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DiMauro

Showing results (461-470 of 942) with videos related to

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Archives of Neurology|May 11, 2005
New DGK gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndromeMichelangelo Mancuso, Silvio Ferraris, Jacklyn Pancrudo, et al.
The Journal of Pediatrics|March 1, 1993
Maternally inherited Leigh syndromeE Ciafaloni, F M Santorelli, S Shanske, et al.
Spine|April 8, 2025
The Impact of Standardized Operating Room Process versus Dedicated Team on Outcomes in Pediatric Spinal Deformity SurgeryVishal Sarwahi, Effat Rahman, Katherine Eigo, et al.
Scientific Reports|August 5, 2017
MiR-23-TrxR1 as a novel molecular axis in skeletal muscle differentiationNeri Mercatelli, Simona Fittipaldi, Elisa De Paola, et al.
Muscle & Nerve|April 9, 2014
Mitochondrial myopathy with dystrophic features due to a novel mutation in the MTTM geneLorenzo Peverelli, Carl A Gold, Ali B Naini, et al.
Antioxidants (Basel, Switzerland)|July 27, 2022
<i>Moringa oleifera</i> Leaf Extract Protects C2C12 Myotubes against H<sub>2</sub>O<sub>2</sub>-Induced Oxidative StressRoberta Ceci, Mariateresa Maldini, Mark E Olson, et al.
Animals : an Open Access Journal From MDPI|September 11, 2019
Prediction of Milk Coagulation Properties and Individual Cheese Yield in Sheep Using Partial Least Squares RegressionMassimo Cellesi, Fabio Correddu, Maria Grazia Manca, et al.
Neuromuscular Disorders : NMD|June 26, 1999
A new mutation in the myophosphorylase gene (Asn684Tyr) in a Spanish patient with McArdle's diseaseA L Andreu, C Bruno, L Tamburino, et al.
Muscle & Nerve|July 27, 1999
A new mutation in the regulatory domain of the myophosphorylase gene affecting protein dimer contactJ Gamez, R Fernandez, C Bruno, et al.
Human Molecular Genetics|December 1, 1994
Aberrant splicing in adult onset glycogen storage disease type II (GSDII): molecular identification of an IVS1 (-13T-->G) mutation in a majority of patients and a novel IVS10 (+1GT-->CT) mutationM L Huie, A S Chen, S Tsujino, et al.
Pageof 95

Showing results (461-470 of 942) with videos related to

Sort By:
Pageof 95
Archives of Neurology|May 11, 2005
New DGK gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndromeMichelangelo Mancuso, Silvio Ferraris, Jacklyn Pancrudo, et al.
The Journal of Pediatrics|March 1, 1993
Maternally inherited Leigh syndromeE Ciafaloni, F M Santorelli, S Shanske, et al.
Spine|April 8, 2025
The Impact of Standardized Operating Room Process versus Dedicated Team on Outcomes in Pediatric Spinal Deformity SurgeryVishal Sarwahi, Effat Rahman, Katherine Eigo, et al.
Scientific Reports|August 5, 2017
MiR-23-TrxR1 as a novel molecular axis in skeletal muscle differentiationNeri Mercatelli, Simona Fittipaldi, Elisa De Paola, et al.
Muscle & Nerve|April 9, 2014
Mitochondrial myopathy with dystrophic features due to a novel mutation in the MTTM geneLorenzo Peverelli, Carl A Gold, Ali B Naini, et al.
Antioxidants (Basel, Switzerland)|July 27, 2022
<i>Moringa oleifera</i> Leaf Extract Protects C2C12 Myotubes against H<sub>2</sub>O<sub>2</sub>-Induced Oxidative StressRoberta Ceci, Mariateresa Maldini, Mark E Olson, et al.
Animals : an Open Access Journal From MDPI|September 11, 2019
Prediction of Milk Coagulation Properties and Individual Cheese Yield in Sheep Using Partial Least Squares RegressionMassimo Cellesi, Fabio Correddu, Maria Grazia Manca, et al.
Neuromuscular Disorders : NMD|June 26, 1999
A new mutation in the myophosphorylase gene (Asn684Tyr) in a Spanish patient with McArdle's diseaseA L Andreu, C Bruno, L Tamburino, et al.
Muscle & Nerve|July 27, 1999
A new mutation in the regulatory domain of the myophosphorylase gene affecting protein dimer contactJ Gamez, R Fernandez, C Bruno, et al.
Human Molecular Genetics|December 1, 1994
Aberrant splicing in adult onset glycogen storage disease type II (GSDII): molecular identification of an IVS1 (-13T-->G) mutation in a majority of patients and a novel IVS10 (+1GT-->CT) mutationM L Huie, A S Chen, S Tsujino, et al.
Pageof 95