-
1
-
-
0031574989
-
New and classical risk factors-the Munster heart study (PROCAM)
-
1 Assmann G, Schulte H, Cullen P. New and classical risk factors-the Munster heart study (PROCAM). Eur J Med Res 1997; 2:237-242.
-
(1997)
Eur J Med Res
, vol.2
, pp. 237-242
-
-
Assmann, G.1
Schulte, H.2
Cullen, P.3
-
2
-
-
0019520249
-
Lipoproteins, cardiovascular disease, and death. The framingham study
-
2 Gordon T, Kannel WB, Castelli WP, Dawber TR. Lipoproteins, cardiovascular disease, and death. The Framingham study. Arch Intern Med 1981; 141:1128-1131.
-
(1981)
Arch Intern Med
, vol.141
, pp. 1128-1131
-
-
Gordon, T.1
Kannel, W.B.2
Castelli, W.P.3
Dawber, T.R.4
-
3
-
-
0023232216
-
Helsinki heart study: Primary-prevention trial with gemfibrozil in middle-aged men with dyslipidemia. Safety of treatment, changes in risk factors, and incidence of coronary heart disease
-
3 Frick MH, Elo O, Haapa K, Heinonen OP, Heisalmi P, Helo P, et al. Helsinki heart study: primary-prevention trial with gemfibrozil in middle-aged men with dyslipidemia. Safety of treatment, changes in risk factors, and incidence of coronary heart disease. N Engl J Med 1987; 317:1237-1245.
-
(1987)
N Engl J Med
, vol.317
, pp. 1237-1245
-
-
Frick, M.H.1
Elo, O.2
Haapa, K.3
Heinonen, O.P.4
Heisalmi, P.5
Helo, P.6
-
4
-
-
0031574989
-
New and classical risk factors-the Munster heart study (PROCAM)
-
4 Assmann G, Schulte H, Cullen P. New and classical risk factors-the Munster heart study (PROCAM). Eur J Med Res 1997; 2:237-242.
-
(1997)
Eur J Med Res
, vol.2
, pp. 237-242
-
-
Assmann, G.1
Schulte, H.2
Cullen, P.3
-
5
-
-
0023263185
-
Coronary risk prediction in adults (the Framingham heart study)
-
published erratum appears in Am J Cardiol 1987 1;60A11
-
5 Wilson PW, Castelli WP, Kannel WB. Coronary risk prediction in adults (the Framingham Heart Study) [published erratum appears in Am J Cardiol 1987 1;60A11]. Am J Cardiol 1987; 59:91G-94G.
-
(1987)
Am J Cardiol
, vol.59
-
-
Wilson, P.W.1
Castelli, W.P.2
Kannel, W.B.3
-
6
-
-
0019302053
-
Construction of a genetic linkage map in man using restriction fragment length polymorphisms
-
6 Botstein D, White RL, Skolnick M, Davis RW. Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am J Hum Genet 1980; 32:314-331.
-
(1980)
Am J Hum Genet
, vol.32
, pp. 314-331
-
-
Botstein, D.1
White, R.L.2
Skolnick, M.3
Davis, R.W.4
-
7
-
-
0009686779
-
Molecular genetics approach to polygenic disease results from atherosclerosis research
-
Galton DJ, Assman G (eds.). Plenum Press New York
-
7 Funke H, Von Eckardstein A, Assmanan G. Molecular genetics approach to polygenic disease results from atherosclerosis research. In: Galton DJ, Assman G (eds.) DNA Polymorphisms as Disease Markers. Plenum Press New York, 15-25 1991.
-
(1991)
DNA Polymorphisms as Disease Markers
, pp. 15-25
-
-
Funke, H.1
Von Eckardstein, A.2
Assmanan, G.3
-
8
-
-
0023915850
-
The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes
-
8 Thompson EA, Deeb S, Walker D, Motulsky AG. The detection of linkage disequilibrium between closely linked markers: RFLPs at the AI-CIII apolipoprotein genes. Am J Hum Genet 1988; 42:113-124.
-
(1988)
Am J Hum Genet
, vol.42
, pp. 113-124
-
-
Thompson, E.A.1
Deeb, S.2
Walker, D.3
Motulsky, A.G.4
-
10
-
-
0022918434
-
Association of apolipoprotein E polymorphism, low-density lipoprotein cholesterol and coronary artery disease
-
10 Lenzen HJ, Assmann G, Buchwalsky R, Schulte H. Association of apolipoprotein E polymorphism, low-density lipoprotein cholesterol and coronary artery disease. Clin Chem 1986; 32:778-781.
