-
1
-
-
1542361567
-
Assessing low levels of high-density lipoprotein cholesterol as a risk factor in coronary heart disease: a working group report and update
-
Gotto Jr. A.M., and Brinton E.A. Assessing low levels of high-density lipoprotein cholesterol as a risk factor in coronary heart disease: a working group report and update. J Am Coll Cardiol 43 (2004) 717-724
-
(2004)
J Am Coll Cardiol
, vol.43
, pp. 717-724
-
-
Gotto Jr., A.M.1
Brinton, E.A.2
-
2
-
-
0030480126
-
Apolipoprotein-mediated removal of cellular cholesterol and phospholipids
-
Oram J.F., and Yokoyama S. Apolipoprotein-mediated removal of cellular cholesterol and phospholipids. J Lipid Res 37 (1996) 2473-2491
-
(1996)
J Lipid Res
, vol.37
, pp. 2473-2491
-
-
Oram, J.F.1
Yokoyama, S.2
-
3
-
-
0033860421
-
How high-density lipoprotein protects against the effects of lipid peroxidation
-
Mackness M.I., Durrington P.N., and Mackness B. How high-density lipoprotein protects against the effects of lipid peroxidation. Curr Opin Lipidol 11 (2000) 383-388
-
(2000)
Curr Opin Lipidol
, vol.11
, pp. 383-388
-
-
Mackness, M.I.1
Durrington, P.N.2
Mackness, B.3
-
4
-
-
0032813808
-
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
-
Brooks-Wilson A., Marcil M., Clee S.M., et al. Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat Genet 22 (1999) 336-345
-
(1999)
Nat Genet
, vol.22
, pp. 336-345
-
-
Brooks-Wilson, A.1
Marcil, M.2
Clee, S.M.3
-
5
-
-
0030933460
-
The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes
-
Kuivenhoven J.A., Pritchard H., Hill J., Frohlich J., Assmann G., and Kastelein J. The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes. J Lipid Res 38 (1997) 191-205
-
(1997)
J Lipid Res
, vol.38
, pp. 191-205
-
-
Kuivenhoven, J.A.1
Pritchard, H.2
Hill, J.3
Frohlich, J.4
Assmann, G.5
Kastelein, J.6
-
6
-
-
0036234218
-
The effects of altered apolipoprotein A-I structure on plasma HDL concentration
-
Sorci-Thomas M.G., and Thomas M.J. The effects of altered apolipoprotein A-I structure on plasma HDL concentration. Trends Cardiovasc Med 12 (2002) 121-128
-
(2002)
Trends Cardiovasc Med
, vol.12
, pp. 121-128
-
-
Sorci-Thomas, M.G.1
Thomas, M.J.2
-
7
-
-
33645422718
-
Role of apoA-I, ABCA1, LCAT, and SR-BI in the biogenesis of HDL
-
Zannis V.I., Chroni A., and Krieger M. Role of apoA-I, ABCA1, LCAT, and SR-BI in the biogenesis of HDL. J Mol Med 84 (2006) 276-294
-
(2006)
J Mol Med
, vol.84
, pp. 276-294
-
-
Zannis, V.I.1
Chroni, A.2
Krieger, M.3
-
8
-
-
0033920731
-
Apolipoprotein A-I: structure-function relationships
-
Frank P.G., and Marcel Y.L. Apolipoprotein A-I: structure-function relationships. J Lipid Res 41 (2000) 853-872
-
(2000)
J Lipid Res
, vol.41
, pp. 853-872
-
-
Frank, P.G.1
Marcel, Y.L.2
-
9
-
-
38949162597
-
Characterization of high density lipoprotein particles in familial apolipoprotein A-I deficiency
-
Santos R.D., Schaefer E.J., Asztalos B.F., et al. Characterization of high density lipoprotein particles in familial apolipoprotein A-I deficiency. J Lipid Res 49 (2008) 349-357
-
(2008)
J Lipid Res
, vol.49
, pp. 349-357
-
-
Santos, R.D.1
Schaefer, E.J.2
Asztalos, B.F.3
-
10
-
-
33646433424
-
