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Cancer Letters
|
February 12, 1998
Translational research studies of erbB oncogenes: selection strategies for breast cancer treatment
B H Brandt, A Beckmann, F Gebhardt, 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.
Journal of Lipid Research
|
February 1, 1997
An improved method for quantification of cholesterol and cholesteryl esters in human monocyte-derived macrophages by high performance liquid chromatography with identification of unassigned cholesteryl ester species by means of secondary ion mass spectrometry
P Cullen, M Fobker, K Tegelkamp, 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.
Deutsche Medizinische Wochenschrift (1946)
|
May 17, 2000
[Knowledge about stroke among the German population]
B M Weltermann, A Rogalewski, J Homann, et al.
Human Molecular Genetics
|
January 1, 1995
Deficiency of lecithin:cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT gene
H Wiebusch, P Cullen, J S Owen, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
November 1, 1994
Plasma Lp(a) levels correlate with number, severity, and length-extension of coronary lesions in male patients undergoing coronary arteriography for clinically suspected coronary atherosclerosis
T Budde, C Fechtrup, E Bösenberg, et al.
Molecular Biology & Medicine
|
June 1, 1986
Polymorphisms in the apolipoprotein AI-CIII gene complex
R T Coleman, P A Gonzalez, H Funke, et al.
Revista Clinica Espanola
|
November 1, 1988
[Detection and treatment of lipid disorders]
G Assmann, J Davignon, A Fernández-Cruz, et al.
Page
of 50
Search research articles
Search
Showing results (361-370 of 495) with videos related to
Sort By:
Page
of 50
Cancer Letters
|
February 12, 1998
Translational research studies of erbB oncogenes: selection strategies for breast cancer treatment
B H Brandt, A Beckmann, F Gebhardt, 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.
Journal of Lipid Research
|
February 1, 1997
An improved method for quantification of cholesterol and cholesteryl esters in human monocyte-derived macrophages by high performance liquid chromatography with identification of unassigned cholesteryl ester species by means of secondary ion mass spectrometry
P Cullen, M Fobker, K Tegelkamp, 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.
Deutsche Medizinische Wochenschrift (1946)
|
May 17, 2000
[Knowledge about stroke among the German population]
B M Weltermann, A Rogalewski, J Homann, et al.
Human Molecular Genetics
|
January 1, 1995
Deficiency of lecithin:cholesterol acyltransferase due to compound heterozygosity of two novel mutations (Gly33Arg and 30 bp ins) in the LCAT gene
H Wiebusch, P Cullen, J S Owen, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
November 1, 1994
Plasma Lp(a) levels correlate with number, severity, and length-extension of coronary lesions in male patients undergoing coronary arteriography for clinically suspected coronary atherosclerosis
T Budde, C Fechtrup, E Bösenberg, et al.
Molecular Biology & Medicine
|
June 1, 1986
Polymorphisms in the apolipoprotein AI-CIII gene complex
R T Coleman, P A Gonzalez, H Funke, et al.
Revista Clinica Espanola
|
November 1, 1988
[Detection and treatment of lipid disorders]
G Assmann, J Davignon, A Fernández-Cruz, et al.
Page
of 50