-
(1986)
Clin Chem
, vol.32
, pp. 778-781
-
-
Lenzen, H.J.1
Assmann, G.2
Buchwalsky, R.3
Schulte, H.4
-
11
-
-
0027223301
-
An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3' untranslated region polymorphisms
-
11 Dammerman M, Sandkuhl LA, Halaas JL, Chung W, Breslow JL. An apolipoprotein CIII haplotype protective against hypertriglyceridemia is specified by promoter and 3' untranslated region polymorphisms. Proc Natl Acad Sci (USA) 1993; 90:4562-4566.
-
(1993)
Proc Natl Acad Sci (USA)
, vol.90
, pp. 4562-4566
-
-
Dammerman, M.1
Sandkuhl, L.A.2
Halaas, J.L.3
Chung, W.4
Breslow, J.L.5
-
12
-
-
0030937346
-
Complex genetic contribution of the apoptosis AI-CIII-AIV gene cluster to familial combined hyperlipidemia: Identification of different susceptibility haplotypes
-
12 Dallinga-Thie GM, Van Linde-Sibenius TM, Rotter JI, Cantor RM, X, Lusis AJ, De BT. Complex genetic contribution of the apoptosis AI-CIII-AIV gene cluster to familial combined hyperlipidemia: identification of different susceptibility haplotypes. J Clin Invest 1997; 99:953-961.
-
(1997)
J Clin Invest
, vol.99
, pp. 953-961
-
-
Dallinga-Thie, G.M.1
Van Linde-Sibenius, T.M.2
Rotter, J.I.3
Cantor, R.M.4
Lusis, A.J.5
De, B.T.6
-
13
-
-
0023806703
-
DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster
-
13 Antonarakis SE, Oettgen P, Chakravarti A, Halloran SL, Hudson RR, Feisee L, Karathanasis SK. DNA polymorphism haplotypes of the human apolipoprotein APOA1-APOC3-APOA4 gene cluster. Hum Genet 1988; 80:265-273.
-
(1988)
Hum Genet
, vol.80
, pp. 265-273
-
-
Antonarakis, S.E.1
Oettgen, P.2
Chakravarti, A.3
Halloran, S.L.4
Hudson, R.R.5
Feisee, L.6
Karathanasis, S.K.7
-
14
-
-
0021918948
-
Mutation in LDL receptor: Alu-alu recombination deletex onons encoding transmembrane and cytoplasmic domains
-
14 Lehrmann MA, Schneider WJ, S-Dhoff TC, Brown MS, Goldstein JL, Russell DW. Mutation in LDL receptor: alu-alu recombination deletex onons encoding transmembrane and cytoplasmic domains. Science 1985; 227:140-146.
-
(1985)
Science
, vol.227
, pp. 140-146
-
-
Lehrmann, M.A.1
Schneider, W.J.2
S-Dhoff, T.C.3
Brown, M.S.4
Goldstein, J.L.5
Russell, D.W.6
-
15
-
-
0020556158
-
A DNA insertion in the apolipoprotein AI gene of patients with premature atherosclerosis
-
15 Karathanasis SK, Zannis VI, Breslow JL. A DNA insertion in the apolipoprotein AI gene of patients with premature atherosclerosis. Nature 1983; 305:823-825.
-
(1983)
Nature
, vol.305
, pp. 823-825
-
-
Karathanasis, S.K.1
Zannis, V.I.2
Breslow, J.L.3
-
16
-
-
0025340464
-
Lecithin cholesterol acyl transferase deficiency: Molecular analysis of a mutated allele
-
16 Taramelli R, Pontoglio M, Candiani G, Ottolenghi S, Dieplinger H, Catapano A, Albers J, et al. Lecithin cholesterol acyl transferase deficiency: molecular analysis of a mutated allele. Hum Genet 1990; 85:195-199.
