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Marina Mora

Showing results (51-60 of 122) with videos related to

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Journal of Neuropathology and Experimental Neurology|February 24, 2011
Human neurotrophin receptor p75NTR defines differentiation-oriented skeletal muscle precursor cells: implications for muscle regenerationEmanuela Colombo, Stefania Romaggi, Enzo Medico, et al.
Journal of Neuropathology and Experimental Neurology|June 4, 2008
The kinesin superfamily motor protein KIF4 is associated with immune cell activation in idiopathic inflammatory myopathiesPia Bernasconi, Cristina Cappelletti, Francesca Navone, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|July 8, 2018
Exosomes and exosomal miRNAs from muscle-derived fibroblasts promote skeletal muscle fibrosisSimona Zanotti, Sara Gibertini, Flavia Blasevich, et al.
Journal of Cachexia, Sarcopenia and Muscle|January 29, 2020
Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy patientsDaniele Capitanio, Manuela Moriggi, Enrica Torretta, et al.
Biochemical and Biophysical Research Communications|January 11, 2015
A rare mutation in MYH7 gene occurs with overlapping phenotypeLucia Ruggiero, Chiara Fiorillo, Sara Gibertini, et al.
Neuromuscular Disorders : NMD|March 5, 2017
Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvementSara Missaglia, Lorenzo Maggi, Marina Mora, et al.
Pharmacological Research|July 2, 2021
Targeting HDAC8 to ameliorate skeletal muscle differentiation in Duchenne muscular dystrophyMarco Spreafico, Marco Cafora, Cinzia Bragato, et al.
Molecular Genetics and Metabolism Reports|January 11, 2017
Pure myopathy with enlarged mitochondria associated to a new mutation in <i>MTND2</i> geneAlice Zanolini, Ana Potic, Franco Carrara, et al.
Frontiers in Cell and Developmental Biology|March 15, 2021
Gain-of-Function STIM1 L96V Mutation Causes Myogenesis Alteration in Muscle Cells From a Patient Affected by Tubular Aggregate MyopathyElena Conte, Alessandra Pannunzio, Paola Imbrici, et al.
Frontiers in Microbiology|February 8, 2021
Unravelling the Role of Rumen Microbial Communities, Genes, and Activities on Milk Fatty Acid Profile Using a Combination of Omics ApproachesSokratis Stergiadis, Irene Cabeza-Luna, Marina Mora-Ortiz, et al.
Pageof 13

Showing results (51-60 of 122) with videos related to

Sort By:
Pageof 13
Journal of Neuropathology and Experimental Neurology|February 24, 2011
Human neurotrophin receptor p75NTR defines differentiation-oriented skeletal muscle precursor cells: implications for muscle regenerationEmanuela Colombo, Stefania Romaggi, Enzo Medico, et al.
Journal of Neuropathology and Experimental Neurology|June 4, 2008
The kinesin superfamily motor protein KIF4 is associated with immune cell activation in idiopathic inflammatory myopathiesPia Bernasconi, Cristina Cappelletti, Francesca Navone, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|July 8, 2018
Exosomes and exosomal miRNAs from muscle-derived fibroblasts promote skeletal muscle fibrosisSimona Zanotti, Sara Gibertini, Flavia Blasevich, et al.
Journal of Cachexia, Sarcopenia and Muscle|January 29, 2020
Comparative proteomic analyses of Duchenne muscular dystrophy and Becker muscular dystrophy muscles: changes contributing to preserve muscle function in Becker muscular dystrophy patientsDaniele Capitanio, Manuela Moriggi, Enrica Torretta, et al.
Biochemical and Biophysical Research Communications|January 11, 2015
A rare mutation in MYH7 gene occurs with overlapping phenotypeLucia Ruggiero, Chiara Fiorillo, Sara Gibertini, et al.
Neuromuscular Disorders : NMD|March 5, 2017
Late onset of neutral lipid storage disease due to novel PNPLA2 mutations causing total loss of lipase activity in a patient with myopathy and slight cardiac involvementSara Missaglia, Lorenzo Maggi, Marina Mora, et al.
Pharmacological Research|July 2, 2021
Targeting HDAC8 to ameliorate skeletal muscle differentiation in Duchenne muscular dystrophyMarco Spreafico, Marco Cafora, Cinzia Bragato, et al.
Molecular Genetics and Metabolism Reports|January 11, 2017
Pure myopathy with enlarged mitochondria associated to a new mutation in <i>MTND2</i> geneAlice Zanolini, Ana Potic, Franco Carrara, et al.
Frontiers in Cell and Developmental Biology|March 15, 2021
Gain-of-Function STIM1 L96V Mutation Causes Myogenesis Alteration in Muscle Cells From a Patient Affected by Tubular Aggregate MyopathyElena Conte, Alessandra Pannunzio, Paola Imbrici, et al.
Frontiers in Microbiology|February 8, 2021
Unravelling the Role of Rumen Microbial Communities, Genes, and Activities on Milk Fatty Acid Profile Using a Combination of Omics ApproachesSokratis Stergiadis, Irene Cabeza-Luna, Marina Mora-Ortiz, et al.
Pageof 13