异纤毛的

We compared the effect of sevoflurane on ciliary beat frequency with that of halothane and isoflurane using purified andcultured rat tracheal epithelial cells.

我们用纯化培养的大鼠气管上皮细胞比较了七氟烷与氟烷和异氟烷对纤毛活动频率的影响。

Background— Primary ciliary dyskinesia is a recessie genetic disorder that is characterized by sinopulmonary disease and reflects abnormal ciliary structure and function. Situs inersus totalis occurs in 50% of PCD patients (Kartagener's syndrome in PCD), and there are a few reports of PCD with heterotaxy, such as cardioascular anomalies.

背景 先天性纤毛运动异常症是以呼吸道感染和纤毛结构与功能不正常为特征的隐性遗传性疾病。50% PCD患者易发生完全性内脏异位(如PCD中的Kartagener综合征)，有小部分PCD伴有心脏旋转不良等心血管异常现象。

By phenotype observation, combined with root tipchromosome counting, PMC MI pairing analysis and chromosome C-banding, a ditelosomic addition line 94K227 and a disomic addition line 94K280 was identified among BC2F2 and BC2F3 population respectively.C-banding results showed that 94K227 contains 1 pair of long arms in chromosome B, and 94K280 contains 1 pair of chromosome D from R.

用普通小麦-纤毛鹅观草双倍体与普通小麦中国春连续回交两次，然后连续自交，通过形态观察、根尖细胞染色体计数、花粉母细胞减数分裂中期Ⅰ染色体配对分析及染色体C－分带，在BC2F3和BC2F3群体中，分别筛选到一个端二体异附加系94K227和一个二体异附加系94K280，其中C-分带显示94K227添加的是纤毛鹅观草染色体B的一对长臂， 94K280添加的是纤毛鹅观草的一对染色体D。

Methods and Results— The prealence of heterotaxic defects was determined in 337 PCD patients by retrospectie reiew of radiographic and ultrasound data.

方法与结果-内脏异位缺陷的发病率被用来决定337原发性纤毛运动障碍患者通过超声，放射数据回顾性研究

Fancy gold-plated dangling earrings with facetted White Opal crystals.

花式镀金悬垂耳环与facetted白欧泊水晶。

This essay chooses the study aim from biology teachers in middle school in Shi Jiazhuang which tells us that most of the middle school biology teachers in Shi Jiazhuang have the"burnout", lower successfulness, individualize.

本文选取石家庄市初中生物教师作为研究对象，运用问卷调查的方法对石家庄市初中生物教师职业倦怠的现状进行调查，调查结果发现，石家庄市初中生物教师这一群体普遍存在职业倦怠，情感枯竭程度偏高，成就感偏低，去个性化程度最为严重。