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David-Alexandre Tregouet

Showing results (21-30 of 53) with videos related to

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Human Molecular Genetics|July 5, 2011
High prevalence of laminopathies among patients with metabolic syndromeAnne Dutour, Patrice Roll, Bénédicte Gaborit, et al.
BMC Medical Genetics|May 29, 2009
Lack of association between polymorphisms of the IL18R1 and IL18RAP genes and cardiovascular risk: the MORGAM ProjectMarie-Lise Grisoni, Carole Proust, Mervi Alanne, et al.
Thrombosis and Haemostasis|July 30, 2011
Association of vitronectin and plasminogen activator inhibitor-1 levels with the risk of metabolic syndrome and type 2 diabetes mellitus. Results from the D.E.S.I.R. prospective cohortMarie-Christine Alessi, Viviane Nicaud, Ilse Scroyen, et al.
European Journal of Human Genetics : EJHG|July 17, 2008
Haplotypic analysis of tag SNPs of the interleukin-18 gene in relation to cardiovascular disease events: the MORGAM ProjectMarie-Lise Grisoni, Carole Proust, Mervi Alanne, et al.
Plos One|March 23, 2012
MFGE8 does not influence chorio-retinal homeostasis or choroidal neovascularization in vivoWilliam Raoul, Lucie Poupel, David-Alexandre Tregouet, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 14, 2004
In-depth haplotype analysis of ABCA1 gene polymorphisms in relation to plasma ApoA1 levels and myocardial infarctionDavid-Alexandre Tregouet, Sylvain Ricard, Viviane Nicaud, et al.
Circulation|July 27, 2005
Genetic analysis of the interleukin-18 system highlights the role of the interleukin-18 gene in cardiovascular diseaseLaurence Tiret, Tiphaine Godefroy, Edith Lubos, et al.
Pediatric Blood & Cancer|January 5, 2026
Genomics of Long-Term Complications of Childhood Leukemia: Rationale and Design of the GenLEA StudyMathilde Veneziano-Broccia, Gerard Michel, Jean-Hugues Dalle, et al.
Clinical Pharmacology and Therapeutics|April 30, 2004
Pharmacogenetics of acenocoumarol pharmacodynamicsSandrine Morin, Laurent Bodin, Marie-Anne Loriot, et al.
Blood|May 28, 2020
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic diseaseKarl C Desch, Ayse B Ozel, Matt Halvorsen, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Human Molecular Genetics|July 5, 2011
High prevalence of laminopathies among patients with metabolic syndromeAnne Dutour, Patrice Roll, Bénédicte Gaborit, et al.
BMC Medical Genetics|May 29, 2009
Lack of association between polymorphisms of the IL18R1 and IL18RAP genes and cardiovascular risk: the MORGAM ProjectMarie-Lise Grisoni, Carole Proust, Mervi Alanne, et al.
Thrombosis and Haemostasis|July 30, 2011
Association of vitronectin and plasminogen activator inhibitor-1 levels with the risk of metabolic syndrome and type 2 diabetes mellitus. Results from the D.E.S.I.R. prospective cohortMarie-Christine Alessi, Viviane Nicaud, Ilse Scroyen, et al.
European Journal of Human Genetics : EJHG|July 17, 2008
Haplotypic analysis of tag SNPs of the interleukin-18 gene in relation to cardiovascular disease events: the MORGAM ProjectMarie-Lise Grisoni, Carole Proust, Mervi Alanne, et al.
Plos One|March 23, 2012
MFGE8 does not influence chorio-retinal homeostasis or choroidal neovascularization in vivoWilliam Raoul, Lucie Poupel, David-Alexandre Tregouet, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|February 14, 2004
In-depth haplotype analysis of ABCA1 gene polymorphisms in relation to plasma ApoA1 levels and myocardial infarctionDavid-Alexandre Tregouet, Sylvain Ricard, Viviane Nicaud, et al.
Circulation|July 27, 2005
Genetic analysis of the interleukin-18 system highlights the role of the interleukin-18 gene in cardiovascular diseaseLaurence Tiret, Tiphaine Godefroy, Edith Lubos, et al.
Pediatric Blood & Cancer|January 5, 2026
Genomics of Long-Term Complications of Childhood Leukemia: Rationale and Design of the GenLEA StudyMathilde Veneziano-Broccia, Gerard Michel, Jean-Hugues Dalle, et al.
Clinical Pharmacology and Therapeutics|April 30, 2004
Pharmacogenetics of acenocoumarol pharmacodynamicsSandrine Morin, Laurent Bodin, Marie-Anne Loriot, et al.
Blood|May 28, 2020
Whole-exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic diseaseKarl C Desch, Ayse B Ozel, Matt Halvorsen, et al.
Pageof 6