Natural-derived compounds and their mechanisms in potential autosomal dominant polycystic kidney disease (ADPKD) treatment
Author:
Funder
Fundamental Research Grant Scheme
Publisher
Springer Science and Business Media LLC
Subject
Physiology (medical),Nephrology,Physiology
Link
https://link.springer.com/content/pdf/10.1007/s10157-021-02111-x.pdf
Reference77 articles.
1. Grantham JJ, Chapman AB, Torres VE. Volume progression in autosomal dominant polycystic kidney disease: the major factor determining clinical outcomes. Clin J Am Soc Nephrol. 2006;1(1):148–57.
2. Chebib FT, Torres VE. Autosomal dominant polycystic kidney disease: core curriculum 2016. Am J Kidney Dis. 2016;67(5):792–810.
3. Torres VE, Harris PC. Strategies targeting cAMP signaling in the treatment of polycystic kidney disease. J Am Soc Nephrol. 2014;25(1):18–32.
4. Mustafa RA, Alan SJ. Burden of proof for tolvaptan in ADPKD: did REPRISE provide the answer? Clin J Am Soc Nephrol. 2018;13(7):1107–9.
5. Blair HA, Keating GM. Tolvaptan: a review in autosomal dominant polycystic kidney disease. Drugs. 2015;75(15):1797–806.
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1. Ouabain enhances renal cyst growth in a slowly progressive mouse model of autosomal dominant polycystic kidney disease;American Journal of Physiology-Renal Physiology;2023-12-01
2. Plant-derived compounds for treating autosomal dominant polycystic kidney disease;Frontiers in Nephrology;2023-02-03
3. Comparative Efficacy of Pharmacological Treatments for Adults With Autosomal Dominant Polycystic Kidney Disease: A Systematic Review and Network Meta-Analysis of Randomized Controlled Trials;Frontiers in Pharmacology;2022-05-18
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