{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Magaletta ME"],"funding":["NIDDK NIH HHS","NIAID NIH HHS"],"pagination":["457"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8786836"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["13(1)"],"pubmed_abstract":["Maldevelopment of the pharyngeal endoderm, an embryonic tissue critical for patterning of the pharyngeal region and ensuing organogenesis, ultimately contributes to several classes of human developmental syndromes and disorders. Such syndromes are characterized by a spectrum of phenotypes that currently cannot be fully explained by known mutations or genetic variants due to gaps in characterization of critical drivers of normal and dysfunctional development. Despite the disease-relevance of pharyngeal endoderm, we still lack a comprehensive and integrative view of the molecular basis and gene regulatory networks driving pharyngeal endoderm development. To close this gap, we apply transcriptomic and chromatin accessibility single-cell sequencing technologies to generate a multi-omic develop"],"journal":["Nature communications"],"pubmed_title":["Integration of single-cell transcriptomes and chromatin landscapes reveals regulatory programs driving pharyngeal organ development."],"pmcid":["PMC8786836"],"funding_grant_id":["U01 DK104218","T32 AI132152","R01 AI132963"],"pubmed_authors":["Aliee H","Kernfeld EM","Parsons TJ","Lobo M","Huey JD","Magaletta ME","Theis FJ","Maehr R"],"additional_accession":[]},"is_claimable":false,"name":"Integration of single-cell transcriptomes and chromatin landscapes reveals regulatory programs driving pharyngeal organ development.","description":"Maldevelopment of the pharyngeal endoderm, an embryonic tissue critical for patterning of the pharyngeal region and ensuing organogenesis, ultimately contributes to several classes of human developmental syndromes and disorders. Such syndromes are characterized by a spectrum of phenotypes that currently cannot be fully explained by known mutations or genetic variants due to gaps in characterization of critical drivers of normal and dysfunctional development. Despite the disease-relevance of pharyngeal endoderm, we still lack a comprehensive and integrative view of the molecular basis and gene regulatory networks driving pharyngeal endoderm development. To close this gap, we apply transcriptomic and chromatin accessibility single-cell sequencing technologies to generate a multi-omic develop","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Jan","modification":"2026-07-16T16:07:00.476Z","creation":"2025-04-06T03:55:08.894Z"},"accession":"S-EPMC8786836","cross_references":{"pubmed":["35075189"],"doi":["10.1038/s41467-022-28067-4"]}}