-
1
-
-
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., Bierman, E.L. and Motulsky, A.G. (1973) 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, 1544-1568.
-
(1973)
J. Clin. Invest.
, vol.52
, pp. 1544-1568
-
-
Goldstein, J.L.1
Schrott, H.G.2
Hazzard, W.R.3
Bierman, E.L.4
Motulsky, A.G.5
-
2
-
-
0015914934
-
Family study of serum lipids and lipoproteins in coronary heart-disease
-
Nikkila, E.A. and Aro, A. (1973) Family study of serum lipids and lipoproteins in coronary heart-disease. Lancet, 1, 954-959.
-
(1973)
Lancet
, vol.1
, pp. 954-959
-
-
Nikkila, E.A.1
Aro, A.2
-
3
-
-
0025970749
-
Familial combined hyperlipidaemia linked to the apolipoprotein AI-CII-AIV gene cluster on chromosome 11q23-q24
-
Wojciechowski, A.P., Farrall, M., Cullen, P., Wilson, T.M., Bayliss, J.D., Farren, B., Griffin, B.A., Caslake, M.J., Packard, C.J., Shepherd, J. et al. (1991) Familial combined hyperlipidaemia linked to the apolipoprotein AI-CII-AIV gene cluster on chromosome 11q23-q24. Nature, 349, 161-164.
-
(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
-
4
-
-
0032698344
-
Linkage of a candidate gene locus to familial combined hyperlipidemia: Lecithin: Cholesterol acyltransferase on 16q
-
Aouizerat, B.E., Allayee, H., Cantor, R.M., Dallinga-Thie, G.M., Lanning, C.D., de Bruin, T.W., Lusis, A.J. and Rutter, J.I. (1999) Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin: Cholesterol acyltransferase on 16q. Arterioscler. Thromb. Vasc. Biol., 19, 2730-2736.
-
(1999)
Arterioscler. Thromb. Vasc. Biol.
, vol.19
, pp. 2730-2736
-
-
Aouizerat, B.E.1
Allayee, H.2
Cantor, R.M.3
Dallinga-Thie, G.M.4
Lanning, C.D.5
de Bruin, T.W.6
Lusis, A.J.7
Rutter, J.I.8
-
5
-
-
0033362160
-
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels
-
Pajukanta, P., Terwilliger, J.D., Perola, M., Hiekkalinna, T., Nuotio, I., Ellonen, P., Parkkonen, M., Hartiala, J., Ylitalo, K., Pihlajamaki, J. et al. (1999) Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels. Am. J. Hum. Genet., 64, 1453-1463.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1453-1463
-
-
Pajukanta, P.1
Terwilliger, J.D.2
Perola, M.3
Hiekkalinna, T.4
Nuotio, I.5
Ellonen, P.6
Parkkonen, M.7
Hartiala, J.8
Ylitalo, K.9
Pihlajamaki, J.10
-
6
-
-
12144287541
-
Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1)
-
Pajukanta, P., Lilja, H.E., Sinsheimer, J.S., Cantor, R.M., Lusis, A.J., Gentile, M., Duan, X.J., Soro-Paavonen, A., Naukkarinen, J., Saarela, J. et al. (2004) Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1). Nat. Genet., 36, 371-376.
-
(2004)
Nat. Genet.
, vol.36
, pp. 371-376
-
-
Pajukanta, P.1
Lilja, H.E.2
Sinsheimer, J.S.3
Cantor, R.M.4
Lusis, A.J.5
Gentile, M.6
Duan, X.J.7
Soro-Paavonen, A.8
Naukkarinen, J.9
Saarela, J.10
-
7
-
-
4344641316
-
Variation in USF1 shows haplotype effects, gene:gene and gene: Environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II
-
Putt, W., Palmen, J., Nicaud, V., Tregouet, D.A., Tahri-Daizadeh, N., Flavell, D.M., Humphries, S.E. and Talmud, P.J. (2004) Variation in USF1 shows haElotype effects, gene:gEne and gene: environment associations with glucose and lipid parameters in the European Atherosclerosis Research Study II. Hum. Mol. Genet., 13, 1587-1597.
-
(2004)
Hum. Mol. Genet.
