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K Reeve

Showing results (71-80 of 93) with videos related to

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Cell Reports|August 11, 2021
3D neuronal mitochondrial morphology in axons, dendrites, and somata of the aging mouse hippocampusJulie Faitg, Clay Lacefield, Tracey Davey, et al.
Human Molecular Genetics|May 21, 2010
OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA moleculesPatrick Yu-Wai-Man, Kamil S Sitarz, David C Samuels, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 15, 2021
Astrocytic Changes in Mitochondrial Oxidative Phosphorylation Protein Levels in Parkinson's DiseaseChun Chen, Emily Mossman, Philippa Malko, et al.
CMAJ Open|July 21, 2021
Community implementation of the 3 Wishes Project: an observational study of a compassionate end-of-life care initiative for critically ill patientsBrenda K Reeve, Brittany B Dennis, William Dechert, et al.
Cell Death & Disease|July 17, 2015
Aggregated α-synuclein and complex I deficiency: exploration of their relationship in differentiated neuronsA K Reeve, M H R Ludtmann, P R Angelova, et al.
The Journal of Experimental Biology|August 2, 2022
Acoustic and postural displays in a miniature and transparent teleost fish, Danionella draculaRose L Tatarsky, Zilin Guo, Sarah C Campbell, et al.
Nucleic Acids Research|May 2, 2016
Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositisKarolina A Rygiel, Helen A Tuppen, John P Grady, 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.
Brain : a Journal of Neurology|December 23, 2011
Sensory neuronopathy in patients harbouring recessive polymerase γ mutationsNichola Z Lax, Roger G Whittaker, Philippa D Hepplewhite, et al.
Neurobiology of Disease|December 21, 2020
Hippocampal network hyperexcitability in young transgenic mice expressing human mutant alpha-synucleinClare Tweedy, Nathan Kindred, Joshua Curry, et al.
Pageof 10

Showing results (71-80 of 93) with videos related to

Sort By:
Pageof 10
Cell Reports|August 11, 2021
3D neuronal mitochondrial morphology in axons, dendrites, and somata of the aging mouse hippocampusJulie Faitg, Clay Lacefield, Tracey Davey, et al.
Human Molecular Genetics|May 21, 2010
OPA1 mutations cause cytochrome c oxidase deficiency due to loss of wild-type mtDNA moleculesPatrick Yu-Wai-Man, Kamil S Sitarz, David C Samuels, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 15, 2021
Astrocytic Changes in Mitochondrial Oxidative Phosphorylation Protein Levels in Parkinson's DiseaseChun Chen, Emily Mossman, Philippa Malko, et al.
CMAJ Open|July 21, 2021
Community implementation of the 3 Wishes Project: an observational study of a compassionate end-of-life care initiative for critically ill patientsBrenda K Reeve, Brittany B Dennis, William Dechert, et al.
Cell Death & Disease|July 17, 2015
Aggregated α-synuclein and complex I deficiency: exploration of their relationship in differentiated neuronsA K Reeve, M H R Ludtmann, P R Angelova, et al.
The Journal of Experimental Biology|August 2, 2022
Acoustic and postural displays in a miniature and transparent teleost fish, Danionella draculaRose L Tatarsky, Zilin Guo, Sarah C Campbell, et al.
Nucleic Acids Research|May 2, 2016
Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositisKarolina A Rygiel, Helen A Tuppen, John P Grady, 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.
Brain : a Journal of Neurology|December 23, 2011
Sensory neuronopathy in patients harbouring recessive polymerase γ mutationsNichola Z Lax, Roger G Whittaker, Philippa D Hepplewhite, et al.
Neurobiology of Disease|December 21, 2020
Hippocampal network hyperexcitability in young transgenic mice expressing human mutant alpha-synucleinClare Tweedy, Nathan Kindred, Joshua Curry, et al.
Pageof 10