Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2255
Gene Symbol: FGF10
FGF10
0.070 Biomarker disease BEFREE Elevated expression of miR-421 was evident, while Fgf10 was poorly expressed in BPD. upregulation of miR-421 and silence of Fgf10 aggravated inflammatory response in lung tissue and promoted lung cell apoptosis in BPD. 31144392 2019
Entrez Id: 2255
Gene Symbol: FGF10
FGF10
0.070 AlteredExpression disease BEFREE Finally, we evaluated changes in FGF10, surfactant protein C (SFTPC), platelet endothelial cell adhesion molecule (PECAM) and alpha-smooth muscle actin 2 (α-SMA) expression in human lung samples from patients suffering from BPD. 30566624 2019
Entrez Id: 2255
Gene Symbol: FGF10
FGF10
0.070 Biomarker disease BEFREE <i>Fgf10</i> signaling is dysregulated in different human lung diseases including bronchopulmonary dysplasia (BPD), idiopathic pulmonary fibrosis (IPF), and chronic obstructive pulmonary disease (COPD), suggesting that dysregulation of the FGF10 pathway is critical to the pathogenesis of several human lung diseases. 30319693 2018
Entrez Id: 2255
Gene Symbol: FGF10
FGF10
0.070 Biomarker disease BEFREE Here we review the cellular and molecular mechanisms linking FGF10 to multiple lung diseases, from bronchopulmonary dysplasia in extremely preterm neonates, cystic fibrosis in children, and chronic adult lung disorders. 30429870 2018
Entrez Id: 2255
Gene Symbol: FGF10
FGF10
0.070 Biomarker disease BEFREE Thus, to investigate the protective effects of FGF-10 on hyperoxia induced BPD in neonatal mice will provide a new strategy for the treatment of BPD. 28861146 2017
Entrez Id: 2255
Gene Symbol: FGF10
FGF10
0.070 Biomarker disease BEFREE Fgf10 deficiency is causative for lethality in a mouse model of bronchopulmonary dysplasia. 27770432 2017
Entrez Id: 2255
Gene Symbol: FGF10
FGF10
0.070 AlteredExpression disease BEFREE Reduced FGF-10 expression may therefore link the innate immune system and impaired lung development in bronchopulmonary dysplasia. 17071719 2007