CUBN variants uncouple proteinuria from kidney function
Author:
Publisher
Springer Science and Business Media LLC
Subject
Nephrology
Link
http://www.nature.com/articles/s41581-019-0242-4.pdf
Reference10 articles.
1. Roscioni, S. S., Heerspink, H. J. L. & de Zeeuw, D. Microalbuminuria: target for renoprotective therapy PRO. Kidney Int. 86, 40–49 (2014).
2. Bedin, M. et al. Human C-terminal CUBN variants associate with chronic proteinuria and normal renal function. J. Clin. Invest. https://doi.org/10.1172/JCI129937 (2019).
3. Jayasinghe, K. et al. Isolated proteinuria due to CUBN homozygous mutation – challenging the investigative paradigm. BMC Nephrol. 20, 330 (2019).
4. Kashtan, C. E. et al. Clinical practice recommendations for the treatment of Alport syndrome: a statement of the Alport Syndrome Research Collaborative. Pediatr. Nephrol. 28, 5–11 (2013).
5. Brenner, B. M. et al. Effects of losartan on renal and cardiovascular outcomes in patients with type 2 diabetes and nephropathy. N. Engl. J. Med. 345, 861–869 (2001).
Cited by 3 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. Isolated benign persistent proteinuria with novel association of CUBN (cubilin) variants;Clinical Case Reports;2023-06
2. Four missense genetic variants in CUBN are associated with higher levels of eGFR in non-diabetes but not in diabetes mellitus or its subtypes: A genetic association study in Europeans;Frontiers in Endocrinology;2023-02-28
3. Podocytopathy and Glomerular Basement Membrane Anomalies in Two Patients With Cubilin Gene Mutations;Cureus;2023-02-07
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