-
1
-
-
0022549920
-
A receptor-mediated pathway for cholesterol homeostasis
-
Brown MS, Goldstein JL: A receptor-mediated pathway for cholesterol homeostasis. Science 1986; 232: 34-47
-
(1986)
Science
, vol.232
, pp. 34-47
-
-
Brown, M.S.1
Goldstein, J.L.2
-
2
-
-
0027515626
-
Cost-effectiveness considerations in the treatment of heterozygous familial hypercholesterolemia
-
Goldman L, Goldman PA, Williams LW et al: Cost-effectiveness considerations in the treatment of heterozygous familial hypercholesterolemia. Am J Cardiol 1993; 72: 75D-79D
-
(1993)
Am J Cardiol
, vol.72
-
-
Goldman, L.1
Goldman, P.A.2
Williams, L.W.3
-
3
-
-
0027153371
-
Cholesterol lowering and mortality: The importance of considering the initial level of risk
-
Davey-Smith G, Song F, Sheldon TA: Cholesterol lowering and mortality: the importance of considering the initial level of risk. BMJ 1993; 306: 1367-1373
-
(1993)
BMJ
, vol.306
, pp. 1367-1373
-
-
Davey-Smith, G.1
Song, F.2
Sheldon, T.A.3
-
4
-
-
0027241856
-
The pathogenesis of atherosclerosis: A perspective for the 1990's
-
Ross R: The pathogenesis of atherosclerosis: a perspective for the 1990's. Nature 1993; 362: 801-809
-
(1993)
Nature
, vol.362
, pp. 801-809
-
-
Ross, R.1
-
5
-
-
0028330005
-
Genetic susceptibility to death from coronary heart disease in a study of twins
-
Marenberg ME, Risch N, Berman LF et al: Genetic susceptibility to death from coronary heart disease in a study of twins. N Engl J Med 1994; 330: 1041-1046
-
(1994)
N Engl J Med
, vol.330
, pp. 1041-1046
-
-
Marenberg, M.E.1
Risch, N.2
Berman, L.F.3
-
6
-
-
0027380997
-
Familial hypercholesterolemia in French Canadians: Taking advantage of a "founder effect"
-
Davignon J, Roy M: Familial hypercholesterolemia in French Canadians: taking advantage of a "founder effect." Am J Cardiol 1993; 72: 6D-10D
-
(1993)
Am J Cardiol
, vol.72
-
-
Davignon, J.1
Roy, M.2
-
7
-
-
0028245754
-
Apolipoprotein E in hyperlipidemia
-
Walden CC, Hegele RA: Apolipoprotein E in hyperlipidemia. Ann Intern Med 1994; 120: 1026-1036
-
(1994)
Ann Intern Med
, vol.120
, pp. 1026-1036
-
-
Walden, C.C.1
Hegele, R.A.2
-
8
-
-
0000107028
-
Genetic markers for studies of atherosclerosis and related risk factors
-
Lusis AJ, Rotter JI, Sparkes RS (eds): Monograph in Human Genetics series, Karger, Basel, Switzerland
-
Mehrabian M, Lusis AJ: Genetic markers for studies of atherosclerosis and related risk factors. In Lusis AJ, Rotter JI, Sparkes RS (eds): Molecular Genetics of Coronary Artery Disease: Candidate Genes and Processes in Atherosclerosis, Monograph in Human Genetics series, Karger, Basel, Switzerland, 1992: 363-418
-
(1992)
Molecular Genetics of Coronary Artery Disease: Candidate Genes and Processes in Atherosclerosis
, pp. 363-418
-
-
Mehrabian, M.1
Lusis, A.J.2
-
9
-
-
0343473644
-
Alternative genetic strategies for predicting risk of atherosclerosis
-
Sing CF, Haviland MB, Templeton AR et al: Alternative genetic strategies for predicting risk of atherosclerosis. Atherosclerosis 1994; 109: 333
-
(1994)
Atherosclerosis
, vol.109
, pp. 333
-
