MARALDI, NADIR
MARALDI, NADIR
DIPARTIMENTO DI SCIENZE BIOMEDICHE E NEUROMOTORIE
MARALDI N; Maraldi NM.; N. Maraldi; Nadir M. Maraldi; N.M. MARALDI; MARALDI M
A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome
2007 Maraldi NM; Capanni C; Mattioli E; Columbaro M; Squarzoni S; Parnaik WK; Wehnert M; Lattanzi G.
A-type lamins and signaling: The PI 3-kinase/Akt pathway moves forward.
2009 Marmiroli S; Bertacchini J; Beretti F; Cenni V; Guida M; De Pol A; Maraldi NM; Lattanzi G.
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy.
2005 Filesi I; Gullotta F; Lattanzi G; D'Apice MR; Capanni C; Nardone AM; Columbaro M; Scarano G; Mattioli E; Sabatelli P; Maraldi NM; Biocca S; Novelli G.
Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment
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 pre-lamin A processing is a common mechanism leading to lipodystrophy.
2005 Capanni C; Mattioli E; Columbaro M; Lucarelli E; Parnaik VK; Novelli G; Wehnert M; Cenni V; Maraldi NM; Squarzoni S; Lattanzi G.
Analysis of intracellular and intraviral localization of the human cytomegalovirus UL53 protein
2002 Dal Monte P.; Pignatelli S.; Zini N.; Maraldi N.M.; Perret E.; Prevost M.C.; Landini M.P.
Ankrd2/ARPP is a novel Akt2 specific substrate and regulates myogenic differentiation upon cellular exposure to H(2)O(2
2011 Cenni V; Bavelloni A; Beretti F; Tagliavini F; Manzoli L; Lattanzi G; Maraldi NM; Cocco L; Marmiroli S;
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria.
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;
Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration
2010 Grumati P; Coletto L; Sabatelli P; Cescon M; Angelin A; Bertaggia E; Blaauw B; Urciuolo A; Tiepolo T; Merlini L; Maraldi NM; Bernardi P; Sandri M; Bonaldo P
Cathepsin k antisense inhibition of cell polarization and bone resorption in human osteoclast
2004 Avnet S.; Lamolinara A.; Zini N.; Solimando L.; Quacquaruccio G.; Maraldi N.M.; Baldini N.; Giunti A.
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse.
2009 Rimessi P; Sabatelli P; Fabris M; Braghetta P; Bassi E; Spitali P; Vattemi G; Tomelleri G; Mari L; Perrone D; Medici A; Neri M; Bovolenta M; Martoni E; Maraldi NM; Gualandi F; Merlini L; Ballestri M; Tondelli L; Sparnacci K; Bonaldo P; Caputo A; Laus M; Ferlini A.
Cell-specific expression of the epm1 (cystatin B) gene in developing rat cerebellum.
2005 Riccio M;Santi S;Dembic M;Di Giaimo R;Cipollini E;Costantino-Ceccarini E;Ambrosetti D;Maraldi NM;Melli M
Cellular and molecular events during chondrogenesis of human mesenchymal stromal cells grown in a three-dimensional hyaluronan based scaffold
2005 Lisignoli G.; Cristino S.; Piacentini A.; Toneguzzi S.; Grassi F.; Cavallo C.; Zini N.; Solimando L.; Maraldi N.M.; Facchini A.
Collagen VI myopathies: from the animal model to the clinical trial.
2009 Maraldi NM; Sabatelli P; Columbaro M; Zamparelli A; Manzoli FA; Bernardi P; Bonaldo P; Merlini L.
Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 loci.
2004 Demir E; Ferreiro A; Sabatelli P; Allamand V; Makri S; Echenne B; Maraldi M; Merlini L; Topaloglu H; Guicheney P.
Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype.
2007 Lombardi F; Gullotta F; Columbaro M; Filareto A; D'Adamo M; Vielle A; Guglielmi V; Nardone AM; Azzolini V; Grosso E; Lattanzi G; D'Apice MR; Masala S; Maraldi NM; Sbraccia P; Novelli G.
Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies.
2012 Sabatelli P; Palma E; Angelin A; Squarzoni S; Urciuolo A; Pellegrini C; Tiepolo T; Bonaldo P; Gualandi F; Merlini L; Bernardi P; Maraldi NM.
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies
2008 Merlini L; Angelin A; Tiepolo T; Braghetta P; Sabatelli P; Zamparelli A; Ferlini A; Maraldi NM; Bonaldo P; Bernardi P.
