Schematic representation of the NOS1AP gene with exons (black 1-10) and... | Download Scientific Diagram
Disruption of nNOS-NOS1AP protein-protein interactions suppresses neuropathic pain in mice. - Abstract - Europe PMC
Recessive NOS1AP variants impair actin remodeling and cause glomerulopathy in humans and mice | Science Advances
CAPON/NOS1AP Antibody
IJMS | Free Full-Text | NOS1AP O-GlcNAc Modification Involved in Neuron Apoptosis Induced by Excitotoxicity
NOS1AP protein (human) - STRING interaction network
Locus zoom plots of the NOS1AP gene region showing SNP p-values from... | Download Scientific Diagram
New kid on the block: NOS1AP is a newly recognized genetic cause of steroid-resistant nephrotic syndrome in infants - Kidney International
NOS1AP Is a Genetic Modifier of the Long-QT Syndrome | Circulation
Frontiers | Overexpression of Isoforms of Nitric Oxide Synthase 1 Adaptor Protein, Encoded by a Risk Gene for Schizophrenia, Alters Actin Dynamics and Synaptic Function
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization | Nature Genetics
Neuronal nitric oxide synthase (NOS1) and its adaptor, NOS1AP, as a genetic risk factors for psychiatric disorders - Freudenberg - 2015 - Genes, Brain and Behavior - Wiley Online Library
Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls | BMC Medical Genetics | Full Text
The epigenome, 4D nucleome and next-generation neuropsychiatric pharmacogenomics | Pharmacogenomics
NOS1AP is a novel molecular target and critical factor in TDP-43 pathology
Neuronal nitric oxide synthase (NOS1) and its adaptor, NOS1AP, as a genetic risk factors for psychiatric disorders - Freudenberg - 2015 - Genes, Brain and Behavior - Wiley Online Library
Hippocampal overexpression of NOS1AP promotes endophenotypes related to mental disorders - eBioMedicine
Neuronal nitric oxide synthase (NOS1) and its adaptor, NOS1AP, as a genetic risk factors for psychiatric disorders - Freudenberg - 2015 - Genes, Brain and Behavior - Wiley Online Library
IJMS | Free Full-Text | NOS1AP Interacts with α-Synuclein and Aggregates in Yeast and Mammalian Cells
NOS1AP Gene - GeneCards | CAPON Protein | CAPON Antibody
Cardiac muscle-restricted partial loss of Nos1ap expression has limited impact on electro- and echo-cardiographic features | bioRxiv
ExonSkipDB: functional annotation of exon skipping event in human - Search
The genetic variation rs12143842 in NOS1AP increases idiopathic ventricular tachycardia risk in Chinese Han populations | Scientific Reports
NOS1AP - an overview | ScienceDirect Topics
NOS1AP - Wikipedia
NOS1AP Gene - GeneCards | CAPON Protein | CAPON Antibody
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