, vol.13
, pp. 1587-1597
-
-
Putt, W.1
Palmen, J.2
Nicaud, V.3
Tregouet, D.A.4
Tahri-Daizadeh, N.5
Flavell, D.M.6
Humphries, S.E.7
Talmud, P.J.8
-
8
-
-
0033593229
-
Essential role in vivo of upstream stimulatory factors for a normal dietary response of the fatty acid synthase gene in the liver
-
Casado, M., Vallet, V.S., Kahn, A. and Vaulont, S. (1999) Essential role in vivo of upstream stimulatory factors for a normal dietary response of the fatty acid synthase gene in the liver. J. Biol. Chem. 274, 2009-2013.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 2009-2013
-
-
Casado, M.1
Vallet, V.S.2
Kahn, A.3
Vaulont, S.4
-
9
-
-
0033556309
-
Cooperative binding of upstream stimulatory factor and hepatic nuclear factor 4 drives the transcription of the human apolipoprotein A-II gene
-
Ribeiro, A., Pastier, D., Kardassis, D., Chambaz, J. and Cardot, P. (1999) Cooperative binding of upstream stimulatory factor and hepatic nuclear factor 4 drives the transcription of the human apolipoprotein A-II gene. J. Biol. Chem., 274, 1216-1225.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 1216-1225
-
-
Ribeiro, A.1
Pastier, D.2
Kardassis, D.3
Chambaz, J.4
Cardot, P.5
-
10
-
-
0030447827
-
Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasia
-
Groenen, P.M., Garcia, E., Debeer, P., Devriendt, K., Fryns, J.P. and Van de Ven, W.J. (1996) Structure, sequence, and chromosome 19 localization of human USF2 and its rearrangement in a patient with multicystic renal dysplasia. Genomics, 38, 141-148.
-
(1996)
Genomics
, vol.38
, pp. 141-148
-
-
Groenen, P.M.1
Garcia, E.2
Debeer, P.3
Devriendt, K.4
Fryns, J.P.5
Van de Ven, W.J.6
-
11
-
-
0042074140
-
Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: A case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study
-
Hopkins, P.N., Heiss, G., Ellison, R.C., Province, M.A., Pankow, J.S., Eckfeldt, J.H. and Hunt, S.C. (2003) Coronary artery disease risk in familial combined hyperlipidemia and familial hypertriglyceridemia: A case-control comparison from the National Heart, Lung, and Blood Institute Family Heart Study. Circulation, 108, 519-523.
-
(2003)
Circulation
, vol.108
, pp. 519-523
-
-
Hopkins, P.N.1
Heiss, G.2
Ellison, R.C.3
Province, M.A.4
Pankow, J.S.5
Eckfeldt, J.H.6
Hunt, S.C.7
-
12
-
-
0033772073
-
Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus
-
Horikawa, Y., Oda, N., Cox, N.J., Li, X., Orho-Melander, M., Hara, M., Hinokio, Y., Lindner, T.H., Mashima, H., Schwarz, P.E. et al. (2000) Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus. Nat. Genet., 26, 163-175.
-
(2000)
Nat. Genet.
, vol.26
, pp. 163-175
-
-
Horikawa, Y.1
Oda, N.2
Cox, N.J.3
Li, X.4
Orho-Melander, M.5
Hara, M.6
Hinokio, Y.7
Lindner, T.H.8
Mashima, H.9
Schwarz, P.E.10
-
13
-
-
0034785352
-
Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease
-
Rioux, J.D., Daly, M.J., Silverberg, M.S., Lindblad, K., Steinhart, H., Cohen, Z., Delmonte, T., Kocher, K., Miller, K., Guschwan, S. et al. (2001) Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease. Nat. Genet., 29, 223-228.
-
(2001)
Nat. Genet.
, vol.29
, pp. 223-228
-
-
Rioux, J.D.1
Daly, M.J.2
Silverberg, M.S.3
Lindblad, K.4
Steinhart, H.5
Cohen, Z.6
Delmonte, T.7
Kocher, K.8
Miller, K.9
Guschwan, S.10
-
14
-
-
1842535898
-
USF1 on trial
-
Shoulders, C.C. (2004) USF1 on trial. Nat. Genet., 36, 322-323.
-
(2004)
Nat. Genet.
, vol.36
, pp. 322-323
-
-
Shoulders, C.C.1
-
15
-
-
0028869928
-
Upstream stimulatory factor proteins are major components of the glucose response complex of the L-type pyruvate kinase gene promoter
-
Lefrancois-Martinez, A.M., Martinez, A., Antoine, B., Raymondjean, M. and Kahn, A. (1995) Upstream stimulatory factor proteins are major components of the glucose response complex of the L-type pyruvate kinase gene promoter. J. Biol. Chem., 270, 2640-2643.
