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NOS1AP encodes a cytosolic protein that binds to the signaling molecule, neuronal nitric oxide synthase (nNOS). Additionally we are shipping NOS1AP Antibodies (64) and many more products for this protein.
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Results suggest that NOS1AP variants are associated with various forms of depression in schizophrenia and are more prevalent in males.
The study suggested that rs3751284 and rs348624 in the NOS1AP gene might be susceptibility loci for sudden unexplained death during daily activities.
report of the association of common NOS1AP polymorphisms with sudden unexplained nocturnal death syndrome in the southern Chinese Han population. These findings suggest that the A allele of rs12567209 and haplotype GCTA may serve as a protective modifier.
The A allele of rs12567209 in NOS1AP may serve as an independent predictor of all-cause death and SCD (show SCD Proteins) in patients with CHF.
This study suggested that NOS1 (show NOS1 Proteins) and NOS1AP were associated with schizophrenia.
We further localized NOS1AP to cardiomyocyte intercalated discs (IDs (show IDS Proteins)) and demonstrate that overexpression of NOS1AP in cardiomyocytes leads to altered cellular electrophysiology.
This is the first study reporting that a variant of the NOS1AP gene is associated with PTSD. Our data also suggest that a genetic variant in NOS1AP may increase the susceptibility to severe depression in patients with PTSD and increased risk for suicide.
rs10918859 of the NOS1AP gene is associated with CHD (show CHDH Proteins) in Han Chinese. In addition, here we report a gender effect in the association between rs10918859 of the NOS1AP gene and CHD (show CHDH Proteins).
In atherosclerosis, NOS1AP variants were associated with QT in CAU, with weaker evidence for selected variants in HIS and CHN. Location of significant SNPs varied across ancestry.
Decreased NOS1AP expression in rs10494366 TT and rs10918594 CC homozygotes may underlie shorter repolarization times.Myocardial tissue for gene expression analysis was obtained from extracted cardiac implantable electronic device.
Capon expression is increased in skeletal muscle by position, repair, NOS activity, and dystrophy.
long-term expression of cocaine-induced behavioral sensitization in females (adolescent and adult) is nNOS (show NOS1 Proteins)-independent, unlike previous finding in adult males.
This gene encodes a cytosolic protein that binds to the signaling molecule, neuronal nitric oxide synthase (nNOS). This protein has a C-terminal PDZ-binding domain that mediates interactions with nNOS and an N-terminal phosphotyrosine binding (PTB) domain that binds to the small monomeric G protein, Dexras1. Studies of the related mouse and rat proteins have shown that this protein functions as an adapter protein linking nNOS to specific targets, such as Dexras1 and the synapsins. Alternative splicing results in multiple transcript variants encoding different isoforms.
nitric oxide synthase 1 (neuronal) adaptor protein
, carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein
, carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like
, C-terminal PDZ domain ligand of neuronal nitric oxide synthase (CAPON)
, C-terminal PDZ ligand of neuronal nitric oxide synthase protein
, ligand of neuronal nitric oxide synthase with carboxyl-terminal PDZ domain
, nitric oxide synthase 1 adaptor protein
, C-terminal PDZ domain ligand of neuronal nitric oxide synthase