This session highlights innovations from molecular mechanisms to drug development and clinical trials in biliary physiology and genetic and metabolic conditions. This session will spotlight cholangiocyte biology from scaffolding to repair. Gain insight into mechanisms and therapautics for A1AT deficiency, Wilson Disease, and hemachromatosis.
Objectives
1. Evaluate emerging therapies for metabolic and genetic liver disease.
2. Describe basic science mechanisms of cholangiocyte development and repair and implications for therapeutic targets.
3. Integrate basic, translational, and clinical studies for treatment of biliary disorders and genetic/metabolic liver disease.