Differential diagnosis of familial high density lipoprotein deficiency syndromes
-
von Eckardstein A. Differential diagnosis of familial high density lipoprotein deficiency syndromes. Atherosclerosis 186 (2006) 231-239
-
(2006)
Atherosclerosis
, vol.186
, pp. 231-239
-
-
von Eckardstein, A.1
-
11
-
-
33947151023
-
Role of LCAT in HDL remodeling: investigation of LCAT deficiency states
-
Asztalos B.F., Schaefer E.J., Horvath K.V., et al. Role of LCAT in HDL remodeling: investigation of LCAT deficiency states. J Lipid Res 48 (2007) 592-599
-
(2007)
J Lipid Res
, vol.48
, pp. 592-599
-
-
Asztalos, B.F.1
Schaefer, E.J.2
Horvath, K.V.3
-
12
-
-
1242285439
-
Cross-linking and lipid efflux properties of apoA-I mutants suggest direct association between apoA-I helices and ABCA1
-
Chroni A., Liu T., Fitzgerald M.L., Freeman M.W., and Zannis V.I. Cross-linking and lipid efflux properties of apoA-I mutants suggest direct association between apoA-I helices and ABCA1. Biochemistry 43 (2004) 2126-2139
-
(2004)
Biochemistry
, vol.43
, pp. 2126-2139
-
-
Chroni, A.1
Liu, T.2
Fitzgerald, M.L.3
Freeman, M.W.4
Zannis, V.I.5
-
13
-
-
0037470173
-
The central helices of ApoA-I can promote ATP-binding cassette transporter A1 (ABCA1)-mediated lipid efflux. Amino acid residues 220-231 of the wild-type ApoA-I are required for lipid efflux in vitro and high density lipoprotein formation in vivo
-
Chroni A., Liu T., Gorshkova I., et al. The central helices of ApoA-I can promote ATP-binding cassette transporter A1 (ABCA1)-mediated lipid efflux. Amino acid residues 220-231 of the wild-type ApoA-I are required for lipid efflux in vitro and high density lipoprotein formation in vivo. J Biol Chem 278 (2003) 6719-6730
-
(2003)
J Biol Chem
, vol.278
, pp. 6719-6730
-
-
Chroni, A.1
Liu, T.2
Gorshkova, I.3
-
14
-
-
0034693064
-
Specific binding of ApoA-I, enhanced cholesterol efflux, and altered plasma membrane morphology in cells expressing ABC1
-
Wang N., Silver D.L., Costet P., and Tall A.R. Specific binding of ApoA-I, enhanced cholesterol efflux, and altered plasma membrane morphology in cells expressing ABC1. J Biol Chem 275 (2000) 33053-33058
-
(2000)
J Biol Chem
, vol.275
, pp. 33053-33058
-
-
Wang, N.1
Silver, D.L.2
Costet, P.3
Tall, A.R.4
-
15
-
-
30944435268
-
A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians
-
Dastani Z., Dangoisse C., Boucher B., et al. A novel nonsense apolipoprotein A-I mutation (apoA-I(E136X)) causes low HDL cholesterol in French Canadians. Atherosclerosis 185 (2006) 127-136
-
(2006)
Atherosclerosis
, vol.185
, pp. 127-136
-
-
Dastani, Z.1
Dangoisse, C.2
Boucher, B.3
-
16
-
-
9144250425
-
A novel two nucleotide deletion in the apolipoprotein A-I gene, apoA-I Shinbashi, associated with high density lipoprotein deficiency, corneal opacities, planar xanthomas, and premature coronary artery disease
-
Ikewaki K., Matsunaga A., Han H., et al. A novel two nucleotide deletion in the apolipoprotein A-I gene, apoA-I Shinbashi, associated with high density lipoprotein deficiency, corneal opacities, planar xanthomas, and premature coronary artery disease. Atherosclerosis 172 (2004) 39-45
-
(2004)
Atherosclerosis
, vol.172
, pp. 39-45
-
-
Ikewaki, K.1
Matsunaga, A.2
Han, H.3
|