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观察的人

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Method] Puncture into Attain long sheath of CS through left infraclavicular vein,guided by CS pipe,take sheath into CS,make reverse contrast of heart vein with Attain saccule contrast pipe,put the left ventricle electric pole into the vein through sheath,then bring it into right ventricle apex and right cardiac ear through the electric pole of right ventricle and atrium,connect it with 3-cavity pulse generator,which is buried under left chest skin.

双心室起搏治疗心力衰竭的临床观察"版权属于原作者所有!请勿将"双心室起搏治疗心力衰竭的临床观察用于商业用途![目的]观察双心室起搏治疗心力衰竭临床疗效。[方法]经左锁骨下静脉穿刺送入Attain冠状静脉窦长鞘,在CS导管的导引下,将鞘送人CS,用Attain球囊造影导管进行心脏静脉逆行造影,将左心室电极经长鞘放入选择的静脉,送人右心室及右心房电极至右室心尖和右心耳。

Get high purity DCs by Cultured plastic-adherent monocytes isolated from healthy human peripheral blood with GM-CSF and IL-4 for 7 days. To observe the morphology of DCs by inverted phase contrast microscope ,electron microscope and laser confocal microscope. Analyse phenotype of DCs with flow cytometry. Investigate the endocytosis ability of DCs as a group by Horseradish peroxidase endocytosis assay. To appraise allogeneic mixed lymphocytes reaction of DCs by MTT reduction assay. Analyse the levels of IL-12 and TNF in liquids of cultured medium by ELISA and MTT reduction assay respectively. Soluble antigens of HCCs was obtained by 3 freeze-and-thaw cycles. Biological characteristics of HC soluble antigens pulsed DCs were monitored by flow cytometry. According to MTT reduction assay estimated the cell proliferation of self lymphocytes activated by HC antigens pulsed DCs. Get high purity BCG HSP 70 protein by SDS-PAGE electrophoresis and determined its biological activity with ELISA. Analyse phenotype of antigen pulsed DCs primed by BCG HSP70 with flow cytometry. By MTT reduction assay estimated the cell proliferation of self lymphocytes and the MLR of DC based vaccine. Analyse expression of HLA-DR molecule on surface of HCC lines. The IFN-γ mRNA in lymphocytes after actived by DC vaccine and the Fas-L expression on DC and DC vaccine primed lymphocytes were detected by in situ hybridization and flow cytometry respectively. Specific cytotoxity lysis of T lymphocytes and nonspecific inhibition of liquids in culture medium against HCC lines were also tested. Detect expression of hAFP on four HCC lines with Cell-ELISA. Induce apoptosis of HCCs with actinomycin-D. Interaction of DCs and apoptotic cells was observed under transmission electron microscope. Growth inhibition test of DC against HCC lines was also performed. Establish the nude mouse model bearing human HC xenografts and indentify the characteristic of tumour by histochemistry and immunohistochemistry techniques. Prevent and treat transplanted human HC on nude mouse with Freezing and anabiotic HC specific lymphocytes.

