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P Benlian

Showing results (21-30 of 51) with videos related to

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Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1985
[Elevation of intraplatelet free Ca2+ in primary hypertension in man and the rat]K H Le Quan Sang, P Benlian, C Duval, et al.
Journal of Hypertension. Supplement : Official Journal of the International Society of Hypertension|December 1, 1985
Platelet cytosolic free calcium concentration in primary hypertensionK H Le Quan Sang, P Benlian, C Kanawati, et al.
Human Genetics|July 1, 1991
Recurrent mutation at aa 792 in the LDL receptor gene in a French patientN Loux, P Benlian, D Pastier, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 24, 1998
The 19th annual meeting of the European Lipoprotein ClubA F Stalenhoef, K Aalto-Setälä, V W Armstrong, et al.
American Journal of Human Genetics|August 1, 1996
Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiencyP Benlian, L Foubert, E Gagné, et al.
Human Mutation|January 1, 1993
Identification of the haplotype associated with the APOB-3500 mutation in a French hypercholesterolemic subject: further support for a unique European ancestral mutationN Loux, B Saint-Jore, G Collod, et al.
Human Mutation|January 1, 1997
A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestryL Foubert, T Bruin, J L De Gennes, et al.
Journal of Lipid Research|August 3, 1999
Apolipoprotein A-I kinetics in heterozygous familial hypercholesterolemia: a stable isotope studyR Frénais, K Ouguerram, C Maugeais, et al.
Journal Francais D'Ophtalmologie|June 12, 2009
[Epidemiology of age related macular degeneration]N Leveziel, C Delcourt, J Zerbib, et al.
Atherosclerosis|September 16, 1999
Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144E M Teh, J W Chisholm, P J Dolphin, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1985
[Elevation of intraplatelet free Ca2+ in primary hypertension in man and the rat]K H Le Quan Sang, P Benlian, C Duval, et al.
Journal of Hypertension. Supplement : Official Journal of the International Society of Hypertension|December 1, 1985
Platelet cytosolic free calcium concentration in primary hypertensionK H Le Quan Sang, P Benlian, C Kanawati, et al.
Human Genetics|July 1, 1991
Recurrent mutation at aa 792 in the LDL receptor gene in a French patientN Loux, P Benlian, D Pastier, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|January 24, 1998
The 19th annual meeting of the European Lipoprotein ClubA F Stalenhoef, K Aalto-Setälä, V W Armstrong, et al.
American Journal of Human Genetics|August 1, 1996
Complete paternal isodisomy for chromosome 8 unmasked by lipoprotein lipase deficiencyP Benlian, L Foubert, E Gagné, et al.
Human Mutation|January 1, 1993
Identification of the haplotype associated with the APOB-3500 mutation in a French hypercholesterolemic subject: further support for a unique European ancestral mutationN Loux, B Saint-Jore, G Collod, et al.
Human Mutation|January 1, 1997
A single Ser259Arg mutation in the gene for lipoprotein lipase causes chylomicronemia in Moroccans of Berber ancestryL Foubert, T Bruin, J L De Gennes, et al.
Journal of Lipid Research|August 3, 1999
Apolipoprotein A-I kinetics in heterozygous familial hypercholesterolemia: a stable isotope studyR Frénais, K Ouguerram, C Maugeais, et al.
Journal Francais D'Ophtalmologie|June 12, 2009
[Epidemiology of age related macular degeneration]N Leveziel, C Delcourt, J Zerbib, et al.
Atherosclerosis|September 16, 1999
Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144E M Teh, J W Chisholm, P J Dolphin, et al.
Pageof 6