Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 142 Records) |
Query Trace: PON2[original query] |
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A Meta-Analysis on the Relationship of the PON Genes and Alzheimer Disease. Journal of geriatric psychiatry and neurology 2017 Jan 891988717731825. Nie Yi, Luo Danyang, Yang Min, Wang Yi, Xiong Li, Gao Li, Liu Yan, Liu H |
Sonographic evaluation of atherosclerosis burden in carotid arteries of ischemic stroke patients and its relation to paraoxonase 1 and 2, MTHFR and AT1R genetic variants. Journal of the neurological sciences 2017 Jul 378 146-151. Hernández-Socorro Carmen Rosa, Rodríguez-Esparragón Francisco Javier, Celli Jennifer, López-Fernández Juan Carl |
Cross-sectional associations between genetic polymorphisms in metabolic enzymes and longer leukocyte telomere length induced by omethoate. Oncotarget 2017 Oct 8 (46): 80638-80644. Duan Xiaoran, Yang Yongli, Wang Sihua, Feng Xiaolei, Wang Tuanwei, Wang Pengpeng, Liu Suxiang, Li Lei, Li Guoyu, Yao Wu, Cui Liuxin, Wang W |
Interactions between superoxide dismutase and paraoxonase polymorphic variants in nonsyndromic cleft lip with or without cleft palate in the Brazilian population. Environmental and molecular mutagenesis 2018 Sep . Machado Renato Assis, de Oliveira Silva Carolina, Persuhn Darlene Camati, de Melo Cavalcanti Dantas Vanessa, de Almeida Reis Silvia Regina, Wu Tao, Line Sergio Roberto, Martelli-Junior Hercilio, Graner Edgard, Coletta Ricardo |
Association of PON2 Gene Polymorphisms (Ser311Cys and Ala148Gly) With the Risk of Developing Type 2 Diabetes Mellitus in the Chinese Population. Frontiers in endocrinology 2018 9 9 495. Ren Huan, Tan Sheng-Lan, Liu Mou-Ze, Banh Hoan L, Luo Jian-Qu |
Association between Q192R polymorphism in the PON1 gene and statin responses in cardiac patients. Annals of medicine and surgery (2012) 2018 Jul 31 1-5. Abd Elgwad Eman R, Behiry Eman G, Swailem Fathy M, Ameen Seham G, Abdelhasib Dalia M, Abd Elhamid Rabab |
Study of the association of 17 lipid-related gene polymorphisms with coronary heart disease. Anatolian journal of cardiology 2018 Jun 19 (6): 360-367. Wu Nan, Liu Guili, Huang Yi, Liao Qi, Han Liyuan, Ye Huandan, Duan Shiwei, Chen Xiaom |
Paraoxonase 1 (PON1)-L55M among common variants in the coding region of the paraoxonase gene family may contribute to the glycemic control in type 2 diabetes. Clinica chimica acta; international journal of clinical chemistry 2018 May 484 40-46. Mahrooz Abdolkarim, Hashemi-Soteh Mohammad Bagher, Heydari Masoud, Boorank Ruzbeh, Ramazani Fatemeh, Mahmoudi Ali, Kianmehr Anvarsadat, Alizadeh Ah |
PON2 and PPARG polymorphisms as biomarkers of risk for coronary heart disease. Biomarkers in medicine 2018 Feb . González-Castro Thelma Beatriz, Tovilla-Zárate Carlos Alfonso, Juárez-Rojop Isela Esther, Hernández-Díaz Yazmín, López-Narváez María Lilia, Rodríguez-Pérez Candelario, González-Hernández Yahaira Karina, Ramos-Méndez Miguel Áng |
Association of PON2 and PON3 polymorphism with risk of developing cataract. Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society 0 33 (2): 153-158. Baig Amena, Ata-Ur-Rehman , Zarina Shamsh |
Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients. Neurogenetics 2019 8 20 (4): 197-208. Narain Priyam, Padhi Aditya K, Dave Upma, Mishra Dibyakanti, Bhatia Rohit, Vivekanandan Perumal, Gomes Jam |
[A clinical and genetic analysis of risk factors for the development of acute and chronic cerebral ischemia]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2019 119 (3. Vyp. 2): 62-67. Anisimova A V, Gunchenko A S, Ikonnikova A Yu, Galkin S S, Avdonina M A, Nasedkina T |
Association of SOD2 A16V and PON2 S311C polymorphisms with polycystic ovary syndrome in Chinese women. Journal of endocrinological investigation 2019 Jan . Liu Q, Liu H, Bai H, Huang W, Zhang R, Tan J, Guan L, Fan |
Paraoxonase-2 variants potentially influence insulin resistance, beta-cell function, and their interrelationships with alanine aminotransferase in type 2 diabetes. Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2018 23 107. Qujeq Durdi, Mahrooz Abdolkarim, Alizadeh Ahad, Boorank Ruzb |
Mendelian randomization analysis identified genes pleiotropically associated with the risk and prognosis of COVID-19. medRxiv : the preprint server for health sciences 2020 9 . Liu Di, Yang Jingyun, Feng Bowen, Lu Wenjin, Zhao Chuntao, Li Lizh |