用GM-CSF和IL-4从健康人外周血诱导DC;分别用倒置相差显微镜、电子显微镜及激光共聚焦显微镜观察DC形态;流式细胞术检测DC表型;HRP吞噬实验测定DC的群体内吞能力;MTT法检测同种异体混合淋巴细胞反应;ELISA法和MTT法分别测定DC培养上清液中IL-12和TNF水平;冻融法制备肝癌细胞可溶性抗原;流式细胞术检测负载肝癌可溶性抗原后DC的生物学特性;MTT法检测DC负载肝癌抗原后对自身淋巴细胞增殖的影响;SDS-PAGE制备电泳纯化BCG HSP70并鉴定纯度,ELISA测定活性;流式细胞术检测负载抗原DC经BCGHSP 70活化后的表型;MTT法检测肝癌DC疫苗对自身淋巴细胞增殖的影响和混合淋巴细胞反应;流式细胞术检测肝癌细胞表面HLA-DR表达;MTT法检测肝癌DC疫苗对自身淋巴细胞的活化;原位杂交法检测肝癌DC疫苗活化后的淋巴细胞IFN-γmRNA表达;流式细胞术检测DC和肝癌DC疫苗活化后淋巴细胞表面Fas-L;MTT法分别检测肝癌DC疫苗活化的淋巴细胞和其培养上清对肝癌细胞的特异性杀伤和非特异性抑制作用;Cell-ELISA检测人肝癌细胞hAFP表达;MTT法检测负载AFP表位肽和凋亡肝癌细胞DC对自身淋巴细胞增殖的影响;ELISA法和MTT法分别测定活化后淋巴细胞培养上清中TNF和IL-12水平;肝癌细胞凋亡的诱导和检测;DC吞噬凋亡肝癌细胞后的电子显微镜观察;DC对肝癌细胞的生长抑制试验;人肝癌裸鼠皮下移植瘤动物模型的建立及其组织学和免疫组织化学鉴定;DC及肝癌特异性淋巴细胞预防和治疗人肝癌裸鼠皮下移植瘤;冻存和复苏后的肝癌特异性淋巴细胞预防和治疗人肝癌裸鼠皮下移植瘤。

The case coming from: In January, 2005~2006 year in December post-natal making a house-call 214 at the beginning of parturient woman, discovered nipple chapping is 92 people, stochastically divides into it the observation group 46 people; Comparison group 46 people, two groups of ages between 25~36 year old, state of health not obvious difference.

案例来自:2005年1月~2006年12月产后访视的214位初产妇,发现乳头皲裂者为92人,将其随机分为观察组46人;对照组46人,两组年龄均在25~36岁之间,健康状况无明显差异。观察组每次哺乳前用清水擦洗,哺乳后用棉签蘸蛋黄油涂擦乳头,如此反复,坚持1~2月,对照组每次哺乳前

The case coming from: In January, 2005~2006 year in December post-natal making a house-call 214 at the beginning of parturient woman, discovered nipple chapping is 92 people, stochastically divides into it the observation group 46 people; Comparison group 46 people, two groups of ages between 25~36 year old, state of health not obvious difference.

内容摘要:案例来自:2005年1月~2006年12月产后访视的214位初产妇,发现乳头皲裂者为92人,将其随机分为观察组46人;对照组46人,两组年龄均在25~36岁之间,健康状况无明显差异。观察组每次本站声明:本文章收录自互联网,文章版权归原作者所有!

The case coming from: In January, 2005~2006 year in December post-natal making a house-call 214 at the beginning of parturient woman, discovered nipple chapping is 92 people, stochastically divides into it the observation group 46 people; Comparison group 46 people, two groups of ages between 25~36 year old, state of health not obvious difference.

案例来自:2005年1月~2006年12月产后访视的214位初产妇,发现乳头皲裂者为92人,将其随机分为观察组46人;对照组46人,两组年龄均在25~36岁之间,健康状况无明显差异。观察组每次哺乳前用清水擦洗,哺乳后用棉签蘸蛋黄油涂擦乳头,如此反复,坚持1~2月,对照组每次哺乳前后用常规方法,清水擦洗乳头。

Following studies had been performed:(1)repetitive WLT and real-time ultrasonography had been performed to 18 HS and 40 FD toassess the reproducibility and influencing factors.(2) correlations of WLT with symptomscore and electrogastrography had been analysed.(3) differences ofWLT between HS and FD had been compared.(4) methophenolane andimmunohistochemistry stain of gastric fundus mucosa biopsy from 40 FD patients hadbeen performed to analyse the correlations of symptom score and WLT with count andactivity of mast cells, 5-HT level, and H.Pylori infectious status.(5) the effect of oralsumatriptan to proximal stomach function in 10 HS and 10 FD had been assessed, so as toestablish the possible regulating mechanism of fundic relaxation, explore the therapeuticpotential and feasibility of sumatriptan on FD.Results:I. Evaluation of WLT and its application in FD management.

