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Der Internist
|
August 1, 1980
[Prediction and early diagnosis of coronary disease. Prospective epidemiologic study of industrial workers in Westphalia]
G Assmann, W Oberwittler, H Schulte, et al.
Nucleic Acids Research
|
November 11, 1986
Deletion polymorphism 5' to the human apolipoprotein AI (apo AI) gene
P M Frossard, R T Coleman, A A Protter, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
December 1, 1994
A nonsense mutation in the apolipoprotein A-I gene is associated with high-density lipoprotein deficiency and periorbital xanthelasmas
R Römling, A von Eckardstein, H Funke, et al.
Personalized Medicine
|
May 23, 2018
Platform evaluation for rapid genotyping of CYP2C9 and VKORC1 alleles
Victoria A Joshi, Elizabeth Duffy, Birgit H Funke, et al.
Nucleic Acids Research
|
May 27, 1986
Pvu II RFLP in the 5' of the human apolipoprotein B gene
P M Frossard, P A Gonzalez, A A Protter, et al.
Arteriosclerosis (Dallas, Tex.)
|
September 1, 1984
Uptake of apolipoprotein E-containing high density lipoproteins by hepatic parenchymal cells
H Funke, J Boyles, K H Weisgraber, et al.
Clinical Genetics
|
August 1, 1996
A novel missense mutation (Gly2Arg) in the human lysosomal acid lipase gene is found in individuals with and without cholesterol ester storage disease (CESD)
H Wiebusch, S Muntoni, H Funke, et al.
Human Mutation
|
January 1, 1996
Compound heterozygosity for a known (D250N) and a novel (E410K) missense mutation in the C-terminal domain of lipoprotein lipase causes familial chylomicronemia
H Wiebusch, H Funke, T Bruin, et al.
Vox Sanguinis
|
March 4, 2009
Gene expression in the detection of autologous blood transfusion in sports--a pilot study
T Pottgiesser, Y O Schumacher, H Funke, et al.
Journal of Lipid Research
|
June 1, 1990
Normolipemic dysbetalipoproteinemia and hyperlipoproteinemia type III in subjects homozygous for a rare genetic apolipoprotein E variant (apoE1)
A Steinmetz, N Assefbarkhi, C Eltze, et al.
Page
of 21
Search research articles
Search
Showing results (91-100 of 203) with videos related to
Sort By:
Page
of 21
Der Internist
|
August 1, 1980
[Prediction and early diagnosis of coronary disease. Prospective epidemiologic study of industrial workers in Westphalia]
G Assmann, W Oberwittler, H Schulte, et al.
Nucleic Acids Research
|
November 11, 1986
Deletion polymorphism 5' to the human apolipoprotein AI (apo AI) gene
P M Frossard, R T Coleman, A A Protter, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
December 1, 1994
A nonsense mutation in the apolipoprotein A-I gene is associated with high-density lipoprotein deficiency and periorbital xanthelasmas
R Römling, A von Eckardstein, H Funke, et al.
Personalized Medicine
|
May 23, 2018
Platform evaluation for rapid genotyping of CYP2C9 and VKORC1 alleles
Victoria A Joshi, Elizabeth Duffy, Birgit H Funke, et al.
Nucleic Acids Research
|
May 27, 1986
Pvu II RFLP in the 5' of the human apolipoprotein B gene
P M Frossard, P A Gonzalez, A A Protter, et al.
Arteriosclerosis (Dallas, Tex.)
|
September 1, 1984
Uptake of apolipoprotein E-containing high density lipoproteins by hepatic parenchymal cells
H Funke, J Boyles, K H Weisgraber, et al.
Clinical Genetics
|
August 1, 1996
A novel missense mutation (Gly2Arg) in the human lysosomal acid lipase gene is found in individuals with and without cholesterol ester storage disease (CESD)
H Wiebusch, S Muntoni, H Funke, et al.
Human Mutation
|
January 1, 1996
Compound heterozygosity for a known (D250N) and a novel (E410K) missense mutation in the C-terminal domain of lipoprotein lipase causes familial chylomicronemia
H Wiebusch, H Funke, T Bruin, et al.
Vox Sanguinis
|
March 4, 2009
Gene expression in the detection of autologous blood transfusion in sports--a pilot study
T Pottgiesser, Y O Schumacher, H Funke, et al.
Journal of Lipid Research
|
June 1, 1990
Normolipemic dysbetalipoproteinemia and hyperlipoproteinemia type III in subjects homozygous for a rare genetic apolipoprotein E variant (apoE1)
A Steinmetz, N Assefbarkhi, C Eltze, et al.
Page
of 21