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Per Eriksson

Showing results (261-270 of 368) with videos related to

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Nature Communications|April 17, 2026
Rare regulatory mutations disrupt mesenchymal molecular programs driving endocardial cushion formation in bicuspid aortic valveArtemy Zhigulev, Andrey Buyan, Enikő Lázár, et al.
Molecular Medicine (Cambridge, Mass.)|March 15, 2012
A CYP26B1 polymorphism enhances retinoic acid catabolism and may aggravate atherosclerosisOlesya Krivospitskaya, Ali Ateia Elmabsout, Eva Sundman, et al.
Annals of the Rheumatic Diseases|February 2, 2012
Association between genetic variants in the tumour necrosis factor/lymphotoxin α/lymphotoxin β locus and primary Sjogren's syndrome in Scandinavian samplesAnne Isine Bolstad, Stephanie Le Hellard, Gudlaug Kristjansdottir, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 31, 2012
Common and low-frequency genetic variants in the PCSK9 locus influence circulating PCSK9 levelsEkaterina Chernogubova, Rona Strawbridge, Hovsep Mahdessian, et al.
Regulatory Peptides|February 1, 2005
Human neuropeptide Y signal peptide gain-of-function polymorphism is associated with increased body mass index: possible mode of functionBo Ding, Björn Kull, Zhurong Liu, et al.
Plos One|December 19, 2013
Association of TERC and OBFC1 haplotypes with mean leukocyte telomere length and risk for coronary heart diseaseCécilia G Maubaret, Klelia D Salpea, Casey E Romanoski, et al.
Journal of the American Heart Association|May 22, 2016
NLRP3 Inflammasome Expression and Activation in Human AtherosclerosisGeena Paramel Varghese, Lasse Folkersen, Rona J Strawbridge, et al.
JACC. Basic to Translational Science|May 13, 2026
FOXC1 Controls Smooth Muscle Cell Differentiation and Plasticity in Vascular DiseaseUrszula Rykaczewska, Bianca E Suur, Sampath Narayanan, et al.
Genes|October 27, 2020
Genetic Variants Associated with Non-Alcoholic Fatty Liver Disease Do Not Associate with Measures of Sub-Clinical Atherosclerosis: Results from the IMPROVE StudyLuigi Castaldo, Federica Laguzzi, Rona J Strawbridge, et al.
British Journal of Cancer|December 22, 2023
The impact of circulating protein levels identified by affinity proteomics on short-term, overall breast cancer riskFelix Grassmann, Anders Mälarstig, Leo Dahl, et al.
Pageof 37

Showing results (261-270 of 368) with videos related to

Sort By:
Pageof 37
Nature Communications|April 17, 2026
Rare regulatory mutations disrupt mesenchymal molecular programs driving endocardial cushion formation in bicuspid aortic valveArtemy Zhigulev, Andrey Buyan, Enikő Lázár, et al.
Molecular Medicine (Cambridge, Mass.)|March 15, 2012
A CYP26B1 polymorphism enhances retinoic acid catabolism and may aggravate atherosclerosisOlesya Krivospitskaya, Ali Ateia Elmabsout, Eva Sundman, et al.
Annals of the Rheumatic Diseases|February 2, 2012
Association between genetic variants in the tumour necrosis factor/lymphotoxin α/lymphotoxin β locus and primary Sjogren's syndrome in Scandinavian samplesAnne Isine Bolstad, Stephanie Le Hellard, Gudlaug Kristjansdottir, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|March 31, 2012
Common and low-frequency genetic variants in the PCSK9 locus influence circulating PCSK9 levelsEkaterina Chernogubova, Rona Strawbridge, Hovsep Mahdessian, et al.
Regulatory Peptides|February 1, 2005
Human neuropeptide Y signal peptide gain-of-function polymorphism is associated with increased body mass index: possible mode of functionBo Ding, Björn Kull, Zhurong Liu, et al.
Plos One|December 19, 2013
Association of TERC and OBFC1 haplotypes with mean leukocyte telomere length and risk for coronary heart diseaseCécilia G Maubaret, Klelia D Salpea, Casey E Romanoski, et al.
Journal of the American Heart Association|May 22, 2016
NLRP3 Inflammasome Expression and Activation in Human AtherosclerosisGeena Paramel Varghese, Lasse Folkersen, Rona J Strawbridge, et al.
JACC. Basic to Translational Science|May 13, 2026
FOXC1 Controls Smooth Muscle Cell Differentiation and Plasticity in Vascular DiseaseUrszula Rykaczewska, Bianca E Suur, Sampath Narayanan, et al.
Genes|October 27, 2020
Genetic Variants Associated with Non-Alcoholic Fatty Liver Disease Do Not Associate with Measures of Sub-Clinical Atherosclerosis: Results from the IMPROVE StudyLuigi Castaldo, Federica Laguzzi, Rona J Strawbridge, et al.
British Journal of Cancer|December 22, 2023
The impact of circulating protein levels identified by affinity proteomics on short-term, overall breast cancer riskFelix Grassmann, Anders Mälarstig, Leo Dahl, et al.
Pageof 37