×
验证码:
换一张
忘记密码?
记住我
CORC
首页
科研机构
检索
知识图谱
申请加入
托管服务
登录
注册
在结果中检索
科研机构
中国医学科学院 北... [29]
内容类型
期刊论文 [28]
会议论文 [1]
发表日期
2019 [10]
2018 [6]
2017 [2]
2016 [2]
2015 [6]
2014 [2]
更多...
×
知识图谱
CORC
开始提交
已提交作品
待认领作品
已认领作品
未提交全文
收藏管理
QQ客服
官方微博
反馈留言
浏览/检索结果:
共29条,第1-10条
帮助
限定条件
专题:中国医学科学院 北京协和医学院
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:
5
10
15
20
25
30
35
40
45
50
55
60
65
70
75
80
85
90
95
100
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
Genome-wide CRISPR-Cas9 screen reveals selective vulnerability of ATRX-mutant cancers to WEE1 inhibition
期刊论文
2019
作者:
Liang Junbo
;
Zhao Hong
;
Diplas Bill H
;
Liu Song
;
Liu Jianmei
收藏
  |  
浏览/下载:13/0
  |  
提交时间:2020/01/03
Exome sequencing reveals a novel variant in NFX1 causing intracranial aneurysm in a Chinese family
期刊论文
2019
作者:
Ding Xinghuan
;
Zhao Sen
;
Zhang Qianqian
;
Yan Zihui
;
Wang Yang
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2020/01/03
Aneurysm
Genetic
Hemorrhage
Hereditary brain tumor with a homozygous germline mutation in PMS2: pedigree analysis and prenatal screening in a family with constitutional mismatch repair deficiency (CMMRD) syndrome
期刊论文
2019, 卷号: 18, 期号: 2, 页码: 261-265
作者:
Baig, Shahid Mahmood
;
Fatima, Ambrin
;
Tariq, Muhammad
;
Khan, Tahir Naeem
;
Ali, Zafar
收藏
  |  
浏览/下载:30/0
  |  
提交时间:2020/01/03
Constitutional mismatch repair deficiency (CMMRD) syndrome
Hereditary brain tumor
Prenatal diagnosis
Genetic counseling
PMS2
Epithelial SERPINB10, a novel marker of airway eosinophilia in asthma, contributes to allergic airway inflammation
期刊论文
2019, 卷号: 316, 期号: 1, 页码: L245-L254
作者:
Mo, Yuqing
;
Zhang, Kan
;
Feng, Yuchen
;
Yi, Lingling
;
Jiang, Yuxia
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2020/01/03
asthma
airway eosinophilia
CCL26
periostin
serine peptidase inhibitor
clade B
member 10
Sensitive and rapid detection of TERT promoter and IDH mutations in diffuse gliomas
期刊论文
2019, 卷号: 21, 期号: 4, 页码: 440-450
作者:
Diplas, Bill H.
;
Liu, Heng
;
Yang, Rui
;
Hansen, Landon J.
;
Zachem, Alexis L.
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2020/01/03
glioma classification
IDH mutation
qPCR
sequencing
TERT promoter mutation
Protective effect of potassium 2-(l-hydroxypentyl)-benzoate on hippocampal neurons, synapses and dystrophic axons in APP/PS1 mice
期刊论文
2019, 卷号: 236, 期号: 9, 页码: 2761-2771
作者:
Huang, Longjian
;
Zhang, Yong
;
Peng, Yuchen
;
Zhao, Zirun
;
Zhou, Yujun
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2020/01/03
Alzheimer's disease
Potassium 2-(l-hydroxypentyl)-benzoate
Hippocampal
Synapse
Dystrophic axon
APP
PS1 mice
Genetic polymorphisms of PAX1 are functionally associated with different PUMC types of adolescent idiopathic scoliosis in a northern Chinese Han population
期刊论文
2019, 卷号: 688, 页码: 215-220
作者:
Liu, Gang
;
Liu, Sen
;
Li, Xiaoxin
;
Chen, Jia
;
Chen, Weisheng
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2020/01/03
Adolescent idiopathic scoliosis (AIS)
PAX1
Northern Han Chinese
Single nucleotide polymorphism (SNP)
PUMC classification system
Detection of early-stage hepatocellular carcinoma in asymptomatic HBsAg-seropositive individuals by liquid biopsy
期刊论文
2019, 卷号: 116, 期号: 13, 页码: 6308-6312
作者:
Qu, Chunfeng
;
Wang, Yuting
;
Wang, Pei
;
Chen, Kun
;
Wang, Minjie
收藏
  |  
浏览/下载:65/0
  |  
提交时间:2020/01/03
cell free DNA
hepatocellular carcinoma
early detection of cancer
HBsAg-seropositive
Genome-wide profiling of Epstein-Barr virus integration by targeted sequencing in Epstein-Barr virus associated malignancies
期刊论文
2019, 卷号: 9, 期号: 4, 页码: 1115-1124
作者:
Xu Miao
;
Zhang Wei-Long
;
Zhu Qing
;
Zhang Shanshan
;
Yao You-Yuan
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2020/01/03
Epstein-Barr virus (EBV)
nasopharyngeal carcinoma (NPC)
DNA integration
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:34/0
  |  
提交时间:2020/01/03
congenital scoliosis (CS)
16p11.2/TBX6
compound inheritance model
genotype-phenotype correlation
gene dosage
©版权所有 ©2017 CSpace - Powered by
CSpace