Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
Our data support a role for clathrin-independent endocytic machinery in balancing membrane tension, which clarifies the previously reported role of GRAF1 as a tumor suppressor.
|
28834752 |
2017 |
Neoplasms
|
0.060 |
GeneticVariation
|
group |
BEFREE |
Furthermore, the cell-matrix Rho GTPase-encoding ARHGAP26 gene, and MAN1C1, a gene encoding a Golgi mannosidase involved in the maturation of procollagens, emerged as new candidate uterine leiomyoma genes affecting both risk and tumor size.
|
25455875 |
2015 |
Neoplasms
|
0.060 |
Biomarker
|
group |
BEFREE |
GTPase regulator associated with focal adhesion kinase (GRAF), a putative tumor suppressor gene, was revealed with mutations and promoter methylation in AML and myelodysplastic syndrome.
|
21074269 |
2011 |
Neoplasms
|
0.060 |
GeneticVariation
|
group |
BEFREE |
The particular position of the human GRAF gene at 5q31 and the proposed antiproliferative and tumor suppressor properties of its avian homologue suggest that it also might be pathogenetically relevant for hematologic malignancies with deletions of 5q.
|
10908648 |
2000 |
Cerebellar Ataxia
|
0.030 |
Biomarker
|
phenotype |
BEFREE |
Autoantibodies against the RhoGTPase-activating protein 26 (ARHGAP26) were originally identified in the context of subacute autoimmune cerebellar ataxia.
|
30158896 |
2018 |
Cerebellar Ataxia
|
0.030 |
Biomarker
|
phenotype |
BEFREE |
The field of movement disorders with neuronal antibodies keeps expanding with the discovery for example of antibodies against leucine rich glioma inactivated protein 1 (LGI1) and contactin associated protein 2 (Caspr2) in chorea, or antibodies targeting ARHGAP26- or Na/K ATPase alpha 3 subunit (ATP1A3) in cerebellar ataxia.
|
27262149 |
2016 |
Cerebellar Ataxia
|
0.030 |
Biomarker
|
phenotype |
BEFREE |
Here, we report a newly diagnosed anti-Ca/ARHGAP26-IgG-positive patient who presented with recurrent psychotic symptoms but no cerebellar ataxia.
|
26298328 |
2015 |
Patent ductus arteriosus
|
0.020 |
Biomarker
|
disease |
BEFREE |
ARHGAP26-knocked-down human DASMCs showed reduced proliferation and migration, which are both crucial to anatomic closure of DA.
|
30592323 |
2019 |
Tumor Cell Invasion
|
0.020 |
Biomarker
|
phenotype |
BEFREE |
Overall, SMURF1-mediated ubiquitination of ARHGAP26 may promote invasion and migration of ovarian cancer cells via the β-catenin pathway.
|
31004081 |
2019 |
Malignant Neoplasms
|
0.020 |
Biomarker
|
group |
BEFREE |
Prognostic significance of frequent CLDN18-ARHGAP26/6 fusion in gastric signet-ring cell cancer.
|
29961079 |
2018 |
Tumor Cell Invasion
|
0.020 |
AlteredExpression
|
phenotype |
BEFREE |
Ectopic expression of CLDN18-ARHGAP26 promotes the migration and invasion capacities of DGC cells.
|
30361512 |
2018 |
Patent ductus arteriosus
|
0.020 |
AlteredExpression
|
disease |
BEFREE |
ARHGAP26 messenger RNA and protein levels were decreased in patent DA tissue (both P ≤ 0.018).
|
25915513 |
2015 |
Childhood Myelodysplastic Syndrome
|
0.020 |
PosttranslationalModification
|
disease |
BEFREE |
GTPase regulator associated with focal adhesion kinase (GRAF), a putative tumor suppressor gene, was revealed with mutations and promoter methylation in AML and myelodysplastic syndrome.
