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Pubblicazioni - Elisabetta Mattioli

 

 

  1. Cenni, V., Capanni, C., Mattioli, E., Columbaro, M., Wehnert, M., Ortolani, M., Fini, M., Novelli, G., Bertacchini, J., Maraldi, N.M., Marmiroli, S., D'Apice, M.R., Prencipe, S., Squarzoni, S., Lattanzi, G. Rapamycin treatment of Mandibuloacral Dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics (2014) Aging, 6 (9), pp. 755-770. 
  2. Lattanzi, G., Ortolani, M., Columbaro, M., Prencipe, S., Mattioli, E., Lanzarini, C., Maraldi, N.M., 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 (2014) Journal of Cell Science, 127 (1), pp. 147-157. 
  3. Meinke, P., Mattioli, E., Haque, F., Antoku, S., Columbaro, M., Straatman, K.R., Worman, H.J., Gundersen, G.G., Lattanzi, G., Wehnert, M., Shackleton, S. Muscular Dystrophy-Associated SUN1 and SUN2 Variants Disrupt Nuclear-Cytoskeletal Connections and Myonuclear Organization (2014) PLoS Genetics, 10 (9), 18 
  4. Columbaro, M., Mattioli, E., Maraldi, N.M., Ortolani, M., Gasparini, L., D'Apice, M.R., Postorivo, D., Nardone, A.M., Avnet, S., Cortelli, P., Liguori, R., Lattanzi, G. Corrigendum to "Oct-1 recruitment to the nuclear envelope in adult-onset autosomal dominant Leukodystrophy" [Biochim. Biophys. Acta, Mol. Basis Dis. 1832 (3) (March 2013) 411-420] (2013) Biochimica et Biophysica Acta - Molecular Basis of Disease, 1832 (12), p. 2244. 
  5. Columbaro, M., Mattioli, E., Maraldi, N.M., Ortolani, M., Gasparini, L., D'Apice, M.R., Postorivo, D., Nardone, A.M., Avnet, S., Cortelli, P., Liguori, R., Lattanzi, G. Oct-1 recruitment to the nuclear envelope in adult-onset autosomal dominant leukodystrophy (2013) Biochimica et Biophysica Acta - Molecular Basis of Disease, 1832 (3), pp. 411-420. 
  6. Mattioli, E., Columbaro, M., Capanni, C., Maraldi, N.M., Cenni, V., Scotlandi, K., Marino, M.T., Merlini, L., Squarzoni, S., Lattanzi, G. Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle (2011) Cell Death and Differentiation, 18 (8), pp. 1305-1315. 
  7. Avnet, S., Pallotta, R., Perut, F., Baldini, N., Pittis, M.G., Saponari, A., Lucarelli, E., Dozza, B., Greggi, T., Maraldi, N.M., Capanni, C., Mattioli, E., Columbaro, M., Lattanzi, G. Osteoblasts from a mandibuloacral dysplasia patient induce human blood precursors to differentiate into active osteoclasts (2011) Biochimica et Biophysica Acta - Molecular Basis of Disease, 1812 (7), pp. 711-718. 
  8. Maraldi, N.M., Capanni, C., Del Coco, R., Squarzoni, S., Columbaro, M., Mattioli, E., Lattanzi, G., Manzoli, F.A. Muscular laminopathies: Role of prelamin A in early steps of muscle differentiation (2011) Advances in Enzyme Regulation, 51 (1), pp. 246-256. 
  9. Columbaro, M., Mattioli, E., Schena, E., Capanni, C., Cenni, V., Levy, N., Navarro, C.L., Del Coco, R., Squarzoni, S., Camozzi, D., Hutchison, C.J., Wehnert, M., Lattanzi, G. Prelamin A processing and functional effects in restrictive dermopathy (2010) Cell Cycle, 9 (23), pp. 4766-4768
  10. Capanni, C., Del Coco, R., Mattioli, E., Camozzi, D., Columbaro, M., Schena, E., Merlini, L., Squarzoni, S., Maraldi, N.M., Lattanzi, G. Emerin-prelamin A interplay in human fibroblasts (2009) Biology of the Cell, 101 (9), pp. 541-554. 
  11. Araujo-Vilar, D., Lattanzi, G., González-Méndez, B., Costa-Freitas, A.T., 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 (2009) Journal of Medical Genetics, 46 (1), pp. 40-48. 
