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Carlo Minetti

Showing results (121-130 of 190) with videos related to

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Laboratory Investigation; a Journal of Technical Methods and Pathology|February 7, 2008
Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitroMonica Traverso, Elisabetta Gazzerro, Stefania Assereto, et al.
Biochemical and Biophysical Research Communications|March 15, 2008
Clinical and genetic characterization of Chanarin-Dorfman syndromeClaudio Bruno, Enrico Bertini, Maja Di Rocco, et al.
Cell Cycle (Georgetown, Tex.)|December 3, 2011
Hyperactivation of oxidative mitochondrial metabolism in epithelial cancer cells in situ: visualizing the therapeutic effects of metformin in tumor tissueDiana Whitaker-Menezes, Ubaldo E Martinez-Outschoorn, Neal Flomenberg, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 1, 2007
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progressionMario Pescatori, Aldobrando Broccolini, Carlo Minetti, et al.
Journal of Neurology|February 20, 2022
Ocular phenotype and electroretinogram abnormalities in Lafora disease and correlation with disease stageAlessandro Orsini, Daniele Ferrari, Antonella Riva, et al.
The American Journal of Pathology|November 19, 2018
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular DystrophyElisabetta Gazzerro, Serena Baratto, Stefania Assereto, et al.
Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Frontiers in Neurology|October 22, 2021
The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic OutcomeMarco Veneruso, Chiara Fiorillo, Paolo Broda, et al.
Plos One|March 31, 2012
Hyccin, the molecule mutated in the leukodystrophy hypomyelination and congenital cataract (HCC), is a neuronal proteinElisabetta Gazzerro, Simona Baldassari, Caterina Giacomini, et al.
Archives of Neurology|September 14, 2011
Hypomyelination and congenital cataract: broadening the clinical phenotypeRoberta Biancheri, Federico Zara, Andrea Rossi, et al.
Pageof 19

Showing results (121-130 of 190) with videos related to

Sort By:
Pageof 19
Laboratory Investigation; a Journal of Technical Methods and Pathology|February 7, 2008
Caveolin-3 T78M and T78K missense mutations lead to different phenotypes in vivo and in vitroMonica Traverso, Elisabetta Gazzerro, Stefania Assereto, et al.
Biochemical and Biophysical Research Communications|March 15, 2008
Clinical and genetic characterization of Chanarin-Dorfman syndromeClaudio Bruno, Enrico Bertini, Maja Di Rocco, et al.
Cell Cycle (Georgetown, Tex.)|December 3, 2011
Hyperactivation of oxidative mitochondrial metabolism in epithelial cancer cells in situ: visualizing the therapeutic effects of metformin in tumor tissueDiana Whitaker-Menezes, Ubaldo E Martinez-Outschoorn, Neal Flomenberg, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|February 1, 2007
Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progressionMario Pescatori, Aldobrando Broccolini, Carlo Minetti, et al.
Journal of Neurology|February 20, 2022
Ocular phenotype and electroretinogram abnormalities in Lafora disease and correlation with disease stageAlessandro Orsini, Daniele Ferrari, Antonella Riva, et al.
The American Journal of Pathology|November 19, 2018
The Danger Signal Extracellular ATP Is Involved in the Immunomediated Damage of α-Sarcoglycan-Deficient Muscular DystrophyElisabetta Gazzerro, Serena Baratto, Stefania Assereto, et al.
Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Frontiers in Neurology|October 22, 2021
The Role of Muscle Biopsy in Diagnostic Process of Infant Hypotonia: From Clinical Classification to the Genetic OutcomeMarco Veneruso, Chiara Fiorillo, Paolo Broda, et al.
Plos One|March 31, 2012
Hyccin, the molecule mutated in the leukodystrophy hypomyelination and congenital cataract (HCC), is a neuronal proteinElisabetta Gazzerro, Simona Baldassari, Caterina Giacomini, et al.
Archives of Neurology|September 14, 2011
Hypomyelination and congenital cataract: broadening the clinical phenotypeRoberta Biancheri, Federico Zara, Andrea Rossi, et al.
Pageof 19