Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: HMOX2[original query] |
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No genetic association between polymorphisms of heme oxygenase 1 and 2 and Alzheimer's disease in a Japanese population. Dementia and geriatric cognitive disorders 2009 27 (3): 273-7. Shibata Nobuto, Ohnuma Tohru, Baba Hajime, Arai He |
Association of an intronic variant of the heme oxygenase-1 gene with hypertension in northern Chinese Han population. Clinical and experimental hypertension (New York, N.Y. : 1993) 2009 Oct 31 (7): 534-43. Yun Li, Xiaoli Liu, Qi Zhao, Laiyuan Wang, Xiangfeng Lu, Chong Shen, Jianfeng Huang, Shufeng Chen, Hongfan Li, Gu Dongfe |
Lack of association between the c.544G>A polymorphism of the heme oxygenase-2 gene and age-related macular degeneration. Medical science monitor : international medical journal of experimental and clinical research 2011 Aug 17 (8): CR449-455. Wysokinski Daniel, Synowiec Ewelina, Chmielewska Marta, Wozniak Katarzyna, Zaras Ma?gorzata, Sklodowska Anna, Blasiak Janusz, Szaflik Jerzy, Szaflik Jacek Paw |
An association between polymorphism of the heme oxygenase-1 and -2 genes and age-related macular degeneration. Molecular biology reports 2012 Mar 39 (3): 2081-7. Synowiec Ewelina, Szaflik Jerzy, Chmielewska Marta, Wozniak Katarzyna, Sklodowska Anna, Waszczyk Maja, Dorecka Mariola, Blasiak Janusz, Szaflik Jacek Paw |
A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease. Pharmacogenetics and genomics 2011 Jun . Ayuso P, Martínez C, Lorenzo-Betancor O, Pastor P, Luengo A, Jiménez-Jiménez FJ, Alonso-Navarro H, Villalba MT, Agúndez JA, García-Martín E |
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 |
Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor. Medicine 2015 Jun 94 (24): e968. Ayuso Pedro, Agúndez José A G, Alonso-Navarro Hortensia, Martínez Carmen, Benito-León Julián, Ortega-Cubero Sara, Lorenzo-Betancor Oswaldo, Pastor Pau, López-Alburquerque Tomás, García-Martín Elena, Jiménez-Jiménez Félix |
Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis. Scientific reports 2016 Feb 6 20830. Agúndez José A G, García-Martín Elena, Martínez Carmen, Benito-León Julián, Millán-Pascual Jorge, Díaz-Sánchez María, Calleja Patricia, Pisa Diana, Turpín-Fenoll Laura, Alonso-Navarro Hortensia, Pastor Pau, Ortega-Cubero Sara, Ayuso-Peralta Lucía, Torrecillas Dolores, García-Albea Esteban, Plaza-Nieto José Francisco, Jiménez-Jiménez Félix Javi |
Delta-amino-levulinic acid dehydratase gene and essential tremor. European journal of clinical investigation 2017 Mar . Agúndez José A G, García-Martín Elena, Alonso-Navarro Hortensia, Ayuso Pedro, Esguevillas Gara, Benito-León Julián, Ortega-Cubero Sara, Pastor Pau, López-Alburquerque Tomás, Jiménez-Jiménez Félix Javi |
Association between a heme oxygenase-2 genetic variant and risk of Parkinson's disease in Han Chinese. Neuroscience letters 2017 Feb 642 119-122. Tian Sijia, Yang Xinglong, Zhao Quanzhen, Zheng Jinhua, Huang Hongyan, Chen Yalan, An Ran, Xu Yanmi |
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 |
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 |
Identification of sixteen novel candidate genes for late onset Parkinson's disease. Molecular neurodegeneration 2021 6 16 (1): 35. Gialluisi Alessandro, Reccia Mafalda Giovanna, Modugno Nicola, Nutile Teresa, Lombardi Alessia, Di Giovannantonio Luca Giovanni, Pietracupa Sara, Ruggiero Daniela, Scala Simona, Gambardella Stefano, , Iacoviello Licia, Gianfrancesco Fernando, Acampora Dario, D'Esposito Maurizio, Simeone Antonio, Ciullo Marina, Esposito Tere |
A nomogram based on A-to-I RNA editing predicting overall survival of patients with lung squamous carcinoma. BMC cancer 2022 6 22 (1): 715. Liu Li, Liu Jun, Deng Xiaoliang, Tu Li, Zhao Zhuxiang, Xie Chenli, Yang L |
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles.
Nature genetics 2022 02 54 (2): 152-160. Hautakangas Heidi, Winsvold Bendik S, Ruotsalainen Sanni E, Bjornsdottir Gyda, Harder Aster V E, Kogelman Lisette J A, Thomas Laurent F, Noordam Raymond, Benner Christian, Gormley Padhraig, Artto Ville, Banasik Karina, Bjornsdottir Anna, Boomsma Dorret I, Brumpton Ben M, Burgdorf Kristoffer Sølvsten, Buring Julie E, Chalmer Mona Ameri, de Boer Irene, Dichgans Martin, Erikstrup Christian, Färkkilä Markus, Garbrielsen Maiken Elvestad, Ghanbari Mohsen, Hagen Knut, Häppölä Paavo, Hottenga Jouke-Jan, Hrafnsdottir Maria G, Hveem Kristian, Johnsen Marianne Bakke, Kähönen Mika, Kristoffersen Espen S, Kurth Tobias, Lehtimäki Terho, Lighart Lannie, Magnusson Sigurdur H, Malik Rainer, Pedersen Ole Birger, Pelzer Nadine, Penninx Brenda W J H, Ran Caroline, Ridker Paul M, Rosendaal Frits R, Sigurdardottir Gudrun R, Skogholt Anne Heidi, Sveinsson Olafur A, Thorgeirsson Thorgeir E, Ullum Henrik, Vijfhuizen Lisanne S, Widén Elisabeth, van Dijk Ko Willems, , , , Aromaa Arpo, Belin Andrea Carmine, Freilinger Tobias, Ikram M Arfan, Järvelin Marjo-Riitta, Raitakari Olli T, Terwindt Gisela M, Kallela Mikko, Wessman Maija, Olesen Jes, Chasman Daniel I, Nyholt Dale R, Stefánsson Hreinn, Stefansson Kari, van den Maagdenberg Arn M J M, Hansen Thomas Folkmann, Ripatti Samuli, Zwart John-Anker, Palotie Aarno, Pirinen Mat |
The HMOX2 polymorphism contributes to the carotid body chemoreflex in European sea-level residents by regulating hypoxic ventilatory responses. Frontiers in medicine 2022 11 9 1000786. Fabries Pierre, Drogou Catherine, Sauvet Fabien, Nespoulous Olivier, Erkel Marie-Claire, Marchandot Vincent, Bouaziz Walid, Lepetit Benoît, Hamm-Hornez Anne-Pia, Malgoyre Alexandra, Koulmann Nathalie, Gomez-Merino Danielle, Chennaoui Moun |
Heme oxygenase 2 genetic variants alter hormonal and metabolic traits in polycystic ovary syndrome. Endocrine connections 2024 1 . Xinyuan Zhang, Suiyan Li, Hongwei Liu, Huai Bai, Qingqing Liu, Chunyi Yang, Ping F |
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