Acquired Immunodeficiency Syndrome
|
0.010 |
Biomarker
|
group |
BEFREE |
Biopsy samples from five acquired immune deficiency syndrome (AIDS)-Kaposi's sarcomas and one non-AIDS-associated Kaposi's sarcoma were assayed by in situ RNA hybridization onto paraformaldehyde-fixed, paraffin-embedded skin sections for the presence of two fibroblast growth factor gene transcripts, FGFB and FGF5.
|
1987771 |
1991 |
Adenocarcinoma
|
0.010 |
AlteredExpression
|
group |
BEFREE |
As a normal protein with significant overexpression by multiple adenocarcinomas and little normal tissue expression, FGF-5 represents an immunotherapy target with potential utility against a broad array of nonmelanoma cancers.
|
11454700 |
2001 |
Alopecia
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Genetic prediction of male pattern baldness.
|
28196072 |
2017 |
Alopecia, Androgenetic, 1
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Detection and interpretation of shared genetic influences on 42 human traits.
|
27182965 |
2016 |
Alopecia, Androgenetic, 1
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Alopecia, Androgenetic, 2
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Alopecia, Androgenetic, 2
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Detection and interpretation of shared genetic influences on 42 human traits.
|
27182965 |
2016 |
Alopecia, Androgenetic, 3
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Detection and interpretation of shared genetic influences on 42 human traits.
|
27182965 |
2016 |
Alopecia, Androgenetic, 3
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Alopecia, Male Pattern
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Alopecia, Male Pattern
|
0.110 |
Biomarker
|
disease |
BEFREE |
The 63 loci explain ∼39% of the phenotypic variance in MPB and highlight several plausible candidate genes (FGF5, IRF4, DKK2) and pathways (melatonin signalling, adipogenesis) that are likely to be implicated in the key-pathophysiological features of MPB and may represent promising targets for the development of novel therapeutic options.
|
28272467 |
2017 |
Alopecia, Male Pattern
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Detection and interpretation of shared genetic influences on 42 human traits.
|
27182965 |
2016 |
Androgenetic Alopecia
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
GWAS for male-pattern baldness identifies 71 susceptibility loci explaining 38% of the risk.
|
29146897 |
2017 |
Androgenetic Alopecia
|
0.100 |
GeneticVariation
|
disease |
GWASCAT |
Detection and interpretation of shared genetic influences on 42 human traits.
|
27182965 |
2016 |
Atrial Fibrillation
|
0.300 |
Biomarker
|
disease |
CTD_human |
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology.
|
30061737 |
2018 |
Brain Neoplasms
|
0.010 |
Biomarker
|
group |
BEFREE |
In summary, we demonstrate for the first time that FGF5 contributes to the malignant progression of human astrocytic brain tumours by both autocrine and paracrine effects.
|
18362893 |
2008 |
Breast Carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
CONCLUSIONS Our results suggest that FGF5 is an independent protective factor for BC patients.
|
29804124 |
2018 |
Breast Carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
We have identified the TAF/FGF5/FGFR2/c-Src/HER2 axis as an escape pathway responsible for HER2 targeted therapies resistance in breast cancer which can be reversed by FGFR inhibitors.
|
31699826 |
2020 |
Cataract
|
0.100 |
Biomarker
|
disease |
HPO |
|
|
|
Central Serous Chorioretinopathy
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In mouse models of triple negative breast cancer (TNBC), Hedgehog ligand produced by neoplastic cells reprograms cancer-associated fibroblasts (CAFs) to provide a supportive niche for the acquisition of a chemo-resistant, cancer stem cell (CSC) phenotype via FGF5 expression and production of fibrillar collagen.
|
30042390 |
2018 |
Childhood Osteosarcoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
<b>Results:</b> FGF5 was significantly upregulated in OS tissues and cells, and closely associated with poor differentiation, larger tumor size, lymph node metastasis, and advanced TNM stage.
|
31372048 |
2019 |
Childhood Osteosarcoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Taken together, our data indicated that miR-567 may function as a tumor suppressor by negatively regulating FGF5 and be potential therapeutic targets for the treatment of OS.
|
29743851 |
2018 |
Congenital absence of germinal epithelium of testes
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Then, we evaluated the expression of FGF5, a growth factor which is downregulated in SCOS Sertoli cells, in human primary cultured Sertoli cells and testicular tissue.
|
30670081 |
2019 |
Degenerative disorder
|
0.010 |
Biomarker
|
group |
BEFREE |
The goal of these experiments was to evaluate the potential of the fibroblast growth factor family members FGF-5 and FGF-18 to rescue photoreceptors from cell death in retinal degenerative disease.
|
11319911 |
2001 |
Degenerative polyarthritis
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We noted and verified that the expression of fibroblast growth factor-5 (FGF5) was higher in Sertoli cells of OA patients than that of SCOS patients at both transcriptional and translational levels.
|
30670081 |
2019 |