-
1
-
-
0026754815
-
Atherosclerosis of the aorta and coronary arteries and cardiovascular risk factors in persons aged 6 to 30 years and studied at necroscopy (the Bogulusa Heart study)
-
Berenson G.S., Wattigney W.A., Tracy R.E., et al. Atherosclerosis of the aorta and coronary arteries and cardiovascular risk factors in persons aged 6 to 30 years and studied at necroscopy (the Bogulusa Heart study). Am J Cardiol. 70:1992;851-858.
-
(1992)
Am J Cardiol
, vol.70
, pp. 851-858
-
-
Berenson, G.S.1
Wattigney, W.A.2
Tracy, R.E.3
-
2
-
-
0003142545
-
The natural history of coronary atherosclerosis
-
Strong J.P. The natural history of coronary atherosclerosis. Am J Pathol. 40:1962;37-49.
-
(1962)
Am J Pathol
, vol.40
, pp. 37-49
-
-
Strong, J.P.1
-
3
-
-
0027505992
-
Serum cholesterol in young men and subsequent cardiovascular disease
-
Klag M.J., Ford D.E., Mead L.A., et al. Serum cholesterol in young men and subsequent cardiovascular disease. N Engl J Med. 328:1993;313-318.
-
(1993)
N Engl J Med
, vol.328
, pp. 313-318
-
-
Klag, M.J.1
Ford, D.E.2
Mead, L.A.3
-
4
-
-
0018137532
-
Tracking of blood lipids and blood pressures in school age children: The Muscatine study
-
Clarke W.R. Tracking of blood lipids and blood pressures in school age children: the Muscatine study. Circulation. 58:1978;626-663.
-
(1978)
Circulation
, vol.58
, pp. 626-663
-
-
Clarke, W.R.1
-
5
-
-
0026571494
-
Highlights of the report of the expert panel on blood cholesterol levels in children and adolescents
-
National Cholesterol Education Program (NCEP)
-
National Cholesterol Education Program (NCEP). Highlights of the report of the expert panel on blood cholesterol levels in children and adolescents. Pediatrics 1992;89:495-501.
-
(1992)
Pediatrics
, vol.89
, pp. 495-501
-
-
-
7
-
-
0025374073
-
Prevalence and expression of familial combined hyperlipidemia in childhood
-
Cortner J.A., Coates P.M., Gallagher P.R. Prevalence and expression of familial combined hyperlipidemia in childhood. J Ped. 116:1990;514-524.
-
(1990)
J Ped
, vol.116
, pp. 514-524
-
-
Cortner, J.A.1
Coates, P.M.2
Gallagher, P.R.3
-
8
-
-
0035906980
-
The cholesterol quartet
-
Goldstein J.L., Brown M.S. The cholesterol quartet. Science. 292:2001;1310-1316.
-
(2001)
Science
, vol.292
, pp. 1310-1316
-
-
Goldstein, J.L.1
Brown, M.S.2
-
9
-
-
0025611016
-
Diagnosis and management of familial dyslipoproteinemia in children and adolescents
-
Kwiterovich P.O. Jr. Diagnosis and management of familial dyslipoproteinemia in children and adolescents. Pediatr Clin North Am. 37:1990;1489-1523.
-
(1990)
Pediatr Clin North Am
, vol.37
, pp. 1489-1523
-
-
Kwiterovich P.O., Jr.1
-
10
-
-
0027026881
-
Molecular genetics of the LDL receptor gene in familial hypercholesterolemia
-
Hobbs H.H., Brown M.S., Goldstein J.L. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia. Hum Mutat. 1:1992;445-466.
-
(1992)
Hum Mutat
, vol.1
, pp. 445-466
-
-
Hobbs, H.H.1
Brown, M.S.2
Goldstein, J.L.3
-
11
-
-
0032728972
-
Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemia
-
Norman D., Sun X., Bourbon, et al. Characterization of a novel cellular defect in patients with phenotypic homozygous familial hypercholesterolemia. J Clin Invest. 104:1999;619-628.
-
(1999)
J Clin Invest
, vol.104
, pp. 619-628
-
-
Norman, D.1
Sun, X.2
Bourbon3
-
12
-
-
0033012287
-
Characterization of a new form of inherited hypercholesterolemia: Familial recessive hypercholesterolemia
-
Zuliani G., Arca M., Signore A., et al. Characterization of a new form of inherited hypercholesterolemia: familial recessive hypercholesterolemia. Arterioscler Thromb Vasc Biol. 19:1999;802-809.
