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Archives of Internal Medicine|January 25, 2012
Severe high-density lipoprotein deficiency associated with autoantibodies against lecithin:cholesterol acyltransferase in non-Hodgkin lymphomaSara Simonelli, Elisabetta Gianazza, Giuliana Mombelli, et al.Biochimica Et Biophysica Acta|September 2, 2005
High-density lipoproteins attenuate interleukin-6 production in endothelial cells exposed to pro-inflammatory stimuliMonica Gomaraschi, Nicoletta Basilico, Francesca Sisto, et al.Biochemical Pharmacology|December 11, 2012
Off-target effects of thrombolytic drugs: apolipoprotein A-I proteolysis by alteplase and tenecteplaseMonica Gomaraschi, Alice Ossoli, Cecilia Vitali, et al.Cardiovascular Research|July 2, 2013
Inflammation impairs eNOS activation by HDL in patients with acute coronary syndromeMonica Gomaraschi, Alice Ossoli, Elda Favari, et al.The Journal of Biological Chemistry|December 14, 2006
A unique protease-sensitive high density lipoprotein particle containing the apolipoprotein A-I(Milano) dimer effectively promotes ATP-binding Cassette A1-mediated cell cholesterol effluxElda Favari, Monica Gomaraschi, Ilaria Zanotti, et al.Journal of Clinical Lipidology|June 5, 2012
Novel missense variants in LCAT and APOB genes in an Italian kindred with familial lecithin:cholesterol acyltransferase deficiency and hypobetalipoproteinemiaPaola Conca, Silvana Pileggi, Sara Simonelli, et al.Atherosclerosis|June 24, 2003
Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiencyLivia Pisciotta, Roberto Miccoli, Alfredo Cantafora, et al.Biologicals : Journal of the International Association of Biological Standardization|October 22, 2013
Recombinant human LCAT normalizes plasma lipoprotein profile in LCAT deficiencySara Simonelli, Cristina Tinti, Laura Salvini, et al.Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|August 3, 2011
[LCAT deficiency: a nephrological diagnosis]Giuliano Boscutti, Laura Calabresi, Stefano Pizzolitto, et al.Atherosclerosis|February 10, 2009
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a Caucasian kindredLaura Calabresi, Peter Nilsson, Elisa Pinotti, et al.Pageof 7