Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 128 Records) |
Query Trace: NFE2L2[original query] |
---|
Association of NFE2L2 Gene Polymorphisms with Risk and Clinical Characteristics of Acute Type A Aortic Dissection in Han Chinese Population. Oxidative medicine and cellular longevity 2021 2021 5173190. Zhang Yiran, Zheng Qi, Chen Ruoshi, Dai Xiaoyi, Zhu Yimin, Ma Lia |
Correlation of alterations in the KEAP1/CUL3/NFE2L2 pathway with radiation failure in larynx squamous cell carcinoma. Laryngoscope investigative otolaryngology 2021 8 6 (4): 699-707. Sheth Siddharth, Farquhar Douglas R, Schrank Travis P, Stepp Wesley, Mazul Angela, Hayward Michele, Lenze Nicholas, Little Paul, Jo Heejoon, Major M Ben, Chera Bhishamjit S, Zevallos Jose P, Hayes D Ne |
KEAP1/NFE2L2 Mutations of Liquid Biopsy as Prognostic Biomarkers in Patients With Advanced Non-Small Cell Lung Cancer: Results From Two Multicenter, Randomized Clinical Trials. Frontiers in oncology 2021 11 659200. Zhu Hongyuan, Xie Daipeng, Yu Yunfang, Yao Lintong, Xu Bin, Huang Luyu, Wu Shaowei, Li Fasheng, Zheng Yating, Liu Xinyi, Xie Wenzhuan, Huang Mengli, Li Hao, Zheng Shaopeng, Zhang Dongkun, Qiao Guibin, Chan Lawrence W C, Zhou Hai |
Multiomics analysis of tumor mutational burden across cancer types. Computational and structural biotechnology journal 2021 19 5637-5646. Li Lin, Bai Long, Lin Huan, Dong Lin, Zhang Rumeng, Cheng Xiao, Liu Zexian, Ouyang Yi, Ding Kesh |
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 |
Profile of esophageal squamous cell carcinoma mutations in Brazilian patients. Scientific reports 2021 10 11 (1): 20596. Munari Fernanda Franco, Dos Santos Wellington, Evangelista Adriane Feijó, Carvalho Ana Carolina, Pastrez Paula Aguiar, Bugatti Diego, Wohnrath Durval R, Scapulatempo-Neto Cristovam, Guimarães Denise Peixoto, Longatto-Filho Adhemar, Reis Rui Manu |
Genomic Profiling Identified Prognostic Biomarkers of Definitive Chemo-Radiotherapy Response in Esophageal Carcinoma. International journal of radiation oncology, biology, physics 2021 Nov 111 (3S): S13. Li L, Yuan S, Sun J, Yin Y, Cui J, Zhang J, Chen Y, Pang J, Yin J, Shao Y, Yu |
Genetic variation in NFE2L2 is associated with outcome following aneurysmal subarachnoid haemorrhage. European journal of neurology 2022 Sep . Gaastra Ben, Duncan Poppy, Bakker Mark K, Hostettler Isabel C, Alg Varinder S, Houlden Henry, Ruigrok Ynte M, Galea Ian, Tapper Will, Werring David, Bulters Dieder |
ADHD-associated PARK2 copy number variants: A pilot study on gene expression and effects of supplementary deprivation in patient-derived cell lines. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2022 8 189 (7-8): 257-270. Radtke Franziska, Palladino Viola Stella, McNeill Rhiannon V, Chiocchetti Andreas G, Haslinger Denise, Leyh Matthias, Gersic Danijel, Frank Markus, Grünewald Lena, Klebe Stephan, Brüstle Oliver, Günther Katharina, Edenhofer Frank, Kranz Thorsten M, Reif Andreas, Kittel-Schneider Sar |
