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M Rouis

Showing results (31-40 of 38) with videos related to

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Journal of Lipid Research|March 1, 1996
Homozygosity for two point mutations in the lipoprotein lipase (LPL) gene in a patient with familial LPL deficiency: LPL(Asp9-->Asn, Tyr262-->His)M Rouis, P Lohse, K A Dugi, et al.
Genetics and Molecular Research : GMR|July 21, 2010
+294T/C polymorphism in the PPAR-delta gene is associated with risk of coronary artery disease in normolipidemic TunisiansI Jguirim-Souissi, A Jelassi, Y Hrira, et al.
Free Radical Biology & Medicine|June 9, 2004
Thioredoxin reductase 1 is upregulated in atherosclerotic plaques: specific induction of the promoter in human macrophages by oxidized low-density lipoproteinsC Furman, A-K Rundlöf, G Larigauderie, et al.
Circulation|August 3, 1999
Adenovirus-mediated overexpression of tissue inhibitor of metalloproteinase-1 reduces atherosclerotic lesions in apolipoprotein E-deficient miceM Rouis, C Adamy, N Duverger, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 22, 2008
A novel splice site mutation of the LDL receptor gene in a Tunisian hypercholesterolemic familyA Jelassi, M Najah, I Jguirim, et al.
Atherosclerosis|September 2, 2008
Limited mutational heterogeneity in the LDLR gene in familial hypercholesterolemia in TunisiaA Jelassi, I Jguirim, M Najah, et al.
The Journal of Biological Chemistry|May 19, 1995
Overexpression of human lecithin cholesterol acyltransferase leads to hyperalphalipoproteinemia in transgenic miceB L Vaisman, H G Klein, M Rouis, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 17, 2004
REDD2 gene is upregulated by modified LDL or hypoxia and mediates human macrophage cell deathC Cuaz-Pérolin, C Furman, G Larigauderie, et al.
Pageof 4

Showing results (31-40 of 38) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 38 results.
Journal of Lipid Research|March 1, 1996
Homozygosity for two point mutations in the lipoprotein lipase (LPL) gene in a patient with familial LPL deficiency: LPL(Asp9-->Asn, Tyr262-->His)M Rouis, P Lohse, K A Dugi, et al.
Genetics and Molecular Research : GMR|July 21, 2010
+294T/C polymorphism in the PPAR-delta gene is associated with risk of coronary artery disease in normolipidemic TunisiansI Jguirim-Souissi, A Jelassi, Y Hrira, et al.
Free Radical Biology & Medicine|June 9, 2004
Thioredoxin reductase 1 is upregulated in atherosclerotic plaques: specific induction of the promoter in human macrophages by oxidized low-density lipoproteinsC Furman, A-K Rundlöf, G Larigauderie, et al.
Circulation|August 3, 1999
Adenovirus-mediated overexpression of tissue inhibitor of metalloproteinase-1 reduces atherosclerotic lesions in apolipoprotein E-deficient miceM Rouis, C Adamy, N Duverger, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 22, 2008
A novel splice site mutation of the LDL receptor gene in a Tunisian hypercholesterolemic familyA Jelassi, M Najah, I Jguirim, et al.
Atherosclerosis|September 2, 2008
Limited mutational heterogeneity in the LDLR gene in familial hypercholesterolemia in TunisiaA Jelassi, I Jguirim, M Najah, et al.
The Journal of Biological Chemistry|May 19, 1995
Overexpression of human lecithin cholesterol acyltransferase leads to hyperalphalipoproteinemia in transgenic miceB L Vaisman, H G Klein, M Rouis, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|August 17, 2004
REDD2 gene is upregulated by modified LDL or hypoxia and mediates human macrophage cell deathC Cuaz-Pérolin, C Furman, G Larigauderie, et al.
Pageof 4