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

The American journal of cardiology, 2004-01, Vol.93 (2), p.159-164

2004

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

Nature genetics, 1999-08, Vol.22 (4), p.336-345

1999

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

The Journal of biological chemistry, 2004-03, Vol.279 (11), p.9963-9969

2004

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

The Journal of biological chemistry, 2004-02, Vol.279 (9), p.7384-7394

2004

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

The Journal of clinical investigation, 2000-11, Vol.106 (10), p.1263-1270

2000

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cAMP induces ABCA1 phosphorylation activity and promotes cholesterol efflux from fibroblasts

Journal of lipid research, 2002-12, Vol.43 (12), p.2087-2094

2002

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Biogenesis and speciation of nascent apoA-I-containing particles in various cell lines

Journal of lipid research, 2005-08, Vol.46 (8), p.1668-1677

2005

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Increased sphingomyelin content impairs HDL biogenesis and maturation in human Niemann-Pick disease type B

Journal of lipid research, 2006-03, Vol.47 (3), p.622-632

2006

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

Journal of lipid research, 2003-05, Vol.44 (5), p.884-892

2003

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

Current atherosclerosis reports, 2009-09, Vol.11 (5), p.329-333

2009

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

European journal of human genetics : EJHG, 2010-03, Vol.18 (3), p.342-347

2010

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Cellular phospholipid and cholesterol efflux in high-density lipoprotein deficiency

Circulation (New York, N.Y.), 2003-03, Vol.107 (10), p.1366-1371

2003

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Evidence that hepatic lipase deficiency in humans is not associated with proatherogenic changes in HDL composition and metabolism

Journal of lipid research, 2004-08, Vol.45 (8), p.1528-1537

2004

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

Atherosclerosis, 2000-10, Vol.152 (2), p.457-468

2000

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

Canadian journal of cardiology, 2007-12, Vol.23 (14), p.1159-1161

2007

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

BMC medical genetics, 2007-12, Vol.8 (1), p.79-79, Article 79

2007

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Characterization of Oligomeric Human ATP Binding Cassette Transporter A1

The Journal of biological chemistry, 2004-10, Vol.279 (40), p.41529-41536

2004

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

Journal of lipid research, 2001-02, Vol.42 (2), p.249-257

2001

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New insights into the biogenesis of human high-density lipoproteins

Current opinion in lipidology, 2006-06, Vol.17 (3), p.258-267

2006

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Molecular interactions between apoE and ABCA1

Journal of lipid research, 2004-05, Vol.45 (5), p.839-848

2004

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Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol

Journal of lipid research, 2002-11, Vol.43 (11), p.1939-1949

2002

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Molecular interactions between apoE and ABCA1: impact on apoE lipidation

Journal of lipid research, 2004-05, Vol.45 (5), p.839-848

2004

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Characterization of oligomeric human ATP binding cassette transporter A1. Potential implications for determining the structure of nascent high density lipoprotein particles

The Journal of biological chemistry, 2004-10, Vol.279 (40), p.41529-41536

2004

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Identification of a novel human cellular HDL biosynthesis defect

European heart journal, 2009-09, Vol.30 (18), p.2204-2212

2009

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

The Journal of clinical investigation, 2000-11, Vol.106 (10), p.1263-1270

2000

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

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

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

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

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

cAMP induces ABCA1 phosphorylation activity and promotes cholesterol efflux from fibroblasts

Biogenesis and speciation of nascent apoA-I-containing particles in various cell lines

Increased sphingomyelin content impairs HDL biogenesis and maturation in human Niemann-Pick disease type B

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

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

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

Cellular phospholipid and cholesterol efflux in high-density lipoprotein deficiency

Evidence that hepatic lipase deficiency in humans is not associated with proatherogenic changes in HDL composition and metabolism

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

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

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

Characterization of Oligomeric Human ATP Binding Cassette Transporter A1

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

New insights into the biogenesis of human high-density lipoproteins

Molecular interactions between apoE and ABCA1

Truncation mutations in ABCA1 suppress normal upregulation of full-length ABCA1 by 9-cis-retinoic acid and 22-R-hydroxycholesterol

Molecular interactions between apoE and ABCA1: impact on apoE lipidation

Characterization of oligomeric human ATP binding cassette transporter A1. Potential implications for determining the structure of nascent high density lipoprotein particles

Identification of a novel human cellular HDL biosynthesis defect

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

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