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Carlo Minetti

Showing results (91-100 of 190) with videos related to

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Laboratory Investigation; a Journal of Technical Methods and Pathology|June 14, 2016
The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophyStefania Assereto, Rosanna Piccirillo, Serena Baratto, et al.
Biochemical and Biophysical Research Communications|February 15, 2015
Early onset cardiomyopathy associated with the mitochondrial tRNALeu((UUR)) 3271T>C MELAS mutationGiacomo Brisca, Chiara Fiorillo, Claudia Nesti, et al.
Clinical Neuropathology|July 20, 2021
Muscle inflammatory pattern in alpha- and gamma-sarcoglycanopathiesChiara Panicucci, Serena Baratto, Lizzia Raffaghello, et al.
The American Journal of Pathology|March 23, 2010
Therapeutic potential of proteasome inhibition in Duchenne and Becker muscular dystrophiesElisabetta Gazzerro, Stefania Assereto, Andrea Bonetto, et al.
Cell Cycle (Georgetown, Tex.)|July 22, 2008
Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathiesStefania Assereto, Mauro Mastrototaro, Silvia Stringara, et al.
Frontiers in Bioscience (Elite Edition)|December 29, 2009
S100B protein and near infrared spectroscopy in preterm and term newbornsLucia Gabriella Tina, Alessandro Frigiola, Raul Abella, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|December 16, 2018
Muscle Expression of Type I and Type II Interferons Is Increased in Juvenile Dermatomyositis and Related to Clinical and Histologic FeaturesGian Marco Moneta, Denise Pires Marafon, Emiliano Marasco, et al.
The American Journal of Pathology|October 15, 2015
Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X AxisElisabetta Gazzerro, Simona Baldassari, Stefania Assereto, et al.
Biochemical and Biophysical Research Communications|October 10, 2007
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changesRoberta Biancheri, Antonio Falace, Alessandra Tessa, et al.
JIMD Reports|April 10, 2015
Expanding the Clinical and Magnetic Resonance Spectrum of Leukoencephalopathy with Thalamus and Brainstem Involvement and High Lactate (LTBL) in a Patient Harboring a Novel EARS2 MutationRoberta Biancheri, Eleonora Lamantea, Mariasavina Severino, et al.
Pageof 19

Showing results (91-100 of 190) with videos related to

Sort By:
Pageof 19
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 14, 2016
The ubiquitin ligase tripartite-motif-protein 32 is induced in Duchenne muscular dystrophyStefania Assereto, Rosanna Piccirillo, Serena Baratto, et al.
Biochemical and Biophysical Research Communications|February 15, 2015
Early onset cardiomyopathy associated with the mitochondrial tRNALeu((UUR)) 3271T>C MELAS mutationGiacomo Brisca, Chiara Fiorillo, Claudia Nesti, et al.
Clinical Neuropathology|July 20, 2021
Muscle inflammatory pattern in alpha- and gamma-sarcoglycanopathiesChiara Panicucci, Serena Baratto, Lizzia Raffaghello, et al.
The American Journal of Pathology|March 23, 2010
Therapeutic potential of proteasome inhibition in Duchenne and Becker muscular dystrophiesElisabetta Gazzerro, Stefania Assereto, Andrea Bonetto, et al.
Cell Cycle (Georgetown, Tex.)|July 22, 2008
Aquaporin-4 expression is severely reduced in human sarcoglycanopathies and dysferlinopathiesStefania Assereto, Mauro Mastrototaro, Silvia Stringara, et al.
Frontiers in Bioscience (Elite Edition)|December 29, 2009
S100B protein and near infrared spectroscopy in preterm and term newbornsLucia Gabriella Tina, Alessandro Frigiola, Raul Abella, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|December 16, 2018
Muscle Expression of Type I and Type II Interferons Is Increased in Juvenile Dermatomyositis and Related to Clinical and Histologic FeaturesGian Marco Moneta, Denise Pires Marafon, Emiliano Marasco, et al.
The American Journal of Pathology|October 15, 2015
Enhancement of Muscle T Regulatory Cells and Improvement of Muscular Dystrophic Process in mdx Mice by Blockade of Extracellular ATP/P2X AxisElisabetta Gazzerro, Simona Baldassari, Stefania Assereto, et al.
Biochemical and Biophysical Research Communications|October 10, 2007
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changesRoberta Biancheri, Antonio Falace, Alessandra Tessa, et al.
JIMD Reports|April 10, 2015
Expanding the Clinical and Magnetic Resonance Spectrum of Leukoencephalopathy with Thalamus and Brainstem Involvement and High Lactate (LTBL) in a Patient Harboring a Novel EARS2 MutationRoberta Biancheri, Eleonora Lamantea, Mariasavina Severino, et al.
Pageof 19