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浏览/检索结果: 共10条，第1-10条 帮助 限定条件 发表日期：2019     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 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 GENETICS IN MEDICINE, 2019, 卷号: 21, 期号: 7 作者:  Liu, Jiaqi;  Wu, Nan;  Yang, Nan;  Takeda, Kazuki;  Chen, Weisheng 收藏  |  浏览/下载：63/0  |  提交时间：2019/12/05 congenital scoliosis (CS)  16p11.2/TBX6  compound inheritance model  genotype-phenotype correlation  gene dosage   Surrogate model assisted cooperative coevolution for large scale optimization 期刊论文 Applied Intelligence, 2019, 卷号: 49, 页码: 513-531 作者:  Ren, Zhigang;  Pang, Bei;  Wang, Muyi;  Feng, Zuren;  Liang, Yongsheng 收藏  |  浏览/下载：104/0  |  提交时间：2019/11/19 Adaptive differential evolutions  Cooperative co-evolution  Large-scale optimization  Radial Basis Function(RBF)  Surrogate model   TBX6-associated congenital scoliosis as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model. 期刊论文 Genetics in medicine : official journal of the American College of Medical Genetics, 2019 作者:  Jiaqi Liu;  Nan Wu;  Nan Yang;  Kazuki Takeda;  Weisheng Chen 收藏  |  浏览/下载：47/0  |  提交时间：2019/12/13 16p11.2/TBX6  compound  inheritance  model  congenital  scoliosis  (CS)  gene  dosage  genotype-phenotype  correlation   TBX6-associated congenital scoliosis as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model 期刊论文 Genetics in Medicine, 2019 作者:  Jiaqi Liu;  Nan Wu;  Deciphering Disorders Involving Scoliosis and COmorbidities study, Nan Yang;  Kazuki Takeda;  Weisheng Chen 收藏  |  浏览/下载：39/0  |  提交时间：2019/12/13 Surgical approaches and outcomes for cervical myelopathy with increased signal intensity on T2-weighted MRI: a meta-analysis 期刊论文 2019, 卷号: 14, 期号: 1, 页码: 224 作者:  Xu Yuan;  Chen Feng;  Wang Yipeng;  Zhang Jianguo;  Hu Jianhua 收藏  |  浏览/下载：3/0  |  提交时间：2020/01/03 Treatment experience for full-thickness wound dehiscence with cerebrospinal fluid leakage following posterior primary spine surgery Three case reports 期刊论文 2019, 卷号: 98, 期号: 15, 页码: e15126 作者:  Chen Feng;  Shao Qianqian;  Hu Jianhua;  Zhao Yu;  Wang Yipeng 收藏  |  浏览/下载：19/0  |  提交时间：2020/01/03 CSF leakage  full-thickness wound dehiscence  posterior primary spine surgery   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   A high-risk luminal A dominant breast cancer subtype with increased mobility 期刊论文 2019, 卷号: 175, 期号: 2, 页码: 459-472 作者:  Guo, Liping;  Chen, Guoji;  Zhang, Wen;  Zhou, Lulin;  Xiao, Ting 收藏  |  浏览/下载：4/0  |  提交时间：2020/01/03 Breast cancer classification  t-SNE  Biology process  Immune pattern  NETs   CYP2B6 genetic polymorphisms influence chronic obstructive pulmonary disease susceptibility in the Hainan population 期刊论文 INTERNATIONAL JOURNAL OF CHRONIC OBSTRUCTIVE PULMONARY DISEASE, 2019, 卷号: 14, 页码: 2103-2115 作者:  Ding, Yipeng*;  Li, Quanni;  Feng, Qiong;  Xu, Dongchuan;  Wu, Cibing 收藏  |  浏览/下载：8/0  |  提交时间：2019/12/27 *COPD  *CYP2B6  *case-control study  *chronic obstructive pulmonary disease  *gene polymorphisms   TERT gene polymorphisms are associated with chronic obstructive pulmonary disease risk in the Chinese Li population 期刊论文 Molecular Genetics and Genomic Medicine, 2019, 卷号: 7, 期号: 8, 页码: e773 作者:  Ding, Yipeng*;  Li, Quanni;  Wu, Cibing;  Wang, Wei;  Zhao, Jie 收藏  |  浏览/下载：10/0  |  提交时间：2019/12/27 TERT  Chinese Li population  chronic obstructive pulmonary disease  single nucleotide polymorphism (SNP)  susceptibility