T S HANSEN - JoVE Visualize

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Scandinavian Audiology|January 1, 1993

High-frequency air conduction audiometry. Testing of a new low impedance circumaural transducer system in normal young personsT S Hansen, T Brask, S Larsen

Pharmacogenetics|December 1, 1996

Imipramine metabolism in relation to the sparteine oxidation polymorphism--a family studyH Madsen, T S Hansen, K Brøsen

Therapeutic Drug Monitoring|March 5, 1998

A dual label oligonucleotide ligation assay for detection of the CYP2C19*1, CYP2C19*2, and CYP2C19*3 alleles involving time-resolved fluorometryL Bathum, T S Hansen, M Hørder, et al.

American Journal of Medical Genetics|October 16, 1996

Unusual xanthomas in a young patient with heterozygous familial hypercholesterolemia and type III hyperlipoproteinemiaG Feussner, J Dobmeyer, H Nissen, 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.

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 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.

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Showing results (1-10 of 17) with videos related to

Sort By:

Pageof 2

Scandinavian Audiology|January 1, 1993

High-frequency air conduction audiometry. Testing of a new low impedance circumaural transducer system in normal young personsT S Hansen, T Brask, S Larsen

Pharmacogenetics|December 1, 1996

Imipramine metabolism in relation to the sparteine oxidation polymorphism--a family studyH Madsen, T S Hansen, K Brøsen

Therapeutic Drug Monitoring|March 5, 1998

A dual label oligonucleotide ligation assay for detection of the CYP2C19*1, CYP2C19*2, and CYP2C19*3 alleles involving time-resolved fluorometryL Bathum, T S Hansen, M Hørder, et al.

American Journal of Medical Genetics|October 16, 1996

Unusual xanthomas in a young patient with heterozygous familial hypercholesterolemia and type III hyperlipoproteinemiaG Feussner, J Dobmeyer, H Nissen, 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.

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 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.

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