-
(1999)
Arterioscler Thromb Vasc Biol
, vol.19
, pp. 802-809
-
-
Zuliani, G.1
Arca, M.2
Signore, A.3
-
13
-
-
0035906961
-
Autsomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein
-
Garcia C.K., Wilund K., Arca M., et al. Autsomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein. Science. 292:2001;1394-1398.
-
(2001)
Science
, vol.292
, pp. 1394-1398
-
-
Garcia, C.K.1
Wilund, K.2
Arca, M.3
-
14
-
-
0037045847
-
Autosomal recessive hypercholesterolemia in Sardinia, Italy, and mutations in ARH: A clinical and molecular analysis
-
Arca M., Zuliani G., Wilund K., et al. Autosomal recessive hypercholesterolemia in Sardinia, Italy, and mutations in ARH: a clinical and molecular analysis. Lancet. 359:2002;841-847.
-
(2002)
Lancet
, vol.359
, pp. 841-847
-
-
Arca, M.1
Zuliani, G.2
Wilund, K.3
-
15
-
-
0023056989
-
Complete cDNA and derived protein sequence of human apolipoprotein B-100
-
Knott T.J., Wallis S.C., Powell L.M., et al. Complete cDNA and derived protein sequence of human apolipoprotein B-100. Nucleic Acids Res. 14:1986;7501-7503.
-
(1986)
Nucleic Acids Res
, vol.14
, pp. 7501-7503
-
-
Knott, T.J.1
Wallis, S.C.2
Powell, L.M.3
-
16
-
-
0024558892
-
Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100
-
Soria L.F., Ludwig E.H., Clarke H.R., et al. Association between a specific apolipoprotein B mutation and familial defective apolipoprotein B-100. Proc Natl Acad Sci USA. 86:1989;587-591.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 587-591
-
-
Soria, L.F.1
Ludwig, E.H.2
Clarke, H.R.3
-
17
-
-
0016366624
-
Beta-sitosterolemia and xanthomatosis. A newly described lipid storage disease in two sisters
-
Bhattacharyya A.K., Connor W.E. Beta-sitosterolemia and xanthomatosis. A newly described lipid storage disease in two sisters. J Clin Invest. 53:1974;1033-1043.
-
(1974)
J Clin Invest
, vol.53
, pp. 1033-1043
-
-
Bhattacharyya, A.K.1
Connor, W.E.2
-
18
-
-
0018841909
-
Phytosterolemia, xanthomatosis, and premature atherosclerotic arterial disease: A case with high plant sterol absorption, impaired sterol elimination and low cholesterol synthesis
-
Miettinen T.A. Phytosterolemia, xanthomatosis, and premature atherosclerotic arterial disease: a case with high plant sterol absorption, impaired sterol elimination and low cholesterol synthesis. Eur J Clin Invest. 10:1980;27-35.
-
(1980)
Eur J Clin Invest
, vol.10
, pp. 27-35
-
-
Miettinen, T.A.1
-
19
-
-
0019500525
-
Hyperapobetalipoproteinemia in two families with xanthomas and phytosterolemia
-
Kwiterovich P.O. Jr., Bachorik P.S., Smith H.H., et al. Hyperapobetalipoproteinemia in two families with xanthomas and phytosterolemia. Lancet. 1:1981;466-469.
-
(1981)
Lancet
, vol.1
, pp. 466-469
-
-
Kwiterovich P.O., Jr.1
Bachorik, P.S.2
Smith, H.H.3
-
20
-
-
0001003949
-
-
C.R. Scriver, A.L. Beaudet, W.S. Sly, & D. Valle. New York: McGraw-Hill. Chap. 65
-
Bjorkhem I., Boberg M. Scriver C.R., Beaudet A.L., Sly W.S., Valle D. The metabolic bases of inherited disease, vol. 2. 7th ed. 1995;2073 McGraw-Hill, New York. Chap. 65.
-
(1995)
The metabolic bases of inherited disease, vol. 2 7th ed.
, pp. 2073
-
-
Bjorkhem, I.1
Boberg, M.2
-
21
-
-
0018841909
-
Phytosterolemia, xanthomatosis, and premature atherosclerotic arterial disease: A case with high plant sterol absorption, impaired sterol elimination and low cholesterol synthesis
-
Miettinen T.A. Phytosterolemia, xanthomatosis, and premature atherosclerotic arterial disease: a case with high plant sterol absorption, impaired sterol elimination and low cholesterol synthesis. Eur J Clin Invest. 10:1980;27-35.
