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ICH was induced by the injection of 50 ul autologous blood into the right caudate nucleus, while 50 μl natural saline was injected in the control group. The rats were killed after 6h, 24h, 2d, 3d, 5d and 7d respectively, the morphology changes of nerve cell oncosis and count by electron microscope and the immunohistochemical method and computer image analysis were performed in rats brain by using antibody of VEGF.

采用二步法制备大鼠脑出血模型,脑出血组注入自体血50μl,对照组注入等量生理盐水,分别于6、24h、2、3、5、7d后处死,行HE染色和免疫组化染色观察脑内VEGF表达变化;电镜下观察胀亡细胞形态学变化并计数。

The item adopts biology engineering technique, withdrawing micromolecule peptide , amino acids, glycoprotein etc. from three-month sheep's ovary embryos and whole blood of cyetic horses. The product contains ovarin, sheep embryo and PMSG, these biological ingredients are great demanded by female. It can repair ovary cell, keep hairdressing, defering consenescence and reducing female disease occurrence.

项目采用生物工程技术,对三个月羊卵巢胚胎,孕马血提取小分子肽,氨基酸,糖蛋白等,产品含有卵巢素,羊胎素,PMSG等大量女性需要的生物活性成份,修复卵巢细胞,美容养颜,延缓更年期,减少女性疾病发生。

Results The injection of mixed bacteria caused a pathological alteration of oviductal wall, such as edema in mucous, shortened cilia of epithelium, inflammatory cell infiltrating, dilation and hyperraemia in blood capillary within lamina propria and obstruction of oviductal lumen.

结果 在使用混合菌接种后,小鼠输卵管管壁结构发生改变,主要包括黏膜层水肿、上皮细胞顶端纤毛变短或消失、固有层炎性细胞浸润、毛细血管充血、管腔狭窄甚至闭塞。

Results; The injection of mixed bacteria caused a pathological alteration of oviductal wall, such as edema in mucous, shortened cilia of epithelium, inflammatory cell infiltrating, dilation and hyperraemia in blood capillary within lamina propria and obstruction of oviductal lumen. These pathological changes were recovered following the treatment of FGST intragastrically administrated.

结果 在使用混合菌接种后,小鼠输卵管管壁结构发生改变,主要包括黏膜层水肿、上皮细胞顶端纤毛变短或消失、固有层炎性细胞浸润、毛细血管充血、管腔狭窄甚至闭塞。;附归参汤;长期给药后明显使上述病理改变向正常组织转归。

TyPe II collagen induced arthritisln the rat ank1e joint andoVathumin as antigen induced arthritis WA in the rabbit knee joint wereestab1ish2 Qualitative evaluation of me in skin, muscle, synovium, cedilagearound joint and blood was performed by OMA3 The CIA rats were treated on day 7 after hind paw swelling and erythemaAnimals were injected intravenously with ase at a dose of 10mg/kg,tWenty minuots 1ater, one ankle of the rats random1y assigned was exPosedlaser irradiation at l00J/cm fOr l000 seconds, and another ankle wasM grouP wihout laser The other two groups is unmanipulatedcontrol group and untreated CIA group Bimaleolar ankle widthmeasuremellts were taken in all animals every tWo days using amicrometer The histopathology of the ank1e Joint was assessed at day 21after disease onset4 The pro1iferating cell nuclear antigen WCNA of CIA treated by PDT andthe HMME group without laser was doterdrined by immunohistochemiStry5 The AfA rabbits were treated on day 7 after knee swelling and erythemaThe theraPy invo1ved lntravenous injection of l0mg/kg HMME, fOl1owedby 20 minues period in dim light, and transdermal light treatment with\l00 J/cm2 fOr l000 seconds The inner sides of the treated Anees wereirradiated at first, and then the outer side did 24 hours later, the synovialtissue of the Anees joint were removed and in situ cel1 aPoptosis wasdetCCted With tednal deoxync1eotidyl transferase-mediated dUTP nickend labelingR6suIt8:l The pathologic changes of CIA and AIA include subsynovial inflammation,opovial hyPerplasia, pannus formation, cartilage and bone destructionresemble RA.2 The studies demonstrated that there are different uptake of HMME withinskin, muscle, synovium, cartilage and b1ood, and the synovium cou1draPidly uPtake more ase than skin and cartilage at the firSt 30 minuesaller intravenous injection of HMME3 The bimaleolar anke width had no different among PDT treated group,H group withollt 1aser and untreated CIA group But hlstologicalevaluation showed statiStical1y significallt reductions in synovialhyperplasia, pannus formation and cart1lage reosion, bone destruction andtotal score in PDT treated group4 Image analysis showed that the ratlo bforeen the areas of the coufltedobect to that of the entire area in PDTtreated grOup is lower than that in conirol group, but the integrated oPticaldensity had no different between the two groups5 Imape analysis showed that the ratio between the area of the countedobject to that of the e

