Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Disease and ECE1[original query] |
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| Endothelin-converting enzyme-1 promoter polymorphisms and susceptibility to sporadic late-onset Alzheimer's disease in a Chinese population. Disease markers 2009 27 (5): 5. Jin Zhao, Luxiang Chi, Huadong Zhou, Yanjiang Wang, Zhiqiang Xu, Hongyuan Cao, Lihua Huang, Xu |
| No replication of genetic association between candidate polymorphisms and Alzheimer's disease. Neurobiology of aging 2011 Aug 32 (8): 1443-51. Cousin Emmanuelle, Macé Sandrine, Rocher Corinne, Dib Colette, Muzard Gaëlle, Hannequin Didier, Pradier Laurent, Deleuze Jean-François, Génin Emmanuelle, Brice Alexis, Campion Dominiq |
| Genetic analysis of genes involved in amyloid-ß degradation and clearance in Alzheimer's disease. Journal of Alzheimer's disease : JAD 2012 28 (3): 553-9. Natunen Teemu, Helisalmi Seppo, Vepsäläinen Saila, Sarajärvi Timo, Antikainen Leila, Mäkinen Petra, Herukka Sanna-Kaisa, Koivisto Anne Maria, Haapasalo Annakaisa, Soininen Hilkka, Hiltunen Mik |
| ECE1 polymorphisms may contribute to the susceptibility of sporadic congenital heart disease in a Chinese population. DNA and cell biology 2012 Aug 31 (8): 1425-30. Wang Yu, Liu Yiming, Peng Wei, Wang Meilin, Sun Jian, Zhang Zhengdong, Mo Xumi |
| The role of ECE1 variants in cognitive ability in old age and Alzheimer's disease risk. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Sep 159B (6): 696-709. Hamilton Gillian, Harris Sarah E, Davies Gail, Liewald David C, Tenesa Albert, Payton Antony, Horan Michael A, Ollier William E R, Pendleton Neil, , Starr John M, Porteous David, Deary Ian |
| Influence of Coding Variability in APP-Aß Metabolism Genes in Sporadic Alzheimer's Disease. PloS one 2016 11 (6): e0150079. Sassi Celeste, Ridge Perry G, Nalls Michael A, Gibbs Raphael, Ding Jinhui, Lupton Michelle K, Troakes Claire, Lunnon Katie, Al-Sarraj Safa, Brown Kristelle S, Medway Christopher, Lord Jenny, Turton James, , Morgan Kevin, Powell John F, Kauwe John S, Cruchaga Carlos, Bras Jose, Goate Alison M, Singleton Andrew B, Guerreiro Rita, Hardy Jo |
| Association of Gene Polymorphisms of Some Endothelial Factors with Stent Reendothelization after Elective Coronary Artery Revascularization. Bulletin of experimental biology and medicine 2021 6 171 (2): 194-197. Timizheva K B, Azova M M, Aissa A Ait, Aghajanyan A V, Tskhovrebova L V, Blagonravov M |
| Exome sequencing identifies novel genes and variants in patients with Hirschsprung disease. Journal of pediatric surgery 2022 12 . Gunadi , Kalim Alvin Santoso, Iskandar Kristy, Marcellus , Puspitarani Dyah Ayu, Diposarosa Rizki, Makhmudi Akhmad, Astuti Galuh Dyah N |
| Mutation analysis of the ECE1 gene in late-onset Alzheimer's disease. Neurobiology of aging 2023 6 129 58-61. Zhanfang Sun, Cheng Zhao, Xueming Liu, Peng Zhang, Xiang Wang, Xiao Man, Zhen Li, Yifeng Du, Xiangqian Che, Yuanyuan Xia |
| Susceptibility of ECE1 polymorphisms to Hirschsprung's disease in southern Chinese children. Frontiers in pediatrics 2023 1 10 1056938. Lan Chaoting, Liu Yanqing, Wu Xiao, Wang Bingtong, Xin Songqing, He Qiuming, Zhong Wei, Liu Zipe |
| The Analysis of ECE1 and PPARG Variants in the Development of Osteopenia and Osteoporosis in Postmenopausal Women. Biomedicines 2024 7 12 (7): . Izabela Uzar, Anna Bogacz, Ma?gorzata ?uszczy?ska, Marlena Wolek, Katarzyna Kotrych, Andrzej Modrzejewski, Bogus?aw Czerny, Pawe? Zi?tek, Adam Kami?s |
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