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Pubblicazioni - Elisabetta Mattioli

 

 

  1. Giovanna Lattanzi, Camilla Pellegrini, Marta Columbaro, Elisa Schena, Sabino Prencipe, Davide Andrenacci, Patricia Iozzo, Maria Angela Guzzardi, Cristina Capanni, Elisabetta Mattioli, Manuela Loi, David Araujo-Vilar, Stefano Squarzoni, Saverio Cinti, Paolo Morselli, Assuero Giorgetti, Laura Zanotti, and Alessandra Gambineri.  Altered adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue . Exp Mol Med 2019
  2. Mattioli E1,2, Andrenacci D1,2, Mai A3, Valente S3, Robijns J4, De Vos WH4, Capanni C1,2, Lattanzi G1,2 Statins and Histone Deacetylase Inhibitors Affect Lamin A/C - Histone Deacetylase 2  Interaction in Human Cells. Frontiers. gen 2019
  3. Jiang Z, Cinti C, Taranta M, Mattioli E, Schena E, Singh S, Khurana R, Lattanzi G, Tsinoremas NF, Capobianco E. Network assessment of demethylation treatment in melanoma: Differential transcriptome-methylome and antigen profile signatures. PLoS One. 2018 Nov 28;13(11)
  4. Mattioli 1,2, Marta Columbaro 2, Mohammed Hakim Jafferali 3, Elisa Schena1,4, Einar Hallberg 5 and Giovanna Lattanzi 1,2,* Samp1 Mislocalization in Emery-Dreifuss Muscular Dystrophy. Cells 2018 oct 
  5. Elisabetta Mattioli, Davide Andrenacci, Cecilia Garofalo, Sabino Prencipe, Katia Scotlandi, Daniel Remondini, Davide Gentilini, Anna Maria Di Blasio, Sergio Valente,Emanuela Scarano, Lucia Cicchilitti, Giulia Piaggio, Antonello Mai, Giovanna Lattanzi. Altered modulation of Lamin A/C-HDAC2 interaction and p21 expression during oxidative stress response in HGPS . Aging cell 2018 aug
  6. Chiara Gargiuli, Elisa Schena, Elisabetta Mattioli, Marta Columbaro, Maria Rosaria D'Apice, Giuseppe Novelli,Tiziana Greggi, and Giovanna Lattanzi . Lamins and bone disorders: current understanding and perspectives. Oncotarget. 2018 Apr
  7. Meinke P, Mattioli E, Haque F, Antoku S, Columbaro M, Straatman KR, Worman HJ, Gundersen GG, Lattanzi G, Wehnert M, Shackleton S. Muscular Dystrophy-Associated SUN1 and SUN2 Variants Disrupt Nuclear-Cytoskeletal Connections and Myonuclear Organization. PLoS Genet. 2014 sept 
  8. Camozzi D, Capanni C, Cenni V, Mattioli E, Columbaro M, Squarzoni S, Lattanzi G. Diverse lamin-dependent mechanisms interact to control chromatin dynamics: Focus on laminopathies. Nucleus. 2014 Sep 2;5(5).
  9. Vittoria Cenni , Cristina Capanni, Elisabetta Mattioli , Marta Columbaro,   Manfred Wehnert, Michela Ortolani, Milena Fini, Giuseppe Novelli, Jessika Bertacchini, Nadir M. Maraldi, Sandra Marmiroli, Maria Rosaria D’Apice, Sabino Prencipe, Stefano Squarzoni, and Giovanna Lattanzi. Rapamycin treatment of Mandibuloacral Dysplasia cells rescues localization of chromatin associated proteins and cell cycle dynamics. Aging 2014   
  10. Lattanzi G, Ortolani M, Columbaro M, Prencipe S, Mattioli E, Lanzarini C, Maraldi NM, Cenni V, Garagnani P, Salvioli S, Storci G, Bonafè M, Capanni C, Franceschi C. Lamins are rapamycin targets that impact human longevity: a study in centenarians .J Cell Sci. 2014 Jan 1;127(Pt 1):147-57. doi: 10.1242/jcs.133983.
