Human Genome Epidemiology Literature Finder
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Records 1 - 24 (of 24 Records) |
| Query Trace: Disease and GCG[original query] |
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| Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a UK population. Brain : a journal of neurology 2001 Mar 124 (Pt 3): 522-6. Hill M E, Creed G A, McMullan T F, Tyers A G, Hilton-Jones D, Robinson D O, Hammans S |
| [Study on gene mutations of alpha-thalassemia in the South of China]. Zhongguo shi yan xue ye xue za zhi / Zhongguo bing li sheng li xue hui = Journal of experimental hematology / Chinese Association of Pathophysiology 2003 Feb 11 (1): 54-60. Duan Shan, Li Hong-Yi, Chen Zheng, Chen Su-Qin, Bi Xiong-Jie, Chen Lu-Ming, Du Chuan-S |
| Patient interleukin-18 GCG haplotype associates with improved survival and decreased transplant-related mortality after unrelated-donor bone marrow transplantation. British journal of haematology 2004 Sep 126 (5): 704-10. Cardoso Sandra M P, DeFor Todd E, Tilley Louise A, Bidwell Jeffrey L, Weisdorf Daniel J, MacMillan Margaret |
| Association of IL-6 gene polymorphisms and COPD in a Spanish population. Respiratory medicine 2008 Dec 102 (12): 1805-11. Córdoba-Lanús Elizabeth, de-Torres Juan-Pablo, López-Aguilar Celeste, Rodríguez-Pérez María-Cristo, Maca-Meyer Nicole, Montejo-de-Garcini Angela, Aguirre-Jaime Armando, Pérez-Méndez Lina, Casanova Ci |
| Influence of interleukin 18 promoter polymorphisms in susceptibility to Kawasaki disease in Taiwan. The Journal of rheumatology 2008 Jul 35 (7): 1408-13. Hsueh Kai-Chung, Lin Ying-Ju, Chang Jeng-Sheng, Wan Lei, Tsai Yu-Hsin, Tsai Chang-Hai, Tsai Fuu-J |
| Genotype and haplotype analysis of cell cycle genes in sporadic colorectal cancer in the Czech Republic. Human mutation 2009 Apr 30 (4): 661-8. Polakova V, Pardini B, Naccarati A, Landi S, Slyskova J, Novotny J, Vodickova L, Bermejo J L, Hanova M, Smerhovsky Z, Tulupova E, Kumar R, Hemminki K, Vodicka |
| A Multinomial Ordinal Probit Model with Singular Value Decomposition Method for a Multinomial Trait. Journal of probability and statistics 2012 2012 . Kwon Soonil, Goodarzi Mark O, Taylor Kent D, Cui Jinrui, Chen Y-D Ida, Rotter Jerome I, Hsueh Willa, Guo Xiuqi |
| Association of ALOX5AP haplotypes with susceptibility to coronary artery disease in a Chinese Han population. European journal of internal medicine 2012 Jul 23 (5): e119-23. Li Yi, Li Zhidong, Zhang Xiaolin, Yan Chenghui, Kang Jian, Liang Zhenyang, Liu Shaowei, Feng Xueyao, Han Yali |
| Effect of genetic polymorphism of ALOX15 on aspirin-exacerbated respiratory disease. International archives of allergy and immunology 2012 159 (2): 157-61. Song Young-Sin, Yang Eun-Mi, Kim Seung-Hyun, Jin Hyun Jung, Park Hae-S |
| CD36 gene variants and their association with type 2 diabetes in an Indian population. Diabetes technology & therapeutics 2013 Aug 15 (8): 680-7. Gautam Sunaina, Pirabu Loganathan, Agrawal Chandra G, Banerjee Monis |
| Glucagon gene polymorphism modifies the effects of smoking and physical activity on risk of type 2 diabetes mellitus in Han Chinese. Gene 2014 Jan 534 (2): 352-5. Li Linlin, Gao Kaiping, Zhao Jingzhi, Feng Tianping, Yin Lei, Wang Jinjin, Wang Chongjian, Li Chunyang, Wang Yan, Wang Qian, Zhai Yujia, You Haifei, Ren Yongcheng, Wang Bingyuan, Hu Dongshe |
| Polymorphism of IL37 gene as a protective factor for autoimmune thyroid disease. Journal of molecular endocrinology 2015 Sep . Yan Ni, Meng Shuai, Song Ronghua, Qin Qiu, Wang Xuan, Yao Qiuming, Jiang Yanfei, Jiang Wenjuan, Shi Liangfeng, Xu Jian, Zhang Jin |
| Toll-like receptor 4 gene polymorphism is associated with chronic periodontitis. International journal of clinical and experimental medicine 2015 8 (4): 6186-92. Ding Yuan-Sheng, Zhao Yue, Xiao Yuan-Yuan, Zhao Ga |