-
(1990)
Hum Genet
, vol.85
, pp. 195-199
-
-
Taramelli, R.1
Pontoglio, M.2
Candiani, G.3
Ottolenghi, S.4
Dieplinger, H.5
Catapano, A.6
Albers, J.7
-
17
-
-
0025819206
-
A molecular defect causing fish eye disease: An amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity
-
17 Funke H, Von EA, Pritchard PH, Albers JJ, Kastelein JJ, Droste C, Assmann G. A molecular defect causing fish eye disease: an amino acid exchange in lecithin-cholesterol acyltransferase (LCAT) leads to the selective loss of alpha-LCAT activity. Proc Natl Acad Sci USA 1991; 88:4855-4859.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 4855-4859
-
-
Funke, H.1
Von, E.A.2
Pritchard, P.H.3
Albers, J.J.4
Kastelein, J.J.5
Droste, C.6
Assmann, G.7
-
18
-
-
0024415898
-
Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins
-
18 Brown ML, Inazu A, Hester CB, Agellon LB, Mann C, Whitlock ME, et al. Molecular basis of lipid transfer protein deficiency in a family with increased high-density lipoproteins. Nature 1989; 342:448-451.
-
(1989)
Nature
, vol.342
, pp. 448-451
-
-
Brown, M.L.1
Inazu, A.2
Hester, C.B.3
Agellon, L.B.4
Mann, C.5
Whitlock, M.E.6
-
19
-
-
0030878439
-
Genetic determinants of high density lipoprotein levels
-
19 Funke H. Genetic determinants of high density lipoprotein levels. Curr Opin Lipidol 1997; 8:189-196.
-
(1997)
Curr Opin Lipidol
, vol.8
, pp. 189-196
-
-
Funke, H.1
-
20
-
-
0026470990
-
Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia
-
20 Wetterau JR, Aggerbeck LP, Bourma ME, Eisenberg C, Munck A, Hermier M, et al. Absence of microsomal triglyceride transfer protein in individuals with abetalipoproteinemia. Science 1992; 258:999-1001.
-
(1992)
Science
, vol.258
, pp. 999-1001
-
-
Wetterau, J.R.1
Aggerbeck, L.P.2
Bourma, M.E.3
Eisenberg, C.4
Munck, A.5
Hermier, M.6
-
21
-
-
0023056989
-
Complete cDNA and derived protein sequence of human apolipoprotein B-100
-
21 Knott TJ, Wallis SC, Powell LM, Pease RJ, Lusis AJ, Blackhart B, et al. Complete cDNA and derived protein sequence of human apolipoprotein B-100. Nucleic Acids Res 1986; 14:7501-7503.
-
(1986)
Nucleic Acids Res
, vol.14
, pp. 7501-7503
-
-
Knott, T.J.1
Wallis, S.C.2
Powell, L.M.3
Pease, R.J.4
Lusis, A.J.5
Blackhart, B.6
-
22
-
-
0023636242
-
cDNA sequence of human apolipoprotein(a) is homologous to plasminogen
-
22 Mclean JW, Tomlinson JE, Kuang WJ, Eaton DL, Chen EY, Fless GM, et al. cDNA sequence of human apolipoprotein(a) is homologous to plasminogen. Nature 1987; 330: 132-137.
-
(1987)
Nature
, vol.330
, pp. 132-137
-
-
Mclean, J.W.1
Tomlinson, J.E.2
Kuang, W.J.3
Eaton, D.L.4
Chen, E.Y.5
Fless, G.M.6
-
23
-
-
0001665337
-
Surface location and high affinity for calcium of a 500-kd liver membrane protein closely related to the LDL-receptor suggest a physiological role as lipoprotein receptor
-
23 Herz J, Hamann U, Rogne S, Myklebost O, Gausepohl H, Stanley KK. Surface location and high affinity for calcium of a 500-kd liver membrane protein closely related to the LDL-receptor suggest a physiological role as lipoprotein receptor. EMBO J 1988; 7:4119-4127.
-
(1988)
EMBO J
, vol.7
, pp. 4119-4127
-
-
Herz, J.1
Hamann, U.2
Rogne, S.3
Myklebost, O.4
Gausepohl, H.5
Stanley, K.K.6
-
24
-
-
0024368085
-
RNA editing: A novel mechanism for regulating lipid transport from the intestine
-
24 Scott J, Wallis SC, Davies MS, Wynne JK, Powell LM, Driscoll DM. RNA editing: a novel mechanism for regulating lipid transport from the intestine. Gut 1989; 30 Spec No:35-43.
-
(1989)
Gut
, vol.30
, pp. 35-43
-
-
Scott, J.1
Wallis, S.C.2
Davies, M.S.3
Wynne, J.K.4
Powell, L.M.5
Driscoll, D.M.6
-
25
-
-
0025902231
-
Inhibition of early atherogenesis in transgenic mice by human apolipoprotein AI
-
25 Rubin EM, Krauss RM, Spangler EA, Verstuyft JG, Clift SM. Inhibition of early atherogenesis in transgenic mice by human apolipoprotein AI. Nature 1991; 353:265-267.
