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Literature Workspace

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1 reference

Research article 2025 Reviewed MVA Hackathon 2026 — BUB1B

Translational readthrough therapy for ADPKD induces polycystin1 expression and partially rescues functional deficits in PKD1 mutant cells

Elena Torban, Lucie Canaff, Sima Babayeva and 5 more Scientific Reports

Autosomal-Dominant Polycystic Kidney Disease, ADPKD, is the most common genetic kidney disease affecting 1:1000 people worldwide. It is caused by mutations in the PKD1 (~ 80%) or PKD2 gene (~ 15%). Although the germline … abstract via Europe PMC

Evidence snapshot note: Torban et al. — PKD1 readthrough and partial cellular rescue. Model: Human HEK293 PKD1 reporters and WT9-12 cells; other-gene evidence. Where: Figures 1H-I, 4, 5 and 6; published 2025-11-22 · cited by MVA-RT-TRANSFER-009

  • Therapy
  • Aminoglycosides
  • Readthrough Drugs
  • Autosomal-dominant Polycystic Kidney Disease

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KBot · Research guide

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