HuGE Literature Finder
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| Association of the lncRNA-GAS5 promoter region rs145204276 polymorphism with sevoflurane maintenance anesthesia outcomes on patients undergoing laparoscopic cholecystectomy. Saudi medical journal 2023 2 44 (2): 137-144. Zhang Panpan, Sha Zhanmi |
| Association of Catalase Gene Polymorphisms with Idiopathic Nephrotic Syndrome in a Chinese Pediatric Population. Laboratory medicine 2022 Aug . Shi Jianrong, Li Wei, Tao Ran, Zhou Dongming, Guo Yajun, Fu Haidong, Sun Anna, Zhang Junfeng, Mao Jianh |
| Evaluation of Relationship Between SOD1 50-bp Deletion Gene Polymorphism, Cu, Zn Level, and Viscosity in Postmenopausal Osteoporosis Patients with Vertebral Fractures. Biological trace element research 2022 Mar . Soyocak Ahu, Doganer Fulya, Duzgun Ergun Dilek, Budak Metin, Turgut Co?an Didem, Ozgen Mer |
| Deletion allele of Apo B gene is associated with higher inflammation, oxidative stress and dyslipidemia in obese type 2 diabetic patients: an analytical cross-sectional study. BMC endocrine disorders 2022 3 22 (1): 73. Mokhtary Nasim, Mousavi Seyedeh Neda, Sotoudeh Gity, Qorbani Mostafa, Dehghani Maryam, Koohdani Fari |
| [Association of AGT, ACE, NOS3, TNF, MMP9, CYBA polymorphism with subclinical arterial wall changes]. Kardiologiia 2021 Mar 61 (3): 57-65. Akopyan A A, Kirillova K I, Strazhesko I D, Samokhodskaya L M, Orlova Ya |
| A New Hypothesis for Type 1 Diabetes Risk: The At-Risk Allele at rs3842753 Associates With Increased Beta-Cell INS Messenger RNA in a Meta-Analysis of Single-Cell RNA-Sequencing Data. Canadian journal of diabetes 2021 5 45 (8): 775-784.e2. Wang Su, Flibotte Stephane, Camunas-Soler Joan, MacDonald Patrick E, Johnson James |
| Susceptibility to preeclampsia is associated with a 50-bp insertion/deletion polymorphism at the promoter region of the SOD1 gene. Journal of the Turkish German Gynecological Association 2021 12 22 (4): 268-272. Namdari Somayeh, Saadat Mosta |
| SKAP2, a Candidate Gene for Type 1 Diabetes, Regulates ?-Cell Apoptosis and Glycemic Control in Newly Diagnosed Patients. Diabetes 2020 Nov . Fløyel Tina, Meyerovich Kira, Prause Michala C, Kaur Simranjeet, Frørup Caroline, Mortensen Henrik B, Nielsen Lotte B, Pociot Flemming, Cardozo Alessandra K, Størling Joach |
| Nuclear factor NF-?B1 functional promoter polymorphism and its expression conferring the risk of Type 2 diabetes-associated dyslipidemia. Mammalian genome : official journal of the International Mammalian Genome Society 2020 Aug . Chatterjee Tanima, De Debasmita, Chowdhury Subhankar, Bhattacharyya Maitr |
| Genetic Variation in SOD1 Gene Promoter Ins/Del and Its Influence on Oxidative Stress in Beta Thalassemia Major Patients. International journal of hematology-oncology and stem cell research 2020 5 14 (2): 110-117. Tripathi Poonam, Agarwal Sarita, Sarangi Aditya Narayan, Tewari Satyendra, Mandal Kaus |
| Uncoupling Protein 2 as genetic risk factor for systemic lupus erythematosus: association with malondialdehyde levels and intima media thickness. Minerva cardioangiologica 2020 6 68 (6): 609-618. Gambino Caterina M, Accardi Giulia, Aiello Anna, Caruso Calogero, Carru Ciriaco, Gioia Bruno G, Guggino Giuliana, Rizzo Sergio, Zinellu Angelo, Ciaccio Marcello, Candore Giuseppi |
| 50?bp deletion in promoter superoxide dismutase 1 gene and increasing risk of cardiovascular disease in Mashhad stroke and heart atherosclerotic disorder cohort study. BioFactors (Oxford, England) 2019 Oct . Darroudi Susan, Tajbakhsh Amir, Esmaily Habibollah, Ghazizadeh Hamideh, Zamani Parvin, Sadabadi Fatemeh, Tayefi Maryam, Tayefi Batool, Fereydouni Narges, Mouhebati Mohsen, Akbari Sark Noushin, Avan Amir, Ferns Gordon A, Mohammadpour Amir H, Asadi Zahra, Ghayour-Mobarhan Maj |
| Whole-exome sequencing identifies a novel INS mutation causative of maturity-onset diabetes of the young 10. Journal of molecular cell biology 2017 Aug . Yan Jing, Jiang Feng, Zhang Rong, Xu Tongfu, Zhou Zhou, Ren Wei, Peng Danfeng, Liu Yong, Hu Cheng, Jia Weipi |
| A 50-bp Ins/Del polymorphism at the promoter region of the superoxide dismutase-1 and bipolar disorder type 1. Nordic journal of psychiatry 2017 Jul 1-4. Kordestanian Nazanin, Saadat Mosta |
