Body Height
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Leveraging Polygenic Functional Enrichment to Improve GWAS Power.
|
30595370 |
2019 |
von Willebrand's factor (lab test)
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Ischemic stroke is associated with the ABO locus: the EuroCLOT study.
|
23381943 |
2013 |
Neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
Xenograft models were used to measure the effect of UNC5A knockdown on tumor growth and metastasis.
|
29720215 |
2018 |
Liver carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Such data indicate that cooperation between the UPR and UNC5A depletion as previously observed by ourselves in HCC patients samples may foster liver cancer development and growth.
|
29277614 |
2018 |
Liver carcinoma
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
UNC5A transcript was found strongly downregulated in HCC samples (33-fold; P<0.0001) as compared with non-HCC samples.
|
28783179 |
2017 |
Neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
Together, these data suggest an important role for UNC5A, a candidate tumor suppressor, in predicting response to DNA damage induced by chemotherapeutic drug and regulating cell death in bladder cancer.
|
24737586 |
2014 |
Colorectal Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Immunostaining was performed for Netrin-1 (deleted in colorectal carcinoma [DCC], UNC5A) and GDNF receptors (rearranged during transfection [Ret], glycosylphosphatidylinositol-linked cell surface receptors [GFRα1, GFRα2, GFRα3]).
|
30811036 |
2019 |
Malignant neoplasm of breast
|
0.010 |
Biomarker
|
disease |
BEFREE |
Tissue microarray and immunohistochemistry were utilized to determine the prognostic value of UNC5A in breast cancer.
|
29720215 |
2018 |
Neoplasm Metastasis
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Xenograft models were used to measure the effect of UNC5A knockdown on tumor growth and metastasis.
|
29720215 |
2018 |
Breast Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Tissue microarray and immunohistochemistry were utilized to determine the prognostic value of UNC5A in breast cancer.
|
29720215 |
2018 |
Mammary Neoplasms
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Consistent with in vitro results, UNC5A expression negatively correlated with EGFR expression in breast tumors, and lower expression of UNC5A, particularly in ERα<sup>+</sup>/PR<sup>+</sup>/HER2<sup>-</sup> tumors, was associated with poor outcome.
|
29720215 |
2018 |
Secondary Neoplasm
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Knockdown of the E2-inducible UNC5A resulted in altered basal gene expression affecting plasma membrane integrity and ERα signaling, as evident from ligand-independent activity of ERα, altered turnover of phosphorylated ERα, unique E2-dependent expression of genes effecting histone demethylase activity, enhanced upregulation of E2-inducible genes such as BCL2, and E2-independent tumorigenesis accompanied by multiorgan metastases.
|
29720215 |
2018 |
Malignant Neoplasms
|
0.010 |
Biomarker
|
group |
BEFREE |
The present study investigated crosstalks between HCV infection and UNC5A, a netrin-1 dependence receptor that is inactivated in cancer.
|
28783179 |
2017 |
Glioma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Taken together, these results suggested netrin-1 promotes glioma cell proliferation by activating NF-κB signaling via UNC5A, netrin-1 may be a potential therapeutic target for the treatment of glioma.
|
28710382 |
2017 |
Hepatitis C
|
0.010 |
Biomarker
|
disease |
BEFREE |
Consistent results were obtained in vitro showing HCV-dependent depletion of UNC5A in HCV-infected hepatocyte-like cells and in primary human hepatocytes.
|
28783179 |
2017 |
Liver Cirrhosis
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
UNC5A mRNA is downregulated in F2 (3-fold; P=0.009), in F3 (10-fold, P=0.0004) and more dramatically so in F4/cirrhosis (44-fold; P<0.0001) histological stages of HCV(+) hepatic lesions compared to histologically matched HCV(-) tissues.
|
28783179 |
2017 |
Myasthenia Gravis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Antibodies against Netrin-1 receptors (DCC and UNC5a) and Caspr2 often coexist and associate with thymoma in patients with neuromyotonia and myasthenia gravis.
|
28251919 |
2017 |
Thymoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Antibodies against Netrin-1 receptors (DCC and UNC5a) and Caspr2 often coexist and associate with thymoma in patients with neuromyotonia and myasthenia gravis.
|
28251919 |
2017 |
Isaacs syndrome
|
0.010 |
Biomarker
|
disease |
BEFREE |
Antibodies against Netrin-1 receptors (DCC and UNC5a) and Caspr2 often coexist and associate with thymoma in patients with neuromyotonia and myasthenia gravis.
|
28251919 |
2017 |
Primary malignant neoplasm
|
0.010 |
Biomarker
|
group |
BEFREE |
The present study investigated crosstalks between HCV infection and UNC5A, a netrin-1 dependence receptor that is inactivated in cancer.
|
28783179 |
2017 |
Hepatocarcinogenesis
|
0.010 |
Biomarker
|
disease |
BEFREE |
Such data argue for the evaluation of the implication of UNC5A in liver carcinogenesis.
|
28783179 |
2017 |
Cirrhosis
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
UNC5A mRNA is downregulated in F2 (3-fold; P=0.009), in F3 (10-fold, P=0.0004) and more dramatically so in F4/cirrhosis (44-fold; P<0.0001) histological stages of HCV(+) hepatic lesions compared to histologically matched HCV(-) tissues.
|
28783179 |
2017 |
Malignant neoplasm of urinary bladder
|
0.010 |
Biomarker
|
disease |
BEFREE |
Together, these data suggest an important role for UNC5A, a candidate tumor suppressor, in predicting response to DNA damage induced by chemotherapeutic drug and regulating cell death in bladder cancer.
|
24737586 |
2014 |
Bladder Neoplasm
|
0.010 |
Biomarker
|
disease |
BEFREE |
Together, these data suggest an important role for UNC5A, a candidate tumor suppressor, in predicting response to DNA damage induced by chemotherapeutic drug and regulating cell death in bladder cancer.
|
24737586 |
2014 |
Carcinoma of bladder
|
0.010 |
Biomarker
|
disease |
BEFREE |
Together, these data suggest an important role for UNC5A, a candidate tumor suppressor, in predicting response to DNA damage induced by chemotherapeutic drug and regulating cell death in bladder cancer.
|
24737586 |
2014 |