-
Sing, C.F.1
Haviland, M.B.2
Templeton, A.R.3
-
10
-
-
0027322448
-
Lipid lowering and plaque regression
-
Brown GB, Zhao X-Q, Sacco D et al: Lipid lowering and plaque regression. Circulation 1993; 87: 1781-1791
-
(1993)
Circulation
, vol.87
, pp. 1781-1791
-
-
Brown, G.B.1
Zhao, X.-Q.2
Sacco, D.3
-
11
-
-
0027987849
-
Randomized trial of cholesterol lowering in 4444 patients with coronary heart disease: The Scandinavian Simvastatin Survival study
-
Simvastatin Survival Study Group: Randomized trial of cholesterol lowering in 4444 patients with coronary heart disease: the Scandinavian Simvastatin Survival study. Lancet 1994; 344: 1383-1389
-
(1994)
Lancet
, vol.344
, pp. 1383-1389
-
-
-
12
-
-
0042166678
-
Patterns of atherosclerosis and rates of progression
-
DeBakey ME: Patterns of atherosclerosis and rates of progression. Atherosclerosis 1978; 3: 1-56
-
(1978)
Atherosclerosis
, vol.3
, pp. 1-56
-
-
Debakey, M.E.1
-
13
-
-
0012352178
-
Changes in the cells of atherosclerotic lesions as advanced lesions evolve in coronary arteries of children and young adults
-
Glagov S, Newman WP, Schaffer SA (eds): Springer, New York
-
Stary HC: Changes in the cells of atherosclerotic lesions as advanced lesions evolve in coronary arteries of children and young adults. In Glagov S, Newman WP, Schaffer SA (eds): Pathobiology of the Human Atherosclerotic Plaque, Springer, New York, 1990: 93-106
-
(1990)
Pathobiology of the Human Atherosclerotic Plaque
, pp. 93-106
-
-
Stary, H.C.1
-
14
-
-
0024496082
-
Clinical application of deoxyribonucleic acid markers in a Utah family with hypercholesterolemia
-
Hegele RA, Emi M, Wu LL et al: Clinical application of deoxyribonucleic acid markers in a Utah family with hypercholesterolemia. Am J Cardiol 1989; 63: 109-112
-
(1989)
Am J Cardiol
, vol.63
, pp. 109-112
-
-
Hegele, R.A.1
Emi, M.2
Wu, L.L.3
-
15
-
-
0025845115
-
Normal plasma cholesterol in an 88-year-old man who eats 25 eggs a day
-
Kern F Jr: Normal plasma cholesterol in an 88-year-old man who eats 25 eggs a day. N Engl J Med 1991; 324: 896-899
-
(1991)
N Engl J Med
, vol.324
, pp. 896-899
-
-
Kern Jr., F.1
-
16
-
-
0028090414
-
Genetic dissection of complex traits
-
Lander ES, Schork NJ: Genetic dissection of complex traits. Science 1994; 265: 2037-2048
-
(1994)
Science
, vol.265
, pp. 2037-2048
-
-
Lander, E.S.1
Schork, N.J.2
-
17
-
-
0021148795
-
Immunohistochemical localization of apoprotein B in aortas from hyperlipemic swine: Preferential accumulation in lesion-prone areas
-
Feldman DL, Hoff H, Gerrity RG: Immunohistochemical localization of apoprotein B in aortas from hyperlipemic swine: preferential accumulation in lesion-prone areas. Arch Pathol Lab Med 1984; 108: 817-822
-
(1984)
Arch Pathol Lab Med
, vol.108
, pp. 817-822
-
-
Feldman, D.L.1
Hoff, H.2
Gerrity, R.G.3
-
18
-
-
0019491124
-
The role of the monocyte in atherogenesis. 1. Transition of blood-borne monocytes into foam cells in fatty lesions
-
Gerrity RG: The role of the monocyte in atherogenesis. 1. Transition of blood-borne monocytes into foam cells in fatty lesions. Am J Pathol 1981; 103: 181-190
