机构

• 上海营养与健康研究所 [5]
• 金属研究所 [2]
• 合肥物质科学研究院 [2]
• 昆明动物研究所 [2]
• 计算技术研究所 [1]
• 化学研究所 [1]
• 更多

采集方式

• OAI收割 [19]
• iSwitch采集 [1]

内容类型

• 期刊论文 [20]

发表日期

• 2022 [3]
• 2021 [1]
• 2019 [2]
• 2018 [5]
• 2017 [2]
• 2016 [1]
• 更多

学科主题

• Cell Biolo... [2]
• Genetics &... [2]
• Abnormal p... [1]
• General & ... [1]
• Science & ... [1]

筛选

浏览/检索结果: 共20条，第1-10条 帮助 条数/页： 5101520253035404550556065707580859095100 排序方式： 请选择题名升序题名降序提交时间升序提交时间降序作者升序作者降序发表日期升序发表日期降序 A novel pathogenic deletion in ISPD causes Walker-Warburg syndrome in a Chinese family 期刊论文  OAI收割 GENES & GENOMICS, 2022, 页码: 7 作者:  Shi, Yuting;  Fu, Yimei;  Tao, Zhouteng;  Yong, Wenjing;  Peng, Huirong   |  收藏  |  浏览/下载：38/0  |  提交时间：2022/09/30 ISPD  Congenital hydrocephalus  Walker-Warburg syndrome  Exome sequencing  Mutation   Cross Analysis of Genomic-Pathologic Features on Multiple Primary Hepatocellular Carcinoma 期刊论文  OAI收割 FRONTIERS IN GENETICS, 2022, 卷号: 13, 页码: 9 作者:  Ren, Fei;  Wang, Depin;  Zhang, Xueyuan;  Zhao, Na;  Wang, Xiaowen   |  收藏  |  浏览/下载：21/0  |  提交时间：2023/07/12 hepatocellular carcinoma  whole exome sequencing  whole slide images  molecular profiling and subtyping  hepatitis B virus   Tumor-infiltrating lymphocytes-based subtypes and genomic characteristics of EBV-associated lymphoepithelioma-like carcinoma 期刊论文  OAI收割 JOURNAL OF PATHOLOGY, 2022 作者:  Yin, WenJuan;  Jin, JiaoYue;  Bao, Hua;  Chen, HanLin;  Wang, CanMing   |  收藏  |  浏览/下载：41/0  |  提交时间：2022/12/23 lymphoepithelioma-like carcinomas  TILs quantification  classification  whole exome sequencing  targeted therapy   Neoantigen load as a prognostic and predictive marker for stage II/III non-small cell lung cancer in Chinese patients 期刊论文  OAI收割 THORACIC CANCER, 2021 作者:  Gong, Lei;  He, Ronghui;  Xu, Yanjun;  Luo, Taobo;  Jin, Kaixiu   |  收藏  |  浏览/下载：81/0  |  提交时间：2021/08/31 biomarker  neoantigen load  NSCLC  prognosis  whole exome sequencing   Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese 期刊论文  OAI收割 NATIONAL SCIENCE REVIEW, 2019, 卷号: 6, 期号: 2, 页码: 257-274 作者:  Zhang, Deng-Feng;  Fan, Yu;  Xu, Min;  Wang, Guihong;  Wang, Dong   |  收藏  |  浏览/下载：78/0  |  提交时间：2019/07/11 Alzheimer's disease  whole-exome sequencing  C7  neuroimaging  complement system   Genome-Wide Association Study of Tacrolimus Pharmacokinetics Identifies Novel Single Nucleotide Polymorphisms in the Convalescence and Stabilization Periods of Post-transplant Liver Function 期刊论文  OAI收割 FRONTIERS IN GENETICS, 2019, 卷号: 10, 期号: -, 页码: 528 作者:  Liu, Yuan;  Li, Lei;  Ou, Baochi;  Fan, Junwei;  Peng, Zhihai   |  收藏  |  浏览/下载：18/0  |  提交时间：2020/12/09 GWAS  CYP3A5  exome  tacrolimus  FAM26F   Identification of LBX2 as a novel causal gene of atrial septal defect 期刊论文  OAI收割 INTERNATIONAL JOURNAL OF CARDIOLOGY, 2018, 卷号: 265, 期号: 1, 页码: 188-194 作者:  Wang, Jing;  Luo, Jing;  Chenc, Qiuhong;  Wang, Xi;  He, Jiangyan   |  收藏  |  浏览/下载：63/0  |  提交时间：2019/07/03 Atrial septal defect  LBX2  Neural crest cells  Whole exome sequencing   Association of vitamin D with risk of type 2 diabetes: A Mendelian randomisation study in European and Chinese adults 期刊论文  OAI收割 PLOS MEDICINE, 2018, 卷号: 15, 期号: 5, 页码: e1002566 作者:  Lu, Ling;  Bennett, Derrick A.;  Millwood, Iona Y.;  Parish, Sarah;  Bragg, Fiona   |  收藏  |  浏览/下载：14/0  |  提交时间：2020/12/09 GWAS  CYP3A5  exome  tacrolimus  FAM26F   Rare Copy Number Variants Identify Novel Genes in Sporadic Total Anomalous Pulmonary Vein Connection 期刊论文  OAI收割 FRONTIERS IN GENETICS, 2018, 卷号: 16, 期号: 6, 页码: 559 作者:  Shi, Xin;  Cheng, Liangping;  Jiao, XianTing;  Chen, Bo;  Wang, Jing   |  收藏  |  浏览/下载：27/0  |  提交时间：2020/12/09 congenital heart defects  total anomalous pulmonary venous connection  whole-exome sequencing  copy number variants  pathogenesis   Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis 期刊论文  OAI收割 SCIENCE CHINA-LIFE SCIENCES, 2018, 卷号: 61, 期号: 8, 页码: 947-953 作者:  Wang Rongrong;  Yang Shuanghao;  Xu Ming;  Huang Jia;  Liu Hongyan   |  收藏  |  浏览/下载：33/0  |  提交时间：2021/02/02 RED-CELL MEMBRANE  HEMATOLOGICALLY IMPORTANT MUTATIONS  RENAL TUBULAR-ACIDOSIS  HEMOLYTIC-ANEMIA  BETA-SPECTRIN  CYTOPLASMIC DOMAIN  BAND-3 DEFICIENCY  DISORDERS  ANKYRIN  VARIANTS  hereditary spherocytosis  mutation  ANK1  SPTB  SLC4A1  whole-exome sequencing