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Tumor associated protein N35 was located on the centriole of the chromosomal domain at the S-G2 phage.Conclusions The tumor associated protein N35 might be a tumor cell growth regulator, expressed only it's the cancer cells and related with the proliferation of cancer cells. It is one of tumor markers.

肿瘤相关蛋白N35可能是一种只存在于肿瘤细胞并与其增殖活动密切相关的重要的肿瘤细胞生长调节蛋白,其功能可能与肿瘤细胞无限制增殖活动有关,是肿瘤标志物之一。

The mechanism probably is that Pishang can inhibit the growth, movement and adheresion to extracellular matrix and endothelial cell of liver tumor cells, up-regulate the expression of nm23, down-regulate the expression of CD44, MMP-2, and inhibit the tumor neovascular by supressing the vascular endothelial cell, down-regulating the expression of VEGF, damaging the primitive mesenchymal cells and inhibiting neovascular gemmation.

砒霜具有明显的抗肝癌细胞作用,并有一定的抗侵袭与转移作用,其机制可能与其能抑制肝癌细胞增殖、迁移、阻止肝癌细胞与细胞外基质和内皮细胞粘附、上调肿瘤转移抑制基因nm23表达、下调肿瘤侵袭分子CD44、MMP-2表达以及通过抑制内皮细胞增殖、下调VEGF表达、损伤间充质细胞、阻止新生血管芽生等途径从而抑制肿瘤新生血管形成有关。

It is obvious that callus induction and proliferation of gerbera need growth regulators, and are influenced by varieties and explants of different parts of the plants.

以上结果说明,生长素是非洲菊愈伤组织诱导和增殖所必须的,非洲菊愈伤组织诱导、增殖和芽再生方式受品种及外植体类型的影响。

I will apply Immumohistochemical method to detect proliferating cell nuclear antigen expression of lung adenocarcinoma histiocyte inpatients, and I will study apoptosis of lung adenocarcinoma cells by TUNEL method; calculate PCNALI and ALI; compare and analysis PCNALI and ALI of different patients with different clinic features simultaneously .

例肺腺癌组织中增殖细胞核抗原的表达,同时通过TUNEL法检测肺腺癌细胞凋亡,计算PCNA增殖指数和细胞凋亡指数,对不同临床特点肺腺癌患者的PCNALI、ALI进行比较分析。

The effect of leptin on promoting myoblast proliferation and cell accumulation in the S+G2/M phase were inhibited by TNF-α.

脂肪细胞因子TNFα抑制leptin对猪骨骼肌成肌细胞增殖和增殖期S+G2/M阶段细胞积聚的促进作用;降低leptin对猪骨骼肌成肌细胞分化期间对CK活性和MyoG表达的抑制效应。

The N protein concentration in the supernatants of virus-infected cells were reduced at different levels in all ER and cytoplasma localized intracellular antibody expressing cell lines, however, the intracellular N protein synthesis in above cell lines was not significantly affected.

利用病毒微量滴定免疫荧光方法,对细胞内抗体与病毒的增殖关系进行了研究,证实无论在内质网还是在胞质,抗核蛋白细胞内抗体都能够抑制病毒的增殖,具有抗病毒活性。

Methods Phase-contrast microscopy, cell proliferation assay and wound -closure were used to study the process of cell proliferation and wound healing in a model of human retinal pigment epithelial cell damage.

应用人RPE细胞损伤模型、细胞增殖曲线法,在倒置相差显微镜下观察人RPE细胞在各种条件作用下的损伤愈合与增殖过程。

METHODS: Proliferation, DNA proliferative fraction and DNA ploidy were analyzed by flow cytometry using standard techniques.

应用流式细胞术,分别分析胃癌细胞群体的增殖、DNA增殖分数和倍性。

The methods of sticking tissues piece to culture primary hFCECs and mouse 3T3 fibroblast conditioned medium to culture passage hFCECs were established;2.The Proliferative capacity of corneal limbus hFCECs is better than central hFCECs.3.3T3 conditioned medium could markedly promote the proliferation of epithelial cells

结论一、组织块贴壁法原代培养人胎儿角膜上皮细胞以及小鼠3T3成纤维细胞条件培养液传代培养方法基本建立;二、人胎儿角膜缘部上皮细胞增殖能力优于中央部;三、3T3细胞条件培养液能促进角膜上皮细胞的增殖。

METHODS:Observe the effect of SKR on immunity function in mice,the phagocytotic rate and phagocytotic index,haemolysin in serum,plaque forming cell,and the proliferation of splenocyte following administration SKR for 15 days.

以SK初乳素R-1连续灌胃给药15 d,测定小鼠增强小鼠炭末廓清能力、小鼠血清溶血素抗体水平、血清IL-2含量、抗体生成细胞数、脾淋巴细胞增殖能力等。结果:SK初乳素R-1各剂量组能增强小鼠炭末廓清率和廓清指数,各剂量组均能明显升高小鼠血清溶血素抗体水平(P.01),提高小鼠血清IL-2含量(P.01),促进小鼠抗体细胞形成(P.01),增强ConA诱导的脾淋巴细胞增殖能力(P.01)。

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