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Journal of Clinical Microbiology
|
February 1, 1989
Indirect immunofluorescence test and enzyme-linked immunosorbent assay for detection of Campylobacter pylori
E Schaber, F Umlauft, G Stöffler, et al.
The Journal of Clinical Investigation
|
August 1, 1987
Lipoprotein binding to cultured human hepatoma cells
F Krempler, G M Kostner, W Friedl, et al.
Atherosclerosis
|
June 5, 2004
The role of the A54T polymorphism of the intestinal fatty acid binding protein for lipid levels, insulin sensitivity and carotid atherosclerosis
W Renner, H Pressl, T C Wascher, et al.
Diabetologia
|
March 27, 2002
Insulin sensitivity is impaired in heterozygous carriers of lipoprotein lipase deficiency
B Hölzl, B Iglseder, A Sandhofer, et al.
The Journal of Biological Chemistry
|
September 15, 1992
Nuclease-hypersensitive sites define a region with enhancer activity in the third intron of the human apolipoprotein B gene
B Levy-Wilson, B Paulweber, B P Nagy, et al.
Molecular Cell Biology Research Communications : MCBRC
|
June 21, 2001
An open chromatin structure in a liver-specific enhancer that confers high level expression to human apolipoprotein b transgenes in mice
B Levy-Wilson, B Paulweber, T J Antes, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 17, 2000
Leptin, peroxisome proliferator-activated receptor-gamma, and CCAAT/enhancer binding protein-alpha mRNA expression in adipose tissue of humans and their relation to cardiovascular risk factors
F Krempler, D Breban, H Oberkofler, et al.
International Journal of Obesity (2005)
|
December 13, 2006
The SREBF-1 locus is associated with type 2 diabetes and plasma adiponectin levels in a middle-aged Austrian population
T K Felder, H Oberkofler, R Weitgasser, et al.
Journal of Lipid Research
|
April 29, 2000
Two novel mutations in the lipoprotein lipase gene in a family with marked hypertriglyceridemia in heterozygous carriers. Potential interaction with the polymorphic marker D1S104 on chromosome 1q21-q23
B Hölzl, H G Kraft, H Wiebusch, et al.
The Journal of Clinical Investigation
|
February 1, 1993
Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities
G Miesenböck, B Hölzl, B Föger, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 54) with videos related to
Sort By:
Page
of 6
Journal of Clinical Microbiology
|
February 1, 1989
Indirect immunofluorescence test and enzyme-linked immunosorbent assay for detection of Campylobacter pylori
E Schaber, F Umlauft, G Stöffler, et al.
The Journal of Clinical Investigation
|
August 1, 1987
Lipoprotein binding to cultured human hepatoma cells
F Krempler, G M Kostner, W Friedl, et al.
Atherosclerosis
|
June 5, 2004
The role of the A54T polymorphism of the intestinal fatty acid binding protein for lipid levels, insulin sensitivity and carotid atherosclerosis
W Renner, H Pressl, T C Wascher, et al.
Diabetologia
|
March 27, 2002
Insulin sensitivity is impaired in heterozygous carriers of lipoprotein lipase deficiency
B Hölzl, B Iglseder, A Sandhofer, et al.
The Journal of Biological Chemistry
|
September 15, 1992
Nuclease-hypersensitive sites define a region with enhancer activity in the third intron of the human apolipoprotein B gene
B Levy-Wilson, B Paulweber, B P Nagy, et al.
Molecular Cell Biology Research Communications : MCBRC
|
June 21, 2001
An open chromatin structure in a liver-specific enhancer that confers high level expression to human apolipoprotein b transgenes in mice
B Levy-Wilson, B Paulweber, T J Antes, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
February 17, 2000
Leptin, peroxisome proliferator-activated receptor-gamma, and CCAAT/enhancer binding protein-alpha mRNA expression in adipose tissue of humans and their relation to cardiovascular risk factors
F Krempler, D Breban, H Oberkofler, et al.
International Journal of Obesity (2005)
|
December 13, 2006
The SREBF-1 locus is associated with type 2 diabetes and plasma adiponectin levels in a middle-aged Austrian population
T K Felder, H Oberkofler, R Weitgasser, et al.
Journal of Lipid Research
|
April 29, 2000
Two novel mutations in the lipoprotein lipase gene in a family with marked hypertriglyceridemia in heterozygous carriers. Potential interaction with the polymorphic marker D1S104 on chromosome 1q21-q23
B Hölzl, H G Kraft, H Wiebusch, et al.
The Journal of Clinical Investigation
|
February 1, 1993
Heterozygous lipoprotein lipase deficiency due to a missense mutation as the cause of impaired triglyceride tolerance with multiple lipoprotein abnormalities
G Miesenböck, B Hölzl, B Föger, et al.
Page
of 6