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 2640-2643
-
-
Lefrancois-Martinez, A.M.1
Martinez, A.2
Antoine, B.3
Raymondjean, M.4
Kahn, A.5
-
16
-
-
0030051159
-
Immunochemical characterization and transacting properties of upstream stimulatory factor isoforms
-
Viollet, B., Lefrancois-Martinez, A.M., Henrion, A., Kahn, A., Raymondjean, M. and Martinez, A. (1996) Immunochemical characterization and transacting properties of upstream stimulatory factor isoforms. J. Biol. Chem., 271, 1405-1415.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 1405-1415
-
-
Viollet, B.1
Lefrancois-Martinez, A.M.2
Henrion, A.3
Kahn, A.4
Raymondjean, M.5
Martinez, A.6
-
17
-
-
0036185842
-
The E-box motif in the proximal ABCA1 promoter mediates transcriptional repression of the ABCA1 gene
-
Yang, X.P., Freeman, L.A., Knapper, C.L., Amar, M.J., Remaley, A., Brewer, H.B., Jr and Santamarina-Fojo, S. (2002) The E-box motif in the proximal ABCA1 promoter mediates transcriptional repression of the ABCA1 gene. J. Lipid. Res., 43, 297-306.
-
(2002)
J. Lipid Res.
, vol.43
, pp. 297-306
-
-
Yang, X.P.1
Freeman, L.A.2
Knapper, C.L.3
Amar, M.J.4
Remaley, A.5
Brewer Jr., H.B.6
Santamarina-Fojo, S.7
-
18
-
-
0030731510
-
Molecular variation of the human angiotensinogen core promoter element located between the TATA box and transcription initiation site affects its transcriptional activity
-
Yanai, K., Saito, T., Hirota, K., Kobayashi, H., Murakami, K. and Fukamizu, A. (1997) Molecular variation of the human angiotensinogen core promoter element located between the TATA box and transcription initiation site affects its transcriptional activity. J. Biol. Chem. 272, 30558-30562.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 30558-30562
-
-
Yanai, K.1
Saito, T.2
Hirota, K.3
Kobayashi, H.4
Murakami, K.5
Fukamizu, A.6
-
19
-
-
0037444792
-
Identification of a non-canonical E-box motif as a regulatory element in the proximal promoter region of the apolipoprotein E gene
-
Salero, E., Gimenez, C. and Zafra, F. (2003) Identification of a non-canonical E-box motif as a regulatory element in the proximal promoter region of the apolipoprotein E gene. Biochem. J., 370 979-986.
-
(2003)
Biochem. J.
, vol.370
, pp. 979-986
-
-
Salero, E.1
Gimenez, C.2
Zafra, F.3
-
20
-
-
13444256227
-
Insulin-mediated down-regulation of apolipoprotein A5 gene expression through the phosphatidylinositol 3-kinase pathway: Role of upstream stimulatory factor
-
Nowak, M., Helleboid-Chapman, A., Jakel, H., Martin, G., Duran-Sandoval, D., Staels, B., Rubin, E.M., Pennacchio, L.A., Taskinen, M.R., Fruchart-Najib, J. et al. (2005) Insulin-mediated down-regulation of apolipoprotein A5 gene expression through the phosphatidylinositol 3-kinase pathway: Role of upstream stimulatory factor. Mol. Cell. Biol., 25, 1537-1548.
-
(2005)
Mol. Cell. Biol.
, vol.25
, pp. 1537-1548
-
-
Nowak, M.1
Helleboid-Chapman, A.2
Jakel, H.3
Martin, G.4
Duran-Sandoval, D.5
Staels, B.6
Rubin, E.M.7
Pennacchio, L.A.8
Taskinen, M.R.9
Fruchart-Najib, J.10
-
21
-
-
2542469144
-
Use and abuse of HOMA modeling
-
Wallace, T.M., Levy, J.C. and Matthews, D.R. (2004) Use and abuse of HOMA modeling. Diabetes Care, 27, 1487-1495.
-
(2004)
Diabetes Care
, vol.27
, pp. 1487-1495
-
-
Wallace, T.M.1
Levy, J.C.2
Matthews, D.R.3
-
22
-
-
0025954028
-
In vivo regulation of the activity of the two promoters of the rat acetyl coenzyme-A carboxylase gene
-
Lopez-Casillas, F., Ponce-Castaneda, M.V. and Kim, K.H. (1991) In vivo regulation of the activity of the two promoters of the rat acetyl coenzyme-A carboxylase gene. Endocrinology, 129, 1049-1058.
