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Due to the complexity of the cell jitter, the NonSynchronous Tining Recovery methods are currently not mature With the emphasis being given to the Class A CBR traffic, this paper analyzes the performance of the queueing delay and cell jitter at the source node and intermediate nodes, and discusses the Source Timing Recovery at the destination node in ATM networks Firstly, this paper presents a description of the cell jitter of CBR traffic, and gives the definitions of two kinds of cell jitter regarding the Source Timing Recovery for CBR traffic Then, by using exact mathematical models and analysis methods, this paper analyzes the impact of the factors, such as the capacity of the queueing buffer, the randomness, the deterministic nature and the correlation in cell arrivals of the background traffic sources, on the queueing delay and cell jitter performance of the CBR traffic through Statistical Multiplexitng To obtain an insight into the power spectral distribution and look for better schemes for the depression and filtering of the cell jitter, within the analyses we succeed deriving the power spectrum of the cell jitter for CBR traffic Hence, not only the power spectral distribution of the cell jitter can in the frequency domain be qualitatively understood, but also can the rms (root-meansquare) value of the cell jitter be quantitatively obtained so as to more accurately measure the amplitude of the jitter In the end-to-end performance analysis of the queueing delay and cell jitter, we propose a kind of quasi-periodic cell stream model to characterize the jittered CBR traffic, and present an initial queueing analysis of the CBR traffic following such a model at a generic intermediate node Additionally, we briefly discuss the buildout/playout and Source Timing Recovery functions of the destination node Finally, regarding the Source Timing Recovery of CBR traffic, this paper systematically discusses several important principles of the cell jitter filtering and depression reported in the literature, introduces several implementation schemes of the Source Timing Recovery e.

由于信元抖动的复杂性,非同步定时恢复方法目前还很不成熟。本文针对A类CBR业务流在ATM网络源节点和中间节点的排队时延和信元抖动性能,以及在目的节点的源定时恢复问题作了较为全面的研究。首先,文中描述了CBR业务流的信元抖动,并具体地给出了两种与CBR业务源定时恢复有关的信元抖动的定义。然后,采用了精确的数学模型和分析方法,有针对性地分析了业务背景中信元到达的纯随机性、确定性和相关性以及排队缓存器容量等因素对CBR业务流经过统计复用后的排队时延和信元抖动性能的影响。为了了解信元抖动的功率频谱分布和寻求更好的抑制和滤除抖动的方法,在性能分析中,我们成功地完成了CBR业务流信元抖动的功率谱分析,使得不但可以从频域定性地认识信元抖动的能量分布特性,而且还可以定量地求出信元抖动的均方根值(rms:root-mean-square),以更为准确地衡量抖动的大小。在CBR业务流的多节点端-端排队时延和信元抖动性能分析中,我们提出了一种准周期性(quasi-periodic)信元流模型来描述感染了信元抖动的CBR业务流,并基于这一模型进行了CBR业务流中间节点的初步排队分析。

1、Cur inhibits K562 cells growth and induces cell apoptosis may be correlated with the down-regulation of p210~、inhibition of protein tyrosine phosphorylation and the signaling molecules such as p-Erk1/2、c-myc which are relevant with cell growth and apoptosis; 2、Cur synergizes STI571 to inhibit K562 cell growth and induce cell apoptosis may be correlated with the down-regulation of p210~、inhibition of protein tyrosine phosphorylation and the signaling molecules such as Hsp90、PKC which are relevant with cell growth and apoptosis; 3、Cur reverses the resistance of K562/G01 cells to STI571, and synergizes STI571 to inhibit K562/G01 cell growth and induce cell apoptosis; 4、Cur inhibits human originated CML CD34~+ cell growth、induces cell apoptosis, and enhances STI571 to down-regulate the expression of p210~, finally inhibit cell growth and induce cell apoptosis.

从以上实验结果我们得出如下结论: 1、Cur抑制K562细胞增殖、诱导细胞凋亡的作用可能与其下调p210~、蛋白酪氨酸磷酸化水平以及抑制下游p-Erk1/2、c-myc等信号分子有关; 2、Cur协同STI571抑制K562细胞增殖、诱导细胞凋亡的作用可能与其下调p210~、蛋白酪氨酸磷酸化水平以及抑制Hsp90和下游PKC等信号分子有关; 3、Cur可逆转K562/G01细胞对STI571的耐药性,并与STI571协同抑制K562/G01细胞增殖和诱导凋亡,其抑制K562/G01细胞增殖、诱导细胞凋亡的作用可能与其下调p210~、蛋白酪氨酸磷酸化水平以及抑制下游Procaspase-3和NF-κB等信号分子有关; 4、Cur可抑制来源于CML患者骨髓的CD34~+细胞的增殖并诱导其凋亡,还可协同STI571下调CML CD34~+细胞p210~表达,进而协同抑制细胞增殖、诱导细胞凋亡。