-
(1980)
Eur J Clin Invest
, vol.10
, pp. 27-35
-
-
Miettinen, T.A.1
-
22
-
-
0029112257
-
Sterol absorption and sterol balance in phytosterolemia evaluated by deuterium-labeled sterols: Effect of sitostanol treatment
-
Lutjohann D., Bjorkham I., Beil V.F., von Bergmann K. Sterol absorption and sterol balance in phytosterolemia evaluated by deuterium-labeled sterols: effect of sitostanol treatment. J Lipid Res. 36:1995;1763.
-
(1995)
J Lipid Res
, vol.36
, pp. 1763
-
-
Lutjohann, D.1
Bjorkham, I.2
Beil, V.F.3
Von Bergmann, K.4
-
23
-
-
17744390348
-
Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters
-
Berge K.E., Tian H., Graf G.A., et al. Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters. Science. 290:2000;1771-1775.
-
(2000)
Science
, vol.290
, pp. 1771-1775
-
-
Berge, K.E.1
Tian, H.2
Graf, G.A.3
-
24
-
-
0034915332
-
Two genes that map to the STSL locus cause sitosterolemia: Genomic structure and spectrum of mutations involving Sterolin-1 and Sterolin-2, encoded by ABCG5 and ABCG8, respectively
-
Lu K., Lee M.-H., Hazard S., et al. Two genes that map to the STSL locus cause sitosterolemia: genomic structure and spectrum of mutations involving Sterolin-1 and Sterolin-2, encoded by ABCG5 and ABCG8, respectively. Am J Hum Genet. 69:2001;278-290.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 278-290
-
-
Lu, K.1
Lee, M.-H.2
Hazard, S.3
-
25
-
-
0037166261
-
Regulation of ATP-binding cassette sterol transporters, ABCG5 and ABCG8, by the oxysterol receptors, LXR alpha and beta
-
Repa J.J., Berge K.E., Pomajzl C., Richardson J.A., Hobbs H., Mangelsdorf D.J. Regulation of ATP-binding cassette sterol transporters, ABCG5 and ABCG8, by the oxysterol receptors, LXR alpha and beta. J Biol Chem. 24:2002;18793-18800.
-
(2002)
J Biol Chem
, vol.24
, pp. 18793-18800
-
-
Repa, J.J.1
Berge, K.E.2
Pomajzl, C.3
Richardson, J.A.4
Hobbs, H.5
Mangelsdorf, D.J.6
-
26
-
-
0015796295
-
Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia
-
Goldstein J.L., Schrott H.G., Hazzard W.R., et al. Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia. J Clin Invest. 52:1973;1544-1568.
-
(1973)
J Clin Invest
, vol.52
, pp. 1544-1568
-
-
Goldstein, J.L.1
Schrott, H.G.2
Hazzard, W.R.3
-
27
-
-
0033860359
-
Insulin resistance and cardiovascular disease
-
Ginsberg H.N. Insulin resistance and cardiovascular disease. J Clin Invest. 106:2000;453-458.
-
(2000)
J Clin Invest
, vol.106
, pp. 453-458
-
-
Ginsberg, H.N.1
-
28
-
-
0028905440
-
LDL physical and chemical properties in familial combined hyperlipidemia
-
Hokanson J.E., Krauss R.M., Albers J.J., et al. LDL physical and chemical properties in familial combined hyperlipidemia. Arterioscler Thromb Vasc Biol. 15:1995;452-459.
-
(1995)
Arterioscler Thromb Vasc Biol
, vol.15
, pp. 452-459
-
-
Hokanson, J.E.1
Krauss, R.M.2
Albers, J.J.3
-
29
-
-
0023807047
-
Low-density lipoprotein patterns and risk of myocardial infarction
-
Austin M.A., Breslow J.L., Hennekens C.H., et al. Low-density lipoprotein patterns and risk of myocardial infarction. JAMA. 260:1998;1917-1921.
