Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 42 Records) |
Query Trace: Syndrome and NOS3[original query] |
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The Role of -786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic Syndrome. International journal of endocrinology 2011 2011 458750. Misiak Blazej, Krolik Marta, Kukowka Anna, Lewera Anna, Leszczynski Przemyslaw, Stankiewicz-Olczyk Joanna, Slezak Rysza |
Interaction between endothelial nitric oxide synthase gene polymorphisms (-786T>C, 894G>T and intron 4 a/b) and cardiovascular risk factors in acute coronary syndromes. Archives of medical research 2012 Apr 43 (3): 205-11. da Costa Escobar Piccoli Jacqueline, Manfredini Vanusa, Hamester Fernanda Irma, Bandinelli Josiane Bettim, Turkienicz Ilan Maltz, Chies José Artur Bogo, Peres Alessandra, Bodanese Luiz Carlos, Bogo Maurício Re |
CYP1A1, GCLC, AGT, AGTR1 gene-gene interactions in community-acquired pneumonia pulmonary complications. Molecular biology reports 2013 Nov 40 (11): 6163-76. Salnikova Lyubov E, Smelaya Tamara V, Golubev Arkadiy M, Rubanovich Alexander V, Moroz Viktor |
Association between endothelial nitric oxide synthase gene polymorphism (-786T>C) and interleukin-6 in acute coronary syndrome. Human & experimental toxicology 2014 Apr 33 (4): 396-402. Piccoli J C E, Manfredini V, Faoro D, Farias F M, Bodanese L C, Bogo M |
Association between endothelial nitric oxide synthase polymorphisms and risk of metabolic syndrome. Disease markers 2013 34 (3): 187-97. Liu Chiu-Shong, Huang Ru-Jiun, Sung Fung-Chang, Lin Cheng-Chieh, Yeh Chih-Chi |
Analysis of nitric oxide synthase gene polymorphisms in neonatal respiratory distress syndrome among the Chinese Han population. Italian journal of pediatrics 2014 40 (1): 27. Shen Wei, Du Jiang, Wang Bin, Zeng Qi |
Association of Nitric Oxide Synthase and Matrix Metalloprotease Single Nucleotide Polymorphisms with Preeclampsia and Its Complications. PloS one 2015 10 (8): e0136693. Leonardo Daniela P, Albuquerque Dulcinéia M, Lanaro Carolina, Baptista Letícia C, Cecatti José G, Surita Fernanda G, Parpinelli Mary A, Costa Fernando F, Franco-Penteado Carla F, Fertrin Kleber Y, Costa Maria Lau |
Role of polymorphisms of inducible nitric oxide synthase and endothelial nitric oxide synthase in idiopathic environmental intolerances. Mediators of inflammation 2015 2015 245308. De Luca Chiara, Gugliandolo Agnese, Calabrò Carlo, Currò Monica, Ientile Riccardo, Raskovic Desanka, Korkina Ludmila, Caccamo Danie |
[Pathogenetic significance of C774T single nucleotide polymorphism of the endothelial NO synthase gene in the development of metabolic syndrome]. Biomedit?s?inskai?a? khimii?a? 2016 May 62 (4): 447-52. Fattakhov N S, Vasilenko M A, Skuratovskaia D A, Kulikov D I, Kirienkova E V, Zatolokin P A, Beletskaya M A, Litvinova L |
Association of a NOS3 gene polymorphism with Behçet's disease but not with Vogt-Koyanagi-Harada syndrome in Han Chinese. Molecular vision 2016 22 311-8. Zhou Yan, Yu Hongsong, Hou Shengping, Fang Jing, Qin Jieying, Yuan Gangxiang, Kijlstra Aize, Yang Peize |
Association between functional polymorphisms in the nitric oxide synthase 3 gene and pediatric acute respiratory distress syndrome. Genetics and molecular research : GMR 2016 Sep 15 (3): . Wei L, An Y, Wang |
