in vitro model造句

• A three - dimension in vitro model for angiogenesis of hemangioma
  一种三维血管瘤血管生成体外培养模型的建立
• Objective to investigate the influence of cardiac motion on the measurement of doppler blood flow velocity through an in vitro model
  目的通过体外模拟实验，研究心脏运动对频谱多普勒血流速度测定的影响。
• This new co - culture method might be a promising in vitro model for studies of interactions between endothelial and smooth muscle cells
  此种ec和smc共培养模型模拟了在体时ec和smc之间的结构关系，可以用来研究两种细胞间的相互影响。
• In vitro model system , they found that stable - transfected cell lines which are over - express wnt - 1 or n - cadherin gene could differentiate into neuron - like cells without ra induction
  目前从事的主要研究工作有：小鼠巢蛋白基因表达调控的分子机制；胚胎性癌细胞
• To study the mechanisms of ischemic brain injury the excitotoxicity more thoroughly , and the therapeutic approach of ischemic brain injury , we in this research established the rational in vitro models of brain slice and primary neuronal cultures , searched new nmda receptor antagonists , and analyzed the characteristics of signal transduction triggered by nmda
  为了更加深入地研究脑缺血损伤机制，探讨脑缺血损伤中起主要作用的兴奋性氨基酸毒性一机制及其治疗药物，本研究进一步建立了脑片和神经元水平的体外脑缺血模型；探讨了新类型n ’ md损伤对抗药物；还对nmd的信号转导特点作了分析。
• In the present study , the grass carp ( ctenopharyngodon idellus ) cell line zc - 7901 and the colossoma brachypomum cell line cbs were used as in vitro model systems to study the effects of cold stress on the cell membrane fluidity , the level of cacium ion , the contents of malondialdehyde ( mda ) , the level of c > 2 and the system of antioxidative enzymes in the fish cells
  本文以培养的草鱼( ctenopharyngodonidellus )吻端细胞系zc - 7901和淡水白鲳( colossomabrachypomum )吻端细胞系cbs为模型，研究低温胁迫对其细胞膜流动性、钙离子水平、 atp酶、丙二醛( mda )含量、超氧化物阴离子( o2 - ' )水平以及抗氧化酶系统的影响，以期探讨它们与细胞耐寒性的关系。
• In this report , we mainly covered the following aspects of " tissue organ regeneration and replication in situ " : 1 ) procedures of tissue organd regeneration and replication and replication in clnical practice ; 2 ) the discover and existence of potentiald regenerative cell ( prc ) ; 3 ) the proliferation , differentiation and regeneration law of potential law of potential regenerative cells ; 4 ) study procedure on tissue organ regeneration and replication from prcs in vitro based on the model of full skin organ regeneration in situ after extensive in vitro , set up the method and technology of searching life regenerative substance required in tissue organ regeneration and replication in situ . in this study , first , the whole human body is divided into 206 function units , which are the " tissue organ " in regeneration study . then the histology foundation of tissue organ regeneration and replication in situ is set up . in ordre to prove the existence of the potential regenerative cells and their potential baility and function , we established clinical tracking rechnique of skin organ regeneration in situ ; meanwhile , several tissue organ regeneration and replication in vitro models which represent different kinds of runctions were sucessfully set up , with all these techniques and models , we confirmed : 1 ) the existence , function and ability of pptemtoa regenerative cells ; 2 ) the importance of life regenerative substance ; 3 ) the feasibility of tissue organ regeneration and replication in situ ; 4 ) the big value of tissue organ regeneration and replication in situ in life science and medicine progerss . we also showed the possible foreground of capture cancer with this method and technologh . in this report , nearly 200 photographs of several tissue organ regeneration and replication in situ or in vitro demonstrated the whole process of tissue organ and big organ entities regeneration and replication from cells . the results of tissue organ regeneration and replication in situ mainly include : 1 ) whole skin organ regeneration and replication in situ ; 2 ) gastrointestinal mucosa tissue organ regeneration in vitro ; 3 ) hair follicle tissue organ regeneration in situ or in vitro ; 4 ) never tissue organ regeneration in situ ; 5 ) pancreas tissue organ regeneration and replication in vitro ; 5 ) marrow tissue regeneration in vitro ; 6 ) renal glomerulus and tubule tissue organ tugeneraation in vitro ; 7 ) heart muscle regeneration in vitro , etcl . in order to let more and more people know and understand this technology of tissue organd regeneration and replication in situ , herein , for the first time , we publicize the key points of actualizing this technology . also , we publicized the technology procedures and the frame constitute of life substances . we bilieve this is a big contribution to human science
  本研究报告,重点报道了组织器官的原位再生复制的临床程序,报道了组织潜能再生细胞的发现和存在,以及该细胞的增殖分化和形成组织器官的变化规律.以烧伤后皮肤组织器官的原位再生复制为模型,研究出了体外组织潜能再生细胞复制组织器官的培养方法;以体外组织器官的复制为模型,建立了寻找原位组织器官再生复制所需生命物质的方法和技术.本研究,首先按人体的器官功能,分解为206个功能单位,确立了所复制的人体器官中的组织功能单位为组织器官,从而建立了原位组织器官再生复制的组织学基础.为了验证组织潜能再生细胞的再生潜能,建立了皮肤器官原位再生的实体临床跟踪技术,同时又建立了能代表有关器官功能类别的代表组织器官的原位和体外复制模型,以多组织器官的成功复制确定潜能再生细胞的作用,确定生命研究再生物质的重要性,确定组织器官原位再生复制的可行性,确定了组织器官原位再生复制的生命科学研究和医学进步的重大应用价值,同时展示了用此方法和技术攻克癌症的前景.本研究报告,以近二百幅多个组织器官原位和体外再生复制的实体图片,展示了潜能再生细胞复制的组织器官和大器官司实体;展示了细胞再生复制器官的全过程.真实的报告了组织器官原位再生复制的成果.所公布的主要成果为:皮肤器官的原位再生复制;胃肠黏膜组织器官的原位和体外再生复制;毛囊组织器官的原位和体外再生复制;神经组织器官的原位复制;胰腺组织器官的体外复制;骨髓组织的体外复制;肾小球小管组织器官的体外复制;心肌的体外复制等.为了让更多的人学会和掌握组织器官原位再生复制技术,本报告首次公布实施技术的重要环节和技术流程;首次公布了生命再生物质的框架和组成.作者自费研究成果对人类生命科学的一大贡献
• The originalities of this paper are : 1 , development of a a flow cytometry - based assay for quantitative analysis of cellular proliferation and cytotoxicity in vitro ; 2 , the soluble secretion of k . 562 cell lines reduce the number of pbmc , but promote the activity of pbmc in dose - dependent manner ; 3 , soluble secretion of k562 cell lines can induce the no production by pbmc , but no only plays a part of the role of soluble secretion of k562 cell lines ; 4 , establishing a in vitro model and giving some parameters for sreening and appraising anti - tumor medicine
  本研究的创新点在于： l 、建立了用流式细胞术定量测定细胞增殖和细胞毒性的直接检测技术； 2发现k562可溶性分泌物剂量依赖性地使pbmc细胞数量减少但活性增加； 3 、 k562可溶性分泌物能诱导pbmc产生no ，但是no的作用并不等同于肿瘤上清的全部作用。 4 、为抗肿瘤药物筛选提供了一个体外模型，并明确了一些筛选指标。