chromosome的例句大全

It showed very significant difference in the rate of micronucleus and frequency of chromosome breakage between the adding medicine groups and the control group ( P < 0. 01).

本组资料表明，微核率和染色体断裂频率在各加药组和对照组之间均有非常显著差异（P＜0.01）。

Thus, the NEU-induced primary chromosome breakage may not be repaired by the ligase.

由NEU所诱发的染色体初级断裂不能为连接酶所修复。

Sodium arsenite was also shown to produce increased sister chromatid exchange in CEO cells and increased chromosome breakage in human lymphocytes.

亚砷酸钠还可引起CHO细胞的姐妹染色单体互换率的增加和人类淋巴细胞染色体的断裂和畸变。

The percentage of chromosome breakage cells had no different between test ( l0.67%) and contrast ( 8. 00%, P> 0. 05).

试验组染色体断裂细胞百分率（10.67%）与对照组（8.00%）之间差异不显著（P>0.05）；

If not repaired, the breakage can result in lethality or chromosome breakage, and if misrepaired, it can cause mutation, gene instability and the increased rate of tumorigenesis.

双链断裂得不到修复，细胞将会死亡或发生染色体断裂、丢失，若是错误修复将导致基因突变或基因组不稳定，增加癌症的风险度。

In this study, MMC-induced chromosome breakage tests have been done on 27 healthy controls and 51 patients with bone marrow failure 〔 including 48 patients with aplastic anemia ( AA) and 3 patients with FA before cytogenetic analysis 〕.

本研究通过对我国27例正常人和51例骨髓造血功能衰竭的患者（48例临床诊断为AA，3例临床诊断为FA）进行了丝裂霉素C（MMC）诱导的染色体断裂试验。

Application of Preparation Chromosome with ConA in Closed Breeding Microtus fortis

封闭群东方田鼠染色体制备中ConA的应用技术研究

A chromosome brittleness test was also carried out on 6 exfoliative patients.

对6例剥脱性皮炎进行染色体脆性分析。

Objective : To investigate the relationship between self-generating abortion couples and abnormal chromosome couples.

目的: 探讨自然流产夫妇与染色体异常的关系.

Linkage analysis of two susceptibility loci on chromosome X for autoimmune thyroid disease among the Hans in the north of China

中国北方汉族人群自身免疫性甲状腺疾病与X染色体2个多态位点的连锁分析

An investigation for genetic polymorphisms of 10 STR loci on chromosome X of Chinese Hui nationality population in Ningxia region of China

宁夏回族人群X染色体10个短串联重复序列位点的遗传多态性调查

Loss of heterozygosity on chromosome 3p in breast cancer and precancerous lesion

乳腺癌及癌前病变3号染色体短臂杂合性缺失的研究

Specific loss of heterozygosity of chromosome 3p loci in soft tissue leiomyosarcoma

软组织平滑肌肉瘤染色体3p位点特异性的杂合性缺失

Loss of Heterozygosity at Chromosome 3P~ ( 14-24) in Patients with Breast Cancer

乳腺癌染色体3P~（14-24）区域不同位点杂合缺失的初步分析

Microsatellite instabilities on chromosome 3p in leiomyosarcoma of soft tissue and its clinical significance

软组织平滑肌肉瘤3p微卫星不稳定性及其临床意义

The results showed that the typical expressions of GVHD were observed 4 or 5 days after the injection of donor spleen cells, and specific male Y chromosome fragment was amplified by genomic PCR in female BALC/ c receipts.

结果显示：3注射脾细胞4～5天后，小鼠开始出现GVHD典型体征，第10天受体小鼠体内扩增出雄性供体小鼠Y染色体特异片段。

Chromosome preparation and G-banded karyotype form lymphoblastoid cells have no obvious change.

细胞染色体制备及G显带棱型分析正常.

Serous retinal detachment in an elderly patient with Philadelphia-chromosome-positive acute lymphoblastic leukemia

1例费城染色体阳性的急性成淋巴细胞性白血病的老年患者出现浆液性视网膜脱离

Objective: To fine map quantitative trait loci controlling the cross section area of cervical enlargement on chromosome 15 of mice.

目的：对15号染色体上控制小鼠脊髓颈膨大截面积的数量性状基因座（QTL）进行精细定位。

Inversion operator is presented to generate a new binary chain by randomly selecting two gene positions and inversing the chain between the two positions in a chromosome.

本文还添加了一种倒位算子，即在一条染色体上随机选择两点构成一个子串，首尾倒置形成新子串替代原子串在个体中的位置。