Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Death 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 |
Common genetic variation, residential proximity to traffic exposure, and left ventricular mass: the multi-ethnic study of atherosclerosis. Environmental health perspectives 2010 Jul 118 (7): 962-9. Van Hee Victor C, Adar Sara D, Szpiro Adam A, Barr R Graham, Diez Roux Ana, Bluemke David A, Sheppard Lianne, Gill Edward A, Bahrami Hossein, Wassel Christina, Sale Michele M, Siscovick David S, Rotter Jerome I, Rich Stephen S, Kaufman Joel |
Associations of genetic variants of endothelin with cardiovascular complications in patients with renal failure. BMC nephrology 2017 Sep 18 (1): 291. Kao Chih-Chin, Cheng Shih-Ying, Wu Mei-Yi, Chien Shu-Chen, Lu Hsing-Fang, Hsu Yu-Wen, Zhang Yan-Feng, Wu Mai-Szu, Chang Wei-Chi |
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 |
Association of PHACTR1 intronic variants with the first myocardial infarction and their effect on PHACTR1 mRNA expression in PBMCs. Gene 2021 Jan 145428. Kuveljic Jovana, Djuric Tamara, Stankovic Goran, Dekleva Milica, Stankovic Aleksandra, Alavantic Dragan, Zivkovic Ma |
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