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Human Genetics|September 8, 2022
Nonsense mutation in the novel PERCC1 gene as a genetic cause of congenital diarrhea and enteropathyDina Marek-Yagel, Emily Stenke, Ben Pode-Shakked, et al.
Nature Communications|September 23, 2020
Enteroendocrine cells couple nutrient sensing to nutrient absorption by regulating ion transportHeather A McCauley, Andrea L Matthis, Jacob R Enriquez, et al.
Nature Biomedical Engineering|August 29, 2018
Mechanically induced development and maturation of human intestinal organoids in vivoHolly M Poling, David Wu, Nicole Brown, et al.
Human Mutation|October 21, 2010
Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tractStefania Gimelli, Gianluca Caridi, Silvana Beri, et al.
Journal of Crohn'S & Colitis|August 30, 2024
Eicosatetraynoic Acid Regulates Profibrotic Pathways in an Induced Pluripotent Stem Cell-Derived Macrophage-Human Intestinal Organoid Model of Crohn's DiseaseIngrid Jurickova, Benjamin W Dreskin, Elizabeth Angerman, et al.
Cellular and Molecular Gastroenterology and Hepatology|January 7, 2023
Enteroendocrine Cells Protect the Stem Cell Niche by Regulating Crypt Metabolism in Response to NutrientsHeather A McCauley, Anne Marie Riedman, Jacob R Enriquez, et al.
Thorax|August 19, 2015
β-Blockers are associated with a reduction in COPD exacerbationsSurya P Bhatt, James M Wells, Gregory L Kinney, et al.
Disease Models & Mechanisms|December 17, 2020
Disruption of a hedgehog-foxf1-rspo2 signaling axis leads to tracheomalacia and a loss of sox9+ tracheal chondrocytesTalia Nasr, Andrea M Holderbaum, Praneet Chaturvedi, et al.
Development (Cambridge, England)|April 8, 2024
RFX6 regulates human intestinal patterning and function upstream of PDX1J Guillermo Sanchez, Scott Rankin, Emily Paul, et al.
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