M. Marcil

发表

Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency

C. Sensen, S. Scherer, M. Hayden, 1999, Nature Genetics.

Evidence that hepatic lipase deficiency in humans is not associated with proatherogenic changes in HDL composition and metabolism Published, JLR Papers in Press, June 1, 2004. DOI 10.1194/jlr.M400090-JLR200

B. Lamarche, P. Couture, M. Marcil, 2004, Journal of Lipid Research.

Cellular cholesterol efflux is modulated by phospholipid-derived signaling molecules in familial HDL deficiency/Tangier disease fibroblasts.

J. Genest, M. Marcil, S. Mott, 2001, Journal of lipid research.

High-density lipoproteins: multifunctional vanguards of the cardiovascular system

M. Marcil, L. Krimbou, Brian O'Connell, 2004, Expert review of cardiovascular therapy.

UvA-DARE (Digital Academic Repository) Age and residuel cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes

A. Brooks-Wilson, K. Roomp, T. Suda, 2016 .

Age and residuel cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA 1 heterozygotes

M. Hayden, A. Brooks-Wilson, J. Kastelein, 2000 .

Metabolic factors clustering, lipoprotein cholesterol, apolipoprotein B, lipoprotein (a) and apolipoprotein E phenotypes in premature coronary artery disease in French Canadians.

J. Genest, Y. Latour, P. Connelly, 1997, The Canadian journal of cardiology.

Effect of Fenofibrate on Plasma Lipoprotein Composition and Kinetics in Patients With Complete Hepatic Lipase Deficiency

B. Lamarche, P. Couture, M. Marcil, 2005, Arteriosclerosis, thrombosis, and vascular biology.

Vascular Calcifications in Homozygote Familial Hypercholesterolemia

G. Francis, R. Hegele, R. McPherson, 2008, Arteriosclerosis, thrombosis, and vascular biology.

Cellular cholesterol transport and efflux in fibroblasts are abnormal in subjects with familial HDL deficiency.

J. Genest, J. Oram, M. Marcil, 1999, Arteriosclerosis, thrombosis, and vascular biology.

Conservation of RET proto-oncogene splicing variants and implications for RET isoform function

L. Mulligan, M. Marcil, J. Vanhorne, 2002, Cytogenetic and Genome Research.

High density lipoproteins in health and in disease.

J. Genest, M. Marcil, M. Denis, 1999, Journal of investigative medicine : the official publication of the American Federation for Clinical Research.

Insulin Resistance Syndrome, and Coronary Artery Disease in Men and Women

L. Campeau, B. Gilfix, M. Marcil, 1995 .

New insights into the biogenesis of human high-density lipoproteins

J. Genest, M. Marcil, L. Krimbou, 2006, Current opinion in lipidology.

Surgical strategies for severe calcification of the aorta (porcelain aorta) in two patients with homozygous familial hypercholesterolemia.

K. Lachapelle, A. Omeroglu, J. Genest, 2007, The Canadian journal of cardiology.

Structural and functional properties of human plasma high density-sized lipoprotein containing only apoE particles Published, JLR Papers in Press, March 1, 2003. DOI 10.1194/jlr.M200273-JLR200

J. Genest, H. Chiba, M. Marcil, 2003, Journal of Lipid Research.

Interaction of lecithin:cholesterol acyltransferase (LCAT).alpha 2-macroglobulin complex with low density lipoprotein receptor-related protein (LRP). Evidence for an alpha 2-macroglobulin/LRP receptor-mediated system participating in LCAT clearance.

J. Genest, J. Davignon, M. Marcil, 2001, The Journal of biological chemistry.

Structural and functional properties of human plasma high density-sized lipoprotein containing only apoE particles

J. Genest, H. Chiba, M. Marcil, 2003 .

Biogenesis and speciation of nascent apoA-I-containing particles in various cell lines Published, JLR Papers in Press, May 16, 2005. DOI 10.1194/jlr.M500038-JLR200

J. Genest, M. Marcil, M. Denis, 2005, Journal of Lipid Research.

Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol Published, JLR Papers in Press, August 16, 2002. DOI 10.1194/jlr.M200277-JLR200

A. Brownlie, M. Hayden, J. Kastelein, 2002, Journal of Lipid Research.

Mutations in the ABC 1 gene in familial HDL deficiency with defective cholesterol efflux

C. Sensen, M. Hayden, A. Brooks-Wilson, 1999, The Lancet.

Cellular cholesterol homeostasis in vascular endothelial cells.

