Establishment and Application of Autoradiograph Assay of p38 MAPK Activity

The chromosomal breaks and fragments, univalents of auto-and sex-chromosomal type and translocation multivalents, especially a rare type, namely between an X chromosome and an autosome were increased at diakinesis-metaphase ⅰ.

在中期Ⅰ发现染色体断裂和断片、易位多价体、性染色体和常染色体的单价体频率显著增高。

The incidence rates of chromosome aberration cells, autosome univalent and sex chromosome univalent had no significant difference between the hexaflumuron-treated groups and the negative control ( P> 0.05) in the chromosome aberration test of primary spermatocyte of mice.

氟铃脲各剂量组的小鼠睾丸初级精母细胞染色体畸变细胞率、常染色体单价体发生率和性染色体单价体发生率与阴性对照组比较，差异无统计学意义（P>0.05）。

The reported ( abnormalities) included the numeric and structural abnormalities of X chromosome, 46, XY, 45, X0/ 46, XY, and the structural abnormality of autosome.

染色体异常包括X染色体数目及结构异常，46，XY、45，X0/46，XY以及常染色体结构异常。

Studies about the genetic diversity of Chinese domestic horses and donkeys were mainly concentrated on mitochondrial genome and autosome. Nevertheless, papers on genetic diversity and origins of Y chromosome in horse and donkey are limited.

目前有关中国马和驴品种遗传多样性的研究多数集中在线粒体DNA和常染色体DNA方面，对其Y染色体遗传多样性和起源进化的研究还比较缺乏。

Based on the hereditary properties of NPV resistance, a hypothesis was proposed and confirmed that the resistance is controlled by NN main gene on an autosome and Z+ Z+ minor genes on the sex chromosome.

根据其遗传规律的特殊性，提出常染色体上NN主基因和性染色体上Z+Z+修饰基因控制假设，并得到试验验证。

( 2) The hereditary mode of rolling tongue or pointed tongue was the dominant heredity of single gene of autosome, and the can-rolling type or can-pointed type was the dominant character.

卷舌和尖舌均为常染色体单基因显性遗传，能卷舌型和能尖舌型分别为显性性状；

It is a recessive hereditary disease of autosome to be deaf and dumb. It was analysed through heredity that reducing or preventing consanguineous marriage can reduce the deaf-mute's birth rate.

聋哑是常染色体隐性遗传病，通过遗传分析发现，减少或防止近亲结婚可以降低聋哑人的出生。

It has been shown that the numbers and the morphologies among the autosome pairs in these four breeds nearly coincided, but there were comparatively remarkable differences among the sex-chromosomes.

结果表明，这四个品种中常染色体对间的带纹数目及形态基本一致，而性染色体间的差异却较大。

The segregative rate in generalized anxiety disorder was 0.225, which was not significantly different ( P> 0.05) from the segregation rate 0.25 in autosome recessive inheritance.

广泛性焦虑校正分离率为0.225，与常染色体隐性遗传的分离率0.25相比较，差异无显著性（P>0.05）；

The hereditary mode of handedness or folding leg was likely the dominant heredity of single gene of autosome, and the right type of them was the dominant character.

利手和叠腿很可能均为常染色体单基因遗传，利手右型和叠腿右型分别为显性性状；

Of the 102 cases of oligospermia, 5 ( 4.9%) patients with the inversion and translocation of some fragments of autosome were identified.

102例少精子症病人中，检出异常染色体核型病人5例（4.9%），主要涉及常染色体某些片段的倒位、易位。

And there are 34 cases of autosome abnormalities which is 25% in all examiners and 46% in chromosome abnormalities.

常染色体异常34例，占全部被检者25%，占异常核型46%。

Sex development in human is determined by lots of genes on sex chromosomes and autosome. It can be divided into two stages: sex determination and sex differentiation.

人类性别发育包括性别决定和性别分化两个阶段，是由性染色体和常染色体上一系列性别决定和分化基因调控的。

Pedigree analysis suggests that FASD is a autosome dominant heredity disease.

家谱分析显示，遗传方式符合常染色体显性遗传。

Model and Stability of Autosome Heredity

常染色体遗传模型及稳定性

44 cases ( 35 8%) were abnormal autosome.

44例（358%）为常染色体异常；

The numbers of MiHAs are huge and their coding genes are in the hole genome, including autosome, Y chromosome and mitochondrial gene.

MiHAs数量庞大，其编码基因分布于整个基因组，包括常染色体、Y染色体、线粒体DNA，现已发现的人类MiHAs有十几种。

Cases were autosome abnormalities ( 4.00%).

常染色体异常8例，检出率4.00%。

The winter landslide survey in Ri-Yue gorge of No.109 autostrada

109国道日月峡滑坡调查

In addition, this paper suggests that the managers need synthesize job demand and job control to manage job stress. The managers should not only pay attention to the negative stress, but also pay more attention to positive job stress such as autotelic experience.

另外，本文提出了管理者需要综合工作需求与工作控制两个方面进行工作压力管理，管理者不应只关注消极压力，更要重视自觉体验等积极工作压力的观点。