S R Thompson|S E Humphries - JoVE Visualize

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Atherosclerosis|March 21, 2001

Polymorphisms in the thrombopoietin gene are associated with risk of myocardial infarction at a young ageK E Webb, J F Martin, A Hamsten, et al.

Thrombosis and Haemostasis|September 1, 1995

The 4G/5G genetic polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene is associated with differences in plasma PAI-1 activity but not with risk of myocardial infarction in the ECTIM study. Etude CasTemoins de I'nfarctus du MycocardeS Ye, F R Green, P Y Scarabin, et al.

Atherosclerosis|May 12, 2018

Coronary heart disease mortality in treated familial hypercholesterolaemia: Update of the UK Simon Broome FH registerS E Humphries, J A Cooper, M Seed, et al.

American Journal of Human Genetics|September 1, 1990

Variation at the apolipoprotein (apo) AI-CIII-AIV gene cluster and apo B gene loci is associated with lipoprotein and apolipoprotein levels in Italian childrenC F Xu, M N Nanjee, J Savill, et al.

Journal of Dental Research|January 30, 2015

Upregulation of gingival tissue miR-200b in obese periodontitis subjectsA Z Kalea, R Hoteit, J Suvan, et al.

Atherosclerosis|September 1, 1984

The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemiaS E Humphries, J A Donald, J J McFadden, et al.

Annals of Human Genetics|June 8, 2004

Heritability of C-reactive protein and association with apolipoprotein E genotypes in Japanese AmericansM A Austin, C Zhang, S E Humphries, et al.

Clinical Science (London, England : 1979)|January 1, 1988

A study of the structure of the gene for lecithin: cholesterol acyltransferase in four unrelated individuals with familial lecithin: cholesterol acyltransferase deficiencyS E Humphries, M E Chaves, F Tata, et al.

Prenatal Diagnosis|February 19, 1998

The use of a highly informative CA repeat polymorphism within the abetalipoproteinaemia locus (4q22-24)K E Heath, L A Luong, J V Leonard, et al.

Atherosclerosis|April 2, 2010

All-cause and cardiovascular mortality in treated patients with severe hypertriglyceridaemia: A long-term prospective registry studyH A W Neil, J Cooper, D J Betteridge, et al.

Pageof 34

Showing results (281-290 of 334) with videos related to

Sort By:

Pageof 34

Atherosclerosis|March 21, 2001

Polymorphisms in the thrombopoietin gene are associated with risk of myocardial infarction at a young ageK E Webb, J F Martin, A Hamsten, et al.

Thrombosis and Haemostasis|September 1, 1995

The 4G/5G genetic polymorphism in the promoter of the plasminogen activator inhibitor-1 (PAI-1) gene is associated with differences in plasma PAI-1 activity but not with risk of myocardial infarction in the ECTIM study. Etude CasTemoins de I'nfarctus du MycocardeS Ye, F R Green, P Y Scarabin, et al.

Atherosclerosis|May 12, 2018

Coronary heart disease mortality in treated familial hypercholesterolaemia: Update of the UK Simon Broome FH registerS E Humphries, J A Cooper, M Seed, et al.

American Journal of Human Genetics|September 1, 1990

Variation at the apolipoprotein (apo) AI-CIII-AIV gene cluster and apo B gene loci is associated with lipoprotein and apolipoprotein levels in Italian childrenC F Xu, M N Nanjee, J Savill, et al.

Journal of Dental Research|January 30, 2015

Upregulation of gingival tissue miR-200b in obese periodontitis subjectsA Z Kalea, R Hoteit, J Suvan, et al.

Atherosclerosis|September 1, 1984

The use of polymorphic DNA and protein markers for the third complement component for determining linkage of familial hypercholesterolaemiaS E Humphries, J A Donald, J J McFadden, et al.

Annals of Human Genetics|June 8, 2004

Heritability of C-reactive protein and association with apolipoprotein E genotypes in Japanese AmericansM A Austin, C Zhang, S E Humphries, et al.

Clinical Science (London, England : 1979)|January 1, 1988

A study of the structure of the gene for lecithin: cholesterol acyltransferase in four unrelated individuals with familial lecithin: cholesterol acyltransferase deficiencyS E Humphries, M E Chaves, F Tata, et al.

Prenatal Diagnosis|February 19, 1998

The use of a highly informative CA repeat polymorphism within the abetalipoproteinaemia locus (4q22-24)K E Heath, L A Luong, J V Leonard, et al.

Atherosclerosis|April 2, 2010

All-cause and cardiovascular mortality in treated patients with severe hypertriglyceridaemia: A long-term prospective registry studyH A W Neil, J Cooper, D J Betteridge, et al.

Pageof 34