机构

• 上海营养与健康研究所 [9]
• 上海生物化学与细胞生... [1]
• 植物研究所 [1]

采集方式

• OAI收割 [11]

内容类型

• 期刊论文 [11]

发表日期

• 2019 [1]
• 2018 [4]
• 2017 [4]
• 2015 [1]
• 2013 [1]

学科主题

• Cell Biol... [11]
• Biochemist... [3]
• Biotechnol... [1]
• Geriatrics... [1]
• Oncology [1]

筛选

浏览/检索结果: 共11条，第1-10条 帮助 限定条件 学科主题：Cell Biology     条数/页： 5101520253035404550556065707580859095100 排序方式： 请选择提交时间升序提交时间降序发表日期升序发表日期降序题名升序题名降序作者升序作者降序 H3K14me3 genomic distributions and its regulation by KDM4 family demethylases (vol 28, pg 1, 2018) 期刊论文  OAI收割 CELL RESEARCH, 2019, 卷号: 29, 期号: 1, 页码: 90-90 作者:  Zhao, Bin;  Xu, Wenqi;  Rong, Bowen;  Ye, Xuanjia;  Dai, Ruofei   |  收藏  |  浏览/下载：20/0  |  提交时间：2020/12/09 thyroid  metabolism   Revisiting ovarian cancer microenvironment: a friend or a foe? 期刊论文  OAI收割 PROTEIN & CELL, 2018, 卷号: 9, 期号: 8, 页码: 674-692 作者:  Zhang, Boyi;  Chen, Fei;  Han, Liu;  Gao, Libin;  Sun, Xiaochen   |  收藏  |  浏览/下载：12/0  |  提交时间：2020/12/09 ovarian cancer  stromal cells  tumor microenvironment  therapeutic resistance  ectopic metastasis  combinational treatment  patient stratification   PPM1K Regulates Hematopoiesis and Leukemogenesis through CDC20-Mediated Ubiquitination of MEIS1 and p21 期刊论文  OAI收割 CELL REPORTS, 2018, 卷号: 23, 期号: 5, 页码: 1461-1475 作者:  Liu, Xiaoye;  Zhang, Feifei;  Zhang, Yaping;  Chen, Chiqi;  Zhou, Meiyi   |  收藏  |  浏览/下载：20/0  |  提交时间：2020/12/09 ancestral reconstruction  copper  odorant receptors  orthologs  sulfur   Aging and Alzheimer's disease: Comparison and associations from molecular to system level 期刊论文  OAI收割 AGING CELL, 2018, 卷号: 17, 期号: 5, 页码: UNSP e12802 作者:  Xia, Xian;  Jiang, Quanlong;  McDermott, Joseph;  Han, Jing-Dong J.;  ,   |  收藏  |  浏览/下载：13/0  |  提交时间：2020/12/09 aging  Alzheimer's disease  cell type composition  comparison and association  epigenetics  genetic susceptibility  microglia  system inflammation   Revisiting ovarian cancer microenvironment: a friend or a foe? 期刊论文  OAI收割 PROTEIN & CELL, 2018, 卷号: 9, 期号: 8, 页码: 674-692 作者:  Zhang, Boyi;  Chen, Fei;  Han, Liu;  Gao, Libin;  Sun, Xiaochen   |  收藏  |  浏览/下载：13/0  |  提交时间：2020/12/09 ovarian cancer  stromal cells  tumor microenvironment  therapeutic resistance  ectopic metastasis  combinational treatment  patient stratification   Sodium Butyrate Protects Against High Fat Diet-Induced Cardiac Dysfunction and Metabolic Disorders in Type II Diabetic Mice 期刊论文  OAI收割 JOURNAL OF CELLULAR BIOCHEMISTRY, 2017, 卷号: 118, 期号: 8, 页码: 2395-2408 作者:  Zhang, Ling;  Du, Jianfeng;  Wang, Hao;  Zhao, Yu Tina;  Zhao, Ting C.   |  收藏  |  浏览/下载：8/0  |  提交时间：2020/12/09 HISTONE DEACETYLASE  DIABETES  CARDIOVASCULAR DISEASE  OBESITY  CARDIAC FUNCTION  METABOLIC SYNDROME   Sodium Butyrate Protects Against High Fat Diet-Induced Cardiac Dysfunction and Metabolic Disorders in Type II Diabetic Mice 期刊论文  OAI收割 JOURNAL OF CELLULAR BIOCHEMISTRY, 2017, 卷号: 118, 期号: 8, 页码: 2395-2408 作者:  Zhang, Ling;  Du, Jianfeng;  Wang, Hao;  Zhao, Yu Tina;  Zhao, Ting C.   |  收藏  |  浏览/下载：13/0  |  提交时间：2020/12/09 HISTONE DEACETYLASE  DIABETES  CARDIOVASCULAR DISEASE  OBESITY  CARDIAC FUNCTION  METABOLIC SYNDROME   Antioxidant MMCC ameliorates catch-up growth related metabolic dysfunction 期刊论文  OAI收割 ONCOTARGET, 2017, 卷号: 8, 期号: 59, 页码: 99931-99939 作者:  Ju, Liping;  Tong, Wenxin;  Qiu, Miaoyan;  Zheng, Sheng;  Chen, Ying   |  收藏  |  浏览/下载：10/0  |  提交时间：2020/12/09 catch-up growth  MMCC (MitoQuinone mesylate beta cyclodextrin complex)  mitochondria  metabolic dysfunction  skeletal functions   No association detected between seven common variants in the CDKALI gene and gestational glycemic traits 期刊论文  OAI收割 MOLECULAR AND CELLULAR PROBES, 2017, 卷号: 34, 期号: -, 页码: 64-67 作者:  Ju, Hongfang;  Lin, Rong;  Sun, Yuantian;  Zeng, Liangliang;  Su, Zhenyu   |  收藏  |  浏览/下载：10/0  |  提交时间：2020/12/09 Gestational glycemic traits  CDKALI  Genetic variants   Recurrent gain-of-function USP8 mutations in Cushing's disease 期刊论文  OAI收割 CELL RESEARCH, 2015, 卷号: 25, 期号: 3, 页码: 306-317 作者:  Ma, ZY;  Song, ZJ;  Chen, JH;  Wang, YF;  Li, SQ 收藏  |  浏览/下载：85/0  |  提交时间：2015/07/22 Cushing's disease  pituitary adenomas  USP8  mutation  whole-exome sequencing