Anorexia Nervosa
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Following on from previous work by our group where we showed that early onset anorexia nervosa (AN) and obsessive-compulsive disorder (OCD) shared a common genetic background, the aim of the present study is to assess genetic pleiotropy related to the serotonergic system (SLC6A4, 5HTR2A, 5HTR2C, TPH2, SLC18A1), in a common phenotype such as very-early age of onset.
|
30554102 |
2019 |
Obsessive-Compulsive Disorder
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Following on from previous work by our group where we showed that early onset anorexia nervosa (AN) and obsessive-compulsive disorder (OCD) shared a common genetic background, the aim of the present study is to assess genetic pleiotropy related to the serotonergic system (SLC6A4, 5HTR2A, 5HTR2C, TPH2, SLC18A1), in a common phenotype such as very-early age of onset.
|
30554102 |
2019 |
Adenocarcinoma
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Increased expression of SLC18A1 was found to be associated with a significantly increased survival in patients with adenocarcinoma (p=0.0058), but not those with squamous carcinoma (p=0.96).
|
30194079 |
2018 |
Malignant neoplasm of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The association between smoking, SLC18A1 expression and overall survival in the lung cancer dataset in The Cancer Genome Atlas was evaluated using the Genomic Data Commons Data Portal (https://portal.gdc.cancer.gov), as well as CbioPortal for Cancer Genomics (http://www.cbioportal.org) and the University of California Santa Cruz Xena browser (https://xenabrowser.net).
|
30194079 |
2018 |
Asthenozoospermia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Gene polymorphisms of HTR2A, MAOA and SLC18A1, related to neurotransmission, are individually associated with asthenozoospermia through variation in sperm count and motility, without detectable allelic or genotype interaction.
|
29602729 |
2018 |
Carcinoma of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The association between smoking, SLC18A1 expression and overall survival in the lung cancer dataset in The Cancer Genome Atlas was evaluated using the Genomic Data Commons Data Portal (https://portal.gdc.cancer.gov), as well as CbioPortal for Cancer Genomics (http://www.cbioportal.org) and the University of California Santa Cruz Xena browser (https://xenabrowser.net).
|
30194079 |
2018 |
Primary malignant neoplasm of lung
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
The association between smoking, SLC18A1 expression and overall survival in the lung cancer dataset in The Cancer Genome Atlas was evaluated using the Genomic Data Commons Data Portal (https://portal.gdc.cancer.gov), as well as CbioPortal for Cancer Genomics (http://www.cbioportal.org) and the University of California Santa Cruz Xena browser (https://xenabrowser.net).
|
30194079 |
2018 |
Mental disorders
|
0.010 |
Biomarker
|
group |
BEFREE |
Vesicular monoamine transporter 1 (VMAT1/SLC18A1) is an attractive candidate gene for psychiatric disorders because of its participation in regulation monoamines.
|
28476685 |
2017 |
Colorectal Carcinoma
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
In summary, the germline deletions at SLC18A1 contributed to the development of CRC.
|
28968818 |
2017 |
Abnormal behavior
|
0.010 |
Biomarker
|
phenotype |
BEFREE |
Vesicular monoamine transporter 1 (VMAT1/SLC18A1) is an attractive candidate gene for psychiatric disorders because of its participation in regulation monoamines.
|
28476685 |
2017 |
Major Depressive Disorder
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Diffusion tensor imaging (DTI) and VMAT1 rs1390938" genes_norm="6570">Thr136Ile (rs1390938) genotyping were performed on 103 patients diagnosed with MDD and 83 healthy control participants.
|
28408293 |
2017 |
Autism Spectrum Disorders
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
In the present case-control study, we evaluated the link between three non-synonymous single nucleotide polymorphisms (SNPs) (rs2270641 [Pro4Thr], rs2270637 [rs2270637" genes_norm="6570">Thr98Ser] and rs1390938 [Thr136Ile]) and one intronic SNP (rs2279709) across the VMAT1 gene and ASD in a group of Iranian patients.
