在等渗或高渗负荷下，椎间盘的器官培养模型可以保持器官完整性和细胞活力至少4周。
Organ culture model of intervertebral discs could preserve organ integrity and cell viability at least 4 weeks under iso-osmotic or hyperosmotic loading.
目的是通过器官培养的方法建立大鼠器官型脊髓片培养模型。
The objective is to establish a model of spinal cord organotypic culture in vitroof Sprague Dawlay rat.
目的：建立人牙切片体外器官培养模型。
PURPOSE: To establish human tooth slice organ culture model in vitro.
目的建立人牙胚发育的体外器官培养模型。
Objective to establish an organ culture model of the developing of human tooth germs in vitro.
方法：器官培养、组织学观察和透射电镜观察。
METHODS: Organ culture, light microscopy and electronic microscopy.
本文报告正常状态下金黄地鼠的体外器官培养变化。
This article deals with the organ culture on hamster trachea under the normal condition.
此方法借助于验证精原干细胞迁移的器官培养体系。
The method depends on an organ culture system onto which SSCs are transplanted.
目的：观察器官培养的新生小鼠胸腺内细胞的生长状况。
Objective:TO observe the growth of the cells in thymuses from newborn mice in condition of organ culture.
对不同生长调节物质对河套蜜瓜器官培养的影响进行了研究。
Effects of different growth regulator on organ culture of Cucumis melo var.
目的：通过器官培养的方法建立大鼠器官型脊髓片培养模型。
Objective: To establish a model of spinal cord organotypic culture in vitroof Sprague Dawlay (SD) rat.
通过器官培养体系，作者观察到中脊上皮细胞向鼻侧而不是口腔侧迁移。
Using this organ culture system, we observed the migration of medial edge epithelial cells to the nasal side, but not to the oral side.
目的：建立人牙切片体外器官培养模型，并采用该模型研究尼莫地平对牙本质形成的影响。
PURPOSE: to establish human tooth slice organ culture model in vitro, and to study the effects of nimodipine on dentinogenesis through this model.
红麻的器官培养和原生质体培养是品种快繁、变异体筛选以及体细胞杂交和遗传转化等生物技术育种的基础。
It's organ culture and protoplast culture is important basic technique of rapid clonal propagation, selection of imitative plants, somatic hybridization and genetic transformation.
目的：建立一种可用于体外研究椎间盘退变的椎间盘器官培养模型，探讨渗透压负荷对模型椎间盘细胞活力和代谢的影响。
Conclusion:Organ culture model of intervertebral discs could preserve organ integrity and cell viability at least 4 weeks under iso-osmotic or hyperosmotic loading.
探索并设计一种新型角膜灌流培养系统，进而优化传统器官培养保存中角膜的生存环境，并预测其在角膜保存中应用的可行性。
To find a new type of corneal perfusion culture system, thus improve the survivable environment of keeping cornea in the traditional organ culture and predict the feasibility in cornea preservation.
有的科研人员希望能够利用胚胎干细胞来培养组织和器官。
Some researchers hope to use embryonic stem cell research to grow tissue and organs.
利用干细胞(产生人体几乎全部的组织与器官的细胞)在实验室内培养出检测声音细胞这一类的细胞将戏剧性地改变上述段落所述定论。
Using stem cells — master cells that produce all the body's tissues and organs — to generate these cell types in the laboratory could change that dramatically.
我们真的能够通过细胞培养技术培养出器官吗？
胚胎干细胞是机体的终极管理细胞，培养所有的组织和器官。
Embryonic stem cells are the ultimate master cell of the body, giving rise to all of the tissues and organs.
如果工程师发现了用干细胞培养器官的方法。
目的：探讨长骨器官体外培养的最佳条件。
Objective: To investigate the optimum of organ culture of long bone in vitro.
方法：体外培养胚胎小白鼠小肠器官型植块，并将所有植块分为两组：实验组和对照组。
Method: Cultured the organ-type explants of mouse intestinal tissue in vitro, all the explants were divided into two groups: test group and control group.
采用乳牛外周血液淋巴细胞作短期培养，以空气干燥法制备染色体。对临床诊断为输卵管阻塞牛1例和生殖器官畸形牛5例进行细胞遗传学分析。
Comparetive chromosome studies wore carried out by means of short culture of lymphocytes from peripheral blood of 1 cow with simple salpingo obstruction and 5 cows with reproduction system problems.
爱丁堡大学的研究者通过培养干细胞获得具有肾脏结构的器官。干细胞是用于构建机体的早期细胞。
Researchers at the University of Edinburgh created the organs by manipulating stem cells – early cells which are the building blocks of the body – to form the structure of a kidney.
本文以无刺大果沙棘—太阳品种的幼嫩器官为组织培养的繁殖材料，研究了无刺大果沙棘的组织培养技术。
Using the organ of nonthorny big fruit seabuckthom as the experimental material, this paper studied the technology of the tissue culture of nonthorny big fruit seabuckthom.
感染器官的培养、染色、光纤内视镜以及电子显微镜大幅扩展病理学家所能获得的信息。
Culturing of infectious organisms, staining, fibre-optic endoscopy, and electron microscopy have greatly expanded the information available to the pathologist.
因此在桑离体培养中，可以通过添加硝酸银来控制离体器官发生，进而建立高效再生体系。
So, organogenesis in vitro of mulberry will be controlled in the course of culture by adding AgNO 3, and a highly effective regeneration system will be formed.
因此在桑离体培养中，可以通过添加硝酸银来控制离体器官发生，进而建立高效再生体系。
So, organogenesis in vitro of mulberry will be controlled in the course of culture by adding AgNO 3, and a highly effective regeneration system will be formed.
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