-
(1991)
Nature
, vol.353
, pp. 265-267
-
-
Rubin, E.M.1
Krauss, R.M.2
Spangler, E.A.3
Verstuyft, J.G.4
Clift, S.M.5
-
26
-
-
0026764308
-
Marked reduction of high density lipoprotein cholesterol in mice geneticaly modified to lack apolipoprotein A-I
-
26 Williamson R, Lee D, Hagaman J, Maeda N. Marked reduction of high density lipoprotein cholesterol in mice geneticaly modified to lack apolipoprotein A-I. Proc Natl Acad Sci USA 1992; 89: 7134-7138.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 7134-7138
-
-
Williamson, R.1
Lee, D.2
Hagaman, J.3
Maeda, N.4
-
27
-
-
0027330901
-
Lack of apoA-I is not associated with increased susceptibility to atherosclerosis in mice
-
27 Li H, Reddick RL, Maeda N. Lack of apoA-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
-
28
-
-
0344429365
-
High plasma HDL concentrations associated with enhanced atherosclerosis in transgenic mice overexpressing lecithin-cholesteryl acyltransferase
-
28 Berard AM, Foger B, Remaley A, Shamburek R, Vaisman BL, Talley G, et al. High plasma HDL concentrations associated with enhanced atherosclerosis in transgenic mice overexpressing lecithin-cholesteryl acyltransferase. Nat Med 1997; 3:744-749.
-
(1997)
Nat Med
, vol.3
, pp. 744-749
-
-
Berard, A.M.1
Foger, B.2
Remaley, A.3
Shamburek, R.4
Vaisman, B.L.5
Talley, G.6
-
29
-
-
16044372278
-
Overexpression of lecithin: Cholesterol acyltransferase in transgenic rabbits prevents diet-induced atherosclerosis
-
29 Hoeg JM, Santamarina-Fojo S, Berard AM, Cornhill JF, Herderick EE, Feldman SH, et al. Overexpression of lecithin: cholesterol acyltransferase in transgenic rabbits prevents diet-induced atherosclerosis. Proc Natl Acad Sci USA 1996; 93:11448-11453.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 11448-11453
-
-
Hoeg, J.M.1
Santamarina-Fojo, S.2
Berard, A.M.3
Cornhill, J.F.4
Herderick, E.E.5
Feldman, S.H.6
-
30
-
-
0031916999
-
Mapping a gene for combined hyperlipdiaemia in a mutant mouse strain
-
30 Castellani LW, Weinreb A, Bodnar J, Goto AM, Doolittle M, Mehrabian M, et al. Mapping a gene for combined hyperlipdiaemia in a mutant mouse strain. Nat Genet 1998; 18:374-377.
-
(1998)
Nat Genet
, vol.18
, pp. 374-377
-
-
Castellani, L.W.1
Weinreb, A.2
Bodnar, J.3
Goto, A.M.4
Doolittle, M.5
Mehrabian, M.6
-
31
-
-
0031918837
-
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23
-
31 Pajukanta P, Nuotio I, Terwilliger JD, Porkka KV, Ylitalo K, Pihlajamaki J, et al. Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23. Nat Genet 1998; 18:369-373.
-
(1998)
Nat Genet
, vol.18
, pp. 369-373
-
-
Pajukanta, P.1
Nuotio, I.2
Terwilliger, J.D.3
Porkka, K.V.4
Ylitalo, K.5
Pihlajamaki, J.6
-
32
-
-
0032958470
-
Identification of CD36 (fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats
-
32 Aitman TJ, Glazier AM, Wallace CA, Cooper LD, Norsworthy PJ, Wahid FN, et al. Identification of CD36 (fat) as an insulin-resistance gene causing defective fatty acid and glucose metabolism in hypertensive rats [in process citation]. Nat Genet 1999; 21;76-83.
-
(1999)
Nat Genet
, vol.21
, pp. 76-83
-
-
Aitman, T.J.1
Glazier, A.M.2
Wallace, C.A.3
Cooper, L.D.4
Norsworthy, P.J.5
Wahid, F.N.6
-
33
-
-
0031017322
-
A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2
-
33 Comuzzie AG, Hixson JE, Almasy L, Mitchell BD, Mahaney MC, Dyer TD, et al. A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2. Nat Genet 1997; 15:273-276.