| Mutant DD genotype of NFKB1 gene is associated with the susceptibility and severity of coronary artery disease. Journal of molecular and cellular cardiology 2017 Jan 103 56-64. Luo Jun-Yi, Li Xiao-Mei, Zhou Yun, Zhao Qiang, Chen Bang-Dang, Liu Fen, Chen Xiao-Cui, Zheng Hong, Ma Yi-Tong, Gao Xiao-Ming, Yang Yi-Ni |
| Accounting for Life-Course Exposures in Epigenetic Biomarker Association Studies: Early Life Socioeconomic Position, Candidate Gene DNA Methylation, and Adult Cardiometabolic Risk. American journal of epidemiology 2016 9 184 (7): 520-531. Huang Jonathan Y, Gavin Amelia R, Richardson Thomas S, Rowhani-Rahbar Ali, Siscovick David S, Hochner Hagit, Friedlander Yechiel, Enquobahrie Daniel |
| Association Analysis of Polymorphisms in Genes Related to Oxidative Stress in South Indian Type 2 Diabetic Patients with Retinopathy. Ophthalmic genetics 2015 Aug 1-8. Narne Parimala, Ponnaluri Kamakshi Chaithri, Siraj Mohammed, Ishaq Mohamm |
| Association between an HLA-G 14 bp insertion/deletion polymorphism and non-segmental vitiligo in the Korean population. Archives of dermatological research 2014 Aug 306 (6): 577-82. Jeong K-H, Kim S-K, Kang B-K, Chung J-H, Shin M-K, Lee M |
| Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses. Journal of the American College of Cardiology 2012 Oct 60 (17): 1678-89. Zhang Kuixing, Rao Fangwen, Miramontes-Gonzalez Jose Pablo, Hightower C Makena, Vaught Brian, Chen Yuhong, Greenwood Tiffany A, Schork Andrew J, Wang Lei, Mahata Manjula, Stridsberg Mats, Khandrika Srikrishna, Biswas Nilima, Fung Maple M, Waalen Jill, Middelberg Rita P, Heath Andrew C, Montgomery Grant W, Martin Nicholas G, Whitfield John B, Baker Dewleen G, Schork Nicholas J, Nievergelt Caroline M, O'Connor Daniel |
| Alpha-adrenergic receptor gene polymorphisms and cardiovascular reactivity to stress in Black adolescents and young adults. Psychophysiology 2012 Mar 49 (3): 401-12. Kelsey Robert M, Alpert Bruce S, Dahmer Mary K, Krushkal Julia, Quasney Michael |
| The presence of the -866A/55Val/Ins haplotype in the uncoupling protein 2 (UCP2) gene is associated with decreased UCP2 gene expression in human retina. Experimental eye research 2012 Jan 94 (1): 49-55. de Souza Bianca M, Assmann Taís S, Kliemann Lúcia M, Marcon Alexandre S, Gross Jorge L, Canani Luís H, Crispim Dai |
| Genotype-independent in vivo oxidative stress following a methionine loading test: maximal platelet activation in subjects with early-onset thrombosis. Thrombosis research 2011 Oct 128 (4): e43-8. Di Minno Matteo Nicola Dario, Pezzullo Salvatore, Palmieri Vittorio, Coppola Antonio, D'Angelo Armando, Sampietro Francesca, Cavalca Viviana, Tremoli Elena, Di Minno Giovan |
| Serotonin transporter gene variants and prediction of stress-induced risk for psychological distress. Genes, brain, and behavior 2011 Jul 10 (5): 536-41. Stefanis N C, Mandelli L, Hatzimanolis A, Zaninotto L, Smyrnis N, Avramopoulos D, Evdokimidis I, Serretti |
| [The -108 C/T polymorphism in paraoxonase 1 gene in Chinese patients with polycystic ovary syndrome]. Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition 2011 Jan 42 (1): 24-8. Zhang Feng, Liu Hong-Wei, Fan Ping, Bai Huai, Song |
| Role of p53 gene polymorphism and bladder cancer predisposition in northern India. Cancer biomarkers : section A of Disease markers 2011 9 8 (1): 21-8. Srivastava Priyanka, Jaiswal Praveen K, Singh Vibha, Mittal Rama |
| Role for mitochondrial uncoupling protein-2 (UCP2) in hyperhomocysteinemia and venous thrombosis risk? Clinical chemistry and laboratory medicine : CCLM / FESCC 2008 46 (5): 655-9. Heil Sandra G, Vermeulen Sita H, Van der Rijt-Pisa Brenda J M, den Heijer Martin, Blom Henk |
| Family-based and case-control study of DRD2, DAT, 5HTT, COMT genes polymorphisms in alcohol dependence. Neuroscience letters 2006 Dec 410 (1): 1-5. Samochowiec Jerzy, Kucharska-Mazur Jolanta, Grzywacz Anna, Jab?o?ski Marcin, Rommelspacher Hans, Samochowiec Agnieszka, Sznabowicz Mariusz, Horodnicki Jan, Sagan Leszek, Pe?ka-Wysiecka Justy |
| F2-Isoprostane level is associated with the angiotensin II type 1 receptor -153A/G gene polymorphism. Free radical biology & medicine 2005 Mar 38 (5): 583-8. Ormezzano Olivier, Cracowski Jean-Luc, Mallion Jean-Michel, Poirier Odette, Bessard Janine, Briançon Serge, François Patrice, Baguet Jean Philip |
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- Page last updated:Mar 22, 2023
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