Related Experiment Video
Updated: Jan 14, 2026

Generation and Quantitative Characterization of Functional and Polarized Biliary Epithelial Cysts
Published on: May 16, 2020
[Cystic diseases in pathology practice]
1Service d'anatomie et cytologie pathologiques, hôpital Armand-Trousseau/Pitié-Salpêtrière/Sorbonne Université, 47-83, boulevard de l'Hôpital, 75651 Paris cedex 13, France.
Abstract:
Cystic diseases are a group of diseases characterised by the formation of cysts in some organs, particularly the lungs and kidneys, which progressively lead to respiratory or renal failure, requiring organ transplantation in advanced cases. Understanding the mechanisms of these cystic diseases has led to advances in early detection and the development of new treatments to slow their progression to end-stage failure.
Related Concept Videos
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
Urologic Endoscopic Procedure: Cystoscopic Examination
Cystic Fibrosis: Management
Sinus disease and chronic...
Sputum Studies I: Gram Stain, cytology, and Acid-fast smear and culture
Gram Stain
The Gram Stain is an integral part of sputum studies. It involves the staining of sputum, which permits...
Lysosomal Hydrolases