-
(1998)
JAMA
, vol.260
, pp. 1917-1921
-
-
Austin, M.A.1
Breslow, J.L.2
Hennekens, C.H.3
-
30
-
-
0024315637
-
Apolipoprotein, low density lipoprotein subfraction, and insulin associations with familial combined hyperlipidemia. Study of Utah patients with familial dyslipidemic hypertension
-
Hunt S.C., Wu L.L., Hopkins P.N., et al. Apolipoprotein, low density lipoprotein subfraction, and insulin associations with familial combined hyperlipidemia. Study of Utah patients with familial dyslipidemic hypertension. Arteriosclerosis. 9:1989;335-344.
-
(1989)
Arteriosclerosis
, vol.9
, pp. 335-344
-
-
Hunt, S.C.1
Wu, L.L.2
Hopkins, P.N.3
-
31
-
-
0027183606
-
Insulin resistance and hyperinsulinemia in individuals with small, dense low density lipoprotein particles
-
Reaven G.M., Chen Y.D., Jeppesen J., et al. Insulin resistance and hyperinsulinemia in individuals with small, dense low density lipoprotein particles. J Clin Invest. 92:1993;141-145.
-
(1993)
J Clin Invest
, vol.92
, pp. 141-145
-
-
Reaven, G.M.1
Chen, Y.D.2
Jeppesen, J.3
-
32
-
-
0037013151
-
Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia
-
Allayee H., Krass K.L., Pajunkanta P., et al. Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia. Circ Res. 90:2002;926-931.
-
(2002)
Circ Res
, vol.90
, pp. 926-931
-
-
Allayee, H.1
Krass, K.L.2
Pajunkanta, P.3
-
33
-
-
0031918837
-
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23
-
Pajukanta P., Nuotio I., Terwillinger J.D., et al. Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23. Nat Genet. 18:1998;369-373.
-
(1998)
Nat Genet
, vol.18
, pp. 369-373
-
-
Pajukanta, P.1
Nuotio, I.2
Terwillinger, J.D.3
-
34
-
-
0033984185
-
Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families
-
Pei B., Baron H., Muller-Myhsok B., et al. Support for linkage of familial combined hyperlipidemia to chromosome 1q21-q23 in Chinese and German families. Clin Genet. 57:2000;29-34.
-
(2000)
Clin Genet
, vol.57
, pp. 29-34
-
-
Pei, B.1
Baron, H.2
Muller-Myhsok, B.3
-
35
-
-
0033782243
-
Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study
-
Coon H., Myers R.H., Borecki I.B., et al. Replication of linkage of familial combined hyperlipidemia to chromosome 1q with additional heterogeneous effect of apolipoprotein A-I/C-III/A-IV locus. The NHLBI Family Heart Study. Arterioscler Thromb Vasc Biol. 20:2000;2275-2280.
-
(2000)
Arterioscler Thromb Vasc Biol
, vol.20
, pp. 2275-2280
-
-
Coon, H.1
Myers, R.H.2
Borecki, I.B.3
-
36
-
-
0033362163
-
A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11
-
Aouizerat B.E., Allayee H., Cantor D.M., et al. A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11. Am J Hum Genet. 65:1999;397-412.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 397-412
-
-
Aouizerat, B.E.1
Allayee, H.2
Cantor, D.M.3
-
37
-
-
0034700641
-
The metabolic pathways of high-density lipoprotein, low-density lipoprotein, and triglycerides: A current review
-
Kwiterovich P.O. The metabolic pathways of high-density lipoprotein, low-density lipoprotein, and triglycerides: a current review. Am J Cardiol. 86:2000;5L-10L.
-
(2000)
Am J Cardiol
, vol.86
-
-
Kwiterovich, P.O.1
-
38
-
-
0032913707
-
Dyslipidemia of central obesity and insulin resistance
-
Brunzell J.D., Hokanson J.E. Dyslipidemia of central obesity and insulin resistance. Diabetes Care. 22:1999;C10-C13.
-
(1999)
Diabetes Care
, vol.22
-
-
Brunzell, J.D.1
Hokanson, J.E.2
-
39
-
-
0033038810
-
The relation of overweight to cardiovascular risk factors among children and adolescents: The Bogalusa Heart Study
-
Freedman D.S., Dietz W.H., Srinivasan S.R., Berenson G.S. The relation of overweight to cardiovascular risk factors among children and adolescents: the Bogalusa Heart Study. Pediatrics. 103:1999;1175-1182.
