SMAD3, SMAD family member 3, 4088

N. diseases: 470; N. variants: 95
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004096
Disease: Asthma
Asthma
0.160 Biomarker disease BEFREE CONCLUSIONS The presence of miR-744 repressed bronchial epithelial cells proliferation through mediating the Smad3 pathway by modulating TGF-ß1, providing a promising therapeutic approach for epithelial function in severe asthma. 30903795 2019
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASCAT Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly Distinct. 30929738 2019
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASCAT Shared genetics of asthma and mental health disorders: a large-scale genome-wide cross-trait analysis. 31619474 2019
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease BEFREE Differentially methylated genes associated with asthma included SMAD3, SERPINC1, PROK1, IL13, RUNX3 and TIGIT. 31009112 2019
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASCAT Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study. 30552067 2019
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASCAT Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks. 29273806 2018
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASCAT A genome-wide cross-trait analysis from UK Biobank highlights the shared genetic architecture of asthma and allergic diseases. 29785011 2018
CUI: C0004096
Disease: Asthma
Asthma
0.160 PosttranslationalModification disease BEFREE Moreover, SMAD3 methylation in IIS neonates with maternal asthma was strongly and positively associated with neonatal production of IL-1β, an innate inflammatory mediator. 28011059 2017
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease BEFREE From the 417 genes interacting in these two pathways, 10 showed an excess of nominal associations, including a known asthma susceptibility locus (encoding SMAD family member 3) and other novel candidate genes. 28079285 2017
CUI: C0004096
Disease: Asthma
Asthma
0.160 Biomarker disease BEFREE MiR-23b may function as an inhibitor of asthma airway remodeling by suppressing ASMCs proliferation via direct targeting of Smad3. 28062322 2017
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
CUI: C0004096
Disease: Asthma
Asthma
0.160 Biomarker disease BEFREE We propose that PCDH1 and SMAD3 act in a single pathway in asthma susceptibility that affects sensitivity of the airway epithelium to TGF-β. 26209277 2015
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASCAT Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype. 24388013 2014
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASDB Genome-wide association study to identify genetic determinants of severe asthma. 22561531 2012
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASDB Identification of IL6R and chromosome 11q13.5 as risk loci for asthma. 21907864 2011
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASCAT A large-scale, consortium-based genomewide association study of asthma. 20860503 2010
CUI: C0004096
Disease: Asthma
Asthma
0.160 GeneticVariation disease GWASDB A large-scale, consortium-based genomewide association study of asthma. 20860503 2010