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CAPANNI, CRISTINA

CAPANNI, CRISTINA  

Istituto di Genetica Molecolare "Luigi Luca Cavalli Sforza"  

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Risultati 1 - 20 di 75 (tempo di esecuzione: 0.015 secondi).
Titolo Data di pubblicazione Autore(i) File
All-trans retinoic acid and rapamycin normalize Hutchinson Gilford progeria fibroblast phenotype. 1-gen-2015 Pellegrini, C; Columbaro, M; Capanni, C; D'Apice, Mr; Cavallo, C; Murdocca, M; Lattanzi, G; Squarzoni, S
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy, 1-gen-2005 I. 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;
Altered adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browning 1-gen-2019 Pellegrini, C; Columbaro, M; Schena, E; Prencipe, S; Andrenacci, D; Iozzo, P; Angela Guzzardi, M; Capanni, C; Mattioli, E; Loi, M; Araujovilar, D; Squarzoni, S; Cinti, S; Morselli, P; Giorgetti, A; Zanotti, L; Gambineri, A; Lattanzi, G
Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment. 1-gen-2012 Camozzi, D; D'Apice, Mr; Schena, E; Cenni, V; Columbaro, M; Capanni, C; Maraldi, Nm; Squarzoni, S; Ortolani, M; Novelli, G; Lattanzi, G
Altered lamin A/C phosphorylation in Emery-Dreifuss muscle, 1-gen-2005 Ognibene, A; Cenni, V; Sabatelli, P; Mattioli, E; Marmiroli, S; Capanni, C; Squarzoni, S; Columbaro, M; Maraldi, Nm; Lattanzi, G
Altered Mitochondrial Dynamic in Lymphoblasts and Fibroblasts Mutated for FANCA-A Gene: The Central Role of DRP1 1-gen-2023 Bertola, N; Bruno, S; Capanni, C; Columbaro, M; Mazzarello, An; Corsolini, F; Regis, S; Degan, P; Cappelli, E; Ravera, S
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy, 1-gen-2005 Capanni, C; Mattioli, E; Columbaro, M; Lucarelli, E; Parnaik, Vk; Novelli, G; Wehnert, M; Cenni, V; Maraldi, Nm; Squarzoni, S; Lattanzi, G
Ankrd2 in Mechanotransduction and Oxidative Stress Response in Skeletal Muscle: New Cues for the Pathogenesis of Muscular Laminopathies 1-gen-2019 Cenni, V; Kojic, S; Capanni, C; Faulkner, G; Lattanzi, G
Apoptotic genes as potential markers of metastatic phenotype in human osteosarcoma cell lines. 1-gen-2008 Zucchini, C; Rocchi, A; Manara, Mc; De Sanctis, P; Capanni, C; Bianchini, M; Carinci, P; Scotlandi, K; Valvassori, L
Association of emerin with nuclear and cytoplasmic actin is regulated in differentiating myoblasts. 1-gen-2003 Lattanzi, G; Cenni, V; Marmiroli, S; Capanni, C; Mattioli, E; Merlini, L; Squarzoni, S; Maraldi, Nm
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria. 1-gen-2011 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.
Barrier-to-Autointegration Factor (BAF) evaluation during DNA-damage response. 1-gen-2016 Loi, Manuela; Cenni, Vittoria; Squarzoni, Stefano; Lattanzi, Giovanna; Capanni, Cristina
Barrier-to-Autointegration Factor (BAF) involvement in prelamin A-related chromatin organization changes. 1-gen-2016 Loi, M; Cenni, V; Duchi, S; Squarzoni, S; Lopezotin, C; Foisner, R; Lattanzi, G; Capanni, C
Barrier-to-autointegration factor involvement in prelamin A-related chromatin remodeling 1-gen-2014 Manuela Loi ; Cristina Capanni ; ;Vittoria Cenni ; Roland Foisner ; Stefano Squarzoni ;Giovanna Lattanzi ;.
Barrier-to-autointegration factor involvement in prelamin A-related chromatin remodeling 1-gen-2013 Cristina Capanni ; Vittoria Cenni ; Manuela Loi ; Tokuko Haraguchi ; Roland Foisner ; Nadir M. Maraldi ; Stefano Squarzoni ;Giovanna Lattanzi ;.
Barrier-to-autointegration factor nuclear localization is a common feature in prelamin A accumulating cells under pathological or physiological conditions. 1-gen-2011 Capanni, C; Cenni, V; Novelli, G; Wehnert, M; Squarzoni, S; M Maraldi, N; Lattanzi, G
Barrier-to-autointegration factors nuclear localization and LAP2alpha mislocalization are a common features in laminopathies with defective prelamin A processing. 1-gen-2010 Capanni, C; Columbaro, M; Foisner, R; Novelli, G; Whenert, M; Squarzoni, S; Maraldi, Nm; Lattanzi, G
Changes in vimentin, lamin A/C and mitofilin induce aberrant cell organization in fibroblasts from Fanconi anemia complementation group A (FA-A) patients 1-gen-2013 Capanni C; Bruschi M; Columbaro M; Cuccarolo P; Ravera S; Dufour C; Candiano G; Petretto A; Degan P; Cappelli E.
Characterization of new genetic defects in mad 1-gen-2011 Lattanzi, G; Capanni, C; Mattioli, E; Columbaro, M; Del Coco, R; Camozzi, D; Schena, E; Dapice, Mr; Vielle, A; Lombardi, F; Gullotta, F; Postorivo, D; Nardone, Am; Dadamo, M; Sbraccia, P; Squarzoni, S; Novelli, G; Maraldi, Nm
Characterization of prelamin A forms accumulated in Mandibuloacral Dysplasia and prospects for therapy 1-gen-2008 Schena E; Cenni V; Columbaro M; Camozzi D; Capanni C; Squarzoni S; Vielle A; Greggi T; DApice MR; Novelli G; Maraldi NM; Lattanzi G.