我们主要进行以下几个方面的研究:(1)对18名健康人及40名FD患者重复进行水负荷试验并结合B超声对近端胃的实时监测,评价水负荷试验结果的可靠性并分析其影响因素;(2)观察水负荷试验结果与症状积分及体表胃电结果的相关性;(3)比较FD患者和健康成人水负荷试验结果的差别;(4)对40名FD患者胃底粘膜活检组织进行免疫组化染色和甲苯胺蓝染色,观察FD患者的症状及水负荷试验结果与胃底粘膜肥大细胞、5-HT表达情况及H.pylori感染情况的相关性:(5)观察口服舒马曲坦对10名健康人及10名FD患者近端胃功能的影响,并由此推测胃底舒张运动调节的生理机制,探讨口服舒马曲坦治疗FD的可行性。

Methods After ZTO injection acted on human ovarian cancer SKOV3 cells, the changes in the nucleus were observed by fluorescence microscope, oncosis index was counted by projection electron microscope, the situation of cell DNA breakage was observed by agarose gel electrophoresis, and cell Bcl-2 gene expression was observed by immunohistochemical method.

以不同浓度莪术油注射液作用人卵巢癌SKOV3细胞后,通过荧光显微镜观察细胞核变化、透射电镜计算细胞胀亡指数、琼脂糖凝胶电泳观察细胞DNA断裂情况、免疫组化观察细胞Bcl-2基因的表达。

Methods We established the model of human hair follicle in vitro in Williams E serum-free medium. We can continuously observe morphologic change of hair follicle under an invert microscope. The length of hair follicle was measured by eyepiece micrometer and DNA synthesis rate of human hair follicle in vitro by measuring the rates of incorporation of 3H-TdR.Histology form was observed by Cryo-section and transmission electron microscope.

在Williams E无血清培养基中,建立离体人头皮毛囊培养模型;通过倒置显微镜观察毛囊的形态变化;目镜测微器测量毛囊长度;3H-TdR 掺入检测毛囊DNA合成率;组织学检测用冰冻切片光镜观察和电镜切片透射电镜观察。

Methods: The CD34+ cells and AC133+ cells were gathered by MiniMACS, then the cell factors were divided into 6 groups. Through the ex vivo comparison cultivation under different cell factor combination stimulation, expansion of the CD34+ and AC133+ selection cells was observed and the clone formation of the CD34+ and AC133+ cells was also observed by using Half-solid Methyl cellulose under different cell factor stimulation (in7d, 14d, 21d.). The rate of cell apoptosis was determined.

常规富集人骨髓CD34+及AC133+细胞,应用本研究组设计并已经证实的细胞因子组合方式,对人骨髓CD34+及AC133+富集细胞进行体外对照培养,分别观察CD34+和AC133+富集细胞的扩增情况;应用甲基纤维素半固体培养法,观察不同组别培养7、14、21d CD34+和AC133+富集细胞的集落形成情况及细胞凋亡率。

Methods CD34(superscript +) cells and AC133(superscript +) cells were gathered by MiniMACS, then the cell factors were divided into 6 groups. Through the ex vivo comparison cultivation under different cell factor combination stimulation, expansion of the CD34(superscript +) and AC133(superscript +) selection cells was observed and the clone formation of the CD34(superscript +) and AC133(superscript +) cells was also observed by using Half-solid Methyl cellulose under different cell factor stimulation (during 7d, 14d, 21d.). The rate of cell apoptosis was determined.

常规富集人骨髓CD34及AC133细胞,应用本研究组设计并已经证实的细胞因子组合方式,对人骨髓CD34及AC133富集细胞进行体外对照培养,分别观察CD34和AC133富集细胞的扩增情况;应用甲基纤维素半固体培养法,观察不同组别培养7、14、21d CD34和AC133富集细胞的集落形成情况及细胞凋亡率。

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