{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Afelik S"],"funding":["NIDDK NIH HHS"],"pagination":["1744-53"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3328176"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["139(10)"],"pubmed_abstract":["Early pancreatic morphogenesis is characterized by the transformation of an uncommitted pool of pancreatic progenitor cells into a branched pancreatic epithelium that consists of 'tip' and 'trunk' domains. These domains have distinct molecular signatures and differentiate into distinct pancreatic cell lineages. Cells at the branched tips of the epithelium develop into acinar cells, whereas cells in the trunk subcompartment differentiate into endocrine and duct cells. Recent genetic analyses have highlighted the role of key transcriptional regulators in the specification of these subcompartments. Here, we analyzed in mice the role of Notch signaling in the patterning of multipotent pancreatic progenitor cells through mosaic overexpression of a Notch signaling antagonist, dominant-negative m"],"journal":["Development (Cambridge, England)"],"pubmed_title":["Notch-mediated patterning and cell fate allocation of pancreatic progenitor cells."],"pmcid":["PMC3328176"],"funding_grant_id":["R01 DK061220","R01-DK061220"],"pubmed_authors":["Nieuwoudt S","Afelik S","Deering T","Jensen J","Bukys MA","Qu X","Macdonald RJ","Hasrouni E","Rogers W"],"additional_accession":[]},"is_claimable":false,"name":"Notch-mediated patterning and cell fate allocation of pancreatic progenitor cells.","description":"Early pancreatic morphogenesis is characterized by the transformation of an uncommitted pool of pancreatic progenitor cells into a branched pancreatic epithelium that consists of 'tip' and 'trunk' domains. These domains have distinct molecular signatures and differentiate into distinct pancreatic cell lineages. Cells at the branched tips of the epithelium develop into acinar cells, whereas cells in the trunk subcompartment differentiate into endocrine and duct cells. Recent genetic analyses have highlighted the role of key transcriptional regulators in the specification of these subcompartments. Here, we analyzed in mice the role of Notch signaling in the patterning of multipotent pancreatic progenitor cells through mosaic overexpression of a Notch signaling antagonist, dominant-negative m","dates":{"release":"2012-01-01T00:00:00Z","publication":"2012 May","modification":"2025-05-29T21:26:55.415Z","creation":"2025-05-29T21:26:55.415Z"},"accession":"S-EPMC3328176","cross_references":{"pubmed":["22461559"],"doi":["10.1242/dev.075804"]}}