Sox9 Is a Modifier of the Liver Disease Severity in a Mouse Model of Alagille Syndrome. Hepatology. 2020; 71:1331-1349.
.Molecular regulation of mammalian hepatic architecture. Editor, Wellik DM. Current Topics in Developmental Biology. 2019; 132:91-136.
.De novo formation of the biliary system by TGFβ-mediated hepatocyte transdifferentiation. Nature. 2018; 557:247-251.
.Identification of a Paralog-Specific Notch1 Intracellular Domain Degron. Cell Reports. 2016; 15:1920-1929.
.ASO silencing of a glycosyltransferase, Poglut1 , improves the liver phenotypes in mouse models of Alagille syndrome. Hepatology. 2023; 78:1337-1351.
.Multiple Facets of Cellular Homeostasis and Regeneration of the Mammalian Liver. Annual Review of Physiology. 2023; 85:469-493.
.Modeling Human Bile Acid Transport and Synthesis in Stem Cell-Derived Hepatocytes with a Patient-Specific Mutation. Stem Cell Reports. 2021; 16:309-323.
.Sox9 Is a Modifier of the Liver Disease Severity in a Mouse Model of Alagille Syndrome. Hepatology. 2020; 71:1331-1349.
.Molecular regulation of mammalian hepatic architecture. Editor, Wellik DM. Current Topics in Developmental Biology. 2019; 132:91-136.
.De novo formation of the biliary system by TGFβ-mediated hepatocyte transdifferentiation. Nature. 2018; 557:247-251.
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Stacey S. Huppert, PhD
Associate Professor
UC Department of Pediatrics
Division of Gastroenterology, Hepatology & Nutrition, Division of Developmental Biology, Cincinnati Children's Hospital Medical Center
Mailing Address:
Cincinnati Children’s Hospital Medical Center
3333 Burnet Avenue
Cincinnati, Ohio 45229
Email:
stacey.huppert@cchmc.org
Office Phone: 513-803-3871
Lab Phone: 513-636-4014