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Journal of Lipid Research|September 1, 1994
A novel missense mutation in the C-terminal domain of lipoprotein lipase (Glu410-->Val) leads to enzyme inactivation and familial chylomicronemiaL Previato, O Guardamagna, K A Dugi, et al.The Journal of Clinical Investigation|August 1, 1995
Dominant expression of type III hyperlipoproteinemia. Pathophysiological insights derived from the structural and kinetic characteristics of ApoE-1 (Lys146-->Glu)W A Mann, P Lohse, R E Gregg, et al.The Journal of Clinical Investigation|April 1, 1993
In vivo metabolism of a mutant form of apolipoprotein A-I, apo A-IMilano, associated with familial hypoalphalipoproteinemiaP Roma, R E Gregg, M S Meng, et al.The Journal of Biological Chemistry|July 25, 1986
Human preproapolipoprotein C-II. Analysis of major plasma isoformsS S Fojo, L Taam, T Fairwell, et al.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.The Journal of Biological Chemistry|March 10, 1995
Carboxyl-terminal domain truncation alters apolipoprotein A-I in vivo catabolismH H Schmidt, A T Remaley, J A Stonik, et al.Journal of Lipid Research|October 11, 1990
Apolipoprotein A-I metabolism in subjects with a PstI restriction fragment length polymorphism of the apoA-I gene and familial hypoalphalipoproteinemiaP Roma, R E Gregg, C Bishop, et al.Pageof 4