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Marina Mora

Showing results (71-80 of 122) with videos related to

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Neurology|October 27, 2015
Histologic muscular history in steroid-treated and untreated patients with Duchenne dystrophyLorenzo Peverelli, Silvia Testolin, Luisa Villa, et al.
Revista Medica Del Instituto Mexicano Del Seguro Social|May 10, 2019
Probiotics’ effectiveness on symptoms, histological features and feeding tolerance in ulcerative colitisAdhara Sánchez-Morales, Mayte Fabiola Pérez-Ayala, Margarita Cruz-Martínez, et al.
Neuromuscular Disorders : NMD|January 24, 2007
A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assayAstrid Milic, Nathalie Daniele, Hanns Lochmüller, et al.
Journal of Medical Genetics|July 3, 2015
A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemiaClaudia Di Blasi, Serena Sansanelli, Alessandra Ruggieri, et al.
Archives of Neurology|October 12, 2005
LAMA2 gene analysis in congenital muscular dystrophy: new mutations, prenatal diagnosis, and founder effectClaudia Di Blasi, Daniela Piga, Paolo Brioschi, et al.
Plos One|May 20, 2016
A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ ReleaseMaria Cristina D'Adamo, Luigi Sforna, Sergio Visentin, et al.
Journal of Cellular Physiology|September 25, 2018
HDAC8 regulates canonical Wnt pathway to promote differentiation in skeletal musclesLuca Ferrari, Cinzia Bragato, Loredana Brioschi, et al.
BMC Research Notes|December 15, 2011
Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2Claudia Di Blasi, Emanuela Bellafiore, Mustafa Am Salih, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|September 5, 2017
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expressionSamuele Gherardi, Matteo Bovolenta, Chiara Passarelli, et al.
Neuromuscular Disorders : NMD|February 12, 2013
Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohortMichela Catteruccia, Fabiana Fattori, Valentina Codemo, et al.
Pageof 13

Showing results (71-80 of 122) with videos related to

Sort By:
Pageof 13
Neurology|October 27, 2015
Histologic muscular history in steroid-treated and untreated patients with Duchenne dystrophyLorenzo Peverelli, Silvia Testolin, Luisa Villa, et al.
Revista Medica Del Instituto Mexicano Del Seguro Social|May 10, 2019
Probiotics’ effectiveness on symptoms, histological features and feeding tolerance in ulcerative colitisAdhara Sánchez-Morales, Mayte Fabiola Pérez-Ayala, Margarita Cruz-Martínez, et al.
Neuromuscular Disorders : NMD|January 24, 2007
A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assayAstrid Milic, Nathalie Daniele, Hanns Lochmüller, et al.
Journal of Medical Genetics|July 3, 2015
A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemiaClaudia Di Blasi, Serena Sansanelli, Alessandra Ruggieri, et al.
Archives of Neurology|October 12, 2005
LAMA2 gene analysis in congenital muscular dystrophy: new mutations, prenatal diagnosis, and founder effectClaudia Di Blasi, Daniela Piga, Paolo Brioschi, et al.
Plos One|May 20, 2016
A Calsequestrin-1 Mutation Associated with a Skeletal Muscle Disease Alters Sarcoplasmic Ca2+ ReleaseMaria Cristina D'Adamo, Luigi Sforna, Sergio Visentin, et al.
Journal of Cellular Physiology|September 25, 2018
HDAC8 regulates canonical Wnt pathway to promote differentiation in skeletal musclesLuca Ferrari, Cinzia Bragato, Loredana Brioschi, et al.
BMC Research Notes|December 15, 2011
Variable disease severity in Saudi Arabian and Sudanese families with c.3924 + 2 T > C mutation of LAMA2Claudia Di Blasi, Emanuela Bellafiore, Mustafa Am Salih, et al.
Biochimica Et Biophysica Acta. Gene Regulatory Mechanisms|September 5, 2017
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expressionSamuele Gherardi, Matteo Bovolenta, Chiara Passarelli, et al.
Neuromuscular Disorders : NMD|February 12, 2013
Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohortMichela Catteruccia, Fabiana Fattori, Valentina Codemo, et al.
Pageof 13