A bigenic mouse model of FSGS reveals perturbed pathways in podocytes, mesangial cells and endothelial cells.
第一作者:
Andrew S,Potter
第一单位:
Department of Pediatrics, Division of Developmental Biology, Cincinnati Children's Medical Center, Cincinnati, OH, United States of America.
作者:
医学主题词
衔接蛋白质类, 信号转导(Adaptor Proteins, Signal Transducing);动物(Animals);细胞支架蛋白质类(Cytoskeletal Proteins);疾病模型, 动物(Disease Models, Animal);内皮细胞(Endothelial Cells);肾小球硬化症, 局灶节段性(Glomerulosclerosis, Focal Segmental);肾小球系膜细胞(Mesangial Cells);小鼠(Mice);分子靶向治疗(Molecular Targeted Therapy);突变(Mutation);表型(Phenotype);足细胞(Podocytes);原癌基因蛋白质c-fyn(Proto-Oncogene Proteins c-fyn)
DOI
10.1371/journal.pone.0216261
PMID
31461442
发布时间
2020-07-01
- 浏览1
PloS one
e0216261页
相似文献
- 中文期刊
- 外文期刊
- 学位论文
- 会议论文


换一批



