Tumor Cell Invasion
|
0.020 |
AlteredExpression
|
phenotype |
BEFREE |
Here we show for the first time that blocking expression of the Eph ligand Ephrin B3 inhibits NSCLC cell migration and invasion.
|
27533087 |
2016 |
Tumor Cell Invasion
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Depletion of endogenous ephrin-B3 expression abrogated the increase of migration and invasion induced by EphB2/Fc, indicating increased invasion is dependent on ephrin-B3 activation.
|
16951161 |
2006 |
Glioblastoma Multiforme
|
0.020 |
PosttranslationalModification
|
disease |
BEFREE |
Immunohistochemistry revealed robust staining for phosphorylated ephrin-B and ephrin-B3 in invading glioblastoma cells.
|
16951161 |
2006 |
Glioblastoma Multiforme
|
0.020 |
Biomarker
|
disease |
BEFREE |
The pair EphA4/Ephrin-B3 favors survival of neuronal progenitors of the brain subventricular zone, an area where glioblastoma multiform (GBM) are thought to originate.
|
28423606 |
2017 |
Malignant Neoplasms
|
0.010 |
Biomarker
|
group |
BEFREE |
In conclusion, we show that blocking Ephrin B3 expression inhibits NSCLC proliferation-, migration- and invasion capacity which calls for further studies on interference with Ephrin B3 as a possible therapeutic avenue in this tumor malignancy.
|
27533087 |
2016 |
Diabetes Mellitus, Non-Insulin-Dependent
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
In the present study, we conducted a human genetic study to assess the association of EFNB3 single nucleotide polymorphisms with human hypertension risks, using 3,448 patients with type 2 diabetes from the ADVANCE study (Action in Diabetes and Vascular Disease: Peterax and Diamicron MR Controlled Evaluation).
|
28272517 |
2017 |
Epilepsy
|
0.010 |
Biomarker
|
disease |
BEFREE |
To further clarify the role of ephrin‑B3 in neurogenesis and the reelin pathway in epilepsy, an exogenous ephrin‑B3 clustering stimulator, EphB3‑Fc, was infused into the bilateral hippocampus of the rats post‑SE.
|
29512697 |
2018 |
Glioma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Ephrin-B3 mRNA was up-regulated in migrating cells of four of four glioma cell lines (1.3- to 1.7-fold) and in invading tumor cells of eight of eight biopsy specimens (1.2- to 10.0-fold).
|
16951161 |
2006 |
Hypogonadism
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Analysis of the association of EPHB6, EFNB1 and EFNB3 variants with hypertension risks in males with hypogonadism.
|
30262919 |
2018 |
Status Epilepticus
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In the present study, the expression of ephrin‑B3 in pilocarpine‑induced status epilepticus (SE) rats was investigated.
|
29512697 |
2018 |
Vascular Diseases
|
0.010 |
GeneticVariation
|
group |
BEFREE |
In the present study, we conducted a human genetic study to assess the association of EFNB3 single nucleotide polymorphisms with human hypertension risks, using 3,448 patients with type 2 diabetes from the ADVANCE study (Action in Diabetes and Vascular Disease: Peterax and Diamicron MR Controlled Evaluation).
|
28272517 |
2017 |
B-Cell Lymphomas
|
0.010 |
Biomarker
|
group |
BEFREE |
Immunohistochemical analyses of autotaxin (ATX), ephrin B3, B-cell lymphoma-w (BCLW), and protein tyrosine kinase 2 beta showed them to be expressed in invasive glioma cells.
|
15720813 |
2005 |
Morphologically altered structure
|
0.010 |
Biomarker
|
disease |
BEFREE |
Cells transfected with ephrin-B3 small interfering RNA (siRNA) showed significant morphologic change and decreased invasion in vitro and ex vivo.
|
16951161 |
2006 |
Primary malignant neoplasm
|
0.010 |
Biomarker
|
group |
BEFREE |
In conclusion, we show that blocking Ephrin B3 expression inhibits NSCLC proliferation-, migration- and invasion capacity which calls for further studies on interference with Ephrin B3 as a possible therapeutic avenue in this tumor malignancy.
|
27533087 |
2016 |
Glioblastoma
|
0.020 |
PosttranslationalModification
|
disease |
LHGDN |
Immunohistochemistry revealed robust staining for phosphorylated ephrin-B and ephrin-B3 in invading glioblastoma cells.
|
16951161 |
2006 |
Movement Disorders
|
0.200 |
Biomarker
|
group |
MGD |
|
|
|