CORC

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CORC

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Tumor-infiltrating lymphocytes-based subtypes and genomic characteristics of EBV-associated lymphoepithelioma-like carcinoma 期刊论文
JOURNAL OF PATHOLOGY, 2022
作者:  Yin, WenJuan;  Jin, JiaoYue;  Bao, Hua;  Chen, HanLin;  Wang, CanMing
收藏  |  浏览/下载：23/0  |  提交时间：2022/12/23
Neoantigen load as a prognostic and predictive marker for stage II/III non-small cell lung cancer in Chinese patients 期刊论文
THORACIC CANCER, 2021
作者:  Gong, Lei;  He, Ronghui;  Xu, Yanjun;  Luo, Taobo;  Jin, Kaixiu
收藏  |  浏览/下载：38/0  |  提交时间：2021/08/31
Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese 期刊论文
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：64/0  |  提交时间：2019/07/11
PTCH1 alterations are frequent but other genetic alterations are rare in sporadic odontogenic keratocysts. 期刊论文
Oral diseases, 2019
作者:  Qu Jiafei;  Zhang Jianyun;  Zhang Heyu;  Li Xuefen;  Hong Yingying
收藏  |  浏览/下载：22/0  |  提交时间：2019/12/04
Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese 期刊论文
国家科学评论, 2019, 卷号: 6, 期号: 2
作者:  Zhang Dengfeng;  Fan Yu;  Xu Min;  Wang Guihong;  Wang Dong
收藏  |  浏览/下载：34/0  |  提交时间：2019/12/04
A family with Danon disease caused by a splice site mutation in LAMP2 that generates a truncated protein 期刊论文
MOLECULAR GENETICS & GENOMIC MEDICINE, 2019, 卷号: 7, 期号: 3
作者:  Tang, Lu;  Sun, Minmin;  Pan, Cuizhen;  Shu, Xianhong;  Zhou, Nianwei
收藏  |  浏览/下载：41/0  |  提交时间：2019/12/05
Whole-exome sequencing reveals a novel mutation of MT-ND5 gene in a mitochondrial cardiomyopathy pedigree: Patients who show biventricular hypertrophy, hyperlactacidemia, pulmonary hypertension, and decreased exercise tolerance 期刊论文
ANATOLIAN JOURNAL OF CARDIOLOGY, 2019, 卷号: 21, 期号: 1
作者:  Zhou, Nianwei;  Tang, Lu;  Jiang, Yingying;  Qin, Shengmei;  Cui, Jie
收藏  |  浏览/下载：81/0  |  提交时间：2019/12/05
Identification of the Germline Mutation Profile in Esophageal Squamous Cell Carcinoma by Whole Exome Sequencing 期刊论文
FRONTIERS IN GENETICS, 2019, 卷号: 10
作者:  Deng, Jiaying;  Wang, Xiaoling;  Ye, Junyi;  Zhou, Daizhan;  Liu, Yun
收藏  |  浏览/下载：25/0  |  提交时间：2019/12/05
The Clinical and Genetic Features of Co-occurring Epilepsy and Autism Spectrum Disorder in Chinese Children 期刊论文
FRONTIERS IN NEUROLOGY, 2019, 卷号: 10
作者:  Long, Shasha;  Zhou, Hao;  Li, Shuang;  Wang, Tianqi;  Ma, Yu
收藏  |  浏览/下载：30/0  |  提交时间：2019/12/05
Complement C7 is a novel risk gene for Alzheimer's disease in Han Chinese 期刊论文
NATIONAL SCIENCE REVIEW, 2019, 卷号: 6, 期号: 2
作者:  Zhang, Deng-Feng;  Fan, Yu;  Xu, Min;  Wang, Guihong;  Wang, Dong
收藏  |  浏览/下载：18/0  |  提交时间：2019/12/05

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