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      n型
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  n-type
    4-Amino-piperidine Library: Studies on Synthesis and Activities of Blockers for N-type Calcium Channel
    4-氨基哌啶类N型钙离子通道阻断剂组合库的研究
短句来源
    Objective To investigate the effect of intrathecal administration of ω-conopeptide SO3,a new N-type calcium channel blocker,on the expression of CGRP and substance P in the spinal cord of a rat model of chronic constriction injury(CCI).
    目的通过研究鞘内注射新型N型钙通道阻滞剂ω-芋螺毒素SO3对坐骨神经慢性挤压伤(CCI)模型大鼠脊髓降钙素基因相关肽(CGRP)、P物质(SP)含量的影响,探讨N型钙通道在伤害性信息传递中的作用。
短句来源
    Comparative QSAR Study on a Novel Class of N-type Calcium Channel Blocks
    一类新型N型钙通道阻滞剂的比较定量构效关系研究
短句来源
    2. The P-type (maybe including Q-type) calcium channel accounted for 50% calcium influx into synaptosomes, N-type for about 20%,while L-type didn't change KCl-induced increased intrasynaptosomal calcium concentrations.
    2.P/Q型钙通道约占突触体钙内流的50%,N型钙通道约占20%,而L型钙通道不影响KCl诱发的突触体内钙离子浓度的升高。
短句来源
    2. Pancuronium of lower concentrations (1-40 P mol ?L"1) potentiated the N~type calcium currents dose-dependently without affecting the activating characteristic while higher concentration ( 100 u mol ?L"1 and higher) inhibited the N-type calcium currents.
    2.1-40 μ mol·L~(-1)的泮库溴铵增强全细胞N型钙通道电流。
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  “n型”译为未确定词的双语例句
    While GDP·βS was added to the internal solution,pancuronium 10 μmol/L had no significant effects on calcium currents.
    在电极内液中加入G蛋白的非水解性竞争性拮抗剂GDP·βS后 ,10 μmol/L的泮库溴铵对N型钙电流的增强作用消失。
短句来源
    P/Q-type cal-cium channel antagonist ω-agatoxin IVA had no different effects on increased intrasynaptosomal calcium concentrations with or without 100 μmol/L etomidate,but for N- or L-type cal-cium channel antagonist,it had additional effects when with etomidate.
    P/Q型钙通道阻断剂ω agatoxinIVA在单用或及与加入依托咪酯 10 0 μmol/L合用后对钙内流抑制作用没有差异 ,而L或N型钙通道阻断剂在加入依托咪酯后抑制钙内流作用增加。
短句来源
    Methods: Rat peritoneal macrophages were gathered and separated into four groups: ①Negative control: macrophages treated with α-Bungarotoxin (α-Bgt),special antagonist of α7 subunit of nicotinic cholinergic receptor (α7nAChR).
    方法:采集大鼠腹腔巨噬细胞,分4组进行实验:①阴性对照组:无荧光标记的N型胆碱能受体α7亚基(α7nAChR)的特异性拮抗剂α-银环蛇毒素(α-Bgt)处理巨噬细胞;
短句来源
    P/Q-type calcium channel antagonist co-agatoxin IVA had no different effects on increased intrasynaptosomal calcium concentrations with or without 100uM etomidate, but for N- or L-type calcium channel antagonist,it had additional effects when with etomidate.
    P/Q型钙通道阻断剂(?) -agatoxin IVA在没有或加入100μM依托咪酯后对钙内流抑制没有差异,而L或N型钙通道阻断剂在加入依托咪酯后抑制钙内流作用增加。
短句来源
    Its EC50 was 10. 63 mol L and Hill coefficient was 2.43, which infered 2 molecular pancuronium interacted with 1 nAChR.
    在记录N型钙电流的电极内液中加入2mI’no IL一’G蛋白的非水解性抑制剂GDp·ps后,10 pm。
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  n-type
Since wavelet bases are not available for this general setting, the new idea used here is to apply the discrete Calderón-type reproducing formula associated to para-accretive functions developed in [14].
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However, the ECV measurement of dopant concentration in the underlying lightly doped n-type substrate is significantly influenced by the upper heavily-doped layer.
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Segmentation of p-n junction was performed by implantation of boron (for the n-type Ge) and mechanical grooving of the Li diffusion layer (for the p-type Ge).
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Some n-type semiconductor metal oxide sensors based on WO3 and In2O3 were studied in detecting unsymmetrical dimethylhydrazine (UDMH) vapors.
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One was from the orf215 region of the N-type mtDNA.
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         The effect of the total saponins of panax notogiseng ( PNS ) on transmitter release was studied on mouse diaphragm. The Ca2+ -mediated release evoked by electric stimulation at the nerve terminal or by raised K+ level was markedly reduced by Cd2 + , but not affected by PNS & nifedipine. Also, PNS didn't change the basic frequency of mepp & the Ba2+ entry during depolarization of the terminal. C-ompared with PNS, Cd2 had a significant effect on decreasing Ba2+ entry. These results suggest that PNS can not ch...
            胞内记录神经—终板电位及微终板电位,证明三七总皂甙不影响神经末梢去极化时Ca~(2+)及Ba~(2+)的内流,对同步、非同步及自发性的量子释放均无减弱。由于Cd~(2+)能明显减弱量子释放,而PNS与nifedipine却无作用,提示胆碱能运动神经末梢上参与递质释放的Ca~(2+)通道属于N型Ca~(2+)通道。
文摘来源
         Comparing the rate of polymerization of Cephalosporins with a different structure at C3 or(and) C7 substituent, it is found out that both C3 and C7 substituent could influence the rat of the polymerizacion of type N. The more 7-substituent attracts electrons strongly, the easier the polymerization goes on. However, the inductive effect of 3-substituent influencing the polymerization has a limit, below which raising the effect of attracting electrons of 3-substituent increases the polymerization and above wh...
            通过对不同3位取代基和不同7位取代基的头孢菌素在水溶液中聚合反应速度的比较,发现3位、7位取代基的结构对头孢菌素N型聚合反应速度均有影响。7位取代基的吸电子效应越强,聚合反应速度越快;当3位取代基的吸电子效应不太强时,增大取代基的吸电子效应,聚合反应速度加快;但取代基的吸电子效应超过某一界限,再增大取代基的吸电子效应,聚合反应速度减慢。据此,对头孢菌素N型聚合反应的机制进行了讨论。
文摘来源
         On isolated nonuniform stretched muscle preparation (INSMP) of rat diaphragm, it was found that the sustained depolarization (SD) in endplate area is the predominant response to repetitive stimu1ation after soman intoxication. Both the microelectrode intracellular recording and the extracellular acetylcholine (ACh) iontophoresis were used to investigate the mechanism of SD.The amplitude of ACh potential was used as the criterion of N-ACh receptor to ACh. ACh potential as well asendplate potential could not ...
            在离休大鼠膈肌标本上,细胞内记录终板区微电泳给乙酰胆碱(ACh)的电位,以ACh电位幅度为突触后反应性指标,观察了梭曼中毒后间接串刺激产生终板区持续性去极化反应的性质并分析了其产生的机理。持续性去极化过程中不仅串终板电位消失,ACh电位也消失,持续性去极化之后ACh逐渐恢复。在正常大鼠和肉毒毒素A中毒大鼠膈肌标本上,梭曼中毒后,串ACh电位(5-10Hz)也可诱发与持续性去极化性质相同的去极化反应,结果表明,持续性去极化主要是突触后N型ACh受体对高浓度ACh的一种反应,不支持突触前ACh“再生性”释放的假说。
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