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Patrick F Chinnery

Showing results (291-300 of 473) with videos related to

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Nature Medicine|May 14, 2024
Dynamics of cognitive variability with age and its genetic underpinning in NIHR BioResource Genes and Cognition cohort participantsMd Shafiqur Rahman, Emma Harrison, Heather Biggs, et al.
Annals of Neurology|April 1, 2018
Stem cell modeling of mitochondrial parkinsonism reveals key functions of OPA1Mindaugas Jonikas, Martin Madill, Alexandre Mathy, et al.
Acta Neuropathologica|July 27, 2016
Herpes simplex encephalitis is linked with selective mitochondrial damage; a post-mortem and in vitro studyMałgorzata Wnęk, Lorenzo Ressel, Emanuele Ricci, et al.
Nature Genetics|February 29, 2008
What causes mitochondrial DNA deletions in human cells?Kim J Krishnan, Amy K Reeve, David C Samuels, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2014
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutationsHelen R Griffin, Angela Pyle, Emma L Blakely, et al.
JIMD Reports|February 23, 2013
NDUFS8-related Complex I Deficiency Extends Phenotype from "PEO Plus" to Leigh SyndromeAdela Della Marina, Ulrike Schara, Angela Pyle, et al.
The British Journal of Ophthalmology|March 19, 2017
Childhood-onset Leber hereditary optic neuropathyAnna Majander, Richard Bowman, Joanna Poulton, et al.
Neurology. Genetics|December 22, 2017
Opening One's Eyes to Mosaicism in Progressive External OphthalmoplegiaEwen W Sommerville, Rachel L Jones, Steven A Hardy, et al.
Frontiers in Immunology|October 16, 2018
Exposure of Monocytic Cells to Lipopolysaccharide Induces Coordinated Endotoxin Tolerance, Mitochondrial Biogenesis, Mitophagy, and Antioxidant DefensesJohn D Widdrington, Aurora Gomez-Duran, Angela Pyle, et al.
Human Molecular Genetics|October 19, 2012
Universal heteroplasmy of human mitochondrial DNABrendan A I Payne, Ian J Wilson, Patrick Yu-Wai-Man, et al.
Pageof 48

Showing results (291-300 of 473) with videos related to

Sort By:
Pageof 48
Nature Medicine|May 14, 2024
Dynamics of cognitive variability with age and its genetic underpinning in NIHR BioResource Genes and Cognition cohort participantsMd Shafiqur Rahman, Emma Harrison, Heather Biggs, et al.
Annals of Neurology|April 1, 2018
Stem cell modeling of mitochondrial parkinsonism reveals key functions of OPA1Mindaugas Jonikas, Martin Madill, Alexandre Mathy, et al.
Acta Neuropathologica|July 27, 2016
Herpes simplex encephalitis is linked with selective mitochondrial damage; a post-mortem and in vitro studyMałgorzata Wnęk, Lorenzo Ressel, Emanuele Ricci, et al.
Nature Genetics|February 29, 2008
What causes mitochondrial DNA deletions in human cells?Kim J Krishnan, Amy K Reeve, David C Samuels, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 6, 2014
Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutationsHelen R Griffin, Angela Pyle, Emma L Blakely, et al.
JIMD Reports|February 23, 2013
NDUFS8-related Complex I Deficiency Extends Phenotype from "PEO Plus" to Leigh SyndromeAdela Della Marina, Ulrike Schara, Angela Pyle, et al.
The British Journal of Ophthalmology|March 19, 2017
Childhood-onset Leber hereditary optic neuropathyAnna Majander, Richard Bowman, Joanna Poulton, et al.
Neurology. Genetics|December 22, 2017
Opening One's Eyes to Mosaicism in Progressive External OphthalmoplegiaEwen W Sommerville, Rachel L Jones, Steven A Hardy, et al.
Frontiers in Immunology|October 16, 2018
Exposure of Monocytic Cells to Lipopolysaccharide Induces Coordinated Endotoxin Tolerance, Mitochondrial Biogenesis, Mitophagy, and Antioxidant DefensesJohn D Widdrington, Aurora Gomez-Duran, Angela Pyle, et al.
Human Molecular Genetics|October 19, 2012
Universal heteroplasmy of human mitochondrial DNABrendan A I Payne, Ian J Wilson, Patrick Yu-Wai-Man, et al.
Pageof 48