-
(1997)
Nat Genet
, vol.15
, pp. 273-276
-
-
Comuzzie, A.G.1
Hixson, J.E.2
Almasy, L.3
Mitchell, B.D.4
Mahaney, M.C.5
Dyer, T.D.6
-
34
-
-
0032231709
-
A defect in the regional deposition of adipose tissue (partial lipodystrophy) is encoded by a gene at chromosome 1q
-
34 Jackson SN, Pinkney J, Bargiotta A, Veal CD, Howlett TA, Mcnally PG, et al. A defect in the regional deposition of adipose tissue (partial lipodystrophy) is encoded by a gene at chromosome 1q. Am J Hum Genet 1998; 63:534-540.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 534-540
-
-
Jackson, S.N.1
Pinkney, J.2
Bargiotta, A.3
Veal, C.D.4
Howlett, T.A.5
Mcnally, P.G.6
-
35
-
-
0031932459
-
Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21-22
-
35 Peters JM, Barnes R, Bennett L, Gitomer WM, Bowcock AM, Garg A. Localization of the gene for familial partial lipodystrophy (Dunnigan variety) to chromosome 1q21-22. Nat Genet 1998; 18:292-295.
-
(1998)
Nat Genet
, vol.18
, pp. 292-295
-
-
Peters, J.M.1
Barnes, R.2
Bennett, L.3
Gitomer, W.M.4
Bowcock, A.M.5
Garg, A.6
-
36
-
-
0033555512
-
Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22
-
36 Anderson JL, Khan M, David WS, Mahdavi Z, Nuttall FQ, Krech E, et al. Confirmation of linkage of hereditary partial lipodystrophy to chromosome 1q21-22 [in process citation]. Am J Med Genet 1999; 82:161-165.
-
(1999)
Am J Med Genet
, vol.82
, pp. 161-165
-
-
Anderson, J.L.1
Khan, M.2
David, W.S.3
Mahdavi, Z.4
Nuttall, F.Q.5
Krech, E.6
-
37
-
-
0028899938
-
A nonparametric approach for mapping quantitative trait loci
-
37 Kruglyak L, Lander ES. A nonparametric approach for mapping quantitative trait loci. Genetics 1995; 139:1421-1428.
-
(1995)
Genetics
, vol.139
, pp. 1421-1428
-
-
Kruglyak, L.1
Lander, E.S.2
-
39
-
-
0025019555
-
Linkage strategies for genetically complex traits. i. Multilocus models
-
39 Risch N. Linkage strategies for genetically complex traits. i. Multilocus models [see comments]. Am J Hum Genet 1990; 46:222-228.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 222-228
-
-
Risch, N.1
-
40
-
-
0025008677
-
Linkage strategies for genetically complex traits. ii. The power of affected relative pairs
-
40 Risch N. Linkage strategies for genetically complex traits. ii. The power of affected relative pairs [see comments]. Am J Hum Genet 1990; 46:229-241.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 229-241
-
-
Risch, N.1
-
41
-
-
0025020461
-
Linkage strategies for genetically complex traits. iii. The effect of marker polymorphism on analysis of affected relative pairs
-
published erratum appears in Am J Hum Genet 1992 Sep;51 (3:673-5 [see comments]
-
41 Risch N. Linkage strategies for genetically complex traits. iii. The effect of marker polymorphism on analysis of affected relative pairs [published erratum appears in Am J Hum Genet 1992 Sep;51 (3:673-5] [see comments]. Am J Hum Genet 1990; 46:242-253.
-
(1990)
Am J Hum Genet
, vol.46
, pp. 242-253
-
-
Risch, N.1
-
42
-
-
0029001682
-
Extreme discordant sib pairs for mapping quantitative trait loci in humans
-
42 Risch N, Zhang H. Extreme discordant sib pairs for mapping quantitative trait loci in humans. Science 1995; 268:1584-1589.
-
(1995)
Science
, vol.268
, pp. 1584-1589
-
-
Risch, N.1
Zhang, H.2
-
43
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
43 Risch N, Merikangas K. The future of genetic studies of complex human diseases [see comments]. Science 1996; 273:1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
44
-
-
3643136390
-
Mapping genes for NIDDM. Design of the Finland-United States investigation of NIDDM genetics (FUSION) study
-
44 Valle T, Tuomilehto J, Bergman RN, Ghosh S, Hauser ER, Eriksson J, et al. Mapping genes for NIDDM. Design of the Finland-United States investigation of NIDDM genetics (FUSION) study. Diabetes Care 1998; 21:949-958.
