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prickle cell相关的网络例句

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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。

Results There were more mineralization nodes to form in shorter time in the 1×105/ml cell density group compared with in the 2×105/ml cell density group, but in the 5×105/ml cell density group, there were not, and with the DMEM medium contained β-glycerophosphate sodium and ascorbic acid, mineralization nodes formed more early compared with the DMEM medium.

结果 在培养30天内,条件培养液或常规培养液培养的5×105个/ml组细胞无结节形成;而2×105个/ml组和1×105个/ml组都有钙化结节形成,而且有细胞越少形成结节越早,数量越的趋势;给予条件培养液又较常规培养液培养有结节形成早而多的趋势。

Results There were more mineralization nodes to form in shorter time in the 1×105/ml cell density group cnpared with in the 2×105/ml cell density group, but in the 5×105/ml cell density group, there were not, and with the DMEM medium contained β-glycerophosphate sodium and ascorbic acid, mineralization nodes formed more early cnpared with the DMEM medium.

结果 在培养30天内,条件培养液或常规培养液培养的5×105个/ml组细胞无结节形成;而2×105个/ml组和1×105个/ml组都有钙化结节形成,而且有细胞越少形成结节越早,数量越多的趋势;给予条件培养液又较常规培养液培养有结节形成早而多的趋势。

Results There were more mineralization nodes to form in shorter time in the 1×105/ml cell density group compared with in the 2×105/ml cell density group, but in the 5×105/ml cell density group, there were not, and with the DMEM medium contained β-glycerophosphate sodium and ascorbic acid, mineralization nodes formed more early compared with the DMEM medium.

结果 在培养30天内,条件培养液或常规培养液培养的5×105个/ml组细胞无结节形成;而2×105个/ml组和1×105个/ml组都有钙化结节形成,而且有细胞越少形成结节越早,数量越多的趋势;给予条件培养液又较常规培养液培养有结节形成早而多的趋势。

To effectiely study the effect of these heterotypic cell-to-cell interactions, it is necessary to establish a culture enironment that controls the interactions between multiple cell types.

为了有效地研究这些异型细胞之间的相互作用,建立一个能控制多种细胞间相互作用的环境是非常必要的。

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