Amandine Viau
Paris, France
Last Updated: 09/26/2026
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Found 24 publications
Cilia to basement membrane signaling is a biomechanical driver in models of autosomal dominant polycystic kidney disease.
Journal: The Journal of clinical investigation
Published: June 30, 2026
Segmentation of renal tubules and automatic biomarker quantification in ciliopathy preclinical models.
Journal: Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference
Published: December 03, 2025
Inhibition of the inflammasome ameliorates orthologous polycystic kidney disease.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: November 13, 2025
Ciliogenic pancreatopathy reveals a link between ciliopathies and exocrine pancreatic disease.
Journal: Gut
Published: October 08, 2025
IL1β is induced in nephronophthisis but does not mediate kidney damage.
Journal: Genes & diseases
Published: December 27, 2024
Agonists of prostaglandin E2 receptors as potential first in class treatment for nephronophthisis and related ciliopathies.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 28, 2022
The renal inflammatory network of nephronophthisis.
Journal: Human molecular genetics
Published: December 08, 2021
Ift88, but not Kif3a, is required for establishment of the periciliary membrane compartment.
Journal: Biochemical and biophysical research communications
Published: September 17, 2021
Identification of pathological transcription in autosomal dominant polycystic kidney disease epithelia.
Journal: Scientific reports
Published: March 17, 2021
Loss of PKD1/polycystin-1 impairs lysosomal activity in a CAPN (calpain)-dependent manner.
Journal: Autophagy
Published: September 24, 2020
Last Updated: 09/26/2026