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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.
Life (Basel, Switzerland)
|
January 21, 2022
Spinal Cord Involvement in Adult Mitochondrial Diseases: A Cohort Study
Guido Primiano, Paolo Mariotti, Ida Turrini, et al.
Neurology. Genetics
|
July 11, 2022
Novel <i>TOP3A</i> Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related Diseases
Guido Primiano, Alessandra Torraco, Daniela Verrigni, et al.
The Italian Journal of Biochemistry
|
February 6, 2007
Mutations in structural genes of complex I associated with neurological diseases
Salvatore Scacco, Vittoria Petruzzella, Enrico Bertini, et al.
Annals of Clinical and Translational Neurology
|
February 8, 2024
Biallelic variants in GTPBP3: New patients, phenotypic spectrum, and outcome
Francesca Nardecchia, Rosalba Carrozzo, Alice Innocenti, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
April 18, 2008
Ischemic preconditioning targets the respiration of synaptic mitochondria via protein kinase C epsilon
Kunjan R Dave, R Anthony DeFazio, Ami P Raval, et al.
International Journal of Molecular Sciences
|
April 10, 2014
Frataxin silencing inactivates mitochondrial Complex I in NSC34 motoneuronal cells and alters glutathione homeostasis
Barbara Carletti, Emanuela Piermarini, Giulia Tozzi, et al.
Cerebellum (London, England)
|
November 29, 2022
AFG3L2 Biallelic Mutation: Clinical Heterogeneity in Two Italian Patients
Fabiana Colucci, Marcella Neri, Fernanda Fortunato, et al.
Biochemical and Biophysical Research Communications
|
February 13, 2007
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy
Vittoria Petruzzella, Alessandra Tessa, Alessandra Torraco, et al.
Clinical Genetics
|
March 5, 2022
A novel homozygous variant in COX5A causes an attenuated phenotype with failure to thrive, lactic acidosis, hypoglycemia, and short stature
Alessandra Torraco, Silvia Morlino, Teresa Rizza, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 48) with videos related to
Sort By:
Page
of 5
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.
Life (Basel, Switzerland)
|
January 21, 2022
Spinal Cord Involvement in Adult Mitochondrial Diseases: A Cohort Study
Guido Primiano, Paolo Mariotti, Ida Turrini, et al.
Neurology. Genetics
|
July 11, 2022
Novel <i>TOP3A</i> Variant Associated With Mitochondrial Disease: Expanding the Clinical Spectrum of Topoisomerase III Alpha-Related Diseases
Guido Primiano, Alessandra Torraco, Daniela Verrigni, et al.
The Italian Journal of Biochemistry
|
February 6, 2007
Mutations in structural genes of complex I associated with neurological diseases
Salvatore Scacco, Vittoria Petruzzella, Enrico Bertini, et al.
Annals of Clinical and Translational Neurology
|
February 8, 2024
Biallelic variants in GTPBP3: New patients, phenotypic spectrum, and outcome
Francesca Nardecchia, Rosalba Carrozzo, Alice Innocenti, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
April 18, 2008
Ischemic preconditioning targets the respiration of synaptic mitochondria via protein kinase C epsilon
Kunjan R Dave, R Anthony DeFazio, Ami P Raval, et al.
International Journal of Molecular Sciences
|
April 10, 2014
Frataxin silencing inactivates mitochondrial Complex I in NSC34 motoneuronal cells and alters glutathione homeostasis
Barbara Carletti, Emanuela Piermarini, Giulia Tozzi, et al.
Cerebellum (London, England)
|
November 29, 2022
AFG3L2 Biallelic Mutation: Clinical Heterogeneity in Two Italian Patients
Fabiana Colucci, Marcella Neri, Fernanda Fortunato, et al.
Biochemical and Biophysical Research Communications
|
February 13, 2007
The NDUFB11 gene is not a modifier in Leber hereditary optic neuropathy
Vittoria Petruzzella, Alessandra Tessa, Alessandra Torraco, et al.
Clinical Genetics
|
March 5, 2022
A novel homozygous variant in COX5A causes an attenuated phenotype with failure to thrive, lactic acidosis, hypoglycemia, and short stature
Alessandra Torraco, Silvia Morlino, Teresa Rizza, et al.
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of 5