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Biochemistry|August 5, 2000
Characterization of recombinant wild type and site-directed mutations of apolipoprotein C-III: lipid binding, displacement of ApoE, and inhibition of lipoprotein lipaseH Liu, P J Talmud, L Lins, et al.Journal of Lipid Research|August 1, 1991
Characterization of the discoidal complexes formed between apoA-I-CNBr fragments and phosphatidylcholineB Vanloo, J Morrison, N Fidge, et al.Developmental Biology|February 1, 1985
Acquisition of the heat-shock response and thermotolerance during early development of Xenopus laevisJ J Heikkila, M Kloc, J Bury, et al.The Biochemical Journal|February 26, 1999
Baculovirus expression and biochemical characterization of the human microsomal triglyceride transfer proteinP J Ritchie, A Decout, J Amey, et al.Journal of Lipid Research|August 1, 1995
Association of synthetic peptide fragments of human apolipoprotein A-I with phospholipidsB Vanloo, L Demoor, C Boutillon, et al.The Journal of Biological Chemistry|September 10, 1983
Interaction of the serum amyloid A proteins with phospholipidL L Bausserman, P N Herbert, T Forte, et al.Atherosclerosis|August 26, 1998
Displacement of apo A-I from HDL by apo A-II or its C-terminal helix promotes the formation of pre-beta1 migrating particles and decreases LCAT activationC Labeur, G Lambert, T Van Cauteren, et al.Biochimica Et Biophysica Acta|June 2, 1994
Structural domain of apolipoprotein A-I involved in its interaction with cellsJ Luchoomun, N Theret, V Clavey, et al.Biology|October 27, 2022
Isotopic Niche Analysis of Long-Finned Pilot Whales (Globicephala melas edwardii) in Aotearoa New Zealand WatersBethany Hinton, Karen A Stockin, Sarah J Bury, et al.The Journal of Biological Chemistry|August 5, 1991
Catalytic triad residue mutation (Asp156----Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447----Ter) in a Turkish familyF Faustinella, A Chang, J P Van Biervliet, et al.Pageof 26