-
(1991)
Endocrinology
, vol.129
, pp. 1049-1058
-
-
Lopez-Casillas, F.1
Ponce-Castaneda, M.V.2
Kim, K.H.3
-
23
-
-
0038054341
-
PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes
-
Mootha, V.K., Lindgren, C.M., Eriksson, K.F., Subramanian, A., Sihag, S., Lehar, J., Puigserver, P., Carlsson, E., Ridderstrale, M., Laurila, E. et al. (2003) PGC-1alpha-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes. Nat. Genet., 34, 267-273.
-
(2003)
Nat. Genet.
, vol.34
, pp. 267-273
-
-
Mootha, V.K.1
Lindgren, C.M.2
Eriksson, K.F.3
Subramanian, A.4
Sihag, S.5
Lehar, J.6
Puigserver, P.7
Carlsson, E.8
Ridderstrale, M.9
Laurila, E.10
-
24
-
-
0037224449
-
Identifying distinct classes of bladder carcinoma using microarrays
-
Dyrskjot, L., Thykjaer, T., Kruhoffer, M., Jensen, J.L., Marcussen, N., Hamilton-Dutoit, S., Wolf, H. and Orntoft, T.F. (2003) Identifying distinct classes of bladder carcinoma using microarrays. Nat. Genet. 33, 90-96.
-
(2003)
Nat. Genet.
, vol.33
, pp. 90-96
-
-
Dyrskjot, L.1
Thykjaer, T.2
Kruhoffer, M.3
Jensen, J.L.4
Marcussen, N.5
Hamilton-Dutoit, S.6
Wolf, H.7
Orntoft, T.F.8
-
25
-
-
4444238183
-
Essential role of vascular endothelial growth factor in angiotensin II-induced vascular inflammation and remodeling
-
Zhao, Q., Ishibashi, M., Hiasa, K., Tan, C., Takeshita, A. and Egashira, K. (2004) Essential role of vascular endothelial growth factor in angiotensin II-induced vascular inflammation and remodeling. Hypertension, 44, 264-270.
-
(2004)
Hypertension
, vol.44
, pp. 264-270
-
-
Zhao, Q.1
Ishibashi, M.2
Hiasa, K.3
Tan, C.4
Takeshita, A.5
Egashira, K.6
-
26
-
-
0036321948
-
ATP-binding cassette transporter A1 and cholesterol trafficking
-
Oram, J.F. (2002) ATP-binding cassette transporter A1 and cholesterol trafficking. Curr. Opin. Lipidol., 13, 373-381.
-
(2002)
Curr. Opin. Lipidol.
, vol.13
, pp. 373-381
-
-
Oram, J.F.1
-
27
-
-
0032813808
-
Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency
-
Brooks-Wilson, A., Marcil, M., Clee, S.M., Zhang, L.H., Roomp, K., van Dam, M., Yu, L., Brewer, C., Collins, J.A., Molhuizen, H.O. et al. (1999) Mutations in ABC1 in Tangier disease and familial high-density lipoprotein deficiency. Nat. Genet., 22, 336-345.
-
(1999)
Nat. Genet.
, vol.22
, pp. 336-345
-
-
Brooks-Wilson, A.1
Marcil, M.2
Clee, S.M.3
Zhang, L.H.4
Roomp, K.5
van Dam, M.6
Yu, L.7
Brewer, C.8
Collins, J.A.9
Molhuizen, H.O.10
-
28
-
-
0026592806
-
Spontaneous hypercholesterolemia and arterial lesions in mice lacking apolipoprotein E
-
Zhang, S.H., Reddick, R.L., Piedrahita, J.A. and Maeda, N. (1992) Spontaneous hypercholesterolemia and arterial lesions in mice lacking apolipoprotein E. Science, 258, 468-471.
-
(1992)
Science
, vol.258
, pp. 468-471
-
-
Zhang, S.H.1
Reddick, R.L.2
Piedrahita, J.A.3
Maeda, N.4
-
29
-
-
0025940314
-
Lipoprotein lipase enhances the binding of chylomicrons to low density lipoprotein receptor-related protein
-
Beisiegel, U., Weber, W. and Bengtsson-Olivecrona, G. (1991) Lipoprotein lipase enhances the binding of chylomicrons to low density lipoprotein receptor-related protein. Proc. Natl Acad. Sci. USA, 88, 8342-8346.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 8342-8346
-
-
Beisiegel, U.1
Weber, W.2
Bengtsson-Olivecrona, G.3
-
30
-
-
0024299370
-
Apolipoprotein E: Cholesterol transport protein with expanding role in cell biology
-
Mahley, R.W. (1988) Apolipoprotein E: Cholesterol transport protein with expanding role in cell biology. Science, 240, 622-630.
