Varaico: Literature-Extracted Genetic Variants

Gene:NOS3
Variant:p.N433T
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NOS3

NM_000603.5:p.N433T

Associated Papers

Genetic variants in varicocele-related male infertility: a systematic review and future directions.

Mostafa T et al.

Human Fertility (cambridge, England), 2023

Predicting drug response and toxicity in metastatic colorectal cancer: the role of germline markers.

Bignucolo A et al.

Expert Review of Clinical Pharmacology, 2022

Genetic susceptibility to cerebrovascular disease: A systematic review.

Griessenauer CJ et al.

Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism, 2018

Genetics of Congenital Heart Disease: Past and Present.

Muntean I et al.

Biochemical Genetics, 2017

Polymorphisms of the methylenetetrahydrofolate reductase gene (C677T and A1298C) in the placenta of pregnancies complicated with preeclampsia.

Chedraui P et al.

Gynecological Endocrinology : the Official Journal of the International Society of Gynecological Endocrinology, 2015

Effect of genetic polymorphisms involved in folate metabolism on the concentration of serum folate and plasma total homocysteine (p-tHcy) in healthy subjects after short-term folic acid supplementation: a randomized, double blind, crossover study.

Cabo R et al.

Genes & Nutrition, 2015

Pharmacogenetic considerations for acute lymphoblastic leukemia therapies.

Dulucq S et al.

Expert Opinion on Drug Metabolism & Toxicology, 2014

Endothelial nitric oxide synthase gene polymorphisms and the risk of osteonecrosis of the femoral head in systemic lupus erythematosus.

Kim HS et al.

International Orthopaedics, 2013

Role of NOS3 DNA variants in externalizing behavioral problems observed in childhood leukemia survivors.

Marcoux S et al.

Journal of Pediatric Hematology/oncology, 2013

Polymorphisms in genes involved in folate metabolism and orofacial clefts.

Bhaskar LV et al.

Archives of Oral Biology, 2011

Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes.

Kuehl K et al.

Birth Defects Research. Part A, Clinical and Molecular Teratology, 2010

Endothelial nitric oxide synthetase, methylenetetrahydrofolate reductase polymorphisms, and cardiovascular complications in Tunisian patients with nondiabetic renal disease.

Kerkeni M et al.

Clinical Biochemistry, 2009

Hyperhomocysteinemia and thrombosis: an overview.

Eldibany MM et al.

Archives of Pathology & Laboratory Medicine, 2007

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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."