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Elisabetta Mattioli

Showing results (41-50 of 48) with videos related to

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Journal of Neuromuscular Diseases|April 25, 2022
A Single mtDNA Deletion in Association with a LMNA Gene New Frameshift Variant: A Case ReportVincenzo Montano, Michelangelo Mancuso, Costanza Simoncini, et al.
Neuromuscular Disorders : NMD|June 26, 2007
Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysisStefania Petrini, Adele D'Amico, Patrizio Sale, et al.
Aging|October 18, 2014
Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamicsVittoria Cenni, Cristina Capanni, Elisabetta Mattioli, et al.
Aging Cell|January 4, 2021
Interleukin-6 neutralization ameliorates symptoms in prematurely aged miceStefano Squarzoni, Elisa Schena, Patrizia Sabatelli, et al.
Experimental & Molecular Medicine|August 4, 2019
Altered adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browningCamilla Pellegrini, Marta Columbaro, Elisa Schena, et al.
Bone Reports|December 11, 2023
Clinical and functional characterization of <i>COL2A1</i> p.Gly444Ser variant: From a fetal phenotype to a previously undisclosed postnatal phenotypeEnrica Marchionni, Maria Rosaria D'Apice, Viviana Lupo, et al.
Cells|November 24, 2023
Mineralocorticoid Receptor Antagonism Prevents Type 2 Familial Partial Lipodystrophy Brown Adipocyte DysfunctionElisa Schena, Elisabetta Mattioli, Chiara Peres, et al.
Cells|September 13, 2025
Profibrotic Molecules Are Reduced in CRISPR-Edited Emery-Dreifuss Muscular Dystrophy FibroblastsEleonora Cattin, Elisa Schena, Elisabetta Mattioli, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
Journal of Neuromuscular Diseases|April 25, 2022
A Single mtDNA Deletion in Association with a LMNA Gene New Frameshift Variant: A Case ReportVincenzo Montano, Michelangelo Mancuso, Costanza Simoncini, et al.
Neuromuscular Disorders : NMD|June 26, 2007
Ullrich myopathy phenotype with secondary ColVI defect identified by confocal imaging and electron microscopy analysisStefania Petrini, Adele D'Amico, Patrizio Sale, et al.
Aging|October 18, 2014
Rapamycin treatment of Mandibuloacral dysplasia cells rescues localization of chromatin-associated proteins and cell cycle dynamicsVittoria Cenni, Cristina Capanni, Elisabetta Mattioli, et al.
Aging Cell|January 4, 2021
Interleukin-6 neutralization ameliorates symptoms in prematurely aged miceStefano Squarzoni, Elisa Schena, Patrizia Sabatelli, et al.
Experimental & Molecular Medicine|August 4, 2019
Altered adipocyte differentiation and unbalanced autophagy in type 2 Familial Partial Lipodystrophy: an in vitro and in vivo study of adipose tissue browningCamilla Pellegrini, Marta Columbaro, Elisa Schena, et al.
Bone Reports|December 11, 2023
Clinical and functional characterization of <i>COL2A1</i> p.Gly444Ser variant: From a fetal phenotype to a previously undisclosed postnatal phenotypeEnrica Marchionni, Maria Rosaria D'Apice, Viviana Lupo, et al.
Cells|November 24, 2023
Mineralocorticoid Receptor Antagonism Prevents Type 2 Familial Partial Lipodystrophy Brown Adipocyte DysfunctionElisa Schena, Elisabetta Mattioli, Chiara Peres, et al.
Cells|September 13, 2025
Profibrotic Molecules Are Reduced in CRISPR-Edited Emery-Dreifuss Muscular Dystrophy FibroblastsEleonora Cattin, Elisa Schena, Elisabetta Mattioli, et al.
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