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A Lingenhel

Showing results (1-10 of 21) with videos related to

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International Journal of Obesity (2005)|July 29, 2009
Decrease of Lp(a) during weight reduction in obese children is modified by the apo(a) kringle-IV copy number variationA Brandstätter, A Lingenhel, K Zwiauer, et al.
Genetics|August 3, 1999
Control of ribosomal protein L1 synthesis in mesophilic and thermophilic archaeaA Kraft, C Lutz, A Lingenhel, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 17, 2000
Lipoprotein(a) in homozygous familial hypercholesterolemiaH G Kraft, A Lingenhel, F J Raal, et al.
Atherosclerosis|February 28, 1997
Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defectsF J Raal, G Pilcher, D C Rubinsztein, et al.
Atherosclerosis|August 23, 1996
The relative electrophoretic mobility of apo(a) isoforms depends on the gel system: proposal of a nomenclature for apo(a) phenotypesH G Kraft, A Lingenhel, G Bader, et al.
Nature Genetics|April 7, 1999
Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISHM Erdel, M Hubalek, A Lingenhel, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|September 10, 2004
Decrease of plasma apolipoprotein A-IV during weight reduction in obese adolescents on a low fat dietA Lingenhel, C Eder, K Zwiauer, et al.
Annals of Clinical Biochemistry|May 1, 1997
A modified sodium dodecyl sulphate-agarose gel/immunoblotting method for apolipoprotein(a) phenotyping using alkaline phosphatase-linked chemiluminescent detectionR W Pang, E D Janus, K S Lam, et al.
Annals of the New York Academy of Sciences|January 17, 1995
Genetic architecture of the atherogenic lipoprotein(a)G Utermann, C Haibach, M Trommsdorff, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 1, 1996
Lp(a) levels and atherosclerotic vascular disease in a sample of patients with familial hypercholesterolemia sharing the same gene defectR Carmena, S Lussier-Cacan, M Roy, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
International Journal of Obesity (2005)|July 29, 2009
Decrease of Lp(a) during weight reduction in obese children is modified by the apo(a) kringle-IV copy number variationA Brandstätter, A Lingenhel, K Zwiauer, et al.
Genetics|August 3, 1999
Control of ribosomal protein L1 synthesis in mesophilic and thermophilic archaeaA Kraft, C Lutz, A Lingenhel, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 17, 2000
Lipoprotein(a) in homozygous familial hypercholesterolemiaH G Kraft, A Lingenhel, F J Raal, et al.
Atherosclerosis|February 28, 1997
Statin therapy in a kindred with both apolipoprotein B and low density lipoprotein receptor gene defectsF J Raal, G Pilcher, D C Rubinsztein, et al.
Atherosclerosis|August 23, 1996
The relative electrophoretic mobility of apo(a) isoforms depends on the gel system: proposal of a nomenclature for apo(a) phenotypesH G Kraft, A Lingenhel, G Bader, et al.
Nature Genetics|April 7, 1999
Counting the repetitive kringle-IV repeats in the gene encoding human apolipoprotein(a) by fibre-FISHM Erdel, M Hubalek, A Lingenhel, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|September 10, 2004
Decrease of plasma apolipoprotein A-IV during weight reduction in obese adolescents on a low fat dietA Lingenhel, C Eder, K Zwiauer, et al.
Annals of Clinical Biochemistry|May 1, 1997
A modified sodium dodecyl sulphate-agarose gel/immunoblotting method for apolipoprotein(a) phenotyping using alkaline phosphatase-linked chemiluminescent detectionR W Pang, E D Janus, K S Lam, et al.
Annals of the New York Academy of Sciences|January 17, 1995
Genetic architecture of the atherogenic lipoprotein(a)G Utermann, C Haibach, M Trommsdorff, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 1, 1996
Lp(a) levels and atherosclerotic vascular disease in a sample of patients with familial hypercholesterolemia sharing the same gene defectR Carmena, S Lussier-Cacan, M Roy, et al.
Pageof 3