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T S Hansen

Showing results (11-20 of 27) with videos related to

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Sygeplejersken|August 3, 1988
[Drugs--dosage forms]P Willems, E W Sørensen, T S Hansen, et al.
Thrombosis and Haemostasis|November 19, 1997
A fast and robust dual-label nonradioactive oligonucleotide ligation assay for detection of factor V LeidenA Chakravarty, T S Hansen, M Hørder, et al.
Journal of Environmental Monitoring : JEM|March 17, 2001
Measurements of nitrogen dioxide in Greenland using Palmes diffusion tubesT S Hansen, M Kruse, H Nissen, et al.
Clinical Genetics|September 4, 1998
Mutation screening of the LDLR gene and ApoB gene in patients with a phenotype of familial hypercholesterolemia and normal values in a functional LDL receptor/apolipoprotein B assayH Nissen, S Lestavel, T S Hansen, et al.
Ugeskrift for Laeger|June 25, 1984
[Experience from a local authority clinic for advice on contraception. A consecutive study of 1000 women attending a clinic for advice on contraception in the Municipality of Fredriksberg]E Schroeder, A V Nybo, A Buch, et al.
The Journal of Biological Chemistry|March 17, 1995
The phosphorylated ribosomal protein S7 in Tetrahymena is homologous with mammalian S4 and the phosphorylated residues are located in the C-terminal region. Structural characterization of proteins separated by two-dimensional polyacrylamide gel electrophoresisL Palm, J Andersen, H Rahbek-Nielsen, et al.
Clinical Chemistry|January 1, 1996
R325X mutation in exon 15 of the hydroxymethylbilane synthase gene identified in two Danish families with acute intermittent porphyriaN E Petersen, H Nissen, T S Hansen, et al.
Clinical Genetics|August 26, 1998
Evaluation of a clinically applicable mutation screening technique for genetic diagnosis of familial hypercholesterolemia and familial defective apolipoprotein BH Nissen, A B Hansen, P Guldberg, et al.
Atherosclerosis|January 3, 1997
Detection and characterization of a novel splice mutation in the LDL receptor intron 12 resulting in two different mutant mRNA variantsH Nissen, A B Hansen, P Guldberg, et al.
Clinical Chemistry|March 1, 1995
Robust nonradioactive oligonucleotide ligation assay to detect a common point mutation in the CYP2D6 gene causing abnormal drug metabolismT S Hansen, N E Petersen, A Iitiä, et al.
Pageof 3

Showing results (11-20 of 27) with videos related to

Sort By:
Pageof 3
Sygeplejersken|August 3, 1988
[Drugs--dosage forms]P Willems, E W Sørensen, T S Hansen, et al.
Thrombosis and Haemostasis|November 19, 1997
A fast and robust dual-label nonradioactive oligonucleotide ligation assay for detection of factor V LeidenA Chakravarty, T S Hansen, M Hørder, et al.
Journal of Environmental Monitoring : JEM|March 17, 2001
Measurements of nitrogen dioxide in Greenland using Palmes diffusion tubesT S Hansen, M Kruse, H Nissen, et al.
Clinical Genetics|September 4, 1998
Mutation screening of the LDLR gene and ApoB gene in patients with a phenotype of familial hypercholesterolemia and normal values in a functional LDL receptor/apolipoprotein B assayH Nissen, S Lestavel, T S Hansen, et al.
Ugeskrift for Laeger|June 25, 1984
[Experience from a local authority clinic for advice on contraception. A consecutive study of 1000 women attending a clinic for advice on contraception in the Municipality of Fredriksberg]E Schroeder, A V Nybo, A Buch, et al.
The Journal of Biological Chemistry|March 17, 1995
The phosphorylated ribosomal protein S7 in Tetrahymena is homologous with mammalian S4 and the phosphorylated residues are located in the C-terminal region. Structural characterization of proteins separated by two-dimensional polyacrylamide gel electrophoresisL Palm, J Andersen, H Rahbek-Nielsen, et al.
Clinical Chemistry|January 1, 1996
R325X mutation in exon 15 of the hydroxymethylbilane synthase gene identified in two Danish families with acute intermittent porphyriaN E Petersen, H Nissen, T S Hansen, et al.
Clinical Genetics|August 26, 1998
Evaluation of a clinically applicable mutation screening technique for genetic diagnosis of familial hypercholesterolemia and familial defective apolipoprotein BH Nissen, A B Hansen, P Guldberg, et al.
Atherosclerosis|January 3, 1997
Detection and characterization of a novel splice mutation in the LDL receptor intron 12 resulting in two different mutant mRNA variantsH Nissen, A B Hansen, P Guldberg, et al.
Clinical Chemistry|March 1, 1995
Robust nonradioactive oligonucleotide ligation assay to detect a common point mutation in the CYP2D6 gene causing abnormal drug metabolismT S Hansen, N E Petersen, A Iitiä, et al.
Pageof 3