Human Genome Epidemiology Literature Finder
Records 1 - 4 (of 4 Records) |
Query Trace: Atherosclerosis and LCAT[original query] |
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Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes. Atherosclerosis 2005 Sep 182 (1): 153-9. Pisciotta L, Calabresi L, Lupattelli G, Siepi D, Mannarino MR, Moleri E, Bellocchio A, Cantafora A, Tarugi P, Calandra S, Bertolini S |
Do mutations causing low HDL-C promote increased carotid intima-media thickness? Clinica chimica acta; international journal of clinical chemistry 2007 Feb 377 (1-2): 273-5. Miller Michael, Rhyne Jeffrey, Hong Seung Ho, Friel Gina, Dolinar Christina, Riley Wa |
Increased risk of premature coronary artery disease in Egyptians with ABCA1 (R219K), CETP (TaqIB), and LCAT (4886C/T) genes polymorphism. Journal of clinical lipidology 0 8 (4): 381-9. Abd El-Aziz Tarek A, Mohamed Rasha H, Hagrass Hoda |
CETP and LCAT Gene Polymorphisms Are Associated with High-Density Lipoprotein Subclasses and Acute Coronary Syndrome. Lipids 2018 Feb 53 (2): 157-166. Vargas-Alarcon Gilberto, Perez-Mendez Oscar, Herrera-Maya Gabriel, Garcia-Sanchez Cynthia, Martinez-Rios Marco Antonio, Peña-Duque Marco Antonio, Posadas-Sanchez Rosalinda, Posadas-Romero Carlos, Escobedo Galileo, Fragoso Jose Manu |
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- Page last updated:Apr 22, 2024
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