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And the overgrowth lesions are characterized by epithelial acanthosis, with long, branched rete peg formation, and the excessive accumulation of radiating collagen fibers in the connective tissue layer.

此种疾病在组织学上的特徵为:上皮细胞层数有增厚的发现,并呈现明显的棘状凸出延伸至结缔组织中,在结缔组织中则有大量胶原蛋白堆积而产生纤维化;然而引发牙龈增生的病理机制至今仍不明确。

This study takes the reservoir of the Kela 2 gas field of the Tariam basin, the western China, as an example for understanding the relationship between the porosity and permeability and autogenetic minerals and textures of the clastic rocks on the vertical depth scale. The secondary pores are essential reservoir space in this gas field, moreover, their origin is closely related to dissolution of the frame grain of plagioclase and the cements of calcite.

本文以克拉2气田储层为研究对象,探讨了该区纵向深度上孔隙度、渗透率与矿物组合、结构上的变化,发现次生孔隙是本区储层的重要储集空间,并且与长石骨架颗粒和方解石胶结物的溶蚀密切相关。

In the short-run label can use all the common bolographic anti-false self adhesive identity applies on anti-counterfeiting technology, such as true color hologram, encryption, and synthetic, photochemical micro-kizami technology, such as relief can be an excellent anti-false effect.

在烫印标上可以运用所有在通用全息防伪不干胶标识上采用的防伪技术,比如像素全息、真彩色、合成加密、微刻、光化浮雕等技术,能起到极佳的防伪效果。

The screening was carried out by single strand conformational polymorphorsim : the PCR product precipitation was dissolved in 20μl denaturing and loading buffer (95%+20mMEDTA+ 0.05% bromophenol blue+0.05% xylene cyanol), heat-denatured in 95 ℃ to two single DNA strands.

通过单链构象多态性分析筛查RDS基因突变;沉淀回收的PCR产物以20μl变性上样液(95%甲酰胺+20mMEDTA+0.05%溴酚蓝+0.05%二甲苯蓝)溶解后热变性为两条DNA单链后,上样于8%非变性聚丙烯酰胺凝胶(含5%甘油),700伏电压、4℃电泳16小时。

However, the alternation of light and darlmeS5 every 12 hours was found to be the best for Colletotrichum acutatum.

它们对碳源的利用有较大差异,胶孢炭疽在麦芽糖上生长最好,而尖孢炭疽在甘露醇和乳糖上生长较好。2种炭疽菌对甲基托布津的敏感性差异显著,尖孢炭疽有较强的耐药性。

The total RNA from brain tissue of substantia nigra of PD rats is extracted at the 1st, 2nd, 4th and 8th week and comparison is made between it and that from normal rats. The total RNA, after RNA formaldehyde degenerated sepharose electrophoresis and separation and Northern transfer, is adsorbed unto colloxylin membrane. Then ECL labeled Selenoprotein P and an unknown gene fragment are used as probes to hybridize with the RNA on the colloxylin membrane. And the hybridized result is obtained with enzyme-linked immunosorbent assay. Finally, analysis of OD is made using ONE-Dscan software.

分别提取1周、2周、1月、2月的帕金森大鼠(各8只)黑质区脑组织总RNA,并取相对应时间的正常大鼠的脑组织总RNA作为对照,经RNA甲醛变性琼脂糖凝胶电泳分离后,通过Northern转移,将其吸附在硝酸纤维素膜上,然后利用ECL标记的Selenoprotein P和一段未知基因为探针,与硝酸纤维素膜上的RNA分子进行杂交,再通过显影取得杂交的结果,应用ONE-Dscan软件进行光密度值分析。

This normal thyroid follicle is lined by a cuboidal follicular epithelium with cells that can add or subtract colloid depending upon the degree of stimulation from TSH released by the pituitary gland.

正常甲状腺滤泡内衬立方上皮。这些上皮细胞可分泌或重吸收胶质,这有赖于垂体分泌的TSH的刺激程度。

It is well known that retinal pigment epithelial cells are predominant proliferative cells in PVR which is an excessively wound healing response occurring after RPE cell wounding. The activated RPE cells migrate from their normal, sessile state to vitreous and onto both surfaces of the retina, in which they begin to dedifferentiate, migrate, proliferate, change phenotype and secrete ECM.

既往研究证明视网膜色素上皮(retinal pigmentepithelial,RPE)细胞是参与PVR的主要细胞,PVR是视网膜脱离后RPE细胞损伤的一种自我修复过程,是一种过度的眼内创伤修复反应;RPE细胞在正常位置上处于静止状态,而在某些病理条件下,如视网膜裂孔形成和视网膜脱离后,RPE细胞脱离原位,开始去分化、移行、增生、发生表型转化并分泌胶原等ECM,最终在视网膜前后表面和玻璃体内形成具有收缩能力的增生膜,造成牵拉性视网膜脱离。

It also express in the ependymal cell.2. The immune expression of AQP4 reinforce after MCAO. The relationship between the level of immune expression reinforcement of AQP-4after ischemia and the change of brain water content and ion content is parallel.

结果:1。 AQP4主要分布在脑血管周围的胶质细胞、脑室脉络丛上皮细胞、室管膜细胞的膜上;2。

Mammary gland epithetical cells were taken to analyze the phospholipids ingredients. SDS-Polyacrylamide gel electrophoresis was used for analyzing the membrane protein ingredients. ATPase activities which have important function in mammary protein were also tested.

同时提取乳腺上皮细胞膜,检测了乳腺上皮细胞膜磷脂组分的相对百分含量,并对膜蛋白进行了SDS-PAGE电泳,蛋白质凝胶成像系统对电泳条带进行定性定量分析,对膜蛋白中具有重要功能的ATP酶的活性进行了测定。

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