  12. Capanni, C., Del Coco, R., Squarzoni, S., Columbaro, M., Mattioli, E., Camozzi, D., Rocchi, A., Scotlandi, K., Maraldi, N., Foisner, R., Lattanzi, G. Prelamin A is involved in early steps of muscle differentiation (2008) Experimental Cell Research, 314 (20), pp. 3628-3637. 
  13. Mattioli, E., Columbaro, M., Capanni, C., Santi, S., Maraldi, N.M., D'Apice, M.R., Novelli, G., Riccio, M., Squarzoni, S., Foisner, R., Lattanzi, G. Drugs affecting prelamin A processing: Effects on heterochromatin organization (2008) Experimental Cell Research, 314 (3), pp. 453-462. 
  14. Lattanzi, G., Columbaro, M., Mattioli, E., Cenni, V., Camozzi, D., Wehnert, M., Santi, S., Riccio, M., Del Coco, R., Maraldi, N.M., Squarzoni, S., Foisner, R., Capanni, C. Pre-lamin A processing is linked to heterochromatin organization (2007) Journal of Cellular Biochemistry, 102 (5), pp. 1149-1159. 
  15. Maraldi, N.M., Mattioli, E., Lattanzi, G., Columbaro, M., Capanni, C., Camozzi, D., Squarzoni, S., Manzoli, F.A. Prelamin A processing and heterochromatin dynamics in laminopathies (2007) Advances in Enzyme Regulation, 47, pp. 154-167. 
  16. Petrini, S., D'Amico, A., Sale, P., Lucarini, L., Sabatelli, P., Tessa, A., Giusti, B., Verardo, M., Carrozzo, R., Mattioli, E., Scarpelli, M., Chu, M.-L., Pepe, G., Russo, M.A., Bertini, E. Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysis (2007) Neuromuscular Disorders, 17 (8), pp. 587-596. 
  17. Maraldi, N.M., Capanni, C., Mattioli, E., Columbaro, M., Squarzoni, S., Parnaik, W.K., Wehnert, M., Lattanzi, G. A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome (2007) Acta Biomedica, 78 (SUPPL. 1), pp. 207-215. 
  18. Angelin, A., Tiepolo, T., Sabatelli, P., Grumati, P., Bergamin, N., Golfieri, C., Mattioli, E., Gualandi, F., Ferlini, A., Merlini, L., Maraldi, N.M., Bonaldo, P., Bernardi, P. Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins (2007) Proceedings of the National Academy of Sciences of the United States of America, 104 (3), pp. 991-996. 
  19. Maraldi, N.M., Lattanzi, G., Capanni, C., Columbaro, M., Mattioli, E., Sabatelli, P., Squarzoni, S., Manzoli, F.A. Laminopathies: A chromatin affair (2006) Advances in Enzyme Regulation, 46 (1), pp. 33-49. 
  20. Maraldi, N.M., Lattanzi, G., Capanni, C., Columbaro, M., Merlini, L., Mattioli, E., Sabatelli, P., Squarzoni, S., Manzoli, F.A. Nuclear envelope proteins and chromatin arrangement: A pathogenic mechanism for laminopathies (2006) European Journal of Histochemistry, 50 (1), pp. 1-8. 
  21. 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, N.M. Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the α3(VI) N10-N7 domains (2006) Journal of Cellular Physiology, 206 (1), pp. 160-166. 
  22. Columbaro, M., Capanni, C., Mattioli, E., Novelli, G., Parnaik, V.K., Squarzoni, S., Maraldi, N.M., Lattanzi, G. Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment (2005) Cellular and Molecular Life Sciences, 62 (22), pp. 2669-2678. 
  23. Filesi, I., Gullotta, F., Lattanzi, G., D'Apice, M.R., Capanni, C., Nardone, A.M., Columbaro, M., Scarano, G., Mattioli, E., Sabatelli, P., Maraldi, N.M., Biocca, S., Novelli, G. Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy (2005) Physiological Genomics, 23 (2), pp. 150-158. 
