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icr mouse
    Isolation of ICR Mouse ES Cell from in Vitro Fertilization Blastocyst
    由体外受精囊胚获得ICR小鼠ES细胞
    Isolation and culture of ICR mouse embryonic stem cells and its identification
    ICR小鼠胚胎干细胞的分离、培养及鉴定
    The Effect of Rat Heart Conditioned Medium in Isolation and Cloning of Embryonic Stem Cells from ICR Mouse Embryo
    大鼠心肌条件培养基对ICR小鼠胚胎干细胞分离克隆的影响
    Culture of ICR mouse embryonic fibroblasts and production of feeder layers for embryonic stem cells
    ICR小鼠胚胎成纤维细胞的培养及饲养层的制作
    Comparative Study of Hepatoxicity Induced by Genipposide in SD Rat,Wistar Rat and ICR Mouse
    京尼平苷对SD大鼠,Wistar大鼠与ICR小鼠肝毒性的比较研究
    Studies on Isolation and Cloning of Pluripotent Stem Cells from ICR Mouse Embryos
    ICR小鼠胚胎多能干细胞的分离克隆研究
    And the expression product can alleviate the symptoms of liver trauma of ICR mouse.
    通过对ICR小鼠的急性肝损伤实验,测得蚕蛹表达产物能明显降低肝脏血清酶活性。
    Method ICR mouse is choiced as experimental animal and each group has 12 mice.
    方法 采用ICR小鼠,分10组,每组12只。
    The investigation studyed the effect of Berberine, Baicalin and Astragalus Polysacharin using the two-cell embryos of ICR mouse as explant.
    为探讨小檗碱、黄芩苷、黄芪多糖三种中药成分对小鼠胚胎体外生长发育的效果,本研究以ICR小鼠2-细胞胚胎为试验材料,设计三个试验:小檗碱、黄芩苷、黄芪多糖对小鼠2-细胞胚胎体外培养效果的筛选试验;
    Aim To study the persistence of experimental Escherichia coli O157∶H7 EDL933 strain in ICR mouse Methods ICR mice were inoculated via oral gastric inoculation with 0 1ml~0 9ml of EDL933 strain 7 0×10 8~4 0×10 9CFU/ml;
    方法 ICR小鼠经口感染 ,剂量为 0 1~ 0 9ml(菌悬液浓度为 7 0× 10 8~ 4 0× 10 9CFU/ml) ,并在SPF动物实验室中饲养。 结果 不同实验动物微生物等级的ICR小鼠对EDL933株表现出不同感染类型 ,Ⅰ级小鼠感染未成功 ;
    The ES cell from ICR mouse offer condition for cell differentiation studing.
    ICR小鼠 ES细胞的获得 ,为研究小鼠的 ES细胞分化提供了条件。
    Objective: To establish feeder layer culture system of ICR mouse embryonic fibroblast(MEF) cells for isolation and culturing of embryonic stem(ES) cells.
    目的:建立ICR小鼠胚胎成纤维细胞饲养层培养体系,用于胚胎干细胞建系及研究。
    To investigate the lipid-lowering effect of Lagerstroemia specious seed oil on hyperlipidemia mice. ICR mouse were fed Lagerstroemia specious seed oil(10、20、40 mg/kg)as a test animal and serum triglyceride(TG),cholesterol(TC),high-density lipoprotein(HDLC)and arteriosclerosis indes(AI)were measured.
    为考察大叶紫薇籽油对高脂血症小鼠血清脂质的影响,采用ICR小鼠作为实验动物,口服大叶紫薇籽油(10、20、40 mg/kg),以酶标法测定血清甘油三酯(TG)、总胆固醇(TC)和动脉硬化指数(AI)。
    Methods: ①the ICR mouse was selected as model animal. The mouse model of myocardial infarction was induced by ligating the mouse coronary artery. We mensurated the heart function and blood dynamics to ensure the success of the operation.
    方法:①以ICR小鼠为对象,采用结扎其冠状动脉制备急性心肌梗塞模型,通过对心功能及血流动力学的检测,证明模型制备的成功与否,通过测量梗塞面积,保证手术的稳定性。
    We use ICR mouse as an example to systematically optimize the condition ofmice embryo cryopreservation with solution EG40 ES40 and EFS40 by rapideryopreservative and vitrified method. Other than straw, the cell freezing tubewas firstly adopted. Using EG40 and ES40,The development ratio reached
    本文以EG40、ES40、EFS40为冷冻液,采用快速冷冻法、玻璃化冷冻法,用ICR小鼠对小鼠胚胎冷冻的条件进行了系统的探索,除用冷冻麦管进行冷冻外,首次用细胞冷冻管进行胚胎冷冻。
    Furthermore, it is more easy to isolate embryos and get the ES cells from ICR mouse than Kunming mouse.
    以上结果表明:ICR小鼠比昆明小鼠更易进行ES细胞的建系工作。
    Both ES and EG cells were cultured to determine the factors affecting on isolation, cloning and passage of pluripotent stem cells from ICR mouse embryos.
    本试验对ICR小鼠胚胎多能干细胞的建系工作做了初步探索,为胚胎多能干细胞多种属广泛建系的研究打下一定基础,也为小鼠胚胎多能干细胞的深入研究积累经验并提供借鉴。
    The results attained were as follows: 1.Derivation of Embryonic stem cells from ICR mouse preimplantation embryos.
    1.源于ICR小鼠ICM的ES细胞分离克隆研究
    This provided a necessary condition for the research of the mechanism how IL-1RII regulates IL-1.At meantime, we successfully established ICR mouse endometriosis model with their own endometrial implantation.
    同时,采用自体内膜组织种植方式,我们成功地建立了ICR小鼠Partl南京医科大学硕士学位论文子宫内膜异位症模型。
    Cloning, analyzing the expression of IL-1RII and setting up ICR mouse endometriosis model may provide essential materials for the further studies on cytokines gene transfection of endometriosis cells, especially the study on the mechanism of cytokines network associated with whole cellular and humoral immunity on endometriosis. With these, we might find new target and pathway for biological therapy to endometriosis.
    人IL一IRH基因的克隆和表达以及ICR小鼠子宫内膜异位症模型的建立,为我们深入了解IL一1在子宫内膜异位症病理生理中,尤其是在整个与细胞及体液免疫相关的各种细胞因子网络中的作用机制,发现内异症新的生物治疗靶点莫定了基础。
 

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