三染色体的

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。

The main aberrations of the euchromosomes was chromosome gain, including trisome, tetrasome, and polysome. The gain rates of the four euchromo-some were 84.9%, 77.5%, 63.7% and 83.2%, and the frequencies of polysome for each euchromosome were 24.6%, 34.9%, 23.4% and 31.7%, respectively. Loss of chromosome Y was observed in 61.2% of male patients. The combination of the four chromosome probes 3, 8, 10 and 20 detected 74.5% of ESCC and the combination of 3, 8, 20 and Y detected 85.0%.

发现所测常染色体在食管癌组织中均存在较高的数目畸变率，主要表现为染色体增益，包括三体、四体及多体。4条常染色体3、8、10和20号染色体增益率分别为84.9%、77.5%、63.7%和83.2%，其中多体率各为24.6%、34.9%、23.4%和31.7%。Y染色体在61.2%的男性患者表现缺失。3、8、10和20号探针联合检测食管癌的阳性率为74.5%， 3、8、20和Y染色体探针联合检测男性食管癌的阳性率为85.0%。

Of or relating to the association of three or more homologous chromosomes during the first division of meiosis.

属于在第一时期成熟分裂时三个或者更多的同源染色体的联合的。

Genetics used of the association of three or more homologous chromosomes during the first division of meiosis.

属于在第一时期成熟分裂时三个或者更多的同源染色体的联合的。

Results showed that the PMC meiosis of autotetraploid was similar to the diploid except some particularities. In metaphase Ⅰ, multivalent, quadrivalent, trivalent, bivalent and univalent were observed and some of the chromosomes were found not to rank on the metaphase plate and so did in metaphase Ⅱ cells. In anaphase Ⅰ and anaphase Ⅱ cells, there were lagging chromosomes, chromosome bridge and fragment. During anaphase Ⅱ and telophase Ⅱ, chromosome segregation was not synchronous or equal. At tetrad stage, dyad, triad, tetrad with micronucleus and polyad appeared.

结果表明，同源四倍体花粉母细胞减数分裂过程与二倍体相比，中期Ⅰ染色体构型复杂，有多价体、四价体、三价体、二价体和单价体；中期Ⅰ及中期Ⅱ有部分染色体没有排列在赤道板上；后期Ⅰ及后期Ⅱ出现落后染色体、染色体桥及断片；后期Ⅱ和末期Ⅱ有染色体不同步分离及不等分裂的现象；四分体时期还出现二分体、三分体、含微核的异常四分体及多分体。

Three kinds of embryos' chromosome, including goat fertilization embryo, goat-goat cloned embryo and goat-rabbit cloned embryo were analyzed, The results showed that all of them have 60 chromosomes with same character, all were telocentric chromosome, besides the X-chromosome is the second larger telocentric chromosome.

经对超排获得的山羊受精胚、山羊同种克隆胚和羊-兔异种克隆胚的囊胚期胚胎染色体分析表明，三种来源的胚胎其染色体数目均为60条，且所有常染色体均为端部着丝点染色体，X染色体为第二大的端部着丝点染色体，说明山羊同种克隆胚和山羊-兔异种克隆胚均为山羊的核型，是供体细胞核在不同胞质中的重新编程的结果。4。

Using semi-quantitative RT-PCR, the differential expression profiles of eleven selected genes were confirmed in the ovaries of triploid and diploid. These genes fell in gene categories with a wide range of functions. The results indicated that triploidy affects the dynamic gene regulatory network in triploid ovary. This study established a firm basis for future investigation on characterization of crucial molecular events for normal ovarian development in shrimp.To further dissect exact gene functions for gonad development of shrimp, three differentially expressed genes between diploid and triploid ovary, PCNA (proliferating cell nuclear antigen), CAS/CSE1 (cellular apoptosis susceptibility protein/chromosome segregation 1) and SSRF (spermatogonial stem-cell renewal factor) were characterized on certain aspects.

利用抑制性消减杂交技术，建立了对虾二倍体和三倍体卵巢间的2个消减文库；在正向消减文库(以三倍体卵巢作为实验组，二倍体卵巢作为驱动组)中，鉴定到54个基因；在反向消减文库(以二倍体卵巢为实验组，三倍体卵巢为驱动组)中，鉴定到16个基因；选取11个差异表达的基因，利用半定量RT-PCR的方法对其在二倍体和三倍体卵巢间的表达进行了检测，均能很好地与消减结果相吻合；这些差异基因编码多种功能的蛋白，分析表明染色体的三倍化使三倍体卵巢中的基因调控网络受到了影响；为深入揭示维持卵巢正常发育的关键分子调控事件奠定了基础。

For obtaining the aneuploid in rice,the primary trisomic from triplo-1 to triplo-12 and the aneuploid derived from 1992~1995.From the offspringe of triplo-10, a primary trisomic of chromosome 10 of this variety,an isotetrasomic triplo-10-1 was obtained.

在水稻上，为了获得这类遗传材料，从中籼3037同源三倍体后代产生的非整倍体中，在筛选初级三体的同时，进行了等臂染色体变异材料的筛选。

N l male gamete transmission of trisomic 2,7,9 had the relation with chromosome behavior at meiosis and with the degression of pollen activity.Besides,n l male gamete fertilization ability and 2n l embryo development ability perhaps could influnce it,too.

6.2号、7号、9号三体n 1雄配子传递率与减数分裂过程中染色体的行为和花粉生活力的降低有关，同时，n 1雄配子受精能力、2n 1胚发育能力可能也会影响n＋l雄配子的传递率。

The results showed that: at metaphase I, the homoeologous chromosome pairing among different F1 hybrids ranged from 2.0 to 11.4 bi-valents formed by homoeologous chromosomes per pollen mother cell, and very few multivalents, and even very few bivalents were formed by two chromosomes within one genome rather than homoeologous chromosomes in some PMCs; at anaphase I, all biva-lents were disjoined and most univalents were divided.

结果表明在中期I阶段，这些杂种一代的近缘染色体联会变化很大，每个花粉母细胞中二价体形成的数目从平均2个到11.4个不等，甚至在某些花粉母细胞中，还发现极少的多价体和非部分同源染色体所形成的单基因组内二价体；在后期I时，所有的二价体分离，同时多数单价体也分离，分离的二价体和分离的单价体都移向两极，从而形成两组染色体；因为这时完整花粉母细胞中分离的二价体在两组染色体中总是对应出现，从而根据半二价体上染色体重组的位置可以分析在二价体的四分体时期发生在非姊妹染色体之间的多种染色体交换类型，如单交换、三线双交换、四线双交换、四线三交换和四线多交换。

And Pharaoh spoke to Joseph, saying, Your father and your brothers have come to you.

47：5 法老对约瑟说，你父亲和你弟兄们到你这里来了。

Additionally, the approximate flattening of surface strip using lines linking midpoints on perpendicular lines between geodesic curves and the unconditional extreme value method are discussed.

提出了用测地线方程、曲面上两点间短程线来计算膜结构曲面测地线的方法，同时，采用测地线间垂线的中点连线和用无约束极值法进行空间条状曲面近似展开的分析。