J. Genest, M. Marcil, M. Denis, 2006, The Canadian journal of cardiology.

Molecular interactions between apoE and ABCA1: impact on apoE lipidation.

J. Genest, M. Marcil, M. Denis, 2004, Journal of lipid research.

Molecular and Cellular Physiology of Apolipoprotein A-I Lipidation by the ATP-binding Cassette Transporter A1 (ABCA1)*

M. Bouvier, J. Genest, M. Marcil, 2004, Journal of Biological Chemistry.

Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol

J. Genest, M. Marcil, C. Bernard, 2003, Human Genetics.

Lipoprotein (a) blood levels in unstable angina pectoris, acute myocardial infarction, and after thrombolytic therapy.

J. Genest, M. Marcil, D. Robitaille, 1991, The American journal of cardiology.

High-density lipoproteins: target for cardiovascular disease prevention

J. Genest, M. Marcil, Mohammad Y. Alenezi, 2004 .

Plasma endothelin-1 levels in stable and unstable angina.

P. Théroux, M. Marcil, B. Solymoss, 1993, Cardiology.

Intra‐operative Echographic Localization for Radioactive Ophthalmic Plaques in Choroidal Melanoma

G. Shenouda, C. Corriveau, M. Evans, 2008, Annals of the New York Academy of Sciences.

Risk factors of venous aortocoronary bypass graft disease noted at late symptom-directed angiographic study.

L. Campeau, M. Marcil, L. Pelletier, 1993, The Canadian journal of cardiology.

The place of ferritin among risk factors associated with coronary artery disease

L. Campeau, B. Gilfix, M. Marcil, 1994, Coronary artery disease.

Increased sphingomyelin content impairs HDL biogenesis and maturation in human Niemann-Pick disease type B Published, JLR Papers in Press, November 30, 2005.

A. Lesimple, O. Mamer, J. Genest, 2006, Journal of Lipid Research.

Incidence and clinical characteristics of the metabolic syndrome in patients with coronary artery disease

S. Lévesque, M. Bourassa, L. Campeau, 2003, Coronary artery disease.

Identification of a novel human cellular HDL biosynthesis defect.

J. Genest, M. Marcil, I. Ruel, 2009, European heart journal.

Genetics of high-density lipoproteins

J. Engert, Z. Dastani, J. Genest, 2006, Current opinion in cardiology.

Decreased cellular cholesterol efflux is a common cause of familial hypoalphalipoproteinemia: role of the ABCA1 gene mutations.

J. Genest, M. Marcil, Lu Yu, 2000, Atherosclerosis.

Functional mutations of the ABCA1 gene in subjects of French-Canadian descent with HDL deficiency.

J. Genest, M. Marcil, I. Ruel, 2006, Atherosclerosis.

Age and residual cholesterol efflux affect HDL cholesterol levels and coronary artery disease in ABCA1 heterozygotes.

M. Hayden, A. Brooks-Wilson, J. Kastelein, 2000, The Journal of clinical investigation.

cAMP induces ABCA1 phosphorylation activity and promotes cholesterol efflux from fibroblasts Published, JLR Papers in Press, August 16, 2002. DOI 10.1194/jlr.M200235-JLR200

J. Genest, M. Marcil, M. Denis, 2002, Journal of Lipid Research.

Iodine‐125 Radiotherapy for Choroidal Melanoma

G. Shenouda, C. Corriveau, M. Evans, 2008, Annals of the New York Academy of Sciences.

Lack of association of the apolipoprotein A-I-C-III-A-IV gene XmnI and SstI polymorphisms and of the lipoprotein lipase gene mutations in familial combined hyperlipoproteinemia in French Canadian subjects.

