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To investigate whether the expression of cdc2 and cyclin B1 in spermatogenic cells during spermatogenesis is actually a temperature dependent event, in situ hybridization, Western blotting and immunohistochemistry analysis were used to study the expression of cdc2 and cyclin B1 in normal and cryptorchid testis. Results showed that heat would differentially hurt male germ cells in different developmental stages during spermatogenesis, especially the pachytene primary spermatocytes. Most of spermatogonia in contralateral cryptorchid testis were not harmed fatally by heat as yet, indicating that spermatogonia could resist to beat to a certain extent. In this case spermatogonia could develop to pachytene/diplotene primary spermatocytes, but they could not acquire the ability to complete the transition from mitosis to meiosis, and then appeared to go through apoptosis. Therefore, we could not find the descendants of meiosis: secondary spermatocytes and round spermatids, elongated spermatids and spermatozoon. The abdominal temperature had no significant influence on the transcription of cdc2 and cyclin B1 in the spermatogonia and pachytene/diplotene primary spermatocytes. In normal rabbit testis, cyclin B1 increased in the pachytene/diplotene primary spermatocytes before meiosis and reached its peak in the spermatids.

为了解精子正常发生过程中cdc2和cyclin B1表达的低温依赖性,我们利用原位杂交和免疫组化等方法,研究了正常和隐睾精子发生过程中cdc2和cyclin B1的转录和翻译调控活动,结果表明:(1)热对各阶段的雄性生殖细胞都有损害,粗线期的初级精母细胞尤为敏感,实验性隐睾内的精原细胞尚未完全受到"致命"影响,说明精原细胞对热有一定的耐受性,但即使成为粗线期/双线期初级精母细胞,却未能获得由有丝分裂过渡到减数分裂的能力,呈现不同程度的凋亡,所以在整个切片中找不到源自减数分裂的产物----次级精母细胞、圆形精子细胞,更谈不上长形精子细胞和精子的形成;(2)腹腔高温未明显地影响隐睾精原细胞和粗线期/双线期初级精母细胞中cyclinB1和cdc2的转录,说明高温并不是通过影响cyclin B1和cdc2的转录活动而导致生精过程阻断的;(3)正常兔睾丸组织中,〓在精原细胞和粗线期/双线期精母细胞中均有表达:cyclin B1蛋白在减数分裂前期的粗线期/双线期初级精母细胞中的表达量增加,于变态末期的精子细胞中达高峰。

According to the bone apposition events at the interface, we measured the osteoblast attachment rate with the hemocytometer, the osteoblast growth curve with modified MTT method, the ALPase activity and protein content of cellular layers with modified kinetic method and modified Coomassie'method respectively, and osteocalain content in the cell medium with RIA , at different levels of cell responses, as osteocompatibility indexs.

根据骨内种植体界面的骨愈合过程,分别从成骨细胞反应的不同层次选择了细胞贴壁率、细胞生长曲线、细胞层ALPase活性和蛋白质含量以及细胞培养液中骨钙素的含量作为体外评价材料骨性生物相容性的指标。采用细胞计数板计数法测定细胞贴壁率,采用改良MTT法测定细胞生长曲线。

The former stimulates the cells and transfer the signals into the cells through the ligation with receptors on the cell membrane. The latter, a derivative of nucleotide, causes a cytotoxic effect to suppress thymidylate synthetase activity, and, therefore, to damnify RNA and DNA synthesis.

前者通过与细胞表面的受体结合,把胞外刺激传递到胞内,诱导免疫受体介导的信号级联放大作用,引起一系列免疫效应;后者是是小分子的核苷酸衍生物,可直接进入细胞内,通过抑制胸苷酸合成酶及损伤RNA、DNA等对基因转录和核苷酸代谢产生影响,最后产生细胞毒效应。

Normal functions of the ER could be impaired and that causes endoplasmic reticulam stress.

