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浏览/检索结果: 共8条，第1-8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 Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population 期刊论文 2019, 卷号: 688, 页码: 215-220 作者:  Liu, Gang;  Liu, Sen;  Li, Xiaoxin;  Chen, Jia;  Chen, Weisheng 收藏  |  浏览/下载：4/0  |  提交时间：2020/01/03 Adolescent idiopathic scoliosis (AIS)  PAX1  Northern Han Chinese  Single nucleotide polymorphism (SNP)  PUMC classification system   Genome-wide DNA methylation profile of thymomas and potential epigenetic regulation of thymoma subtypes 期刊论文 2019, 卷号: 41, 期号: 5, 页码: 2762-2774 作者:  Bi, Yalan;  Meng, Yunxiao;  Niu, Yuchen;  Li, Shanqing;  Liu, Hongsheng 收藏  |  浏览/下载：25/0  |  提交时间：2020/01/03 thymomas  differential methylation  integrative analysis  molecular subtypes  tumorigenesis mechanism   Genome-wide profiling of Epstein-Barr virus integration by targeted sequencing in Epstein-Barr virus associated malignancies 期刊论文 2019, 卷号: 9, 期号: 4, 页码: 1115-1124 作者:  Xu Miao;  Zhang Wei-Long;  Zhu Qing;  Zhang Shanshan;  Yao You-Yuan 收藏  |  浏览/下载：9/0  |  提交时间：2020/01/03 Epstein-Barr virus (EBV)  nasopharyngeal carcinoma (NPC)  DNA integration   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：33/0  |  提交时间：2020/01/03 congenital scoliosis (CS)  16p11.2/TBX6  compound inheritance model  genotype-phenotype correlation  gene dosage   Perturbations of BMP/TGF-beta and VEGF/VEGFR signalling pathways in non-syndromic sporadic brain arteriovenous malformations (BAVM) 期刊论文 2018, 卷号: 55, 期号: 10, 页码: 675-684 作者:  Wang, Kun;  Zhao, Sen;  Liu, Bowen;  Zhang, Qianqian;  Li, Yaqi 收藏  |  浏览/下载：6/0  |  提交时间：2020/01/03 brain arteriovenous malformation (bavm)  whole exome sequencing  genetics heterogeneity  vasculogenesis   Functional and In Silico Assessment of GDF3 Gene Variants in a Chinese Congenital Scoliosis Population 期刊论文 2018, 卷号: 24, 页码: 2992-3001 作者:  Chen, Jia;  Li, Xiaoxin;  Niu, Yuchen;  Wu, Zhihong;  Qiu, Guixing 收藏  |  浏览/下载：4/0  |  提交时间：2020/01/03 Computer Simulation  Genetic Variation  Growth Differentiation Factor 3  Molecular Biology  Scoliosis  Transforming Growth Factor beta   Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) 期刊论文 2016, 卷号: 12, 期号: 1, 页码: 1-222 作者:  Klionsky, Daniel J.;  Abdelmohsen, Kotb;  Abe, Akihisa;  Abedin, Md Joynal;  Abeliovich, Hagai 收藏  |  浏览/下载：26/0  |  提交时间：2020/01/04 autolysosome  autophagosome  chaperone-mediated autophagy  flux  LC3  lysosome  macroautophagy  phagophore  stress  vacuole   A novel anti-cancer agent icaritin suppresses hepatocellular carcinoma initiation and malignant growth through the IL-6/Jak2/Stat3 pathway 期刊论文 2015, 卷号: 26, 期号: 31, 页码: 67-67 作者:  Zhao, Hong;  Guo, Yuming;  Li, Shu;  Han, Ruiqin;  Ying, Jianming 收藏  |  浏览/下载：5/0  |  提交时间：2020/01/13 Icaritin  HCC  HCC initiating cells  IL-6 receptors  Stat3