Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 50 Records) |
| Query Trace: Disease and NOS1[original query] |
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| Genetic variance in nitric oxide synthase and endothelin genes among children with and without endothelial dysfunction. Journal of translational medicine 2013 11 227. Chatsuriyawong Siriporn, Gozal David, Kheirandish-Gozal Leila, Bhattacharjee Rakesh, Khalyfa Ahamed A, Wang Yang, Hakonarson Hakon, Keating Brendan, Sukhumsirichart Wasana, Khalyfa Abdelna |
| Nitric oxide synthase polymorphisms, gene expression and lung function in chronic obstructive pulmonary disease. BMC pulmonary medicine 2013 13 (1): 64. Aminuddin Farzian, Hackett Tillie-Louise, Stefanowicz Dorota, Saferali Aabida, Paré Peter D, Gulsvik Amund, Bakke Per, Cho Michael H, Litonjua Augusto, Lomas David A, Anderson Wayne H, Beaty Terri H, Silverman Edwin K, Sandford Andrew |
| The genetic contribution of the NO system at the glutamatergic post-synapse to schizophrenia: further evidence and meta-analysis. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2014 Jan 24 (1): 65-85. Weber H, Klamer D, Freudenberg F, Kittel-Schneider S, Rivero O, Scholz C-J, Volkert J, Kopf J, Heupel J, Herterich S, Adolfsson R, Alttoa A, Post A, Grußendorf H, Kramer A, Gessner A, Schmidt B, Hempel S, Jacob C P, Sanjuán J, Moltó M D, Lesch K-P, Freitag C M, Kent L, Reif |
| Nitric oxide synthase (NOS) single nucleotide polymorphisms are associated with coronary heart disease and hypertension in the INTERGENE study. Nitric oxide : biology and chemistry / official journal of the Nitric Oxide Society 2014 May 39 1-7. Levinsson Anna, Olin Anna-Carin, Björck Lena, Rosengren Annika, Nyberg Fredr |
| Pharmacogenomics of 17-alpha hydroxyprogesterone caproate for recurrent preterm birth prevention. American journal of obstetrics and gynecology 2014 Apr 210 (4): 321.e1-321.e21. Manuck Tracy A, Watkins W Scott, Moore Barry, Esplin M Sean, Varner Michael W, Jackson G Marc, Yandell Mark, Jorde Ly |
| Genetic variants in ICAM1, PPARGC1A and MTHFR are potentially associated with different phenotypes of diabetic retinopathy. Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift für Augenheilkunde 2014 232 (3): 156-62. Simões Maria José, Lobo Conceição, Egas Conceição, Nunes Sandrina, Carmona Susana, Costa Miguel Ângelo, Duarte Tânia, Ribeiro Luísa, Faro Carlos, Cunha-Vaz José |
| Organophosphate Pesticide Exposures, Nitric Oxide Synthase Gene Variants, and Gene-Pesticide Interactions in a Case-Control Study of Parkinson's Disease, California (USA). Environmental health perspectives 2015 Sep . Paul Kimberly C, Sinsheimer Janet S, Rhodes Shannon L, Cockburn Myles, Bronstein Jeff, Ritz Bea |
| Identification of gene variants related to the nitric oxide pathway in patients with acute coronary syndrome. Gene 2015 Jul . Umman B, Cakmakoglu B, Cincin Z B, Kocaaga M, Emet S, Tamer S, Gokkusu |
