Lack of association between the eNOS rs1800779 (A/G) polymorphism and the myocardial infarction incidence among the Iraqi Kurdish population.
Journal Of Taibah University Medical Sciences
Khudhur, Zhikal O ZO; Othman, Goran G; Othman, Galawezh O GO; Jafaar, Aziz M AM; Qadir, Mahdi Kh MK; Awla, Harem Kh HK; Qasim, Sara Sh SS; Hadi, Shayma M SM; Khan, Samiha S SS; Noreen, Sobia S; Smail, Shukur W SW
The NESHIE and CP Genetics Resource (NCGR): A database of genes and variants reported in neonatal encephalopathy with suspected hypoxic ischemic encephalopathy (NESHIE) and consequential cerebral palsy (CP).
Genomics
Holborn, Megan A MA; Ford, Graeme G; Turner, Sarah S; Mellet, Juanita J; van Rensburg, Jeanne J; Joubert, Fourie F; Pepper, Michael S MS
Publication Date: 2022-10-18
Variant appearance in text: NOS3: -51-898G>A; rs1800779
Association of endothelial nitric oxide synthase gene variants with preeclampsia.
Reproductive Health
Shaheen, Ghazala G; Jahan, Sarwat S; Bibi, Nousheen N; Ullah, Asmat A; Faryal, Rani R; Almajwal, Ali A; Afsar, Tayyaba T; Al-Disi, Dara D; Abulmeaty, Mahmoud M; Al Khuraif, Abdulaziz Abdullah AA; Arshad, Mohammed M; Razak, Suhail S
The Role of Single Nucleotide Variants of NOS1, NOS2, and NOS3 Genes in the Development of the Phenotype of Migraine and Arterial Hypertension.
Brain Sciences
Moskaleva, Polina V PV; Shnayder, Natalya A NA; Petrova, Marina M MM; Kaskaeva, Daria S DS; Gavrilyuk, Oksana A OA; Radostev, Sergey V SV; Garganeeva, Natalia P NP; Sharavii, Victoria B VB; Vaiman, Elena E EE; Nasyrova, Regina F RF
Sex-Specific Genetic Susceptibility to Adverse Neurodevelopmental Outcome in Offspring of Pregnancies at Risk of Early Preterm Delivery.
American Journal Of Perinatology
Varner, Michael W MW; Costantine, Maged M MM; Jablonski, Kathleen A KA; Rouse, Dwight J DJ; Mercer, Brian M BM; Leveno, Kenneth J KJ; Reddy, Uma M UM; Buhimschi, Catalin C; Wapner, Ronald J RJ; Sorokin, Yoram Y; Thorp, John M JM; Ramin, Susan M SM; Malone, Fergal D FD; Carpenter, Marshall M; O'sullivan, Mary J MJ; Peaceman, Alan M AM; Dudley, Donald J DJ; Caritis, Steve N SN; ,
Genetic Variation, Magnesium Sulfate Exposure, and Adverse Neurodevelopmental Outcomes Following Preterm Birth.
American Journal Of Perinatology
Clark, Erin A S EAS; Weiner, Steven J SJ; Rouse, Dwight J DJ; Mercer, Brian M BM; Reddy, Uma M UM; Iams, Jay D JD; Wapner, Ronald J RJ; Sorokin, Yoram Y; Malone, Fergal D FD; O'Sullivan, Mary J MJ; Peaceman, Alan M AM; Hankins, Gary D V GDV; Dudley, Donald J DJ; Caritis, Steve N SN; ,
Deep-targeted sequencing of endothelial nitric oxide synthase gene exons uncovers exercise intensity and ethnicity-dependent associations with post-exercise hypotension.
Physiological Reports
Pescatello, Linda S LS; Schifano, Elizabeth D ED; Ash, Garrett I GI; Panza, Gregory A GA; Corso, Lauren M L LML; Chen, Ming-Hui MH; Deshpande, Ved V; Zaleski, Amanda A; Cilhoroz, Burak B; Farinatti, Paulo P; Taylor, Beth A BA; O'Neill, Rachel J RJ; Thompson, Paul D PD
Candidate gene analysis in pathogenesis of surgically and non-surgically treated necrotizing enterocolitis in preterm infants.
