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d and c相关的网络例句

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与 d and c 相关的网络例句 [注:此内容来源于网络,仅供参考]

The preliminary bioassary showed that at the concentration of 100μg/mL, the inhibitory rate of compounds Ⅴc to Fusarium graminearum was 81.3%;Ⅳe to Fusarium oxysporium was 83.4%;Ⅴe and Ⅴf to Cercospora sorghi were 79.7% and 72.4% respectively;Ⅳd to Fusarium graminearum and Fusarium oxysporium were 68.9% and 65.7% respectively.

初步生物测试结果表明:在质量浓度为100μgmL下,化合物Ⅴc对小麦赤霉病菌的抑制率达到了81.3%;化合物Ⅳe对马铃薯干腐病菌的抑制率达到了83.4%;化合物Ⅴe,Ⅴf对玉米弯孢病菌的抑制率也分别达到了79.7%和72.4%;化合物Ⅳd对小麦赤霉病菌和马铃薯干腐病菌的抑制率分别达到了68.9%和65.7%。

Objective To explore the relationships between the levels of C-reactive protein and D- dimeride and the onset 、development and prognosis of acute cerebral infartion and their significance in the treatment .

目的 探究C-反应蛋白和D-二聚体水平与急性脑梗死起病、发展及预后的关系,明确其在治疗急性脑梗死中的临床意义。

In the present study changes of NOS positive cells after injection of LPS and apoptotic ependymal cells, the relationship between expression of immediate early gene c-fos and astrocytes, and comparison of changes between SFO and rest regions of the brain in different time-points were investigated with NADPH-d histochemistry, apoptosis in SITU detection of TUNEL, TEM and SEM, fluorescein double labeling of immunohistochemistry, and laser scanning confocal microscope .

为了证实穹窿下器在脑内免疫调节系统中的作用,在本研究当中,应用了NADPH-d的组化方法、TUNEL末端标记法、扫描及透射电镜方法、免疫组织化学的荧光双标法及激光扫描共聚焦显微镜技术,来研究在腹腔内给予大肠杆菌内毒素后,脑内的一氧化氮合酶细胞的变化、室管膜细胞的凋亡、早期即刻基因c-fos的表达与星形胶质细胞之间的关系,以及穹窿下器与其它脑区相比较时的特异性改变。

Taking mRNA from ephebic Bombyx mandarina as templates,the cDNA of four troponin I isoforms was cloned by RT-PCR,named TnI-A,TnI-B,TnI-C and TnI-D(GenBank accession numbers:FJ785828,FJ785829,F3785830 and FJ890515 )respectively.Sequence homology comparison and functional prediction of the amino acids encoded by the four TnI gene isoforms in Bombyx mandarina indicate that they have characteristics of troponin families.

与电子克隆到的相应的家蚕TnI亚型比较分析,结果显示:野桑蚕与家蚕TnI-B有相同的氨基酸,TnI-A和TnI-C有一个氨基酸的差别,而在家蚕中没有电子克隆到与野桑蚕TnI-D相同的亚型。3。

In the A and B figures, small grape-like tissue covered over all the epiglottic area that is hypertrophic lymphoid tonsil. More advanced the fiberoptic laryngoscope during spontaneous inspiration phase, larynx and vocal cord can be visualized in the C and D figures. We must emphasize that endotracheal intubation and even artificial ventilation was hardly performed under direct laryngocopy and general anesthesia.

图片A和B中,覆盖整个会厌部的葡萄息肉状物就是濔漫增生的舌底部淋巴组织增生,当光纤内视镜随著病人自主呼吸向内向下移动,吐气时可以见到图片C和D中喉头及声带的开合,由於在全身麻醉下无自主呼吸时此病人咽喉部位的似帘幕状遮蔽特殊结构造成之困难插管甚至是困难通气。

In the A and B figures, small grape - like tissue covered over all the epiglottic area that is hypertrophic lymphoid tonsil . More advanced the fiberoptic laryngoscope during spontaneous inspiration phase, larynx and vocal cord can be visualized in the C and D figures. We must emphasize that endotracheal intubation and even artificial ventilation was hardly performed under direct laryngocopy and general anesthesia .+{{: congress:2008:abstract:c01-1. jpg

图片A和B中,覆盖整个会厌部的葡萄息肉状物就是濔漫增生的舌底部淋巴组织增生,当光纤内视镜随著病人自主呼吸向内向下移动,吐气时可以见到图片C和D中喉头及声带的开合,由於在全身麻醉下无自主呼吸时此病人咽喉部位的似帘幕状遮蔽特殊结构造成之困难插管甚至是困难通气。

METHODS: Sixty healthy Sprague-Dawley rats were randomly divided into 3 groups: 6 rats in normal control group, 6 rats in EGb treating normal IOP group, and the other 48 rats were established chronic high IOP models of rats by cauterizing two episcleral veins. The n 30 rats satisfying experimental level were selected and randomly divided into five groups: 6 rats in physiological brine treating group, and the other 24 rats were divided into four experimental groups according to the dose of EGb: group A, EGb 50mg/; group B, EGb 100mg/; group C, EGb 150mg/; and group D EGb 200mg/. After the treating time of 1 month, the rats were sacrificed on schedule.