Cyclosporine A in Ullrich congenital muscular dystrophy: long-term results.
2011 Merlini L; Sabatelli P; Armaroli A; Gnudi S; Angelin A; Grumati P; Michelini ME; Franchella A; Gualandi F; Bertini E; Maraldi NM; Ferlini A; Bonaldo P; Bernardi P.
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria.
2009 Dominici S; Fiori V; Magnani M; Schena E; Capanni C; Camozzi D; D'Apice MR; Le Dour C; Auclair M; Caron M; Novelli G; Vigouroux C; Maraldi NM; Lattanzi G.
Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
---|---|---|---|---|---|---|
A pathogenic mechanism leading to partial lipodistrophy and prospects for pharmacological treatment of insulin resistance syndrome | Maraldi NM; Capanni C; Mattioli E; Columbaro M; Squarzoni S; Parnaik WK; Wehnert M; Lattanzi G. | 2007-01-01 | ACTA BIO-MEDICA DE L'ATENEO PARMENSE | - | 1.01 Articolo in rivista | - |
A-type lamins and signaling: The PI 3-kinase/Akt pathway moves forward. | Marmiroli S; Bertacchini J; Beretti F; Cenni V; Guida M; De Pol A; Maraldi NM; Lattanzi G. | 2009-01-01 | JOURNAL OF CELLULAR PHYSIOLOGY | - | 1.01 Articolo in rivista | - |
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy. |
Filesi I; Gullotta F; Lattanzi G; D'Apice MR; Capanni C; Nardone AM; Columbaro M; Scarano G; Mat...tioli E; Sabatelli P; Maraldi NM; Biocca S; Novelli G. |
2005-01-01 | PHYSIOLOGICAL GENOMICS | - | 1.01 Articolo in rivista | - |
Altered chromatin organization and SUN2 localization in mandibuloacral dysplasia are rescued by drug treatment | Camozzi D; D'Apice MR; Schena E; Cenni V; Columbaro M; Capanni C; Maraldi NM; Squarzoni S; Ortola...ni M; Novelli G; Lattanzi G. | 2012-01-01 | HISTOCHEMISTRY AND CELL BIOLOGY | - | 1.01 Articolo in rivista | - |
Altered pre-lamin A processing is a common mechanism leading to lipodystrophy. |
Capanni C; Mattioli E; Columbaro M; Lucarelli E; Parnaik VK; Novelli G; Wehnert M; Cenni V; Mara...ldi NM; Squarzoni S; Lattanzi G. |
2005-01-01 | HUMAN MOLECULAR GENETICS | - | 1.01 Articolo in rivista | - |
Analysis of intracellular and intraviral localization of the human cytomegalovirus UL53 protein | Dal Monte P.; Pignatelli S.; Zini N.; Maraldi N.M.; Perret E.; Prevost M.C.; Landini M.P. | 2002-01-01 | JOURNAL OF GENERAL VIROLOGY | - | 1.01 Articolo in rivista | - |
Ankrd2/ARPP is a novel Akt2 specific substrate and regulates myogenic differentiation upon cellular exposure to H(2)O(2 | Cenni V; Bavelloni A; Beretti F; Tagliavini F; Manzoli L; Lattanzi G; Maraldi NM; Cocco L; Marmir...oli S; | 2011-01-01 | MOLECULAR BIOLOGY OF THE CELL | - | 1.01 Articolo in rivista | - |
Autophagic degradation of farnesylated prelamin A as a therapeutic approach to lamin-linked progeria. | 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; | 2011-01-01 | EUROPEAN JOURNAL OF HISTOCHEMISTRY | - | 1.01 Articolo in rivista | - |
Autophagy is defective in collagen VI muscular dystrophies, and its reactivation rescues myofiber degeneration | Grumati P; Coletto L; Sabatelli P; Cescon M; Angelin A; Bertaggia E; Blaauw B; Urciuolo A; Tiepol...o T; Merlini L; Maraldi NM; Bernardi P; Sandri M; Bonaldo P | 2010-01-01 | NATURE MEDICINE | - | 1.01 Articolo in rivista | - |
Cathepsin k antisense inhibition of cell polarization and bone resorption in human osteoclast | Avnet S.; Lamolinara A.; Zini N.; Solimando L.; Quacquaruccio G.; Maraldi N.M.; Baldini N.; Giunt...i A. | 2004-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
