S R Thompson|S E Humphries - JoVE Visualize

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Arthritis and Rheumatism|February 24, 2001

A functional polymorphic variant in the interleukin-6 gene promoter associated with low bone resorption in postmenopausal womenS L Ferrari, P Garnero, S Emond, et al.

Nucleic Acids Research|July 11, 1995

Electrophoresis for genotyping: temporal thermal gradient gel electrophoresis for profiling of oligonucleotide dissociationI N Day, S D O'Dell, I D Cash, et al.

Somatic Cell and Molecular Genetics|November 1, 1984

Gene for apolipoprotein CII is on human chromosome 19M Jeanpierre, D Weil, M C Hors-Cayla, et al.

Annals of Human Genetics|April 17, 1998

Development of a microsatellite-based approach to co-segregation analysis of familial hypercholesterolaemic kindredsL Haddad, L B Day, J Attwood, et al.

Atherosclerosis|December 1, 1991

Apolipoprotein B gene polymorphisms are associated with lipid levels in men of South Asian descentH H Renges, D B Wile, P M McKeigue, et al.

Disease Markers|May 1, 1992

Plasma fibrinogen levels and fibrinogen genotype in non-insulin dependent diabeticsC Snowden, R Houlston, M F Laker, et al.

Annals of Clinical Biochemistry|January 1, 1985

Possible applications of recombinant DNA technology to the diagnosis and study of variants of alpha 1-antitrypsinN Kalsheker, D Chiswell, A Markham, et al.

The Journal of Clinical Endocrinology and Metabolism|May 10, 2001

Angiotensin-I converting enzyme genotype-dependent benefit from hormone replacement therapy in isometric muscle strength and bone mineral densityD Woods, G Onambele, R Woledge, et al.

Human Genetics|January 1, 1985

The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase)S E Humphries, F Tata, I Henry, et al.

Journal of Medical Genetics|July 1, 1997

The effects of genotype and infant weight on adult plasma levels of fibrinogen, factor VII, and LDL cholesterol are additiveJ A Henry, M Bolla, C Osmond, et al.

Pageof 34

Showing results (141-150 of 334) with videos related to

Sort By:

Pageof 34

Arthritis and Rheumatism|February 24, 2001

A functional polymorphic variant in the interleukin-6 gene promoter associated with low bone resorption in postmenopausal womenS L Ferrari, P Garnero, S Emond, et al.

Nucleic Acids Research|July 11, 1995

Electrophoresis for genotyping: temporal thermal gradient gel electrophoresis for profiling of oligonucleotide dissociationI N Day, S D O'Dell, I D Cash, et al.

Somatic Cell and Molecular Genetics|November 1, 1984

Gene for apolipoprotein CII is on human chromosome 19M Jeanpierre, D Weil, M C Hors-Cayla, et al.

Annals of Human Genetics|April 17, 1998

Development of a microsatellite-based approach to co-segregation analysis of familial hypercholesterolaemic kindredsL Haddad, L B Day, J Attwood, et al.

Atherosclerosis|December 1, 1991

Apolipoprotein B gene polymorphisms are associated with lipid levels in men of South Asian descentH H Renges, D B Wile, P M McKeigue, et al.

Disease Markers|May 1, 1992

Plasma fibrinogen levels and fibrinogen genotype in non-insulin dependent diabeticsC Snowden, R Houlston, M F Laker, et al.

Annals of Clinical Biochemistry|January 1, 1985

Possible applications of recombinant DNA technology to the diagnosis and study of variants of alpha 1-antitrypsinN Kalsheker, D Chiswell, A Markham, et al.

The Journal of Clinical Endocrinology and Metabolism|May 10, 2001

Angiotensin-I converting enzyme genotype-dependent benefit from hormone replacement therapy in isometric muscle strength and bone mineral densityD Woods, G Onambele, R Woledge, et al.

Human Genetics|January 1, 1985

The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase)S E Humphries, F Tata, I Henry, et al.

Journal of Medical Genetics|July 1, 1997

The effects of genotype and infant weight on adult plasma levels of fibrinogen, factor VII, and LDL cholesterol are additiveJ A Henry, M Bolla, C Osmond, et al.

Pageof 34