Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 50 Records) |
| Query Trace: Disease and HMOX1[original query] |
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| 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 |
| Lead-Related Genetic Loci, Cumulative Lead Exposure and Incident Coronary Heart Disease: The Normative Aging Study. PloS one 2016 11 (9): e0161472. Ding Ning, Wang Xin, Weisskopf Marc G, Sparrow David, Schwartz Joel, Hu Howard, Park Sung Ky |
| 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 |
| Genetic polymorphism of heme oxygenase 1 promoter in the occurrence and severity of chronic obstructive pulmonary disease: a meta-analysis. Journal of cellular and molecular medicine 2016 Dec . Zhou Hongbin, Ying Xiwang, Liu Yuanshun, Ye Sa, Yan Jianping, Li Yaqi |
| Serum Bilirubin Levels and Promoter Variations in HMOX1 and UGT1A1 Genes in Patients with Fabry Disease. Oxidative medicine and cellular longevity 2017 2017 9478946. Jirásková Alena, Bortolussi Giulia, Dostálová Gabriela, Eremiášová Lenka, Gola? Lubor, Danzig Vilém, Linhart Aleš, Vítek Lib |
| Association of the haem oxygenase-1 gene with inflammatory bowel disease. Swiss medical weekly 2017 8 147 w14456. Lin Zhenwu, Hao Han, Hegarty John P, Lin Tony R, Wang Yunhua, Harris Leonard R, Xu He N, Wu Rongling, Thomas Neal J, Floros Joan |
| Roles of APOL1 G1 and G2 variants in sickle cell disease patients: kidney is the main target. British journal of haematology 2017 10 179 (2): 323-335. Kormann Raphaël, Jannot Anne-Sophie, Narjoz Céline, Ribeil Jean-Antoine, Manceau Sandra, Delville Marianne, Joste Valentin, Prié Dominique, Pouchot Jacques, Thervet Eric, Courbebaisse Marie, Arlet Jean-Beno |
| Clinical and genetic predictors of renal dysfunctions in sickle cell anaemia in Cameroon. British journal of haematology 2017 May . Geard Amy, Pule Gift D, Chetcha Chemegni Bernard, Ngo Bitoungui Valentina J, Kengne Andre P, Chimusa Emile R, Wonkam Ambroi |
| 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 |
| Fetal Microsatellite in the Heme Oxygenase 1 Promoter Is Associated With Severe and Early-Onset Preeclampsia. Hypertension (Dallas, Tex. : 1979) 2017 Dec . Kaartokallio Tea, Utge Siddheshwar, Klemetti Miira M, Paananen Jussi, Pulkki Kari, Romppanen Jarkko, Tikkanen Ilkka, Heinonen Seppo, Kajantie Eero, Kere Juha, Kivinen Katja, Pouta Anneli, Lakkisto Päivi, Laivuori Hanne |
| 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 |
| Heme oxygenase 1 polymorphism, occupational vapor, gas, dust, and fume exposure and chronic obstructive pulmonary disease in a Danish population-based study. Scandinavian journal of work, environment & health 2019 Aug . Würtz Else Toft, Brasch-Andersen Charlotte, Steffensen Rudi, Hansen Jens Georg, Malling Tine Halsen, Schlünssen Vivi, Omland Øyvi |
| Association of Genetic Variations in NRF2, NQO1, HMOX1, and MT with Severity of Coronary Artery Disease and Related Risk Factors. Cardiovascular toxicology 2019 Jul . Sarutipaiboon Ingkarat, Settasatian Nongnuch, Komanasin Nantarat, Kukongwiriyapan Upa, Sawanyawisuth Kittisak, Intharaphet Phongsak, Senthong Vichai, Settasatian Chat |
| Implication of HMOX1 and CCR5 genotypes on clinical phenotype of Egyptian patients with sickle cell anemia. Annals of hematology 2019 Apr . Bakr Salwa, Khorshied Mervat, Talha Noha, Jaffer Karim Yahia, Soliman Nohair, Eid Khaled, El-Ghamrawy Mo |
| Genetic Polymorphisms in Sepsis and Cardiovascular Disease: Do Similar Risk Genes Suggest Similar Drug Targets? Chest 2019 Jan . Nakada Taka-Aki, Takahashi Waka, Nakada Emiri, Shimada Tadanaga, Russell James A, Walley Keith |
| Polymorphisms in the heme oxygenase-1 and bone morphogenetic protein receptor type 1b genes and estimated glomerular filtration rate in Brazilian sickle cell anemia patients. Hematology, transfusion and cell therapy 2020 May . Chinedu Okeke, Tonassé Wouitchékpo Vincent, Albuquerque Dulcinéia Martins, Domingos Igor de Farias, Araújo Aderson da Silva, Bezerra Marcos André Cavalcanti, Sonati Maria de Fátima, Santos Magnun Nueldo Nunes D |
