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Arteriosclerosis, Thrombosis, and Vascular Biology|December 20, 2008
Despite antiatherogenic metabolic characteristics, SCD1-deficient mice have increased inflammation and atherosclerosisMarcia L E MacDonald, Miranda van Eck, Reeni B Hildebrand, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|July 10, 2012
Human ATP-binding cassette G1 controls macrophage lipoprotein lipase bioavailability and promotes foam cell formationMaryline Olivier, Michael W Tanck, Ruud Out, et al.Atherosclerosis|June 21, 2016
Abca1 deficiency protects the heart against myocardial infarction-induced injuryMieke C Louwe, Bart Lammers, Miguel A Frias, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|October 30, 2010
Macrophage adipose triglyceride lipase deficiency attenuates atherosclerotic lesion development in low-density lipoprotein receptor knockout miceBart Lammers, Prakash G Chandak, Elma Aflaki, et al.Circulation|August 31, 2006
Both hepatic and extrahepatic ABCA1 have discrete and essential functions in the maintenance of plasma high-density lipoprotein cholesterol levels in vivoRoshni R Singaraja, Miranda Van Eck, Nagat Bissada, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|May 1, 2010
Restoration of high-density lipoprotein levels by cholesteryl ester transfer protein expression in scavenger receptor class B type I (SR-BI) knockout mice does not normalize pathologies associated with SR-BI deficiencyReeni B Hildebrand, Bart Lammers, Illiana Meurs, et al.The New England Journal of Medicine|January 14, 2011
Genetic variant of the scavenger receptor BI in humansMenno Vergeer, Suzanne J A Korporaal, Remco Franssen, et al.Atherosclerosis|August 16, 2011
Hypocholesterolemia, foam cell accumulation, but no atherosclerosis in mice lacking ABC-transporter A1 and scavenger receptor BIYing Zhao, Marieke Pennings, Carlos L J Vrins, et al.Journal of Lipid Research|April 27, 2013
Farnesoid X receptor activation increases cholesteryl ester transfer protein expression in humans and transgenic miceThomas Gautier, Willeke de Haan, Jacques Grober, et al.Plos One|June 1, 2014
Mutation in KERA identified by linkage analysis and targeted resequencing in a pedigree with premature atherosclerosisStephanie Maiwald, Suthesh Sivapalaratnam, Mahdi M Motazacker, et al.Pageof 16