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   in the cells 的翻译结果: 查询用时:0.103秒
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in the cells     
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  在细胞内
     When growing anaerobically in the light using sulfide as electron donor, strain HD_1, HD_2 and HD_4 deposited sulfur granules in the cells.
     菌株HD_1、HD_2和HD_4在厌氧光照条件下利用硫化物,且在细胞内贮存硫粒。
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     In the first one, the cells were cultured at four levels of cadmium (0, 50, 100, 180 μmol/L) and one level of phosphorus (2.5 mmol/L) to investigate the effect of cadmium on the accumulation and distribution of phosphorus in the cells;
     共设置两组试验:一组设4个镉水平(0,50,100,180μmol/L)和1个磷水平(2.5mmol/L),主要研究镉对磷在细胞内积累和分布的影响;
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     After incubation in conventional medium for 24 h over 90% WSA and 70% of the 3H-Liposomes still remained in the cells, while only 35% of the 125I-Trastuzumab remained.
     细胞摄取125ITrastuzumabWSA3H脂质体后,在普通培养液中培养24和48h,分别有90%、67%的WSA滞留在细胞内
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     (2) The metabolic behaviour of oxHDL2 in the cells is similar to HDL2. Both of them do not take a lysosomal pathway.
     (2)ox-HDL2在细胞内代谢方式与HDL2相似,均没有经历溶酶体分解途径。
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     Dox accumulation in the Har-resistant HL60 cells treated by Tet was increased. CONCLUSION: Dox resistance in the Har-resistant HL60 cells treated by Tet or Dau was reduced, due to the increase of Dox accumulation in the cells.
     结论:Tet和Dau减低抗Har的HL60细胞对Dox的抗性,其机制是增加Dox在细胞内积聚。
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  在细胞
     Recombination of TK gene in the cells was examined by blot hybridization and sensitivity of A549-TK cells to GCV was observed in vitro.
     斑点杂交检测外源基因在细胞中整合,并体外观察A549-TK对GCV的敏感性。
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     Moreover, a similar amount of PpIX was found in the cells incubated with 0.2 mmol/L He ALA or 2 mmol/L ALA and a similar level of cell survival was reached following light exposure.
     实验发现 ,0 .2mmol/L的He ALA药物浓度与 2mmol/LALA的药物浓度在细胞中生成的PpIX含量相当 ;
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     e. ,the expressed products of different R genes in the cells are reviewed.
     综述了不同基因表达产物-R蛋白在细胞中的定位及其相应的功能。
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     Methods Decoy-ODNs targeting AP-1 were designed and synthesized. NIH3T3 cells were transfected by cationic liposomes. The distribution of Decoy-ODNs in the cells was investigated.
     方法 设计合成针对AP 1的Decoy ODNs,用阳离子脂质体转染NIH3T3细胞 ,观察Decoy ODNs在细胞中的分布 ;
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     They perform different functions in the cells. RNA polymerase Ⅰ synthesizes the three largest rRNAs, 5.8S , 18S and 28S rRNA. RNA polymerase Ⅱ mainly produces mRNA encoding proteins, and RNA polymerase Ⅲ makes 5S rRNA and tRNAs , as well as a few small nuclear RNAs.
     在细胞中它们的功能各不相同:RNA聚合酶Ⅰ负责催化合成5.8S、18S和28S rRNA,RNA聚合酶Ⅱ主要负责mRNA的转录合成,而RNA聚合酶Ⅲ则负责催化5S rRNA、tRNA、多数的Sn RNA以及某些病毒基因(如VA基因)等的转录。
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  于细胞
     Results In the cells of Lovo/EGFP and 3T3/EGFP-VP3 group, EGFP was fairly well-distributed in whole cell. No change was found in cell morphology and apoptosis rate on transfected cells than natural ones.
     结果在Lovo/EGFP组和3T3/EGFP-VP3组细胞中,EGFP均匀分布于细胞中,细胞形态无明显变化,细胞凋亡率较非转染细胞组亦无明显增加。
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     The grey density of Du increased than that of in Con,they were 0.22±0.04μm 2 and 0.14±0.04μm-2(P<0.01) An abounding endoplasmic reticulum and mitoebondria with a lugher dense groundplasm were found in the cells The secretory granules labelled with 5 nm colloidal gold particles usually scattered in basal cytoplasma.
     β-EP阳性细胞灰度密度增大为0.22±0.04μm-2,与Con组0.14±0.04μm-2相比,差异显著,(P<0.01); 细胞内内质网和线粒体丰富,基质密度增高,5nm胶体金标记的颗粒散在于细胞基部。
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     Conclusion:Catalase reversed the effect of DMNQ on EC/CUHK1 and EC/CUHK1(As-) cells. It was concluded that the susceptibility of esophageal cells to arsenic trioxide-induced apoptosis is determined by ROS level in the cells.
     过氧化氢酶 (catalase)可逆转 DMNQ的效应。 结论 :食管癌细胞株 EC/ CUHK1、EC/ CUHK1(As- )对 As2 O3 促凋亡的敏感性决定于细胞固有的 ROS水平
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     Growth curve was shifted downward and proliferative index (PI) was obviously lower in the cells by octreotide and TGF-α , compared with the cells by TGF-α (P<0.01).
     两者同时作用于细胞较TGF-α单独作用,细胞生长曲线下移,增殖指数(PI)值明显降低(P<0.01)。
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     one week later, there was a significant increase of melanin content in the cells (P< 0 05), with darker and larger melanin particles, which tended to be gathered at the centre of the cells, forming a cap like structure.
     紫外线照射后1周,浅表角质层细胞黑素含量明显增加,与照射前比较有统计学差异(P<005)。 同时观察到角质层细胞内黑素颗粒增大,颜色增深,黑素颗粒倾向集聚于细胞中心,形成帽状现象。
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  后细胞
     Results The recombinant adenovirus Ad/siRNA/COX-2 was successfully constructed. Ninty six hours after Ad/ siRNA/COX 2 transfecting into Eca 109 cells,COX-2 mRNA was reduced by 71.7%,and PGE2 concentration in the cells culture supernatant was decreased by 62.0%.
     结果重组腺病毒 Ad/siRNA/COX-2构建成功,转染 Eca-109细胞后,细胞 COX-2 mRNA 水平下降71.7%(P<0.01),培养液上清 PGE2浓度下降62.0%(P<0.01);
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     Results:The grey level ratio of RANKL mRNA expression to β-actin in untreated OBs was 0.32,that in the cells infected by 107 and 109 CFU/ml of Pe for 24 h was increased to 1.73 and 2.24 respectively.
     结果以107和109CFU/mlPe作用成骨细胞24h后,细胞表达RANKLmRNA与βactin的mRNA灰度值的比值分别为1.73、2.44。 大鼠头盖骨细胞基础表达RANKLmRNA为0.32。
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     Expression of Survivin protein in the cells treated with SB at 2.500 mmol/L was detected by immunohistochemistry SP method.
     采用免疫组织化学SP法检测2.500mmol/LSB作用24h、48h、72h后细胞抗凋亡蛋白Survivin表达的变化。
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     The levels of IL-2 and IFN-γ se- cretion enhanced significantly in the cells with lactadherin functional peptide in comparison with those in the untreated cells (P = 0.0394, P = 0.0082, respectively), but IL-4 secretion had no marked change.
     给予乳凝集素处理后细胞培养上清中IL-2(P=0.0394)和IFN-γ(P=0.0082)的含量高于未处理细胞组,而IL-4没有显著的增高;
短句来源
     RESULTS:The PGE 2 level in the cells cultured supernatant decreased by NIM in a concentration and time dependent manner.
     结果 :NIM处理A 5 49细胞后 ,细胞培养上清液PGE2 水平下降 ,呈浓度和时间依赖性 ;
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  in the cells
Enzyme activity was revealed in the cells grown on medium with elemental sulfur or in the presence of various sulfide minerals and concentrates of sulfide ores.
      
