Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6370
Gene Symbol: CCL25
CCL25
0.010 AlteredExpression disease BEFREE To investigate the expression of CCL21 and CCL25 in different types of CRS and their significance in CRS development. 31825941 2020
Entrez Id: 6366
Gene Symbol: CCL21
CCL21
0.010 AlteredExpression disease BEFREE To investigate the expression of CCL21 and CCL25 in different types of CRS and their significance in CRS development. 31825941 2020
Entrez Id: 51364
Gene Symbol: ZMYND10
ZMYND10
0.030 Biomarker disease BEFREE This study assessed safety and efficacy of EDS-FLU in a large population with moderate-tosevere CRS with or without nasal polyps (CRSwNP, CRSsNP). 31815255 2020
Entrez Id: 406938
Gene Symbol: MIR146A
MIR146A
0.010 Biomarker disease BEFREE Importantly, C-miR146a showed efficacy in dampening severe inflammation in clinically relevant models of chimeric antigen receptor (CAR) T-cell-induced cytokine release syndrome (CRS). 31805184 2020
Entrez Id: 7124
Gene Symbol: TNF
TNF
0.100 GeneticVariation disease BEFREE Chronic rhinosinusitis (CRS) is a frequently observed condition in patients with immunodeficiency secondary to tumor necrosis factor alpha inhibitors (TNFαis). 31794110 2020
Entrez Id: 51364
Gene Symbol: ZMYND10
ZMYND10
0.030 Biomarker disease BEFREE EDS-FLU has demonstrated significant improvement in managing symptoms and polyps in CRS. 31789927 2020
Entrez Id: 85480
Gene Symbol: TSLP
TSLP
0.030 GeneticVariation disease BEFREE This study was performed to determine whether there was any association between abnormal DNA methylation of a thymic stromal lymphopoietin (TSLP) locus and pathogenesis of chronic rhinosinusitis (CRS). 31768185 2019
Entrez Id: 2077
Gene Symbol: ERF
ERF
0.440 Biomarker disease BEFREE These cell lines provide good materials to understand the roles of ERF in development, trophoblast differentiation and craniosynostosis for further studies. 31743839 2019
Entrez Id: 10631
Gene Symbol: POSTN
POSTN
0.090 Biomarker disease BEFREE As for CRS, we discussed the studies that investigated nasal nitric oxide (nNO), pendrin, and periostin. 31731479 2019
Entrez Id: 5172
Gene Symbol: SLC26A4
SLC26A4
0.020 Biomarker disease BEFREE As for CRS, we discussed the studies that investigated nasal nitric oxide (nNO), pendrin, and periostin. 31731479 2019
Entrez Id: 1490
Gene Symbol: CCN2
CCN2
0.010 Biomarker disease BEFREE Meanwhile, the CTGF-LRP pathway might be one of the therapeutic targets for myocardial infarction caused type 2 CRS which showed a positive change after BXYS treatment and is worthy of further exploration. 31708787 2019
Entrez Id: 3123
Gene Symbol: HLA-DRB1
HLA-DRB1
0.020 Biomarker disease BEFREE By multivariable analysis, only pretransplant disease status (hazard ratio, HR: 6.84, P = .005) and HLA-DRB1 mismatching (HR: 17.19, P = .003) remained independent predictors of grade ≥3 CRS. 31702882 2020
Entrez Id: 930
Gene Symbol: CD19
CD19
0.100 Biomarker disease BEFREE These data support the contention that early intervention with tocilizumab and/or corticosteroids in subjects with early signs of CRS is without negative impact on the antitumor potency of CD19 CAR T cells. 31697826 2019
Entrez Id: 3604
Gene Symbol: TNFRSF9
TNFRSF9
0.010 Biomarker disease BEFREE Here, we report on the low incidence of severe cytokine release syndrome (CRS) in a subject treated with a CAR T-cell product composed of a defined ratio CD4:CD8 T-cell composition with a 4-1BB:zeta CAR targeting CD19 who also recieved early intervention treatment. 31697826 2019
Entrez Id: 8600
Gene Symbol: TNFSF11
TNFSF11
0.110 Biomarker disease BEFREE CRS mouse models were treated with anti-RANKL. 31693309 2019
Entrez Id: 4982
Gene Symbol: TNFRSF11B
TNFRSF11B
0.020 AlteredExpression disease BEFREE RANKL was upregulated whereas decoy receptor osteoprotegerin (OPG) was downregulated in CRS. 31693309 2019
Entrez Id: 383
Gene Symbol: ARG1
ARG1
0.010 AlteredExpression disease BEFREE Thus, the present study investigates the activity of arginase I (ARG1) and II (ARG2) in CRS and its possible involvement in the pathogenesis of this disease. 31683763 2019
Entrez Id: 384
Gene Symbol: ARG2
ARG2
0.010 AlteredExpression disease BEFREE Increased ARG2 expression was found in patients with CRS without nasal polyposis (FR 3.14 ± 1.16 vs. 1.31 ± 0.21, <i>p</i> = 0.0175), in non-allergic CRS (FR 2.55 ± 0.52 vs. 1.31 ± 0.21, <i>p</i> = 0.005), and non-asthmatic CRS (FR 2.42 ± 0.57 vs. 1.31 ± 0.21, <i>p</i> = 0.028). 31683763 2019
Entrez Id: 871
Gene Symbol: SERPINH1
SERPINH1
0.010 Biomarker disease BEFREE HSP47 is increased in patients with CRS without nasal polyps. 31664133 2019
Entrez Id: 4318
Gene Symbol: MMP9
MMP9
0.070 AlteredExpression disease BEFREE MMP-1 and MMP-9 expression was increased in the nasal tissues of smokers with asthma and CRS via real-time PCR and western blot. 31653934 2019
Entrez Id: 4312
Gene Symbol: MMP1
MMP1
0.020 AlteredExpression disease BEFREE MMP-1 and MMP-9 expression was increased in the nasal tissues of smokers with asthma and CRS via real-time PCR and western blot. 31653934 2019
Entrez Id: 6278
Gene Symbol: S100A7
S100A7
0.030 AlteredExpression disease BEFREE The reported differential expression patterns and activities of psoriasin and calgranulins suggest that S100 proteins exert unique and concerted roles in mediating immunity in different subtypes of CRS. 31644435 2020
Entrez Id: 6280
Gene Symbol: S100A9
S100A9
0.020 Biomarker disease BEFREE Psoriasin (S100A7) and calgranulins (S100A8, S100A9, and S100A12) are S100 proteins that have been studied for their immune-mediating responses to pathogens within the context of CRS. 31644435 2020
Entrez Id: 6283
Gene Symbol: S100A12
S100A12
0.020 Biomarker disease BEFREE Psoriasin (S100A7) and calgranulins (S100A8, S100A9, and S100A12) are S100 proteins that have been studied for their immune-mediating responses to pathogens within the context of CRS. 31644435 2020
Entrez Id: 2263
Gene Symbol: FGFR2
FGFR2
0.700 GeneticVariation disease BEFREE Crouzon syndrome (CS), which results from fibroblast growth factor receptor 2 mutations, is associated with craniosynostosis, exophthalmos, and other symptoms. 31640617 2019