-
(1998)
Diabetes Care
, vol.21
, pp. 949-958
-
-
Valle, T.1
Tuomilehto, J.2
Bergman, R.N.3
Ghosh, S.4
Hauser, E.R.5
Eriksson, J.6
-
45
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
45 Kruglyak L, Daly MJ, Reeve-Daly MP, Lander ES. Parametric and nonparametric linkage analysis: a unified multipoint approach. Am J Hum Genet 1996; 58:1347-1363.
-
(1996)
Am J Hum Genet
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
46
-
-
16044374799
-
Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish familes
-
46 Mahtani MM, Widen E, Lehto M, Thomas J, Mccarthy M, Brayer J, et al. Mapping of a gene for type 2 diabetes associated with an insulin secretion defect by a genome scan in Finnish familes [see comments]. Nat Genet 1996; 14:90-94.
-
(1996)
Nat Genet
, vol.14
, pp. 90-94
-
-
Mahtani, M.M.1
Widen, E.2
Lehto, M.3
Thomas, J.4
Mccarthy, M.5
Brayer, J.6
-
47
-
-
17344371519
-
A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10
-
47 Hager J, Dina C, Francke S, Dubois S, Houari M, Vatin V, et al. A genome-wide scan for human obesity genes reveals a major susceptibility locus on chromosome 10. Nat Genet 1998; 20:304-308.
-
(1998)
Nat Genet
, vol.20
, pp. 304-308
-
-
Hager, J.1
Dina, C.2
Francke, S.3
Dubois, S.4
Houari, M.5
Vatin, V.6
-
48
-
-
0025970749
-
Familial combined hyperlipidemia is linked to the apolipoprotein AI-CIII-AIV gene cluster on chromosome 11q23-Q24
-
48 Wojciechowski AP, Farrall ML, Cullen P, Wilson TME, Bayliss JD, Farren B, et al. Familial combined hyperlipidemia is linked to the apolipoprotein AI-CIII-AIV gene cluster on chromosome 11q23-Q24. Nature 1991; 349:161-164.
-
(1991)
Nature
, vol.349
, pp. 161-164
-
-
Wojciechowski, A.P.1
Farrall, M.L.2
Cullen, P.3
Wilson, T.M.E.4
Bayliss, J.D.5
Farren, B.6
-
49
-
-
17344368404
-
Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy
-
published erratum appears in Nat Genet 1998 Nov;20(3).312
-
49 Rust S, Walter M, Funke H, Von EA, Cullen P, Kroes HY, et al. Assignment of Tangier disease to chromosome 9q31 by a graphical linkage exclusion strategy [published erratum appears in Nat Genet 1998 Nov;20(3).312]. Nat Genet 1998; 20:96-98.
-
(1998)
Nat Genet
, vol.20
, pp. 96-98
-
-
Rust, S.1
Walter, M.2
Funke, H.3
Von, E.A.4
Cullen, P.5
Kroes, H.Y.6
-
50
-
-
0030941803
-
The SREBP pathway; regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor
-
50 Brown MS, Goldstein JL. The SREBP pathway; regulation of cholesterol metabolism by proteolysis of a membrane-bound transcription factor. Cell 1997; 89:331-340.
-
(1997)
Cell
, vol.89
, pp. 331-340
-
-
Brown, M.S.1
Goldstein, J.L.2
-
51
-
-
0029972133
-
Control of apolipoprotein AI gene expression through synergistic interactions between hepatocyte nuclear factors 3 and 4
-
51 Harnish DC, Malik S, Kilbourne E, Costa R, Karathanasis SK. Control of apolipoprotein AI gene expression through synergistic interactions between hepatocyte nuclear factors 3 and 4. J Biol Chem 1996; 271:13621-13628.
-
(1996)
J Biol Chem
, vol.271
, pp. 13621-13628
-
-
Harnish, D.C.1
Malik, S.2
Kilbourne, E.3
Costa, R.4
Karathanasis, S.K.5
-
52
-
-
0030007427
-
ADD1/SREBP1 promotes adipocyte differentiation and gene expression linked to fatty acid metabolism
-
52 Kim JB, Spiegelman BM. ADD1/SREBP1 promotes adipocyte differentiation and gene expression linked to fatty acid metabolism. Genes Dev 1996; 10:1096-1107.
