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Nadir M Maraldi

Showing results (11-20 of 41) with videos related to

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Molecular Biology of the Cell|July 9, 2011
Ankrd2/ARPP is a novel Akt2 specific substrate and regulates myogenic differentiation upon cellular exposure to H(2)O(2)Vittoria Cenni, Alberto Bavelloni, Francesca Beretti, et al.
Advances in Enzyme Regulation|November 2, 2010
Muscular laminopathies: role of prelamin A in early steps of muscle differentiationNadir M Maraldi, Cristina Capanni, Rosalba Del Coco, et al.
Human Molecular Genetics|March 19, 2009
Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic miceElena Palma, Tania Tiepolo, Alessia Angelin, et al.
Experimental & Molecular Medicine|January 30, 2004
Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibitionCristina Capanni, Patrizia Sabatelli, Elisabetta Mattioli, et al.
Neurobiology of Disease|September 3, 2005
Cell-specific expression of the epm1 (cystatin B) gene in developing rat cerebellumMassimo Riccio, Spartaco Santi, Maja Dembic, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 26, 2008
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathiesLuciano Merlini, Alessia Angelin, Tania Tiepolo, et al.
Cell Cycle (Georgetown, Tex.)|September 1, 2012
Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistributionCristina Capanni, Stefano Squarzoni, Vittoria Cenni, et al.
Experimental Cell Research|November 5, 2003
Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcriptionCristina Capanni, Vittoria Cenni, Elisabetta Mattioli, et al.
Experimental Cell Research|December 21, 2007
Drugs affecting prelamin A processing: effects on heterochromatin organizationElisabetta Mattioli, Marta Columbaro, Cristina Capanni, et al.
Human Molecular Genetics|April 22, 2005
Altered pre-lamin A processing is a common mechanism leading to lipodystrophyCristina Capanni, Elisabetta Mattioli, Marta Columbaro, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Molecular Biology of the Cell|July 9, 2011
Ankrd2/ARPP is a novel Akt2 specific substrate and regulates myogenic differentiation upon cellular exposure to H(2)O(2)Vittoria Cenni, Alberto Bavelloni, Francesca Beretti, et al.
Advances in Enzyme Regulation|November 2, 2010
Muscular laminopathies: role of prelamin A in early steps of muscle differentiationNadir M Maraldi, Cristina Capanni, Rosalba Del Coco, et al.
Human Molecular Genetics|March 19, 2009
Genetic ablation of cyclophilin D rescues mitochondrial defects and prevents muscle apoptosis in collagen VI myopathic miceElena Palma, Tania Tiepolo, Alessia Angelin, et al.
Experimental & Molecular Medicine|January 30, 2004
Dysferlin in a hyperCKaemic patient with caveolin 3 mutation and in C2C12 cells after p38 MAP kinase inhibitionCristina Capanni, Patrizia Sabatelli, Elisabetta Mattioli, et al.
Neurobiology of Disease|September 3, 2005
Cell-specific expression of the epm1 (cystatin B) gene in developing rat cerebellumMassimo Riccio, Spartaco Santi, Maja Dembic, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 26, 2008
Cyclosporin A corrects mitochondrial dysfunction and muscle apoptosis in patients with collagen VI myopathiesLuciano Merlini, Alessia Angelin, Tania Tiepolo, et al.
Cell Cycle (Georgetown, Tex.)|September 1, 2012
Familial partial lipodystrophy, mandibuloacral dysplasia and restrictive dermopathy feature barrier-to-autointegration factor (BAF) nuclear redistributionCristina Capanni, Stefano Squarzoni, Vittoria Cenni, et al.
Experimental Cell Research|November 5, 2003
Failure of lamin A/C to functionally assemble in R482L mutated familial partial lipodystrophy fibroblasts: altered intermolecular interaction with emerin and implications for gene transcriptionCristina Capanni, Vittoria Cenni, Elisabetta Mattioli, et al.
Experimental Cell Research|December 21, 2007
Drugs affecting prelamin A processing: effects on heterochromatin organizationElisabetta Mattioli, Marta Columbaro, Cristina Capanni, et al.
Human Molecular Genetics|April 22, 2005
Altered pre-lamin A processing is a common mechanism leading to lipodystrophyCristina Capanni, Elisabetta Mattioli, Marta Columbaro, et al.
Pageof 5