Adult Liver Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Taken together, our findings identify the DHX9-NONO-SFPQ complex as a key regulator manipulating the oncogenic splicing switch of BIN1 and as a candidate therapeutic target in liver cancer.
|
31815296 |
2019 |
Liver and Intrahepatic Biliary Tract Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Taken together, our findings identify the DHX9-NONO-SFPQ complex as a key regulator manipulating the oncogenic splicing switch of BIN1 and as a candidate therapeutic target in liver cancer.
|
31815296 |
2019 |
Malignant neoplasm of liver
|
0.010 |
Biomarker
|
disease |
BEFREE |
Taken together, our findings identify the DHX9-NONO-SFPQ complex as a key regulator manipulating the oncogenic splicing switch of BIN1 and as a candidate therapeutic target in liver cancer.
|
31815296 |
2019 |
Malignant Pleural Mesothelioma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We aimed to determine the expression of BIN1 and IDO1, their association with other markers and impact on overall survival (OS) in MPM.
|
30885349 |
2019 |
Gestational Diabetes
|
0.010 |
GeneticVariation
|
phenotype |
BEFREE |
No significant associations of the genetic variants rs744373 in BIN1, rs11136000 in CLU, or rs3818361 in CR1 were found with GDM, T2DM or IGT, but rs3851179 in PICALM was associated with an increased risk of GDM.
|
28316001 |
2017 |
Impaired glucose tolerance
|
0.010 |
GeneticVariation
|
phenotype |
BEFREE |
The aim of this study was to examine whether the variants of some candidate genes involved in the development of AD, namely BIN1 (rs744373), CLU (rs11136000), CR1 (rs3818361), and PICALM (rs3851179), are related to several disorders of glucose metabolism-gestational diabetes (GDM), T2DM and impaired glucose tolerance (IGT).
|
28316001 |
2017 |
Colitis
|
0.010 |
Biomarker
|
disease |
BEFREE |
In this study, we offer preclinical proof of concept for a monoclonal antibody (mAb) targeting the Bin1 protein that blunts UC pathogenicity in a mouse model of experimental colitis.
|
26195312 |
2016 |
Colorectal Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Our results suggest that a therapy based on Bin1 monoclonal antibody supporting mucosal barrier function and protecting integrity of the lymphoid follicle could offer a novel strategy to treat UC and possibly limit risks of colorectal cancer.
|
26195312 |
2016 |
Diabetes Mellitus, Non-Insulin-Dependent
|
0.010 |
Biomarker
|
disease |
BEFREE |
Although preliminary and require further replications, our findings support a contribution of BIN1 to individual differences in episodic memory performance among T2D patients.
|
26947052 |
2016 |
Epilepsy, Temporal Lobe
|
0.010 |
Biomarker
|
disease |
BEFREE |
Our data indicate that poor memory performance in patients with TLE strongly corresponds to distinctly altered neuronal transcript signatures, which - as demonstrated for BIN1 - can correlate with a particular allelic promoter variant.
|
26631617 |
2016 |
Hematological Disease
|
0.010 |
Biomarker
|
group |
BEFREE |
This study shows a novel deregulated mechanism in CML patients, indicating BIN1 and RIN1 as players in the maintenance of the abnormal RTK signaling in this hematological disease.
|
26194865 |
2016 |
Myeloid Leukemia, Chronic
|
0.010 |
Biomarker
|
disease |
BEFREE |
In order to provide another proof in favor of BIN1 and RIN1 endocytosis function in CML, we demonstrated that Imatinib induced, in K562 cell line, BIN1-RIN1 upregulation accompanied by a parallel AXL receptor internalization into cytoplasmic compartment.
|
26194865 |
2016 |
Malignant neoplasm of colon and/or rectum
|
0.010 |
Biomarker
|
disease |
BEFREE |
Our results suggest that a therapy based on Bin1 monoclonal antibody supporting mucosal barrier function and protecting integrity of the lymphoid follicle could offer a novel strategy to treat UC and possibly limit risks of colorectal cancer.
|
26195312 |
2016 |
Parkinson Disease
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Our results suggest that alterations in the BIN1 locus, previously associated with Alzheimer disease, may modify the AAO of GBA-associated PD.
|
26233692 |
2015 |
Sezary Syndrome
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We recently demonstrated that BIN1 transcript levels are significantly downregulated in CD4(+)CD7(-) Sezary cells from patients with Sezary syndrome (SS), a subtype of cutaneous T-cell lymphoma (CTCL).
|
25578476 |
2015 |
Solid Neoplasm
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
BIN1 attenuation has been reported in several solid tumors; however, the role of BIN1 in lymphomagenesis remains unexplored.
|
25578476 |
2015 |
Leukemogenesis
|
0.010 |
Biomarker
|
disease |
BEFREE |
BIN1 attenuation has been reported in several solid tumors; however, the role of BIN1 in lymphomagenesis remains unexplored.
|
25578476 |
2015 |
Familial lichen amyloidosis
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
The direction of association at APOE, CLU, and BIN1 loci was the same for participants with PCA and posterior AD.
|
24670887 |
2014 |
Dementia
|
0.010 |
Biomarker
|
disease |
BEFREE |
BIN1 declined with age in a cohort of non-dementia control cases between 25 and 88 years but the correlation was not significant (rs=-0.449, p=0.081).
|
24205320 |
2013 |
Rhabdoid Tumor
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Functionally, we demonstrate that re-expression of BIN1 specifically compromises the proliferation of SNF5-deficient RT cell lines.
|
22544318 |
2012 |
Hepatocarcinogenesis
|
0.010 |
Biomarker
|
disease |
BEFREE |
In the present study, we investigated the expression and prognostic role of BIN1 in primary HCC and evaluated the function of BIN1 in hepatocarcinogenesis.
|
22281836 |
2012 |
Congenital Myotonic Dystrophy
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
We found that alternative splicing of the bridging integrator-1 (BIN1) pre-mRNA is altered in skeletal muscle samples of people with CDM1, DM1 and DM2.
|
21623381 |
2011 |
Malignant tumor of colon
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In primary colon cancer, the strong expression of IDO existed in 9/71 cases (12.7%), while the strong expression of Bin1 existed in 33/71 cases (46.5%).
|
19695096 |
2009 |
Colon Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In primary colon cancer, the strong expression of IDO existed in 9/71 cases (12.7%), while the strong expression of Bin1 existed in 33/71 cases (46.5%).
|
19695096 |
2009 |
Neoplastic Cell Transformation
|
0.010 |
Biomarker
|
phenotype |
LHGDN |
Bin1 attenuation in breast cancer is correlated to nodal metastasis and reduced survival.
|
17218774 |
2007 |