| On the role of NOS1 ex1f-VNTR in ADHD-allelic, subgroup, and meta-analysis. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Jun . Weber Heike, Kittel-Schneider Sarah, Heupel Julia, Weißflog Lena, Kent Lindsey, Freudenberg Florian, Alttoa Aet, Post Antonia, Herterich Sabine, Haavik Jan, Halmøy Anne, Fasmer Ole B, Landaas Elisabeth T, Johansson Stefan, Cormand Bru, Ribasés Marta, Sánchez-Mora Cristina, Ramos-Quiroga Josep Antoni, Franke Barbara, Lesch Klaus-Peter, Reif Andre |
| Genetic association of NOS1 exon18, NOS1 exon29, ABCB1 1236C/T, and ABCB1 3435C/T polymorphisms with the risk of Parkinson's disease: A meta-analysis. Medicine 2016 Oct 95 (40): e4982. Huang Hongbin, Peng Cong, Liu Yong, Liu Xu, Chen Qicong, Huang Zunn |
| Association of a neuronal nitric oxide synthase gene polymorphism with levodopa-induced dyskinesia in Parkinson's disease. Nitric oxide : biology and chemistry 2017 Jun . Santos-Lobato Bruno Lopes, Borges Vanderci, Ferraz Henrique Ballalai, Mata Ignacio Fernandez, Zabetian Cyrus P, Tumas Vit |
| Genetics of Aggression in Alzheimer's Disease (AD). Frontiers in aging neuroscience 2017 9 87. Lukiw Walter J, Rogaev Evgeny |
| Rs2910164 in microRNA?146a confers an elevated risk of depression in patients with coronary artery disease by modulating the expression of NOS1. Molecular medicine reports 2018 Apr . Zhang Xinling, Huo Qianqian, Sun Wei, Zhang Chunxiang, Wu Zongyin, Xing Bing, Li Qia |
| Variation of genes involved in oxidative and nitrosative stresses in depression. European psychiatry : the journal of the Association of European Psychiatrists 2017 Dec 48 38-48. Wigner Paulina, Czarny Piotr, Synowiec Ewelina, Bijak Micha?, Bia?ek Katarzyna, Talarowska Monika, Galecki Piotr, Szemraj Janusz, Sliwinski Toma |
| Clinical-Pharmacogenetic Predictive Models for Time to Occurrence of Levodopa Related Motor Complications in Parkinson's Disease. Frontiers in genetics 2019 10 461. Redenšek Sara, Jenko Bizjan Barbara, Trošt Maja, Dolžan Vi |
| Role of Genomic Biomarkers in Increasing Fetal Hemoglobin Levels Upon Hydroxyurea Therapy and in ?-Thalassemia Intermedia: A Validation Cohort Study. Hemoglobin 2019 5 43 (1): 27-33. Kolliopoulou Alexandra, Siamoglou Stavroula, John Anne, Sgourou Argyro, Kourakli Alexandra, Symeonidis Argiris, Vlachaki Efthymia, Chalkia Panagiota, Theodoridou Stamatia, Ali Bassam R, Katsila Theodora, Patrinos George P, Papachatzopoulou Adamant |
| The association of Intron 4 VNTR and Glu298Asp polymorphisms of the nitric oxide synthetase 3 gene and vasculogenic erectile dysfunction in Turkish men. Systems biology in reproductive medicine 2019 Apr 1-7. Arda Ersan, Ay Arzu, Akdere Hakan, Akdeniz Es |
| Genetic variability of inflammation and oxidative stress genes does not play a major role in the occurrence of adverse events of dopaminergic treatment in Parkinson's disease. Journal of neuroinflammation 2019 Feb 16 (1): 50. Redenšek Sara, Flisar Dušan, Kojovic Maja, Kramberger Milica Gregoric, Georgiev Dejan, Pirtošek Zvezdan, Trošt Maja, Dolžan Vi |
| Identification of exon skipping events associated with Alzheimer's disease in the human hippocampus. BMC medical genomics 2019 2 12 (Suppl 1): 13. Han Seonggyun, Miller Jason E, Byun Seyoun, Kim Dokyoon, Risacher Shannon L, Saykin Andrew J, Lee Younghee, Nho Kwangsik, |
