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浏览/检索结果: 共16条，第1-10条 帮助 限定条件 专题：中国医学科学院 北京协和医学院    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 Successful treatment of central nervous system involved Erdheim-Chester disease by intermediate-dose cytarabine as first-line therapy 期刊论文 2019, 页码: 1-4 作者:  Wang Ji-Nuo;  Qiu Yu;  Niu Na;  Zhang Yan;  Li Jian 收藏  |  浏览/下载：21/0  |  提交时间：2020/01/03 Chronic Urotensin-II Administration Improves Whole-Body Glucose Tolerance in High-Fat Diet-Fed Mice 期刊论文 2019, 卷号: 10, 页码: 453 作者:  Chen, Xi;  Yin, Lin;  Jia, Wei-hua;  Wang, Nuo-qi;  Xu, Chun-yang 收藏  |  浏览/下载：38/0  |  提交时间：2020/01/03 urotensin-II  high-fat diet  glucose tolerance  skeletal muscle  adipose tissue  mitochondrion   Early or deferred treatment of smoldering multiple myeloma: a meta-analysis on randomized controlled studies 期刊论文 2019, 卷号: 11, 页码: 5599-5611 作者:  Zhao, Ai-Lin;  Shen, Kai-Ni;  Wang, Ji-Nuo;  Huo, Lan-Qing;  Li, Jian 收藏  |  浏览/下载：8/0  |  提交时间：2020/01/03 smoldering multiple myeloma  early treatment  lenalidomide  meta-analysis   Application of next-generation sequencing to screen for pathogenic mutations in 123 unrelated Chinese patients with Marfan syndrome or a related disease 期刊论文 2019 作者:  Li Jiacheng;  Lu Chaoxia;  Wu Wei;  Liu Yaping;  Wang Rongrong 收藏  |  浏览/下载：19/0  |  提交时间：2020/01/03 FBN1 mutation  Marfan syndrome  genotype-phenotype correlations  next-generation sequencing   Glucose consumption assay discovers coptisine with beneficial effect on diabetic mice 期刊论文 2019, 卷号: 859, 页码: 172523 作者:  Shi, Li-li;  Jia, Wei-hua;  Zhang, Li;  Xu, Chun-yang;  Chen, Xi 收藏  |  浏览/下载：9/0  |  提交时间：2020/01/03 Coptisine  Diabetes  Glucose consumption  AMPK  Mitochondrion  Natural compound   TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model 期刊论文 2019, 卷号: 21, 期号: 7, 页码: 1548-1558 作者:  Liu, Jiaqi;  Wu, Nan;  Yang, Nan;  Takeda, Kazuki;  Chen, Weisheng 收藏  |  浏览/下载：36/0  |  提交时间：2020/01/03 congenital scoliosis (CS)  16p11.2/TBX6  compound inheritance model  genotype-phenotype correlation  gene dosage   A novel MAF missense mutation leads to congenital nuclear cataract by impacting the transactivation of crystallin and noncrystallin genes 期刊论文 2019, 卷号: 692, 页码: 113-118 作者:  Si, Nuo;  Song, Zixun;  Meng, Xiaolu;  Li, Xinru;  Xiao, Wei 收藏  |  浏览/下载：5/0  |  提交时间：2020/01/03 Congenital cataract  MAF  Extended homology region  Crystallins  Noncrystallins   Increased activated regulatory T cell subsets and aging Treg-like cells in multiple myeloma and monoclonal gammopathy of undetermined significance: a case control study 期刊论文 2018, 卷号: 18, 页码: 187 作者:  Wang, Ji-nuo;  Cao, Xin-xin;  Zhao, Ai-lin;  Cai, Hao;  Wang, Xuan 收藏  |  浏览/下载：9/0  |  提交时间：2020/01/03 Multiple myeloma  Monoclonal gammopathy of undetermined significance  Immune dysfunction  Regulatory T cell   Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies 期刊论文 2018, 卷号: 16, 期号: 1, 页码: 241 作者:  Lu, Chaoxia;  Wu, Wei;  Liu, Fang;  Yang, Kunqi;  Li, Jiacheng 收藏  |  浏览/下载：17/0  |  提交时间：2020/01/03 Inherited cardiomyopathy  Mutation  Next generation sequencing  TTN   FUNCTIONAL CHARACTERIZATION OF NOVEL SLC5A2 VARIANTS IN CHINESE PATIENTS WITH FAMILIAL RENAL GLUCOSURIA 会议论文 NEPHROLOGY DIALYSIS TRANSPLANTATION, 2018-05-01 作者:  Xu, Lubin;  Nuo, Si;  Zhao, Yumo;  Tian, Dongli;  Tang, Xueqing 收藏  |  浏览/下载：3/0  |  提交时间：2020/01/03