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Results Stratum ganglionare nervi optici and inner nuclear layer became thinner under light microscope,and there was pyknosis and mitochondria vacuolization under electron microscope after reperfusion for 6 hours.

结果 再灌注6 h后，光镜下模型组视网膜神经节细胞层、内核层变薄，电镜下出现核固缩，线粒体空泡化。

Using Scan Electron Microscope and Metallography Microscope to analyze the organization and appearance of the abraded face of the composite materials.

利用SEM和金相显微镜分析复合材料组织及磨面形貌。

Morphological changes of aortas'tissues and SMCs had been observed under microscope and electro-microscope.

光镜及电镜下观察了动脉组织及SMCs形态学改变。

As exposed to optics microscope and inverted microscope,compared to control,SW480 cells with Giemsa staining that treated with the H2RA(cimetidine、nizatidine) took on malignance declining as crimpled firstly,cellular bulk and heteromorphism dimimished,the amount of rounded cell manifolded,nucleolus bulk lessened,dyeing thin,the amount of nucleolus decreased,partial cell organs manifest side-gathering phenomenon on chromatin,and the link between SW480 cell is loosened , subsequently partial rounded cell is floated.When the H2RA(cimetidine 40μM、nizatidine 20μM) against SW480 cells after 3 day,SW480 cells change roundly,nucleolus smashed,shrinking nucleolus came into being,and part of those not adhibited cell wall.

在光镜和倒置相差显微镜下，与对照组相比，经姬姆萨染色观察，西咪替丁、尼扎替丁处理的SW480细胞，先发生皱缩，体积变小，异形性减少，细胞变圆数目增多，细胞核变小，染色变淡，核仁数量减少，部分可见染色质边集现象；细胞间连接疏松，随后部分变圆细胞浮起。40μM西咪替丁及20μM尼扎替丁连续处理3天后，SW480细胞全部变圆，细胞核碎裂，固缩微核形成，部分不再贴壁。

The surface and the cross-section of the alloy films before and after hydrogenation were observed by scanning electron microscope and atomic force microscope, which showed that the lower reflection observed in the dehydrogenated film is due to the rough surface originating from the first hydrogenation.

利用扫描电子显微镜和原子力显微镜观察了吸放氢前后薄膜的表面及剖面形貌。

The adjacent region in 3mm diameter was eradiated in various ways: exposed directly to light, through AcrySof one piece IOL, PMMA IOL,AcrySof Natural IOL, and without light. Then the eye cups were cultured for 48h. Lastly, tissue and cell structure were observed with light microscope and transmission electron microscope.

在无菌条件下将新鲜离体猪眼制成眼杯，利用显微镜光源对视网膜后极部照射，使相应视网膜蓝光光照强度为30J/cm2或40J/cm2，进行单独光照、透过Acrysof一片I0L、透过Acrysof Natu-ral，照射后培养48h，对相应部位视网膜组织，HE染色光镜、透射电镜下观察。

MethodsHuman embryonic lens epithelial cells were cultured by the explanting culture methods. An inverted phase contrast microscope, electron microscope and immunocytochemistry were used to study the growth specialties of the human embryonic lens epithelial cells.

方法组织块贴壁法培养人胚晶状体上皮细胞，通过倒置相差显微镜、透射电子显微镜，采用免疫细胞化学法分析人胚晶状体上皮细胞的生长特性。

Optical microscope, electron microscope and FCM were used to analyse the apoptosis of Hela cell treated with different concentration of DM9811 fermentation filtrates. FCM was used to analyse the cell cycle of the differently treated Hela cells.

用光镜、电镜和流式细胞仪分析不同浓度乳酸杆菌DM9811发酵滤液对Hela细胞凋亡的诱导效果；用流式细胞仪分析不同浓度乳酸杆菌DM9811发酵滤液对Hela细胞细胞周期的影响。

Thirdly, the influences of HDTMA on the algal physiological functions were measured and the micro-structures of algae stressed by HDTMA and flocculated with organo-clay particles were observed separately through transmission electron microscope and scanning electron microscope.

另外，测定了 HDTMA 胁迫下藻细胞生理指标的变化，借助电镜观察等手段分析了 HDTMA 改性粘土去除赤潮生物的机理。

For further studying the genetic mechanism of the reproductive isolation phenomenon of interspecific hybrid, paraffin sections of testes from 13 sexually mature male mules (Equus asinus×Equus caballus) and 12 hinnies (Equus caballus×Equus asinus) were prepared, and the samples of Giemsa meiosis and AgNO 3 synaptonemal complexes were observed and compared with spermatocyte meiosis of horse and donkey under light microscope and electronic microscope.

为了进一步探讨种间杂种生殖隔离现象的遗传机理，本研究采用性成熟公骡的睾丸为材料，制备组织切片和减数分裂联会复合体标本进行观察，发现个别性腺发育较好的个体虽然减数分裂存在大量异常，但确有少数精母细胞完成了减数分裂并产生精子。

This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

扫描电镜观察多杀性巴氏杆菌细菌幽灵和菌落形成单位评价遗传灭活率。