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Cristina Capanni - Pubblicazioni

  1. Pellegrini C, Columbaro M, Capanni C, D'Apice MR, Cavallo C, Murdocca M, Lattanzi G, Squarzoni S. All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype. Oncotarget. 2015 Oct 6;6(30):29914-28. doi: 10.18632/oncotarget.4939.
  2. Piva R, Lambertini E, Manferdini C, Capanni C, Penolazzi L, Gabusi E, Paolella F, Lolli A, Angelozzi M, Lattanzi G, Lisignoli G. Slug transcription factor and nuclear Lamin B1 are upregulated in osteoarthritic chondrocytes. Osteoarthritis Cartilage. 2015 Jul;23(7):1226-30. doi: 10.1016/j.joca.2015.03.015. 
  3. 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-Oct;5(5):427-40. doi: 10.4161/nucl.36289. Review. 
  4. Cenni V, Capanni C, Mattioli E, Columbaro M, Wehnert M, Ortolani M, Fini M, Novelli G, Bertacchini J, Maraldi NM, Marmiroli S, D'Apice MR, Prencipe S, Squarzoni S, Lattanzi G. Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamics. Aging (Albany NY). 2014 Sep;6(9):755-70. 
  5. Ravera S, Capanni C, Tognotti D, Bottega R, Columbaro M, Dufour C, Cappelli E, Degan P. Inhibition of metalloproteinase activity in FANCA is linked to altered oxygen metabolism. J Cell Physiol. 2015 Mar;230(3):603-9. doi: 10.1002/jcp.24778.
  6. Columbaro M, Ravera S, Capanni C, Panfoli I, Cuccarolo P, Stroppiana G, Degan P, Cappelli E. Treatment of FANCA cells with resveratrol and N-acetylcysteine: a  comparative study. PLoS One. 2014 Aug 15;9(7):e104857. doi: 10.1371/journal.pone.0104857. 
  7. 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. 
  8. Capanni C, Bruschi M, Columbaro M, Cuccarolo P, Ravera S, Dufour C, Candiano G, Petretto A, Degan P, Cappelli E. Changes in vimentin, lamin A/C and mitofilin  induce aberrant cell organization in fibroblasts from Fanconi anemia complementation group A (FA-A) patients. Biochimie. 2013 Oct;95(10):1838-47. doi: 10.1016/j.biochi.2013.06.024. 
  9. Ravera S, Vaccaro D, Cuccarolo P, Columbaro M, Capanni C, Bartolucci M, Panfoli I, Morelli A, Dufour C, Cappelli E, Degan P. Mitochondrial respiratory chain Complex I defects in Fanconi anemia complementation group A. Biochimie. 2013 Oct;95(10):1828-37. doi: 10.1016/j.biochi.2013.06.006. 
  10. Capanni C, Squarzoni S, Cenni V, D'Apice MR, Gambineri A, Novelli G, Wehnert  M, Pasquali R, Maraldi NM, Lattanzi G. Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistribution. Cell Cycle. 2012  Oct 1;11(19):3568-77. doi: 10.4161/cc.21869.
  11. Camozzi D, D'Apice MR, Schena E, Cenni V, Columbaro M, Capanni C, Maraldi NM, Squarzoni S, Ortolani M, Novelli G, Lattanzi G. Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment.  Histochem Cell Biol. 2012 Oct;138(4):643-51. doi: 10.1007/s00418 012-0977-5. 
  12. Benedetti S, Bernasconi P, Bertini E, Biagini E, Boriani G, Capanni C, Carboni N, Cenacchi G, Columbaro M, D'Adamo M, D'Amico A, D'Apice MR, Fontana M,  Gambineri A, Lattanzi G, Liguori R, Maraldi NM, Mazzanti L, Mercuri E, Mongini T, Morandi LO, Neri I, Nigro G, Novelli G, Ortolani M, Pasquali R, Pini A, Petrini S, Politano L, Previtali S, Pucci L, Rapezzi C, Ricci G, Rodolico C, Sbraccia P,  Scarano E, Siciliano G, Squarzoni S, Toscano A, Vercelli L, Ziacchi M. The empowerment of translational research: lessons from laminopathies. Orphanet J Rare Dis. 2012 Jun 12;7:37. 
  13. Cenni V, Capanni C, Columbaro M, Ortolani M, D'Apice MR, Novelli G, Fini M, Marmiroli S, Scarano E, Maraldi NM, Squarzoni S, Prencipe S, Lattanzi G. Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria. Eur J Histochem. 2011 Oct 19;55(4):e36. doi: 10.4081/ejh.2011.e36. Erratum in: Eur J Histochem. 2013;57(4):e42. 
  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. doi: 10.1016/j.bbadis.2011.03.006. 