-
(1981)
Am J Pathol
, vol.103
, pp. 181-190
-
-
Gerrity, R.G.1
-
19
-
-
0024603895
-
Beyond cholesterol: Modifications of low-density lipoproteins that increase its atherogenicity
-
Steinberg D, Parasarathy S, Carew TE et al: Beyond cholesterol: modifications of low-density lipoproteins that increase its atherogenicity. N Engl J Med 1989; 320: 915-924
-
(1989)
N Engl J Med
, vol.320
, pp. 915-924
-
-
Steinberg, D.1
Parasarathy, S.2
Carew, T.E.3
-
20
-
-
0002906795
-
Adhesive interactions of the blood cells and the vascular wall
-
Colman RW, Hirsch J, Marder VJ (eds): JB Lippincott, Philadelphia
-
Hawiger J: Adhesive interactions of the blood cells and the vascular wall. In Colman RW, Hirsch J, Marder VJ (eds): Hemostasis and Thrombosis: Basic Principles and Clinical Practice, JB Lippincott, Philadelphia, 1994: 762-796
-
(1994)
Hemostasis and Thrombosis: Basic Principles and Clinical Practice
, pp. 762-796
-
-
Hawiger, J.1
-
21
-
-
0002996869
-
Plaque ruptures, their genesis and their role in supraplaque thrombosis and atherogenesis
-
Glagov S, Newman WP, Schaffer SA (eds): Springer, New York
-
Constantinides P: Plaque ruptures, their genesis and their role in supraplaque thrombosis and atherogenesis. In Glagov S, Newman WP, Schaffer SA (eds): Pathobiology of the Human Atherosclerotic Plaque, Springer, New York, 1990: 393-411
-
(1990)
Pathobiology of the Human Atherosclerotic Plaque
, pp. 393-411
-
-
Constantinides, P.1
-
22
-
-
0001474759
-
Familial disorders of high density lipoprotein metabolism
-
Scriver CR, Beardet al, Sly WS et al (eds): McGraw Hill, New York
-
Breslow JL: Familial disorders of high density lipoprotein metabolism. In Scriver CR, Beardet al, Sly WS et al (eds): The Metabolic Basis of Inherited Diseases, McGraw Hill, New York, 1989: 1251-1266
-
(1989)
The Metabolic Basis of Inherited Diseases
, pp. 1251-1266
-
-
Breslow, J.L.1
-
23
-
-
0002744944
-
Familial high density lipoprotein deficiency: Tangier disease
-
Scriver CR, Beaudet al, Sly WS et al (eds): McGraw Hill, New York
-
Assmann G, Schmitz G, Brewer HB Jr: Familial high density lipoprotein deficiency: Tangier disease. In Scriver CR, Beaudet al, Sly WS et al (eds): The Metabolic Basis of Inherited Diseases, McGraw Hill, New York, 1989: 1267-1282
-
(1989)
The Metabolic Basis of Inherited Diseases
, pp. 1267-1282
-
-
Assmann, G.1
Schmitz, G.2
Brewer Jr., H.B.3
-
24
-
-
0029046821
-
The lowdown on lipoprotein lipase
-
Funke H, Assmann G: The lowdown on lipoprotein lipase. Nat Genet 1995; 10: 6-7
-
(1995)
Nat Genet
, vol.10
, pp. 6-7
-
-
Funke, H.1
Assmann, G.2
-
25
-
-
0025941724
-
Cholesterol transport between cells and high density lipoproteins
-
Johnson WJ, Mahlberg FH, Rothblat GH et al: Cholesterol transport between cells and high density lipoproteins. Biochim Biophys Acta 1991; 1085: 273-298
-
(1991)
Biochim Biophys Acta
, vol.1085
, pp. 273-298
-
-
Johnson, W.J.1
Mahlberg, F.H.2
Rothblat, G.H.3
-
26
-
-
0025902231
-
Inhibition of early atherogenesis in transgenic mice by human apolipoprotein A-I
