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Identification and characterization of new gain-of-function mutations in the PCSK9 gene responsible for autosomal dominant hypercholesterolemia.
Abifadel M, Guerin M, Benjannet S, Rabès JP, Le Goff W, Julia Z, Hamelin J, Carreau V, Varret M, Bruckert E, Tosolini L, Meilhac O, Couvert P, Bonnefont-Rousselot D, Chapman J, Carrié A, Michel JB, Prat A, Seidah NG, Boileau C. Abifadel M, et al. Among authors: bruckert e. Atherosclerosis. 2012 Aug;223(2):394-400. doi: 10.1016/j.atherosclerosis.2012.04.006. Epub 2012 May 17. Atherosclerosis. 2012. PMID: 22683120
Action of ciprofibrate in type IIb hyperlipoproteinemia: modulation of the atherogenic lipoprotein phenotype and stimulation of high-density lipoprotein-mediated cellular cholesterol efflux.
Guerin M, Le Goff W, Frisdal E, Schneider S, Milosavljevic D, Bruckert E, Chapman MJ. Guerin M, et al. Among authors: bruckert e. J Clin Endocrinol Metab. 2003 Aug;88(8):3738-46. doi: 10.1210/jc.2003-030191. J Clin Endocrinol Metab. 2003. PMID: 12915663 Clinical Trial.
Prevention campaigns for cardiovascular disease.
Bruckert E, Chapman J. Bruckert E, et al. Lancet. 2003 Nov 22;362(9397):1767-8. doi: 10.1016/S0140-6736(03)14871-4. Lancet. 2003. PMID: 14643142 No abstract available.
Metabolic syndrome features small, apolipoprotein A-I-poor, triglyceride-rich HDL3 particles with defective anti-apoptotic activity.
de Souza JA, Vindis C, Hansel B, Nègre-Salvayre A, Therond P, Serrano CV Jr, Chantepie S, Salvayre R, Bruckert E, Chapman MJ, Kontush A. de Souza JA, et al. Among authors: bruckert e. Atherosclerosis. 2008 Mar;197(1):84-94. doi: 10.1016/j.atherosclerosis.2007.08.009. Epub 2007 Sep 14. Atherosclerosis. 2008. PMID: 17868679
465 results