Epigenetics and autosomal dominant polycystic kidney disease
Author:
Funder
Polycystic Kidney Disease Foundation, Children's Research Institute
National Institutes of Health
Publisher
Elsevier BV
Subject
Molecular Biology,Molecular Medicine
Reference80 articles.
1. Autosomal dominant polycystic kidney disease;Gabow;Am. J. Kidney Dis.,1993
2. Genetic heterogeneity of polycystic kidney disease in Europe;Peters;Contrib. Nephrol.,1992
3. Polycystin-L is a calcium-regulated cation channel permeable to calcium ions;Chen;Nature,1999
4. Polycystin-2, the protein mutated in autosomal dominant polycystic kidney disease (ADPKD), is a Ca2+-permeable nonselective cation channel;Gonzalez-Perrett;Proc. Natl Acad. Sci. USA,2001
5. Co-assembly of polycystin-1 and -2 produces unique cation-permeable currents;Hanaoka;Nature,2000
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1. DNA methyltransferase 1 (DNMT1) promotes cyst growth and epigenetic age acceleration in autosomal dominant polycystic kidney disease;Kidney International;2024-08
2. Benzothiazole derivatives as histone deacetylase inhibitors for the treatment of autosomal dominant polycystic kidney disease;European Journal of Medicinal Chemistry;2024-05
3. Transcription factor FoxM1 promotes cyst growth in PKD1 mutant ADPKD;Human Molecular Genetics;2022-11-02
4. Predicting Progression of Autosomal Dominant Polycystic Kidney Disease by Changes in the Telomeric Epigenome;Cells;2022-10-20
5. Chromatin Methylation Abnormalities in Autosomal Dominant Polycystic Kidney Disease;Frontiers in Medicine;2022-07-05
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