{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Xu Y"],"funding":["Clinical Discipline Project of Shanghai Pudong","China Postdoctoral Science Foundation","National Natural Science Foundation of China"],"pagination":["e2305631"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC10987150"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["11(13)"],"pubmed_abstract":["Stem cell-derived pancreatic progenitors (SC-PPs), as an unlimited source of SC-derived β (SC-β) cells, offers a robust tool for diabetes treatment in stem cell-based transplantation, disease modeling, and drug screening. Whereas, PDX1<sup>+</sup>/NKX6.1<sup>+</sup> PPs enhances the subsequent endocrine lineage specification and gives rise to glucose-responsive SC-β cells in vivo and in vitro. To identify the regulators that promote induction efficiency and cellular function maturation, single-cell RNA-sequencing is performed to decipher the transcriptional landscape during PPs differentiation. The comprehensive evaluation of functionality demonstrated that manipulating LINC MIR503HG using CRISPR in PP cell fate decision can improve insulin synthesis and secretion in mature SC-β cells, wit"],"journal":["Advanced science (Weinheim, Baden-Wurttemberg, Germany)"],"pubmed_title":["LINC MIR503HG Controls SC-β Cell Differentiation and Insulin Production by Targeting CDH1 and HES1."],"pmcid":["PMC10987150"],"funding_grant_id":["PWYts 2021-06","82372133","2021M690085","82001860","82070654","82272170","82001977"],"pubmed_authors":["Mao S","Lu Y","Zhang M","Yuan J","Wang L","Jiang Z","Fan H","Yu B","Huang Y","Wan J","Wang Z","Xu Y","Zhu S"],"additional_accession":[]},"is_claimable":false,"name":"LINC MIR503HG Controls SC-β Cell Differentiation and Insulin Production by Targeting CDH1 and HES1.","description":"Stem cell-derived pancreatic progenitors (SC-PPs), as an unlimited source of SC-derived β (SC-β) cells, offers a robust tool for diabetes treatment in stem cell-based transplantation, disease modeling, and drug screening. Whereas, PDX1<sup>+</sup>/NKX6.1<sup>+</sup> PPs enhances the subsequent endocrine lineage specification and gives rise to glucose-responsive SC-β cells in vivo and in vitro. To identify the regulators that promote induction efficiency and cellular function maturation, single-cell RNA-sequencing is performed to decipher the transcriptional landscape during PPs differentiation. The comprehensive evaluation of functionality demonstrated that manipulating LINC MIR503HG using CRISPR in PP cell fate decision can improve insulin synthesis and secretion in mature SC-β cells, wit","dates":{"release":"2024-01-01T00:00:00Z","publication":"2024 Apr","modification":"2025-04-05T14:46:09.263Z","creation":"2024-12-04T06:20:44.247Z"},"accession":"S-EPMC10987150","cross_references":{"pubmed":["38243869"],"doi":["10.1002/advs.202305631"]}}