The mutants varied in Cr(VI) resistance, the degree of chromium accumulation in the cells (from 0.1 to 11.6 mg/g dry cells), and the degree of Cr(VI) reduction (from 50% to complete disappearance of bichromate from the culture liquid).
      
Treatment with ambiol enhanced the differentiation of the internal membrane system of plastids in the cells of original and transgenic plants, especially the tubular membrane systems.
      
The concentration of eight kinds of catechins in solution decreased by 29.6-47.6%, respectively; some catechins were absorbed and accumulated by yeast cells, but the amount in the cells was very low during the fermentation process.
      
Specific attention is given to regulation of enzymes of antioxidative defense, operating in the cells of strict anaerobes under the conditions of oxidative stress caused by oxygen, superoxide anion, or hydrogen peroxide.
      
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1. The albino mice were used for this study. The Golgi apparatus in the cells of the epididymis and the vas deferens of normal, starved, and refed animals were studied.2. The amount of the Golgi elements can be maintained by feeding, not only by the sex hormone.3. The Golgi apparatus may be regarded as a product of food assimilation, not a definite cell organ.4. It is suggested that the Golgi apparatus has similar organ with that of mitochondria and secretion granules, but with different quantity...

1. The albino mice were used for this study. The Golgi apparatus in the cells of the epididymis and the vas deferens of normal, starved, and refed animals were studied.2. The amount of the Golgi elements can be maintained by feeding, not only by the sex hormone.3. The Golgi apparatus may be regarded as a product of food assimilation, not a definite cell organ.4. It is suggested that the Golgi apparatus has similar organ with that of mitochondria and secretion granules, but with different quantity of lipoids.

