Hematuria
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
%dRBCs (<i>P</i>=0.0001) and UF-%sRBCs (<i>P</i>=0.0006) differed between the GN and NGN groups in patients with isolated hematuria but without proteinuria.
|
30623619 |
2019 |
Neoplasms
|
0.090 |
Biomarker
|
group |
BEFREE |
Neogenin is closely related to the human tumor suppressor gene deleted in colorectal cancer and plays a role in mammary morphogenesis.
|
25416629 |
2014 |
Malignant Neoplasms
|
0.040 |
Biomarker
|
group |
BEFREE |
Neogenin has been documented as playing an important role in cancer development.
|
25998984 |
2015 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
Neogenin has been documented as playing an important role in cancer development.
|
25998984 |
2015 |
Malignant neoplasm of breast
|
0.020 |
Biomarker
|
disease |
BEFREE |
Neogenin may serve as a potential diagnostic marker and therapeutic target for breast cancer.
|
25998984 |
2015 |
Breast Carcinoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Neogenin may serve as a potential diagnostic marker and therapeutic target for breast cancer.
|
25998984 |
2015 |
Neoplasms
|
0.090 |
Biomarker
|
group |
BEFREE |
NEO1 and DCC are also tumor suppressors that can inhibit metastasis by acting as dependence receptors.
|
30858446 |
2019 |
Leukemia, Myelocytic, Acute
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21.
|
19665076 |
2009 |
Adult Acute Myeloblastic Leukemia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21.
|
19665076 |
2009 |
Childhood Acute Myeloid Leukemia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21.
|
19665076 |
2009 |
Neoplasms
|
0.090 |
Biomarker
|
group |
BEFREE |
A second new hypothesis is based on evidence that serine proteases can deplete cells of the tumour suppressors Deleted in Colorectal Cancer (DCC) and neogenin.
|
29526577 |
2018 |
Tumor Progression
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Although NEO1 and its ligands are involved in tumor progression, their precise role in tumor cell survival and migration remain unclear.
|
28038459 |
2017 |
Osteoporosis, Postmenopausal
|
0.010 |
Biomarker
|
disease |
BEFREE |
Among these 11 genes, three genes (OSTF1, ADRB1 and NEO1) were speculated to serve roles in PMOP by regulating the balance between bone formation and bone resorption, while two genes (GPR87 and GPR116) may be involved in PMOP by regulating the nuclear factor‑κB signaling pathway.
|
30569177 |
2019 |
Malignant Neoplasms
|
0.040 |
Biomarker
|
group |
BEFREE |
By immunohistochemical analysis of 69 primary and 16 paired initial and recurrent glioma sections, we found that the loss of neogenin did not only correlate negatively with glioma malignancy (n = 69, p<0.01), but also glioma recurrence (n = 16, p<0.05).
|
22666451 |
2012 |
Primary malignant neoplasm
|
0.040 |
Biomarker
|
group |
BEFREE |
By immunohistochemical analysis of 69 primary and 16 paired initial and recurrent glioma sections, we found that the loss of neogenin did not only correlate negatively with glioma malignancy (n = 69, p<0.01), but also glioma recurrence (n = 16, p<0.05).
|
22666451 |
2012 |
Glioma
|
0.010 |
PosttranslationalModification
|
disease |
BEFREE |
By Methylation specific polymerase chain reaction (MSP), we reported that neogenin promoter was methylated in 31.0% (9/29) gliomas, but absent in 3 kinds of glioma cell lines.
|
22666451 |
2012 |
Blood Protein Measurement
|
0.100 |
GeneticVariation
|
phenotype |
GWASCAT |
Co-regulatory networks of human serum proteins link genetics to disease.
|
30072576 |
2018 |
Glioblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Collectively, these results suggest that miR-18a may regulate biological behavior of human glioblastoma cells by targeting neogenin, and miR-18a can serve as a potential target in the treatment of glioblastoma.
|
24657544 |
2014 |
Adult Glioblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Collectively, these results suggest that miR-18a may regulate biological behavior of human glioblastoma cells by targeting neogenin, and miR-18a can serve as a potential target in the treatment of glioblastoma.
|
24657544 |
2014 |
Childhood Glioblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Collectively, these results suggest that miR-18a may regulate biological behavior of human glioblastoma cells by targeting neogenin, and miR-18a can serve as a potential target in the treatment of glioblastoma.
|
24657544 |
2014 |
Glioblastoma Multiforme
|
0.020 |
Biomarker
|
disease |
BEFREE |
Collectively, these results suggest that miR-18a may regulate biological behavior of human glioblastoma cells by targeting neogenin, and miR-18a can serve as a potential target in the treatment of glioblastoma.
|
24657544 |
2014 |
Acute monocytic/monoblastic leukemia
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Described here is the case of a 2(1/2)-year-old girl with AML-M5 and 51 chromosomes characterized by double tetrasomy of chromosomes 8 and 21 and also a neocentric derivative chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter).
|
19665076 |
2009 |
Neoplasms
|
0.090 |
Biomarker
|
group |
BEFREE |
Expression of the tumour suppressor Deleted in Colorectal Cancer (DCC) and the related protein neogenin is reduced by the mammalian serine protease chymotrypsin or the bacterial serine protease subtilisin, with increased cell migration.
|
30403907 |
2019 |
Neuroblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Furthermore, NTN4 was shown to act as a cell adhesion molecule required for the migration induced by Neogenin-1 (NEO1) in SK-N-SH neuroblastoma cells.
|
30160193 |
2019 |
Central neuroblastoma
|
0.020 |
Biomarker
|
disease |
BEFREE |
Furthermore, NTN4 was shown to act as a cell adhesion molecule required for the migration induced by Neogenin-1 (NEO1) in SK-N-SH neuroblastoma cells.
|
30160193 |
2019 |