Rapid cell selected, regional, rows or columns: the mouse click to select the current cell; click the region to be selected first cell, and then drag the mouse to the last cell can be two selected region between; worksheet click the Select All button, you can select the current worksheet; hold down the Ctrl click or drag using the mouse, you can select multiple nonadjacent cells or regional; select a region first cell, hold down the Shift key click on the angle of regional cells, can be between the selected rectangular area; click the line number can be selected corresponding to the entire line; click out the corresponding label can be selected out of the whole; along its line number or a list of drag the mouse, or to select the first row or first column, hold down the Shift key to select the end of the row or column, you can select a number of adjacent rows or columns; first select the first row or first column, and then hold down the Ctrl key to select other non-adjacent rows or columns; If you want to increase or decrease in the activities of the cell area can be selected by holding down the Shift key click the lower right corner of the region the last cell, the cell activities and the click between the cells will become a rectangular area to select a new region.

快速选中单元格、区域、行或列:鼠标单击可以将当前单元格选中;单击待选中区域的第一个单元格,然后拖动鼠标至最后一个单元格,可以将两者之间的区域选中;单击工作表的全选按钮,可以将当前工作表选中;按住 Ctrl 单击或使用鼠标拖动,可以选中不相邻的多个单元格或区域;选中某区域的第一个单元格,按住 Shift 键单击区域对角的单元格,可以将两者之间的矩形区域选中;单击行号可将对应的整行选中;单击列标号可将对应的整列选中;沿行号或列表号拖动鼠标,或者先选中第一行或第一列,按住 Shift 键选中结束行或列,就可以选中相邻的多个行或列;先选中第一行或第一列,然后按住 Ctrl 键选中其他不相邻的行或列;如果您想增加或减少活动区域中的单元格,可以按住 Shift 键单击选中区域右下角的最后一个单元格,活动单元格和所单击的单元格之间的矩形区域就会成为新的选中区域。

Higher Ca distributed in bulliformcell than in mesophyll cell and bundle sheath cell of dune reed, higher Mg distributedin mesophyll cell and higher K, Na and Cl distributed in sheath cell HigherNa and Mg distributed in mesophyll than in bulliform cell and bundle sheathcell of light salt meadow reed, and higher K, Ca and Cl distributed in itsbundle sheath cell. Higher Na and Mg distributed in bulliform cell than in mesophyllcell and bundle sheath cell of heavy salt meadow reed, higher K, Ca and Cl distributedin its mesophyll cell. This paper discussed the distribution conditions of theabove five ions in leaf cell of the four reed ecotypes and the meaning ofphysiological adaptation to habitat in detail.

沙丘芦苇的泡状细胞内Ca分布较叶肉细胞和鞘细胞高,叶细胞内Mg分布较高,在鞘细胞内K,Na和Cl布较高;轻度盐化草甸芦苇叶肉细胞内分布了较多的Na和Mg,在鞘细胞内K,Ca和C1分布较叶肉细胞和泡状细胞高;而重度盐化草甸芦苇泡状细胞内分布了较多的Na和Mg,叶肉细胞分布了较多的K,Ca和Cl;详细讨论了以上五种离子在不同生态型芦苇叶片内不同细胞类型的分布状况与环境适应的意义。

The area is small to the highest ( conversion efficiency 13 - 15%, some have achieved more than 20%) of monocrystalline silicon solar energy cell conversion efficiency, and output power is big, and stability is good, grows ( generally can reach more than 20 years ) service life, but the raw and processed material cost height, the weak light specific property is wronger, and production technology is complicated, hence the selling price is also higher; The polycrystalline silicon solar energy cell is basic identical with the function characteristic of monocrystalline silicon solar energy cell; The conversion efficiency of non- brilliant silicon solar cell than hangs down ( simples about 6 - 8%), the area is than greatly, but because of his raw and processed material cost than hanging down, can be easy to big area industrialize production, what will have hope to be used the generally big area to generate electricity from now on most will be this kind of application that battery is along with manufacture technique and new material, in a single day the practical package photoelectricity conversion efficiency of its big area achieves more than the 10-15%, and the price of every tile electric power-generating equipment is fallen 1 - 2 U.S.dollar of time, and just is enough to that the solar energy cell efficiency that big area the getting extensive use will constantly replace in now convention certainly special use and the laboratory of sources of energy s will high get many.

