Alcoholic Intoxication, Chronic
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
This study provides data from a sample of ethnically homogeneous unrelated Caucasian subjects for future meta-analyses and suggests that the increased platelet MAO-B activity might be used as independent peripheral indicator of alcohol dependence, while COMT Val108/158Met polymorphism is associated with increased suicidality and early onset of alcohol dependence.
|
25035107 |
2014 |
Alcoholic Intoxication, Chronic
|
0.390 |
Biomarker
|
disease |
PSYGENET |
This study provides data from a sample of ethnically homogeneous unrelated Caucasian subjects for future meta-analyses and suggests that the increased platelet MAO-B activity might be used as independent peripheral indicator of alcohol dependence, while COMT Val108/158Met polymorphism is associated with increased suicidality and early onset of alcohol dependence.
|
25035107 |
2014 |
Alcoholic Intoxication, Chronic
|
0.390 |
GeneticVariation
|
disease |
BEFREE |
Our aim was to test whether MAOA-LPR influences the impact of CSA on alcoholism and ASPD in a sample of 291 women, 50% of whom have experienced CSA; we also tested whether haplotypes covering the region where both MAOA and monoamine oxidase B (MAOB) genes are located predict risk of alcoholism and ASPD better than the MAOA-LPR locus alone.
|
17592478 |
2008 |
Alcoholic Intoxication, Chronic
|
0.390 |
Biomarker
|
disease |
PSYGENET |
Our aim was to test whether MAOA-LPR influences the impact of CSA on alcoholism and ASPD in a sample of 291 women, 50% of whom have experienced CSA; we also tested whether haplotypes covering the region where both MAOA and monoamine oxidase B (MAOB) genes are located predict risk of alcoholism and ASPD better than the MAOA-LPR locus alone.
|
17592478 |
2008 |
Alcoholic Intoxication, Chronic
|
0.390 |
Biomarker
|
disease |
PSYGENET |
A case group of males with type 2 alcoholism (N=59) and a control group of healthy males (N=282), both of Croatian origin, were analyzed for the frequency distribution of polymorphisms in 5HT transporter (5HTT-VNTR2, 5HTT-LPR), monoamine oxidase A (MAOA-uVNTR) and B (MAOB-A/G) and tryptophan hydroxylase 1 (TPH1 A218C) and 2 (TPH2 G-703T) genes.
|
18405071 |
2008 |
Alcoholic Intoxication, Chronic
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
In the present study platelet monoamine oxidase B (MAO-B) activity was investigated in 76 male type 1 alcohol-dependent subjects with and without a family history of alcoholism.
|
12414550 |
2003 |
Alcoholic Intoxication, Chronic
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
Low platelet monoamine oxidase B (MAO-B) activity and the presence of the Taq1 A1 allele of the dopamine D2 receptor (DRD2) gene have independently been proposed as 'biological/genetic' markers for alcoholism.
|
11022024 |
2000 |
Alcoholic Intoxication, Chronic
|
0.390 |
Biomarker
|
disease |
PSYGENET |
Low platelet monoamine oxidase B (MAO-B) activity and the presence of the Taq1 A1 allele of the dopamine D2 receptor (DRD2) gene have independently been proposed as 'biological/genetic' markers for alcoholism.
|
11022024 |
2000 |
Alcoholic Intoxication, Chronic
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
The four phenotypes considered were a factor describing medical symptoms of alcohol dependency, a factor describing a psychological profile correlated with susceptibility to alcoholism, monoamine oxidase B (MAOB) activity and an average measurement of the P3 component of event-related potentials (ERP) at the Fp electrode placements.
|
10597455 |
1999 |
Alcoholic Intoxication, Chronic
|
0.390 |
Biomarker
|
disease |
PSYGENET |
The four phenotypes considered were a factor describing medical symptoms of alcohol dependency, a factor describing a psychological profile correlated with susceptibility to alcoholism, monoamine oxidase B (MAOB) activity and an average measurement of the P3 component of event-related potentials (ERP) at the Fp electrode placements.
|
10597455 |
1999 |
Alcoholic Intoxication, Chronic
|
0.390 |
Biomarker
|
disease |
BEFREE |
The present results in brain tissue contrast with previous reports of decreased MAO-B enzymatic activity in platelets of alcoholics, but strongly agree with recent genetic studies on MAO-B status in alcoholism.
|
9394121 |
1997 |
Alcoholic Intoxication, Chronic
|
0.390 |
AlteredExpression
|
disease |
BEFREE |
Reduced MAOB activity has been found in type-II alcoholism and in cigarette smokers.
|
9326944 |
1997 |
Alcoholic Intoxication, Chronic
|
0.390 |
Biomarker
|
disease |
BEFREE |
Thus, MAOB is not a biological/genetic marker of alcoholism sensu stricto but is rather a biological/genetic marker of an underlying pathophysiologic process leading to alcoholism and other psychiatric illness.
|
8154672 |
1994 |
Alcoholic Intoxication, Chronic
|
0.390 |
GeneticVariation
|
disease |
BEFREE |
In order to determine the role of the MAO genes in alcoholism we have measured MAO-B activity and typed two simple sequence repeats (one in the MAO-A gene and one in the MAO-B gene) in a sample of 133 unrelated alcoholics, 300 subjects from 30 two- and three-generation pedigrees ascertained through an alcoholic proband, and 92 normal controls.
|
8974315 |
1994 |