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4.4 Polycystic kidney disease (PKD) and urinary tract infections PKD is an autosomal dominant genetic kidney disease characterized by the progressive development of cysts in renal epithelial cells, ultimately leading to end-stage renal disease (ESRD)

After that, the selenium content in the solution was measured by an ICP-MS

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In addition, expression of IGF-1 and IGF-2 mRNA increased following acute deletion of IR in primary chondrocytes (Figure 4d and 4e)