  15. Maraldi NM, Capanni C, Cenni V, Fini M, Lattanzi G. Laminopathies and lamin-associated signaling pathways. J Cell Biochem. 2011 Apr;112(4):979-92. doi:10.1002/jcb.22992. 
  16. 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. doi: 10.1038/cdd.2010.183. 
  17. 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. 
  18. 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. doi:10.1016/j.advenzreg.2010.09.006.
  19. Muscari C, Capanni C, Giordano E, Stefanelli C, Bonavita F, Stanic I, Bonafè  F, Caldarera CM, Guarnieri C. Leupeptin preserves cardiac nitric oxide synthase 3 during reperfusion following long-term cardioplegia. J Surg Res. 2010 Nov;164(1):e27-35. doi: 10.1016/j.jss.2010.05.041. 
  20. Capanni C, Cenni V, Haraguchi T, Squarzoni S, Schüchner S, Ogris E, Novelli G, Maraldi N, Lattanzi G. Lamin A precursor induces barrier-to-autointegration factor nuclear localization. Cell Cycle. 2010 Jul 1;9(13):2600-10. doi: 10.4161/cc.9.13.12080. 
  21. Dominici S, Fiori V, Magnani M, Schena E, Capanni C, Camozzi D, D'Apice MR, Le Dour C, Auclair M, Caron M, Novelli G, Vigouroux C, Maraldi NM, Lattanzi G. Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria. Eur J Histochem. 2009 Jan-Mar;53(1):43-52.
  22. 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 Sep;101(9):541-54. doi: 10.1042/BC20080175. 
  23. 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. Exp Cell Res. 2008 Dec 10;314(20):3628-37. doi: 10.1016/j.yexcr.2008.09.026. 
  24. Camozzi D, Pignatelli S, Valvo C, Lattanzi G, Capanni C, Dal Monte P, Landini MP. Remodelling of the nuclear lamina during human cytomegalovirus infection: role of the viral proteins pUL50 and pUL53. J Gen Virol. 2008 Mar;89(Pt3):731-40. doi: 10.1099/vir.0.83377-0. 
  25. Maraldi NM, Capanni C, Lattanzi G, Camozzi D, Facchini A, Manzoli FA. SREBP1  interaction with prelamin A forms: a pathogenic mechanism for lipodystrophic laminopathies. Adv Enzyme Regul. 2008;48:209-23. 
  26. Zucchini C, Rocchi A, Manara MC, De Sanctis P, Capanni C, Bianchini M, Carinci P, Scotlandi K, Valvassori L. Apoptotic genes as potential markers of metastatic phenotype in human osteosarcoma cell lines. Int J Oncol. 2008 Jan;32(1):17-31. 
  27. 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. 
  28. 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. 
  29. 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.
  30. 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;47:154-67. 
  31. Maraldi NM, Lattanzi G, Capanni C, Columbaro M, Mattioli E, Sabatelli P, Squarzoni S, Manzoli FA. Laminopathies: a chromatin affair. Adv Enzyme Regul. 2006;46:33-49. Epub 2006 Jul 18. Review. 
  32. 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;50(1):1-8. Review. 
  33. Squarzoni S, Sabatelli P, Capanni C, Lattanzi G, Rutigliano C, Columbaro M, Mattioli E, Rocca M, Maraldi NM. Emerin increase in regenerating muscle fibers. Eur J Histochem. 2005 Oct-Dec;49(4):355-62.
  34. 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;62(22):2669-78.
  35. Maraldi NM, Lattanzi G, Squarzoni S, Capanni C, Cenni V, Manzoli FA. Implications for nuclear organization and gene transcription of lamin A/C specific mutations. Adv Enzyme Regul. 2005;45:1-16. Epub 2005 Sep 26. 
  36. Filesi I, Gullotta F, Lattanzi G, D'Apice MR, Capanni C, Nardone AM, Columbaro M, Scarano G, Mattioli E, Sabatelli P, Maraldi NM, Biocca S, Novelli G. Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy. Physiol Genomics. 2005 Oct 17;23(2):150-8.
  37. 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;206(1):160-
  38. Capanni C, Mattioli E, Columbaro M, Lucarelli E, Parnaik VK, Novelli G, Wehnert M, Cenni V, Maraldi NM, Squarzoni S, Lattanzi G. Altered pre-lamin A processing is a common mechanism leading to lipodystrophy. Hum Mol Genet. 2005 Jun 1;14(11):1489-502. Epub 2005 Apr 20. 
  39. Cenni V, Sabatelli P, Mattioli E, Marmiroli S, Capanni C, Ognibene A, Squarzoni S, Maraldi NM, Bonne G, Columbaro M, Merlini L, Lattanzi G. Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in  Emery-Dreifuss muscular dystrophy. J Med Genet. 2005 Mar;42(3):214-20. 
  40. 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;203(2):319-27. Review.
