Disruption of Robo2-Baiap2 integrated signaling drives cystic disease

Hereditary renal cystic diseases are characterized by defects in primary cilia of renal tubular epithelial cells and abnormality of tubular epithelium, which ultimately result in the development of renal cysts. However, the mechanism leading from abnormality of the tubular epithelium to cystogenesis...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:JCI Insight
Main Authors: Li, Qinggang, Cui, Shaoyuan, Ma, Qian, Liu, Ying, Yu, Hongyu, Geng, GuangRui, Agborbesong, Ewud, Ren, Chongyu, Wei, Kai, Zhang, Yingjie, Yang, Jurong, Bai, Xueyuan, Cai, Guangyan, Xie, Yuansheng, Li, Xiaogang, Chen, Xiangmei
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2019
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6795383/
https://ncbi.nlm.nih.gov/pubmed/31534052
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/jci.insight.127602
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados