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H Funke

Showing results (81-90 of 203) with videos related to

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The Journal of Dairy Research|May 1, 1991
Bacteriological investigations of clinical mastitis in heifers in SwedenP Jonsson, S O Olsson, A S Olofson, et al.
The Journal of Molecular Diagnostics : JMD|January 1, 2013
Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic eraPolakit Teekakirikul, Melissa A Kelly, Heidi L Rehm, et al.
Thrombosis Research|February 1, 1995
Impact of polymorphisms in the alpha- and beta-fibrinogen gene on plasma fibrinogen concentrations of coronary heart disease patientsJ Heinrich, H Funke, S Rust, et al.
Herz|December 28, 1999
[Congenital and "acquired QT syndromes]W Haverkamp, E Schulze-Bahr, G Mönnig, et al.
Lancet (London, England)|September 9, 1995
Genetically determined absence of HDL-cholesterol and coronary atherosclerosisR Navalesi, R Miccoli, L Odoguardi, et al.
Zeitschrift Fur Kardiologie|July 17, 1999
The LQT syndromes--current status of molecular mechanismsE Schulze-Bahr, H Wedekind, W Haverkamp, et al.
Biochimica Et Biophysica Acta|October 19, 1999
Cloning and functional characterization of the bovine endothelin-converting enzyme-1a promoterH D Orzechowski, C M Richter, H Funke-Kaiser, et al.
European Journal of Pediatrics|February 1, 1997
Marked changes of lipid levels during puberty in a patient with lipoprotein lipase deficiencyH Bucher, S Rampini, R W James, et al.
The Journal of Clinical Investigation|January 1, 1991
A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacitiesH Funke, A von Eckardstein, P H Pritchard, et al.
Atherosclerosis|January 3, 1997
The replacement of arginine by cysteine at residue 151 in apolipoprotein A-I produces a phenotype similar to that of apolipoprotein A-IMilanoE Bruckert, A von Eckardstein, H Funke, et al.
Pageof 21

Showing results (81-90 of 203) with videos related to

Sort By:
Pageof 21
The Journal of Dairy Research|May 1, 1991
Bacteriological investigations of clinical mastitis in heifers in SwedenP Jonsson, S O Olsson, A S Olofson, et al.
The Journal of Molecular Diagnostics : JMD|January 1, 2013
Inherited cardiomyopathies: molecular genetics and clinical genetic testing in the postgenomic eraPolakit Teekakirikul, Melissa A Kelly, Heidi L Rehm, et al.
Thrombosis Research|February 1, 1995
Impact of polymorphisms in the alpha- and beta-fibrinogen gene on plasma fibrinogen concentrations of coronary heart disease patientsJ Heinrich, H Funke, S Rust, et al.
Herz|December 28, 1999
[Congenital and "acquired QT syndromes]W Haverkamp, E Schulze-Bahr, G Mönnig, et al.
Lancet (London, England)|September 9, 1995
Genetically determined absence of HDL-cholesterol and coronary atherosclerosisR Navalesi, R Miccoli, L Odoguardi, et al.
Zeitschrift Fur Kardiologie|July 17, 1999
The LQT syndromes--current status of molecular mechanismsE Schulze-Bahr, H Wedekind, W Haverkamp, et al.
Biochimica Et Biophysica Acta|October 19, 1999
Cloning and functional characterization of the bovine endothelin-converting enzyme-1a promoterH D Orzechowski, C M Richter, H Funke-Kaiser, et al.
European Journal of Pediatrics|February 1, 1997
Marked changes of lipid levels during puberty in a patient with lipoprotein lipase deficiencyH Bucher, S Rampini, R W James, et al.
The Journal of Clinical Investigation|January 1, 1991
A frameshift mutation in the human apolipoprotein A-I gene causes high density lipoprotein deficiency, partial lecithin: cholesterol-acyltransferase deficiency, and corneal opacitiesH Funke, A von Eckardstein, P H Pritchard, et al.
Atherosclerosis|January 3, 1997
The replacement of arginine by cysteine at residue 151 in apolipoprotein A-I produces a phenotype similar to that of apolipoprotein A-IMilanoE Bruckert, A von Eckardstein, H Funke, et al.
Pageof 21