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P Amouyel

Showing results (191-200 of 225) with videos related to

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Human Genetics|July 8, 1999
Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's diseaseF Wavrant-DeVrièze, J C Lambert, L Stas, et al.
Journal of Human Hypertension|August 30, 2000
Association of hypertensive status and its drug treatment with lipid and haemostatic factors in middle-aged men: the PRIME studyP Marques-Vidal, M Montaye, B Haas, et al.
Neurology|August 19, 2011
Systemic chemokine levels, coronary heart disease, and ischemic stroke events: the PRIME studyF Canouï-Poitrine, G Luc, Z Mallat, et al.
Human Molecular Genetics|August 13, 1998
Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's diseaseJ C Lambert, C Berr, F Pasquier, et al.
Journal of Human Hypertension|September 6, 2002
Efficacy of very low dose perindopril 2 mg/indapamide 0.625 mg combination on left ventricular hypertrophy in hypertensive patients: the P.I.C.X.E.L. study rationale and designP Gosse, O Dubourg, P Guéret, et al.
Molecular Psychiatry|March 16, 2011
Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sitesN Brouwers, C Van Cauwenberghe, S Engelborghs, et al.
Molecular Psychiatry|June 21, 2007
Evidence for the association of the S100beta gene with low cognitive performance and dementia in the elderlyJ-C Lambert, S Ferreira, J Gussekloo, et al.
Human Molecular Genetics|September 26, 2000
The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's diseaseJ C Lambert, L Goumidi, F W Vrièze, et al.
Scientific Reports|March 8, 2019
Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutationM Ibrahim-Kosta, P Suchon, F Couturaud, et al.
European Heart Journal|October 26, 1999
Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE groupP Charron, F Tesson, O Poirier, et al.
Pageof 23

Showing results (191-200 of 225) with videos related to

Sort By:
Pageof 23
Human Genetics|July 8, 1999
Association between coding variability in the LRP gene and the risk of late-onset Alzheimer's diseaseF Wavrant-DeVrièze, J C Lambert, L Stas, et al.
Journal of Human Hypertension|August 30, 2000
Association of hypertensive status and its drug treatment with lipid and haemostatic factors in middle-aged men: the PRIME studyP Marques-Vidal, M Montaye, B Haas, et al.
Neurology|August 19, 2011
Systemic chemokine levels, coronary heart disease, and ischemic stroke events: the PRIME studyF Canouï-Poitrine, G Luc, Z Mallat, et al.
Human Molecular Genetics|August 13, 1998
Pronounced impact of Th1/E47cs mutation compared with -491 AT mutation on neural APOE gene expression and risk of developing Alzheimer's diseaseJ C Lambert, C Berr, F Pasquier, et al.
Journal of Human Hypertension|September 6, 2002
Efficacy of very low dose perindopril 2 mg/indapamide 0.625 mg combination on left ventricular hypertrophy in hypertensive patients: the P.I.C.X.E.L. study rationale and designP Gosse, O Dubourg, P Guéret, et al.
Molecular Psychiatry|March 16, 2011
Alzheimer risk associated with a copy number variation in the complement receptor 1 increasing C3b/C4b binding sitesN Brouwers, C Van Cauwenberghe, S Engelborghs, et al.
Molecular Psychiatry|June 21, 2007
Evidence for the association of the S100beta gene with low cognitive performance and dementia in the elderlyJ-C Lambert, S Ferreira, J Gussekloo, et al.
Human Molecular Genetics|September 26, 2000
The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's diseaseJ C Lambert, L Goumidi, F W Vrièze, et al.
Scientific Reports|March 8, 2019
Minor allele of the factor V K858R variant protects from venous thrombosis only in non-carriers of factor V Leiden mutationM Ibrahim-Kosta, P Suchon, F Couturaud, et al.
European Heart Journal|October 26, 1999
Identification of a genetic risk factor for idiopathic dilated cardiomyopathy. Involvement of a polymorphism in the endothelin receptor type A gene. CARDIGENE groupP Charron, F Tesson, O Poirier, et al.
Pageof 23