Varaico: Literature-Extracted Genetic Variants

Gene:NOS3
Variant:p.V827M
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NOS3

NM_000603.5:p.V827M

Associated Papers

Bicuspid Aortic Valve: Old and Novel Gene Contribution to Disease Onset and Complications.

Sticchi E et al.

Diagnostics (basel, Switzerland), 2025

Methionine synthetase A2756G and Cystathionine-β-synthase 844ins68 polymorphisms and coronary artery disease: A meta-analysis.

Li YY et al.

The American Journal of the Medical Sciences, 2025

Functional mutation, splice, distribution, and divergence analysis of impactful genes associated with heart failure and other cardiovascular diseases.

Mhatre I et al.

Scientific Reports, 2023

37798313 (PubMed )
Supplement: 41598_2023_44127_MOESM2_ESM.pdf

Whole-exome sequencing in searching for novel variants associated with the development of high altitude pulmonary edema.

Chen M et al.

Gene, 2023

Endothelial Nitric Oxide Synthase Gene Polymorphisms Increase Risk of Deep Vein Thrombosis by Altering Homocysteine Levels.

Akhter MS et al.

Clinical Laboratory, 2022

Interplay of physical activity and genetic variants of the endothelial lipase on cardiovascular disease risk factors.

Salazar-Tortosa DF et al.

Pediatric Research, 2022

Structural and functional alterations of nitric oxide synthase 3 due to missense variants associate with high-altitude pulmonary edema through dynamic study.

Kanipakam H et al.

Journal of Biomolecular Structure & Dynamics, 2021

Mutations in PCYT2 disrupt etherlipid biosynthesis and cause a complex hereditary spastic paraplegia.

Vaz FM et al.

Brain : a Journal of Neurology, 2019

31637422 (PubMed )
Supplement: awz291_supplementary_data.zip › awz291-Suppl_data › Supplementary_Data2.pdf

PRIMA-1MET-induced neuroblastoma cell death is modulated by p53 and mycn through glutathione level.

Mlakar V et al.

Journal of Experimental & Clinical Cancer Research : Cr, 2019

30755224 (PubMed )
Supplement: 13046_2019_1066_MOESM1_ESM.xlsx › LAN6

Screening of the NOS3 gene identifies the variants 894G/T, 1998C/G and 2479G/A to be associated with acute onset ischemic stroke in young Asian Indians.

Akhter MS et al.

Journal of the Neurological Sciences, 2014

Multiple gene dysfunctions lead to high cancer-susceptibility: evidences from a whole-exome sequencing study.

He ML et al.

American Journal of Cancer Research, 2011

A genetic association analysis of cognitive ability and cognitive ageing using 325 markers for 109 genes associated with oxidative stress or cognition.

Harris SE et al.

Bmc Genetics, 2007

17601350 (PubMed )
Supplement: 1471-2156-8-43-S1.doc
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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."