Quantification of muscle mitochondrial oxidative phosphorylation enzymes <i>via</i> histochemical staining of blue native polyacrylamide gels

Elisabetta Zerbetto, Lodovica Vergani, Federica Dabbeni‐Sala

Electrophoresis

Biased Incorporation of Ribonucleotides on the Mitochondrial L-Strand Accounts for Apparent Strand-Asymmetric DNA Replication

Mingyao Yang, Mark Bowmaker, Aurelio Reyes, +5

Cell

DnaMitochondrial BiogenesisMitochondrial FunctionNatural SciencesGenetics +5

Disruption of skeletal muscle mitochondrial network genes and miRNAs in amyotrophic lateral sclerosis

Aaron P. Russell, Shogo Wada, Lodovica Vergani, +11

Neurobiology of Disease

Amyotrophic Lateral SclerosisMitochondrial FunctionGeneticsGene ExpressionMedicine +2

Spinal and bulbar muscular atrophy: Skeletal muscle pathology in male patients and heterozygous females

Gianni Sorarú, Carla D’Ascenzo, Alberto Polo, +7

Journal of the Neurological Sciences

Muscle PathologyKinesiologySkeletal MuscleMedicineMale Patients +10

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency

Rikke Katrine Jentoft Olsen, Eliška Koňaříková, Teresa Anna Giancaspero, +45

The American Journal of Human Genetics

Human skeletal muscle atrophy in amyotrophic lateral sclerosis reveals a reduction in Akt and an increase in atrogin‐1

Bertrand Léger, Lodovica Vergani, Gianni Sorarú, +6

The FASEB Journal

Motor DysfunctionMuscle AtrophySkeletal MuscleCell Muscle AtrophyMuscle Atrophy Model +19

The Mitochondrial Fission Protein hFis1 Requires the Endoplasmic Reticulum Gateway to Induce Apoptosis

Emilie Alirol, Dominic I. James, Denise Huber, +4

Molecular Biology of the Cell

MitophagyApoptosisCell DeathMolecular BiologyMitochondrial Biology +17

MtDNA Mutations Associated with Leber′s Hereditary Optic Neuropathy: Studies on Cytoplasmic Hybrid (Cybrid) Cells

Lodovica Vergani, Andrea Martinuzzi, Valério Carelli, +6

Biochemical and Biophysical Research Communications

Neurodegenerative DiseasesMolecular NeuroscienceMtdna Mutations AssociatedOphthalmologyGenetic Disorder +10

Inhibition of mitochondrial fission favours mutant over wild-type mitochondrial DNA

Adriana Malena, Emanuele Loro, Miriam Di Re, +2

Human Molecular Genetics

BiologyGenome InstabilityMitochondrial FunctionMitochondrial DynamicMedicine +12

Overexpression of microRNA-206 in the skeletal muscle from myotonic dystrophy type 1 patients

Stefano Gambardella, Fabrizio Rinaldi, Saverio Massimo Lepore, +6

Journal of Translational Medicine