The molecular and genetic aspects of adolescent girls anomalous uterine bleeding: the role of endothelial dysfunction syndrome. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2016 Oct 32 (sup2): 23-26. Melkozerova O A, Bashmakova N V, Volkova E V, Tretyakova T B, Tsyvian P |
Splenomegaly and Its Associations with Genetic Polymorphisms and Treatment Outcome in Colorectal Cancer Patients Treated with Adjuvant FOLFOX. Cancer research and treatment : official journal of Korean Cancer Association 2016 Jul 48 (3): 990-7. Kim Mi-Jung, Han Sae-Won, Lee Dae-Won, Cha Yongjun, Lee Kyung-Hun, Kim Tae-Yong, Oh Do-Youn, Kim Se Hyung, Im Seock-Ah, Bang Yung-Jue, Kim Tae-Y |
Association of Glu298Asp Polymorphism of Endothelial NO Synthase Gene with Metabolic Syndrome Development: a Pilot Study. Bulletin of experimental biology and medicine 2017 Mar . Fattakhov N S, Skuratovskaya D A, Vasilenko M A, Kirienkova E V, Zatolokin P A, Mironyuk N I, Litvinova L |
Haplotype analysis of endothelial nitric oxide synthase (NOS3) genetic variants and metabolic syndrome in healthy subjects and schizophrenia patients. International journal of obesity (2005) 2018 Jun . Fattakhov Nikolai, Smirnova Liudmila, Atochin Dmitriy, Parshukova Daria, Skuratovskaia Daria, Painter Quinn, Zatolokin Pavel, Semke Arkadiy, Litvinova Larisa, Ivanova Svetla |
Novel West syndrome candidate genes in a Chinese cohort. CNS neuroscience & therapeutics 2018 4 24 (12): 1196-1206. Peng Jing, Wang Ying, He Fang, Chen Chen, Wu Li-Wen, Yang Li-Fen, Ma Yu-Ping, Zhang Wen, Shi Zi-Qing, Chen Chao, Xia Kun, Guo Hui, Yin Fei, Pang N |
High levels of chemerin associated with variants in the NOS3 and APOB genes in rural populations of Ouro Preto, Minas Gerais, Brazil. Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas 2020 53 (6): e9113. Batista A P, Barbosa K F, Masioli C Z, Queiroz E M, Marinho C C, Cândido A P C, Machado-Coelho G L |
NOS3 Gene rs1799983 and rs2070744 Polymorphisms in Patients with Unstable Angina. Journal of vascular research 2020 Mar 1-7. Pawlik Andrzej, B?aszczyk Halina, Ra? Monika, Maciejewska-Skrendo Agnieszka, Safranow Krzysztof, Dziedziejko Violet |
The incidence of NOS3 gene polymorphisms on newborns with large and small birth weight. Molecular biology reports 2020 Oct . de Aragão Santos Thaysa Walléria, Dos Santos Catena Andriu, da Silva Mattos Sandra, de Lima Filho José Luiz, Gondim Martins Danyelly Brunes |
Potential Role of eNOS Genetic Variants in Ischemic Heart Disease Susceptibility and Clinical Presentation. Journal of cardiovascular development and disease 2021 Sep 8 (9): . Severino Paolo, D'Amato Andrea, Prosperi Silvia, Magnocavallo Michele, Mariani Marco Valerio, Netti Lucrezia, Birtolo Lucia Ilaria, De Orchi Paolo, Chimenti Cristina, Maestrini Viviana, Miraldi Fabio, Lavalle Carlo, Caputo Viviana, Palmirotta Raffaele, Mancone Massimo, Fedele Frances |
Association of NOS3-c.894G>T transversion with susceptibility to metabolic syndrome in Azar-cohort population: A case-control study and in silico analysis of the SNP molecular effects. Iranian journal of basic medical sciences 2021 5 24 (3): 408-419. Seyedrezazadeh Ensiyeh, Faramarzi Elnaz, Bakhtiyari Nasim, Ansarin Atefeh, Gilani Neda, Amiri-Sadeghan Amir, Seyyedi Maryam, Ansarin Khalil, Aftabi Youn |
