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Rosalba Carrozzo

Showing results (1-10 of 118) with videos related to

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Electrophoresis|October 27, 2007
Functional assays in high-resolution clear native gels to quantify mitochondrial complexes in human biopsies and cell linesIlka Wittig, Rosalba Carrozzo, Filippo M Santorelli, et al.
Biochimica Et Biophysica Acta|June 20, 2006
Supercomplexes and subcomplexes of mitochondrial oxidative phosphorylationIlka Wittig, Rosalba Carrozzo, Filippo M Santorelli, et al.
Journal of Child Neurology|May 17, 2011
Infantile-onset disorders of mitochondrial replication and protein synthesisCélia Nogueira, Rosalba Carrozzo, Laura Vilarinho, et al.
Genes|February 13, 2021
Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic ApproachesMichela Di Nottia, Daniela Verrigni, Alessandra Torraco, et al.
Neurogenetics|November 15, 2005
Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patientSimona Lucioli, Klaus Hoffmeier, Rosalba Carrozzo, et al.
Molecular and Cellular Neurosciences|June 19, 2003
Human melanoma/NG2 chondroitin sulfate proteoglycan is expressed in the sarcolemma of postnatal human skeletal myofibers. Abnormal expression in merosin-negative and Duchenne muscular dystrophiesStefania Petrini, Alessandra Tessa, Rosalba Carrozzo, et al.
Annals of Neurology|December 21, 2005
Subcomplexes of human ATP synthase mark mitochondrial biosynthesis disordersRosalba Carrozzo, Ilka Wittig, Filippo M Santorelli, et al.
Neuropediatrics|May 24, 2012
Mitochondrial neurogastrointestinal encephalomyopathy: novel pathogenic mutations in thymidine phosphorylase gene in two Italian brothersLaura Libernini, Chiara Lupis, Mario Mastrangelo, et al.
Biochimica Et Biophysica Acta. General Subjects|October 20, 2022
Silencing of the mitochondrial ribosomal protein L-24 gene activates the oxidative stress response in Caenorhabditis elegansGraziella Ficociello, Emily Schifano, Michela Di Nottia, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 29, 2018
The impact of biomarkers analysis in the diagnosis of Niemann-Pick C disease and acid sphingomyelinase deficiencyFederica Deodato, Sara Boenzi, Roberta Taurisano, et al.
Pageof 12

Showing results (1-10 of 118) with videos related to

Sort By:
Pageof 12
Electrophoresis|October 27, 2007
Functional assays in high-resolution clear native gels to quantify mitochondrial complexes in human biopsies and cell linesIlka Wittig, Rosalba Carrozzo, Filippo M Santorelli, et al.
Biochimica Et Biophysica Acta|June 20, 2006
Supercomplexes and subcomplexes of mitochondrial oxidative phosphorylationIlka Wittig, Rosalba Carrozzo, Filippo M Santorelli, et al.
Journal of Child Neurology|May 17, 2011
Infantile-onset disorders of mitochondrial replication and protein synthesisCélia Nogueira, Rosalba Carrozzo, Laura Vilarinho, et al.
Genes|February 13, 2021
Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic ApproachesMichela Di Nottia, Daniela Verrigni, Alessandra Torraco, et al.
Neurogenetics|November 15, 2005
Introducing a novel human mtDNA mutation into the Paracoccus denitrificans COX I gene explains functional deficits in a patientSimona Lucioli, Klaus Hoffmeier, Rosalba Carrozzo, et al.
Molecular and Cellular Neurosciences|June 19, 2003
Human melanoma/NG2 chondroitin sulfate proteoglycan is expressed in the sarcolemma of postnatal human skeletal myofibers. Abnormal expression in merosin-negative and Duchenne muscular dystrophiesStefania Petrini, Alessandra Tessa, Rosalba Carrozzo, et al.
Annals of Neurology|December 21, 2005
Subcomplexes of human ATP synthase mark mitochondrial biosynthesis disordersRosalba Carrozzo, Ilka Wittig, Filippo M Santorelli, et al.
Neuropediatrics|May 24, 2012
Mitochondrial neurogastrointestinal encephalomyopathy: novel pathogenic mutations in thymidine phosphorylase gene in two Italian brothersLaura Libernini, Chiara Lupis, Mario Mastrangelo, et al.
Biochimica Et Biophysica Acta. General Subjects|October 20, 2022
Silencing of the mitochondrial ribosomal protein L-24 gene activates the oxidative stress response in Caenorhabditis elegansGraziella Ficociello, Emily Schifano, Michela Di Nottia, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 29, 2018
The impact of biomarkers analysis in the diagnosis of Niemann-Pick C disease and acid sphingomyelinase deficiencyFederica Deodato, Sara Boenzi, Roberta Taurisano, et al.
Pageof 12