Search Results - "Maraldi, N.M."

Nuclear damages and oxidative stress: new perspectives for laminopathies by Lattanzi, G, Marmiroli, S, Facchini, A, Maraldi, N M

“…Mutations in genes encoding nuclear envelope proteins, particularly LMNA encoding the A-type lamins, cause a broad range of diverse diseases, referred to as…”
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Bent spine syndrome due to myofibrillar myopathy by Valentino, M.L, Columbaro, M, Avoni, P, Bisulli, F, Maraldi, N.M, Liguori, R

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Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria by Cenni, V, Capanni, C, Columbaro, M, Ortolani, M, D'Apice, M R, Novelli, G, Fini, M, Marmiroli, S, Scarano, E, Maraldi, N M, Squarzoni, S, Prencipe, S, Lattanzi, G

“…Farnesylated prelamin A is a processing intermediate produced in the lamin A maturation pathway. Accumulation of a truncated farnesylated prelamin A form,…”
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Erratum - Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria by Cenni, V., Capanni, C., Columbaro, M., Ortolani, M., D'Apice, M.R., Novelli, G., Fini, M., Marmiroli, S., Scarano, E., Maraldi, N.M., Squarzoni, S., Prencipe, S., Lattanzi, G.

“…We refer to our article by Vittoria Cenni et al. published in the European Journal of Histochemistry…”
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P2.3 Monoamine oxidase inhibitors reduce mitochondrial ROS accumulation and dysfunction in patients with collagen VI myopathies by Menazza, S, Zulian, A, Sabatelli, P, Maraldi, N.M, Merlini, L, Bonaldo, P, Bernardi, P, Di Lisa, F, Canton, M

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EM.I.2 Toward a mitochondrial therapy of collagen VI muscular dystrophies by Bernardi, P, Bonaldo, P, Sabatelli, P, Maraldi, N.M, Merlini, L

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O.17 Autophagy thwarts collagen VI muscular dystrophies by Grumati, P, Coletto, L, Sabatelli, P, Cescon, M, Angelin, A, Bertaggia, E, Blaauw, B, Urciuolo, A, Merlini, L, Maraldi, N.M, Bernardi, P, Sandri, M, Bonaldo, P

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P2.7 Collagen VI alpha5 and alpha6 chains expression in human muscle by Sabatelli, P, Martoni, E, Gara, S.K, Squarzoni, S, Zamparelli, A, Paulsson, M, Wagener, R, Gualandi, F, Pellegrini, C, Merlini, L, Ferlini, A, Maraldi, N.M

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P1.28 Dystrophin mediates melanocytes attachment to dermal-epidermal junction in human skin by Pellegrini, C, Gualandi, F, Manzati, E, Merlini, L, Michelini, M.E, Benassi, L, Ferlini, A, Maraldi, N.M, Sabatelli, P

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Basic fibroblast growth factor enhances in vitro mineralization of rat bone marrow stromal cells grown on non-woven hyaluronic acid based polymer scaffold by Lisignoli, G., Zini, N., Remiddi, G., Piacentini, A., Puggioli, A., Trimarchi, C., Fini, M., Maraldi, N.M., Facchini, A.

“…A biodegradable non-woven hyaluronic acid polymer scaffold (Hyaff ® 11) was analysed in vitro as a carrier vehicle for differentiation and mineralization of…”
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EM.P.5.04 Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice by Tiepolo, T, Palma, E, Angelin, A, Sabatelli, P, Maraldi, N.M, Basso, E, Forte, A.M, Bernardi, P, Bonaldo, P

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EM.P.5.02 Role of mitochondria in the pathogenesis of muscular dystrophies by Palma, E, Angelin, A, Tiepolo, T, Sabatelli, P, Maraldi, N.M, Merlini, L, Bonaldo, P, Bernardi, P

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M.P.1.01 Pilot trial with cyclosporin A in patients with collagen VI myopathies by Merlini, L, Angelin, A, Tiepolo, T, Braghetta, P, Sabatelli, P, Zamparelli, A, Armaroli, A, Michelini, M.E, Ferlini, A, Maraldi, N.M, Bonaldo, P, Bernardi, P

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EM.P.4.03 Extensive sequencing of COL6A genes in a cohort of 65 patients with collagen type VI related myopathies. Focus on splicing mutations causing Ullrich congenital muscular dystrophy by Martoni, E, Urciuolo, A, Trabanelli, C, Fabris, M, Sabatelli, P, Bertini, E, Mercuri, E, Maraldi, N.M, Bernardi, P, Bonaldo, P, Merlini, L, Ferlini, A, Gualandi, F

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EM.P.5.01 Gene expression and proteome profiles in Col6a1−/− mice, a model of Ullrich congenital muscular dystrophy (UCMD) by Bovolenta, M, De Palma, S, Vasso, M, Maraldi, N.M, Gualandi, F, Merlini, L, Sabatelli, P, Tiepolo, T, Bonaldo, P, Bernardi, P, Gelfi, C, Ferlini, A

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Nuclear changes in a case of X-linked Emery-Dreifuss muscular dystrophy by Ognibene, A., Sabatelli, P., Petrini, S., Squarzoni, S., Riccio, M., Santi, S., Villanova, M., Palmeri, S., Merlini, L., Maraldi, N.M.

“…Ultrastructural alterations in the nuclear architecture were found in skeletal muscle and skin cultured cells from a patient affected by X‐linked…”
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62 Multifractal and Topological Analysis of Trabecular Bone Structure Related to Osteoporosis by Santoro, R, Servizi, G, Turchetti, G, Busacca, M, Vanel, D, Maraldi, N.M, Canini, R, Albisinni, U

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Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery–Dreifuss muscular dystrophy patients and carriers by Sabatelli, P, Squarzoni, S, Petrini, S, Capanni, C, Ognibene, A, Cartegni, L, Cobianchi, F, Merlini, L, Toniolo, D, Maraldi, N.M

“…Emery–Dreifuss muscular dystrophy (EMD) is an inherited myopathy characterised by muscle contractures, progressive muscle wasting and weakness, with…”
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Ultrastructural changes in muscle cells of patients with collagen VI-related myopathies by Tagliavini, F., Sardone, F., Squarzoni, S., Maraldi, N.M., Merlini, L., Faldini, C., Sabatelli, P.

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Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies by Tagliavini, F., Pellegrini, C., Sardone, F., Squarzoni, S., Paulsson, M., Wagener, R., Gualandi, F., Trabanelli, C., Ferlini, A., Merlini, L., Santi, S., Maraldi, N.M., Faldini, C., Sabatelli, P.

“…Collagen VI is a non-fibrillar collagen present in the extracellular matrix (ECM) as a complex polymer; the mainly expressed form is composed of α1, α2 and α3…”
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