M. Hayden, J. Genest, J. Davignon, 1996, Journal of lipid research.

The therapeutic potential of high-density lipoprotein mimetic agents in coronary artery disease

J. Tardif, A. Nigam, P. Meyer, 2009, Current atherosclerosis reports.

Is the decreased high-density lipoprotein cholesterol in the metabolic syndrome due to cellular lipid efflux defect?

J. Genest, M. Marcil, D. Blank, 2004, The Journal of clinical endocrinology and metabolism.

WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels.

T. Lehtimäki, R. Cantor, M. Laakso, 2008, American journal of human genetics.

Disorders of high‐density lipoprotein biogenesis

I. Iatan, Z. Dastani, J. Genest, 2008 .

Identification of a Novel C5L2 Variant (S323I) in a French Canadian Family With Familial Combined Hyperlipemia

D. Gaudet, K. Cianflone, J. Engert, 2006, Arteriosclerosis, thrombosis, and vascular biology.

A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians.

P. Pajukanta, R. Hegele, J. Engert, 2006, Atherosclerosis.

Genetic lipoprotein disorders and coronary atherosclerosis

J. Genest, G. Thanassoulis, M. Marcil, 2005, Current atherosclerosis reports.

Cellular Phospholipid and Cholesterol Efflux in High-Density Lipoprotein Deficiency

J. Genest, M. Marcil, L. Krimbou, 2003, Circulation.

Severe familial HDL deficiency in French-Canadian kindreds. Clinical, biochemical, and molecular characterization.

J. Frohlich, J. Genest, J. Davignon, 1995, Arteriosclerosis, thrombosis, and vascular biology.

Fine mapping and association studies of a high-density lipoprotein cholesterol linkage region on chromosome 16 in French-Canadian subjects

Swneke D. Bailey, T. Hudson, J. Rioux, 2010, European Journal of Human Genetics.

Evidence for a Gene Influencing High-Density Lipoprotein Cholesterol on Chromosome 4q31.21

C. Plaisier, P. Pajukanta, J. Engert, 2005, Arteriosclerosis, thrombosis, and vascular biology.

Apolipoprotein A-I Activates Cellular cAMP Signaling through the ABCA1 Transporter*

J. Genest, M. Marcil, M. Denis, 2004, Journal of Biological Chemistry.

Effect of increasing metabolic syndrome score on atherosclerotic risk profile and coronary artery disease angiographic severity.

S. Lévesque, M. Bourassa, L. Campeau, 2004, The American journal of cardiology.

Characterization of Oligomeric Human ATP Binding Cassette Transporter A1

M. Bouvier, J. Genest, M. Marcil, 2004, Journal of Biological Chemistry.

Long-term rates of cardiovascular events in patients with the metabolic syndrome according to severity of coronary-angiographic alterations

S. Lévesque, M. Bourassa, L. Campeau, 2009, Coronary artery disease.

Relation of coronary artery disease in women < 60 years of age to the combined elevation of serum lipoprotein (a) and total cholesterol to high-density cholesterol ratio.

L. Campeau, B. Gilfix, M. Marcil, 1993, The American journal of cardiology.

Sphingomyelin phosphodiesterase-1 (SMPD1) coding variants do not contribute to low levels of high-density lipoprotein cholesterol

J. Engert, Z. Dastani, J. Genest, 2007, BMC Medical Genetics.

Interaction of Lecithin:Cholesterol Acyltransferase (LCAT)·α2-Macroglobulin Complex with Low Density Lipoprotein Receptor-related Protein (LRP)

M. Marcil, L. Krimbou, J. Davignon, 2001, The Journal of Biological Chemistry.

WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels.

T. Lehtimäki, R. Cantor, M. Laakso, 2008, American journal of human genetics.

Fasting hyperinsulinism, insulin resistance syndrome, and coronary artery disease in men and women.

L. Campeau, B. Gilfix, M. Marcil, 1995, The American journal of cardiology.