Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

P Benlian

Showing results (41-50 of 51) with videos related to

Pageof 6
Sort By:
Human Mutation|January 1, 1994
Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestriesY Ma, M S Liu, D Chitayat, et al.
Journal of Lipid Research|February 1, 1995
Homozygous deletion of exon 9 causes lipoprotein lipase deficiency: possible intron-Alu recombinationP Benlian, J Etienne, J L de Gennes, et al.
Journal of Cardiovascular Pharmacology|January 1, 1986
Active Na+ and Ca+ transport, Na+-Ca2+ exchange, and intracellular Na+ and Ca2+ content in young spontaneously hypertensive ratsM David-Dufilho, M G Pernollet, H LeQuan Sang, et al.
Human Mutation|January 1, 1992
Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism methodN Loux, B Saint-Jore, G Collod, et al.
Journal of Lipid Research|November 28, 1997
Relationship between lipoprotein lipase and high density lipoprotein cholesterol in mice: modulation by cholesteryl ester transfer protein and dietary statusS M Clee, H Zhang, N Bissada, et al.
Vision Research|April 22, 1999
Exclusion of the apoE gene in autosomal dominant retinitis pigmentosaE H Souied, P Benlian, J M Rozet, et al.
Human Mutation|January 1, 1996
Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100P Benlian, J L de Gennes, F Dairou, et al.
Clinical Chemistry|April 12, 2000
Comparison of a new method for the direct and simultaneous assessment of LDL- and HDL-cholesterol with ultracentrifugation and established methodsP Benlian, C Cansier, G Hennache, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 25, 2001
Apolipoprotein B Arg3500Gln mutation prevalence in children with hypercholesterolemia: a French multicenter studyS Viola, P Benlian, A Morali, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
Ethnic variation and in vivo effects of the -93t-->g promoter variant in the lipoprotein lipase geneE Ehrenborg, S M Clee, S N Pimstone, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Human Mutation|January 1, 1994
Recurrent missense mutations at the first and second base of codon Arg243 in human lipoprotein lipase in patients of different ancestriesY Ma, M S Liu, D Chitayat, et al.
Journal of Lipid Research|February 1, 1995
Homozygous deletion of exon 9 causes lipoprotein lipase deficiency: possible intron-Alu recombinationP Benlian, J Etienne, J L de Gennes, et al.
Journal of Cardiovascular Pharmacology|January 1, 1986
Active Na+ and Ca+ transport, Na+-Ca2+ exchange, and intracellular Na+ and Ca2+ content in young spontaneously hypertensive ratsM David-Dufilho, M G Pernollet, H LeQuan Sang, et al.
Human Mutation|January 1, 1992
Screening for new mutations in the LDL receptor gene in seven French familial hypercholesterolemia families by the single strand conformation polymorphism methodN Loux, B Saint-Jore, G Collod, et al.
Journal of Lipid Research|November 28, 1997
Relationship between lipoprotein lipase and high density lipoprotein cholesterol in mice: modulation by cholesteryl ester transfer protein and dietary statusS M Clee, H Zhang, N Bissada, et al.
Vision Research|April 22, 1999
Exclusion of the apoE gene in autosomal dominant retinitis pigmentosaE H Souied, P Benlian, J M Rozet, et al.
Human Mutation|January 1, 1996
Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100P Benlian, J L de Gennes, F Dairou, et al.
Clinical Chemistry|April 12, 2000
Comparison of a new method for the direct and simultaneous assessment of LDL- and HDL-cholesterol with ultracentrifugation and established methodsP Benlian, C Cansier, G Hennache, et al.
Journal of Pediatric Gastroenterology and Nutrition|September 25, 2001
Apolipoprotein B Arg3500Gln mutation prevalence in children with hypercholesterolemia: a French multicenter studyS Viola, P Benlian, A Morali, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology|December 31, 1997
Ethnic variation and in vivo effects of the -93t-->g promoter variant in the lipoprotein lipase geneE Ehrenborg, S M Clee, S N Pimstone, et al.
Pageof 6