  11. Starke S, Meinke P, Camozzi D, Mattioli E, Pfaeffle R, Siekmeyer M, Hirsch W, Horn LC, Paasch U, Mitter D, Lattanzi G, Wehnert M, Kiess W. Progeroid laminopathy with restrictive dermopathy-like features caused by an isodisomic LMNA mutation p.R435C. Aging (Albany NY). 2013 Jun;5(6):445-59
  12. Columbaro M, Mattioli E, Maraldi NM, Ortolani M, Gasparini L, D'Apice MR, Postorivo D, Nardone AM, Avnet S, Cortelli P, Liguori R, Lattanzi G. Oct-1 recruitment to the nuclear envelope in adult-onset autosomal dominant leukodystrophy. Biochim Biophys Acta. 2013 Mar;1832(3):411-20. doi: 10.1016/j.bbadis.2012.12.006. Epub 2012 Dec 20
  13. Mattioli E, Columbaro M, Capanni C, Maraldi NM, Cenni V, Scotlandi K, Marino MT, Merlini L, Squarzoni S, Lattanzi G. Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle. Cell Death Differ. 2011 Aug;18(8):1305-15. Epub 2011 Feb 11   
  14. Avnet S, Pallotta R, Perut F, Baldini N, Pittis MG, Saponari A, Lucarelli E, Dozza B, Greggi T, Maraldi NM, Capanni C, Mattioli E, Columbaro M, Lattanzi G. Osteoblasts from a mandibuloacral dysplasia patient induce human blood precursors to differentiate into active osteoclasts. Biochim Biophys Acta. 2011 Jul;1812(7):711-8. Epub 2011 Mar 16
  15. Columbaro M, Mattioli E, Schena E, Capanni C, Cenni V, Levy N, Navarro CL, Del Coco R, Squarzoni S, Camozzi D, Hutchison CJ, Wehnert M, Lattanzi G. Prelamin A processing and functional effects in restrictive dermopathy.Cell Cycle. 2010 Dec 1;9(23):4766-8. Epub 2010 Dec 1
  16. Maraldi NM, Capanni C, Del Coco R, Squarzoni S, Columbaro M, Mattioli E, Lattanzi G, Manzoli FA. Muscular laminopathies: role of prelamin A in early steps of muscle differentiation. Adv Enzyme Regul. 2011;51(1):246-56. Epub 2010 Oct 28
  17. Capanni C, Del Coco R, Mattioli E, Camozzi D, Columbaro M, Schena E, Merlini L, Squarzoni S, Maraldi NM, Lattanzi G. Emerin-prelamin A interplay in human fibroblasts . Biol Cell. 2009 Mar 26.
  18. Araújo-Vilar D, Lattanzi G, González-Méndez B, Costa-Freitas AT, Prieto D, Columbaro M, Mattioli E, Victoria B, Martínez-Sánchez N, Ramazanova A, Fraga M, Beiras A, Forteza J, Domínguez-Gerpe L, Calvo C, Lado-Abeal J. Site-dependent differences in both prelamin A and adipogenic genes in subcutaneous adipose tissue of patients with type 2 familial partial lipodystrophy. J Med Genet. 2009 Jan;46(1):40-8.
  19. Capanni C, Del Coco R, Squarzoni S, Columbaro M, Mattioli E, Camozzi D, Rocchi A, Scotlandi K, Maraldi N, Foisner R, Lattanzi G. ExpPrelamin A is involved in early steps of muscle differentiation. Cell Res. 2008 Dec 10;314(20):3628-37.
  20. Mattioli E, Columbaro M, Capanni C, Santi S, Maraldi NM, D'Apice MR, Novelli G,    Riccio M, Squarzoni S, Foisner R, Lattanzi G. Drugs affecting prelamin A processing: Effects on heterochromatin organization. Exp Cell Res. 2008 Feb 1;314(3):453-62.
  21. Lattanzi G, Columbaro M, Mattioli E, Cenni V, Camozzi D, Wehnert M, Santi S, Riccio M, Del Coco R, Maraldi NM, Squarzoni S, Foisner R, Capanni C. Pre-Lamin A processing is linked to heterochromatin organization. J Cell Biochem. 2007 Dec 1;102(5):1149-59.
  22. Petrini S, D'Amico A, Sale P, Lucarini L, Sabatelli P, Tessa A, Giusti B, Verardo M, Carrozzo R, Mattioli E, Scarpelli M, Chu ML, Pepe G, Russo MA, Bertini E Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysis. Neuromuscul Disord. 2007 Aug;17(8):587-96. 
  23. Maraldi NM, Capanni C, Mattioli E, Columbaro M, Squarzoni S, Parnaik WK, Wehnert M, Lattanzi G. A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome. Acta Biomed. 2007;78 Suppl 1:207-15
  24. Alessia Angelin, Tania Tiepolo, Patrizia Sabatelli, Paolo Grumati, Natascha Bergamin, Cristina Golfieri, Elisabetta Mattioli, Francesca Gualandi, Alessandra Ferlini, Luciano Merlini, Nadir M. Maraldi, Paolo Bonaldo, and Paolo Bernardi. Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins. PNAS Jan 2007
  25. Maraldi NM, Mattioli E, Lattanzi G, Columbaro M, Capanni C, Camozzi D, Squarzoni S, Manzoli FA. Prelamin A processing and heterochromatin dynamics in laminopathies Adv Enzyme Regul. 2007
  26. Maraldi NM, Lattanzi G, Capanni C, Columbaro M, Mattioli E, Sabatelli P, Squarzoni S, Manzoli FA.  Laminopathies: A chromatin affair. Adv Enzyme Regul. 2006 Jul.
