC〓F〓代中,通过根尖有丝分裂和花粉母细胞减数分裂中期Ⅰ观察选出4个2n=56,PMC MI染色体构型为28Ⅱ的八倍体小偃麦;14个2n=44,PMC MI染色体构型为22Ⅱ的双体异附加系;3个2n=43,PMC MI染色体构型为21Ⅱ+1Ⅰ的单体异附加系;1个2n=42,PMC MI染色体构型为21Ⅱ的异代换系。

X chromosome was a large submetacentric chromosome. Y chromosome was a small metacentric chromosome.The relative length of chromosome was measured by AutoCAD software. The relative length of autosomes ranged from 1.545% to 4.921% in Yanbian yellow cattle and from 1.637% to 5.855% in Liyan hybrid cattle.

结果表明,延边黄牛和利延杂交牛二倍体染色体数目2n=60,公牛核型为2n=60,XY,母牛为2n=60,XX,其中29对常染色体均为端着丝粒染色体,X染色体为较大的亚中着丝粒染色体,Y染色体为较小的中着丝粒染色体。

It was found that the chromosomes involved in translocation were chromosome 10 and 11 in stead of chromosome 9 and 12 as being compared with the karyotype of Nipponbare.So we consider that the chromosome 9 and 12 in the present rice chromosome numbering system could be chromosome 10 and 11 according to their length,arm ratio and the relationship with nucleolus.

结果表明,该易位系的易位染色体并非第9和第12染色体,而是第10和第11染色体,从而认为目前国际上统一编号的第9、12染色体,根据染色体的实际长度可能分别为第10、11染色体。

Biomass and WUE1 of wheat with R chromosome set is largest in all diploidy material, and that with B chromosome set is least in all diploidy material. Meanwhile, the root growth of wheat with A and B chromosome set is largest, and that with D chromosome set is least in all diploid material.

N、P影响了干旱下玉米叶片的气体交换能力,表现为提高了干旱下玉米叶片的气孔导度和光合速率,且N的作用要大于P的作用;N具有同时降低玉米叶片光合作用的气孔和非气孔限制的作用,而P提高玉米光合则主要是由于降低了干旱下的非气孔限制。

This text is mainly about the analysis of the palindromes of Y chromosome. We mainly used DOTTER program for detailed comparison of two sequences to obtain these results. The main contents are as follows:Chapter one mainly introduces the whole characteristics of human Y chromosome;Chapter two mainly describes the characteristics, functions and recombination modes of the palindromes in Y chromosome;Chapter three mainly analyses the symmetries of 8 palindromes of Y chromosome, we find a mechanism of symmetry breaking in P2 palindrome from a detailed analysis;initially introduces other 7 palindromes.

本文主要借助于DOTTER程序对Y染色体的回文序列进行分析,主要内容如下:第一章主要介绍人类Y染色体的整体特征;第二章主要描述Y染色体中回文序列的特征、功能及重组模式;第三章主要是对Y染色体8个回文序列的对称性分析,主要对P2回文进行了详细分析,提出了P2回文的对称性发生破缺的机理;对其他7个回文进行了初步分析。

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