-
(1996)
Genes Dev
, vol.10
, pp. 1096-1107
-
-
Kim, J.B.1
Spiegelman, B.M.2
-
53
-
-
0030590074
-
Molecular cloning, expression and characterization of human peroxisome proliferator activated receptors gamma 1 and gamma 2
-
53 Elbrecht A, Chen Y, Cullinan CA, Hayes N, Leibowitz M, Moller DE, Berger J. Molecular cloning, expression and characterization of human peroxisome proliferator activated receptors gamma 1 and gamma 2. Biochem Biophys Res Commun 1996; 224:431-437.
-
(1996)
Biochem Biophys Res Commun
, vol.224
, pp. 431-437
-
-
Elbrecht, A.1
Chen, Y.2
Cullinan, C.A.3
Hayes, N.4
Leibowitz, M.5
Moller, D.E.6
Berger, J.7
-
54
-
-
0032540012
-
PPAR-gamma promotes monocyte/macrophage differentiation and uptake of oxidized LDL
-
54 Tontonoz P, Nagy L, Alvarez JG, Thomazy VA, Evans RM. PPAR-gamma promotes monocyte/macrophage differentiation and uptake of oxidized LDL. Cell 1998; 93:241-252.
-
(1998)
Cell
, vol.93
, pp. 241-252
-
-
Tontonoz, P.1
Nagy, L.2
Alvarez, J.G.3
Thomazy, V.A.4
Evans, R.M.5
-
55
-
-
0031667938
-
Activators of the nuclear receptor PPAR-gamma enhance colon polyp formation
-
55 Saez E, Tontonoz P, Nelson MC, Alvarez JG, Ming UT, Baird SM, et al. Activators of the nuclear receptor PPAR-gamma enhance colon polyp formation. Nat Med 1998; 4:1058-1061.
-
(1998)
Nat Med
, vol.4
, pp. 1058-1061
-
-
Saez, E.1
Tontonoz, P.2
Nelson, M.C.3
Alvarez, J.G.4
Ming, U.T.5
Baird, S.M.6
-
56
-
-
0032502689
-
Estrogen regulation of the apolipoprotein AI gene promoter through transcription cofactor sharing
-
56 Harnish DC, Evans MJ, Scicchitano MS, Bhat RA, Karathanasis SK. Estrogen regulation of the apolipoprotein AI gene promoter through transcription cofactor sharing. J Biol Chem 1998; 273:9270-9278.
-
(1998)
J Biol Chem
, vol.273
, pp. 9270-9278
-
-
Harnish, D.C.1
Evans, M.J.2
Scicchitano, M.S.3
Bhat, R.A.4
Karathanasis, S.K.5
-
57
-
-
0032584567
-
Regulation of a transcription factor network required for differentiation and metabolism
-
57 Duncan SA, Navas MA, Dufort D, Rossant J, Stoffel M. Regulation of a transcription factor network required for differentiation and metabolism. Science 1998; 281:692-695.
-
(1998)
Science
, vol.281
, pp. 692-695
-
-
Duncan, S.A.1
Navas, M.A.2
Dufort, D.3
Rossant, J.4
Stoffel, M.5
-
58
-
-
0032524459
-
Multiple parameters determine the specificity of transcriptional response by nuclear receptors HNF-4, ARP-1, PPAR, RAR and RXR through common response elements
-
58 Nakshatri H, Bhat-Nakshatri P. Multiple Parameters Determine The specificity of transcriptional response by nuclear receptors HNF-4, ARP-1, PPAR, RAR and RXR through common response elements. Nucleic Acids Res 1998; 26:2491-2499.
-
(1998)
Nucleic Acids Res
, vol.26
, pp. 2491-2499
-
-
Nakshatri, H.1
Bhat-Nakshatri, P.2
-
59
-
-
0013199471
-
Cholesterol and bile acid metabolism are impaired in mice lacking the nuclear oxysterol receptor LXR alpha
-
59 Peet DJ, Turley SD, Ma W, Janowski BA, Lobaccaro JM, Hammer RE, Mangelsdorf DJ. Cholesterol and bile acid metabolism are impaired in mice lacking the nuclear oxysterol receptor LXR alpha. Cell 1998; 93:693-704.
-
(1998)
Cell
, vol.93
, pp. 693-704
-
-
Peet, D.J.1
Turley, S.D.2
Ma, W.3
Janowski, B.A.4
Lobaccaro, J.M.5
Hammer, R.E.6
Mangelsdorf, D.J.7
-
60
-
-
0018939225
-
Mevinolin: A highly potent competitive inhibitor of hydroxymethylglutaryl-coenzyme a reductase and a cholesterol-lowering agent
-
60 Alberts AW, Chen J, Kuron G, Hunt V, Huff J, Huffman C, et al. Mevinolin: a highly potent competitive inhibitor of hydroxymethylglutaryl-coenzyme a reductase and a cholesterol-lowering agent. Proc Natl Acad Sci USA 1980; 77:3957-3961.
