Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 42 Records) |
| Query Trace: Disease and NOS2[original query] |
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| The (CCTTT)n microsatellite polymorphism in the nitric oxide synthase 2 gene may influence bladder cancer pathogenesis. The Journal of urology 2010 Nov 184 (5): 2150-7. Ryk Charlotta, Steineck Gunnar, Wiklund N Peter, Nyberg Tommy, de Verdier Petra |
| Ser608Leu polymorphisms in the nitric oxide synthase-2 gene may influence urinary bladder cancer pathogenesis. Scandinavian journal of urology and nephrology 2011 Nov 45 (5): 319-25. Ryk Charlotta, Wiklund N Peter, Nyberg Tommy, De Verdier Petra |
| Association between recurrent aphthous stomatitis and inheritance of a single-nucleotide polymorphism of the NOS2 gene encoding inducible nitric oxide synthase. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology 2011 Oct 40 (9): 715-20. Karasneh Jumana A, Darwazeh Azmi M G, Hassan Ahmad F, Thornhill Mart |
| Association of NOS2 and potential effect of VEGF, IL6, CCL2 and IL1RN polymorphisms and haplotypes on susceptibility to GCA--a simultaneous study of 130 potentially functional SNPs in 14 candidate genes. Rheumatology (Oxford, England) 2012 May 51 (5): 841-51. Enjuanes Anna, Benavente Yolanda, Hernández-Rodríguez José, Queralt Carme, Yagüe Jordi, Jares Pedro, de Sanjosé Silvia, Campo Elias, Cid Maria |
| 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 |
| No association of IFNG+874T/A SNP and NOS2A-954G/C SNP variants with nitric oxide radical serum levels or susceptibility to tuberculosis in a Brazilian population subset. BioMed research international 2013 2013 901740. Leandro Ana Cristina C S, Rocha Márcia Andrade, Lamoglia-Souza Andreia, VandeBerg John L, Rolla Valeria Cavalcanti, Bonecini-Almeida Maria da Glor |
| Association analysis of nitric oxide synthases: NOS1, NOS2A and NOS3 genes, with multiple sclerosis. Annals of human biology 2013 Jul 40 (4): 368-75. AlFadhli Suad, Mohammed Eiman M A, Al Shubaili Asmah |
| Genetic associations of psoriasis in a Pakistani population. The British journal of dermatology 2013 Mar . Shaiq PA, Stuart PE, Latif A, Schmotzer C, Kazmi AH, Khan MS, Azam M, Tejasvi T, Voorhees JJ, Raja GK, Elder JT, Qamar R, Nair RP |
| 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 |
| Association of candidate gene polymorphisms and TGF-beta/IL-10 levels with malaria in three regions of Cameroon: a case-control study. Malaria journal 2014 13 236. Apinjoh Tobias O, Anchang-Kimbi Judith K, Njua-Yafi Clarisse, Ngwai André N, Mugri Regina N, Clark Taane G, Rockett Kirk A, Kwiatkowski Dominic P, Achidi Eric A, |
| 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 |
| Association analysis of GWAS and candidate gene loci in a Pakistani population with psoriasis. Molecular immunology 2015 Mar 64 (1): 190-4. Munir Saeeda, ber Rahman Simeen, Rehman Sadia, Saba Nusrat, Ahmad Wasim, Nilsson Staffan, Mazhar Kehkashan, Naluai Åsa Torinss |
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture.
