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Author Report for: Arca M

No contact information in database for Arca M

    Title: The Fibrinogen-like Domain of ANGPTL3 Facilitates Lipolysis in 3T3-L1 Cells by Activating the Intracellular Erk Pathway
    Bini S, Pecce V, Di Costanzo A, Polito L, Ghadiri A, Minicocci I, Tambaro F, Covino S, Arca M, D'Erasmo L
    Ref: Biomolecules, 12:, 2022 : PubMed


    Title: Lysosomal acid lipase activity and liver fibrosis in the clinical continuum of non-alcoholic fatty liver disease
    Baratta F, Pastori D, Tozzi G, D'Erasmo L, Di Costanzo A, Arca M, Ettorre E, Ginanni Corradini S, Violi F and Del Ben M <1 more author(s)>
    Ref: Liver Int, 39:2301, 2019 : PubMed


    Title: Depletion in LpA-I:A-II particles enhances HDL-mediated endothelial protection in familial LCAT deficiency
    Gomaraschi M, Ossoli A, Castelnuovo S, Simonelli S, Pavanello C, Balzarotti G, Arca M, Di Costanzo A, Sampietro T and Calabresi L <4 more author(s)>
    Ref: J Lipid Res, 58:994, 2017 : PubMed


    Title: Neutral Lipid Storage Diseases: clinical/genetic features and natural history in a large cohort of Italian patients
    Pennisi EM, Arca M, Bertini E, Bruno C, Cassandrini D, D'Amico A, Garibaldi M, Gragnani F, Maggi L and Angelini C <10 more author(s)>
    Ref: Orphanet J Rare Dis, 12:90, 2017 : PubMed


    Title: Contribution of mutations in low density lipoprotein receptor (LDLR) and lipoprotein lipase (LPL) genes to familial combined hyperlipidemia (FCHL): A reappraisal by using a resequencing approach
    Minicocci I, Prisco C, Montali A, Di Costanzo A, Ceci F, Pigna G, Arca M
    Ref: Atherosclerosis, 242:618, 2015 : PubMed


    Title: Genetic variants in adipose triglyceride lipase influence lipid levels in familial combined hyperlipidemia
    Nanni L, Quagliarini F, Megiorni F, Montali A, Minicocci I, Campagna F, Pizzuti A, Arca M
    Ref: Atherosclerosis, 213:206, 2010 : PubMed


    Title: Clinical and genetic characterization of Chanarin-Dorfman syndrome.
    Bruno C, Bertini E, Di Rocco M, Cassandrini D, Ruffa G, De Toni T, Seri M, Spada M, Li Volti G and Minetti C <6 more author(s)>
    Ref: Biochemical & Biophysical Research Communications, 369:1125, 2008 : PubMed


    Title: Novel mutations in the adipose triglyceride lipase gene causing neutral lipid storage disease with myopathy
    Campagna F, Nanni L, Quagliarini F, Pennisi E, Michailidis C, Pierelli F, Bruno C, Casali C, Dimauro S, Arca M
    Ref: Biochemical & Biophysical Research Communications, 377:843, 2008 : PubMed


    Title: The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families
    Calabresi L, Pisciotta L, Costantin A, Frigerio I, Eberini I, Alessandrini P, Arca M, Bon GB, Boscutti G and Franceschini G <17 more author(s)>
    Ref: Arterioscler Thromb Vasc Biol, 25:1972, 2005 : PubMed


    Title: Genetic study of common variants at the Apo E, Apo AI, Apo CIII, Apo B, lipoprotein lipase (LPL) and hepatic lipase (LIPC) genes and coronary artery disease (CAD): variation in LIPC gene associates with clinical outcomes in patients with established CAD
    Baroni MG, Berni A, Romeo S, Arca M, Tesorio T, Sorropago G, Di Mario U, Galton DJ
    Ref: BMC Med Genet, 4:8, 2003 : PubMed


    Title: Common variants in the lipoprotein lipase gene, but not those in the insulin receptor substrate-1, the beta3-adrenergic receptor, and the intestinal fatty acid binding protein-2 genes, influence the lipid phenotypic expression in familial combined hyperlipidemia
    Campagna F, Montali A, Baroni MG, Maria AT, Ricci G, Antonini R, Verna R, Arca M
    Ref: Metabolism, 51:1298, 2002 : PubMed


    Title: The common mutations in the lipoprotein lipase gene in Italy: effects on plasma lipids and angiographically assessed coronary atherosclerosis
    Arca M, Campagna F, Montali A, Barilla F, Mangieri E, Tanzilli G, Seccareccia F, Campa PP, Ricci G, Pannitteri G
    Ref: Clin Genet, 58:369, 2000 : PubMed


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Mail to: Nicolas Lenfant, Thierry Hotelier, Yves Bourne, Pascale Marchot and Arnaud Chatonnet.
Please cite: Lenfant 2013 Nucleic.Acids.Res. or Marchot Chatonnet 2012 Prot.Pept Lett.
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