Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 162 Records) |
Query Trace: NOS1[original query] |
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[Effects of Nitric Oxide Synthase-1 Exon 1f-VNTR Gene Polymorphism on the Clinical Symptoms of Alcohol Dependence,Impulsivity and Comorbid Attention Deficit Hyperactivity Disorder]. Turk psikiyatri dergisi = Turkish journal of psychiatry 2019 30 (2): 82-89. Karakaya ?brahim, Gürel ?eref Can, Ayhan Yavuz, Ka?ifo?lu Mehmet Ali, Karahan Sevilay, Babao?lu Melih Önder, Göka Erol, Dilbaz Hilmiye Nesrin, Ulu? Berna Diclenur, Demir Ba?ar |
Nitric oxide synthase genotype interacts with stressful life events to increase aggression in male subjects in a population-representative sample. European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2019 Aug . O'Leary Aet, Laas Kariina, Vaht Mariliis, Kiive Evelyn, Veidebaum Toomas, Reif Andreas, Harro Jaan |
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 |
Genetic Association Study of Restless Legs Syndrome in Chinese Population. European neurology 2019 May 81 (1-2): 47-55. Chen Jie, Luo Qi, Li Gen, Huang Yumeng, Ma Jianfa |
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 |
IL1B polymorphism is associated with essential tremor in Chinese population. BMC neurology 2019 May 19 (1): 99. Chen Jie, Huang Pei, He Yachao, Shen Junyi, Du Juanjuan, Cui Shishuang, Chen Shengdi, Ma Jianfa |
Influence of two functional polymorphisms in NOS1 on baseline cortisol and working memory in healthy subjects. Nitric oxide : biology and chemistry 2019 Apr 88 45-49. Roth N J, Zipperich S, Kopf J, Deckert J, Reif |
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 |
Association between polymorphisms of NOS1, NOS2 and NOS3 genes and suicide behavior: a systematic review and meta-analysis. Metabolic brain disease 2019 Mar . González-Castro Thelma Beatriz, Genis-Mendoza Alma Delia, Tovilla-Zárate Carlos Alfonso, Juárez-Rojop Isela Esther, López-Narvaez María Lilia, Pérez-Hernández Nonanzit, Rodríguez-Pérez José Manuel, Martínez-Magaña José Jai |
Genetic Risk Factors for Essential Tremor: A Review. Tremor and other hyperkinetic movements (New York, N.Y.) 2020 Jun 10 4. Siokas Vasileios, Aloizou Athina-Maria, Tsouris Zisis, Liampas Ioannis, Aslanidou Paraskevi, Dastamani Metaxia, Brotis Alexandros G, Bogdanos Dimitrios P, Hadjigeorgiou Georgios M, Dardiotis Efthimi |
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 |
Neural correlates of NOS1 ex1f-VNTR allelic variation in panic disorder and agoraphobia during fear conditioning and extinction in fMRI. NeuroImage. Clinical 2020 Apr 27 102268. Ridderbusch Isabelle C, Yang Yunbo, Weber Heike, Reif Andreas, Herterich Sabine, Ströhle Andreas, Pfleiderer Bettina, Arolt Volker, Wittchen Hans-Ulrich, Lueken Ulrike, Kircher Tilo, Straube Benjam |
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 |
NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis. Cardiovascular research 2020 2 117 (2): 472-483. Ronchi Carlotta, Bernardi Joyce, Mura Manuela, Stefanello Manuela, Badone Beatrice, Rocchetti Marcella, Crotti Lia, Brink Paul, Schwartz Peter J, Gnecchi Massimiliano, Zaza Anton |
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 |
Defective Allele of the Neuronal Nitric Oxide Synthase Gene Increases Insulin Resistance During Acute Phase of Myocardial Infarction. International journal of general medicine 2021 14 3669-3676. Nóbrega Otávio T, Campos-Staffico Alessandra M, Oliveira Elayne Kelen, Munhoz Daniel B, Moura Filipe A, Carvalho Luis Sérgio F, Soares Alexandre Anderson S M, Gomes Ciro M, Tonet-Furioso Audrey C, Sposito Andrei C, |
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 (NOS2) gene polymorphism c.1832C>T (Ser608Leu) associated with nitrosative stress in Fanconi anaemia. Molecular biology reports 2021 Mar . George Merin, Solanki Avani, Mohanty Purvi, Dhangar Somprakash, Rajendran Aruna, Mohan Sheila, Vundinti Babu R |
Inhibition-directed multimodal imaging fusion patterns in adults with ADHD and its potential underlying "gene-brain-cognition" relationship. CNS neuroscience & therapeutics 2021 3 27 (6): 664-673. Guo Xiaojie, Liu Lu, Li Tiantian, Zhao Qihua, Li Hui, Huang Fang, Wang Yanfei, Qian Qiujin, Cao Qingjiu, Wang Yufeng, Calhoun Vince D, Sui Jing, Sun |
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 |
Association Analysis of Neuronal Nitric Oxide Synthase 1 Gene Polymorphism With Psychopathological Symptoms in Chronic Ketamine Users. Frontiers in psychiatry 2020 11 580771. Chen Jiansong, Zhang Minling, Zhou Chao, Ding Yi, Fan Ni, He Hong |
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 |
Genetic Analysis of RASD1 as a Candidate Gene for Schizophrenia. Balkan medical journal 2022 10 39 (6): 422-428. Durmaz Ceren Damla, Karabulut Halil Gürhan, Saka Meram Can, Sucularl? Ceren, Gümü? Akay Güvem, Atba?o?lu Cem, Ilg?n Ruhi Hati |
Absence of a significant interaction of two common NOS1 and 5-HTT polymorphisms on sensorimotor gating in humans. Physiological research 2021 12 70 (S3): S387-S395. Rovný R, Marko M, Minárik G, Rie?anský |
Uncovering associations between mental illness diagnosis, nitric oxide synthase gene variation, and peripheral nitric oxide concentration. Brain, behavior, and immunity 2022 1 101 275-283. McNeill Rhiannon V, Kehrwald Christopher, Brum Murielle, Knopf Katrin, Brunkhorst-Kanaan Nathalie, Etyemez Semra, Koreny Carolin, Bittner Robert A, Freudenberg Florian, Herterich Sabine, Reif Andreas, Kittel-Schneider Sar |
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 |
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 |
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 |
Interaction between HTR2A rs3125 and negative life events in suicide attempts among patients with major depressive disorder: a cross-sectional study. BMC psychiatry 2024 4 24 (1): 249. Jian-Yue Pang, Yi-Ping Wang, Hui-Min Teng, Jin He, Rui Luo, Si-Meng Feng, Wei-Hua Yue, Heng-Fen |
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- Page last updated:Apr 16, 2024
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