Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Abnormalities and LCAT[original query] |
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Increased risk of coronary artery disease in Caucasians with extremely low HDL cholesterol due to mutations in ABCA1, APOA1, and LCAT. Biochimica et biophysica acta 2012 Mar 1821 (3): 416-24. Tietjen Ian, Hovingh G Kees, Singaraja Roshni, Radomski Chris, McEwen Jason, Chan Elden, Mattice Maryanne, Legendre Annick, Kastelein John J P, Hayden Michael |
Identification of genetic variants of lecithin cholesterol acyltransferase in individuals with high HDL-C levels. Molecular medicine reports 2014 Jul 10 (1): 496-502. Naseri Mohsen, Hedayati Mehdi, Daneshpour Maryam Sadat, Bandarian Fatemeh, Azizi Fereido |
Single nucleotide polymorphisms in LCAT may contribute to dyslipidaemia in HIV-infected individuals on HAART in a Ghanaian population. Scientific reports 2020 11 10 (1): 19419. Bani Simon Bannison, Danquah Kwabena Owusu, Obirikorang Christian, Owiredu William K B A, Quaye Lawrence, Muonir Der Edmund, Acheampong Emmanuel, Adams Yussif, Dapare Peter Paul M, Banyeh Moses, Anto Enoch Odame, Sakyi Samuel Asamo |
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- Page last updated:Apr 22, 2024
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