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浏览/检索结果: 共17条，第1-10条 帮助 限定条件 发表日期：2016    专题：西安交通大学    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 Exome sequencing identified FGF12 as a novel candidate gene for Kashin-Beck disease 期刊论文 FUNCTIONAL & INTEGRATIVE GENOMICS, 2016, 卷号: 16, 页码: 13-17 作者:  Zhang, Feng;  Dai, Lanlan;  Lin, Weimin;  Wang, Wenyu;  Liu, Xuanzhu 收藏  |  浏览/下载：4/0  |  提交时间：2019/11/26 Genome-wide association study  Fibroblast growth factor  Kashin-Beck disease  Exome sequencing   Comparative analysis of signaling pathways in peripheral blood from patients with Kashin-Beck disease and osteoarthritis 期刊论文 EXPERIMENTAL AND THERAPEUTIC MEDICINE, 2016, 卷号: 12, 期号: [db:dc_citation_issue], 页码: 4077-4084 作者:  Ning, Yujie;  Wang, Xi;  Wang, Sen;  Guo, Xiong 收藏  |  浏览/下载：6/0  |  提交时间：2019/12/02 peripheral mononuclear cell  osteoarthritis  signaling pathway  Kashin-Beck disease  differentially expressed gene   Relationship of microRNA 616 gene polymorphism with prognosis in patients with premature coronary artery disease 期刊论文 INTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS, 2016, 卷号: 54, 期号: [db:dc_citation_issue], 页码: 899-903 作者:  Zhang, Yan;  Wang, Shijie;  Li, Yongqin;  Zhang, Chunyan;  Xue, Jiahong 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/02 premature coronary artery disease  microRNA  single nucleotide polymorphism   The haplotype of UBE2L3 gene is associated with Hashimoto's thyroiditis in a Chinese Han population 期刊论文 BMC ENDOCRINE DISORDERS, 2016, 卷号: 16, 期号: [db:dc_citation_issue] 作者:  Wang, Yu;  Zhu, Yuan-feng;  Wang, Qiong;  Xu, Jing;  Yan, Ni 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/02 Graves' disease (GD)  Single-nucleotide polymorphism (SNP)  Autoimmune thyroid disease (AITDs)  Hashimoto's thyroiditis (HT)  Ubiquitin conjugating enzyme E2L3 (UBE2L3)   Association of human leukocyte antigen DRB1 polymorphism and tuberculosis: a meta-analysis 期刊论文 INTERNATIONAL JOURNAL OF TUBERCULOSIS AND LUNG DISEASE, 2016, 卷号: 20, 期号: [db:dc_citation_issue], 页码: 121-U187 作者:  Yang, P-L.;  He, X-J.;  Zang, Q-J.;  Li, H-P.;  Wang, G-Y. 收藏  |  浏览/下载：3/0  |  提交时间：2019/12/02 human leukocyte antigen DRB1 (HLA-DRB1)  gene polymorphism  meta-analysis  TB   Integrative analysis of genome-wide association studies and gene expression profiles identified candidate genes for osteoporosis in Kashin-Beck disease patients 期刊论文 OSTEOPOROSIS INTERNATIONAL, 2016, 卷号: 27, 期号: [db:dc_citation_issue], 页码: 1041-1046 作者:  Wen, Y.;  Guo, X.;  Hao, J.;  Xiao, X.;  Wang, W. 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/02 Pleiotropy  Genome-wide association study  Gene expression profile  Kashin-Beck disease  Osteoporosis   A bivariate genome-wide association study identifies ADAM12 as a novel susceptibility gene for Kashin-Beck disease 期刊论文 SCIENTIFIC REPORTS, 2016, 卷号: 6, 期号: [db:dc_citation_issue] 作者:  Hao, Jingcan;  Wang, Wenyu;  Wen, Yan;  Xiao, Xiao;  He, Awen 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/02 Increased expression of EHF via gene amplification contributes to the activation of HER family signaling and associates with poor survival in gastric cancer 期刊论文 CELL DEATH & DISEASE, 2016, 卷号: 7, 期号: [db:dc_citation_issue] 作者:  Shi, Jing;  Qu, Yiping;  Li, Xinru;  Sui, Fang;  Yao, Demao 收藏  |  浏览/下载：2/0  |  提交时间：2019/12/02 NPR-C gene polymorphism is associated with increased susceptibility to coronary artery disease in Chinese Han population: a multicenter study 期刊论文 ONCOTARGET, 2016, 卷号: 7, 期号: [db:dc_citation_issue], 页码: 33662-33674 作者:  Hu, Qin;  Liu, Qiji;  Wang, Shasha;  Zhen, Xi;  Zhang, Zhimian 收藏  |  浏览/下载：4/0  |  提交时间：2019/12/02 coronary artery disease  natriuretic peptide receptor C  single nucleotide polymorphisms  susceptibility gene  Pathology Section  genome-wide association studies   Associations between dopamine D2 receptor gene polymorphisms and schizophrenia risk: a PRISMA compliant meta-analysis 期刊论文 NEUROPSYCHIATRIC DISEASE AND TREATMENT, 2016, 卷号: 12, 期号: [db:dc_citation_issue], 页码: 3129-3144 作者:  He, Hairong;  Wu, Huanhuan;  Yang, Lihong;  Gao, Fan;  Fan, Yajuan 收藏  |  浏览/下载：10/0  |  提交时间：2019/12/02 polymorphisms  schizophrenia  dopamine D2 receptor