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移植型和基因工程型乳腺癌动物模型研究进展 被引量:3
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作者 程宇凌 敖竹君 陈伟 《遵义医学院学报》 2016年第3期319-325,共7页
乳腺癌是导致女性死亡的重要原因,其死亡率占女性恶性肿瘤死亡率的第2位,仅次于肺癌。因此寻求新的、有效的治疗方法以防止肿瘤细胞的增殖及转移,并阐明其潜在的分之机制,有助于降低癌症患者的死亡率。乳腺癌小鼠模型是乳腺肿瘤学研究... 乳腺癌是导致女性死亡的重要原因,其死亡率占女性恶性肿瘤死亡率的第2位,仅次于肺癌。因此寻求新的、有效的治疗方法以防止肿瘤细胞的增殖及转移,并阐明其潜在的分之机制,有助于降低癌症患者的死亡率。乳腺癌小鼠模型是乳腺肿瘤学研究的基础。乳腺癌动物模型对研究乳腺癌的发生、发展及治疗等方面具有重要作用。本文将介绍关于移植型和基因工程型小鼠乳腺癌模型在人类乳腺癌的应用,并着重讨论该两种动物模型系统的局限性和新的攻克方法。 展开更多
关键词 乳腺癌 动物模型 移植型 基因工程型
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Chloroplast Genetic Engineering in Higher Plants 被引量:1
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作者 张景昱 张嫄 宋艳茹 《Acta Botanica Sinica》 CSCD 2003年第5期509-516,共8页
Chloroplast genetic engineering, with several advantages over nuclear genetic engineering, is now regarded as an attractive new technology in basic and applied research, including deepening our understanding of plasti... Chloroplast genetic engineering, with several advantages over nuclear genetic engineering, is now regarded as an attractive new technology in basic and applied research, including deepening our understanding of plastid genome, engineering plant metabolic system, generating transplastomic plants with higher resistance to insect, disease, drought and herbicide and bioproducing of antibodies and vaccines. In this review, the principle and operating system for chloroplast genetic engineering and its application in higher plants have been discussed. 展开更多
关键词 chloroplast genetic engineering transplastomic plants plastid genome
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HIGH DENSITY CULTIVATION OF GENETICALLY-ENGINEERED CHO CELL LINES WITH MICROCARRIER CULTURE SYSTEMS 被引量:1
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作者 肖成祖 黄子才 +2 位作者 刘凤云 郭志霞 高丽华 《Chinese Medical Sciences Journal》 CAS CSCD 1994年第2期71-74,共4页
Genetically-engineered CHO cell lines, rβ- 13 and CLF-8B2, were cultivated with the MC- 1 microcarrier culture system. The cell density could be enhanced by increasing the concentration of microcarrier. At a microcar... Genetically-engineered CHO cell lines, rβ- 13 and CLF-8B2, were cultivated with the MC- 1 microcarrier culture system. The cell density could be enhanced by increasing the concentration of microcarrier. At a microcarrier concentration of 10 mg/ml. the cell density could reach 4 to 5 × 106 cells/ml. It was shown that these cell lines would spontaneously release from the microcarrier to attach to and proliferate on fresh microcarriers. We were thus able to scale up cultivation using a simple method. i. e. by adding fresh microcarriers and medium directly into the culture system to about 2, 4 or 8 times the original volume. Using a perfusion culture system. we have successfully cultivated CLF-8B2 cells in a 2 L bioreactor for several weeks at medium perfusion rates of 0. 5 to 3working volumes. Prourokinase was stably secreted. 展开更多
关键词 MC -1 type microcarrier CHO cell lines HuIFN-β
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