单晶硅太阳能电池转换效率最高(转换效率13~15%,有的已达到20%以上),面积小,输出功率大,稳定性好,使用寿命长(一般可达20年以上),但原材料成本较高,弱光特性较差,生产工艺复杂,故售价也较高;多晶硅太阳能电池与单晶硅太阳能电池的性能特点基本相同;非晶硅太阳能电池的转换效率较低(约6~8%左右),面积较大,但因其原材料成本较低,可便于大面积工业化生产,今后最有希望用于一般大面积发电的将是这种电池。随着制造技术和新材料的应用,一旦它的大面积实用组件光电转换效率达到10-15%以上,每瓦发电设备的价格降到1~2美元时,便足以大面积得到广泛应用并将不断取代现在常规能源。当然特殊用途和实验室中的太阳能电池效率要高得多。

In the gravid uterus, The CKs immunolabelling were detected in glandular cell, luminal epithelial cell, traphoblast cell, endoblastic cell and allantoic cell; Vimentin immunolabelling were detected in stromal cell and endoblastic cell; CK7 immunolabelling were not detected in any tissue of the yak utenus but in endoblastic cell and some luminal epithelial cell.

对分离得到的子宫内膜基质细胞和子宫内膜腺上皮细胞进行免疫组织化学标记的结果显示在体外子宫内膜基质细胞表达泛角蛋白,子宫内膜腺上皮细胞表达波形蛋白,并且这一特性不因为传代而发生丢失。

2B8a was weakly reactive to neutrophils (23.72%) and negative for T cells, NK, DC, RBC and Plt. The antibody reacted to all 3 marrow CD34+ cells with an average positive rate of 39.33% while it was negative for G-CSF-mobilized CD34+ peripheral blood stem/progenitor cells (PBSC, 1.25%). Cell line analysis showed that the antibody notably reacted to three out of 4 cell lines (Raji, SMS-SB, Nalm-6 and Nall-1) with the positive rates of 98.78%, 98.61%, 94.93% respectively and weakly to one of them with 5.68% in B lineage cell lines and monoblastic cell line (U937, 67.78%) while it was only weakly positive or negative for other myeloid leukemia cell lines including Meg01 (33.40%), HL-60 (29.70%),K562 (28.19%), KG1a (16.23 %) and HEL92.1.7 (8.02%). Among 4 T lineage leukemia,5 neuroblastoma and 1 colon cancer cell lines tested, only Molt-3 was found weakly positive (31.40%) for 2B8a, while the remaining 3 T cell lines (Molt4, JM and CCRF-CEM), 5 neuroblastoma cell lines (LA-N1, KCNR, BE, SK-N-SH, SK-N-AS) and the colon cancer cell line (HR8348) tested were negative.

结果表明: 2B8a抗原在外周血B细胞上表达(3/3例,平均阳性细胞数为26.29 %),而在T淋巴细胞和NK细胞上不表达(0/3例);在粒细胞和单核细胞上阳性表达均为2/3例,平均阳性细胞数分别是23.72 %和59.84 %;在DC细胞、红细胞和血小板上均不表达(0/3例)。2B8a抗原在骨髓CD34+细胞上的阳性表达是3/3例,平均阳性细胞数39.33 %,而在G-CSF动员的外周血CD34+细胞上的阳性表达仅1/3例,平均阳性细胞数为1.25 %。2B8a抗原在B系细胞系Raji、SMS-SB、Nalm-6和Nall-1上的平均阳性细胞数分别为98.78 %、98.61 %、94.93 %和5.68 %;在T系细胞系Molt-3上的平均阳性细胞数为31.40 %,而在Molt-4、JM和CCRF-CEM 细胞上不表达;在髓系细胞系U937、Meg-01、HL-60、K562、KG1a和HEL92.1.7上的平均阳性细胞数分别为67.78 %、33.40 %、29.70 %、28.19 %、16.23 %和8.02 %;在神经母细胞瘤细胞系SK-N-SH、KCNR、BE、LAN-1和SK-N-AS细胞以及结肠癌细胞系HR8348细胞上均不表达,而在羊膜细胞系FL细胞上呈一定的阳性表达,平均阳性细胞数为45.03%。

Cell line analysis showed that the antibody notably reacted to three out of 4 cell lines (Raji, SMS-SB, Nalm-6 and Nall-1) with the positive rates of 98.78%, 98.61%, 94.93% respectively and weakly to one of them with 5.68% in B lineage cell lines and monoblastic cell line (U937, 67.78%) while it was only weakly positive or negative for other myeloid leukemia cell lines including Meg01 (33.40%), HL-60 (29.70%),K562 (28.19%), KG1a (16.23 %) and HEL92.1.7 (8.02%). Among 4 T lineage leukemia,5 neuroblastoma and 1 colon cancer cell lines tested, only Molt-3 was found weakly positive (31.40%) for 2B8a, while the remaining 3 T cell lines (Molt4, JM and CCRF-CEM), 5 neuroblastoma cell lines (LA-N1, KCNR, BE, SK-N-SH, SK-N-AS) and the colon cancer cell line (HR8348) tested were negative.

