Glycosphingolipid metabolism and polycystic kidney disease
Author:
Publisher
Elsevier BV
Subject
Cell Biology
Reference108 articles.
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2. Polycystic kidney disease;Bergmann;Nat. Rev. Dis. Primers,2018
3. Molecular pathways and therapies in autosomal-dominant polycystic kidney disease;Saigusa;Physiology,2015
4. Targeting Glucosylceramide synthesis in the treatment of rare and common renal disease;Shayman;Semin. Nephrol.,2018
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1. Sphingolipids and Chronic Kidney Disease;Journal of Clinical Medicine;2024-08-26
2. 2,8-Dihydroxyadenine-induced nephropathy causes hexosylceramide accumulation with increased mTOR signaling, reduced levels of protective SirT3 expression and impaired renal mitochondrial function;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2024-01
3. Renal ciliopathies: promising drug targets and prospects for clinical trials;Expert Opinion on Therapeutic Targets;2023-05-04
4. Targeting Glycosphingolipid Metabolism in ADPKD: Another Roadblock for Treatment;American Journal of Kidney Diseases;2023-05
5. Venglustat, a Novel Glucosylceramide Synthase Inhibitor, in Patients at Risk of Rapidly Progressing ADPKD: Primary Results of a Double-Blind, Placebo-Controlled, Phase 2/3 Randomized Clinical Trial;American Journal of Kidney Diseases;2023-05
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