  27. Squarzoni S, Sabatelli P, Bergamin N, Guicheney P, Demir E, Merlini L, Lattanzi G, Ognibene A, Capanni C, Mattioli E, Columbaro M, Bonaldo P, Maraldi NM. Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the alpha3(VI) N10-N7 domains. J Cell Physiol. 2006 Jan
  28. Maraldi NM, Lattanzi G, Capanni C, Columbaro M, Merlini L, Mattioli E, Sabatelli P, Squarzoni S, Manzoli FA. Nuclear envelope proteins and chromatin arrangement: a pathogenic mechanism for laminopathies. Eur J  Histochem. 2006 Jan-Mar
  29. Squarzoni, P. Sabatelli, C. Capanni, G. Lattanzi, M. Rocca, C. Rutigliano, M. Columbaro, E. Mattioli, N.M. Maraldi. Emerin increase in regenerating muscle fibres. Eur. J. Histochem. 2005  Oct-Dec.
  30. Columbaro M, Capanni C, Mattioli E, Novelli G, Parnaik VK, Squarzoni S, Maraldi NM, Lattanzi G. Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment. Cell Mol Life Sci. 2005 Nov.
  31. Filesi, F. Gullotta, G. Lattanzi, M.R D’Apice, C. Capanni, A.M Nardone, M. Columbaro, G. Scarano, E. Mattioli, P. Sabatelli, N.M Maraldi, S. Biocca, G. Novelli. Alterations of nuclear envelope and chromatin organization in mandibuloacral dyslasia, a rare form of laminopathy. Physiol Genomics  2005 July. 
  32. Capanni, E. Mattioli, M. Columbaro, E. Lucarelli, V. K. Parnaik, G. Novelli, M. Wehnert, V. Cenni,  N. M. Maraldi, S. Squarzoni, G. Lattanzi. Altered pre-lamin A processing is a common mechanism leading to lipodystrophy. Hum. Mol. Genet., 2005 June.
  33. Maraldi NM, Squarzoni S, Sabatelli P, Capanni C, Mattioli E, Ognibene A, Lattanzi G.  Laminopathies: involvement of structural nuclear proteins in the pathogenesis of an increasing number of human diseases. J Cell Physiol. 2005 May.
  34. V. Cenni, P. Sabatelli,  E. Mattioli , S. Marmiroli, C. Capanni, A. Ognibene, S. Squarzoni ,N.M. Maraldi ,G. Bonne , M. Columbaro, L. Merlini, G. Lattanzi .Lamin A N-terminal phosphorylation is associated with myoblast activation impairment in Emery-Dreyfuss muscular dystrophy. J. Med. Genet. 2005 Mar.
  35. C.Capanni, P. Sabatelli, E. Mattioli, A. Ognibene, M. Columbaro, G. Lattanzi, L. Merlini, C. Minetti, N.M. Maraldi, S. Squarzoni. Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition. Exp. Mol. Med., 2003 Dec. 
  36. C. Capanni, V. Cenni, E. Mattioli, P. Sabatelli A. Ognibene, M. Columbaro, V. K. Parnaik, M. Wehnert, N.M. Maraldi, S. Squarzoni, G Lattanzi. Failure of lamin A/C to functionally assemble in the R482L mutated familial partial lipodistrophy fibroblasts: altered inter-molecolar interaction with emerin and implications for gene transcription. Exp. Cell Res., 2003 Nov. 
  37. N.M. Maraldi, G Lattanzi, P Sabatelli, A. Ognibene, M. Columbaro, C. Capanni, C. Rutigliano, E. Mattioli, S. Suqarzoni. Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology. Eur. J. Histochem. 2003.
  38. Lattanzi G, Cenni V, Marmiroli S, Capanni C, Mattioli E, Merlini L, Squarzoni S, Maraldi NM. Association of emerin with nuclear and citoplasmic actin is regulated in differentiating myoblasts. Biochem Biophys Res Commun 2003 Apr. 
  39. Zhang RZ, Sabatelli P, Pan TC, Squarzoni S, Mattioli E, Bertini E, Pepe G, Chu ML. Effects on collagen VI mRNA stability and microfibrillar assembly of three COL6A2 mutations in two families with Ullrich congenital muscolar dystrophy. J Biol Chem., 2002 Nov. 
  40. M. Columbaro, E. Mattioli, G. Lattanzi, C. Rutigliano, A. Ognibene, N.M. Maraldi, S. Squarzoni. Staurosporin treatment and serum starvation promote the cleavage of emerin in cultured mouse myoblasts: involvement of a caspase-dependent mechanism. FEBS Lett., 2001 Dec.
  41. P. Sabatelli, P. Bonaldo, G. Lattanzi, P. Breghetta, N. Bergamin, C. Capanni, E. Mattioli, M. Columbaro, A. Ognibene, G. Pepe, E. Bertini, L. Merlini, N.M Maraldi, S. Squarzoni. Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts. Matrix Biol., 2001 Nov.
  42. Talim B, Ognibene A, Mattioli E, Richard I, Anderson LV, Merlini L. Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2A. Neurology., 2001 Mar.


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