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Inactivation of miR-100 combined with arsenic treatment enhances the malignant transformation of BEAS-2B cells via stimulating epithelial -mesenchymal transition
Yang, Jia; Chen, Zhijun; Wang, Xinyi; Xu, Mo; Fang, Haoshu; Li, Feifei; Liu, Yakun; Jiang, Yu; Ding, Yi; Li, Juan
刊名CANCER BIOLOGY & THERAPY
2017
卷号18期号:12页码:965-973
关键词Carcinogenesis lung cancer micro RNA miR-100
DOI10.1080/15384047.2017.1345393
URL标识查看原文
公开日期[db:dc_date_available]
内容类型期刊论文
URI标识http://www.corc.org.cn/handle/1471x/4590880
专题山东大学
作者单位1.Shandong Univ, Sch Med, Dept Anesthesia, Jinan, Shandong, Peoples R China.
2.[Yang, Jia
3.Chen, Zhijun
4.Wang, Xinyi
5.Xu, Mo
6.Fan
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GB/T 7714
Yang, Jia,Chen, Zhijun,Wang, Xinyi,et al. Inactivation of miR-100 combined with arsenic treatment enhances the malignant transformation of BEAS-2B cells via stimulating epithelial -mesenchymal transition[J]. CANCER BIOLOGY & THERAPY,2017,18(12):965-973.
APA Yang, Jia.,Chen, Zhijun.,Wang, Xinyi.,Xu, Mo.,Fang, Haoshu.,...&Wang, Siying.(2017).Inactivation of miR-100 combined with arsenic treatment enhances the malignant transformation of BEAS-2B cells via stimulating epithelial -mesenchymal transition.CANCER BIOLOGY & THERAPY,18(12),965-973.
MLA Yang, Jia,et al."Inactivation of miR-100 combined with arsenic treatment enhances the malignant transformation of BEAS-2B cells via stimulating epithelial -mesenchymal transition".CANCER BIOLOGY & THERAPY 18.12(2017):965-973.
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