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Patrick F Chinnery

Showing results (341-350 of 473) with videos related to

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Science Advances|December 8, 2021
Mitochondrial DNA heteroplasmy is modulated during oocyte development propagating mutation transmissionHaixin Zhang, Marco Esposito, Mikael G Pezet, et al.
Neurology. Genetics|April 29, 2016
Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhoodDavid Lewis-Smith, Kimberli J Kamer, Helen Griffin, et al.
Brain : a Journal of Neurology|December 11, 2007
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenanceGavin Hudson, Patrizia Amati-Bonneau, Emma L Blakely, et al.
The Journal of Clinical Investigation|November 5, 2003
Mitochondrial DNA mutations in human colonic crypt stem cellsRobert W Taylor, Martin J Barron, Gillian M Borthwick, et al.
Plos One|October 3, 2013
Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegiaCynthia Yu-Wai-Man, Fiona E Smith, Michael J Firbank, et al.
European Heart Journal. Cardiovascular Imaging|November 7, 2012
Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriersMatthew G D Bates, Kieren G Hollingsworth, Jane H Newman, et al.
Neurology. Genetics|April 12, 2016
Respiratory chain deficiency in nonmitochondrial diseaseAngela Pyle, Helen J Nightingale, Helen Griffin, et al.
Science (New York, N.Y.)|October 9, 2025
Ubiquitin-mediated mitophagy regulates the inheritance of mitochondrial DNA mutationsMichele Frison, Brandon S Lockey, Yu Nie, et al.
Neurology|April 22, 2021
[<sup>11</sup>C]PK11195-PET Brain Imaging of the Mitochondrial Translocator Protein in Mitochondrial DiseaseJelle van den Ameele, Young T Hong, Roido Manavaki, et al.
Human Mutation|February 27, 2016
MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial DiseaseLishuang Shen, Maria Angela Diroma, Michael Gonzalez, et al.
Pageof 48

Showing results (341-350 of 473) with videos related to

Sort By:
Pageof 48
Science Advances|December 8, 2021
Mitochondrial DNA heteroplasmy is modulated during oocyte development propagating mutation transmissionHaixin Zhang, Marco Esposito, Mikael G Pezet, et al.
Neurology. Genetics|April 29, 2016
Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhoodDavid Lewis-Smith, Kimberli J Kamer, Helen Griffin, et al.
Brain : a Journal of Neurology|December 11, 2007
Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenanceGavin Hudson, Patrizia Amati-Bonneau, Emma L Blakely, et al.
The Journal of Clinical Investigation|November 5, 2003
Mitochondrial DNA mutations in human colonic crypt stem cellsRobert W Taylor, Martin J Barron, Gillian M Borthwick, et al.
Plos One|October 3, 2013
Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegiaCynthia Yu-Wai-Man, Fiona E Smith, Michael J Firbank, et al.
European Heart Journal. Cardiovascular Imaging|November 7, 2012
Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriersMatthew G D Bates, Kieren G Hollingsworth, Jane H Newman, et al.
Neurology. Genetics|April 12, 2016
Respiratory chain deficiency in nonmitochondrial diseaseAngela Pyle, Helen J Nightingale, Helen Griffin, et al.
Science (New York, N.Y.)|October 9, 2025
Ubiquitin-mediated mitophagy regulates the inheritance of mitochondrial DNA mutationsMichele Frison, Brandon S Lockey, Yu Nie, et al.
Neurology|April 22, 2021
[<sup>11</sup>C]PK11195-PET Brain Imaging of the Mitochondrial Translocator Protein in Mitochondrial DiseaseJelle van den Ameele, Young T Hong, Roido Manavaki, et al.
Human Mutation|February 27, 2016
MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial DiseaseLishuang Shen, Maria Angela Diroma, Michael Gonzalez, et al.
Pageof 48