  24. Capanni, C., Mattioli, E., Columbaro, M., Lucarelli, E., Parnaik, V.K., Novelli, G., Wehnert, M., Cenni, V., Maraldi, N.M., Squarzoni, S., Lattanzi, G. Altered pre-lamin A processing is a common mechanism leading to lipodystrophy (2005) Human Molecular Genetics, 14 (11), pp. 1489-1502. 
  25. Maraldi, N.M., 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 (2005) Journal of Cellular Physiology, 203 (2), pp. 319-327. 
  26. Cenni, V., Sabatelli, P., Mattioli, E., Marmiroli, S., Capanni, C., Ognibene, A., Squarzoni, S., Maraldi, N.M., Bonne, G., Columbaro, M., Merlini, L., Lattanzi, G. Lamin A N-terminal phosphorylation is associated with myoblast activation: Impairment in Emery-Dreifuss muscular dystrophy (2005) Journal of Medical Genetics, 42 (3), pp. 214-220. 
  27. Capanni, C., Sabatelli, P., Mattioli, E., Ognibene, A., Columbaro, M., Lattanzi, G., Merlini, L., Minetti, C., Maraldi, N.M., Squarzoni, S. Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition (2003) Experimental and Molecular Medicine, 35 (6), pp. 538-544. 
  28. Capanni, C., Cenni, V., Mattioli, E., Sabatelli, P., Ognibene, A., Columbaro, M., Parnaik, V.K., Wehnert, M., Maraldi, N.M., Squarzoni, S., Lattanzi, G. Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: Altered intermolecular interaction with emerin and implications for gene transcription (2003) Experimental Cell Research, 291 (1), pp. 122-134. 
  29. Lattanzi, G., Cenni, V., Marmiroli, S., Capanni, C., Mattioli, E., Merlini, L., Squarzoni, S., Maraldi, N.M. Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts (2003) Biochemical and Biophysical Research Communications, 303 (3), pp. 764-770. 
  30. Maraldi, N.M., Lattanzi, G., Sabatelli, P., Ognibene, A., Columbaro, M., Capanni, C., Rutigliano, C., Mattioli, E., Squarzoni, S. Immunocytochemistry of nuclear domains and Emery-Dreifuss muscular dystrophy pathophysiology (2003) European Journal of Histochemistry, 47 (1), pp. 3-16. 
  31. Zhang, R.-Z., Sabatelli, P., Pan, T.-C., Squarzoni, S., Mattioli, E., Bertini, E., Pepe, G., Chu, M.-L. Effects on collagen VI mRNA stability and microfibrillar assembly of three COL6A2 mutations in two families with Ullrich congenital muscular dystrophy (2002) Journal of Biological Chemistry, 277 (46), pp. 43557-43564. 
  32. Columbaro, M., Mattioli, E., Lattanzi, G., Rutigliano, C., Ognibene, A., Maraldi, N.M., Squarzoni, S. Staurosporine treatment and serum starvation promote the cleavage of emerin in cultured mouse myoblasts: Involvement of a caspase-dependent mechanism (2001) FEBS Letters, 509 (3), pp. 423-429. 
  33. Merlini, L., Kaplan, J.-C., Navarro, C., Kalaydjieva, L., Leturcq, F., Tournev, I., Guergueltcheva, V., Politano, L., Gresham, D., Santos, M., Teijeira, S., Mattioli, E. The limb-girdle muscular dystrophy 2C in Gypsies (2001) Acta Myologica, 20 (DEC.), pp. 188-191. 
  34. Sabatelli, P., Bonaldo, P., Lattanzi, G., Braghetta, P., Bergamin, N., Capanni, C., Mattioli, E., Columbaro, M., Ognibene, A., Pepe, G., Bertini, E., Merlini, L., Maraldi, N.M., Squarzoni, S. Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts (2001) Matrix Biology, 20 (7), pp. 475-486. 
  35. Talim, B., Ognibene, A., Mattioli, E., Richard, I., Anderson, L.V.B., Merlini, L. Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2A (2001) Neurology, 56 (5), pp. 692-693. 

 


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