  41. Capanni C, Sabatelli P, Mattioli E, Ognibene A, Columbaro M, Lattanzi G, Merlini L, Minetti C, Maraldi NM, Squarzoni S. Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibition. Exp Mol Med. 2003 Dec 31;35(6):538-44. 
  42. Capanni C, Cenni V, Mattioli E, Sabatelli P, Ognibene A, Columbaro M, Parnaik VK, Wehnert M, Maraldi NM, 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. Exp Cell Res. 2003 Nov 15;291(1):122-34. 
  43. Sabatelli P, Columbaro M, Mura I, Capanni C, Lattanzi G, Maraldi NM, Beltran-Valero de Barnabè D, van Bokoven H, Squarzoni S, Merlini L. Extracellular matrix and nuclear abnormalities in skeletal muscle of a patient with Walker-Warburg syndrome caused by POMT1 mutation. Biochim Biophys Acta. 2003 May 20;1638(1):57-62. 
  44. Maraldi NM, 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. Eur J Histochem. 2003;47(1):3-16. Review. 
  45. Lattanzi G, Cenni V, Marmiroli S, Capanni C, Mattioli E, Merlini L, Squarzoni S, Maraldi NM. Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts. Biochem Biophys Res Commun. 2003 Apr 11;303(3):764-70. 
  46. Merlini L, Carbone I, Capanni C, Sabatelli P, Tortorelli S, Sotgia F, Lisanti MP, Bruno C, Minetti C. Familial isolated hyperCKaemia associated with a new mutation in the caveolin-3 (CAV-3) gene. J Neurol Neurosurg Psychiatry. 2002 Jul;73(1):65-7. Erratum in: J Neurol Neurosurg Psychiatry 2003 Jan;74(1):142.
  47. 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 NM, Squarzoni S. Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts. Matrix Biol. 2001 Nov;20(7):475-86. 
  48. Sabatelli P, Lattanzi G, Ognibene A, Columbaro M, Capanni C, Merlini L, Maraldi NM, Squarzoni S. Nuclear alterations in autosomal-dominant Emery-Dreifuss muscular dystrophy. Muscle Nerve. 2001 Jun;24(6):826-9. 
  49. Lattanzi G, Ognibene A, Sabatelli P, Capanni C, Toniolo D, Columbaro M, Santi S, Riccio M, Merlini L, Maraldi NM, Squarzoni S. Emerin expression at the early stages of myogenic differentiation. Differentiation. 2000 Dec;66(4-5):208-17.
  50. Squarzoni S, Sabatelli P, Capanni C, Petrini S, Ognibene A, Toniolo D, Cobianchi F, Zauli G, Bassini A, Baracca A, Guarnieri C, Merlini L, Maraldi NM. Emerin presence in platelets. Acta Neuropathol. 2000 Sep;100(3):291-8.
  51. Flamigni F, Facchini A, Capanni C, Stefanelli C, Tantini B, Caldarera CM. p44/42 mitogen-activated protein kinase is involved in the expression of ornithine decarboxylase in leukaemia L1210 cells. Biochem J. 1999 Jul 15;341 (Pt 2):363-9. 
  52. Muscari C, Pappagallo M, Ferrari D, Giordano E, Capanni C, Caldarera CM, Guarnieri C. Simultaneous detection of reduced and oxidized glutathione in tissues and mitochondria by capillary electrophoresis. J Chromatogr B Biomed Sci  Appl. 1998 Apr 10;707(1-2):301-7. PubMed PMID: 9613963.
  53. Sabatelli P, Squarzoni S, Petrini S, Capanni C, Ognibene A, Cartegni L, Cobianchi F, Merlini L, Toniolo D, Maraldi NM. Oral exfoliative cytology for the  non-invasive diagnosis in X-linked Emery-Dreifuss muscular dystrophy patients and carriers. Neuromuscul Disord. 1998 Apr;8(2):67-71. 
  54. Capanni C, Squarzoni S, Petrini S, Villanova M, Muscari C, Maraldi NM, Guarnieri C, Caldarera CM. Increase of neuronal nitric oxide synthase in rat skeletal muscle during ageing. Biochem Biophys Res Commun. 1998 Apr 7;245(1):216-9. 
  55. Flamigni F, Marmiroli S, Capanni C, Stefanelli C, Guarnieri C, Caldarera CM. Phosphatidylinositol 3-kinase is required for the induction of ornithine decarboxylase in leukemia cells stimulated to growth. Biochem Biophys Res Commun. 1997 Oct 29;239(3):729-33.
  56. Neri LM, Santi S, Cinti C, Sabatelli P, Valmori A, Capanni C, Capitani S, Stuppia L, Maraldi NM. Multiple fluorescence and reflectance simultaneous detection by confocal microscopy of HaeIII digested DNA sequences. Eur J Cell Biol. 1996 Sep;71(1):120-8. 

 


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