Human Genome Epidemiology Literature Finder
Records 1 - 13 (of 13 Records) |
Query Trace: Syndrome and NOS1[original query] |
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Physician-diagnosed asthma and acute chest syndrome: associations with NOS polymorphisms. Pediatric pulmonology 2007 Apr 42 (4): 332-8. Duckworth Laurie, Hsu Lewis, Feng Hua, Wang Jianwei, Sylvester James E, Kissoon Niranjan, Sandler Eric, Lima John |
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome. Movement disorders : official journal of the Movement Disorder Society 2008 Feb 23 (3): 350-8. Winkelmann Juliane, Lichtner Peter, Schormair Barbara, Uhr Manfred, Hauk Stephanie, Stiasny-Kolster Karin, Trenkwalder Claudia, Paulus Walter, Peglau Ines, Eisensehr Ilonka, Illig Thomas, Wichmann H-Erich, Pfister Hildegard, Golic Jelena, Bettecken Thomas, Pütz Benno, Holsboer Florian, Meitinger Thomas, Müller-Myhsok Bertr |
Polymorphisms of interleukin-1 Beta and interleukin-17Alpha genes are associated with restless legs syndrome. Biological research for nursing 2014 Apr 16 (2): 143-51. Hennessy Mary Dawn, Zak Rochelle S, Gay Caryl L, Pullinger Clive R, Lee Kathryn A, Aouizerat Bradley |
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 |
Neuronal nitric oxide synthase (nNOS, NOS1) rs693534 and rs7977109 variants and risk for restless legs syndrome. Journal of neural transmission (Vienna, Austria : 1996) 2015 Jun 122 (6): 819-23. Jiménez-Jiménez Félix Javier, Alonso-Navarro Hortensia, Martínez Carmen, Zurdo Martín, Turpín-Fenoll Laura, Millán-Pascual Jorge, Adeva-Bartolomé Teresa, Cubo Esther, Navacerrada Francisco, Rojo-Sebastián Ana, Rubio Lluisa, Calleja Marisol, Plaza-Nieto José Francisco, Pilo-de-la-Fuente Belén, Arroyo-Solera Margarita, García-Albea Esteban, García-Martín Elena, Agúndez José A |
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 |
Targeted next generation sequencing approach identifies eighteen new candidate genes in normosmic hypogonadotropic hypogonadism and Kallmann syndrome. Molecular and cellular endocrinology 2016 12 437 86-96. Quaynor Samuel D, Bosley Maggie E, Duckworth Christina G, Porter Kelsey R, Kim Soo-Hyun, Kim Hyung-Goo, Chorich Lynn P, Sullivan Megan E, Choi Jeong-Hyeon, Cameron Richard S, Layman Lawrence |
Genetics of Aggression in Alzheimer's Disease (AD). Frontiers in aging neuroscience 2017 9 87. Lukiw Walter J, Rogaev Evgeny |
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 |
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 |
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 |
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 |
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- Page last updated:Nov 30, 2023
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