Cationic PMMA nanoparticles bind and deliver antisense oligoribonucleotides allowing restoration of dystrophin expression in the mdx mouse. | Rimessi P; Sabatelli P; Fabris M; Braghetta P; Bassi E; Spitali P; Vattemi G; Tomelleri G; Mari L...; Perrone D; Medici A; Neri M; Bovolenta M; Martoni E; Maraldi NM; Gualandi F; Merlini L; Ballestri M; Tondelli L; Sparnacci K; Bonaldo P; Caputo A; Laus M; Ferlini A. | 2009-01-01 | MOLECULAR THERAPY | - | 1.01 Articolo in rivista | - |
Cell-specific expression of the epm1 (cystatin B) gene in developing rat cerebellum. | Riccio M;Santi S;Dembic M;Di Giaimo R;Cipollini E;Costantino-Ceccarini E;Ambrosetti D;Maraldi NM;...Melli M | 2005-01-01 | NEUROBIOLOGY OF DISEASE | - | 1.01 Articolo in rivista | - |
Cellular and molecular events during chondrogenesis of human mesenchymal stromal cells grown in a three-dimensional hyaluronan based scaffold | Lisignoli G.; Cristino S.; Piacentini A.; Toneguzzi S.; Grassi F.; Cavallo C.; Zini N.; Solimando... L.; Maraldi N.M.; Facchini A. | 2005-01-01 | BIOMATERIALS | - | 1.01 Articolo in rivista | - |
Collagen VI myopathies: from the animal model to the clinical trial. | Maraldi NM; Sabatelli P; Columbaro M; Zamparelli A; Manzoli FA; Bernardi P; Bonaldo P; Merlini L. | 2009-01-01 | ADVANCES IN ENZYME REGULATION | - | 1.01 Articolo in rivista | - |
Collagen VI status and clinical severity in Ullrich congenital muscular dystrophy: phenotype analysis of 11 families linked to the COL6 loci. | Demir E; Ferreiro A; Sabatelli P; Allamand V; Makri S; Echenne B; Maraldi M; Merlini L; Topaloglu... H; Guicheney P. | 2004-01-01 | NEUROPEDIATRICS | - | 1.01 Articolo in rivista | - |
Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype. |
Lombardi F; Gullotta F; Columbaro M; Filareto A; D'Adamo M; Vielle A; Guglielmi V; Nardone AM; A...zzolini V; Grosso E; Lattanzi G; D'Apice MR; Masala S; Maraldi NM; Sbraccia P; Novelli G. |
2007-01-01 | THE JOURNAL OF CLINICAL ENDOCRINOLOGY AND METABOLISM | - | 1.01 Articolo in rivista | - |
Critical evaluation of the use of cell cultures for inclusion in clinical trials of patients affected by collagen VI myopathies. | Sabatelli P; Palma E; Angelin A; Squarzoni S; Urciuolo A; Pellegrini C; Tiepolo T; Bonaldo P; Gua...landi F; Merlini L; Bernardi P; Maraldi NM. | 2012-01-01 | JOURNAL OF CELLULAR PHYSIOLOGY | - | 1.01 Articolo in rivista | - |
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathies |
Merlini L; Angelin A; Tiepolo T; Braghetta P; Sabatelli P; Zamparelli A; Ferlini A; Maraldi NM; ...Bonaldo P; Bernardi P. |
2008-01-01 | PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA | - | 1.01 Articolo in rivista | - |
Cyclosporine A in Ullrich congenital muscular dystrophy: long-term results. | Merlini L; Sabatelli P; Armaroli A; Gnudi S; Angelin A; Grumati P; Michelini ME; Franchella A; Gu...alandi F; Bertini E; Maraldi NM; Ferlini A; Bonaldo P; Bernardi P. | 2011-01-01 | OXIDATIVE MEDICINE AND CELLULAR LONGEVITY | - | 1.01 Articolo in rivista | - |
Different prelamin A forms accumulate in human fibroblasts: a study in experimental models and progeria. | Dominici S; Fiori V; Magnani M; Schena E; Capanni C; Camozzi D; D'Apice MR; Le Dour C; Auclair M;... Caron M; Novelli G; Vigouroux C; Maraldi NM; Lattanzi G. | 2009-01-01 | EUROPEAN JOURNAL OF HISTOCHEMISTRY | - | 1.01 Articolo in rivista | - |