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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 lines
Ilka Wittig, Rosalba Carrozzo, Filippo M Santorelli, et al.
Biochimica Et Biophysica Acta
|
June 20, 2006
Supercomplexes and subcomplexes of mitochondrial oxidative phosphorylation
Ilka Wittig, Rosalba Carrozzo, Filippo M Santorelli, et al.
Journal of Child Neurology
|
May 17, 2011
Infantile-onset disorders of mitochondrial replication and protein synthesis
Célia Nogueira, Rosalba Carrozzo, Laura Vilarinho, et al.
Genes
|
February 13, 2021
Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic Approaches
Michela 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 patient
Simona 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 dystrophies
Stefania Petrini, Alessandra Tessa, Rosalba Carrozzo, et al.
Annals of Neurology
|
December 21, 2005
Subcomplexes of human ATP synthase mark mitochondrial biosynthesis disorders
Rosalba 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 brothers
Laura 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 elegans
Graziella 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 deficiency
Federica Deodato, Sara Boenzi, Roberta Taurisano, et al.
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of 12
Search research articles
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Showing results (1-10 of 118) with videos related to
Sort By:
Page
of 12
Electrophoresis
|
October 27, 2007
Functional assays in high-resolution clear native gels to quantify mitochondrial complexes in human biopsies and cell lines
Ilka Wittig, Rosalba Carrozzo, Filippo M Santorelli, et al.
Biochimica Et Biophysica Acta
|
June 20, 2006
Supercomplexes and subcomplexes of mitochondrial oxidative phosphorylation
Ilka Wittig, Rosalba Carrozzo, Filippo M Santorelli, et al.
Journal of Child Neurology
|
May 17, 2011
Infantile-onset disorders of mitochondrial replication and protein synthesis
Célia Nogueira, Rosalba Carrozzo, Laura Vilarinho, et al.
Genes
|
February 13, 2021
Mitochondrial Dynamics: Molecular Mechanisms, Related Primary Mitochondrial Disorders and Therapeutic Approaches
Michela 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 patient
Simona 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 dystrophies
Stefania Petrini, Alessandra Tessa, Rosalba Carrozzo, et al.
Annals of Neurology
|
December 21, 2005
Subcomplexes of human ATP synthase mark mitochondrial biosynthesis disorders
Rosalba 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 brothers
Laura 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 elegans
Graziella 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 deficiency
Federica Deodato, Sara Boenzi, Roberta Taurisano, et al.
Page
of 12