Association of Variants of the NFE2L2 Gene with Metabolic and Kidney Function Parameters in Patients with Diabetes and/or Hypertension. Genetic testing and molecular biomarkers 2022 7 26 (7-8): 382-390. Gómez-García Erika Fabiola, Cortés-Sanabria Laura, Cueto-Manzano Alfonso Martín, Vidal-Martínez Midori Ariana, Medina-Zavala R Susana, López-Leal Jorge, Rentería-Padilla Josué, Mendoza-Carrera Francis |
Applications of molecular barcode sequencing for the detection of low-frequency variants in circulating tumour DNA from hepatocellular carcinoma. Liver international : official journal of the International Association for the Study of the Liver 2022 7 42 (10): 2317-2326. Lee Hye Won, Kim Esl, Cho Kyung Joo, Park Hye Jung, Seo Jieun, Lee Hyeonah, Baek Eunha, Choi Jong Rak, Han Kwang-Hyub, Lee Seung-Tae, Park Jun Yo |
Survival Outcomes and Treatment Patterns in Patients With NFE2L2 and/or KEAP1 Mutation-Positive Advanced Squamous Cell NSCLC Using a Real-World Clinico-Genomic Database. Clinical lung cancer 2022 6 23 (6): 487-497. Wu Yanyu, Yin Yu, Crossland Victoria, Vincent Sylvie, Paik Paul K, Lineberry Neil, Faller Douglas |
Multi-omics analysis identifies distinct subtypes with clinical relevance in lung adenocarcinoma harboring KEAP1/NFE2L2. Journal of Cancer 2022 4 13 (5): 1512-1522. Yang Xiaodong, Li Ming, Chen Zhencong, Fan Xiaobin, Guo Liang, Jin Bo, Huang Yiwei, Wang Qun, Wu Liang, Zhan Che |
TIMP3 Gene Polymorphisms of -1296 T > C and -915 A > G Increase the Susceptibility to Arsenic-Induced Skin Cancer: A Cohort Study and In Silico Analysis of Mutation Impacts. International journal of molecular sciences 2022 12 23 (23): . Wu Meei-Maan, Chen Chi-Wei, Chen Chiu-Yi, Lee Chih-Hung, Chou Mark, Hsu Ling-I, Lee Te-Chang, Chen Chien-J |
The Role of Single-Nucleotide Polymorphisms in Cholangiocarcinoma: A Systematic Review. Cancers 2022 12 14 (23): . Wang Guanwu, Heij Lara Rosaline, Liu Dong, Dahl Edgar, Lang Sven Arke, Ulmer Tom Florian, Luedde Tom, Neumann Ulf Peter, Bednarsch J |
Integrated analysis of racial disparities in genomic architecture identifies a trans-ancestry prognostic subtype in bladder cancer. Molecular oncology 2022 12 . Zhang Baifeng, Jia Peilin, Wang Jiayin, Pei Guangsheng, Wang Changxi, Pei Shimei, Li Xiangchun, Zhao Zhongming, Yi Xin, Guan Xin-Yuan, Huang |
A novel cuproptosis-related gene signature of prognosis and immune microenvironment in head and neck squamous cell carcinoma cancer. Journal of cancer research and clinical oncology 2022 11 149 (1): 203-218. Jiang Xu, Ke Jing, Jia Lifeng, An Xiang, Ma Haiyu, Li Zhongwan, Yuan W |
Targeting NFE2L2/KEAP1 Mutations in Advanced NSCLC With the TORC1/2 Inhibitor TAK-228. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2022 10 . Paik Paul K, Fan Pang-Dian, Qeriqi Besnik, Namakydoust Azadeh, Daly Bobby, Ahn Linda, Kim Rachel, Plodkowski Andrew, Ni Ai, Chang Jason, Fanaroff Rachel, Ladanyi Marc, de Stanchina Elisa, Rudin Charles |
Cuproptosis Combined with lncRNAs Predicts the Prognosis and Immune Microenvironment of Breast Cancer. Computational and mathematical methods in medicine 2022 10 2022 5422698. Zhang Liangping, Zhang Yujun, Bao Jianhang, Gao Wenshuo, Wang Dong, Pan H |
