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湖南大学 [5]
湖南农业大学 [2]
复旦大学上海医学院 [2]
上海中医药大学 [2]
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期刊论文 [15]
发表日期
2017 [15]
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CEP78 is mutated in a distinct type of Usher syndrome
期刊论文
JOURNAL OF MEDICAL GENETICS, 2017, 卷号: 54, 期号: 3
作者:
Fu, Qing
;
Xu, Mingchu
;
Chen, Xue
;
Sheng, Xunlun
;
Yuan, Zhisheng
收藏
  |  
浏览/下载:8/0
  |  
提交时间:2019/12/05
GUCA1A mutation causes maculopathy in a five-generation family with a wide spectrum of severity
期刊论文
GENETICS IN MEDICINE, 2017, 卷号: 19, 期号: 8
作者:
Chen, Xue
;
Sheng, Xunlun
;
Zhuang, Wenjuan
;
Sun, Xiantao
;
Liu, Guohua
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/05
GUCA1A
maculopathy
medical genetics
ophthalmology
pathogenic mechanism
Efficacy and Safety of Niaoduqing Particles for Delaying Moderate-to-severe Renal Dysfunction: A Randomized, Double-blind, Placebo-controlled, Multicenter Clinical Study
期刊论文
中华医学杂志, 2017, 卷号: 130, 期号: 20
作者:
Ying Zheng
;
Guangyan Cai
;
Liqun He
;
Hongli Lin
;
Xiaohong Cheng
收藏
  |  
浏览/下载:9/0
  |  
提交时间:2019/12/05
Chronic Kidney Disease
Moderate-to-severe Renal Dysfunction
Niaoduqing Particles
Randomized Controlled Trial
Traditional Chinese Medicine
Analysis of Factors Associated with Death in Maintenance Hemodialysis Patients: A Multicenter Study in China
期刊论文
中华医学杂志, 2017, 卷号: 130, 期号: 8
作者:
Ni Zhaohui
;
Song Kangkang
;
Zhao Delong
;
Wang Yuanda
;
Wang Yong
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2019/12/05
Hemodialysis
Mortality
Risk Factors
Risk Factor Analysis for AKI Including Laboratory Indicators: a Nationwide Multicenter Study of Hospitalized Patients
期刊论文
KIDNEY & BLOOD PRESSURE RESEARCH, 2017, 卷号: 42, 页码: 761-773
作者:
Nie, Sasa
;
Feng, Zhe
;
Tang, Li
;
Wang, Xiaolong
;
He, Yani
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/11/26
Epidemiology
Acute kidney injury
Serum uric acid
Risk factors
Mortality
Tacrolimus Monotherapy after Intravenous Methylprednisolone in Adults with Minimal Change Nephrotic Syndrome
期刊论文
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2017, 卷号: 28, 期号: 4, 页码: 1286-1295
作者:
Li, Xiayu
;
Liu, Zhangsuo
;
Wang, Li
;
Wang, Rong
;
Ding, Guohua
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2019/12/12
Atomic scale g-C3N4/Bi2WO6 2D/2D heterojunction with enhanced photocatalytic degradation of ibuprofen under visible light irradiation
期刊论文
Applied Catalysis B: Environmental, 2017, 卷号: 209, 页码: 285-294
作者:
Wang, Jiajia
;
Tang, Lin*
;
Zeng, Guangming
;
Deng, Yaocheng
;
Liu, Yani
收藏
  |  
浏览/下载:3/0
  |  
提交时间:2019/12/23
Atomic scale
2D/2D heterojunction
Monolayer Bi2WO6
Ultrathin g-C3N4 nanosheets
Photocatalysis
Construction of Plasmonic Ag and Nitrogen-Doped Graphene Quantum Dots Codecorated Ultrathin Graphitic Carbon Nitride Nanosheet Composites with Enhanced Photocatalytic Activity: Full-Spectrum Response Ability and Mechanism Insight
期刊论文
ACS Applied Materials and Interfaces, 2017, 卷号: 9, 期号: 49, 页码: 42816-42828
作者:
Deng, Yaocheng
;
Tang, Lin*
;
Feng, Cheugyang
;
Zeng, Guanming*
;
Wang, Jiajia
收藏
  |  
浏览/下载:11/0
  |  
提交时间:2019/12/23
full-spectrum light
nitrogen-doped graphene quantum dot
surface plasmon resonance
tetracycline
upconversion effect
Tacrolimus Monotherapy after Intravenous Methylprednisolone in Adults with Minimal Change Nephrotic Syndrome
期刊论文
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2017, 卷号: 28, 期号: 4
作者:
Huo, Bengang
;
Wang, Rong
;
Ding, Guohua
;
Fu, Ping
;
Du, Juan
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2019/12/05
CEP78 is mutated in a distinct type of Usher syndrome
期刊论文
2017, 卷号: 54, 期号: 3, 页码: 190-195
作者:
Fu, Qing
;
Xu, Mingchu
;
Chen, Xue
;
Sheng, Xunlun
;
Yuan, Zhisheng
收藏
  |  
浏览/下载:4/0
  |  
提交时间:2020/01/04
CEP78
Usher syndrome
cone-rod dystrophy
next-generation sequencing
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