Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Syndrome and EDN1[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 |
| Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease. Human genetics 2008 Apr 123 (3): 307-13. Wiltshire Steven, Powell Brenda L, Jennens Michelle, McCaskie Pamela A, Carter Kim W, Palmer Lyle J, Thompson Peter L, McQuillan Brendan M, Hung Joseph, Beilby John |
| Maternal EDN1 G5665T polymorphism influences circulating endothelin-1 levels and plays a role in determination of preeclampsia phenotype. Journal of hypertension 2009 Oct 27 (10): 2044-50. Aggarwal Pardeep Kumar, Jain Vanita, Srinivasan Radhika, Jha Vivekana |
| The -974C>A (rs3087459) gene polymorphism in the endothelin gene (EDN1) is associated with risk of developing acute coronary syndrome in Mexican patients. Gene 2014 Jun 542 (2): 258-62. Vargas-Alarcon Gilberto, Vallejo Maite, Posadas-Romero Carlos, Juarez-Rojas Juan G, Martinez-Rios Marco Antonio, Peña-Duque Marco Antonio, Carrillo-Sanchez Silvia, Perez-Mendez Oscar, Fragoso José Manu |
| Association between endothelin?1 and fibromyalgia syndrome. Molecular medicine reports 2017 Aug . Nah Seong-Su, Lee Hwayoung, Hong Yeongseon, Im Jiyun, Won Hansol, Chang Sung-Hae, Kim Hyung-Ki, Kwon Jun-Tack, Kim Hak-J |
| Protein Z and Endothelin-1 genetic polymorphisms in pediatric Egyptian sickle cell disease patients. Journal of clinical laboratory analysis 2018 Feb 32 (2): . Khorshied Mervat M, Mohamed Nohair S, Hamza Rania S, Ali Rasha M, El-Ghamrawy Mona |
| Genetic Susceptibility to Postdiarrheal Hemolytic-Uremic Syndrome After Shiga Toxin-Producing Escherichia coli Infection: A Centers for Disease Control and Prevention FoodNet Study. The Journal of infectious diseases 2018 03 217 (6): 1000-1010. Kallianpur Asha R, Bradford Yuki, Mody Rajal K, Garman Katie N, Comstock Nicole, Lathrop Sarah L, Lyons Carol, Saupe Amy, Wymore Katie, Canter Jeffrey A, Olson Lana M, Palmer Amanda, Jones Timothy |
| [Endothelin-1 rs5370 gene polymorphism in primary nephrotic syndrome: A case-control study]. Anales de pediatria 2020 Dec . Rizk Hoda, Hammad Ayman, El-Said Afaf, Wahba Yah |
| Endothelin-1 rs9296344 associates with the susceptibility of childhood primary nephrotic syndrome. Journal of clinical laboratory analysis 2020 Jan e23134. Zhang Ruifeng, Yang Huandan, Zhu Bingbing, Yuan Tingting, Peng Qianqian, Lv Juan, Qiu Shan, Zhou Suqin, Li Yan, Zhong Zhaow |
| Gene variants associated with obstructive sleep apnea (OSA) in relation to sudden infant death syndrome (SIDS). International journal of legal medicine 2021 Feb . Kerz J, Schürmann P, Rothämel T, Dörk T, Klintschar |
| Endothelin-1 RS5370 gene polymorphism in primary nephrotic syndrome: A case-control study. Anales de pediatria 2021 12 95 (6): 406-412. Rizk Hoda, Hammad Ayman, El-Said Afaf, Wahba Yah |
| Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance. Anais da Academia Brasileira de Ciencias 2021 11 93 (suppl 4): e20210618. Janssen Luísa P, Medeiros Liciane F, Souza Andressa DE, Silva Juliana |
| Genetic variant in the 5' untranslated region of endothelin1 (EDN1) gene in children with primary nephrotic syndrome. Journal of biochemical and molecular toxicology 2021 Nov e22963. Yahia Sohier, Hammad Ayman, El-Gilany Abdel-Hady, El-Assmy Mohamed, El-Tanbouly Rasha, Elsaid Afaf M, Elmoursi Lamiaa Z, Elshazli Rami M, Shoaib Rasha |
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