Molecular And Cellular Biochemistry
Szpecht, Dawid D; Neumann-Klimasińska, Natalia N; Błaszczyński, Michał M; Seremak-Mrozikiewicz, Agnieszka A; Kurzawińska, Grażyna G; Cygan, Dorothy D; Szymankiewicz, Marta M; Drews, Krzysztof K; Gadzinowski, Janusz J
Editor's Highlight: Modifying Role of Endothelial Function Gene Variants on the Association of Long-Term PM2.5 Exposure With Blood DNA Methylation Age: The VA Normative Aging Study.
Toxicological Sciences : An Official Journal Of The Society Of Toxicology
Nwanaji-Enwerem, Jamaji C JC; Bind, Marie-Abele MA; Dai, Lingzhen L; Oulhote, Youssef Y; Colicino, Elena E; Di, Qian Q; Just, Allan C AC; Hou, Lifang L; Vokonas, Pantel P; Coull, Brent A BA; Weisskopf, Marc G MG; Baccarelli, Andrea A AA; Schwartz, Joel D JD
Are Immune Modulating Single Nucleotide Polymorphisms Associated with Necrotizing Enterocolitis?
Scientific Reports
Franklin, Ashanti L AL; Said, Mariam M; Cappiello, Clint D CD; Gordish-Dressman, Heather H; Tatari-Calderone, Zohreh Z; Vukmanovic, Stanislav S; Rais-Bahrami, Khodayar K; Luban, Naomi L C NL; Devaney, Joseph M JM; Sandler, Anthony D AD
Association between polymorphisms in NOS3 and KCNH2 and social memory.
Frontiers In Neuroscience
Henningsson, Susanne S; Zettergren, Anna A; Hovey, Daniel D; Jonsson, Lina L; Svärd, Joakim J; Cortes, Diana S DS; Melke, Jonas J; Ebner, Natalie C NC; Laukka, Petri P; Fischer, Håkan H; Westberg, Lars L
Angiogenesis related genes NOS3, CD14, MMP3 and IL4R are associated to VEGF gene expression and circulating levels in healthy adults.
Bmc Medical Genetics
Saleh, Abdelsalam A; Stathopoulou, Maria G MG; Dadé, Sébastien S; Ndiaye, Ndeye Coumba NC; Azimi-Nezhad, Mohsen M; Murray, Helena H; Masson, Christine C; Lamont, John J; Fitzgerald, Peter P; Visvikis-Siest, Sophie S
Interaction between arsenic exposure from drinking water and genetic polymorphisms on cardiovascular disease in Bangladesh: a prospective case-cohort study.
Environmental Health Perspectives
Wu, Fen F; Jasmine, Farzana F; Kibriya, Muhammad G MG; Liu, Mengling M; Cheng, Xin X; Parvez, Faruque F; Islam, Tariqul T; Ahmed, Alauddin A; Rakibuz-Zaman, Muhammad M; Jiang, Jieying J; Roy, Shantanu S; Paul-Brutus, Rachelle R; Slavkovich, Vesna V; Islam, Tariqul T; Levy, Diane D; VanderWeele, Tyler J TJ; Pierce, Brandon L BL; Graziano, Joseph H JH; Ahsan, Habibul H; Chen, Yu Y
Genetic association analyses of nitric oxide synthase genes and neural tube defects vary by phenotype.
Birth Defects Research. Part B, Developmental And Reproductive Toxicology
Soldano, Karen L KL; Garrett, Melanie E ME; Cope, Heidi L HL; Rusnak, J Michael JM; Ellis, Nathen J NJ; Dunlap, Kaitlyn L KL; Speer, Marcy C MC; Gregory, Simon G SG; Ashley-Koch, Allison E AE
Nitric oxide synthase polymorphisms, gene expression and lung function in chronic obstructive pulmonary disease.
Bmc Pulmonary Medicine
Aminuddin, Farzian F; Hackett, Tillie-Louise TL; Stefanowicz, Dorota D; Saferali, Aabida A; Paré, Peter D PD; Gulsvik, Amund A; Bakke, Per P; Cho, Michael H MH; Litonjua, Augusto A; Lomas, David A DA; Anderson, Wayne H WH; Beaty, Terri H TH; Silverman, Edwin K EK; Sandford, Andrew J AJ
A Novel Mathematical Approach to Define the Genes/SNPs Conferring Risk or Protection in Sporadic Amyotrophic Lateral Sclerosis Based on Auto Contractive Map Neural Networks and Graph Theory.
