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

Besides the fingerprint authorized storage volume FU-Disk s safety, the auto-run FU-Software features FU-Lock, Favorites and Synchronize between PC folder with Bio Crypto Flash and all the stored data will be auto encrypted.

除FU盘的指纹认证安全存储功能外,自动运行的FU软件还可实现FU锁功能、收藏夹功能以及同步个人电脑文件夹和生物加密闪存盘的功能,所有存储数据将被自动加密。

The codA gene encodes cytosine deaminase, which can deaminate nontoxic compound 5-fluorocytosine (5-FC) to the highly cytotoxic compound 5-fluorouracil (5-FU). 5-FU can influence the cells survival through interference with the synthesis metabolism of the RNA and DNA.

codA基因在细菌体内编码胞嘧啶脱氨酶,CD能把对细胞无毒的5-氟胞嘧啶(5-FC)脱氨成为有毒的5-氟尿嘧啶(5-FU)。5-FU通过干扰RNA和DNA的合成代谢从而影响细胞的生存。

Methods: 100KunMing mice were divided into four groups randomly, each group included 25 mice inoculated EAC cells. The mice were treatedby celiac injection with saline solution , L-Arg , 5-Fu, L-Arg + 5-Fu respectively in each group . The natural survival time andthe average hydroperitoneum capacity were recorded for each group before the mice were killed.

将100只昆明小鼠随机分成4组,接种EAC细胞,依照分组向腹腔注射生理盐水、L-Arg、5-Fu、L-Arg+5-Fu,同时记录各组小鼠自然存活时间、处死时平均腹水量。

Methods:The SD rats were each given a catheterization of jejunostomy and an inoculation of Walker-256 carcinosarcoma cells subcutaneously. Thirty-six rats were randomized into 3 groups: Group A (balance amino acid+NS), Group B (balance amino acid +5-Fu), Group C (complex amino acids of arginine-enriched and leucine-enriched+5-Fu).

SD大鼠空肠造瘘,皮下接种Walker-256癌肉瘤,36只接种成功之大鼠随机分为A组、B组(平衡氨基酸+ 5-Fu组)、C组(富含亮氨酸及精氨酸的不平衡氨基酸+ 5-Fu组)。

Single proton emission computer tomography and X-Ray film were taken to observe the allocation of the drugs.Results (1) Pelvic and periaortic nodal 5-FU concentrations of RP were 60~106 and 76~119 times of that of IP respectively.(2) The nodal 5-FU concentrations on repeated injection side were 16~20 times of that on control sides of RP.(3) There was no complications or adverse effect observed.(4) 5-FU was allocated to the space including the external iliac, internal iliac, obturator, deep inguinal and common iliac lymph nodes and also up to the periaortic lymph nodes.

结果 (1)腹主动脉旁淋巴结5-FU浓度,腹膜后化疗是腹腔化疗的76~119倍;盆腔淋巴结5-FU的浓度,腹膜后化疗是腹腔化疗的66~106倍;(2)腹膜后化疗重复注药,注药侧5-FU浓度为未注药侧的16~20倍;(3)腹膜后化疗与腹腔化疗均无明显的毒副作用;(4)经盆腔腹膜外间隙给药,药物能从盆腔上行至腹主动脉旁淋巴结及其周围。

RESULTS: Tumor sizes decreased steadily and tumors disappeared within the first week after 5-FU treatment; and at the same time 75 mg/kg 5-FU also had side effects on peripherial blood cells.

Hb含量在5-FU治疗后第1天也出现降低,由化疗前的(133 7)g/L降为(112 9)g/L,差异有统计学意义(P〈0.01),随后Hb含量持续在低水平,治疗后15d逐渐恢复至化疗前水平。75mg/kg的5-Fu对荷瘤小鼠血小板的抑制作用不明显,反而在治疗后第1、11天出现2次血小板一过性增高(P〈0.01)。

Results 5-FU inhibits growth of Lovo cells; it is found that within a limited dosage and period of time, there has been an obvious increase in apoptosis cells under the photomechanical scope; the analysis of Lovo cells by FCM showed that after the induction of 5-FU, the percentage of apoptosis cells has increased; and FCM also displays dosage and time effects. Electrophoresis was obviously in a stripe shape of trapeziform.

结果 5-FU能抑制 Lovo细胞生长,在一定剂量和时间范围内,通过光镜观察,见凋亡细胞明显增多,经5-FU诱导后,用FCM 分析 Lovo细胞,发现凋亡百分率增加并显示剂量和时间效应。

Compared with 5-FU-H20,the active toxity of 5-FU-CH was examined preliminarily. The LD50 were 216mg/kg and 600mg/kg,respectively.

同时,本文以5-FU-H.0为参比制剂,对5-FU-CH制剂的急性毒性进行了初步研究,测得其半数致死量LD。

MethodsPolyprenols separated and purified from ginkgobiloba L were administered alone and in combination with 5 Fu,CTX and PDD,and in contrast with 5 Fu,CTX and PDD alone,the experiments were carried out on mouse transplanted Heps and EC.

方法从银杏叶中分离纯化聚戊烯醇,分别与氟脲嘧啶(5 Fu)、环磷酰胺和顺铂联合应用,对移植性Heps和EC荷瘤小鼠进行抑瘤实验,并与 5 Fu、CTX和PDD单独用药比较。

And ZNF397nf function as transcription repressors. The different transcriptional regulation activity of the nf isoforms and their interaction with the fu isoforms would contribute to the complexity of the transcription regulation. To further examine the biological function of interaction between different isoforms we also analyze the potential role of ZNF191 and ZNF434 on signaling pathway. We found that ZNF191fu can significantly enhance the HSE-luciferase activity, while ZNF434fu can enhance the AP1-luciferase activity, then we analyze whether the nf isoforms have impact on the fu isoforms.

而这些成员的nf剪接本与它们对应的fu剪接本的转录调控功能有所不同,其中ZNF191nf与ZNF434nf剪接本的转录调控活性相对它们的fu剪接本显著降低,呈现较弱的转录抑制作用,但ZNF447nf剪接本却呈现出显著的转录激活作用,同时ZNF397nf剪接本则表现出显著的转录抑制作用,ZNF396nf剪接本的转录调控作用与其fu剪接本相当。nf剪接本这种与fu剪接本不尽相同的转录调控活性以及能与fu剪接本互作的能力,大大增加了转录调控作用的复杂性,这使得通过少量的转录因子作用来实现众多基因时空表达的不同成为可能。

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