Stephen Duncan

Affiliations: 
Cell Biology, Neurobiology, and Anatomy Medical College of Wisconsin, Milwaukee, WI, United States 
Area:
Cell Biology, Human Development, Molecular Biology
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"Stephen Duncan"
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Publications

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Doueiry C, Kappler CS, Martinez-Morant C, et al. (2024) A PNPLA3-Deficient iPSC-Derived Hepatocyte Screen Identifies Pathways to Potentially Reduce Steatosis in Metabolic Dysfunction-Associated Fatty Liver Disease. International Journal of Molecular Sciences. 25
Blaszkiewicz J, Duncan SA. (2024) Use of stem cell-derived hepatocytes to model liver disease. Journal of Hepatology
Kurz J, Weiss AC, Lüdtke TH, et al. (2022) GATA6 is a crucial factor for Myocd expression in the visceral smooth muscle cell differentiation program of the murine ureter. Development (Cambridge, England). 149
Heslop JA, Pournasr B, Duncan SA. (2022) Chromatin remodeling is restricted by transient GATA6 binding during iPSC differentiation to definitive endoderm. Iscience. 25: 104300
Heslop JA, Pournasr B, Liu JT, et al. (2021) GATA6 defines endoderm fate by controlling chromatin accessibility during differentiation of human-induced pluripotent stem cells. Cell Reports. 35: 109145
Pournasr B, Duncan SA. (2020) Generation of isogenic Propionyl-CoA carboxylase beta subunit (PCCB) deficient induced pluripotent stem cell lines. Stem Cell Research. 48: 101953
Heslop JA, Duncan SA. (2020) FoxA factors: the chromatin key and doorstop essential for liver development and function. Genes & Development. 34: 1003-1004
Corbett JL, Duncan SA. (2019) iPSC-Derived Hepatocytes as a Platform for Disease Modeling and Drug Discovery. Frontiers in Medicine. 6: 265
DeLaForest A, Di Furio F, Jing R, et al. (2018) HNF4A Regulates the Formation of Hepatic Progenitor Cells from Human iPSC-Derived Endoderm by Facilitating Efficient Recruitment of RNA Pol II. Genes. 10
Heslop JA, Duncan SA. (2018) The use of human pluripotent stem cells for modelling liver development and disease. Hepatology (Baltimore, Md.)
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