-
Rubin EM, Krauss RM, Spangler EA et al: Inhibition of early atherogenesis in transgenic mice by human apolipoprotein A-I. Nature 1991; 353: 265-267
-
(1991)
Nature
, vol.353
, pp. 265-267
-
-
Rubin, E.M.1
Krauss, R.M.2
Spangler, E.A.3
-
27
-
-
0028280609
-
The properties of HDL in genetically engineered mice
-
Schultz JR, Rubin EM: The properties of HDL in genetically engineered mice. Curr Opin Lipidol 1994; 5: 126-137
-
(1994)
Curr Opin Lipidol
, vol.5
, pp. 126-137
-
-
Schultz, J.R.1
Rubin, E.M.2
-
28
-
-
0027330901
-
Lack of apo A-I is not associated with increased susceptibility to atherosclerosis in mice
-
Li H, Reddick RL, Maeda N: Lack of apo A-I is not associated with increased susceptibility to atherosclerosis in mice. Arterioscler Thromb 1993; 13: 1814-1821
-
(1993)
Arterioscler Thromb
, vol.13
, pp. 1814-1821
-
-
Li, H.1
Reddick, R.L.2
Maeda, N.3
-
29
-
-
0344189687
-
DNA within the apolipoprotein A-I/C-III/A-IV-encoding gene cluster of certain patients with atherosclerosis
-
Karathanasis SK, Ferris E, Haddad IA: DNA within the apolipoprotein A-I/C-III/A-IV-encoding gene cluster of certain patients with atherosclerosis. Proc Natl Acad Sci USA 1987; 84: 7198-7202
-
(1987)
Proc Natl Acad Sci USA
, vol.84
, pp. 7198-7202
-
-
Karathanasis, S.K.1
Ferris, E.2
Haddad, I.A.3
-
30
-
-
0026101257
-
A frameshift mutation in the human apo A-I gene causes high density lipoprotein deficiency, partial lecithin:cholesterol acyl transferase deficiency and corneal opacities
-
Funke H, von Eckardstein A, Pritchard PH et al: A frameshift mutation in the human apo A-I gene causes high density lipoprotein deficiency, partial lecithin:cholesterol acyl transferase deficiency and corneal opacities. J Clin Invest 1991; 87: 371-376
-
(1991)
J Clin Invest
, vol.87
, pp. 371-376
-
-
Funke, H.1
Von Eckardstein, A.2
Pritchard, P.H.3
-
31
-
-
0027429343
-
High density lipoprotein deficiency with xanthomas: A defect in reverse cholesterol transport caused by a point mutation in the apolipoprotein A-I gene
-
Lackner KJ, Dieplinger H, Nowicka G et al: High density lipoprotein deficiency with xanthomas: a defect in reverse cholesterol transport caused by a point mutation in the apolipoprotein A-I gene. J Clin Invest 1993; 92: 2262-2273
-
(1993)
J Clin Invest
, vol.92
, pp. 2262-2273
-
-
Lackner, K.J.1
Dieplinger, H.2
Nowicka, G.3
-
32
-
-
0028170617
-
A nonsense mutation in the apolipoprotein A-I gene is associated with high-density lipoprotein deficiency and periorbital xanthelasmas
-
Romling R, von Eckardstein A, Funke H et al: A nonsense mutation in the apolipoprotein A-I gene is associated with high-density lipoprotein deficiency and periorbital xanthelasmas. Arterioscler Thromb 1994; 14: 1915-1922
-
(1994)
Arterioscler Thromb
, vol.14
, pp. 1915-1922
-
-
Romling, R.1
Von Eckardstein, A.2
Funke, H.3
-
33
-
-
0028157828
-
Apolipoprotein A-I Q[-2]X causing isolated apolipoprotein A-I deficiency in a family with analphalipoproteinemia
-
Ng DS, Leiter LA, Vezina C et al: Apolipoprotein A-I Q[-2]X causing isolated apolipoprotein A-I deficiency in a family with analphalipoproteinemia. J Clin Invest 1994; 93: 223-229
