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The Pharmacogenomics Journal
|
August 28, 2002
Efficient discovery of single-nucleotide polymorphisms in coding regions of human genes
G Hu, B Modrek, H M F Riise Stensland, et al.
American Journal of Human Genetics
|
June 19, 2001
Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups
M Perola, M Ohman, T Hiekkalinna, et al.
Atherosclerosis
|
March 21, 1997
Serum complement and familial combined hyperlipidemia
K Ylitalo, K V Porkka, S Meri, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
March 17, 2001
Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL
P Pajukanta, J S Bodnar, R Sallinen, et al.
Journal of Medical Genetics
|
April 14, 2005
A male-specific quantitative trait locus on 1p21 controlling human stature
S Sammalisto, T Hiekkalinna, E Suviolahti, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
May 1, 1997
No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families
P Pajukanta, K V Porkka, M Antikainen, et al.
Nature Genetics
|
April 16, 1998
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23
P Pajukanta, I Nuotio, J D Terwilliger, et al.
American Journal of Human Genetics
|
April 17, 1999
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels
P Pajukanta, J D Terwilliger, M Perola, et al.
Diabetologia
|
November 1, 2007
TCF7L2 is associated with high serum triacylglycerol and differentially expressed in adipose tissue in families with familial combined hyperlipidaemia
A Huertas-Vazquez, C Plaisier, D Weissglas-Volkov, et al.
American Journal of Human Genetics
|
November 15, 2000
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland
P Pajukanta, M Cargill, L Viitanen, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
The Pharmacogenomics Journal
|
August 28, 2002
Efficient discovery of single-nucleotide polymorphisms in coding regions of human genes
G Hu, B Modrek, H M F Riise Stensland, et al.
American Journal of Human Genetics
|
June 19, 2001
Quantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups
M Perola, M Ohman, T Hiekkalinna, et al.
Atherosclerosis
|
March 21, 1997
Serum complement and familial combined hyperlipidemia
K Ylitalo, K V Porkka, S Meri, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
March 17, 2001
Fine mapping of Hyplip1 and the human homolog, a potential locus for FCHL
P Pajukanta, J S Bodnar, R Sallinen, et al.
Journal of Medical Genetics
|
April 14, 2005
A male-specific quantitative trait locus on 1p21 controlling human stature
S Sammalisto, T Hiekkalinna, E Suviolahti, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
May 1, 1997
No evidence of linkage between familial combined hyperlipidemia and genes encoding lipolytic enzymes in Finnish families
P Pajukanta, K V Porkka, M Antikainen, et al.
Nature Genetics
|
April 16, 1998
Linkage of familial combined hyperlipidaemia to chromosome 1q21-q23
P Pajukanta, I Nuotio, J D Terwilliger, et al.
American Journal of Human Genetics
|
April 17, 1999
Genomewide scan for familial combined hyperlipidemia genes in finnish families, suggesting multiple susceptibility loci influencing triglyceride, cholesterol, and apolipoprotein B levels
P Pajukanta, J D Terwilliger, M Perola, et al.
Diabetologia
|
November 1, 2007
TCF7L2 is associated with high serum triacylglycerol and differentially expressed in adipose tissue in families with familial combined hyperlipidaemia
A Huertas-Vazquez, C Plaisier, D Weissglas-Volkov, et al.
American Journal of Human Genetics
|
November 15, 2000
Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland
P Pajukanta, M Cargill, L Viitanen, et al.
Page
of 3