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Stefano Squarzoni
Stefano Squarzoni
IGM CNR
Verified email at area.bo.cnr.it
Title
Cited by
Cited by
Year
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy
C Capanni, E Mattioli, M Columbaro, E Lucarelli, VK Parnaik, G Novelli, ...
Human molecular genetics 14 (11), 1489-1502, 2005
2532005
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment
M Columbaro, C Capanni, E Mattioli, G Novelli, VK Parnaik, S Squarzoni, ...
Cellular and molecular life sciences 62, 2669-2678, 2005
1882005
Intramembrane protein distribution in cell cultures is affected by 50 Hz pulsed magnetic fields
F Bersani, F Marinelli, A Ognibene, A Matteucci, S Cecchi, S Santi, ...
Bioelectromagnetics: Journal of the Bioelectromagnetics Society, The Society …, 1997
1691997
Fretting wear in a modular neck hip prosthesis
M Viceconti, M Baleani, S Squarzoni, A Tonil
Journal of Biomedical Materials Research: An Official Journal of The Society …, 1997
1661997
Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy
L Cartegni, MR Di Barletta, R Barresi, S Squarzoni, P Sabatelli, N Maraldi, ...
Human molecular genetics 6 (13), 2257-2264, 1997
1651997
Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts
P Sabatelli, P Bonaldo, G Lattanzi, P Braghetta, N Bergamin, C Capanni, ...
Matrix Biology 20 (7), 475-486, 2001
1462001
Autosomal recessive myosclerosis myopathy is a collagen VI disorder
L Merlini, E Martoni, P Grumati, P Sabatelli, S Squarzoni, A Urciuolo, ...
Neurology 71 (16), 1245-1253, 2008
1412008
Early diagnosis of ceramic liner fracture: guidelines based on a twelve-year clinical experience
A Toni, F Traina, S Stea, A Sudanese, M Visentin, B Bordini, S Squarzoni
JBJS 88 (suppl_4), 55-63, 2006
1412006
Diverse lamin-dependent mechanisms interact to control chromatin dynamics: Focus on laminopathies
D Camozzi, C Capanni, V Cenni, E Mattioli, M Columbaro, S Squarzoni, ...
Nucleus 5 (5), 427-440, 2014
1292014
Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts
G Lattanzi, V Cenni, S Marmiroli, C Capanni, E Mattioli, L Merlini, ...
Biochemical and biophysical research communications 303 (3), 764-770, 2003
1142003
Nuclear changes in a case of X‐linked Emery‐Dreifuss muscular dystrophy
A Ognibene, P Sabatelli, S Petrini, S Squarzoni, M Riccio, S Santi, ...
Muscle & Nerve: Official Journal of the American Association of …, 1999
1141999
Lamin A/C sustains PcG protein architecture, maintaining transcriptional repression at target genes
E Cesarini, C Mozzetta, F Marullo, F Gregoretti, A Gargiulo, M Columbaro, ...
Journal of Cell Biology 211 (3), 533-551, 2015
1072015
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria
V Cenni, C Capanni, M Columbaro, M Ortolani, MR D'Apice, G Novelli, ...
European journal of histochemistry: EJH 55 (4), 2011
1072011
Expression of the collagen VI α5 and α6 chains in normal human skin and in skin of patients with collagen VI-related myopathies
P Sabatelli, SK Gara, P Grumati, A Urciuolo, F Gualandi, R Curci, ...
Journal of Investigative Dermatology 131 (1), 99-107, 2011
982011
Expression of collagen VI α5 and α6 chains in human muscle and in Duchenne muscular dystrophy-related muscle fibrosis
P Sabatelli, F Gualandi, SK Gara, P Grumati, A Zamparelli, E Martoni, ...
Matrix Biology 31 (3), 187-196, 2012
972012
Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle
E Mattioli, M Columbaro, C Capanni, NM Maraldi, V Cenni, K Scotlandi, ...
Cell Death & Differentiation 18 (8), 1305-1315, 2011
962011
Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for …
C Capanni, V Cenni, E Mattioli, P Sabatelli, A Ognibene, M Columbaro, ...
Experimental cell research 291 (1), 122-134, 2003
922003
Nuclear alterations in autosomal‐dominant Emery‐Dreifuss muscular dystrophy
P Sabatelli, G Lattanzi, A Ognibene, M Columbaro, C Capanni, L Merlini, ...
Muscle & Nerve: Official Journal of the American Association of …, 2001
922001
Dominant and recessive COL6A1 mutations in Ullrich scleroatonic muscular dystrophy
B Giusti, L Lucarini, V Pietroni, S Lucioli, B Bandinelli, P Sabatelli, ...
Annals of neurology 58 (3), 400-410, 2005
882005
Pre‐Lamin A processing is linked to heterochromatin organization
G Lattanzi, M Columbaro, E Mattioli, V Cenni, D Camozzi, M Wehnert, ...
Journal of cellular biochemistry 102 (5), 1149-1159, 2007
872007
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