Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: ECE1[original query] |
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Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development. Pediatric research 2004 Sep 56 (3): 391-5. Weese-Mayer Debra E, Berry-Kravis Elizabeth M, Zhou Lili, Maher Brion S, Curran Mark E, Silvestri Jean M, Marazita Mary |
Genes encoding endothelin-converting enzyme-1 and endothelin-1 interact to influence blood pressure in women: the EVA study. Journal of hypertension 2004 Apr 22 (4): 739-43. Funalot Benoît, Courbon Dominique, Brousseau Thierry, Poirier Odette, Berr Claudine, Cambien François, Amouyel Philippe, Schwartz Jean-Charles, Ducimetière Pierre, |
Association of single nucleotide polymorphisms in endothelin family genes with the progression of atherosclerosis in patients with essential hypertension. Journal of human hypertension 2007 Nov 21 (11): 883-92. Yasuda H, Kamide K, Takiuchi S, Matayoshi T, Hanada H, Kada A, Yang J, Miwa Y, Yoshii M, Horio T, Yoshihara F, Nakamura S, Nakahama H, Tei C, Miyata T, Kawano |
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 |
The role of the kallikrein-kinin system genes in the salt sensitivity of blood pressure: the GenSalt Study. American journal of epidemiology 2012 Oct 176 Suppl 7 S72-80. Gu Dongfeng, Zhao Qi, Kelly Tanika N, Hixson James E, Rao Dabeeru C, Cao Jie, Chen Jing, Li Jianxin, Chen Jichun, Ji Xu, Hu Dongsheng, Wang Xushan, Liu De-Pei, He Jia |
Variation in genes in the endothelin pathway and endothelium-dependent and endothelium-independent vasodilation in an elderly population. Acta physiologica (Oxford, England) 2013 May 208 (1): 88-94. Lind L, Syvänen A-C, Axelsson T, Lundmark P, Hägg S, Larsson |
Polymorphisms of ECE1 may contribute to susceptibility to ischemic stroke in Han Chinese of Northern China. Cell biochemistry and biophysics 2014 Jun 69 (2): 237-46. Sui Rubo, He Zhi |
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 between ECE1 gene polymorphisms and risk of intracerebral haemorrhage. The Journal of international medical research 2016 Jun 44 (3): 444-52. Zeng Yi, Ma Mingming, Liu Baoqiong, Xia Jian, Xu Hongwei, Liu Yunhai, Du Xiaoping, Hu Zhiping, Yang Qidong, Zhang |
Identification of novel alleles associated with insulin resistance in childhood obesity using pooled-DNA genome-wide association study approach. International journal of obesity (2005) 2017 Nov . Kotnik P, Knapi? E, Kokošar J, Kova? J, Jerala R, Battelino T, Horvat |
Noncardiac genetic predisposition in sudden infant death syndrome. Genetics in medicine : official journal of the American College of Medical Genetics 2018 Aug . Gray Belinda, Tester David J, Wong Leonie Ch, Chanana Pritha, Jaye Amie, Evans Jared M, Baruteau Alban-Elouen, Evans Margaret, Fleming Peter, Jeffrey Iona, Cohen Marta, Tfelt-Hansen Jacob, Simpson Michael A, Ackerman Michael J, Behr Elijah |
The -839(A/C) Polymorphism in the ECE1 Isoform b Promoter Associates With Osteoporosis and Fractures. Journal of the Endocrine Society 2019 Nov 3 (11): 2041-2050. Hansen Karen E, Johnson Michael G, Carter Tonia C, Mayer John, Keuler Nicholas S, Blank Robert |
Association of ECE1 gene polymorphisms and essential hypertension risk in the Northern Han Chinese: A case-control study. Molecular genetics & genomic medicine 2020 Feb e1188. Wang Hao, Liu Jielin, Liu Kuo, Liu Ya, Wen Jie, Wang Zuoguang, Wen Shaoj |
Genetic Examination for Fetuses with Increased Fetal Nuchal Translucency by Genomic Technology. Cytogenetic and genome research 2020 2 160 (2): 57-62. Xue Shuya, Yan Huanchen, Chen Jingsi, Li Nan, Wang Jiayan, Liu Yu, Zhang Huimin, Li Shaoying, Zhang Wei, Chen Dunjin, Chen M |
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 |
Interactions between PDA-associated polymorphisms and genetic ancestry alter ductus arteriosus gene expression. Pediatric research 2021 4 91 (4): 903-911. Clyman Ronald I, Hills Nancy K, Dagle John M, Murray Jeffrey C, Kelsey Keeg |
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 |
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- Page last updated:Apr 16, 2024
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