-
2
-
-
0026762806
-
Familial lipoprotein disorders in patients with premature coronary artery disease
-
(1992)
Circulation
, vol.85
, pp. 2025-2033
-
-
Genest J.J., Jr.1
Martin-Munley, S.S.2
McNamara, J.R.3
Ordovas, J.M.4
Jenner, J.5
Myers, R.H.6
Silberman, S.R.7
Wilson, P.W.8
Salem, D.N.9
Schaefer, E.J.10
-
4
-
-
0031918837
-
Linkage of familial combined hyperlipidemia to chromosome 1q21-q23
-
(1998)
Nat Genet
, vol.18
, pp. 369-373
-
-
Pajukanta, P.1
Nuotio, I.2
Terwilliger, J.D.3
Porkka, K.V.K.4
Ylitalo, K.5
Pihlajamaki, J.6
Suomalainen, A.J.7
Syvanen, A.-C.8
Lehtimaki, T.9
Viikari, J.S.A.10
-
5
-
-
0031916999
-
Mapping a gene for combined hyperlipidaemia in a mutant mouse strain
-
(1998)
Nat Genet
, vol.18
, pp. 374-377
-
-
Castellani, L.W.1
Weinreb, A.2
Bodnar, J.3
Gotto, A.M.4
Doolittle, M.5
Mehrabian, M.6
Demant, P.7
Lusis, A.J.8
-
6
-
-
0025970749
-
Familial combined hyperlipidemia linked to the apolipoprotein AI-CII-AIV gene cluster on chromosome 11q23-q24
-
(1991)
Nature
, vol.349
, pp. 161-164
-
-
Wojciechowski, A.P.1
Farrall, M.2
Cullen, P.3
Wilson, T.M.4
Bayliss, J.D.5
Farren, B.6
Griffin, B.A.7
Caslake, M.J.8
Packard, C.J.9
Shepherd, J.10
-
7
-
-
0032231670
-
Families with familial combined hyperlipidemia and families enriched for coronary artery disease share genetic determinants for the atherogenic lipoprotein phenotype
-
(1998)
Am J Hum Genet
, vol.63
, pp. 577-585
-
-
Alayee, H.1
Aouizerat, B.E.2
Cantor, R.M.3
Dallinga-Thie, G.M.4
Krauss, R.M.5
Lanning, C.D.6
Rotter, J.I.7
Lusis, A.J.8
De Bruin, T.W.9
-
10
-
-
0031797460
-
Haplotypes of the apoA-I/C-III/A-IV gene cluster and familial combined hyperlipidemia
-
(1998)
Arterioscler Thromb Vasc Biol
, vol.18
, pp. 1810-1817
-
-
Tahvanainen, E.1
Pajukanta, P.2
Porkka, K.3
Nieminen, S.4
Ikavalko, L.5
Nuotio, I.6
Taskinen, M.R.7
Peltonen, L.8
Ehnholm, C.9
-
14
-
-
17444444680
-
Gender-related association between the -93T→G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia
-
(1998)
Atherosclerosis
, vol.138
, pp. 91-99
-
-
Hoffer, M.J.1
Bredie, S.J.2
Snieder, H.3
Reymer, P.W.4
Demacker, P.N.5
Havekes, L.M.6
Boomsma, D.I.7
Stalenhoef, A.F.8
Frants, R.R.9
Kastelein, J.J.10
-
16
-
-
0029142759
-
A frequently occurring mutation in the lipoprotein lipase gene (Asn291Ser) contributes to the expression of familial combined hyperlipidemia
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1543-1549
-
-
Reymer, P.W.1
Groenemeyer, B.E.2
Gagne, E.3
Miao, L.4
Appelman, E.E.5
Seidel, J.C.6
Kromhout, D.7
Bijvoet, S.M.8
Van de Oever, K.9
Bruin, T.10
-
18
-
-
16944363110
-
No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families
-
(1997)
Arterioscler Thromb Vasc Biol
, vol.17
, pp. 841-850
-
-
Pajukanta, P.1
Porkka, K.V.2
Antikainen, M.3
Taskinen, M.R.4
Perola, M.5
Murtomaki-Repo, S.6
Ehnholm, S.7
Nuotio, I.8
Suurinkeroinen, L.9
Lahdenkari, A.T.10
-
19
-
-
0029941114
-
NHLBI family heart study: Objectives and design
-
(1996)
Am J Epidemiol
, vol.143
, pp. 1219-1228
-
-
Higgins, M.1
Province, M.2
Heiss, G.3
Eckfeldt, J.4
Ellison, R.C.5
Folsom, A.R.6
Rao, D.C.7
Sprafka, M.8
Williams, R.9
-
20
-
-
0007678820
-
-
NHLBI Family Heart Study: Manuals of Procedure. St. Louis, Mo: Washington University
-
(1993)
-
-
-
24
-
-
15844419531
-
Quantitative trait locus mapping of human blood pressure to a genetic region at or near the lipoprotein lipase gene locus on chromosome 8p22
-
(1996)
J Clin Invest
, vol.97
, pp. 2111-2118
-
-
Wu, D.A.1
Bu, X.2
Warden, C.H.3
Shen, D.D.4
Jeng, C.Y.5
Sheu, W.H.6
Fuh, M.M.7
Katsuya, T.8
Dzau, V.J.9
Reaven, G.M.10
-
31
-
-
85037950271
-
-
Pedigree Analysis Package, Revision 4.0. Salt Lake City, Utah: Department of Human Genetics, University of Utah
-
(1994)
-
-
Hasstedt, S.J.1
-
34
-
-
85037927699
-
-
SAS User's Guide, Version 6.03. Cary, NC: Statistical Analysis Institute
-
(1988)
-
-
-
36
-
-
2542509443
-
The human apM-1, an adipocyte-specific gene linked to the family of TNF's and to genes expressed in activated T cells, is mapped to chromosome 1q21.3-q23, a susceptibility locus identified for familial combined hyperlipidemia (FCH)
-
(1999)
Biochem Biophys Res Commun
, vol.260
, pp. 416-425
-
-
Schaffler, A.1
Orso, E.2
Palitzsch, K.D.3
Buchler, C.4
Drobnik, W.5
Furst, A.6
Scholmerich, J.7
Schmitz, G.8
|