Tumor Cell Invasion
|
0.030 |
Biomarker
|
phenotype |
BEFREE |
Stem cell transcription factor NANOG controls cell migration and invasion via dysregulation of E-cadherin and FoxJ1 and contributes to adverse clinical outcome in ovarian cancers.
|
22945654 |
2013 |
Allergic rhinitis (disorder)
|
0.030 |
Biomarker
|
disease |
BEFREE |
To investigate the association between single nucleotide polymorphisms (SNPs) of human FOXJ1 and allergic rhinitis, we scanned the whole human FOXJ1 gene, including the promoter region, by direct sequencing of DNA from 32 individuals.
|
16518568 |
2006 |
Hydrocephalus
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Heterozygous de novo mutations in FOXJ1, which encodes a well-known member of the forkhead transcription factors important for ciliogenesis of motile cilia, cause a motile ciliopathy that is characterized by hydrocephalus internus, chronic destructive airway disease, and randomization of left/right body asymmetry.
|
31630787 |
2019 |
Carcinogenesis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
FOXJ1, a member of the FOX family, has been found to participate in tumorigenesis.
|
31062413 |
2019 |
Ciliopathies
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Heterozygous de novo mutations in FOXJ1, which encodes a well-known member of the forkhead transcription factors important for ciliogenesis of motile cilia, cause a motile ciliopathy that is characterized by hydrocephalus internus, chronic destructive airway disease, and randomization of left/right body asymmetry.
|
31630787 |
2019 |
Ciliopathies
|
0.020 |
GeneticVariation
|
disease |
BEFREE |
Therefore, based on this FOXJ1 network study we have predicted important effectors in the motile cilia interactome, which are possibly associated with ciliary biology and/or function and are likely to further our understanding of the pathophysiology in ciliopathies like PCD.
|
30881373 |
2019 |
Carcinoma
|
0.020 |
AlteredExpression
|
group |
BEFREE |
We concluded that FOXJ1 was expressed in low quantities in bladder epithelial carcinoma, which was closely correlated with the biological characteristics of the tumor.
|
29434839 |
2018 |
Hydrocephalus
|
0.020 |
Biomarker
|
disease |
BEFREE |
Mechanistic analyses revealed a novel NF-κB-independent IKK2 activity stabilizing Foxj1 in mature ECs, and we found that known IKK2 inhibitors including viruses and growth factors robustly induced Foxj1 degradation, EC de-differentiation, and hydrocephalus.
|
29695808 |
2018 |
Malignant neoplasm of stomach
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Additionally, FOXJ1 was overexpressed in GC tissues and cell lines, and its expression was negatively correlated with that of miR-6852 in GC tissues.
|
30214548 |
2018 |
Stomach Carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Additionally, FOXJ1 was overexpressed in GC tissues and cell lines, and its expression was negatively correlated with that of miR-6852 in GC tissues.
|
30214548 |
2018 |
Carcinoma of bladder
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
The link between FOXJ1 expression level in bladder carcinoma and tumor recurrence.
|
29434839 |
2018 |
Carcinoma of bladder
|
0.020 |
Biomarker
|
disease |
BEFREE |
Targeting FOXJ1 could be a potential therapeutic strategy in bladder cancer.
|
29129693 |
2018 |
Tumor Progression
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
The role of FOXJ1 in cancer progression is still elusive and controversial.
|
28209947 |
2017 |
Carcinoma
|
0.020 |
AlteredExpression
|
group |
BEFREE |
Anaplastic ependymomas as well as choroid plexus carcinomas show decreased FOXJ1 expression and its associated ciliogenesis programme genes.
|
26690880 |
2016 |
Malignant neoplasm of stomach
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
We thus investigated FOXJ1 expression in gastric cancer and analyzed its correlations with tumor progression and prognosis.
|
24809300 |
2015 |
Neoplasm Metastasis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
In addition, the relation between FOXJ1 and metastasis was investigated in another 40 pairs of primary lesions and corresponding lymph node metastases.
|
24809300 |
2015 |
Tumor Progression
|
0.020 |
AlteredExpression
|
phenotype |
BEFREE |
We thus investigated FOXJ1 expression in gastric cancer and analyzed its correlations with tumor progression and prognosis.
|
24809300 |
2015 |
Carcinogenesis
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
However, the role of FOXJ1 in tumorigenesis remains largely unknown or even conflicting.
|
24809300 |
2015 |
Stomach Carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
Decreased FOXJ1 expression was significantly correlated with clinic stage, lymph node metastasis, and distant metastasis, and lower FOXJ1 expression independently predicted shorter survival time in gastric carcinoma.
|
24809300 |
2015 |
Malignant neoplasm of breast
|
0.020 |
Biomarker
|
disease |
BEFREE |
Recent studies suggested that FOXJ1 may function as a tumor suppressor gene in breast cancer.
|
22488567 |
2013 |
Neoplasm Metastasis
|
0.020 |
GeneticVariation
|
phenotype |
BEFREE |
Multivariate analysis indicated that tumor grade (P < 0.0001), metastasis (P = 0.0451), tumor size (P = 0.0459), FOXJ1 (P = 0.0011), and Ki-67 (P = 0.0006) were independent prognostic markers for HCC.
|
22488567 |
2013 |
Breast Carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Recent studies suggested that FOXJ1 may function as a tumor suppressor gene in breast cancer.
|
22488567 |
2013 |
Malignant neoplasm of breast
|
0.020 |
Biomarker
|
disease |
BEFREE |
By conducting this initial screen on EMT6 cells and applying protein function and genomic structure criteria to genes identified as upregulated in response to 5-azadC/TSA, we were able to identify two characterized breast cancer TSGs (Timp3 and Rprm) and four putative TSGs (Atp1B2, Dusp2, FoxJ1 and Smpd3) silenced in this line.
|
18836996 |
2009 |
Breast Carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
By conducting this initial screen on EMT6 cells and applying protein function and genomic structure criteria to genes identified as upregulated in response to 5-azadC/TSA, we were able to identify two characterized breast cancer TSGs (Timp3 and Rprm) and four putative TSGs (Atp1B2, Dusp2, FoxJ1 and Smpd3) silenced in this line.
|
18836996 |
2009 |
Laryngeal Squamous Cell Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
FOXJ1 knockdown suppressed glycolysis in LSCC cells, which was illustrated by the reduced glucose consumption and lactate production.
|
31062413 |
2019 |