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Page 1
Serum complement and familial combined hyperlipidemia.
Ylitalo K, Porkka KV, Meri S, Nuotio I, Suurinkeroinen L, Vakkilainen J, Pajukanta P, Viikari JS, Peltonen L, Ehnholm C, Taskinen MR. Ylitalo K, et al. Among authors: pajukanta p. Atherosclerosis. 1997 Mar 21;129(2):271-7. doi: 10.1016/s0021-9150(96)06054-6. Atherosclerosis. 1997. PMID: 9105570
No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families.
Pajukanta P, Porkka KV, Antikainen M, Taskinen MR, Perola M, Murtomäki-Repo S, Ehnholm S, Nuotio I, Suurinkeroinen L, Lahdenkari AT, Syvänen AC, Viikari JS, Ehnholm C, Peltonen L. Pajukanta P, et al. Arterioscler Thromb Vasc Biol. 1997 May;17(5):841-50. doi: 10.1161/01.atv.17.5.841. Arterioscler Thromb Vasc Biol. 1997. PMID: 9157946
Phenotype expression in familial combined hyperlipidemia.
Porkka KV, Nuotio I, Pajukanta P, Ehnholm C, Suurinkeroinen L, Syvänne M, Lehtimäki T, Lahdenkari AT, Lahdenperä S, Ylitalo K, Antikainen M, Perola M, Raitakari OT, Kovanen P, Viikari JS, Peltonen L, Taskinen MR. Porkka KV, et al. Among authors: pajukanta p. Atherosclerosis. 1997 Sep;133(2):245-53. doi: 10.1016/s0021-9150(97)00134-2. Atherosclerosis. 1997. PMID: 9298685
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23.
Pajukanta P, Nuotio I, Terwilliger JD, Porkka KV, Ylitalo K, Pihlajamäki J, Suomalainen AJ, Syvänen AC, Lehtimäki T, Viikari JS, Laakso M, Taskinen MR, Ehnholm C, Peltonen L. Pajukanta P, et al. Nat Genet. 1998 Apr;18(4):369-73. doi: 10.1038/ng0498-369. Nat Genet. 1998. PMID: 9537421
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels.
Pajukanta P, Terwilliger JD, Perola M, Hiekkalinna T, Nuotio I, Ellonen P, Parkkonen M, Hartiala J, Ylitalo K, Pihlajamäki J, Porkka K, Laakso M, Viikari J, Ehnholm C, Taskinen MR, Peltonen L. Pajukanta P, et al. Am J Hum Genet. 1999 May;64(5):1453-63. doi: 10.1086/302365. Am J Hum Genet. 1999. PMID: 10205279 Free PMC article.
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.
Pajukanta P, Cargill M, Viitanen L, Nuotio I, Kareinen A, Perola M, Terwilliger JD, Kempas E, Daly M, Lilja H, Rioux JD, Brettin T, Viikari JS, Rönnemaa T, Laakso M, Lander ES, Peltonen L. Pajukanta P, et al. Am J Hum Genet. 2000 Dec;67(6):1481-93. doi: 10.1086/316902. Epub 2000 Nov 13. Am J Hum Genet. 2000. PMID: 11078477 Free PMC article.
157 results