Association between Genetic Variants in NOS2 and TNF Genes with Congenital Zika Syndrome and Severe Microcephaly. Viruses 2021 02 13 (2): . Gomes Julia A, Sgarioni Eduarda, Boquett Juliano A, Terças-Trettel Ana Cláudia P, da Silva Juliana H, Ribeiro Bethânia F R, Galera Marcial F, de Oliveira Thalita M, Carvalho de Andrade Maria Denise F, Carvalho Isabella F, Schüler-Faccini Lavínia, Vianna Fernanda S |
Association of Aquaporin-3, Aquaporin-7, NOS3 and CYBA polymorphisms with hypertensive disorders in women. Pregnancy hypertension 2021 3 24 44-49. da Silva Inês Vieira, Santos Ana Carolina, Matos Andreia, Pereira da Silva Alda, Soveral Graça, Rebelo Irene, Bicho Manu |
Common Endothelial Nitric Oxide Synthase Single Nucleotide Polymorphisms are not Related With the Risk for Restless Legs Syndrome. Frontiers in pharmacology 2021 12 618989. Jiménez-Jiménez Félix Javier, Agúndez Blanca G, Gómez-Tabales Javier, Alonso-Navarro Hortensia, Turpín-Fenoll Laura, Millán-Pascual Jorge, Díez-Fairén Mónica, Álvarez Ignacio, Pastor Pau, Calleja Marisol, García-Ruiz Rafael, Navarro-Muñoz Santiago, Recio-Bermejo Marta, Plaza-Nieto José Francisco, García-Albea Esteban, García-Martín Elena, Agúndez José A |
Association between nitric oxide synthase 3 genetic variant and acute kidney injury following pediatric cardiac surgery. American heart journal 2022 8 254 57-65. Kikano Sandra, Breeyear Joseph, Aka Ida, Edwards Todd L, Van Driest Sara L, Kannankeril Prince |
CELSR1 Risk Alleles in Familial Bicuspid Aortic Valve and Hypoplastic Left Heart Syndrome. Circulation. Genomic and precision medicine 2022 2 15 (2): e003523. Theis Jeanne L, Niaz Talha, Sundsbak Rhianna S, Fogarty Zachary C, Bamlet William R, Hagler Donald J, Olson Timothy |
The Association of PLAUR Genotype and Soluble suPAR Serum Level with COVID-19-Related Lung Damage Severity. International journal of molecular sciences 2022 12 23 (24): . Nekrasova Ludmila A, Shmakova Anna A, Samokhodskaya Larisa M, Kirillova Karina I, Stoyanova Simona S, Mershina Elena A, Nazarova Galina B, Rubina Kseniya A, Semina Ekaterina V, Kamalov Armais |
Glu298Asp variant of the endothelial nitric oxide synthase gene and acute coronary syndrome or premature coronary artery disease: A systematic review and meta-analysis. Nitric oxide : biology and chemistry 2023 7 138-139 85-95. Himanshu Rai, Sean Fitzgerald, J J Coughlan, Mark Spence, Roisin Colleran, Michael Joner, Robert A Byr |
NOS3 (rs61722009) gene variants testing in prediction of COVID-19 pneumonia severity. Nitric oxide : biology and chemistry 2023 4 134-135 44-48. Fishchuk Liliia, Rossokha Zoia, Pokhylko Valeriy, Cherniavska Yuliia, Dubitska Olha, Vershyhora Viktoriia, Tsvirenko Svitlana, Kovtun Serhii, Gorovenko Natali |
Genetic Susceptibility to Tardive Dyskinesia and Cognitive Impairments in Chinese Han Schizophrenia: Role of Oxidative Stress-Related and Adenosine Receptor Genes. Neuropsychiatric disease and treatment 2023 11 19 2499-2509. Qiaona Jiang, Xiaofei Zhang, Xiaohui Lu, Yanzhe Li, Chenghao Lu, Jinghui Chi, Yanyan Ma, Xiaomei Shi, Lili Wang, Shen |
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- Page last updated:Apr 22, 2024
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