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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)

Indeed, the numbers of total PSCs and activated PSCs were significantly increased upon LOsG treatment

Impaired virus clearance, compromised immune response and increased mortality in type 2 diabetic mice infected with West Nile virus

NTZ-200 was close to NAC and 4-PBA effects concerning hepatic SOD activity (Figure 3C), yet it was less effective than both concerning hepatic GSH (Figure 3B)

GDP-exchange inhibition assays confirmed DJX-A-KM s shortest linker best preserved MRTX849s inhibitory activity against KRAS G12C (Supplementary Table 3)

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