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   human fetal 的翻译结果: 查询用时:0.264秒
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human fetal     
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  人胎
     IL-6、IL-1β and TNFα induce the expression of c-fos and c -jun in human fetal cere-bral neurons
     IL-6、IL-1β、TNFα对人胎大脑神经细胞c-fos、c-jun的表达调控
短句来源
     Effect of IL-6、IL-1β、TNFα on the Growth of Human Fetal Cerebral Neurons in vitro
     IL-6、IL-1β、TNFα对人胎大脑神经细胞体外生长的影响
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     Effect of Mifepristone on the Ultrastructure of Human Fetal Umbilical Vein and ER、PR、ET-1 and eNOS
     米非司酮对人胎脐静脉超微结构及ER、PR、ET-1和eNOS的影响
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     Effect of 3,5,3′-Triiodothyronine on Tubulin Development of Human Fetal Cerebral Neuron in Vitro
     3,5,3′-三碘甲腺原氨酸对人胎大脑神经细胞培养物微管蛋白发育的影响
短句来源
     DIFFERENTIATION OF HUMAN FETAL LIVER CD34~+ CELLS INTO NEURONAL CELLS INDUCED BY β-ME AND BHA IN VITRO
     β-ME和BHA体外诱导人胎肝CD34~+细胞向神经组织细胞分化研究
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  人胎儿
     Methods Human fetal MMSCs were isolated and cultured with in vitro cell culture technique; MMSCs were induced on 1% Matrigel as matrix,2.5μmol/ml AZA pretreatment for 10-12h,HGF 10ng/ml+FGF4 10ng/ml+HGM medium in vitro;
     方法采用体外细胞培养技术,分离培养人胎儿MMSCs,在1%Matrigel做基质,2.5μmol/ml AZA预处理10~12h,HGF 10ng/ml+FGF4 10ng/ml+HGM培养基中诱导。
短句来源
     Results:The concentrations (pg/100mg wet tissue) of AVP( n =12) and OT( n =13) in extracts of human fetal thymus were ( x±s )47.64±45.14 and 83.35±55.89,respectively.
     结果:人胎儿胸腺组织提取液中AVP(12例)和OT(13例)的含量(pg/100mg湿重组织)(x±s)分别为47.64±45.14和83.35±55.89。
短句来源
     Methods:SP immunocytochemical technique was used to observe the expression of TGF-β1, PCNA in Leydig cells, Sertoli cells and spermatogenic cells of human fetal testis from 12th to 28th week.
     方法:采用SP免疫细胞化学技术检测12~28周人胎儿睾丸间质细胞、支持细胞、生精细胞TGF-β1、PCNA的表达情况。
短句来源
     Effects of As_2O_3, MNNG and B(a)P on Epithelia of Human Fetal Tracheae and Rat Tracheae in Organ Culture
     As_2O_3、MNNG和B(a)P对人胎儿及大鼠气管上皮的致癌前病变作用
短句来源
     EXPRESSION OF TGF-β1 AND PCNA DURING THE DEVELOPMENT OF HUMAN FETAL TESTIS
     人胎儿睾丸发生过程中TGF-β1与PCNA的表达
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  人胚
     CD_2,CD_3 ,CD_4 and CD_8 McAbs Regulates Cytotoxic Activity of Human Fetal Thymocyte Induced by rHuIL-2
     CD_2、CD_3、CD_4和CD_8四种McAb对rHuIL-2诱导人胚胸腺细胞杀伤功能的调节作用
短句来源
     Expression of IL-1,1L-1ra,and IL-6 in Human Fetal Schwann Cells
     人IL-1、IL-1ra及IL-6在人胚雪旺细胞中的表达
短句来源
     Each mouse in group B and C were injected Human fetal fibroblast(HF) and Dulbecco modified Eagle medium(DMEM) 0.5 ml respectively.
     B组为HF对照组,C组为DMEM对照组,分别腹腔注射人胚成纤维细胞(Human fetal fibroblast,HF)细胞悬液、改良Eagle培养液(Dulbecco modified Eagle medium,DMEM)各0.5ml/只。
短句来源
     The regulatory effect of CD_2,CD_3,CD_4 and CD_8 McAbs on human fetal thymocyte cytotoxic activity induced by rHuIL-2 was investigated.
     本文观察了人胚胸腺细胞(16~40周龄)对CD_2、CD_3、CD_4和CD_8四种McAb诱导的增殖反应及这四种McAb对rHuIL-2诱导的人胚胸腺细胞杀伤功能的影响。
短句来源
     Expression of phospholipase-γ1in human fetal tissues
     磷脂酶C-γ1在人胚组织中的表达
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  人胚胎
     BACKGROUND & AIM: To study the mutation of ras genes induced by 3-chloro-4-(dichloromethyl)-5-hydroxy-25H -furanone (MX) in human fetal hepatocytes (L-02) in vitro.
     背景与目的:研究饮水氯化消毒副产物3-氯-4-二氯甲基-5-羟基-2(5氢)-呋喃酮(3-chloro-4-(dichloromethyl)-5-hydroxy-2[5H]-furanone,MX)对体外培养的人胚胎肝细胞(L-02细胞)ras基因突变的诱导。
短句来源
     RESULTS:After the induction of β ME+RA,CD34+cells from human fetal liver were neuronal phenotype,and expressed neuron specific protein.
     结果:培养的人胚胎肝CD34+细胞经β-ME+RA诱导后,细胞表现神经元样细胞形态,表达神经细胞特异蛋白。
短句来源
     Molecular Cloning of cDNA of Dopamine D_2 Receptor from Human Fetal Brain
     人胚胎脑多巴胺D_2受体基因的克隆
短句来源
     Human fetal CD34~+cells differentiating into nerve cells in vitro
     人胚胎CD34~+细胞体外向神经细胞分化的实验研究
短句来源
     To study the effects of nerve growth factor (NGF) on proliferation and DNA synthesis and apoptosis of cultured human fetal retinal pigment epithelium (RPE) cells, the cultured RPE cells were treated with NGF of different concentrations for 48h.
     用培养的人胚胎视网膜色素上皮(Retinal pigment epithelium,RPE)细胞研究神经生长因子(Nerve growth factor,NGF)对其增殖、DNA合成及凋亡的影响。
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  human fetal
The human novel gene of ZNF322 is cloned from human fetal cDNA library using the primers on the basis of the ZNF322 sequence analyzed with computer.
      