|
28476685 |
2017 |
Tumour budding
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
In LCM samples, similar observations were obtained that the expression levels of SLC18A1 in the tumor buddings, cancer cells in the center of primary tumor, and stroma of both tumor budding and cancer cells were lower than normal intestinal epithelial and stromal cells (fold change = 0.17-0.62, 0.12-0.57 and 0.37-0.68, respectively).
|
28968818 |
2017 |
Alcohol withdrawal syndrome
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
This study shows that genetic variants in VMAT1, including the functional SNP rs1390938, contribute to the severity of AW in patients of European descent.
|
26876819 |
2016 |
Chlamydia Infections
|
0.010 |
AlteredExpression
|
group |
BEFREE |
Altered protein distributions together with down-regulation of VMAT1 suggest that chlamydial infection may influence vesicular transport.
|
21883697 |
2011 |
Benign Prostatic Hyperplasia
|
0.010 |
Biomarker
|
disease |
BEFREE |
Here, we demonstrate that VAT-1 is a novel pathogenic factor in BPH associated with cell proliferation.
|
21394740 |
2011 |
Alzheimer's Disease
|
0.010 |
GeneticVariation
|
disease |
BEFREE |
Molecular genetics and developmental studies have identified 21 genes in this region (ADRA1A, ARHGEF10, CHRNA2, CHRNA6, CHRNB3, DKK4, DPYSL2, EGR3, FGF17, FGF20, FGFR1, FZD3, LDL, NAT2, NEF3, NRG1, PCM1, PLAT, PPP3CC, SFRP1 and VMAT1/SLC18A1) that are most likely to contribute to neuropsychiatric disorders (schizophrenia, autism, bipolar disorder and depression), neurodegenerative disorders (Parkinson's and Alzheimer's disease) and cancer.
|
19204725 |
2009 |
Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
VAT-1 is overexpressed in glioblastomas and functionally involved in glioma cell migration, representing a new component involved in glioma invasion
|
19508442 |
2009 |
Glioma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
VAT-1 is overexpressed in glioblastomas and functionally involved in glioma cell migration, representing a new component involved in glioma invasion
|
19508442 |
2009 |
Neuroblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
By microarray expression analysis (Affymetrix HU133A) important players in the noradrenalin biosynthesis pathway (DBH, DDC, GATA2, GATA3, PHOX2A, PHOX2B, SLC6A2 SLC18A1 and TH) were found to be among the top ranked genes in showing lower expression in unfavorable NB tumor types as compared to favorable ones.
|
19212675 |
2009 |
Adult Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Increased VAT-1 mRNA and protein levels were found in glioblastoma tissues and cell lines compared with normal human brain.
|
19508442 |
2009 |
Childhood Glioblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
Increased VAT-1 mRNA and protein levels were found in glioblastoma tissues and cell lines compared with normal human brain.
|
19508442 |
2009 |
Neurodegenerative Disorders
|
0.010 |
GeneticVariation
|
group |
BEFREE |
Molecular genetics and developmental studies have identified 21 genes in this region (ADRA1A, ARHGEF10, CHRNA2, CHRNA6, CHRNB3, DKK4, DPYSL2, EGR3, FGF17, FGF20, FGFR1, FZD3, LDL, NAT2, NEF3, NRG1, PCM1, PLAT, PPP3CC, SFRP1 and VMAT1/SLC18A1) that are most likely to contribute to neuropsychiatric disorders (schizophrenia, autism, bipolar disorder and depression), neurodegenerative disorders (Parkinson's and Alzheimer's disease) and cancer.
|
19204725 |
2009 |
Central neuroblastoma
|
0.010 |
AlteredExpression
|
disease |
BEFREE |
By microarray expression analysis (Affymetrix HU133A) important players in the noradrenalin biosynthesis pathway (DBH, DDC, GATA2, GATA3, PHOX2A, PHOX2B, SLC6A2 SLC18A1 and TH) were found to be among the top ranked genes in showing lower expression in unfavorable NB tumor types as compared to favorable ones.
|
19212675 |
2009 |
Tumor Cell Invasion
|
0.010 |
AlteredExpression
|
phenotype |
BEFREE |
VAT-1 is overexpressed in glioblastomas and functionally involved in glioma cell migration, representing a new component involved in glioma invasion
|
19508442 |
2009 |