Patrizia Sabatelli
Patrizia Sabatelli
Unknown affiliation
Verified email at area.bo.cnr.it
Title
Cited by
Cited by
Year
Mitochondrial dysfunction and apoptosis in myopathic mice with collagen VI deficiency
WA Irwin, N Bergamin, P Sabatelli, C Reggiani, A Megighian, L Merlini, ...
Nature genetics 35 (4), 367-371, 2003
4392003
Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration
P Grumati, L Coletto, P Sabatelli, M Cescon, A Angelin, E Bertaggia, ...
Nature medicine 16 (11), 1313, 2010
4082010
POMT2 mutations cause α-dystroglycan hypoglycosylation and Walker-Warburg syndrome
J van Reeuwijk, M Janssen, C van den Elzen, DBV De Bernabé, ...
Journal of medical genetics 42 (12), 907-912, 2005
3822005
Ullrich scleroatonic muscular dystrophy is caused by recessive mutations in collagen type VI
OC Vanegas, E Bertini, RZ Zhang, S Petrini, C Minosse, P Sabatelli, ...
Proceedings of the National Academy of Sciences 98 (13), 7516-7521, 2001
2982001
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies
L Merlini, A Angelin, T Tiepolo, P Braghetta, P Sabatelli, A Zamparelli, ...
Proceedings of the National Academy of Sciences 105 (13), 5225-5229, 2008
1952008
Mitochondrial dysfunction in the pathogenesis of Ullrich congenital muscular dystrophy and prospective therapy with cyclosporins
A Angelin, T Tiepolo, P Sabatelli, P Grumati, N Bergamin, C Golfieri, ...
Proceedings of the National Academy of Sciences 104 (3), 991-996, 2007
1832007
EMILIN-1 deficiency induces elastogenesis and vascular cell defects
M Zanetti, P Braghetta, P Sabatelli, I Mura, R Doliana, A Colombatti, ...
Molecular and cellular biology 24 (2), 638-650, 2004
1792004
Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophy
E Demir, P Sabatelli, V Allamand, A Ferreiro, B Moghadaszadeh, ...
The American Journal of Human Genetics 70 (6), 1446-1458, 2002
1692002
Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human
M Neri, S Torelli, S Brown, I Ugo, P Sabatelli, L Merlini, P Spitali, ...
Neuromuscular Disorders 17 (11-12), 913-918, 2007
1622007
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
1461997
Preclinical PK and PD studies on 2′-O-methyl-phosphorothioate RNA antisense oligonucleotides in the mdx mouse model
H Heemskerk, C De Winter, P Van Kuik, N Heuvelmans, P Sabatelli, ...
Molecular Therapy 18 (6), 1210-1217, 2010
1362010
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
1192001
Emilin1 deficiency causes structural and functional defects of lymphatic vasculature
C Danussi, P Spessotto, A Petrucco, B Wassermann, P Sabatelli, ...
Molecular and cellular biology 28 (12), 4026-4039, 2008
1152008
The 180-kDa isoform of topoisomerase II is localized in the nucleolus and belongs to the structural elements of the nucleolar remnant
N Zini, AM Martelli, P Sabatelli, S Santi, GCBA RICOTTI, NM MARALOI, ...
Experimental cell research 200, 460-466, 1992
1151992
The cyclophilin inhibitor Debio 025 normalizes mitochondrial function, muscle apoptosis and ultrastructural defects in Col6a1−/− myopathic mice
T Tiepolo, A Angelin, E Palma, P Sabatelli, L Merlini, L Nicolosi, F Finetti, ...
British journal of pharmacology 157 (6), 1045-1052, 2009
1112009
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy
I Filesi, F Gullotta, G Lattanzi, MR D'Apice, C Capanni, AM Nardone, ...
Physiological genomics 23 (2), 150-158, 2005
1112005
Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice
E Palma, T Tiepolo, A Angelin, P Sabatelli, NM Maraldi, E Basso, ...
Human molecular genetics 18 (11), 2024-2031, 2009
1052009
Muscle interstitial fibroblasts are the main source of collagen VI synthesis in skeletal muscle: implications for congenital muscular dystrophy types Ullrich and Bethlem
Y Zou, RZ Zhang, P Sabatelli, ML Chu, CG Bönnemann
Journal of Neuropathology & Experimental Neurology 67 (2), 144-154, 2008
1012008
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
981999
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
862003
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