Pluripotent stem cells exhibiting similar characteristics can be isolated from human fetal bone marrow, heart, liver, muscle, lu
      
In this study, we further isolated pluripotent stem cells from human fetal heart, liver, muscle, lung, derma, kidney, and fat and then analyzed the characteristics and function of these stem cells.
      
Little is known about the expression characteristics of the various kinds of possible markers in hepatic stem cells (HSCs) and other HSC-related cells in human fetal liver in various developmental stages.
      
Identification of the OCT4-pg1 retrogene and NANOG gene expression in the human fetal eye
      
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A simple and reliable procedure for the isolation of pure DNA from human fetal liver is described.A high pure and natural DNA with an average molecular weight of 4 ×106 can be easily obtained after the sample is treated with SDS and trypsin and fractionated by a sepharose 4B column.The product meets the requirement for general research work of molecular biology.

本文报道一种从人胎肝抽提纯化DNA简易可靠的方法。样品经去垢剂(SDS)及蛋白酶处理后,通过珠状琼脂糖凝胶层析柱,得到天然状、大分子和高纯度的DNA。分子量约为4×10~6,符合一般分子生物学研究要求。

This paper is undertaken to establish a rapid radioimmunoassay method, namely an improved quantitative radio-countercurrent-immunoelectrophoresis. Substances with various moleoular weights and charges were chosen: insulin, human serum albumin, human fetal alpha-fetoprotein and the surface antigen of hepatitis B virus. Trial-assays of the above antigens were carried out repeatedly by the improved method. The whole procedure can be completed within 3~5 hrs for Ins, HSA and AFP and 6~7 hrs for HBsAg respectively....

This paper is undertaken to establish a rapid radioimmunoassay method, namely an improved quantitative radio-countercurrent-immunoelectrophoresis. Substances with various moleoular weights and charges were chosen: insulin, human serum albumin, human fetal alpha-fetoprotein and the surface antigen of hepatitis B virus. Trial-assays of the above antigens were carried out repeatedly by the improved method. The whole procedure can be completed within 3~5 hrs for Ins, HSA and AFP and 6~7 hrs for HBsAg respectively. It has been shown that the improved method possesses the advantages of high sensitivity and accuracy, extreme simplioity and rapidity, as well as satisfactory reproducibility. Therefore it is expected to be widely used in the trace amount estimations of various antigens migrating from the cathode towards the anode including small molecules, macremolecules, as well as virus particles.

改进后的放射对流免疫定量电泳不仅具有简易、快速和灵敏度高等优点,而且重复性好。本文选用胰岛素、人血清白蛋白、人胎儿AFP和HBsAg四种抗原-抗体系统对这一技术进行了考验,均获得了满意的结果。对HBsAg的定量测定只需6~7小时,另三种抗原需时更短,约3~5小时。因此认为这一技术有可能发展成为适合临床、科研需要的快速、精确的超微量定量手段。

This paper is undertaken to establish a rapid radioimmunoassay method,namelyan improved quantitative radio-countercurrent-immunceleotrophoresis.Substanceswith various molecular weights and charges were chosen:insulin,human serumalbumin,human fetal alpha-fetoprotein and the surface antigen of hepatitis B virus.Trial-assays of the above antigens were carried out repeatedly by the improvedmethod.The whole procedure can be completed within 3~5 hrs for Ins,HSA andAFP and 6~7 hrs for HBsAg respectively.It has...

This paper is undertaken to establish a rapid radioimmunoassay method,namelyan improved quantitative radio-countercurrent-immunceleotrophoresis.Substanceswith various molecular weights and charges were chosen:insulin,human serumalbumin,human fetal alpha-fetoprotein and the surface antigen of hepatitis B virus.Trial-assays of the above antigens were carried out repeatedly by the improvedmethod.The whole procedure can be completed within 3~5 hrs for Ins,HSA andAFP and 6~7 hrs for HBsAg respectively.It has been shown that the improvedmethod possesses the advantages of high sensitivity and accuracy,extreme simplicityand rapidity,as well as satisfactory reproducibility.Therefore it is expected to bewidely used in the trace amount estimations of various antigens migrating from thecathode towards the anode including small molecules,macromolecules,as well asvirus particles.

改进后的放射对流免疫定量电泳不仅具有简易、快速和灵敏度高等优点,而且重复性好。本文选用胰岛素、人血清白蛋白、人胎儿AFP 和HBsAg 四种抗原-抗体系统对这一技术进行了考验,均获得了满意的结果。对HBsAg 的定量测定只需6~7小时,另三种抗原需时更短,约3~5小时。因此认为这一技术有可能发展成为适合临床、科研需要的快速、精确的超微量定量手段。

 
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