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科研机构
华南理工大学 [83]
内容类型
期刊论文 [38]
会议论文 [36]
会议 [9]
发表日期
2017 [11]
2016 [7]
2015 [7]
2014 [4]
2013 [5]
2012 [4]
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Bandpass Class-F Power Amplifier Based on Multifunction Hybrid Cavity-Microstrip Filter
期刊论文
IEEE TRANSACTIONS ON CIRCUITS AND SYSTEMS II-EXPRESS BRIEFS, 2017, 卷号: 64, 页码: 742-746
作者:
Guo, Qing-Yi[1]
;
Zhang, Xiu Yin[1]
;
Xu, Jin-Xu[1]
;
Li, Yuan Chun[1]
;
Xue, Quan[2,3]
收藏
  |  
浏览/下载:12/0
  |  
提交时间:2019/04/24
Class-F power amplifier (PA)
complex impedance conversion
high efficiency
hybrid cavity-microstrip bandpass filter (BPF)
Modeling of expanded granular sludge bed reactor using artificial neural network (EI收录)
期刊论文
Journal of Environmental Chemical Engineering, 2017, 卷号: 5, 页码: 2142-2150
作者:
Yi-Fan, Hu[1]
;
Chang-Zhu, Yang[1]
;
Jin-Feng, Dan[1]
;
Wen-Hong, Pu[1]
;
Jia-Kuang, Yang[1]
收藏
  |  
浏览/下载:5/0
  |  
提交时间:2019/04/24
Alkalinity
Chemical oxygen demand
Damage detection
Fatty acids
Forecasting
Granular materials
Mean square error
Neural networks
Optimization
pH effects
Redox reactions
Structural optimization
Surface properties
Volatile fatty acids
Melatonin alleviates lipopolysaccharide-compromised integrity of blood-brain barrier through activating AMP-activated protein kinase in old mice
期刊论文
AGING CELL, 2017, 卷号: 16, 页码: 414-421
作者:
Wang, Xiaona[1,2]
;
Xue, Gai-Xiu[3]
;
Liu, Wen-Cao[4]
;
Shu, Hui[1,2]
;
Wang, Mengwei[1,2]
收藏
  |  
浏览/下载:14/0
  |  
提交时间:2019/04/24
AMPK
blood-brain barrier
lipopolysaccharide
Melatonin
old mice
tight junction protein
MicroRNA-21 Mediates Angiotensin II-Induced Liver Fibrosis by Activating NLRP3 Inflammasome/IL-1 beta Axis via Targeting Smad7 and Spry1
期刊论文
ANTIOXIDANTS & REDOX SIGNALING, 2017, 卷号: 27, 页码: 1-20
作者:
Ning, Zuo-Wei[1]
;
Luo, Xiao-Ying[1]
;
Wang, Guo-Zhen[1]
;
Li, Yang[1]
;
Pan, Miao-Xia[2]
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2019/04/24
microRNA 21
angiotensin II
angiotensin-(1-7)
NLRP3 inflammasome
reactive oxygen species
liver fibrosis
Spleen atrophy related immune system changes attributed to infection of Angiostrongylus cantonensis in mouse model
期刊论文
PARASITOLOGY RESEARCH, 2017, 卷号: 116, 页码: 577-587
作者:
Liu, Zhen[1,2]
;
Wu, Yu[1,2]
;
Feng, Ying[3]
;
Wu, Feng[1,2]
;
Liu, Rui-Feng[1]
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/04/24
Angiostrongylus cantonensis
CNS
Spleen atrophy
Treg cells
CD28
CD38
miR-106b-5p promotes renal cell carcinoma aggressiveness and stem-cell-like phenotype by activating Wnt/beta-catenin signalling
期刊论文
ONCOTARGET, 2017, 卷号: 8, 页码: 21461-21471
作者:
Lu, Jun[1]
;
Wei, Jin-Huan[1]
;
Feng, Zi-Hao[1]
;
Chen, Zhen-Hua[1]
;
Wang, Yong-Qian[2]
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2019/04/24
miR-106b-5p
stemness
wnt signalling
tumorigenesis
renal cell carcinoma
Two heterozygous mutations identified in one Chinese patient with bilateral macular coloboma
期刊论文
MOLECULAR MEDICINE REPORTS, 2017, 卷号: 16, 页码: 2505-2510
作者:
Li, Tao[1]
;
Lin, Ying[1]
;
Gao, Hongbin[2,3]
;
Chen, Chuan[1,4]
;
Zhu, Yi[1,4]
收藏
  |  
浏览/下载:29/0
  |  
提交时间:2019/04/24
macular coloboma
bestrophin 1
regulating synaptic membrane exocytosis 1
mutation
macular atrophy
Bestrophin 1 gene analysis and associated clinical findings in a Chinese patient with Best vitelliform macular dystrophy
期刊论文
MOLECULAR MEDICINE REPORTS, 2017, 卷号: 16, 页码: 4751-4755
作者:
Lin, Ying[1]
;
Li, Tao[1]
;
Gao, Hongbin[2,3]
;
Lian, Yu[1]
;
Chen, Chuan[1,4]
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2019/04/24
best vitelliform macular dystrophy
bestrophin 1
VMD2
mutation
single nucleotide polymorphism
HLA-A*24:02 as a common risk factor for antiepileptic drug-induced cutaneous adverse reactions
期刊论文
NEUROLOGY, 2017, 卷号: 88, 页码: 2183-2191
作者:
Shi, Yi-Wu[1,2,4,5]
;
Min, Fu-Li[1,2,4,5,6]
;
Zhou, Dong[7]
;
Qin, Bin[8,9]
;
Wang, Juan[1,2,4,5,10]
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/04/24
C278F mutation in FGFR2 gene causes two different types of syndromic craniosynostosis in two Chinese patients
期刊论文
MOLECULAR MEDICINE REPORTS, 2017, 卷号: 16, 页码: 5333-5337
作者:
Lin, Ying[1]
;
Gao, Hongbin[2,3]
;
Ai, Siming[1]
;
Eswarakumar, Jacob V. P.[4]
;
Chen, Chuan[1,5]
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/04/24
craniosynostosis
fibroblast growth factor receptor 2
gene
mutation
Peters anomaly
Pfeiffer syndrome
Crouzon syndrome
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