治疗组在大鼠出现踝关节红肿后1周,炎症达到高峰时进行PDT治疗。随机治疗大鼠一侧的踝关节,另。2。一一侧作单纯HMME 对照。治疗方法是大鼠麻醉后尾静脉注入 HMME10ngkg,20分钟后踝关节照光,激光波长627.sum,功率密度 100mwcm',照射时间1000秒,能量密度100)/。治疗后避光喂养72 小时。隔日一次测量大鼠的踝关节左右横径,治疗后两周取关节进行病理d 观察。 4。大鼠CIA模型用上述方法进行PDT治疗后,治疗组和单纯HMME 组用兔疫组化SP法检测石蜡切片的核增殖抗原。 5。兔AIA模型在关节炎出现第七天进行PDT治疗,随机治疗一侧膝关节,另一侧作自身对照。兔耳静脉注入I'arrainrelomg/Kg,20分钟后,膝关节用金蒸气激光照射,激光能量密度100)儿旷。24 /J'时后取膝关节滑膜作病理检查,并用脱氧核昔酸末端转移酶介导的缺口末端标记法原位检测凋亡细胞。结果: 1。模型观察:CIA大鼠炎症高峰期滑膜下炎细胞浸润明显,滑膜细胞明显增殖,炎症达到高峰后二周,血管缀形成,并侵蚀和破坏软骨和骨, CIA模型病理改变与人类RA相似。兔AIA模型膝关节滑膜病理可见滑膜细胞增生,滑膜下炎细胞浸润,也与人类RA滑膜改变相似。 2。关节周围组织中光敏剂含量的测定结果表明,各组织对HMME 的吸收速度和吸收量不同,荧光值一时间曲线不同,滑膜组织比皮肤和软骨对 HMME的吸收多,在 2 0分钟时即有明显差异。 3.PDT对CIA模型的治疗结果表明:PDT治疗后关节炎组、单纯 HMME组和治疗组踝关节左右横径统计学检验差异没有显著性,但病理评分PDT治疗组滑膜增生、血管资形成及软骨破坏、骨破坏和总分比关节炎对照组和HMME对照组好,统计学检验差异有显著性。。3_军医进修学院硕士学位论文中文摘要 4.PDT治疗组PCNA阳性细胞较对照组少,图像分析结果表明面密度(阳性染色的面积总和与统计视野面积的比值)治疗组小于对照组,统计学检验差异有显著性。。 5.PDT治疗组凋亡阳性细胞较对照组明显增多,图像分析结果单位视野内阳性细胞数和面密度PDT治疗组高于对照组,统计学检验差异有显著性。凋亡细胞核直径PDT治疗组较小,与对照组相比,统计学检验差异有显著性。结论:二。CIA、AIA的病理改变类似人类RA,可作为研究RA病因、发病机制、检查及治疗方法的模型。 2。各组织对HMME的吸收速度和吸收量不同,滑膜组织比皮。

These results suggest that the activate spleen-energy method can achieve appetitive purpose by not only affecting the gastrointestinal tract function in periphery, but also regulating the process of ingestion in brain. The basic research about ingestion indicate: one hand, after food enters the gastro-intestinal tract, the endocrine cell of the intestinal tract is activated and secrete many kinds of brains intestines peptide, the level of the brain intestines peptide in blood as the periphery signal spreads to the central nervous system regions that control digest and feeding behavior. On the other hand, it has been shown that dorsal parabranchial neurons, containing CCK-8S, extend fibers to the VMH and are involved in the inhibition of feeding .

关于摄食控制的基础研究表明,一方面食物进入胃肠道后,激活肠道的内分泌细胞,分泌多种脑肠肽如CCK-8S,这些脑肠肽在血中的水平作为外周信号可通过&肠—脑轴&传入中枢神经系统介导消化和摄食行为的部位,影响摄食中枢神经元的活动调节动物的摄食行为;另一方面中枢神经元可合成释放内源性的神经肽直接作用于摄食中枢神经元调节摄食,如中枢鳃旁体神经元的神经纤维就可延伸到达VMH,并且合成释放内源性的CCK-8S。

Objective: To explore the difference of IL-12 produced by human peripherial blood monocyte-derived dentritic cell between in asthmatic subjects and in healthy volunteers,and its influence on Th1/Th2 balance.

目的 :探讨过敏性哮喘病人和正常人外周血单个核细胞来源树突状细胞(dendriticcell ,DC)产生IL 12的差异,及其对Th1/Th2平衡的影响。

The proposed automated analysis was implemented on peripherial blood lymphocyte subsets from 307 samples stained and prepared in an identical way and it was capable of identifying all cell subsets present in each sample studied that could also be detected in the same data files by an expert operator.

计划通过仪器自动分析取自307例样本的外周血淋巴亚群,这些样本的染色和制备都是用一种相同的方法,也可以由专业的操作人员识别每个样本中所有的细胞亚群百分比,以及检测每个样本数据中的文件。

Results In RT-PCR analysis of the peripherial blood, 45%(18 out 40) of CRC patients, 10%(2 out 20) of CRP patients were positive for CEA mRNA, respectively. All 40 healthy individuals were negative for CEA mRNA expression. The detection of CEA mRNA was significantly correlated with TNM stage of CRC patients, while there were no significant relationship between the CEA mRNA expression and the malignant extent of cell differentiation.

结果 40例结肠癌患者外周血中CEA mRNA表达的阳性率为45.0%(18/40),而健康对照组均为阴性,两者比较有显著性差异(P.01);20例结肠息肉患者中CEA mRNA表达阳性率为10%(2/20);CEA mRNA阳性表达率与肿瘤分期相关,而与肿瘤细胞分化程度并不相关。

Objective To explore the possibility of pharmacodynamic monitoring of cyclosporine immuno-suppression by measuring T-cell functions in peripheral whole blood.

目的:以不同的T淋巴细胞功能标志物作为药效动力学指标。探讨环孢素免疫抑制作用监测的可能性。

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Breath, muscle contraction of the buttocks; arch body, as far as possible to hold his head, right leg straight towards the ceiling (peg-leg knee in order to avoid muscle tension).

呼气,收缩臀部肌肉;拱起身体,尽量抬起头来,右腿伸直朝向天花板(膝微屈,以避免肌肉紧张)。

The cost of moving grain food products was unchanged from May, but year over year are up 8%.

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However, to get a true quote, you will need to provide detailed personal and financial information.

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