| Clinical and Clinical-Pharmacogenetic Models for Prediction of the Most Common Psychiatric Complications Due to Dopaminergic Treatment in Parkinson's Disease. The international journal of neuropsychopharmacology 2020 7 23 (8): 496-504. Redenšek Sara, Jenko Bizjan Barbara, Trošt Maja, Dolžan Vi |
| 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 |
| Genetic factors in treatment-related cardiovascular complications in survivors of childhood acute lymphoblastic leukemia. Pharmacogenomics 2021 9 22 (14): 885-901. Petrykey Kateryna, Rezgui Aziz M, Guern Mathilde Le, Beaulieu Patrick, St-Onge Pascal, Drouin Simon, Bertout Laurence, Wang Fan, Baedke Jessica L, Yasui Yutaka, Hudson Melissa M, Raboisson Marie-Josée, Laverdière Caroline, Sinnett Daniel, Andelfinger Gregor U, Krajinovic Ma |
| Single-Nucleotide Polymorphisms in Oxidative Stress-Related Genes and the Risk of a Stroke in a Polish Population-A Preliminary Study. Brain sciences 2021 Mar 11 (3): . Synowiec Ewelina, Wigner Paulina, Cichon Natalia, Watala Cezary, Czarny Piotr, Saluk-Bijak Joanna, Miller Elzbieta, Sliwinski Tomasz, Zielinska-Nowak Ewa, Bijak Mich |
| Nitric Oxide Synthase 2 Promoter Polymorphism Is a Risk Factor for Allergic Asthma in Children. Medicina (Kaunas, Lithuania) 2021 12 57 (12): . Nowakowska Joanna, Sobkowiak Paulina, Br?borowicz Anna, Mrówczy?ska Magdalena, Wojsyk-Banaszak Irena, Szczepankiewicz Aleksand |
| Variation of genes encoding nitric oxide synthases and antioxidant enzymes as potential risks of multiple sclerosis development: a preliminary study. Scientific reports 2022 Jun 12 (1): 10603. Wigner Paulina, Dziedzic Angela, Synowiec Ewelina, Miller Elzbieta, Bijak Michal, Saluk-Bijak Joan |
| The rs2682826 Polymorphism of the NOS1 Gene Is Associated with the Degree of Disability of Erectile Dysfunction. Life (Basel, Switzerland) 2023 5 13 (5): . Leticia Perticarrara Ferezin, Cezar Kayzuka, Vitória Carolina Rondon Pereira, Murilo Ferreira de Andrade, Carlos Augusto Fernandes Molina, Silvio Tucci, Jose Eduardo Tanus-Santos, Riccardo Lacchi |
| Quantitative and causal analysis for inflammatory genes and the risk of Parkinson's disease. Frontiers in immunology 2023 3 14 1119315. Yi Minhan, Li Jiaxin, Jian Shijie, Li Binbin, Huang Zini, Shu Li, Zhang Yu |
| Variation in Exon 29 of the NOS1 Gene Does Not Contribute to Parkinson's Disease in the North Karnataka Population. Cureus 2023 10 15 (9): e45347. Rudragouda Bulagouda, Smita Hegde, Rajat Hegde, Ashwini Hiremath, G M Wali, Gurushantappa S Kadak |
| Caffeine Consumption and Interaction with ADORA2A, CYP1A2 and NOS1 Variants Do Not Influence Age at Onset of Machado-Joseph Disease. Cerebellum (London, England) 2024 7 . Ana Carolina Martins, Jordânia Dos Santos Pinheiro, Luciana Szinwelski, Eduardo Rockenbach Cidade, Danilo Fernando Santin, Laura Damke Proença, Bruna Almeida Araújo, Maria Luiza Saraiva-Pereira, Laura Bannach Jard |
| Interaction between Caffeine Consumption & Genetic susceptibility in Parkinson's disease: a systematic review. Ageing research reviews 2024 6 102381. Yujuan Yang, Zhi-Dong Zhou, Ling Xiao Yi, Brendan Jen-Wei Tan, Eng-King T |
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