lumacaftor and Polycystic-Kidney--Autosomal-Recessive

lumacaftor has been researched along with Polycystic-Kidney--Autosomal-Recessive* in 1 studies

Other Studies

1 other study(ies) available for lumacaftor and Polycystic-Kidney--Autosomal-Recessive

ArticleYear
Ameliorating liver disease in an autosomal recessive polycystic kidney disease mouse model.
    American journal of physiology. Gastrointestinal and liver physiology, 2023, 05-01, Volume: 324, Issue:5

    Systemic and portal hypertension, liver fibrosis, and hepatomegaly are manifestations associated with autosomal recessive polycystic kidney disease (ARPKD), which is caused by malfunctions of fibrocystin/polyductin (FPC). The goal is to understand how liver pathology occurs and to devise therapeutic strategies to treat it. We injected 5-day-old

    Topics: Animals; Cystic Fibrosis Transmembrane Conductance Regulator; Heat-Shock Proteins; Humans; Liver Cirrhosis; Mice; Polycystic Kidney, Autosomal Recessive; Receptors, Cell Surface

2023