结果表明: 2B8a抗原在外周血B细胞上表达(3/3例,平均阳性细胞数为26.29 %),而在T淋巴细胞和NK细胞上不表达(0/3例);在粒细胞和单核细胞上阳性表达均为2/3例,平均阳性细胞数分别是23.72 %和59.84 %;在DC细胞、红细胞和血小板上均不表达(0/3例)。2B8a抗原在骨髓CD34+细胞上的阳性表达是3/3例,平均阳性细胞数39.33 %,而在G-CSF动员的外周血CD34 细胞上的阳性表达仅1/3例,平均阳性细胞数为1.25 %。2B8a抗原在B系细胞系Raji、SMS-SB、Nalm-6和Nall-1上的平均阳性细胞数分别为98.78 %、98.61 %、94.93 %和5.68 %;在T系细胞系Molt-3上的平均阳性细胞数为31.40 %,而在Molt-4、JM和CCRF-CEM 细胞上不表达;在髓系细胞系U937、Meg-01、HL-60、K562、KG1a和HEL92.1.7上的平均阳性细胞数分别为67.78 %、33.40 %、29.70 %、28.19 %、16.23 %和8.02 %;在神经母细胞瘤细胞系SK-N-SH、KCNR、BE、LAN-1和SK-N-AS细胞以及结肠癌细胞系HR8348细胞上均不表达,而在羊膜细胞系FL细胞上呈一定的阳性表达,平均阳性细胞数为45.03%。

In accordance with the Provisions on the Protection of Geographical Indication Products issued by National Bureau of Quality Inspection, by the end of 2009, 21 kinds of products in the province had obtained the protection of national geographical indication products including Zanhuang Chinese Date in Shijiazhuang Area; Shacheng Grape Wine, and Xuanghua Milk Grape in Zhangjiakou Area; Shanzhuang Old Wine, Weichang Potato, Chengde Guoguang Apple in Chengde Area; Changli Grape Wine, Lulong Silk Noddles, and Shimen Walnut in Qinhuangdao Area; Lixian County Chinese Yam, and Rongcheng Bamboo Shoot in Baoding Area; Botou Pear, Cangzhou Golden-Silk Jujube, and Huanghua Winter Dater in Cangzhou Area; Ningjin Pear in Xingtai Area; Shexian County Walnut, Shexian County Pepper, Weixian County Pear, Yongnian Garlic, and Wu'an Millet in Handan Area; and Jingdong Chestnut (including the administration regions of Qianxi, Qian'an and Zunhua in Tangshan Area, Funing, Qinglong, and Lulong in Qinhuangdao Area, Xinglong, Kuangcheng, Pingquan, Chengde, Luanping, and Fengning in Chengde Area).

按照国家质检总局颁布的《地理标志产品保护规定》,截至2009年底,我省石家庄地区赞皇大枣;张家口地区沙城葡萄酒、宣化牛奶葡萄;承德地区山庄老酒、围场马铃薯、承德国光苹果;秦皇岛地区昌黎葡萄酒、卢龙粉丝、石门核桃;保定地区蠡县麻山药、容城绿竹笋;沧州地区泊头鸭梨、沧州金丝小枣、黄骅冬枣;邢台地区宁晋鸭梨;邯郸地区涉县核桃、涉县花椒、魏县鸭梨、永年大蒜、武安小米;京东板栗(唐山地区的迁西、迁安、遵化,秦皇岛地区的抚宁、青龙、卢龙,承德地区的兴隆、宽城、平泉、承德、栾平、丰宁等行政区域)共计21种产品已获得国家地理标志产品保护。

Beijing Real Estate and Construction Bar Association Professional Committee of Liu Hua, deputy director of the Law Society: The contract agreement in the area, it seems to me there are at least two flaws: First, it agreed to construction area for the sale area, construction area is passed and the pool area and the area, and in this contract on the pool area also lacks transparency, developers will not tell you specific assessments where the location of the area, the specific area is the number, which for him provided an opportunity for fraud; Secondly, the contract agreed by the parties, permit the forecast area of 3% error, if the pool size increases as long as no more than 3%, you can only increase the pool for this increase the size back the principal.

北京地产及建造界律师协会专业委员会刘华副主任律师公会:合同协议,在该地区,在我看来至少有两个缺陷:第一,它同意建筑面积的销售区,建筑面积是通过和游泳池区和地区,并在此合同的游泳池也缺乏透明度,开发商不会告诉你具体评估那里的位置,面积,具体领域是的数目,这为他提供了一个机会,欺诈;其次,该合同约定,允许预测面积的3 %的错误,如果池大小的增加,只要不超过3%,你只能增加池的大小增加本金。

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