性异常

On one hand, it changes the distribution of meridional wind, thus the geostrophic vortivity develops in the ridge region on the south of the subtropical high at 500 hPa. On the other hand, it causes inhomogeneity of the vertical distribution of diabetic heating, triggering anomalous cyclonic circulation between two ridges and anticyclonic circulation in the ridge region on the south.

这一方面改变了经向风的分布，使500 hPa副高南侧脊线区域地转涡度平流项发展；另一方面引起非绝热加热垂直分布不均匀，在两脊线之间诱生一异常气旋性环流，在南侧脊线区生成异常反气旋环流。

Uni- or bilateral radial ray malformation including thenar hypoplasia, thumb hypoplasia/aplasia, triphalangeal, preaxial polydactyly, clubhand, deviation of the forearms, Duane anomaly, sensorineural or conductive deafness, and renal abnormalities

单侧或双侧桡骨线变形包括手掌发育不良，拇指发育不良/发育不全，三指节畸形，轴前并指畸形，畸形手，前臂偏斜，Duane异常，感觉神经性或传导性耳聋，和肾的异常。

Seismicity trend before the earthquake was forecasted according to seismicity feature and commensurable characteristics of strong earthquake activities of Sichuan and Yunnan areas.Since Oct., 1995, a lot of kinds of the anomalies with large amplitude, such as radon and CO2 contents in groundwater and groundwater level etc.synchronized in a wide range of western Yunnan, especially along Zhongdian—Nanjian seismic area. The characteristics of these short-term anomalies are introduced and analysed.

根据川滇地区地震活动特征和可公度性计算结果，在该次地震前对地震大形势进行了预测。1995年10月以后，滇西北地区出现了大面积、大幅度、多手段的同步异常，其中以水氡、水位和CO2异常为主，沿中甸─南涧地震区分布较为集中。

Gene mutations were detected in 25 patients and a 18-year-old girl among 16 families. Trinucleotide repeats of CAG were 73～79. The fragments of abnormal alleles were 380～402bp, and all patients were heterozygous. The copy numbers of normal alleles were 18～40, fragments from 202～270bp. SCV reduction was much obvious compared to MCV, MCV and SCV in lower limb ?ere much more slow than that in upper's. BAEP, VEP were also delayed in latency. The anticipation in parental sex bias were much more obvioius than that in matental's. Cerebellar ataxia was most severe, the next were dysarthria and bulging eyes. Amytrophy was seen only in bed ridden patients. Cerebellar atrophy was more severe than brain stem, cord atrophy was n't observed in all MJD.

结果检出10个家系25例病人及1例症状前18岁女孩有MJD基因突变，CAG三核苷酸重复73～79次，异常等位基因片段长380～402bp，均为杂合子；正常人CAG三核苷酸重复18～40次，等位片段长200～270bp，电生理发现MJD的SCV减慢比MCV明显，而下肢的MCV、SCV又较上肢明显，BAEP、VEP均有不同程度的潜伏期延长或波的异常；MJD的父亲遗传早于母亲，进展也较块，临床以小脑性共济失调为突出症状，其次为构音障碍、突眼等，肌肉萎缩仅见于晚期病人；MRI示小脑萎缩较明显，脑干萎缩并不严重，未见明显的颈髓萎缩。

Cases of eosinophilia were collected and chromosome specimens of bone marrow cells were prepared by 24hour culture, and Gbanding technique was used for karyotyping.

为探讨染色体异常克隆在嗜酸性粒细胞增多症诊断和鉴别诊断中的意义及克隆性嗜酸性粒细胞增多症涉及的染色体异常，收集了65例嗜酸性粒细胞增多患者的骨髓标本，培养24小时，采用G显带进行核型分析。

The aim of study was to investigate the importance of chromosome aberration in differential diagnosis of eosinophilia and the chromosomal aberrations involved in patients with clonal eosinophilia. 65 cases of eosinophilia were collected and chromosome specimens of bone marrow cells were prepared by 24hour culture, and Gbanding technique was used for karyotyping.

为探讨染色体异常克隆在嗜酸性粒细胞增多症诊断和鉴别诊断中的意义及克隆性嗜酸性粒细胞增多症涉及的染色体异常，收集了65例嗜酸性粒细胞增多患者的骨髓标本，培养24小时，采用G显带进行核型分析。

Theories concerning drug addiction dominantly consist of Hedonics, Abnormal Learning, Motivation-sensitization and Dysfunction of Prefrontal Cortex. Models of Self-administration and Conditioned Place Preference are often applied to study drug addiction.

药物成瘾的理论假说主要包括：享乐学说、异常性学习学说、动机-敏感化学说和额叶功能异常学说；且该研究中经常采用的动物模型有自我给药模型、条件化位置偏好模型等。

Results:All of the cases studied,38 cases were abnormal(82.6%).Their magnetic resonance imagings manifested encephalatrophy、leukodystrophy、cerebromalacia、cerebral maldevelopment,and infections of the central nervous system.

结果：46例中，MRI异常38例(82.6%)，脑萎缩、脑白质病变、脑软化灶、先天畸形、中枢神经系统感染等是脑性瘫痪常见的MRI异常表现。

In addition, we presume that the role of different MMPs is distinct in various stages of EMs development. The difference of subjects which is resulted by the genetic difference of MMP-1 has the association with the risk of EMs, and the abnormal expression of protein may have relation with the development of EMs; The abnormal expression of MMP-3 has a very important role in the development of EMs; As a protein of endothelial expression, MMP-7 may participate in the development of EMs, endometrial cells with high-expression MMP-7 easily take place ectopic implantation in the blood of menstruate countercurrented and increase the risk of EMs; It is not confirmed in our study that there are the association of MMP-9 with the risk of EMs, but in view of other study, we will further evaluate the role of MMP-9 in the development of EMs.

且推测不同的MMPs基因在子宫内膜异位症发生和发展的不同阶段作用不同，MMP-1基因的遗传差异所导致的个体差异与子宫内膜异位症发病风险的个体差异相关，其蛋白的异常表达还可能与子宫内膜异位症的进展相关；MMP-3基因的异常表达在子宫内膜异位症的发展中起重要作用；MMP-7作为一个上皮性表达的蛋白，可能对子宫内膜异位症的发生起重要作用，带有MMP-7高表达的在位子宫内膜细胞更易在经血逆流中"异位"种植，增加个体子宫内膜异位症的发病风险；MMP-9虽然在本研究中没有被证实与子宫内膜异位症的发生和发展有相关性，但鉴于其它相关研究，有待于从其它方法证实MMP-9在子宫内膜异位症进展中的作用。

Results Metaphyseal chondrodysplasia is a rare osteopathy that would lead to short limb type pygmy or mutilation bone disease .

结果 干骺端软骨发育异常是一种较罕见的全身短管状骨干骺端软骨发育异常导致短肢型侏儒或致残性体质性骨病。

However, as the name（read－only memory）implies, CD disks cannot be written onorchanged in any way.

然而，正如其名字所指出的那样，CD盘不能写，也不能用任何方式改变其内容。

Galvanizes steel pallet is mainly export which suits standard packing of European Union, the North America. galvanizes steel pallet is suitable to heavy rack. Pallet surface can design plate type, corrugated and the gap form, satisfies the different requirements.

镀锌钢托盘多用于出口，替代木托盘，免薰蒸，符合欧盟、北美各国对出口货物包装材料的法令要求；喷涂钢托盘适用于重载上货架之用，托盘表面根据需要制作成平板状、波纹状及间隔形式，满足不同的使用要求。