Human Genome Epidemiology Literature Finder
Records 1 - 12 (of 12 Records) |
Query Trace: Syndrome and HMOX1[original query] |
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Heme oxygenase-1 microsatellite polymorphism and haplotypes are associated with the development of acute respiratory distress syndrome. Intensive care medicine 2009 Aug 35 (8): 1343-51. Sheu Chau-Chyun, Zhai Rihong, Wang Zhaoxi, Gong Michelle N, Tejera Paula, Chen Feng, Su Li, Thompson B Taylor, Christiani David |
Transforming growth factor beta 2 and heme oxygenase 1 genes are risk factors for the cerebral malaria syndrome in Angolan children. PloS one 2010 5 (6): e11141. Sambo Maria Rosário, Trovoada Maria Jesus, Benchimol Carla, Quinhentos Vatúsia, Gonçalves Lígia, Velosa Rute, Marques Maria Isabel, Sepúlveda Nuno, Clark Taane G, Mustafa Stefan, Wagner Oswald, Coutinho António, Penha-Gonçalves Carl |
Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease. Blood 2012 Nov 120 (18): 3822-8. Bean Christopher J, Boulet Sheree L, Ellingsen Dorothy, Pyle Meredith E, Barron-Casella Emily A, Casella James F, Payne Amanda B, Driggers Jennifer, Trau Heidi A, Yang Genyan, Jones Kimberly, Ofori-Acquah Solomon F, Hooper W Craig, DeBaun Michael |
Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Restless Legs Syndrome. Medicine 2015 Aug 94 (34): e1448. García-Martín Elena, 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, Ortega-Cubero Sara, Pastor Pau, Calleja Marisol, Plaza-Nieto José Francisco, Pilo-de-la-Fuente Belén, Arroyo-Solera Margarita, García-Albea Esteban, Agúndez José A |
Prediction of feature genes in trauma patients with the TNF rs1800629 A allele using support vector machine. Computers in biology and medicine 2015 Sep 64 24-9. Chen Guoting, Han Ning, Li Guofeng, Li Xin, Li Guang, Liu Yangzhou, Wu Wei, Wang Yong, Chen Yanxi, Sun Guixin, Li Zengchun, Li Qinchu |
Association of HMOX1 and NQO1 Polymorphisms with Metabolic Syndrome Components. PloS one 2015 10 (5): e0123313. Martínez-Hernández Angélica, Córdova Emilio J, Rosillo-Salazar Oscar, García-Ortíz Humberto, Contreras-Cubas Cecilia, Islas-Andrade Sergio, Revilla-Monsalve Cristina, Salas-Labadía Consuelo, Orozco Lore |
Genetics of restless legs syndrome: An update. Sleep medicine reviews 2018 06 39 108-121. Jiménez-Jiménez Félix J, Alonso-Navarro Hortensia, García-Martín Elena, Agúndez José A |
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 |
Heme oxygenase-1 repeat polymorphism in septic acute kidney injury. PloS one 2019 14 (5): e0217291. Vilander Laura M, Vaara Suvi T, Donner Kati M, Lakkisto Päivi, Kaunisto Mari A, Pettilä Ville, |
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 |
Association of Serum Bilirubin and Functional Variants of Heme Oxygenase 1 and Bilirubin UDP-Glucuronosyl Transferase Genes in Czech Adult Patients with Non-Alcoholic Fatty Liver Disease. Antioxidants (Basel, Switzerland) 2021 12 10 (12): . Petrtýl Jaromír, Dvo?ák Karel, St?íteský Jan, Lení?ek Martin, Jirásková Alena, Šmíd Václav, Haluzík Martin, Br?ha Radan, Vítek Lib |
Association of Low Serum Bilirubin Concentrations and Promoter Variations in the UGT1A1 and HMOX1 Genes with Type 2 Diabetes Mellitus in the Czech Population. International journal of molecular sciences 2023 7 24 (13): . Alena Jirásková, Jan Škrha, Libor Vít |
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- Page last updated:Mar 25, 2024
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