Prognostic Value and Immune Infiltration Analysis of Nuclear Factor Erythroid-2 Family Members in Ovarian Cancer. BioMed research international 2022 1 2022 8672258. Dou Rui, Wang Xiong, Zhang J |
Comprehensive analyses of the clinicopathological features and genomic mutations of combined hepatocellular-cholangiocarcinoma. Hepatology research : the official journal of the Japan Society of Hepatology 2023 9 . Takashi Ito, Takamichi Ishii, Haruhiko Takeda, Shinji Sumiyoshi, Katsuhiro Tomofuji, Satoshi Wakama, Kenta Makino, Hiroshi Horie, Ken Kumagai, Atsushi Takai, Elena Yukie Uebayashi, Satoshi Ogiso, Ken Fukumitsu, Hironori Haga, Hiroshi Seno, Etsuro Hata |
Towards Understanding the Key Signature Pathways Associated from Differentially Expressed Gene Analysis in an Indian Prostate Cancer Cohort. Diseases (Basel, Switzerland) 2023 5 11 (2): . Nidhi Shukla, Bhumandeep Kour, Devendra Sharma, Maneesh Vijayvargiya, T C Sadasukhi, Krishna Mohan Medicherla, Babita Malik, Bhawana Bissa, Sugunakar Vuree, Nirmal Kumar Lohiya, Prashanth Suravajha |
Noninvasive genomic profiling of somatic mutations in oral cavity cancers. Oral oncology 2023 4 140 106372. Xi Yuanxin, Negrao Marcelo V, Akagi Keiko, Xiao Weihong, Jiang Bo, Warner Sarah C, Dunn Joe Dan, Wang Jing, Symer David E, Gillison Maura |
Quantitative and causal analysis for inflammatory genes and the risk of Parkinson's disease. Frontiers in immunology 2023 3 14 1119315. Yi Minhan, Li Jiaxin, Jian Shijie, Li Binbin, Huang Zini, Shu Li, Zhang Yu |
Identification of molecular subtypes and a risk model based on inflammation-related genes in patients with low grade glioma. Heliyon 2023 12 9 (12): e22429. Cheng Long, Ya Song, Yimin Pan, Changwu |
Decreased DNA repair capacity caused by exposure to metal mixtures is modulated by the PARP1 rs1136410 variant in newborns from a polluted metropolitan area. Environmental research 2023 11 241 117631. Marvin Paz-Sabillón, Nereida Montes-Castro, Luisa Torres-Sánchez, Luz M Del Razo, Emilio J Córdova, Betzabet Quintanilla-Ve |
A Transcriptomic Approach Outperforms Mutational Analysis to Identify KEAP1/NFE2L2 Pathway Activation in Patients With NSCLC. Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer 2023 10 18 (11): 1431-1433. Sara Hijazo-Pechero, Cristina Muñoz-Pinedo, Ernest Nad |
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 |
Analysis of Tumor Mutational Burden, Progression-Free Survival, and Local-Regional Control in Patents with Locally Advanced Non-Small Cell Lung Cancer Treated With Chemoradiation and Durvalumab. JAMA network open 2023 1 6 (1): e2249591. Lebow Emily S, Shepherd Annemarie, Eichholz Jordan E, Offin Michael, Gelblum Daphna Y, Wu Abraham J, Simone Charles B, Schoenfeld Adam J, Jones David R, Rimner Andreas, Chaft Jamie E, Riaz Nadeem, Gomez Daniel R, Shaverdian Nar |
Prevalence and Associations of Co-occurrence of NFE2L2 Mutations and Chromosome 3q26 Amplification in Lung Cancer. Global medical genetics 2024 4 11 (2): 150-158. Jinfeng Liu, Sijie Liu, Dan Li, Hongbin Li, Fan Zha |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: