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COLUMBARO, MARTA

COLUMBARO, MARTA  

Istituto di Genetica Molecolare "Luigi Luca Cavalli Sforza"  

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Risultati 1 - 16 di 16 (tempo di esecuzione: 0.011 secondi).
Titolo Data di pubblicazione Autore(i) File
A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome 1-gen-2007 Maraldi, Nm; Capanni, C; Mattioli, E; Columbaro, M; Squarzoni, S; Parnaik, Wk; Wehnert, M; Lattanzi, G
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 expression of the MCSP/NG2 chondroitin sulfate proteoglycan in collagen VI deficiency, 1-gen-2005 S. PETRINI; A. TESSA; W.B. STALLCUP; P. SABATELLI; M. PESCATORI; B. GIUSTI; R. CARROZZO; M. VERARDO; N. BERGAMIN; M. COLUMBARO; C. BERNARDINI; L. MERLINI; G. PEPE; P. BONALDO; E. BERTINI;
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
ATP depletion inhibits thymocyte apoptosis 1-gen-1996 Stefanelli, C; Robuffo, I; Bonavita, F; Stanic, I; Columbaro, M; Farruggia, C; Pignatti, C; Rossoni, C; Caldarera, C M; Falcieri, E
Compound heterozygosity for mutations in LMNA in a patient with myopathic and lipodystrophic Mandibuloacral Dysplasia type A phenotype. 1-gen-2007 Lombardi, F; Gullotta, F; Columbaro, M; Filareto, A; Dadamo, M; Vielle, A; Guglielmi, V; Nardone, Am; Azzolini, V; Grosso, E; Lattanzi, G; Dapice, Mr; Masala, S; Maraldi, Nm; Sbraccia, P; Novelli, G
Drugs affecting prelamin A processing: Effects on heterochromatin organization. 1-gen-2008 Mattioli E; Columbaro M; Capanni C; Santi S; Maraldi NM; D'Apice MR; Novelli G; Riccio M; Squarzoni S; Foisner R; Lattanzi G.
Emerin increase in regenerating muscle fibers, 1-gen-2005 Squarzoni, S; Sabatelli, P; Capanni, C; Lattanzi, G; Rutigliano, C; Columbaro, M; Mattioli, E; Rocca, M; Maraldi, Nm
Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2, 1-gen-2005 L. MERLINI; P. SABATELLI; M. COLUMBARO; E. BONIFAZI; V. PISANI; R. MASSA; G. NOVELLI;
Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery-Dreifuss muscular dystrophy, 1-gen-2005 Cenni, V; Sabatelli, P; Mattioli, E; Marmiroli, S; Capanni, C; Ognibene, A; Squarzoni, S; Maraldi, Nm; Bonne, G; Columbaro, M; Merlini, L; Lattanzi, G
Laminopathies: a chromatin affair, 1-gen-2006 Maraldi, Nm; Lattanzi, G; Capanni, C; Columbaro, M; Mattioli, E; Sabatelli, P; Squarzoni, S; Manzoli, Fa
Nuclear envelope proteins and chromatin arrangem ent: a pathogenic mechanism for laminopathies, 1-gen-2006 Maraldi, Nm; Lattanzi, G; Capanni, C; Columbaro, M; Merlini, L; Mattioli, E; Sabatelli, P; Squarzoni, S; Manzoli, Fa
Prelamin A is involved in early steps of muscle differentiation. 1-gen-2008 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 processing and heterochromatin dynamics in laminopathies. 1-gen-2007 Maraldi, Nm; Mattioli, E; Lattanzi, G; Columbaro, M; Capanni, C; Camozzi, D; Squarzoni, S; Manzoli, Fa
Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment, 1-gen-2005 Columbaro, M; Capanni, C; Mattioli, E; Novelli, G; Parnaik, Vk; Squarzoni, S; Maraldi, Nm; Lattanzi, G
Ultrastructural defects of collagen VI filaments in an Ullrich syndrome patient with loss of the alpha3(VI) N10-N7 domains, 1-gen-2006 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