-
(1999)
Pediatrics
, vol.103
, pp. 1175-1182
-
-
Freedman, D.S.1
Dietz, W.H.2
Srinivasan, S.R.3
Berenson, G.S.4
-
40
-
-
0032958470
-
Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats
-
Aitman T.J., Glazier A.M., Wallace C.A., et al. Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats. Nat Genet. 21:1999;76-83.
-
(1999)
Nat Genet
, vol.21
, pp. 76-83
-
-
Aitman, T.J.1
Glazier, A.M.2
Wallace, C.A.3
-
41
-
-
0032958470
-
Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats
-
Aitman T.J., Glazier A.M., Wallace C.A., et al. Identification of Cd36 (Fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats. Nat Genet. 21:1999;76-83.
-
(1999)
Nat Genet
, vol.21
, pp. 76-83
-
-
Aitman, T.J.1
Glazier, A.M.2
Wallace, C.A.3
-
42
-
-
0032693236
-
Genetics of Cd36 and the clustering of multiple cardiovascular risk factors in spontaneous hypertension
-
Pravenec M., Zidek V., Simakova M., et al. Genetics of Cd36 and the clustering of multiple cardiovascular risk factors in spontaneous hypertension. J Clin Invest. 103:1999;1651-1657.
-
(1999)
J Clin Invest
, vol.103
, pp. 1651-1657
-
-
Pravenec, M.1
Zidek, V.2
Simakova, M.3
-
43
-
-
0036309976
-
Factors of insulin resistance syndrome - Related phenotypes are linked to genetic locations on chromosomes 6 and 7 in nondiabetic Americans
-
Arya R., Blangero J., Williams K., et al. Factors of insulin resistance syndrome - related phenotypes are linked to genetic locations on chromosomes 6 and 7 in nondiabetic Americans. Diabetes. 51:2002;841-847.
-
(2002)
Diabetes
, vol.51
, pp. 841-847
-
-
Arya, R.1
Blangero, J.2
Williams, K.3
-
44
-
-
0033942570
-
A major susceptibility locus influencing plasma triglyceride concentrations is located on chromosome 15q in Mexican Americans
-
Duggirala R., Blangero J., Almasy L., et al. A major susceptibility locus influencing plasma triglyceride concentrations is located on chromosome 15q in Mexican Americans. Am J Hum Genet. 66:2000;1237-1245.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1237-1245
-
-
Duggirala, R.1
Blangero, J.2
Almasy, L.3
-
45
-
-
0002330773
-
Familial lipoprotein lipase deficiency and other causes of chylomicronemia syndrome
-
C.R. Scriver, A.L. Beaudet, W.S. Sly, & D. Valle. New York: McGraw-Hill
-
Brunzell J.D. Familial lipoprotein lipase deficiency and other causes of chylomicronemia syndrome. Scriver C.R., Beaudet A.L., Sly W.S., Valle D. The molecular basis of inherited disease. 1989;1165 McGraw-Hill, New York.
-
(1989)
The molecular basis of inherited disease
, pp. 1165
-
-
Brunzell, J.D.1
-
46
-
-
0031718707
-
Familial lipoprotein lipase deficiency in infancy: Clinical, biochemical, and molecular study
-
Feoli-Fonseca J.C., Levy E., Godard M., et al. Familial lipoprotein lipase deficiency in infancy: clinical, biochemical, and molecular study. J Ped. 133:1998;417-423.
-
(1998)
J Ped
, vol.133
, pp. 417-423
-
-
Feoli-Fonseca, J.C.1
Levy, E.2
Godard, M.3
-
47
-
-
0030804675
-
Therapeutic response to medium-chain triglycerides and ω-3 fatty acids in a patient with the familial chylomicronemia syndrome
-
Rouis M., Dugi K.A., Previato L., et al. Therapeutic response to medium-chain triglycerides and ω-3 fatty acids in a patient with the familial chylomicronemia syndrome. Arterioscler Thromb Vasc Biol. 17:1997;1400-1414.
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 1400-1414
-
-
Rouis, M.1
Dugi, K.A.2
Previato, L.3
-
48
-
-
0024397097
-
Structure of the human lipoprotein lipase gene
-
Deeb S.S., Peng R. Structure of the human lipoprotein lipase gene. Biochemistry. 28:1989;4131-4135.
-
(1989)
Biochemistry
, vol.28
, pp. 4131-4135
-
-
Deeb, S.S.1
Peng, R.2
-
49
-
-
0023090942
-
Human lipoprotein lipase complementary DNA sequence
-
Wion K.L., Kirchgessner T.G., Lusis A., et al. Human lipoprotein lipase complementary DNA sequence. Science. 235:1987;1638-1641.