-
(1994)
J Clin Invest
, vol.93
, pp. 223-229
-
-
Ng, D.S.1
Leiter, L.A.2
Vezina, C.3
-
34
-
-
0027377974
-
Psychological and ethical considerations in screening for disease
-
Quaid KA: Psychological and ethical considerations in screening for disease. Am J Cardiol 1993; 72: 64D-67D
-
(1993)
Am J Cardiol
, vol.72
-
-
Quaid, K.A.1
-
35
-
-
0025773298
-
Interaction between variant apolipoproteins C-II and E that affects plasma lipoprotein concentrations
-
Hegele RA, Breckenridge WC, Cox DW et al: Interaction between variant apolipoproteins C-II and E that affects plasma lipoprotein concentrations. Arterioscler Thromb 1991; 11: 1303-1309
-
(1991)
Arterioscler Thromb
, vol.11
, pp. 1303-1309
-
-
Hegele, R.A.1
Breckenridge, W.C.2
Cox, D.W.3
-
36
-
-
0025864444
-
Effects of three genetic loci in a family with multiple lipoprotein phenotypes
-
Emi M, Hegele RA, Hopkins PN et al: Effects of three genetic loci in a family with multiple lipoprotein phenotypes. Arterioscler Thromb 1991; 11: 1303-1309
-
(1991)
Arterioscler Thromb
, vol.11
, pp. 1303-1309
-
-
Emi, M.1
Hegele, R.A.2
Hopkins, P.N.3
-
37
-
-
0028900876
-
A polymorphism of the paraoxonase gene associated with variation in plasma lipoproteins in a genetic isolate
-
Hegele RA, Brunt JH, Connelly PW: A polymorphism of the paraoxonase gene associated with variation in plasma lipoproteins in a genetic isolate. Arterioscler Thromb Vasc Biol 1995; 15: 89-95
-
(1995)
Arterioscler Thromb Vasc Biol
, vol.15
, pp. 89-95
-
-
Hegele, R.A.1
Brunt, J.H.2
Connelly, P.W.3
-
39
-
-
0028037134
-
Variation at the hepatic lipase and apolipoprotein AI/CIII/AIV loci is a major cause of genetically determined variation in plasma HDL cholesterol levels
-
Cohen JC, Wang Z, Grundy SM et al: Variation at the hepatic lipase and apolipoprotein AI/CIII/AIV loci is a major cause of genetically determined variation in plasma HDL cholesterol levels. J Clin Invest 1994; 94: 2377-2384
-
(1994)
J Clin Invest
, vol.94
, pp. 2377-2384
-
-
Cohen, J.C.1
Wang, Z.2
Grundy, S.M.3
-
40
-
-
0027162816
-
Hepatic lipase deficiency: Clinical, biochemical and molecular genetic characteristics
-
Hegele RA, Little JA, Vezina C et al: Hepatic lipase deficiency: clinical, biochemical and molecular genetic characteristics. Arterioscler Thromb 1993; 13: 720-728
-
(1993)
Arterioscler Thromb
, vol.13
, pp. 720-728
-
-
Hegele, R.A.1
Little, J.A.2
Vezina, C.3
-
41
-
-
0027447964
-
The role of genome type-environment interaction and time in understanding the impact of genetic polymorphism on lipid metabolism
-
Zerba KE, Sing CF: The role of genome type-environment interaction and time in understanding the impact of genetic polymorphism on lipid metabolism. Curr Opin Lipidol 1993; 4: 152-162
-
(1993)
Curr Opin Lipidol
, vol.4
, pp. 152-162
-
-
Zerba, K.E.1
Sing, C.F.2
-
42
-
-
0000639606
-
From complexity to perplexity
-
Horgan J: From complexity to perplexity. Sci Am 1995; 272: 104-109
-
(1995)
Sci Am
, vol.272
, pp. 104-109
-
-
Horgan, J.1
|