|
21074269 |
2011 |
Adult Myelodysplastic Syndrome
|
0.020 |
PosttranslationalModification
|
disease |
BEFREE |
GTPase regulator associated with focal adhesion kinase (GRAF), a putative tumor suppressor gene, was revealed with mutations and promoter methylation in AML and myelodysplastic syndrome.
|
21074269 |
2011 |
Malignant Neoplasms
|
0.020 |
AlteredExpression
|
group |
BEFREE |
The aim of this study was to investigate the expression level of GRAF gene in those patients with myeloid malignancies including acute myeloid leukemia (AML), myelodysplastic syndrome (MDS) and chronic myeloid leukemia (CML).
|
20704716 |
2010 |
Childhood Myelodysplastic Syndrome
|
0.020 |
PosttranslationalModification
|
disease |
BEFREE |
In contrast to normal tissues, which tested negative for GRAF promoter methylation, 11 of 29 (38%) bone marrow samples from patients with acute myeloid leukaemia or myelodysplastic syndrome were positive.
|
16404424 |
2006 |
Adult Myelodysplastic Syndrome
|
0.020 |
PosttranslationalModification
|
disease |
BEFREE |
In contrast to normal tissues, which tested negative for GRAF promoter methylation, 11 of 29 (38%) bone marrow samples from patients with acute myeloid leukaemia or myelodysplastic syndrome were positive.
|
16404424 |
2006 |
Malignant neoplasm of breast
|
0.010 |
Biomarker
|
disease |
BEFREE |
Consistent with the tumor suppressive role of claudins shown in mice, in humans, claudin-low breast cancer has been described as a distinct entity with a poor prognosis, and claudin-18-Rho GTPase activating protein 26 (CLDN18-ARHGAP26) fusion protein as a driver gene aberration in diffuse-type gastric cancer due to effects on RhoA.
|
31332482 |
2019 |
Malignant neoplasm of stomach
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The circ-ARHGAP26 expression was elevated in HGC-27 (P < 0.001), AGS (P < 0.001), SGC-7901 (P < 0.01), BGC-823 (P < 0.05) and NCI-N87 (P < 0.05) GC cell lines compared to GSE-1 cells.
|
30719998 |
2019 |
Secondary malignant neoplasm of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
ARHGAP26 upregulation in A2780 cells also inhibited lung metastasis in vivo.
|
31004081 |
2019 |
Breast Carcinoma
|
0.010 |
Biomarker
|
disease |
BEFREE |
Consistent with the tumor suppressive role of claudins shown in mice, in humans, claudin-low breast cancer has been described as a distinct entity with a poor prognosis, and claudin-18-Rho GTPase activating protein 26 (CLDN18-ARHGAP26) fusion protein as a driver gene aberration in diffuse-type gastric cancer due to effects on RhoA.
|
31332482 |
2019 |
Stomach Carcinoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The circ-ARHGAP26 expression was elevated in HGC-27 (P < 0.001), AGS (P < 0.001), SGC-7901 (P < 0.01), BGC-823 (P < 0.05) and NCI-N87 (P < 0.05) GC cell lines compared to GSE-1 cells.
|
30719998 |
2019 |
Carcinoma, Signet Ring Cell
|
0.010 |
Biomarker
|
disease |
BEFREE |
Overall, this study provides insights into the clinical and genomic features of SRCC, and highlights the importance of frequent CLDN18-ARHGAP26/6 fusions in chemotherapy response for SRCC.
|
29961079 |
2018 |
Impaired cognition
|
0.010 |
Biomarker
|
disease |
BEFREE |
Anti-ARHGAP26 Autoantibodies Are Associated With Isolated Cognitive Impairment.
|
30158896 |
2018 |
Primary malignant neoplasm
|
0.010 |
Biomarker
|
group |
BEFREE |
Prognostic significance of frequent CLDN18-ARHGAP26/6 fusion in gastric signet-ring cell cancer.
|
29961079 |
2018 |