Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease-Reference-Cited by-同舟云学术

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Cystin, a novel cilia-associated protein, is disrupted in the cpk mouse model of polycystic kidney disease

Published:2002-02-15 Issue:4 Volume:109 Page:533-540
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Hou Xiaoying,Mrug Michal,Yoder Bradley K.,Lefkowitz Elliot J.,Kremmidiotis Gabriel,D’Eustachio Peter,Beier David R.,Guay-Woodford Lisa M.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference58 articles.

1. Autosomal Dominant Polycystic Kidney Disease

2. Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21–cen

Cited by 163 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. SHCBP1 Overexpression Aggravates Pancreatitis by Triggering the Loss of Primary Cilia;DNA and Cell Biology;2024-03-01

2. Pkd2 Deficiency in Embryonic Aqp2+ Progenitor Cells Is Sufficient to Cause Severe Polycystic Kidney Disease;Journal of the American Society of Nephrology;2024-01-23

3. TRP channels in renal disease. Lessons from Polycystin-2 (TRPP2);TRP Channels as Therapeutic Targets;2024

4. CFTR and PC2, partners in the primary cilia in autosomal dominant polycystic kidney disease;American Journal of Physiology-Cell Physiology;2023-09-01

5. Cystin is required for maintaining fibrocystin (FPC) levels and safeguarding proteome integrity in mouse renal epithelial cells;The FASEB Journal;2023-06-15

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