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浏览/检索结果: 共5条，第1-5条 帮助 限定条件 专题：上海健康医学院    第一署名单位    第一作者单位    通讯作者单位     已选(0)清除 条数/页：5101520253035404550556065707580859095100   排序方式：请选择作者升序作者降序题名升序题名降序发表日期升序发表日期降序提交时间升序提交时间降序 Macrophage-derived CCL18 promotes osteosarcoma proliferation and migration by upregulating the expression of UCA1 期刊论文 JOURNAL OF MOLECULAR MEDICINE-JMM, 2019, 卷号: 97, 期号: 1 作者:  Su, Yang;  Zhou, Yan;  Sun, Yuan-jue;  Wang, Ya-Ling;  Yin, Jun-yi 收藏  |  浏览/下载：19/0  |  提交时间：2019/12/06 CCL18  Osteosarcoma  Macrophage  UCA1  EP300  Metastasis   Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review. 期刊论文 Neuromuscular disorders : NMD, 2019, 卷号: 29, 期号: 4 作者:  Tian Wo-Tu;  Luan Xing-Hua;  Zhou Hai-Yan;  Zhang Chao;  Huang Xiao-Jun 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/06 Congenital disorder of glycosylation  Glycogen storage disease  PGM1  Whole exome sequencing   The study of exercise tests in paroxysmal kinesigenic dyskinesia. 期刊论文 Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology, 2018, 卷号: 129, 期号: 11 作者:  Zhou Hai-Yan;  Zhan Fei-Xia;  Tian Wo-Tu;  Zhang Chao;  Wang Yan 收藏  |  浏览/下载：14/0  |  提交时间：2019/12/06 Compound muscle action potential  Hypokalaemic periodic paralysis  Long exercise test  Paroxysmal kinesigenic dyskinesia  Proline-rich transmembrane protein 2  Short exercise test   Progressive myoclonus epilepsy without renal failure in a Chinese family with a novel mutation in SCARB2 gene and literature 期刊论文 SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2018, 卷号: 57 作者:  Tian, Wo-Tu;  Liu, Xiao-Li;  Xu, Yang-Qi;  Huang, Xiao-Jun;  Zhou, Hai-Yan 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/06 Changes in F-18-FDG uptake within minutes after chemotherapy in a rabbit VX2 tumor model 期刊论文 JOURNAL OF NUCLEAR MEDICINE, 2008, 卷号: 49, 期号: 2 作者:  Song, Shao-Li;  Liu, Jian-Jun;  Huang, Gang;  Wang, Zhao-Hai;  Song, Yan-Yan 收藏  |  浏览/下载：1/0  |  提交时间：2019/12/06 F-18-FDG PET/CT  cisplatin  chemosensitivity  VX2 tumors