-
(1987)
Science
, vol.235
, pp. 1638-1641
-
-
Wion, K.L.1
Kirchgessner, T.G.2
Lusis, A.3
-
50
-
-
0035033247
-
Lipoprotein lipase (LPL) deficiency: A new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of the reported mutations: 75% are clustered in exons 5 and 6
-
Gilbert T., Rouis M., Griglio S., et al. Lipoprotein lipase (LPL) deficiency: a new patient homozygote for the preponderant mutation Gly188Glu in the human LPL gene and review of the reported mutations: 75% are clustered in exons 5 and 6. Ann Genet. 44:2001;25-32.
-
(2001)
Ann Genet
, vol.44
, pp. 25-32
-
-
Gilbert, T.1
Rouis, M.2
Griglio, S.3
-
52
-
-
0023133252
-
Apolipoprotein E isoform phenotyping methodology and population frequency with identification of apoE1 and apoE5 isoforms
-
Ordovas J.M., Litwack-Klein L., Wilson P.W., et al. Apolipoprotein E isoform phenotyping methodology and population frequency with identification of apoE1 and apoE5 isoforms. J Lipid Res. 28:1987;371-380.
-
(1987)
J Lipid Res
, vol.28
, pp. 371-380
-
-
Ordovas, J.M.1
Litwack-Klein, L.2
Wilson, P.W.3
-
53
-
-
0025816694
-
Influences of common variants of apolipoprotein E on measures of lipid metabolism in a sample selected for health
-
Xhignesse M., Lussier-Cacan S., Sing C.F., et al. Influences of common variants of apolipoprotein E on measures of lipid metabolism in a sample selected for health. Arterioscler Thromb. 11:1991;1100-1110.
-
(1991)
Arterioscler Thromb
, vol.11
, pp. 1100-1110
-
-
Xhignesse, M.1
Lussier-Cacan, S.2
Sing, C.F.3
-
54
-
-
0035718503
-
Determinants of lipid level variability in French-Canadian children with familial hypercholesterolemia
-
Lambert M., Assouline L., Feoli-Fonseca J.C., et al. Determinants of lipid level variability in French-Canadian children with familial hypercholesterolemia. Arterioscler Thromb Vasc Biol. 21:2001;979-984.
-
(2001)
Arterioscler Thromb Vasc Biol
, vol.21
, pp. 979-984
-
-
Lambert, M.1
Assouline, L.2
Feoli-Fonseca, J.C.3
-
55
-
-
0025187754
-
Association of hypercholesterolemia and apolipoprotein E4 in school children
-
Yanagi H., Shimakura Y., Yamanouchi Y., et al. Association of hypercholesterolemia and apolipoprotein E4 in school children. Clin Genet. 38:1990;264-269.
-
(1990)
Clin Genet
, vol.38
, pp. 264-269
-
-
Yanagi, H.1
Shimakura, Y.2
Yamanouchi, Y.3
-
56
-
-
0038278510
-
The apolipoprotein ε 4 allele confers additional risk in children with familial hypercholesterolemia
-
Wiegman A., Sijbrands E.J., Rodenburg J., et al. The apolipoprotein ε 4 allele confers additional risk in children with familial hypercholesterolemia. Pediat Res. 53:2003;1008-1012.
-
(2003)
Pediat Res
, vol.53
, pp. 1008-1012
-
-
Wiegman, A.1
Sijbrands, E.J.2
Rodenburg, J.3
-
57
-
-
0032898483
-
Frequent occurrence of hypoalphalipoproteinemia due to mutant apolipoprotein A-1 gene in the population: A population based study
-
Yamakawa-Kobayashi K., Yanagi H., Fukayama H., et al. Frequent occurrence of hypoalphalipoproteinemia due to mutant apolipoprotein A-1 gene in the population: a population based study. Hum Mol Gen. 8:1999;331-336.
-
(1999)
Hum Mol Gen
, vol.8
, pp. 331-336
-
-
Yamakawa-Kobayashi, K.1
Yanagi, H.2
Fukayama, H.3
-
58
-
-
0021344194
-
Human apolipoprotein A-I and C-III genes reside in the p11-q13 region of chromosome 11
-
Law S.W., Gray G., Brewer H.B. Jr., et al. Human apolipoprotein A-I and C-III genes reside in the p11-q13 region of chromosome 11. Biochem Biophys Res Commun. 118:1984;934-942.
