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...

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Publicat a:JCI Insight
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 2019
Matèries:
Research Article
Accés en línia: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
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