Neurology Research International
Buscema, Massimo M; Penco, Silvana S; Grossi, Enzo E
Pharmacogenetic association of NOS3 variants with cardiovascular disease in patients with hypertension: the GenHAT study.
Plos One
Zhang, Xue X; Lynch, Amy I AI; Davis, Barry R BR; Ford, Charles E CE; Boerwinkle, Eric E; Eckfeldt, John H JH; Leiendecker-Foster, Catherine C; Arnett, Donna K DK
Genomewide association study using a high-density single nucleotide polymorphism array and case-control design identifies a novel essential hypertension susceptibility locus in the promoter region of endothelial NO synthase.
Hypertension (Dallas, Tex. : 1979)
Salvi, Erika E; Kutalik, Zoltán Z; Glorioso, Nicola N; Benaglio, Paola P; Frau, Francesca F; Kuznetsova, Tatiana T; Arima, Hisatomi H; Hoggart, Clive C; Tichet, Jean J; Nikitin, Yury P YP; Conti, Costanza C; Seidlerova, Jitka J; Tikhonoff, Valérie V; Stolarz-Skrzypek, Katarzyna K; Johnson, Toby T; Devos, Nabila N; Zagato, Laura L; Guarrera, Simonetta S; Zaninello, Roberta R; Calabria, Andrea A; Stancanelli, Benedetta B; Troffa, Chiara C; Thijs, Lutgarde L; Rizzi, Federica F; Simonova, Galina G; Lupoli, Sara S; Argiolas, Giuseppe G; Braga, Daniele D; D'Alessio, Maria C MC; Ortu, Maria F MF; Ricceri, Fulvio F; Mercurio, Maurizio M; Descombes, Patrick P; Marconi, Maurizio M; Chalmers, John J; Harrap, Stephen S; Filipovsky, Jan J; Bochud, Murielle M; Iacoviello, Licia L; Ellis, Justine J; Stanton, Alice V AV; Laan, Maris M; Padmanabhan, Sandosh S; Dominiczak, Anna F AF; Samani, Nilesh J NJ; Melander, Olle O; Jeunemaitre, Xavier X; Manunta, Paolo P; Shabo, Amnon A; Vineis, Paolo P; Cappuccio, Francesco P FP; Caulfield, Mark J MJ; Matullo, Giuseppe G; Rivolta, Carlo C; Munroe, Patricia B PB; Barlassina, Cristina C; Staessen, Jan A JA; Beckmann, Jacques S JS; Cusi, Daniele D
Genetic Association Analysis of NOS3 and Methamphetamine-Induced Psychosis Among Japanese.
Current Neuropharmacology
Okochi, T T; Kishi, T T; Ikeda, M M; Kitajima, T T; Kinoshita, Y Y; Kawashima, K K; Okumura, T T; Tsunoka, T T; Fukuo, Y Y; Inada, T T; Yamada, M M; Uchimura, N N; Iyo, M M; Sora, I I; Ozaki, N N; Ujike, H H; Iwata, N N
Association of fetal inflammation and coagulation pathway gene polymorphisms with neurodevelopmental delay at age 2 years.
American Journal Of Obstetrics And Gynecology
Clark, Erin A S EA; Mele, Lisa L; Wapner, Ronald J RJ; Spong, Catherine Y CY; Sorokin, Yoram Y; Peaceman, Alan A; Iams, Jay D JD; Leveno, Kenneth J KJ; Harper, Margaret M; Caritis, Steve N SN; Miodovnik, Menachem M; Mercer, Brian M BM; Thorp, John M JM; Ramin, Susan M SM; Carpenter, Marshall M; Rouse, Dwight J DJ; ,
Endothelial nitric oxide synthase gene variants and primary open-angle glaucoma: interactions with sex and postmenopausal hormone use.
Investigative Ophthalmology & Visual Science
Kang, Jae Hee JH; Wiggs, Janey L JL; Rosner, Bernard A BA; Hankinson, Susan E SE; Abdrabou, Wael W; Fan, Bao Jian BJ; Haines, Jonathan J; Pasquale, Louis R LR
Relation of candidate genes that encode for endothelial function to migraine and stroke: the Stroke Prevention in Young Women study.
Stroke
MacClellan, Leah R LR; Howard, Timothy D TD; Cole, John W JW; Stine, O Colin OC; Giles, Wayne H WH; O'Connell, Jeffery R JR; Wozniak, Marcella A MA; Stern, Barney J BJ; Mitchell, Braxton D BD; Kittner, Steven J SJ