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Mucous membrane protective screen is formed by the join between cell of alvine mucous membrane and cell, atrophy of cell of alvine mucous membrane, wither dies, cellular connective can send alvine path to connect flabbily appear a gender to increase, provide passageway; chemical protective screen for the bacterium inside bowel and toxin the digestive juice that shows epithelial excretive mucus and alvine memory are in bowel and digest enzymatic the chemistry that waits for material to reach its to develop.

黏膜屏障由肠黏膜细胞和细胞间的连接构成,肠黏膜细胞萎缩、凋亡、细胞连接的松弛可致肠道通透性增加,为肠内细菌及毒素提供通道;化学屏障指肠上皮细胞分泌的黏液及肠内存在的消化液和消化酶等物质及其发挥的化学功能。

METHODS: A model of T cell activation and proliferation was established by stimulated the cells with Con A.T cells were treated with different concentrations of CPT. The expression of CD69, the early marker of CD3(superscript +) T cell activation, was measured by FACS. The proliferation index was determined by carboxyl fluorescin diacetate succinmidyl ester by flow cytometry. The cell-cycle distribution was analyzed by propidium iodide staining.

以ConA刺激小鼠T淋巴细胞,建立小鼠T淋巴细胞活化、增殖的模型,以不同浓度的CPT作用于该模型,流式细胞术检测T细胞早期活化标志CD69分子的表达;以活体染料羧基荧光素乙酰乙酸染色流式细胞术分析CPT在ConA刺激下小鼠淋巴细胞的增殖相关指数;以碘化丙啶染色流式细胞术分析细胞周期的分布情况。

The increases in the cell density in the sutures of the treated groups were higher as compared to the two controlled groups for 3 7 14days indicating that cellular hyperplasia in the expanded sutures were accelerated by the protraction .The cell density in the palatomaxillary sutures and in the frontomaxillary sutures differed in increase ways at the two time points of 21th day and 28th day suggested that the mode of bone formation in the circummaxillary sutures is different from one another..5 The expression of Proliferating Cell Nuclear Antigen were always higher than the controls in the course of this study,which i

而在21、28天时间点两个骨缝与对照组相比在相同时间点增长程度明显不相一致,提示我们不同的上领骨周围骨缝在前牵引作用下改建方式过程可能不一。5、在上领前牵引作用下,上领骨的额领缝内的PCNA的阳性表达一直高于对照组,提示前牵引促进上领骨周围骨缝内细胞增殖活动增强。

Gambogic acid presents powerful anti-leukemia effects through both proliferation inhibition and apoptosis induction. HL-60 cell line was the most sensitive one to gambogic acid of all three leukemia cell line. However, the exact mechanism may vary from one cell line to another.

第三部分藤黄酸对Jurkat白血病细胞核孔蛋白与核磷蛋白的调节作用目的:研究藤黄酸对白血病细胞增殖和凋亡的影响,并探讨其可能的作用机理,为其临床应用提供理论基础。

The Collaborative Program in Developmental Biology is primarily dedicated to research and education in Developmental Biology including amphibian gastrulation, molecular control of hematopoiesis, lymphocyte lineage commitment and cell development, hematopoietic stem cells, lymphocyte development, cell enlargement and cell differentiation, vertebrate embryogenesis, developmental neurobiology.

动物学系发育生物学合作研究组主要致力于两栖动力原肠胚形成,造血作用的分子控制,淋巴细胞血统定型和细胞发育,造血干细胞,淋巴细胞发育,细胞生长和细胞分化,脊椎动物胚形成,发育神经生物学等。

The Collaborative Program in Developmental Biology is primarily dedicated to research and education in Developmental Biology including amphibian gastrulation, molecular control of hematopoiesis, lymphocyte lineage commitment and cell development, hematopoietic stem cells, lymphocyte development, cell enlargement and cell differentiation, vertebrate embryogenesis, developmental neurobiology.

动物学系发育生物学合作研究组主要致力于两栖动力原肠胚形成,造血作用的分子控制,淋巴细胞血统定型和细胞发育,造血干细胞,淋巴细胞发育,细胞生长和细胞分化,脊椎动物胚形成,发育???经生物学等。

The germinative number of horsebeans and peas were raised by 44% with activated water by tourmaline. 200μl 1 X 10~6/ml mouse's H_(22) cell, 200μ 4X 10~6/ml splenic cell, 200μl 1 × 10~6/ml epidermal cell were all inhibited after the action of tourmaline. It is analyzed that the factors which effected the multiplication of the cells included direct action which are tourmaline's electric field, far-infrared, negative ions and solvent ions, and indirect effect which are small water clusters and pH value.

电气石活化水使蚕豆和绿豌豆种子发芽速度均提高44%。0.5g电气石分别对200μl 1×10~6/ml的小白鼠H_(22)肝癌细胞,对200μl 4×10~6/ml小白鼠脾细胞,对200μl 1×10~6/ml的小白鼠表皮细胞的增殖起抑制作用,分析认为,电气石影响细胞增殖的因素包括电场、红外线、负离子和溶出离子对细胞的直接作用和通过改变水分子结构、培养基pH值的间接作用。

The change of α1,2-FT activity in the cell line before and after the tranfection was confirmed by the determination of enzymatic activity. The changes of cell lipid and glucolipid, especially the change of type Ⅱ oligosaccharide, in the cell line before and after the transfection was determined by Thin-Layer Chromatography and TLC immunostaining method, respectively.

通过酶活性测定证明转染前后细胞系α1,2-FT活性的改变,采用薄层层析、薄层层析免疫染色方法测定转染前后细胞脂质及糖脂,特别是Ⅱ型寡糖的变化。

Result When nimodipint dosage was 1×10^(-7)g/L^(-1), the survival rate of the neural stem cell was obviously higher than glutaminic acid in the group (P.01); With gradual increased of the nimodipint dosage, the cell survival rate of the neural stem cell damage model was obviously improved.

结果 当尼莫地平剂量为1×10^(-7)g/L^(-1)时,神经干细胞的存活率明显高于谷氨酸组(P.01);以后随着尼莫地平剂量的逐渐增加,神经干细胞的存活率明显提高。

Setting up the model of glutaminic acid damaging the neural stem cell. After different dosages of nimodipint were used to intervene, cell survival rate of the glutaminic acid nerve stem cell damage model was detected.

在建立谷氨酸对神经干细胞损伤的模型基础上,给予不同剂量的尼莫地平进行干预,测定尼莫地平干预后谷氨酸神经干细胞损伤模型的细胞存活率。

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