CALABRESI, LAURA
CALABRESI, LAURA
Dipartimento di Scienze Farmacologiche e Biomolecolari
A 33-year-old man with nephrotic syndrome and lecithin-cholesterol acyltransferase (LCAT) deficiency. Description of two new mutations in the LCAT gene
2004 G.M. Frasca, L. Soverini, E. Tampieri, G. Franceschini, L. Calabresi, L. Pisciotta, P. Preda, A. Vangelista, S. Stefoni, S. Bertolini
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla)
2015 L. Pisciotta, C. Vitali, E. Favari, P. Fossa, M.P. Adorni, D. Leone, N. Artom, R. Fresa, L. Calabresi, S. Calandra, S. Bertolini
A model structure for the heterodimer apoA-IMilano-apoA-II supports its peculiar susceptibility to proteolysis
2006 A.G. Rocco, L. Mollica, E. Gianazza, L. Calabresi, G. Franceschini, C.R. Sirtori, I. Eberini, A GUERINI ROCCO
A novel homozygous mutation in CETP gene as a cause of CETP deficiency in a caucasian kindred
2009 L. CALABRESI, P. NILSSON, E. PINOTTI, M. GOMARASCHI, E. FAVARI, M.P. ADORNI, F. BERNINI, C.R. SIRTORI, S. CALANDRA, G. FRANCESCHINI, P. TARUGI
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemia
2008 L. Pisciotta, T. Fasano, L. Calabresi, A. Bellocchio, R. Fresa, C. Borrini, S. Calandra, S. Bertolini
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease
2001 S. Bertolini, L. Pisciotta, M. Seri, R. Cusano, A. Cantafora, L. Calabresi, G. Franceschini, R. Ravazzolo, S. Calandra
A proteomic approach to identify novel disease biomarkers in LCAT deficiency
2018 S. Simonelli, A. Ossoli, C. Banfi, C. Pavanello, L. Calabresi, E. Gianazza
A proteomic portrait of atherosclerosis
2013 I. Eberini, R. Wait, L. Calabresi, C. Sensi, I. Miller, E. Gianazza
A structural model for apoA-I Milano (A-IM) in its heterodimeric form with apoA-II (A-II)
2006 A. Guerini Rocco, L. Mollica, E. Gianazza, L. Calabresi, C.R. Sirtori, I. Eberini
A structural model for apolipoprotein A-Imilano (A-IM) in its heterodimeric form with apolipoprotein A-II (A-II)
2006 A. Guerini Rocco, L. Mollica, E. Gianazza, L. Calabresi, C.R. Sirtori, I. Eberini
A unique protease-sensitive high density lipoprotein particle containing the apolipoprotein A-I(Milano) dimer effectively promotes ATP-binding Cassette A1-mediated cell cholesterol efflux
2007 E. Favari, M. Gomaraschi, I. Zanotti, F. Bernini, M. Lee-Rueckert, P.T. Kovanen, C.R. Sirtori, G. Franceschini, L. Calabresi
A woman with low HDL cholesterol and corneal opacity
2012 T. Lucchi, L. Calabresi, A. Pinto, E. Benetti, B. Arosio, S. Simonelli, R. Ratiglia, C. Vergani
ABCA1 and HDL3 are required to modulate smooth muscle cells phenotypic switch after cholesterol loading
2017 S. Castiglioni, M. Monti, L. Arnaboldi, M. Canavesi, G. Ainis Buscherini, L. Calabresi, A. Corsini, S. Bellosta
ABCA1 and HDL3 are Required to Modulate Smooth Muscle Cells Transdifferentiation in a Myocardin-miR143/145-Dependent Process
2016 S. Castiglioni, L. Arnaboldi, A. Vettore, L. Calabresi, A. Corsini, S. Bellosta
Abdominal obesity negatively influences key metrics of reverse cholesterol transport
2022 J. Härdfeldt, M. Cariello, S. Simonelli, A. Ossoli, N. Scalpi, M. Piglionica, E. Pasculli, A. Noia, E. Berardi, P. Suppressa, G. Piazzolla, C. Sabbà, L. Calabresi, A. Moschetta
Abnormal Lipoproteins Trigger Oxidative Stress-Mediated Apoptosis of Renal Cells in LCAT Deficiency
2023 M. Gomaraschi, M. Turri, A. Strazzella, M. Lhomme, C. Pavanello, W. Le Goff, A. Kontush, L. Calabresi, A. Ossoli
Abnormal splicing of ABCA1 per-mRNA in Tangier disease due to a IVS+5G>C mutation in ABCA1 gene
2003 S. Attilia, L. Pisciotta, R. Garuti, P. Tarugi, A. Cantafora, L. Calabresi, J. Tagliabue, S. Maccari, F. Bernini, I. Zanotti, C. Vergani, S. Bertolini, S. Calandra
Acquired lecithin :cholesterol acyltransferase deficiency as a major factor in lowering plasma HDL levels in chronic kidney disease
2015 L. Calabresi, S. Simonelli, P. Conca, G. Busnach, M. Cabibbe, L. Gesualdo, M. Gigante, S. Penco, F. Veglia, G. Franceschini
Activation of lecithin cholesterol acyltransferase by a disulfide-linked apolipoprotein A-I dimer
1997 L. Calabresi, G. Franceschini, A. Burkybile, A. Jonas
Activation of naturally occurring LCAT mutants by a novel activator compound
2020 C. Pavanello, A. Ossoli, M. Turri, A. Strazzella, S. Simonelli, T. Laurenzi, K. Kono, K. Yamada, N. Kiyosawa, I. Eberini, L. Calabresi