PKHD1 protein encoded by the gene for autosomal recessive polycystic kidney disease associates with basal bodies and primary cilia in renal epithelial cells

Mutations of the polycystic kidney and hepatic disease 1 (PKHD1) gene have been shown to cause autosomal recessive polycystic kidney disease (ARPKD), but the cellular functions of the gene product (PKHD1) remain uncharacterized. To illuminate its properties, the spatial and temporal expression patte...

Full beskrivning

Sparad:
Bibliografiska uppgifter
Huvudupphovsmän: Zhang, Ming-Zhi, Mai, Weiyi, Li, Cunxi, Cho, Sae-youll, Hao, Chuanming, Moeckel, Gilbert, Zhao, Runxiang, Kim, Ingyu, Wang, Jikui, Xiong, Huaqi, Wang, Hong, Sato, Yasunori, Wu, Yizhong, Nakanuma, Yasuni, Lilova, Marusia, Pei, York, Harris, Raymond C., Li, Song, Coffey, Robert J., Sun, Le, Wu, Dianqing, Chen, Xing-Zhen, Breyer, Matthew D., Zhao, Zhizhuang Joe, McKanna, James A., Wu, Guanqing
Materialtyp: Artigo
Språk:Inglês
Publicerad: National Academy of Sciences 2004
Ämnen:
Biological Sciences
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC356947/
https://ncbi.nlm.nih.gov/pubmed/14983006
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0400073101
Taggar: Lägg till en tagg
Inga taggar, Lägg till första taggen!

Liknande verk