Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Syndrome and KEAP1[original query] |
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Association of NFE2L2 and KEAP1 haplotypes with amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis & frontotemporal degeneration 2014 Mar 15 (1-2): 130-7. Bergström Petra, von Otter Malin, Nilsson Staffan, Nilsson Ann-Charloth, Nilsson Michael, Andersen Peter M, Hammarsten Ola, Zetterberg Henr |
Genetic variants involved in oxidative stress, base excision repair, DNA methylation, and folate metabolism pathways influence myeloid neoplasias susceptibility and prognosis. Molecular carcinogenesis 2016 Mar . Gonçalves Ana Cristina, Alves Raquel, Baldeiras Inês, Cortesão Emília, Carda José Pedro, Branco Claudia C, Oliveiros Bárbara, Loureiro Luísa, Pereira Amélia, Nascimento Costa José Manuel, Sarmento-Ribeiro Ana Bela, Mota-Vieira Lui |
Evaluation of the role of Nrf2/Keap1 pathway-associated novel mutations and gene expression on antioxidant status in patients with deep vein thrombosis. Experimental and therapeutic medicine 2020 8 20 (2): 868-881. Akin-Bali Dilara Fatma, Eroglu Tamer, Ilk Sedef, Egin Yonca, Kankilic Teom |
Impact on the Clinical Evolution of Patients with COVID-19 Pneumonia and the Participation of the NFE2L2/KEAP1 Polymorphisms in Regulating SARS-CoV-2 Infection. International journal of molecular sciences 2023 1 24 (1): . Soto María Elena, Fuentevilla-Álvarez Giovanny, Palacios-Chavarría Adrián, Vázquez Rafael Ricardo Valdez, Herrera-Bello Héctor, Moreno-Castañeda Lidia, Torres-Paz Yazmín Estela, González-Moyotl Nadia Janet, Pérez-Torres Idalia, Aisa-Alvarez Alfredo, Manzano-Pech Linaloe, Pérez-Torres Israel, Huesca-Gómez Claudia, Gamboa Ricar |
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