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spleen相关的网络例句

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与 spleen 相关的网络例句 [注:此内容来源于网络,仅供参考]

NT-3-ir cells belonged to the stroma cells of spleen and scattered mainly in the periarterial lymphoid sheath, lymphatic follicles and the inner wall of the blood vessels.

NT-3-ir 细胞疾病属于网状细胞疾病,主要散布于动脉周围淋巴鞘、淋巴小结和血管内壁。

Suis was found in all identifiable crypt areas; SS2 also appeard in marginal zone and periarterial lymphoid sheath of spleen, hepatic sinusoid of liver, interstitium of lung; presence of SS2 was at the cortex where histopathological lesions and expression of inflammatory mediators were observed.

实验表明,SS2主要定殖于扁桃体的隐窝附近;在脾的边缘区和动脉周围淋巴鞘附近、淋巴结的生发中心和皮质内、肝血窦、肺间质和肾小体中均可见菌体状荧光颗粒;在脑组织中发生脑膜炎的区域,如皮层等可检出细菌。

When infraction or perisplenitis occurs, however, pain in the region of the spleen may be intense

然而,若发生梗塞或脾周围炎,则脾区疼痛可加剧。

Note that this spleen also shows irregular tan-white fibrous plaques over the purple surface. This "sugar icing" has the name hyaline perisplenitis.

图示脾的紫色表面上也显示有不规则的苍白色纤维性斑片,称为玻璃样脾周围炎。

METHODS: the supernatants of cultured spleen's lymphocytes induced by ConA were injected into mice peritoneally,kinetics of plasma corticotropin releasing hormone,adrenocorticotropic hormone and corticosterone in mice were tested at different time (0.5,1,2,4,6 h),or tissue of hypothalamus pituitarium or adrenal was stimulated with supernatants induced by ConA,and the secretion of CRH, ACTH and CORT were observed.

采用ConA诱导淋巴细胞培养上清液给小鼠腹腔注射,测定不同时间(0.5,1,2,4,6 h)的小鼠血浆中CRH,ACTH,皮质酮产生的动力学,同时在体外用ConA诱导上清液分别与下丘脑,垂体,肾上腺组织共同培养后观察CRH,ACTH,CORT分泌情况。

We found that intravenously administered arginine significantly decreased the spleen weight, the serum interleukin-6 level, and IL-6 production by leukocytes, splenic macrophages, and thymocytes; significantly decreased tumor-necrosis factor-α production of leukocytes and thymocytes; and significantly increased the stimulating index of cell proliferation in T-thymocytes in peritonitic rats.

结果显示,静脉给予arginine显著降低腹膜炎大鼠脾脏重量、血清间白素-6、与白血球、脾脏巨噬细胞及胸腺细胞IL-6分泌量,且显著降低白血球与胸腺细胞肿瘤坏死因子-α分泌量,但显著增加胸腺细胞增生的刺激指数。

Methods The method of replenishing qi to reinforce the spleen and dissolving phlegm to remove turbidity was used,and eight periumbilical points (Tianshu,Huaroumen,Wailing,Yinjiao and Shuifen),points Guanyuan and Zusanli were selected in cooperation with auricular-plaster therapy.In the corresponding period,30 healthy persons were selected for comparison.Changes in FBG,INS,ISI,TC,TG,LDL-C and HDL-C were evaluated after acupuncture in simple obesity patients.Also were changes in waist circumference,hip circumference,waist-to-hip ratio,body weight and BMI,and differences in them between the curative effects on degree Ⅰ and degree Ⅱ obesity.

方法采用&益气健脾,化痰消浊&法,取脐周八穴(天枢、滑肉门、外陵、阴交、水分)、关元、足三里等穴,配合耳穴贴压,并与同期30例健康体检者比较,观察针刺前后单纯性肥胖症患者FBG、INS、ISI、TC、TG、LDL-C、HDL-C的变化;还观察针刺前后单纯性肥胖症患者腰围、臀围、腰臀比、体重、BMI的变化,及其Ⅰ度肥胖、Ⅱ度肥胖的疗效差异。

MethodsThe transplanted tumor model of the mouse S180 sarcoma was established.Fifty mice were randomly divided into five groups,the control group,the CTX group,the Gecko group.They were treated respectively with oral administration of saline,and intraperitoneal injection of CTX 100 mg/kg only one time,oral administration of Gecko in doses of 13.5,9,4.5 g/kg,one time a day.After 14 days,the anti-tumor activity was evaluated by tumor tissue weighing. The impact on immune organ was detected by accounting thymus index, spleen index and the number of peritoneal macrophage which phagocytose chicken red blood cells.The protein express of vascular endothelin growth factor and basic fibroblast growth factor were detected by SABC immunohistochemistry.

方法建立移植瘤小鼠S180肉瘤模型,将50只雌鼠随机分为对照组、环磷酰胺组、壁虎高组、中组、低组共5组,分别给于生理盐水灌胃1次/d,CTX(100 mg/kg)腹腔注射1次,壁虎高、中、低组(13.5,9,4.5 g/kg),每天灌胃1次。14 d后,称取荷瘤小鼠瘤重、胸腺重、脾脏重,计算抑瘤率、胸腺指数、脾脏指数,观察腹腔巨噬细胞吞噬鸡血红细胞实验指标;用SABC免疫组化法检测血管内皮生长因子、碱性成纤维细胞生长因子的蛋白表达,TUNEL方法检测细胞凋亡率。

Cultured for 48 hours, the floating cells were removed and the adherent cells were continued to culture with cytokines including IL-4 and GM-CSF. After 14 days culture, the induced DCs were observed by photics microscope and electron microscope, also co-cultured with native T cells derived from spleen, its stimulating function was detected by MTT assay.

经过光镜,透射电镜观察培养DCs的形态学特征;通过同种T细胞混合培养,采用MTT比色分析法测定不同浓度的DCs发同种T细胞增殖的能力。

Methods Routine immunization of BALB/ c mice by a tansfected cell line 293T/ B7-H4 as antigens.Then the immunized spleen was fused with SP2/0,a kind of plasmocytoma cells, and screen the positive clones by FCS with the 293T/B7-H4 as a positive control while 293T/ mock as the negative control.

以高表达人B7-H4分子的基因转染细胞株293T/B7-H4为免疫原,常规免疫BALB/c小鼠,采用B淋巴细胞杂交瘤技术进行细胞融合,并以该基因转染细胞293T/B7-H4作为阳性筛选细胞,以转空质粒的对照细胞293T/Mock作为阴性对照细胞。

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