内质网是细胞内重要的细胞器,内质网功能的损伤引起ER应激。

1,After transfected the mutated mtDNA of colorectal carcinoma,the mtDNA D-loop region of the transfected cells displays new mutation points.2,The external source pieces of the mutated mtDNA can integrate to nuclear genome after transfection.3,There's no differences in apoptosis between combinations after transfected the mutation of mtDNA in NIH3T3 and LST cells.4,The mutated mtDNA may affect the action mechanism of occurrence and development in colorectal carcinoma through affecting its mtDNA mutation or integrating exogenetic mtDNA to its nuclear which may cause the abnormal expression of oncogene or anti-oncogene.

(1)转染突变的大肠癌细胞mtDNA后转染细胞的mtDNA均可发生多处的突变位点。(2)通过转染后突变的外源性的mtDNA可以整合到核基因组内。(3)突变的mtDNA转染LST细胞及NIH3T3细胞后,不影响转染细胞的凋亡改变。(4)mtDNA的突变可能通过影响体细胞mtDNA的突变和通过外源性mtDNA在核内的整合从而影响癌基因或抑癌基因的表达异常,从而参与肿瘤的发生发展。

1,After transfected the mutated mtDNA of colorectal carcinoma,the mtDNA D-loop region of the transfected cells displays new mutation points.2,The external source pieces of the mutated mtDNA can integrate to nuclear genome after transfection.3,There's no differences in apoptosis between combinations after transfected the mutation of mtDNA in NIH3T3 and LST cells.4,The mutated mtDNA may affect the action mechanism of occurrence and development in colorectal carcinoma through affecting its mtDNA mutation or integrating exogenetic mtDNA to its nuclear which may cause the abnormal expression of oncogene or anti-oncogene.

(1)转染突变的大肠癌细胞mtDNA后转染细胞的mtDNA均可发生多处的突变位点。(2)通过转染后突变的外源性的mtDNA可以整合到核基因组内。(3)突变的mtDNA转染LST细胞及NIH3T3细胞后,不影响转染细胞的凋亡改变。(4)mtDNA的突变可能通过影响体细胞mtDNA的突变和通过外源性mtDNA在核内的整合从而影响癌基因或抑癌基因的表达异常,从而参与肿瘤的发生发展。线粒体DNA;D―环区;突变;质粒;pcDNA3.1;转染

Background: Glycan-binding proteins could regulate many fundamental and important biological functions, including cell recognition, cell signaling pathway, growth, endocytosis, intracellular, apoptosis, cellular differentiation and infection of pathogenic microorganism through the interaction with glycan of glycoprotein or glucolipid.

研究背景:糖结合蛋白(glycan binding proteins,GBPs)通过和糖蛋白糖链或糖脂糖链的相互作用调控细胞间的识别、信号传递、细胞的内吞和细胞内物质的运输、细胞生长、分化以及凋亡、外界病原微生物的感染等一些最基本的也是最主要的生物学功能。

Immunohistochemistrical section: observe the VEGF protein expression in different cells, the positive ratio detected by a morphometrical analysis system was used as the amount of the VEGF protein expression.

免疫组化染色切片:观察不同给药时间股骨头内VEGF的表达情况;高倍视野下(400倍)沿骨小梁表面计数50个成骨细胞中的阳性细胞数,VEGF成骨细胞阳性率=阳性成骨细胞数/50×100%,3次取平均值;计数每个高倍视野软骨细胞中的阳性细胞数,VEGF软骨细胞阳性率=阳性软骨细胞数/软骨细胞总数×100%,5次取平均值。

Over-expression of NaDC3 accelerates the speed rate of energy metabolism and increases intracellular ROS generation by transporting an overdose of tricarboxylic acid cycle intermediates in human renal tubular epithelial cells.

NaDC3过表达可通过转运过多的三羧酸循环中间代谢产物进入细胞内而加快肾小管上皮细胞能量代谢的速率、增加细胞内ROS的产生水平。

Further study demonstrated that peroxynitrite also induced tau nitration in neuroblastoma N2a cell line, and the nitrated tau was accumulated in the cells.

进一步研究发现:用PN处理稳定表达tau蛋白的N2a细胞,可以诱导细胞内tau蛋白的硝基化,而且硝基化的tau蛋白在细胞内发生聚积。

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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。

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