Association of Genetic and Environmental Factors with Non-Alcoholic Fatty Liver Disease in a Chinese Han Population. International journal of environmental research and public health 2020 Jul 17 (14): . Li Zheng, Ye Cheng-Yin, Wang Li, Li Jin-Mei, Yang L |
[Association between PON2 gene polymorphisms and susceptibility to noise-induced hearing loss]. Zhonghua lao dong wei sheng zhi ye bing za zhi = Zhonghua laodong weisheng zhiyebing zazhi = Chinese journal of industrial hygiene and occupational diseases 2020 Feb 38 (2): 128-132. Wu S S, Yu J N, Jiao J, Chen G S, Zhang C Y, Yu S |
Association of Race and Major Adverse Cardiac Events (MACE): The Atherosclerosis Risk in Communities (ARIC) Cohort. Journal of aging research 2020 4 2020 7417242. Franey Ericha G, Kritz-Silverstein Donna, Richard Erin L, Alcaraz John E, Nievergelt Caroline M, Shaffer Richard A, Bhatnagar Vib |
Association between oxidative stress biomarkers and PON and GST polymorphisms as a predictor for susceptibility to the effects of pesticides. International journal of molecular medicine 2020 3 45 (6): 1951-1959. Costa Chiara, Briguglio Giusi, Giambò Federica, Catanoso Rosaria, Teodoro Michele, Caccamo Daniela, Fenga Concetti |
Paraoxonase Role in Human Neurodegenerative Diseases. Antioxidants (Basel, Switzerland) 2020 12 10 (1): . Reichert Cadiele Oliana, Levy Debora, Bydlowski Sergio |
Mendelian randomization analysis identified genes pleiotropically associated with the risk and prognosis of COVID-19. The Journal of infection 2020 12 82 (1): 126-132. Liu Di, Yang Jingyun, Feng Bowen, Lu Wenjin, Zhao Chuntao, Li Lizh |
Susceptibility of PON1/PON2 Genetic Variations to Ischemic Stroke Risk in a Chinese Han Population. Pharmacogenomics and personalized medicine 2020 11 13 563-570. Pan Yuqin, He Bangshun, Sun Huiling, Xu Tao, Pan Bei, Wang Shukui, Mei Yanpi |
Paraoxonase 3 gene polymorphisms are associated with occupational noise-induced deafness: A matched case-control study from China. PloS one 2020 15 (10): e0240615. Zhou Huaping, Zhou Jinpeng, Li Hui, Hui Changye, Bi Ji |
[Complex association analysis of antioxidant genes polymorphic DNA-markers with age in the ethnic group of Abkhazians.]. Advances in gerontology = Uspekhi gerontologii 2021 34 (3): 360-366. Erdman V V, Matua A Z, Nasibullin T R, Tuktarova I A, Goruhchieva F A, Trapsh K Z, Amaba S T, Ahuba L O, Smyr S D, Danilko K V, Viltorova T |
Association Analysis of Candidate Gene Polymorphisms and Tinnitus in Young Musicians. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2021 Jul . Bhatt Ishan Sunilkumar, Dias Raquel, Torkamani A |
Plasma cholinesterase activity is influenced by interactive effect between omethoate exposure and CYP2E1 polymorphisms. Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes 2021 Apr 1-6. Wang Tuanwei, Zhang Hui, Li Lei, Zhang Wenjuan, Wang Qi, Wang W |
Association between human paraoxonase 2 protein and efficacy of acetylcholinesterase inhibiting drugs used against Alzheimer's disease. PloS one 2021 10 16 (10): e0258879. Parween Fauzia, Hossain Md Summon, Singh Kshetra Pal, Gupta Rinkoo De |
Paraoxonase 2 C311S single nucleotide polymorphism is associated with type C lesions in coronary atherosclerosis. Clinical biochemistry 2022 4 105-106 64-69. Paszek El?bieta, Godlewski Jacek, Wo?kow Pawe?, ?mudka Krzysztof, S?owik Agnieszka, Legutko Jacek, Kleczy?ski Paw |
Genetic Variants Associated with Poor Responsiveness to Sulfonylureas in Filipinos with Type 2 Diabetes Mellitus. Journal of the ASEAN Federation of Endocrine Societies 2023 5 38 (1): 31-40. Elizabeth Paz-Pacheco, Jose Nevado, Eva Maria Cutiongco-De La Paz, Gabriel Jasul, Aimee Yvonne Criselle Aman, Elizabeth Laurize Alejandro-Ribaya, Mark David Francisco, Ma Luz Vicenta Guanzon, May Uyking-Naranjo, Cecille Añonuevo-Cruz, Maria Patricia Deanna Maningat, Cristina Jaring, Paulette Nacpil-Dominguez, Aniza Pala-Mohamad, Abigail Uy-Canto, John Paul Quisumbing, Annabelle Marie Lat, Diane Carla Bernardo, Noemie Marie Mansibang, Vincent Sean Ribaya, Karell Jo Angelique Calpito, Julius Patrick Ferrer, Jessica Biwang, Jodelyn Melegrito, Christian Deo Deguit, Carlos Emmanuel Paner |
A whole exome sequencing study to identify rare variants in multiplex families with alcohol use disorder. Frontiers in psychiatry 2023 11 14 1216493. Shirley Y Hill, Joseph Host |
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- Page last updated:Mar 25, 2024
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