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binary cell相关的网络例句

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与 binary cell 相关的网络例句 [注:此内容来源于网络,仅供参考]

A method for cold transportation of goods that are placed in a hollow-walled refrigerating container, comprising the following steps: storage of a pumpable solution of tiny ice crystals, known as binary ice, having a given composition and temperature, in a binary ice store until said binary ice is used for refrigerating or filling purposes; the optionally filled wall of the refrigerating container that is to be used is emptied via an outlet valve for the binary ice; binary ice is allowed to circulate inside the refrigerating container via filling instruments that are supplied with binary ice from the binary ice store until the temperature of the wall drops to a given temperature, whereby the heated fluid that is discharged from the outlet valve is fed to a binary ice fluid store; the wall of the refrigerating container is filled with a given amount of binary ice; the refrigerating container is decoupled from the filling instruments; the binary fluid that result from the melted binary ice is returned to a corresponding binary fluid store in order to produce new binary ice from said binary fluid.

一种置于一中空壁制冷容器里的制品的冷运输用的方法包括下列诸步骤:将一种具有一预定的组成和温度的可被泵送的小的冰晶体的溶液保存在一个二元冰储槽中,直到所述的二元冰用于制冷或充填目的;通过一二元冰出口阀将待被使用的一制冷容器的随意被充填的壁排空;用二元冰充入该制冷容器的被排空的壁内;通过充填器具使该二元冰在该制冷容器里循环,这循环由来自二元冰储槽的二元冰供给,直到壁温下降到一预定值,从而从该出口阀放出的被加热的流体被提供给一个二元冰流体储槽;将一给定量的二元冰充入该制冷容器的壁里;从诸充填器具上拆离该制冷容器;将从溶化的二元冰形成的二元流体返回到一相应的二元流体储槽内,以便从所述的二元流体制取新的二元冰。

Make signal be called binary system numeral to make for the make of binary system signal, the binary system make and is divided into a binary system to move key to control(2 ASK), the binary system Pin move key to control(2 FSK), the binary system mutually move key to control(2 PSK) with bad cent the binary system mutually move key to control(2 DPSK) etc. variety basic type, this topic main is numeral the frequency make and call Pin to move key to control.

调制信号为二进制信号的调制称为二进制数字调制,二进制调制又分为二进制幅移键控(2ASK)、二进制频移键控(2FSK)、二进制相移键控(2PSK)和差分二进制相移键控(2DPSK)等多种基本的类型,本课题主要是数字频率调制又称频移键控。

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。

The entire theory systems of the punctured binary sequence pair and the punctured binary array pair are built, which include the perfect punctured binary sequence pair theory, the perfect punctured binary array pair theory, the quasi-perfect and double quasi-perfect binary array pair theory, and the punctured binary complementary sequence pair theory.

定义了屏蔽二进序列偶、最佳屏蔽二进序列偶和奇周期最佳屏蔽二进序列偶,研究了它们的变换性质和存在的组合允许条件,并用这些性质和条件,搜索出若干最佳屏蔽二进序列偶和奇周期最佳屏蔽二进序列偶。

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。

The relationships among perfect punctured binary array pair, quasi-perfect and double quasi-perfect punctured binary array pair is presented. Specially, when first and second dimension period of the punctured binary array pair are odd, the perfect punctured binary array pair, quasi-perfect and double quasi-perfect punctured binary array are able to change each other.

定义了准最佳屏蔽二进阵列偶和双准最佳屏蔽二进阵列偶,研究了它们的变换性质和频谱特性,给出了它们存在的组合允许条件,利用这些组合允许条件,有效地搜索出若干准最佳屏蔽二进阵列偶和双准最佳屏蔽二进阵列偶。

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 samples were smeared on slides and stained with Giemsas stain. The stained smears were observed microscopically and photographed. It showed that except typical trophozoites in binary fission. the following trophozoites of abnormal morphs were also observed. for instance abnormal trophozoites with binary fission; enlarged trophozoites with round and irregular shaped eosinophilic bodies in the cell plasma; enlarged cells containing round and irregular shaped eosinophilic bodies and flagella; enlarged cells which contain 6 or 8 nuclear-like bodies and flagella, 3 or 4 embryonic forms of daughter trophozoite in one mother trophozoite; 4 trophozoite embryonic forms with fused plasma 3 trophozoites with fused plasma;4 trophozoites with fused plasma; a pair of trophozoite with binary fission fused with another trophozoite;2 pairs of trophozoite with binary fission fused each other; a trophozoite with 1 nuclear only.

结果 除观察到典型的营二分裂法繁殖的贾第虫滋养体外,还可见到多种形态异常的虫体,包括;虫体呈非典型二分裂;滋养体胀大,胞质中有团块状和不规则形状的嗜酸性物质;在胀大的贾第虫细胞内含有团块状和不规则形状的嗜酸性物质以及鞭毛;在胀大的贾第虫细胞内含有6或8个核状物以及鞭毛;在一个母体细胞中含有3或4个子体细胞的雏形;胞质互相融合的4个滋养体的雏形;胞质互相触合的3个滋养体,胞质互相融合的4个滋养体;1对营二分裂的滋养体与另一个滋养休互相融合;2对营二分裂的滋养体互相融合;仅有1个细胞核的滋养体。

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%。

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