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科研机构
西安交通大学 [2]
金属研究所 [2]
山东大学 [1]
湖南大学 [1]
内容类型
期刊论文 [6]
发表日期
2018 [6]
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Polarized M2c macrophages have a promoting effect on the epithelial-to-mesenchymal transition of human renal tubular epithelial cells.
期刊论文
Immunobiology, 2018, 卷号: 223, 页码: 826-833
作者:
Chen Zhao
;
Dong Fengming
;
Lu Jiamei
;
Wei Linting
;
Tian Lifang
收藏
  |  
浏览/下载:15/0
  |  
提交时间:2019/11/26
Epithelial-to-mesenchymal transition (EMT)
Renal tubular epithelial cell
Renal fibrosis
Macrophage
Epithelial C5aR1 Signaling Enhances Uropathogenic Escherichia coil Adhesion to Human Renal Tubular Epithelial Cells
期刊论文
FRONTIERS IN IMMUNOLOGY, 2018, 卷号: 9
作者:
Song, Yun
;
Wu, Kun-Yi
;
Wu, Weiju
;
Duan, Zhao-Yang
;
Gao, Ya-Feng
收藏
  |  
浏览/下载:10/0
  |  
提交时间:2019/11/26
renal tubular epithelial cell
mannosyl residues
C5aR1
uropathogenic Escherichia coli
bacterial adhesion/invasion
Protective Effect of Salidroside Against Diabetic Kidney Disease Through Inhibiting BIM-Mediated Apoptosis of Proximal Renal Tubular Cells in Rats
期刊论文
FRONTIERS IN PHARMACOLOGY, 2018, 卷号: 9
作者:
Guo, Congcong
;
Li, Yun
;
Zhang, Rui
;
Zhang, Yaqin
;
Zhao, Junyu
收藏
  |  
浏览/下载:6/0
  |  
提交时间:2019/12/11
diabetic kidney disease
salidroside
apoptosis
BIM protein
proximal
renal tubular epithelial cell
Preparation and evaluation of anti‐renal fibrosis activity of novel truncated TGF‐β receptor type II
期刊论文
Biotechnology and Applied Biochemistry, 2018, 卷号: Vol.65 No.6, 页码: 834-840
作者:
Haifeng Liu
;
Zhongmin Zhang
;
Yuting Li
;
Xiaoli Wang
;
Yufei Zhang
收藏
  |  
浏览/下载:2/0
  |  
提交时间:2019/12/26
renal
fibrosis
renal
tubular
epithelial
cell
transforming
growth
factor‐beta
receptor
type
II
Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis
期刊论文
SCIENCE CHINA-LIFE SCIENCES, 2018, 卷号: 61, 期号: 8, 页码: 947-953
作者:
Wang Rongrong
;
Yang Shuanghao
;
Xu Ming
;
Huang Jia
;
Liu Hongyan
收藏
  |  
浏览/下载:63/0
  |  
提交时间:2021/02/02
RED-CELL MEMBRANE
HEMATOLOGICALLY IMPORTANT MUTATIONS
RENAL TUBULAR-ACIDOSIS
HEMOLYTIC-ANEMIA
BETA-SPECTRIN
CYTOPLASMIC DOMAIN
BAND-3 DEFICIENCY
DISORDERS
ANKYRIN
VARIANTS
hereditary spherocytosis
mutation
ANK1
SPTB
SLC4A1
whole-exome sequencing
Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis
期刊论文
SCIENCE CHINA-LIFE SCIENCES, 2018, 卷号: 61, 期号: 8, 页码: 947-953
作者:
Wang Rongrong
;
Yang Shuanghao
;
Xu Ming
;
Huang Jia
;
Liu Hongyan
收藏
  |  
浏览/下载:7/0
  |  
提交时间:2021/02/02
RED-CELL MEMBRANE
HEMATOLOGICALLY IMPORTANT MUTATIONS
RENAL TUBULAR-ACIDOSIS
HEMOLYTIC-ANEMIA
BETA-SPECTRIN
CYTOPLASMIC DOMAIN
BAND-3 DEFICIENCY
DISORDERS
ANKYRIN
VARIANTS
hereditary spherocytosis
mutation
ANK1
SPTB
SLC4A1
whole-exome sequencing
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