Human Genome Epidemiology Literature Finder
Records 1 - 17 (of 17 Records) |
Query Trace: Stress and KEAP1[original query] |
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Oncogenic NRF2 mutations in squamous cell carcinomas of oesophagus and skin. The Journal of pathology 2010 Mar 220 (4): 446-51. Kim Yoo Ri, Oh Ji Eun, Kim Min Sung, Kang Mi Ran, Park Sang Wook, Han Ji Youn, Eom Hyeon Seok, Yoo Nam Jin, Lee Sug Hyu |
The NRF2 gene variant, -653G/A, is associated with nephritis in childhood-onset systemic lupus erythematosus. Lupus 2010 Sep 19 (10): 1237-42. Córdova E J, Velázquez-Cruz R, Centeno F, Baca V, Orozco |
Association of Nrf2-encoding NFE2L2 haplotypes with Parkinson's disease. BMC medical genetics 2010 11 (1): 36. von Otter Malin, Landgren Sara, Nilsson Staffan, Celojevic Dragana, Bergström Petra, Håkansson Anna, Nissbrandt Hans, Drozdzik Marek, Bialecka Monika, Kurzawski Mateusz, Blennow Kaj, Nilsson Michael, Hammarsten Ola, Zetterberg Henr |
Nrf2-encoding NFE2L2 haplotypes influence disease progression but not risk in Alzheimer's disease and age-related cataract. Mechanisms of ageing and development 2010 Feb 131 (2): 105-10. von Otter Malin, Landgren Sara, Nilsson Staffan, Zetterberg Madeleine, Celojevic Dragana, Bergström Petra, Minthon Lennart, Bogdanovic Nenad, Andreasen Niels, Gustafson Deborah R, Skoog Ingmar, Wallin Anders, Tasa Gunnar, Blennow Kaj, Nilsson Michael, Hammarsten Ola, Zetterberg Henr |
Relationship between air pollution, NFE2L2 gene polymorphisms and childhood asthma in a Hungarian population. Journal of community genetics 2012 Jan 3 (1): 25-33. Ungvári Ildikó, Hadadi Eva, Virág Viktor, Nagy Adrienne, Kiss András, Kalmár Agnes, Zsigmond Györgyi, Semsei Agnes F, Falus András, Szalai Csa |
Aberrant Keap1 methylation in breast cancer and association with clinicopathological features. Epigenetics : official journal of the DNA Methylation Society 2012 Dec 8 (1): 1. Barbano R, Muscarella LA, Pasculli B, Valori VM, Fontana A, Coco M, la Torre A, Balsamo T, Poeta ML, Marangi GF, Maiello E, Castelvetere M, Pellegrini F, Murgo R, Fazio VM, Parrella P |
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 |
KEAP1 Genetic Polymorphisms Associate with Breast Cancer Risk and Survival Outcomes. Clinical cancer research : an official journal of the American Association for Cancer Research 2015 Apr 21 (7): 1591-601. Hartikainen Jaana M, Tengström Maria, Winqvist Robert, Jukkola-Vuorinen Arja, Pylkäs Katri, Kosma Veli-Matti, Soini Ylermi, Mannermaa Ar |
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 |
A polymorphism in a major antioxidant gene (Kelch-like ECH-associated protein 1) predicts incident cardiovascular events in chronic kidney disease patients: an exploratory study. Journal of hypertension 2016 Mar . Testa Alessandra, Leonardis Daniela, Spoto Belinda, Sanguedolce Maria Cristina, Parlongo Rosa M, Pisano Anna, Giovanni Tripepi, Mallamaci Francesca, Zoccali Carmi |
Mutations in the KEAP1-NFE2L2 Pathway Define a Molecular Subset of Rapidly Progressing Lung Adenocarcinoma. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2019 7 14 (11): 1924-1934. Goeman Frauke, De Nicola Francesca, Scalera Stefano, Sperati Francesca, Gallo Enzo, Ciuffreda Ludovica, Pallocca Matteo, Pizzuti Laura, Krasniqi Eriseld, Barchiesi Giacomo, Vici Patrizia, Barba Maddalena, Buglioni Simonetta, Casini Beatrice, Visca Paolo, Pescarmona Edoardo, Mazzotta Marco, De Maria Ruggero, Fanciulli Maurizio, Ciliberto Gennaro, Maugeri-Saccà Marcel |
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 |
Oxidative stress parameters and keap 1 variants in T2DM: Association with T2DM, diabetic neuropathy, diabetic retinopathy, and obesity. Journal of clinical laboratory analysis 2021 Dec e24163. Khalili Farnaz, Vaisi-Raygani Asad, Shakiba Ebrahim, Kohsari Maryam, Dehbani Maryam, Naseri Rozita, Asadi Soheila, Rahimi Ziba, Rahimi Mehrali, Rahimi Zohr |
Thioredoxin reductase-1 levels are associated with NRF2 pathway activation and tumor recurrence in non-small cell lung cancer. Free radical biology & medicine 2021 Oct 177 58-71. Delgobo Marina, Gonçalves Rosângela Mayer, Delazeri Marco Antônio, Falchetti Marcelo, Zandoná Alessandro, Nascimento das Neves Raquel, Almeida Karoline, Fagundes Adriane Cristina, Gelain Daniel Pens, Fracasso João Isidro, Macêdo Guilherme Baroni de, Priori Leonardo, Bassani Nicklas, Bishop Alexander James Roy, Forcelini Cassiano Mateus, Moreira José Cláudio Fonseca, Zanotto-Filho Alf |
A core Nrf2 gene set defined through comprehensive transcriptomic analysis predicts drug resistance and poor multi-cancer prognosis. bioRxiv : the preprint server for biology 2023 5 . George Luo, Harshita Kumar, Kristin Aldridge, Stevie Rieger, Ethan Jiang, Ernest R Chan, Ahmed Soliman, Haider Mahdi, John J Letter |
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 |
Gestational Diabetes Mellitus (GDM), Hypothyroidism, and Gene Variants (Keap1 Rs11085735) in Patients with Preeclampsia. Reports of biochemistry & molecular biology 2023 1 11 (3): 493-501. Khadir Fatemeh, Rahimi Zohreh, Vaisi-Raygani Asad, Shakiba Ebrahim, Naseri Rozi |
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- Page last updated:Apr 22, 2024
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