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北京大学 [4]
复旦大学上海医学院 [4]
合肥物质科学研究院 [3]
南华大学 [2]
昆明动物研究所 [2]
西安交通大学 [1]
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期刊论文 [22]
会议论文 [1]
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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
lymphoepithelioma-like carcinomas
TILs quantification
classification
whole exome sequencing
targeted therapy
Whole-exome mutational landscape of neuroendocrine carcinomas of the gallbladder
期刊论文
SIGNAL TRANSDUCTION AND TARGETED THERAPY, 2021, 卷号: 6
作者:
Liu, Fatao
;
Li, Yongsheng
;
Ying, Dongjian
;
Qiu, Shimei
;
He, Yong
收藏
  |  
浏览/下载:27/0
  |  
提交时间:2021/04/26
Integrative Proteomic Characterization of Human Lung Adenocarcinoma
期刊论文
CELL, 2020, 卷号: 182, 期号: 1, 页码: 245-+
作者:
Xu, Jun-Yu
;
Zhang, Chunchao
;
Wang, Xiang
;
Zhai, Linhui
;
Ma, Yiming
收藏
  |  
浏览/下载:52/0
  |  
提交时间:2020/12/24
Distinct co-acquired alterations and genomic evolution during TKI treatment in non-small-cell lung cancer patients with or without acquired T790M mutation
期刊论文
ONCOGENE, 2020, 卷号: 39
作者:
Jin, Ying
;
Bao, Hua
;
Le, Xiuning
;
Fan, Xiaojun
;
Tang, Ming
收藏
  |  
浏览/下载:25/0
  |  
提交时间:2020/11/26
Phenotypic variability of SLC7A14 mutations in patients with inherited retinal dystrophy
期刊论文
OPHTHALMIC GENETICS, 2019, 卷号: 40, 期号: 2
作者:
Lia, Jun
;
Guo, Li-Yun
;
Zheng, Sui-Lian
;
Zhu, Qin
;
Duan, Wen-Hua
收藏
  |  
浏览/下载:22/0
  |  
提交时间:2019/12/04
Inherited retinal dystrophy
SLC7A14 gene
targeted exome sequencing
mutations
Mutation and association analyses of dementia-causal genes in Han Chinese patients with early-onset and familial Alzheimer's disease
期刊论文
JOURNAL OF PSYCHIATRIC RESEARCH, 2019, 卷号: 113, 页码: 141-147
作者:
Xu, M
;
Feng, T
;
Yao, YG
;
Shan, BC
;
Tan, LW
收藏
  |  
浏览/下载:245/0
  |  
提交时间:2019/06/14
Identification of a novel COL4A5 mutation in the proband initially diagnosed as IgAN from a Chinese family with X-linked Alport syndrome
期刊论文
Science China Life Sciences, 2019
作者:
Li, Z.*
;
Zhu, P.
;
Huang, H.
;
Pan, Y.
;
Han, P.
收藏
  |  
浏览/下载:18/0
  |  
提交时间:2019/12/27
Alport syndrome
COL4A5
IgA nephropathy
a novel frameshift mutation
targeted exome-based next-generation sequencing
Identification of a novel mutation in the FGFR3 gene in a Chinese family with Hypochondroplasia
期刊论文
GENE, 2018, 卷号: 641, 页码: 355-360
作者:
Chen, Jing
;
Yang, Jiangfei
;
Zhao, Suzhou
;
Ying, Hui
;
Li, Guimei
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/11
Hypochondroplasia (HCH)
Fibroblast growth factor receptor 3 (FGFR3)
Short stature
Targeted exome sequencing (TES)
Missense Variants in HIF1A and LACC1 Contribute to Leprosy Risk in Han Chinese
期刊论文
The American Journal of Human Genetics, 2018, 期号: 102, 页码: 794–805
作者:
Deng-Feng Zhang
;
Dong Wang
;
Yong-Gang Yao
;
Mahadev Malhi
;
Rui Bi
收藏
  |  
浏览/下载:18/0
  |  
提交时间:2018/09/27
Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing
期刊论文
SCIENTIFIC REPORTS, 2017, 卷号: 7
作者:
Wang, Yi
;
Wang, Yimin
;
Du, Xiaonan
;
Bin, Rao
;
Yu, Shanshan
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
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