| [Haplotype Analysis of Oculopharyngeal Muscular Dystrophy (OPMD) Locus in Yakutia]. Genetika 2016 Mar 52 (3): 376-84. Marusin A V, Kurtanov Kh A, Maksimova N R, Svarovskaya M G, Stepanov V |
| The Association Between Clusterin and APOE Polymorphisms and Late-Onset Alzheimer Disease in a Turkish Cohort. Journal of geriatric psychiatry and neurology 2016 Apr . Alayl?o?lu Merve, Gezen-Ak Duygu, Dursun Erdinç, Bilgiç Ba?ar, Hana?as? Ha?met, Ertan Turan, Gürvit Hakan, Emre Murat, Eker Engin, Uysal Ömer, Y?lmazer Sel |
| Association of NIPA1 repeat expansions with amyotrophic lateral sclerosis in a large international cohort. Neurobiology of aging 2019 02 74 234.e9-234.e15. Tazelaar Gijs H P, Dekker Annelot M, van Vugt Joke J F A, van der Spek Rick A, Westeneng Henk-Jan, Kool Lindy J B G, Kenna Kevin P, van Rheenen Wouter, Pulit Sara L, McLaughlin Russell L, Sproviero William, Iacoangeli Alfredo, Hübers Annemarie, Brenner David, Morrison Karen E, Shaw Pamela J, Shaw Christopher E, Panadés Monica Povedano, Mora Pardina Jesus S, Glass Jonathan D, Hardiman Orla, Al-Chalabi Ammar, van Damme Philip, Robberecht Wim, Landers John E, Ludolph Albert C, Weishaupt Jochen H, van den Berg Leonard H, Veldink Jan H, van Es Michael A, |
| Association between arsenic metabolism gene polymorphisms and arsenic-induced skin lesions in individuals exposed to high-dose inorganic arsenic in northwest China. Scientific reports 2018 01 8 (1): 413. Luo Lanrong, Li Yuanyuan, Gao Yanhui, Zhao Lijun, Feng Hongqi, Wei Wei, Qiu Chuanying, He Qian, Zhang Yanting, Fu Songbo, Sun Dianj |
| Analysis of the GCG repeat length in NIPA1 gene in C9orf72-mediated ALS in a large Italian ALS cohort. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2019 7 40 (12): 2537-2540. Corrado Lucia, Brunetti Maura, Di Pierro Alice, Barberis Marco, Croce Roberta, Bersano Enrica, De Marchi Fabiola, Zuccalà Miriam, Barizzone Nadia, Calvo Andrea, Moglia Cristina, Mazzini Letizia, Chiò Adriano, D'Alfonso Sand |
| Low Levels of LRRK2 Gene Expression are Associated with LRRK2 SNPs and Contribute to Parkinson's Disease Progression. Neuromolecular medicine 2020 10 23 (2): 292-304. Y?lmazer Selma, Canda? Esin, Genç Gençer, Alayl?o?lu Merve, ?engül Bü?ra, Gündüz Ay?egül, Apayd?n Hülya, K?z?ltan Güne?, Ertan Sibel, Dursun Erdinç, Gezen-Ak Duy |
| Association of extracellular superoxide dismutase (EC-SOD) polymorphisms with risk of type 2 diabetes mellitus in a Chinese Han population. International journal of clinical and experimental pathology 2020 1 10 (12): 11819-11827. Li Haoyun, Zhang Changmeng, He Li, Zhang Fengjiao, Luo Fang, Yuan Yizhe, Li Qingc |
| 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 |
| Association of Sirtuin Gene Polymorphisms with Susceptibility to Coronary Artery Disease in a North Chinese Population. BioMed research international 2022 2022 4294008. Song Xingfa, Wang Haidong, Wang Chao, Ji Guangquan, Jiang Pei, Liang Donglou, Wang Xiaoji |
| Determinants of plasma levels of proglucagon and the metabolic impact of glucagon receptor signalling: a UK Biobank study. Diabetologia 2024 5 . Marie Winther-Sørensen, Sara L Garcia, Andreas Bartholdy, Maud E Ottenheijm, Karina Banasik, Søren Brunak, Charlotte M Sørensen, Lise Lotte Gluud, Filip K Knop, Jens J Holst, Mette M Rosenkilde, Majken K Jensen, Nicolai J Wewer Albrechts |
| The 3'UTR Polymorphisms in the NLRP3 Gene Associated with the Risk of COPD and Their Putative Effects on the microRNA Mechanism. Genetic testing and molecular biomarkers 2024 5 . Huiyan Wu, Chuting Huang, Yanling Zhang, Xin Yang, Liang Peng, Weipeng |
- Page last reviewed:Feb 1, 2024
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