取健康SD大鼠60只,正常对照组和正常银杏叶治疗组各6只,其余48只采用烧烙法,烙闭大鼠左眼2条浅层巩膜静脉,制作大鼠持续性高眼压模型,从中选出眼压稳定在实验要求水平的大鼠30只,随机分为生理盐水组,治疗A组(每日EGb 50mg/kg)、治疗B 组(每日EGb 100mg/kg)、治疗C 组(每日EGb 150mg/kg)、治疗D 组(每日EGb 200mg/kg),治疗时间为1mo,处死大鼠后做视网膜全层铺片,对RGCL神经元做特异性染色后行神经元计数分析来评估神经元的情况。

METHODS: Sixty healthy Sprague-Dawley rats were randomly divided into 3 groups: 6 rats in normal control group, 6 rats in EGb treating normal IOP group, and the other 48 rats were established chronic high IOP models of rats by cauterizing two episcleral veins. Then 30 rats satisfying experimental level were selected and randomly divided into five groups: 6 rats in physiological brine treating group, and the other 24 rats were divided into four experimental groups according to the dose of EGb: group A, EGb 50mg/; group B, EGb 100mg/; group C, EGb 150mg/; and group D EGb 200mg/. After the treating time of 1 month, the rats were sacrificed on schedule. Flat preparation of whole retinaes was stained distinctively and neuron counting in retinal ganglion cell layer from both eyes of each rat were performed to evaluate neuron situation.

取健康SD大鼠60只,正常对照组和正常银杏叶治疗组各6只,其余48只采用烧烙法,烙闭大鼠左眼2条浅层巩膜静脉,制作大鼠持续性高眼压模型,从中选出眼压稳定在实验要求水平的大鼠30只,随机分为生理盐水组,治疗A组(每日EGb 50mg/kg)、治疗B 组(每日EGb 100mg/kg)、治疗C 组(每日EGb 150mg/kg)、治疗D 组(每日EGb 200mg/kg),治疗时间为1mo,处死大鼠后做视网膜全层铺片,对RGCL神经元做特异性染色后行神经元计数分析来评估神经元的情况。

METHODS: Sixty healthy Sprague-Dawley rats were randomly divided into 3 groups: 6 rats in normal control group, 6 rats in EGb treating normal IOP group, and the other 48 rats were established chronic high IOP models of rats by cauterizing two episcleral veins. The n 30 rats satisfying experimental level were selected and randomly divided into five groups: 6 rats in physiological brine treating group, and the other 24 rats were divided into four experimental groups according to the dose of EGb: group A, EGb 50mg/; group B, EGb 100mg/; group C, EGb 150mg/; and group D EGb 200mg/. After the treating time of 1 month, the rats were sacrificed on schedule. Flat preparation of whole retinaes was stained distinctively and neuron counting in retinal ganglion cell layer from both eyes of each rat were performed to evaluate neuron situation.

取健康SD大鼠60只,正常对照组和正常银杏叶治疗组各6只,其余48只采用烧烙法,烙闭大鼠左眼2条浅层巩膜静脉,制作大鼠持续性高眼压模型,从中选出眼压稳定在实验要求水平的大鼠30只,随机分为生理盐水组,治疗A组(每日EGb 50mg/kg)、治疗B 组(每日EGb 100mg/kg)、治疗C 组(每日EGb 150mg/kg)、治疗D 组(每日EGb 200mg/kg),治疗时间为1mo,处死大鼠后做视网膜全层铺片,对RGCL神经元做特异性染色后行神经元计数分析来评估神经元的情况。

METHODS: Sixty healthy Sprague-Dawley rats were randomly divided into 3 groups: 6 rats in normal control group, 6 rats in EGb treating normal IOP group, and the other 48 rats were established chronic high IOP models of rats by cauterizing two episcleral veins. n 30 rats satisfying experimental level were selected and randomly divided into five groups: 6 rats in physiological brine treating group, and the other 24 rats were divided into four experimental groups according to the dose of EGb: group A, EGb 50mg/; group B, EGb 100mg/; group C, EGb 150mg/; and group D EGb 200mg/. After the treating time of 1 month, the rats were sacrificed on schedule. Flat preparation of whole retinaes was stained distinctively and neuron counting in retinal ganglion cell layer from both eyes of each rat were performed to evaluate neuron situation.

取健康SD大鼠60只,正常对照组和正常银杏叶组各6只,其余48只采用烧烙法,烙闭大鼠左眼2条浅层巩膜静脉,制作大鼠持续性高眼压模型,从中选出眼压稳定在实验要求水平的大鼠30只,随机分为生理盐水组,治疗A组(每日EGb 50mg/kg)、治疗B 组(每日EGb 100mg/kg)、治疗C 组(每日EGb 150mg/kg)、治疗D 组(每日EGb 200mg/kg),治疗时间为1mo,处死大鼠后做视网膜全层铺片,对RGCL神经元做特异性染色后行神经元计数来评估神经元的情况。

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