American journal of human genetics 2015 Nov . Stuart Philip E, Nair Rajan P, Tsoi Lam C, Tejasvi Trilokraj, Das Sayantan, Kang Hyun Min, Ellinghaus Eva, Chandran Vinod, Callis-Duffin Kristina, Ike Robert, Li Yanming, Wen Xiaoquan, Enerbäck Charlotta, Gudjonsson Johann E, Kõks Sulev, Kingo Külli, Esko Tõnu, Mrowietz Ulrich, Reis Andre, Wichmann H Erich, Gieger Christian, Hoffmann Per, Nöthen Markus M, Winkelmann Juliane, Kunz Manfred, Moreta Elvia G, Mease Philip J, Ritchlin Christopher T, Bowcock Anne M, Krueger Gerald G, Lim Henry W, Weidinger Stephan, Weichenthal Michael, Voorhees John J, Rahman Proton, Gregersen Peter K, Franke Andre, Gladman Dafna D, Abecasis Gonçalo R, Elder James |
| Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: A pilot study. Clinica chimica acta; international journal of clinical chemistry 2015 Jan . Carrera Paola, Di Resta Chiara, Volonteri Chiara, Castiglioni Emanuela, Bonfiglio Silvia, Lazarevic Dejan, Cittaro Davide, Stupka Elia, Ferrari Maurizio, Somaschini Marco, |
| 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 |
| Genetic polymorphisms affecting antioxidant enzymes are present in tympanosclerosis patients. The Journal of laryngology and otology 2016 Aug 1-6. Akyigit A, Yalcin ?, Etem E Ö, Kaygusuz I, Karlidag T, Keles E, Celik Z B, Tektemur |
| Genetic basis of TNF-a antagonist associated psoriasis in inflammatory bowel diseases: a genotype-phenotype analysis. Alimentary pharmacology & therapeutics 2016 Mar 43 (6): 697-704. Vedak P, Kroshinsky D, St John J, Xavier R J, Yajnik V, Ananthakrishnan A |
| Polymorphisms in the promoter region of iNOS predispose to rheumatoid arthritis in south Indian Tamils. International journal of immunogenetics 2017 Apr . Negi V S, Mariaselvam C M, Misra D P, Muralidharan N, Fortier C, Charron D, Krishnamoorthy R, Tamouza |
| Inducible nitric oxide synthase 2 promoter polymorphism and malaria disease severity in children in Southern Ghana. PloS one 2018 13 (8): e0202218. Dzodzomenyo Mawuli, Ghansah Anita, Ensaw Nana, Dovie Benjamin, Bimi Langbong, Quansah Reginald, Gyan Ben A, Gyakobo Mawuli, Amoani Benjam |
| 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 |
| [A clinical and genetic analysis of risk factors for the development of acute and chronic cerebral ischemia]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2019 119 (3. Vyp. 2): 62-67. Anisimova A V, Gunchenko A S, Ikonnikova A Yu, Galkin S S, Avdonina M A, Nasedkina T |
| 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 |
| Genomewide Association Study of Acute Anterior Uveitis Identifies New Susceptibility Loci.
Investigative ophthalmology & visual science 2020 Jun 61 (6): 3. Huang Xiu-Feng, Li Zhixiu, De Guzman Erika, Robinson Philip, Gensler Lianne, Ward Michael M, Rahbar Mohammad Hossein, Lee MinJae, Weisman Michael H, Macfarlane Gary J, Jones Gareth T, Klingberg Eva, Forsblad-d'Elia Helena, McCluskey Peter, Wakefield Denis, Coombes Jeff S, Fiatarone Singh Maria A, Mavros Yorgi, Vlahovich Nicole, Hughes David C, Marzo-Ortega Helena, Van der Horste-Bruinsma Irene, O'Shea Finbar, Martin Tammy M, Rosenbaum James, Breban Maxime, Jin Zi-Bing, Leo Paul, Reveille John D, Wordsworth B Paul, Brown Matthew |
| 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 |
| 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 |
| Analysis of selected genetic variants in psoriasis susceptibility and response to treatment. Postepy dermatologii i alergologii 2022 12 39 (5): 934-939. Malinowski Damian, Bia?ecka Monika, Bojko Piotr, Kiszkielis Adriana, Dro?dzik Marek, Kurzawski Mateu |
| Polymorphic Variants of ASS1 Gene Related to Arginine Metabolism and the Risk of HCC. Protein and peptide letters 2023 5 . Kulsoom Bibi, Tehseen Fatima, Saba Sohrab, Ghulam Haider, Shamshad Zarina, Amber Ily |
| Association of nitric oxide synthase gene polymorphism with asthma: A systematic review and meta-analysis. The clinical respiratory journal 2023 4 . Zeru Fan, Tao Liu, Wei |
- Page last reviewed:Feb 1, 2024
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