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Conclusion] The nursing method summed here has obvious cure effect on recovery of patients with anklebone fracture under joint microscope.

结论]本文所总结的护理方法对关节镜下治疗踝关节骨折的手术病人的康复具有明显的疗效。

The histology of chief parts of eyeball and lacrimal gland in Camelus bactrianus was studied with light microscope, and some optic parameters were measured. The eyeball is of anomalistic sphere.

通过光学显微镜对双峰驼Camelus bactrianus眼球的主要结构及附属结构泪腺进行了组织学研究,同时对眼球的一些光学参数进行了测量。

Methods:To produce antihuman DR5 monoclonal antibody(mDRA6) by immunizing BALB/c mice using DR5 protein. The change of DR5 expression after DDPtreated on HL60 cells was detected by FACS. Morphologic changes of HL60 cells were observed under fluorencence microscope. Cytotoxic and apoptotic effects of mDRA6 and DDP on HL60 cells were measured by MTT analysis. DNA fragmentation was detected by agarose gel electrophoresis.

DR5蛋白免疫BALB/c小鼠,融合筛选抗DR5杂交瘤细胞,制备抗DR5单抗——mDRA6;流式细胞术测定顺铂对HL60细胞表面DR5表达及细胞凋亡率;荧光显微镜下观察mDRA6与顺铂协同作用下HL60细胞形态变化;MTT法测定不同浓度的顺铂与mDRA6对HL60细胞存活的影响;琼脂糖凝胶电泳检测mDRA6与顺铂联合对HL60细胞DNA片段化的影响。

The results showed that with treatment of the fixative solution added with antimonite,the free Ca2+ in pear different organs and tissues could be changed into antimonite calcium and precipitated in situ,which,after being stained,appeared as black particles under electronic microscope,whereas such particles could not be observed in the treatment without antimonite.

结果表明:在固定液中加焦锑酸钾处理进行制样,梨树不同器官或组织细胞中的自由态Caa2+,都能生成焦锑酸钙在原部位沉淀,经染色后在电子显微镜下呈现出黑色颗粒,而固定液中不加焦锑酸钾处理的则没有这种颗粒。

After lentectomy through the pupillary hole, the epithelial cells at dorsal iris in Anuran tadpole of Bufo raddei Strauch can undergo transdifferentiation to regenerate a new lens. The morphological changes of lens formation from different regeneration stages were observed with both microcope and transmission electron microscope.

以无尾两栖类花背蟾蜍后肢芽期蝌蚪为实验材料,摘除其左眼晶状体,在再生不同时期固定,石蜡连续切片,苏木精-伊红对染,光镜观察,研究晶状体再生的组织来源;另外,选再生不同时期材料用戊二醛,锇酸固定,透射电镜观察,以研究晶状体再生组织的超微结构变化。

Though, the lateral resolution of CM has been enhanced to be 1.4 times of that of a conventional optical microscope under the same aperture focus ratio, it is still two orders of magnitude lower than the axial resolution of itself.

然而,尽管共焦显微镜的横向分辨力已提高到相同孔焦比的普通光学显微镜的1.4倍,但与其本身的轴向分辨力相比,横向分辨力仍低2个数量级,因此进一步改善共焦显微镜横向分辨力的研究显得尤为迫切。

The operation on the skin and the conjunctiva was performed without using microscope, the dermis and the aponeurosis of the levator muscle of upper eyelid were limited within the ring of the ligature by the line of suture ligatured to form firmly heal which keeps the formed double-fold eyeli...

其法的特征是皮肤面和结膜面均在直视下操作,增加了可信度,缝线结扎后保证了将皮肤的真皮层和提上睑肌的腱膜层均拦在结扎线环内,形成了牢固的粘连愈合,使之形成的重睑沟牢固持久,永不消失。

Cathepsin D and β-tubulin marked with fluorescence were followed in distribution observed by laser scaning microscope, the distribution was from nucleus nearby to cytoplasm and apophysis, which suggested that they took part in traffic in cells.

荧光双标组织蛋白酶D及β-tubulin,共焦激光扫描显微镜下观察,可见二者伴随分布,均由开始的核周分布明显到散在分布于胞质及突起中,说明溶酶体与骨架蛋白密切相关,提示共同参与细胞内的运输。

The result of framework protein and lysosome marked with fluorescence was observed in sym-acorched laser scaning microscope: red fluorescent β-tubulin and green fluorescent eathepsin in nerve cell were seen in distribution in the same sample. The distribution of both was the same, and was located in around nucleus in the early of differentiation, and in cytoplasm and apophysis in the maturity of differentiation.

共焦激光扫描显微镜镜观察荧光双标的骨架蛋白和溶酶体的染色结果:在同一标本上,不同波长的单光激发可分别见到发红色荧光的β-tubulin和发绿色荧光的组织蛋白酶D在神经元内的存在及分布情况,二者的分布区域大致相同,神经元分化初期,较集中分布在核周附近,神经元分化成熟则分布于胞质及突起内。

Methods Laser Confocal Microscope was adopted to measure DNA and RNA of the bone marrow cells marked by AO probe. Influences of arecoline on cell cycle were observed by the Flow Cytometer.

方法采用AO探针标记,激光共聚焦技术检测槟榔碱对骨髓细胞内DNA和RNA的影响;采用流式细胞仪测定槟榔碱对骨髓细胞周期的影响。

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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。

There is no differences of cell proliferation vitality between labeled and unlabeled NSCs.

双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。