Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Tybjaerg-Hansen

Showing results (51-60 of 68) with videos related to

Pageof 7
Sort By:
Atherosclerosis|August 1, 1991
Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemiaP Talmud, A Tybjaerg-Hansen, D Bhatnagar, et al.
Annals of Internal Medicine|September 1, 1997
ACE gene polymorphism as a risk factor for ischemic cerebrovascular diseaseB Agerholm-Larsen, A Tybjaerg-Hansen, R Frikke-Schmidt, et al.
Human Genetics|May 1, 1992
Multipoint linkage analysis of the short arm of chromosome 11 in non-insulin dependent diabetes including maturity onset diabetes of youthS O'Rahilly, P Patel, O J Lehmann, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 11, 1999
Mutations in the lipoprotein lipase gene associated with ischemic heart disease in men. The Copenhagen city heart studyH H Wittrup, A Tybjaerg-Hansen, R Steffensen, et al.
Diabetes|August 1, 1992
Linkage analysis of maturity-onset diabetes of the young with microsatellite polymorphisms. No linkage to ADA or GLUT2 genes in two familiesP Patel, Y M Lo, A Hattersley, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Studies of genetic variability of the uncoupling protein 1 gene in Caucasian subjects with juvenile-onset obesityS A Urhammer, M Fridberg, T I Sørensen, et al.
Diabetologia|March 14, 1998
Organisation of the coding exons and mutational screening of the uncoupling protein 3 gene in subjects with juvenile-onset obesityS A Urhammer, L T Dalgaard, T I Sørensen, et al.
Biochemical and Biophysical Research Communications|April 7, 1997
Amino acid variants in the human leptin receptor: lack of association to juvenile onset obesityS M Echwald, T D Sørensen, T I Sørensen, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|April 1, 1997
Identification of two novel missense mutations in the human OB geneS M Echwald, S B Rasmussen, T I Sørensen, et al.
Atherosclerosis|January 1, 1990
Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten casesA Tybjaerg-Hansen, J Gallagher, J Vincent, et al.
Pageof 7

Showing results (51-60 of 68) with videos related to

Sort By:
Pageof 7
Atherosclerosis|August 1, 1991
Rapid screening for specific mutations in patients with a clinical diagnosis of familial hypercholesterolaemiaP Talmud, A Tybjaerg-Hansen, D Bhatnagar, et al.
Annals of Internal Medicine|September 1, 1997
ACE gene polymorphism as a risk factor for ischemic cerebrovascular diseaseB Agerholm-Larsen, A Tybjaerg-Hansen, R Frikke-Schmidt, et al.
Human Genetics|May 1, 1992
Multipoint linkage analysis of the short arm of chromosome 11 in non-insulin dependent diabetes including maturity onset diabetes of youthS O'Rahilly, P Patel, O J Lehmann, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|June 11, 1999
Mutations in the lipoprotein lipase gene associated with ischemic heart disease in men. The Copenhagen city heart studyH H Wittrup, A Tybjaerg-Hansen, R Steffensen, et al.
Diabetes|August 1, 1992
Linkage analysis of maturity-onset diabetes of the young with microsatellite polymorphisms. No linkage to ADA or GLUT2 genes in two familiesP Patel, Y M Lo, A Hattersley, et al.
The Journal of Clinical Endocrinology and Metabolism|December 17, 1997
Studies of genetic variability of the uncoupling protein 1 gene in Caucasian subjects with juvenile-onset obesityS A Urhammer, M Fridberg, T I Sørensen, et al.
Diabetologia|March 14, 1998
Organisation of the coding exons and mutational screening of the uncoupling protein 3 gene in subjects with juvenile-onset obesityS A Urhammer, L T Dalgaard, T I Sørensen, et al.
Biochemical and Biophysical Research Communications|April 7, 1997
Amino acid variants in the human leptin receptor: lack of association to juvenile onset obesityS M Echwald, T D Sørensen, T I Sørensen, et al.
International Journal of Obesity and Related Metabolic Disorders : Journal of the International Association for the Study of Obesity|April 1, 1997
Identification of two novel missense mutations in the human OB geneS M Echwald, S B Rasmussen, T I Sørensen, et al.
Atherosclerosis|January 1, 1990
Familial defective apolipoprotein B-100: detection in the United Kingdom and Scandinavia, and clinical characteristics of ten casesA Tybjaerg-Hansen, J Gallagher, J Vincent, et al.
Pageof 7