(1)本研究以白鼠为材料,就常态白鼠绝食及再餵之白鼠观察其副睾丸及输精管上皮细胞内之高基體。查得在绝食期内副睾上皮细胞之高基體逐渐減少,由网状體变为颗粒,先集于前端後卽散开,至三十六小时高基體绝少,再餵後復有颗粒出现於前端。 (2)输精管上皮细胞内高基體原作线状,列於细胞前部。绝食十三时後,变为颗粒。俟三十六小时後再餵,卽有许多小粒在细胞前端边缘或卽係高基體 (3)由此结果可知高基體之多寡,既视绝食与否而定,或可谓为食物同化之产物,非固定之细胞器官也。 (4)高基體之起源或与粒线體,及分泌粒同,但其所含类脂質之量不同。

High-frequency titration curves are discussed for various methods of experimental determination (the Q-meter, Z-meter and F-meter methods), using equivalent circuits for C-type and L-type titrating cells. It has been found that for the cases of L-type cell with Q-determination and C-type cell with Z- or F-determination, the quantity measured in the course of titration changes monotonously with .the increase of conductivity of the solution. In these cases, the high-frequency titration curve...

High-frequency titration curves are discussed for various methods of experimental determination (the Q-meter, Z-meter and F-meter methods), using equivalent circuits for C-type and L-type titrating cells. It has been found that for the cases of L-type cell with Q-determination and C-type cell with Z- or F-determination, the quantity measured in the course of titration changes monotonously with .the increase of conductivity of the solution. In these cases, the high-frequency titration curve should be similar in shape to that obtained in an ordinary conductometric titration. Two mistakes appearing in literature are here pointed out. (1) The equivalent parellel circuit and the equivalent series circuit for the C-type titrating cell do give the identical result for the value of the conductance of the solution which gives the maximum loss of high-frequency energy in the cell. (2) The appearance of a maximum high-frequency loss with increasing conduc- tance of the solution in the C-type cell is not the result of the Debye-Falkenhagen effect. The use of Pt wire electrodes in direct contact with solution for high-frequency titration is suggested. Satisfactory titration curves have been obtained with wire electrodes and a series capacitor to act as a C-type cell with much less shielding troubles.

1.對高頻滴定用的C式和L式滴定池,Q表法,Z表法及F表法测定得到的滴定曲線,與溶液電導改變的關係,用等效電路的理論,作了全面的討論。除C式滴定池Q表法測定,文獻中已有討論外,L式滴定池Q表法測定時,和C式滴定池Z表法和F表法測定時,滴定過程中測定的量都與溶液的電導值單調變化。 2.指出了文獻中的錯誤。C式滴定池應用等效串聯電路與等效並聯電路計算的結果,是完全等同的。C式滴定池的高頻電能損耗與溶液中電解質濃度的關係,與Debye-Falkenhagen效應無關。 3.提出了用鉑絲電極直接插入溶液的高頻滴定法。

When a suitable immersion medium, the refractive index of which is not far different from that of the fiber, is chosen and the wave length of light is adjusted to a certain particular value, it is possible to make the refractive index of the immersion medium and of the fiber exactly equal at this particular wave length. By means of an ordinary spectrophotometer with its optical system slightly modified, one can easily determine this particular wave length and consequently find the exact refractive index of the...

When a suitable immersion medium, the refractive index of which is not far different from that of the fiber, is chosen and the wave length of light is adjusted to a certain particular value, it is possible to make the refractive index of the immersion medium and of the fiber exactly equal at this particular wave length. By means of an ordinary spectrophotometer with its optical system slightly modified, one can easily determine this particular wave length and consequently find the exact refractive index of the fiber for sodium light, if the dispersion curve of the immersion liquid and the so-called "λ-factors" of the fiber are known. To carry out the process, a series of immersion media of refractive indices differing by steps of 0.004-0.005 or smaller are required. In this work, the actual immersion media used are mixtures of dibutyl phthalate and tricresyl phosphate of varying composition for liquids of refractive indices ranging from 1.4920 to 1.5545. For higher refractive indices up to 1.5945, solutions of diphenylamine in tricresyl phosphate of varying concentrations are used. The dispersion curves of these liquids, as determined by means of a spectrometer, are shown in Fig. 5. The factors for cellulose fibers are listed in table Ⅰ. The modified optical system of the spectrophotometer is shown in Fig. 2. The presence of layers of parallel fibers immersed in a liquid in the cell C causes some of the incident light to be reflected back and a part of the transmitred light to be deviated from its straight path and hence intercepted by the slit S, placed in front of the photocell C_1. At a certain particular wave length of light, the refractive index of the fiber and of the liquid are the same; therefore the transmitted intensity as indicated by the photocurrent will be at its maximum. Some typical results of measurements are given in Fig. 7. From the value of this particular wave length corresponding to the transmission maximum, the refractive index n_λ can be found and thus corrected in to n_D by means of Table Ⅰ. The results for five different rayons are given in Table Ⅲ. The method is macroscopic, giving the mean refractive index of a fiber sample accurate to +0.0005 in a single determination.

选择一种浸剂,其折光指数与纤维的折光指数相差不远,并调整光波至某一特定波长,可使纤维与浸剂在这一特定波长时的折光指数恰巧相等。作者利用通常的光谱光度计,稍加修改,测得这一特定波长,从而求得纤维的正确折光指数。方法是宏观的,一次测定便可得试样的平均折光指数,精确度也容易达到±0.0005。

 
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