Alzheimer's Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
We have studied the relationship of both these NOS gene polymorphisms to development of AD and dementia with Lewy bodies and find no evidence for association with either condition.
|
11297817 |
2001 |
Alzheimer's Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Administration of the NOS inhibitor L-NG-Nitroarginine methyl ester reversed vasodilation as well as the protective effects of rapamycin on CBF and vasculature integrity, indicating that rapamycin preserves vascular density and CBF in AD mouse brains through NOS activation.
|
23801246 |
2013 |
Alzheimer's Disease
|
0.100 |
AlteredExpression
|
disease |
BEFREE |
Further, this review provide convergent evidence that NO could provide a therapeutic avenue in AD via modulation of the relevant NOS expression.
|
31782366 |
2019 |
Alzheimer's Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
No association was demonstrated for AD and this particular nNOS polymorphism.
|
12210288 |
2002 |
Alzheimer's Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Adopting strategies to reduce the effects of NOS and NOX activities, and improve the actions of UCPs and PPARs may help in the treatment of AD.
|
16873964 |
2006 |
Alzheimer's Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
Our findings indicate that downregulation of miR-132/212 disturbs the balance of S-nitrosylation and induces tau phosphorylation in a NOS1-dependent way, and thereby may contribute to the pathogenesis of AD and other tauopathies.
|
28089352 |
2017 |
Alzheimer's Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Main genes involved in AD include mutational loci (APP, PS1, PS2, TAU) and multiple susceptibility loci (APOE, A2M, AACT, LRP1, IL1A, TNF, ACE, BACE, BCHE, CST3, MTHFR, GSK3B, NOS) distributed across the human genome.
|
12369958 |
2002 |
Alzheimer's Disease
|
0.100 |
Biomarker
|
disease |
BEFREE |
These findings provide further evidence for an association of NOS1 with AD.
|
21098972 |
2011 |
Alzheimer's Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
Therefore, short alleles of the NOS1 exon 1f-VNTR are likely to be susceptibility factors for AD, and interact with the epsilon 4 allele to markedly increase the AD risk.
|
17418914 |
2008 |
Alzheimer's Disease
|
0.100 |
GeneticVariation
|
disease |
BEFREE |
In this study, we analyzed RNA-Seq data of hippocampus brain tissue from Alzheimer's disease (AD; n = 24) and cognitively normal elderly controls (CN; n = 50) and identified three exon skipping events in two genes (RELN and NOS1) as significantly associated with AD (corrected p-value < 0.05 and fold change > 1.5).
|
30704480 |
2019 |
Alzheimer's Disease
|
0.100 |
GeneticVariation
|
disease |
LHGDN |
Association of neuronal nitric oxide synthase C276T polymorphism with Alzheimer's disease.
|
15765269 |
2005 |