{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"submitter":["Heydarian M"],"funding":["Bundesministerium für Bildung und Forschung","NHLBI NIH HHS","International Research Group ‘Role of BMP signaling’","Research Training Group Targets in Toxicology","Helmholtz Foundation"],"pagination":["1176-1186"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC9685723"],"repository":["biostudies-literature"],"omics_type":["Unknown"],"volume":["77(12)"],"pubmed_abstract":["<h4>Introduction</h4>Chronic lung disease, that is, bronchopulmonary dysplasia (BPD) is the most common complication in preterm infants and develops as a consequence of the misguided formation of the gas-exchange area undergoing prenatal and postnatal injury. Subsequent vascular disease and its progression into pulmonary arterial hypertension critically determines long-term outcome in the BPD infant but lacks identification of early, disease-defining changes.<h4>Methods</h4>We link impaired bone morphogenetic protein (BMP) signalling to the earliest onset of vascular pathology in the human preterm lung and delineate the specific effects of the most prevalent prenatal and postnatal clinical risk factors for lung injury mimicking clinically relevant conditions in a multilayered animal model "],"journal":["Thorax"],"pubmed_title":["Relationship between impaired BMP signalling and clinical risk factors at early-stage vascular injury in the preterm infant."],"pmcid":["PMC9685723"],"funding_grant_id":["01KI1010I","GRK2338","K08 HL143051","01KI1010C","01KI07110","NWG VH-NG-829"],"pubmed_authors":["Kamgari N","Pritzke T","Hafner F","Sucre J","Forster K","Hubener C","Spiekerkoetter E","Hilgendorff A","Morty RE","Oak P","Desai TJ","Tian X","Zhang X","Koschlig M","Morrell N","Petrera A","Kirsten H","Kindt A","Sudheendra D","Heydarian M","Gonzalez-Rodriguez E","Ahnert P","Flemmer AW","Yildirim AO"],"additional_accession":[]},"is_claimable":false,"name":"Relationship between impaired BMP signalling and clinical risk factors at early-stage vascular injury in the preterm infant.","description":"<h4>Introduction</h4>Chronic lung disease, that is, bronchopulmonary dysplasia (BPD) is the most common complication in preterm infants and develops as a consequence of the misguided formation of the gas-exchange area undergoing prenatal and postnatal injury. Subsequent vascular disease and its progression into pulmonary arterial hypertension critically determines long-term outcome in the BPD infant but lacks identification of early, disease-defining changes.<h4>Methods</h4>We link impaired bone morphogenetic protein (BMP) signalling to the earliest onset of vascular pathology in the human preterm lung and delineate the specific effects of the most prevalent prenatal and postnatal clinical risk factors for lung injury mimicking clinically relevant conditions in a multilayered animal model ","dates":{"release":"2022-01-01T00:00:00Z","publication":"2022 Dec","modification":"2026-06-15T05:54:15.043Z","creation":"2024-11-12T11:09:18.668Z"},"accession":"S-EPMC9685723","cross_references":{"pubmed":["35580897"],"doi":["10.1136/thoraxjnl-2021-218083"]}}