-
(1980)
Proc Natl Acad Sci USA
, vol.77
, pp. 3957-3961
-
-
Alberts, A.W.1
Chen, J.2
Kuron, G.3
Hunt, V.4
Huff, J.5
Huffman, C.6
-
61
-
-
0003042048
-
Mevinolin, an inhibitor of cholesterol synthesis, induces mRNA for low density lipoprotein receptor in livers of hamsters and rabbits
-
61 Ma PT, Gil G, Sudhof TC, Bilheimer DW, Goldstein JL, Brown MS. Mevinolin, an inhibitor of cholesterol synthesis, induces mRNA for low density lipoprotein receptor in livers of hamsters and rabbits. Proc Natl Acad Sci USA 1986; 83:8370-8374.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 8370-8374
-
-
Ma, P.T.1
Gil, G.2
Sudhof, T.C.3
Bilheimer, D.W.4
Goldstein, J.L.5
Brown, M.S.6
-
62
-
-
0030776160
-
Treatment goals for low-density lipoprotein cholesterol in the secondary prevention of coronary heart disease. Absolute levels or extent of lowering?
-
62 Cullen P, Assmann G. Treatment goals for low-density lipoprotein cholesterol in the secondary prevention of coronary heart disease. absolute levels or extent of lowering? Am J Cardiol 1997; 80:1287-1294.
-
(1997)
Am J Cardiol
, vol.80
, pp. 1287-1294
-
-
Cullen, P.1
Assmann, G.2
-
63
-
-
0028792392
-
High-throughput genotyping using horizontal polyacrylamide gels with wells arranged for microplate array diagonal gel electrophoresis (MADGE)
-
63 Day IN, Humphries SE, Richards S, Norton D, Reid M. High-throughput genotyping using horizontal polyacrylamide gels with wells arranged for microplate array diagonal gel electrophoresis (MADGE). Biotechniques 1995; 19:830-835.
-
(1995)
Biotechniques
, vol.19
, pp. 830-835
-
-
Day, I.N.1
Humphries, S.E.2
Richards, S.3
Norton, D.4
Reid, M.5
-
64
-
-
0031717848
-
A multilocus genotyping assay for cardiovascular disease
-
64 Cheng S, Pallaud C, Grow MA, Scharf SJ, Erlich HA, Kitz W, et al. A multilocus genotyping assay for cardiovascular disease. Clin Chem Lab Med 1998; 36:561-566.
-
(1998)
Clin Chem Lab Med
, vol.36
, pp. 561-566
-
-
Cheng, S.1
Pallaud, C.2
Grow, M.A.3
Scharf, S.J.4
Erlich, H.A.5
Kitz, W.6
-
65
-
-
0027026881
-
Molecular genetics of the LDL receptor gene in familial hypercholesterolemia
-
65 Hobbs HH, Brown MS, Goldstein JL. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia. Hum Mutat 1992; 1:445-446
-
(1992)
Hum Mutat
, vol.1
, pp. 445-446
-
-
Hobbs, H.H.1
Brown, M.S.2
Goldstein, J.L.3
-
66
-
-
0029046417
-
Homozygosity for a splice junction mutation in exon 8 of the gene encoding lysosomal acid lipase
-
A Spanish kindred with cholesterol ester storage disease (CESD)
-
66 Muntoni S, Wiebusch H, Funke H, Ros E, Seedorf U, Assmann G. Homozygosity for a splice junction mutation in exon 8 of the gene encoding lysosomal acid lipase. In: A Spanish kindred with cholesterol ester storage disease (CESD). Hum Genet 1995; 95:491-49.
-
(1995)
Hum Genet
, vol.95
, pp. 491-549
-
-
Muntoni, S.1
Wiebusch, H.2
Funke, H.3
Ros, E.4
Seedorf, U.5
Assmann, G.6
-
67
-
-
0028937337
-
Plasma cholesteryl ester transfer protein and high-density lipoproteins: New insights from molecular genetic studies
-
67 Tall AR. Plasma cholesteryl ester transfer protein and high-density lipoproteins: new insights from molecular genetic studies. J Intern Med 1995; 237:5-12.
-
(1995)
J Intern Med
, vol.237
, pp. 5-12
-
-
Tall, A.R.1
|