-
(1988)
Science
, vol.240
, pp. 622-630
-
-
Mahley, R.W.1
-
31
-
-
0026531139
-
Overexpression of apolipoprotein E in transgenic mice: Marked reduction in plasma lipoproteins except high density lipoprotein and resistance against diet-induced hypercholesterolemia
-
Shimano, H., Yamada, N., Katsuki, M., Shimada, M., Gotoda, T., Harada, K., Murase, T., Fukazawa, C., Takaku, F. and Yazaki, Y. (1992) Overexpression of apolipoprotein E in transgenic mice: Marked reduction in plasma lipoproteins except high density lipoprotein and resistance against diet-induced hypercholesterolemia. Proc. Natl Acad. Sci. USA 89, 1750-1754.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 1750-1754
-
-
Shimano, H.1
Yamada, N.2
Katsuki, M.3
Shimada, M.4
Gotoda, T.5
Harada, K.6
Murase, T.7
Fukazawa, C.8
Takaku, F.9
Yazaki, Y.10
-
32
-
-
0642338120
-
Induction of atherosclerosis by human chylomicron remnants: A hypothesis
-
Wilhelm, M.G. and Cooper, A.D. (2003) Induction of atherosclerosis by human chylomicron remnants: A hypothesis. J. Atheroscler. Thromb., 10, 132-139.
-
(2003)
J. Atheroscler. Thromb.
, vol.10
, pp. 132-139
-
-
Wilhelm, M.G.1
Cooper, A.D.2
-
33
-
-
0042974264
-
Molecular mechanisms of type III hyperlipoproteinemia: The contribution of the carboxy-terminal domain of ApoE can account for the dyslipidemia that is associated with the E2/E2 phenotype
-
Kypreos, K.E., Li, X., van Dijk, K.W., Havekes, L.M. and Zannis, V.I. (2003) Molecular mechanisms of type III hyperlipoproteinemia: The contribution of the carboxy-terminal domain of ApoE can account for the dyslipidemia that is associated with the E2/E2 phenotype. Biochemistry, 42, 9841-9853.
-
(2003)
Biochemistry
, vol.42
, pp. 9841-9853
-
-
Kypreos, K.E.1
Li, X.2
van Dijk, K.W.3
Havekes, L.M.4
Zannis, V.I.5
-
34
-
-
0026718601
-
The role of apolipoprotein E genetic variants in lipoprotein disorders
-
Rall, S.C., Jr and Mahley, R.W. (1992) The role of apolipoprotein E genetic variants in lipoprotein disorders. J. Intern. Med., 231 653-659.
-
(1992)
J. Intern. Med.
, vol.231
, pp. 653-659
-
-
Rall Jr., S.C.1
Mahley, R.W.2
-
35
-
-
11244275436
-
Impaired recycling of apolipoprotein E4 is associated with intracellular cholesterol accumulation
-
Heeren, J., Grewal, T., Laatsch, A., Becker, N., Rinninger, F., Rye, K.A. and Beisiegel, U. (2004) Impaired recycling of apolipoprotein E4 is associated with intracellular cholesterol accumulation. J. Biol. Chem., 279, 55483-55492.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 55483-55492
-
-
Heeren, J.1
Grewal, T.2
Laatsch, A.3
Becker, N.4
Rinninger, F.5
Rye, K.A.6
Beisiegel, U.7
-
36
-
-
0027954497
-
Cloning of human acetyl-CoA carboxylase cDNA
-
Ha, J., Daniel, S., Kong, I.S., Park, C.K., Tae, H.J. and Kim, K.H. (1994) Cloning of human acetyl-CoA carboxylase cDNA. Eur. J. Biochem. 219, 297-306.
-
(1994)
Eur. J. Biochem.
, vol.219
, pp. 297-306
-
-
Ha, J.1
Daniel, S.2
Kong, I.S.3
Park, C.K.4
Tae, H.J.5
Kim, K.H.6
-
37
-
-
18344386779
-
Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families
-
Soro, A., Pajukanta, P., Lilja, H.E., Ylitalo, K., Hiekkalinna, T., Perola, M., Cantor, R.M., Viikari, J.S., Taskinen, M.R. and Peltonen, L. (2002) Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families. Am. J. Hum. Genet., 70, 1333-1340.
-
(2002)
Am. J. Hum. Genet.
, vol.70
, pp. 1333-1340
-
-
Soro, A.1
Pajukanta, P.2
Lilja, H.E.3
Ylitalo, K.4
Hiekkalinna, T.5
Perola, M.6
Cantor, R.M.7
Viikari, J.S.8
Taskinen, M.R.9
Peltonen, L.10
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