N. Duverger

发表

Apolipoprotein specificity for lipid efflux by the human ABCAI transporter.

H. Brewer, A. Remaley, T. Eggerman, 2001, Biochemical and biophysical research communications.

Distribution of subclasses of HDL containing apoA-I without apoA-II (LpA-I) in normolipidemic men and women.

H. Brewer, D. Rader, N. Duverger, 1994, Arteriosclerosis and thrombosis : a journal of vascular biology.

Cholesterol efflux from human monocyte-derived macrophages in the presence of LpA-I:A-II.

S. Skarlatos, H. Kruth, D. Rader, 1995, Biochimica et biophysica acta.

Biochemical characterization of the three major subclasses of lipoprotein A-I preparatively isolated from human plasma.

P. Duchateau, D. Rader, H. Brewer, 1993, Biochemistry.

Characterization of high-density apolipoprotein particles A-I and A-I:A-II isolated from humans with cholesteryl ester transfer protein deficiency.

D. Rader, H. Brewer, T. Ishikawa, 1995, European journal of biochemistry.

Markedly accelerated catabolism of apolipoprotein A-II (ApoA-II) and high density lipoproteins containing ApoA-II in classic lecithin: cholesterol acyltransferase deficiency and fish-eye disease.

D. Rader, J. Frohlich, M. Clerc, 1994, The Journal of clinical investigation.

Role of the hepatic ABCA1 transporter in modulating intrahepatic cholesterol and plasma HDL cholesterol concentrations Published, JLR Papers in Press, November 4, 2002. DOI 10.1194/jlr.M200414-JLR200

H. Brewer, A. Remaley, T. Tansey, 2003, Journal of Lipid Research.

In Vitro Expression of Structural Defects in the Lecithin-Cholesterol Acyltransferase Gene (*)

H. Klein, H. Brewer, S. Marcovina, 1995, The Journal of Biological Chemistry.

Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis.

H. Klein, H. Brewer, S. Marcovina, 1993, The Journal of clinical investigation.

Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83-->stop) and LCAT (tyr156-->asn).

D. Rader, H. Klein, H. Brewer, 1993, Journal of lipid research.

Very low high-density lipoproteins without coronary atherosclerosis

I. Feuerstein, W. Connor, L. Zech, 1993, The Lancet.

Human ATP-binding cassette transporter 1 (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred.

P. Denéfle, H. Brewer, M. Dinger, 1999, Proceedings of the National Academy of Sciences of the United States of America.

Complete genomic sequence of the human ABCA1 gene: analysis of the human and mouse ATP-binding cassette A promoter.

J. Cheng, E. Rubin, P. Denéfle, 2000, Proceedings of the National Academy of Sciences of the United States of America.