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复旦大学上海医学院 [6]
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期刊论文 [21]
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Adjuvant chemotherapy does not benefit patients with esophageal squamous cell carcinoma treated with definitive chemoradiotherapy
期刊论文
RADIATION ONCOLOGY, 2018, 卷号: 13
作者:
Chen, Mingqiu
;
Shen, Minmin
;
Lin, Yu
;
Liu, Pingping
;
Liu, Xiaohong
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/11/21
Concurrent chemoradiotherapy
Survival
Esophageal squamous cell carcinoma
Adjuvant chemotherapy
Long Noncoding RNA FAM201A Mediates the Radiosensitivity of Esophageal Squamous Cell Cancer by Regulating ATM and mTOR Expression via miR-101
期刊论文
Frontiers in Genetics, 2018, 卷号: Vol.9
作者:
Mingqiu Chen
;
Pingping Liu
;
Yuangui Chen
;
Zhiwei Chen
;
Minmin Shen
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/26
ATM
esophageal
squamous
cell
carcinoma
FAM201A
long
noncoding
RNA
miR-101
mTOR
Synthesis of novel hierarchical porous polymers with a nanowire-interconnected network structure from core-shell polymer nanoobjects
期刊论文
SCIENCE CHINA-CHEMISTRY, 2017, 卷号: 60, 期号: 8, 页码: 1084-1089
作者:
Liang, Yeru
;
Ruan, Yingbo
;
Huang, Junlong
;
Peng, Bo
;
Liu, Chen-Yang
收藏
  |  
浏览/下载:23/0
  |  
提交时间:2018/05/02
Hierarchical Porous Polymer
Nanonetwork Structure
One-dimensional Network Unit
Hypercrosslinking
Microporous Heterogeneous Nanowire
The efficacy and toxicities of intensive induction chemotherapy followed by concurrent chemoradiotherapy in nasopharyngeal carcinoma patients with N-3 disease (vol 7, 3668, 2017)
期刊论文
SCIENTIFIC REPORTS, 2017, 卷号: 7
作者:
Zhang, Yingying
;
Chen, Mingqiu
;
Chen, Cheng
;
Kong, Lin
;
Lu, Jiade J.
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
The efficacy and toxicities of intensive induction chemotherapy followed by concurrent chemoradiotherapy in nasopharyngeal carcinoma patients with N-3 disease
期刊论文
SCIENTIFIC REPORTS, 2017, 卷号: 7
作者:
Zhang, Yingying
;
Chen, Mingqiu
;
Chen, Cheng
;
Kong, Lin
;
Lu, Jiade J.
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2019/12/05
A novel mutation of GATA4 (K300T) associated with familial atrial septal defect
期刊论文
GENE, 2016, 卷号: 575, 期号: 2
作者:
Liu, Wei
;
Chen, Jia
;
Qi, Bingyang
;
Zhao, Juan
;
Duan, Ranhui
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/12/05
Ventricular septal defect
Incomplete penetrance
Whole exome sequencing
Post-translational modification
Methylation
A novel mutation of GATA4 (K300T) associated with familial atrial septal defect
期刊论文
Gene, 2015, 卷号: 575, 期号: 2, 页码: 473-477
作者:
Chen, Jia
;
Qi, Bingyang
;
Zhao, Juan
;
Liu, Wei
;
Duan, Ranhui*
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2019/12/03
CHD
congenital heart diseases
ToF
tetralogy of Fallot
ASD
atrial septal defect
VSD
ventricular septal defect
AVSD
atrioventricular septal defect
DCM
dilated cardiomyopathy
HGMD
human gene mutation database
dbSNP
database of Single Nucleotide Polymorphisms
EVSD
Exome Variant Server Database
NLS
nuclear localization signal
SNP
Single nucleotide polymorphism
GATK
Genome Analysis Toolkit
PolyPhen-2
Polymorphism Phenotyping v2
SIFT
Sorting Intolerant From Tolerant
TAD
transcription activation domain
N-Znf
N-terminal zinc finger
C-Znf
C-terminal zinc finger
Ventricular septal defect
Incomplete penetrance
Whole exome sequencing
Post-translational modification
Methylation
Association of Common Polymorphisms in beta 1-adrenergic Receptor With Antihypertensive Response to Carvedilol
期刊论文
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2014, 卷号: 64, 期号: 4
作者:
Zhou, Hui
;
Si, Dayong
;
Wang, Juan
;
Xu, Ying
;
Chen, Xiaoshuai
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/05
carvedilol
beta-adrenergic receptor
ADRB1
antihypertensive therapy
Association of Common Polymorphisms in beta 1-adrenergic Receptor With Antihypertensive Response to Carvedilol
期刊论文
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2014, 卷号: 64, 期号: 4
作者:
Si, Dayong
;
Wang, Juan
;
Xu, Ying
;
Chen, Xiaoshuai
;
Zhang, Mingqiu
收藏
  |  
浏览/下载:8/0
  |  
提交时间:2019/12/05
carvedilol
beta-adrenergic receptor
ADRB1
antihypertensive therapy
Whole exome sequencing identifies a novel EMD mutation in a Chinese family with dilated cardiomyopathy
期刊论文
BMC MEDICAL GENETICS, 2014, 卷号: 15
作者:
Si, Dayong
;
Zhang, Mingqiu
;
Chen, Jia
;
Zheng, Yu
;
Jiao, Haixu
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2019/12/05
Dilated cardiomyopathy
Emery-Dreifuss muscular dystrophy
EMD gene
Novel mutation
Whole exome sequencing
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