N. Maraldi

发表

Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy.

L. Cartegni, N. Maraldi, D. Toniolo, 1997, Human molecular genetics.

Nuclear damages and oxidative stress: new perspectives for laminopathies

N. Maraldi, G. Lattanzi, N. Maraldi, 2012, European journal of histochemistry : EJH.

Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria

G. Novelli, N. Maraldi, C. Capanni, 2011, European journal of histochemistry : EJH.

Emerin expression at the early stages of myogenic differentiation.

C. Capanni, D. Toniolo, A. Ognibene, 2000, Differentiation; research in biological diversity.

Staurosporine treatment and serum starvation promote the cleavage of emerin in cultured mouse myoblasts: involvement of a caspase‐dependent mechanism

N. Maraldi, A. Ognibene, G. Lattanzi, 2001, FEBS letters.

Defective collagen VI α6 chain expression in the skeletal muscle of patients with collagen VI-related myopathies

A. Ferlini, M. Paulsson, P. Sabatelli, 2014, Biochimica et biophysica acta.

Critical Evaluation of the Use of Cell Cultures for Inclusion in Clinical Trials of Patients Affected by Collagen VI Myopathies

P. Bonaldo, P. Bernardi, A. Angelin, 2011, Journal of cellular physiology.

Collagen VI deficiency affects the organization of fibronectin in the extracellular matrix of cultured fibroblasts.

E. Bertini, N. Maraldi, C. Capanni, 2001, Matrix biology : journal of the International Society for Matrix Biology.

Functional domains of the nucleus: implications for Emery–Dreifuss muscular dystrophy

N. Maraldi, A. Ognibene, G. Lattanzi, 2002, Neuromuscular Disorders.

EM.P.5.04 Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic mice

N. Maraldi, P. Bonaldo, P. Bernardi, 2009, Neuromuscular Disorders.

Emerin increase in regenerating muscle fibers.

C. Capanni, G. Lattanzi, M. Columbaro, 2009, European journal of histochemistry : EJH.

Hereditary motor and sensory neuropathy Lom type in an Italian Gypsy family

L. Kalaydjieva, A. Malandrini, M. Villanova, 1998, Neuromuscular Disorders.

Lamin A N-terminal phosphorylation is associated with myoblast activation: impairment in Emery–Dreifuss muscular dystrophy

C. Capanni, A. Ognibene, G. Lattanzi, 2005, Journal of Medical Genetics.

Increase of neuronal nitric oxide synthase in rat skeletal muscle during ageing.

C. Caldarera, S. Petrini, M. Villanova, 1998, Biochemical and biophysical research communications.

Emerin presence in platelets

S. Petrini, G. Zauli, C. Capanni, 2000, Acta Neuropathologica.

Nuclear changes in a case of X‐linked Emery‐Dreifuss muscular dystrophy

S. Petrini, M. Villanova, A. Ognibene, 1999, Muscle & nerve.

Erratum - Autophagic Degradation of Farnesylated Prelamin a as a Therapeutic Approach to Lamin-Linked Progeria

G. Novelli, C. Capanni, G. Lattanzi, 2013, European Journal of Histochemistry : EJH.

Decreased expression of laminin β1 in chromosome 21-linked Bethlem myopathy

A. Malandrini, M. Villanova, P. Sabatelli, 1999, Neuromuscular Disorders.

Decreased expression of laminin beta 1 in chromosome 21-linked Bethlem myopathy.

A. Malandrini, M. Villanova, P. Sabatelli, 1999, Neuromuscular Disorders.

Oral exfoliative cytology for the non-invasive diagnosis in X-linked Emery–Dreifuss muscular dystrophy patients and carriers

L. Cartegni, S. Petrini, C. Capanni, 1998, Neuromuscular Disorders.

Rescue of heterochromatin organization in Hutchinson-Gilford progeria by drug treatment

G. Novelli, N. Maraldi, C. Capanni, 2005, Cellular and Molecular Life Sciences.

Immunocytochemical detection of emerin within the nuclear matrix

L. Cartegni, S. Petrini, D. Toniolo, 1997, Neuromuscular Disorders.

Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle

N. Maraldi, C. Capanni, K. Scotlandi, 2011, Cell Death and Differentiation.

Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria

C. Vigouroux, G. Novelli, M. Magnani, 2009, European journal of histochemistry : EJH.

Localization of dystrophin COOH-terminal domain by the fracture-label technique

M. Maltarello, P. Sabatelli, S. Squarzoni, 1992, The Journal of cell biology.

Considerations on ceramic prosthesis explants.

S. Stea, S. Squarzoni, A. Sudanese, 1992, La Chirurgia degli organi di movimento.

Intracellular detection of laminin α 2 chain in skin by electron microscopy immunocytochemistry: Comparison between normal and laminin α 2 chain deficient subjects

G. Guazzi, A. Malandrini, A. Pini, 1997, Neuromuscular Disorders.

Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria.

C. Vigouroux, G. Novelli, M. Magnani, 2009, European journal of histochemistry : EJH.

Histological and Clinical Survey of Polylactic-Polyglycolic Acid and Dextrane Copolymer in Maxillary Sinus Lift: A Pilot in Vivo Study

N. Maraldi, M. Maltarello, L. Sbordone, 2008, International journal of immunopathology and pharmacology.

Localization of laminin α2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

F. Muntoni, J. Six, L. Palma, 1997, Acta Neuropathologica.