Epigenetics in ADPKD: Understanding Mechanisms and Discovering Treatment
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Codon Publications
Reference130 articles.
1. Genetic Heterogeneity of Polycystic Kidney Disease in Europe1
2. Polycystin-L is a calcium-regulated cation channel permeable to calcium ions
3. Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel
4. Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents
5. Polycystin-2 is an intracellular calcium release channel
Cited by 4 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. The utility of serum neutrophil gelatinase‐associated lipocalin level on predicting autosomal dominant polycystic kidney disease progression;Therapeutic Apheresis and Dialysis;2024-05-21
2. Chromatin Methylation Abnormalities in Autosomal Dominant Polycystic Kidney Disease;Frontiers in Medicine;2022-07-05
3. Molecular Mechanisms of Epigenetic Regulation, Inflammation, and Cell Death in ADPKD;Frontiers in Molecular Biosciences;2022-06-29
4. Renal plasticity revealed through reversal of polycystic kidney disease in mice;Nature Genetics;2021-10-11
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