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Apolipoprotein E_Bethesda: isolation and partial characterization of a variant of human apolipoprotein E isolated from very low density lipoproteinsGHISELLI, G; GREGG, R. E; BRYAN BREWER, H. JR et al.Biochimica et biophysica acta. 1984, Vol 794, Num 2, pp 333-339, issn 0006-3002Article

Cholesterol Efflux and Atheroprotection: Advancing the Concept of Reverse Cholesterol TransportROSENSON, Robert S; BRYAN BREWER, H; REMALEY, Alan T et al.Circulation (New York, N.Y.). 2012, Vol 125, Num 15, pp 1905-1919, issn 0009-7322, 15 p.Article

HDL Measures, Particle Heterogeneity, Proposed Nomenclature, and Relation to Atherosclerotic Cardiovascular EventsROSENSON, Robert S; BRYAN BREWER, H; CHAPMAN, M. John et al.Clinical chemistry (Baltimore, Md.). 2011, Vol 57, Num 3, pp 392-410, issn 0009-9147, 19 p.Article

Three genetic variants of human plasma apolipoprotein A-IV : Apoa-IV-1(Thr³⁴⁷ → Ser), Apoa-IV-0(Lys¹⁶⁷ → Glu,Gln³⁶⁰ → His), and Apoa-IV-3(Glu¹⁶⁵ → Lys)LOHSE, P; KINDT, M. R; RADER, D. J et al.The Journal of biological chemistry (Print). 1991, Vol 266, Num 21, pp 13513-13518, issn 0021-9258, 6 p.Article

Transcriptional regulation of the human lipoprotein lipase gene in 3T3-L1 adipocytesPREVIATO, L; PARROTT, C. L; SANTAMARINA-FOJO, S et al.The Journal of biological chemistry (Print). 1991, Vol 266, Num 28, pp 18958-18963, issn 0021-9258Article

Human apolipoprotein A-I: post-translational modification by fatty acid acylationHOEG, J. M; MENG, M. S; RONAN, R et al.The Journal of biological chemistry (Print). 1986, Vol 261, Num 9, pp 3911-3915, issn 0021-9258Article

Levels of lipoprotein Lp(a) decline with neomycin and niacin treatmentGURAKAR, A; HOEG, J. M; KOSTNER, G et al.Atherosclerosis. 1985, Vol 57, Num 2-3, pp 293-301, issn 0021-9150Article

Distinct hepatic receptors for low density lipoprotein and apolipoprotein E in humansHOEG, J. M; DEMOSKY, S. J. JR; GREGG, R. E et al.Science (Washington, D.C.). 1985, Vol 227, Num 4688, pp 759-761, issn 0036-8075Article

A deletion mutation in the ApoC-II gene (ApoC-II_Nijmegen) of a patient with a deficiency of apolipoprotein C-IIFOJO, S. S; STALENHOEF, A. F. H; MARR, K et al.The Journal of biological chemistry (Print). 1988, Vol 263, Num 34, pp 17913-17916, issn 0021-9258Article

Abnormal in vivo metabolism of apolipoprotein E₄ in humansGREGG, R. E; ZECH, L. A; SCHAEFER, E. J et al.The Journal of clinical investigation. 1986, Vol 78, Num 3, pp 815-821, issn 0021-9738Article

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Isoforms of apolipoprotein A-II in human plasma and thoracic duct lymphLACKNER, K. J; EDGE, S. B; GREGG, R. E et al.The Journal of biological chemistry (Print). 1985, Vol 260, Num 2, pp 703-706, issn 0021-9258Article

Two different allelic mutations in the lecithin : cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency : LCAT (tyr⁸³→stop) and LCAT (tyr¹⁵⁶→asn)KLEIN, H.-G; LOHSE, P; DUVERGER, N et al.Journal of lipid research. 1993, Vol 34, Num 1, pp 49-58, issn 0022-2275Article

Human preproapolipoprotein C-II. Analysis of major plasma isoformsFOJO, S. S; TAAM, L; FAIRWELL, T et al.The Journal of biological chemistry (Print). 1986, Vol 261, Num 21, pp 9591-9594, issn 0021-9258Article

Lipoprotein abnormalities in primary biliary cirrhosis: association with hepatic lipase inhibition as well as altered cholesterol esterificationJAHN, C. E; SCHAEFER, E. J; TAAM, L. A et al.Gastroenterology (New York, NY. 1943). 1985, Vol 89, Num 6, pp 1266-1278, issn 0016-5085Article

Two genes that map to the STSL locus cause sitosterolemia: Genomic structure and spectrum of mutations involving sterolin-1 and sterolin-2, encoded by ABCG5 and ABCG8, respectivelyLU, Kangmo; LEE, Mi-Hye; BRUCKERT, Eric et al.American journal of human genetics. 2001, Vol 69, Num 2, pp 278-290, issn 0002-9297Article