-
(1984)
Biochem Biophys Res Commun
, vol.118
, pp. 934-942
-
-
Law, S.W.1
Gray, G.2
Brewer H.B., Jr.3
-
59
-
-
0019419450
-
Relation between the HDL apoproteins and AI isoproteins in subjects with the AI Milano abnormality
-
Franceschini G., Sisrtori M., Gianfreceshi G., et al. Relation between the HDL apoproteins and AI isoproteins in subjects with the AI Milano abnormality. Metabolism. 30:1981;502-509.
-
(1981)
Metabolism
, vol.30
, pp. 502-509
-
-
Franceschini, G.1
Sisrtori, M.2
Gianfreceshi, G.3
-
60
-
-
0021925271
-
Familial associations of lipids and lipoproteins in a highly consanguineous population: The Limone sul Garda study
-
Gualandri V., Orsini G.B., Cerrone A., et al. Familial associations of lipids and lipoproteins in a highly consanguineous population: the Limone sul Garda study. Metabolism. 34:1984;212-221.
-
(1984)
Metabolism
, vol.34
, pp. 212-221
-
-
Gualandri, V.1
Orsini, G.B.2
Cerrone, A.3
-
61
-
-
0342811295
-
Human ATP-binding cassette transporter a (ABC1): Genomic organization and identification of the genetic defect in the original Tangier disease kindred
-
Remaley A.T., Rust S., Rosier M., et al. Human ATP-binding cassette transporter a (ABC1): genomic organization and identification of the genetic defect in the original Tangier disease kindred. PNAS. 96:1999;12685-12690.
-
(1999)
PNAS
, vol.96
, pp. 12685-12690
-
-
Remaley, A.T.1
Rust, S.2
Rosier, M.3
-
62
-
-
0032813809
-
The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease
-
Bodzioch M., Orso E., Klucken, et al. The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. Nat Genet. 22:1999;347-351.
-
(1999)
Nat Genet
, vol.22
, pp. 347-351
-
-
Bodzioch, M.1
Orso, E.2
Klucken3
-
63
-
-
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. Rust R., Rosier M., Funke H., et al. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nat Genet. 22:1999;352-355.
-
(1999)
Nat Genet
, vol.22
, pp. 336-345
-
-
Brooks-Wilson, A.1
Marcil, M.2
Clee, S.M.3
-
64
-
-
0032813660
-
Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1
-
Rust R., Rosier M., Funke H., et al. Tangier disease is caused by mutations in the gene encoding ATP-binding cassette transporter 1. Nat Genet. 22:1999;352-355.
-
(1999)
Nat Genet
, vol.22
, pp. 352-355
-
-
Rust, R.1
Rosier, M.2
Funke, H.3
-
65
-
-
0030944935
-
Plasma lipoprotein (a) levels and expression of the apolipoprotein (a) gene are dependent on the nucleotide polymorphisms in its 5″-flanking region
-
Suzuki K., Kuriyama M., Saito T., et al. Plasma lipoprotein (a) levels and expression of the apolipoprotein (a) gene are dependent on the nucleotide polymorphisms in its 5″-flanking region. J Clin Invest. 99:1997;1361-1366.
-
(1997)
J Clin Invest
, vol.99
, pp. 1361-1366
-
-
Suzuki, K.1
Kuriyama, M.2
Saito, T.3
-
66
-
-
0018689047
-
Lp (a) phenotypes, other lipoprotein parameters, and a family history of coronary heart disease in middle-aged males
-
Berg K., Dahlen G., Borresen A.L. Lp (a) phenotypes, other lipoprotein parameters, and a family history of coronary heart disease in middle-aged males. Clin Genet. 16:1979;347-352.
-
(1979)
Clin Genet
, vol.16
, pp. 347-352
-
-
Berg, K.1
Dahlen, G.2
Borresen, A.L.3
-
67
-
-
0031152047
-
Lipoprotein (a): Its role in childhood thromboembolism
-
Nowak-Gottl U., Debus O., Findeisen M., et al. Lipoprotein (a): its role in childhood thromboembolism. Pediatrics. 99:(6):1997;E11.
-
(1997)
Pediatrics
, vol.99
, Issue.6
, pp. 11
-
-
Nowak-Gottl, U.1
Debus, O.2
Findeisen, M.3
|