| Association of Genetic Polymorphisms of TGF-?1, HMOX1, and APOL1 With CKD in Nigerian Patients With and Without HIV. American journal of kidney diseases : the official journal of the National Kidney Foundation 2020 Apr . Ekrikpo Udeme E, Mnika Khuthala, Effa Emmanuel E, Ajayi Samuel O, Okwuonu Chimezie, Waziri Bala, Bello Aminu, Dandara Collet, Kengne Andre P, Wonkam Ambroise, Okpechi Ikec |
| Clinical and genetic factors are associated with kidney complications in African children with sickle cell anaemia. British journal of haematology 2021 Sep . Adebayo Oyindamola Christiana, Betukumesu DieuMerci Kabasele, Nkoy Agathe Bikupe, Adesoji Oluyomi Modupe, Ekulu Pepe Mfutu, Van den Heuvel Lambertus P, Levtchenko Elena N, Labarque Veer |
| Endometriosis Is Associated with Functional Polymorphism in the Promoter of Heme Oxygenase 1 (HMOX1) Gene. Cells 2021 Mar 10 (3): . Milewski Lukasz, Sciezynska Aneta, Poninska Joanna, Soszynska Marta, Barcz Ewa, Roszkowski Piotr I, Kaminski Pawel, Wlodarski Pawel, Ploski Rafal, Malejczyk Jac |
| The role of functional polymorphisms in oxidative stress-related genes on early-stage breast cancer survival. The International journal of biological markers 2021 Apr 17246008211011177. Korobeinikova Erika, Ugenskiene Rasa, Insodaite Ruta, Rudzianskas Viktoras, Gudaitiene Jurgita, Juozaityte Elo |
| Association of HMOX-1 with sporadic Alzheimer's disease in southern Han Chinese. European journal of neurology 2021 4 28 (9): 2922-2926. Zhang Bei, Yu Hong-Xiang, Zhi Nan, Cui Can, Han Ying-Ying, Hu Min, Shen Hao, Bao Huan, Li Ga |
| Donor-Derived Myeloid Heme Oxygenase-1 Controls the Development of Graft-Versus-Host Disease. Frontiers in immunology 2021 2 11 579151. Spilleboudt Chloé, De Wilde Virginie, Lewalle Philippe, Cabanne Ludovic, Leclerc Mathieu, Beckerich Florence, Bories Dominique, Cardoso Silvia, Soares Miguel P, Vokaer Benoît, Hougardy Jean-Michel, Flamand Véronique, Racapé Judith, Abramowicz Marc, Maury Sébastien, Le Moine Ala |
| 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 |
| Shorter (GT) repeats in the haem-oxygenase 1 gene promoter are associated with better mid-term survival in subjects with coronary artery disease and abnormal ejection fraction. Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals 2021 Oct 1-16. Liang Kae-Woei, Lee Wen-Jane, Lee Wen-Lieng, Wu Jen-Pey, Sheu Wayne H |
| Subjects with coronary artery disease and reduced ejection fraction have longer (GT) repeats in the heme-oxygenase 1 gene promoter. Heart and vessels 2021 1 36 (5): 615-620. Liang Kae-Woei, Lee Wen-Jane, Lee Wen-Lieng, Wu Jen-Pey, Lee I-Te, Wang Jun-Sing, Sheu Wayne H |
| Association of HMOX-1 rs2071747 with sporadic Parkinson's disease in southern Han Chinese. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 1 43 (6): 3671-3675. Xiong Ran, Zhang B |
| Prevalence and Impact of HMOX1 Polymorphism (rs2071746: A?>?T) in Indian Sickle Cell Disease Patients. Journal of laboratory physicians 2023 10 15 (4): 583-589. Hareram Pandey, Kanwaljeet Singh, Ravi Ranjan, Jasmita Dass, Seema Tyagi, Tulika Seth, Renu Saxena, Manoranjan Mahapat |
| Systematic Review of Genetic Modifiers Associated with the Development and/or Progression of Nephropathy in Patients with Sickle Cell Disease. International journal of molecular sciences 2024 5 25 (10): . Veerle Labarque, Emmanuel Chide Okocha, |
| Genetic Variability in Oxidative Stress, Inflammatory, and Neurodevelopmental Pathways: Impact on the Susceptibility and Course of Spinal Muscular Atrophy. Cellular and molecular neurobiology 2024 10 44 (1): 71. Maruša Barbo, Blaž Koritnik, Lea Leonardis, Tanja Blagus, Vita Dolžan, Metka Ravnik-Glav |
- Page last reviewed:Feb 1, 2024
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